Author: "Yan G" / Language: undetermined - Searchworks@Jio Institute Digital Library Search Results

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249 results on '"Yan G"'

1. Pattern of global spin alignment of ϕ and K*0 mesons in heavy-ion collisions

Author: STAR Collaboration, Abdallah, M. S., Aboona, B. E., Adam, J., Adamczyk, L., Adams, J. R., Adkins, J. K., Agakishiev, G., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Aitbaev, A., Alekseev, I., Anderson, D. M., Aparin, A., Aschenauer, E. C., Ashraf, M. U., Atetalla, F. G., Averichev, G. S., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Behera, A., Bellwied, R., Bhagat, P., Bhasin, A., Bielcik, J., Bielcikova, J., Bordyuzhin, I. G., Brandenburg, J. D., Brandin, A. V., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Chakaberia, I., Chaloupka, P., Chan, B. K., Chang, F-H., Chang, Z., Chatterjee, A., Chattopadhyay, S., Chen, D., Chen, J., Chen, J. H., Chen, X., Chen, Z., Cheng, J., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Daugherity, M., Dedovich, T. G., Deppner, I. M., Derevschikov, A. A., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fawzi, F. M., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Francisco, A., Fu, C., Gagliardi, C. A., Galatyuk, T., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Guryn, W., Hamed, A., Han, Y., Harabasz, S., Harasty, M. D., Harris, J. W., Harrison, H., He, S., He, W., He, X. H., He, Y., Heppelmann, S., Herrmann, N., Hoffman, E., Holub, L., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jena, C., Jentsch, A., Ji, Y., Jia, J., Jiang, K., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kagamaster, S., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kechechyan, A., Kelsey, M., Kikoła, D. P., Kimelman, B., Kincses, D., Kisel, I., Kiselev, A., Knospe, A. G., Ko, H. S., Kochenda, L., Korobitsin, A., Kosarzewski, L. K., Kramarik, L., Kravtsov, P., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Kwasizur, J. H., Lacey, R., Lan, S., Landgraf, J. M., Lauret, J., Lebedev, A., Lednicky, R., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Liang, X., Liang, Y., Licenik, R., Lin, T., Lin, Y., Lisa, M. A., Liu, F., Liu, H., Liu, P., Liu, T., Liu, X., Liu, Y., Liu, Z., Ljubicic, T., Llope, W. J., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Manukhov, S. L., Margetis, S., Markert, C., Matis, H. S., Mazer, J. A., Minaev, N. G., Mioduszewski, S., Mohanty, B., Mondal, M. M., Mooney, I., Morozov, D. A., Mukherjee, A., Nagy, M., Nam, J. D., Nasim, Md., Nayak, K., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Nigmatkulov, G., Niida, T., Nishitani, R., Nogach, L. V., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okorokov, V. A., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Panebratsev, Y., Parfenov, P., Paul, A., Pawlik, B., Pawlowska, D., Perkins, C., Pluta, J., Pokhrel, B. R., Porter, J., Posik, M., Prozorova, V., Pruthi, N. K., Przybycien, M., Putschke, J., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Reed, R., Ritter, H. G., Robotkova, M., Romero, J. L., Roy, D., Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Samigullin, E., Sandweiss, J., Sato, S., Schmidke, W. B., Schmitz, N., Schweid, B. R., Seck, F., Seger, J., Seto, R., Seyboth, P., Shah, N., Shahaliev, E., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, R., Sheikh, A. I., Shen, D. Y., Shi, S. S., Shi, Y., Shou, Q. Y., Sichtermann, E. P., Sikora, R., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Smirnov, N., Söhngen, Y., Solyst, W., Song, Y., Spinka, H. M., Srivastava, B., Stanislaus, T. D. S., Stefaniak, M., Stewart, D. J., Strikhanov, M., Stringfellow, B., Suaide, A. A. P., Sumbera, M., Sun, X. M., Sun, X., Sun, Y., Surrow, B., Svirida, D. N., Sweger, Z. W., Szymanski, P., Tang, A. H., Tang, Z., Taranenko, A., Tarnowsky, T., Thomas, J. H., Timmins, A. R., Tlusty, D., Todoroki, T., Tokarev, M., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Tripathy, S. K., Truhlar, T., Trzeciak, B. A., Tsai, O. D., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vanek, J., Vasiliev, A. N., Vassiliev, I., Verkest, V., Videbæk, F., Vokal, S., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, P., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wieman, H., Wissink, S. W., Witt, R., Wu, J., Wu, Y., Xi, B., Xiao, Z. G., Xie, G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zbroszczyk, H., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: High Energy Physics - Phenomenology, Multidisciplinary, High Energy Physics::Phenomenology, Nuclear Experiment
Abstract: Notwithstanding decades of progress since Yukawa first developed a description of the force between nucleons in terms of meson exchange, a full understanding of the strong interaction remains a major challenge in modern science. One remaining difficulty arises from the non-perturbative nature of the strong force, which leads to the phenomenon of quark confinement at distances on the order of the size of the proton. Here we show that in relativistic heavy-ion collisions, where quarks and gluons are set free over an extended volume, two species of produced vector (spin-1) mesons, namely $\phi$ and $K^{*0}$, emerge with a surprising pattern of global spin alignment. In particular, the global spin alignment for $\phi$ is unexpectedly large, while that for $K^{*0}$ is consistent with zero. The observed spin-alignment pattern and magnitude for the $\phi$ cannot be explained by conventional mechanisms, while a model with a connection to strong force fields, i.e. an effective proxy description within the Standard Model and Quantum Chromodynamics, accommodates the current data. This connection, if fully established, will open a potential new avenue for studying the behaviour of strong force fields.
Published: 2023

2. Recent Progress in Biomarker Bioanalysis and Target Engagement Assessment

Author: Yan G. Ni, Lindsay E. King, and Carmen Fernández‐Metzler
Published: 2022

3. Tomography of ultrarelativistic nuclei with polarized photon-gluon collisions

Author: STAR Collaboration, Abdallah, M. S., Aboona, B. E., Adam, J., Adamczyk, L., Adams, J. R., Adkins, J. K., Agakishiev, G., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Aitbaev, A., Alekseev, I., Anderson, D. M., Aparin, A., Aschenauer, E. C., Ashraf, M. U., Atetalla, F. G., Averichev, G. S., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Behera, A., Bellwied, R., Bhagat, P., Bhasin, A., Bielcik, J., Bielcikova, J., Bordyuzhin, I. G., Brandenburg, J. D., Brandin, A. V., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Chakaberia, I., Chaloupka, P., Chan, B. K., Chang, F-H., Chang, Z., Chatterjee, A., Chattopadhyay, S., Chen, D., Chen, J., Chen, J. H., Chen, X., Chen, Z., Cheng, J., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Daugherity, M., Dedovich, T. G., Deppner, I. M., Derevschikov, A. A., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fawzi, F. M., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Francisco, A., Fu, C., Gagliardi, C. A., Galatyuk, T., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Guryn, W., Hamed, A., Han, Y., Harabasz, S., Harasty, M. D., Harris, J. W., Harrison, H., He, S., He, W., He, X. H., He, Y., Heppelmann, S., Herrmann, N., Hoffman, E., Holub, L., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jena, C., Jentsch, A., Ji, Y., Jia, J., Jiang, K., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kagamaster, S., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kechechyan, A., Kelsey, M., Kikoła, D. P., Kimelman, B., Kincses, D., Kisel, I., Kiselev, A., Klein, S. R., Knospe, A. G., Ko, H. S., Kochenda, L., Korobitsin, A., Kosarzewski, L. K., Kramarik, L., Kravtsov, P., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Kwasizur, J. H., Lacey, R., Lan, S., Landgraf, J. M., Lauret, J., Lebedev, A., Lednicky, R., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Liang, X., Liang, Y., Licenik, R., Lin, T., Lin, Y., Lisa, M. A., Liu, F., Liu, H., Liu, P., Liu, T., Liu, X., Liu, Y., Liu, Z., Ljubicic, T., Llope, W. J., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Manukhov, S. L., Margetis, S., Markert, C., Matis, H. S., Mazer, J. A., Minaev, N. G., Mioduszewski, S., Mohanty, B., Mondal, M. M., Mooney, I., Morozov, D. A., Mukherjee, A., Nagy, M., Nam, J. D., Nasim, Md., Nayak, K., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Nigmatkulov, G., Niida, T., Nishitani, R., Nogach, L. V., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okorokov, V. A., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Panebratsev, Y., Parfenov, P., Paul, A., Pawlik, B., Pawlowska, D., Perkins, C., Pluta, J., Pokhrel, B. R., Porter, J., Posik, M., Prozorova, V., Pruthi, N. K., Przybycien, M., Putschke, J., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Reed, R., Ritter, H. G., Robotkova, M., Romero, J. L., Roy, D., Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Samigullin, E., Sandweiss, J., Sato, S., Schmidke, W. B., Schmitz, N., Schweid, B. R., Seck, F., Seger, J., Seto, R., Seyboth, P., Shah, N., Shahaliev, E., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, R., Sheikh, A. I., Shen, D. Y., Shi, S. S., Shi, Y., Shou, Q. Y., Sichtermann, E. P., Sikora, R., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Smirnov, N., Söhngen, Y., Solyst, W., Song, Y., Spinka, H. M., Srivastava, B., Stanislaus, T. D. S., Stefaniak, M., Stewart, D. J., Strikhanov, M., Stringfellow, B., Suaide, A. A. P., Sumbera, M., Sun, X. M., Sun, X., Sun, Y., Surrow, B., Svirida, D. N., Sweger, Z. W., Szymanski, P., Tang, A. H., Tang, Z., Taranenko, A., Tarnowsky, T., Thomas, J. H., Timmins, A. R., Tlusty, D., Todoroki, T., Tokarev, M., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Tripathy, S. K., Truhlar, T., Trzeciak, B. A., Tsai, O. D., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vanek, J., Vasiliev, A. N., Vassiliev, I., Verkest, V., Videbæk, F., Vokal, S., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, P., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wieman, H., Wissink, S. W., Witt, R., Wu, J., Wu, Y., Xi, B., Xiao, Z. G., Xie, G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zbroszczyk, H., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: Nuclear Theory (nucl-th), Quantum Physics, Multidisciplinary, Nuclear Theory, FOS: Physical sciences, Nuclear Experiment (nucl-ex), Nuclear Experiment, Quantum Physics (quant-ph)
Abstract: A linearly polarized photon can be quantized from the Lorentz-boosted electromagnetic field of a nucleus traveling at ultrarelativistic speed. When two relativistic heavy nuclei pass one another at a distance of a few nuclear radii, the photon from one nucleus may interact through a virtual quark-antiquark pair with gluons from the other nucleus, forming a short-lived vector meson (e.g., ρ 0 ). In this experiment, the polarization was used in diffractive photoproduction to observe a unique spin interference pattern in the angular distribution of ρ 0 → π + π − decays. The observed interference is a result of an overlap of two wave functions at a distance an order of magnitude larger than the ρ 0 travel distance within its lifetime. The strong-interaction nuclear radii were extracted from these diffractive interactions and found to be 6.53 ± 0.06 fm ( 197 Au) and 7.29 ± 0.08 fm ( 238 U), larger than the nuclear charge radii. The observable is demonstrated to be sensitive to the nuclear geometry and quantum interference of nonidentical particles.
Published: 2023

4. The Association between Factor XI Deficiency and the Risk of Bleeding, Cardiovascular, and Venous Thromboembolic Events

Author: Alan R. Shuldiner, Chalothorn Dan, Sarah Sharman Moser, Morton Lori C, Ming-Dauh Wang, Gabriel Chodick, Yan G. Ni, Ophira Salomon, and Jessica J. Jalbert
Subjects: Adult, Male, Venous Thrombosis, medicine.medical_specialty, Factor XI Deficiency, business.industry, MEDLINE, Hemorrhage, Retrospective cohort study, Venous Thromboembolism, Hematology, medicine.disease, Internal medicine, Humans, Medicine, Female, business, Factor XI, Stroke, Retrospective Studies
Abstract: The objective of this study was to assess the relationship between factor XI (FXI) deficiency and the risks of bleeding and cardiovascular (CV) events. We conducted a retrospective cohort study using data from Maccabi Healthcare Services (MHS). We identified adults with FXI deficiency (severe
Published: 2021

5. Fusion Peptide of SARS-CoV-2 Spike Rearranges into a Wedge Inserted in Bilayered Micelles

Author: Rama K. Koppisetti, Steven R. Van Doren, and Yan G. Fulcher
Subjects: Protein Conformation, alpha-Helical, Biochemistry, Micelle, Article, Catalysis, Colloid and Surface Chemistry, Protein structure, Humans, Spin label, Micelles, Phospholipids, Fusion, SARS-CoV-2, Chemistry, Bilayer, COVID-19, Lipid bilayer fusion, General Chemistry, Protein Subunits, Membrane, Spike Glycoprotein, Coronavirus, Helix, Biophysics, Peptides, Hydrophobic and Hydrophilic Interactions, Protein Binding
Abstract: The receptor binding and proteolysis of Spike of SARS-CoV-2 release its S2 subunit to rearrange and catalyze viral-cell fusion. This deploys the fusion peptide for insertion into the cell membranes targeted. We show that this fusion peptide transforms from intrinsic disorder in solution into a wedge-shaped structure inserted in bilayered micelles, according to chemical shifts, 15N NMR relaxation, and NOEs. The globular fold of three helices contrasts the open, extended forms of this region observed in the electron density of compact prefusion states. In the hydrophobic, narrow end of the wedge, helices 1 and 2 contact the fatty acyl chains of phospholipids, according to NOEs and proximity to a nitroxide spin label deep in the membrane mimic. The polar end of the wedge may engage and displace lipid head groups and bind Ca2+ ions for membrane fusion. Polar helix 3 protrudes from the bilayer where it might be accessible to antibodies.
Published: 2021

6. Machinery, regulation and pathophysiological implications of autophagosome maturation

Author: Patrice Codogno, Hong Zhang, and Yan G Zhao
Subjects: Autophagosome, Endosome, Autophagosome maturation, Cellular homeostasis, Endosomes, Review Article, Membrane trafficking, Vacuole, Biology, Phagosomes, Macroautophagy, Autophagy, Humans, Transport Vesicles, Molecular Biology, SARS-CoV-2, Autophagosomes, Neurodegenerative Diseases, Cell Biology, Cell biology, rab GTP-Binding Proteins, Rab, Lysosomes, SNARE Proteins, Protein Processing, Post-Translational, Biogenesis
Abstract: Autophagy is a versatile degradation system for maintaining cellular homeostasis whereby cytosolic materials are sequestered in a double-membrane autophagosome and subsequently delivered to lysosomes, where they are broken down. In multicellular organisms, newly formed autophagosomes undergo a process called ‘maturation’, in which they fuse with vesicles originating from endolysosomal compartments, including early/late endosomes and lysosomes, to form amphisomes, which eventually become degradative autolysosomes. This fusion process requires the concerted actions of multiple regulators of membrane dynamics, including SNAREs, tethering proteins and RAB GTPases, and also transport of autophagosomes and late endosomes/lysosomes towards each other. Multiple mechanisms modulate autophagosome maturation, including post-translational modification of key components, spatial distribution of phosphoinositide lipid species on membranes, RAB protein dynamics, and biogenesis and function of lysosomes. Nutrient status and various stresses integrate into the autophagosome maturation machinery to coordinate the progression of autophagic flux. Impaired autophagosome maturation is linked to the pathogenesis of various human diseases, including neurodegenerative disorders, cancer and myopathies. Furthermore, invading pathogens exploit various strategies to block autophagosome maturation, thus evading destruction and even subverting autophagic vacuoles (autophagosomes, amphisomes and autolysosomes) for survival, growth and/or release. Here, we discuss the recent progress in our understanding of the machinery and regulation of autophagosome maturation, the relevance of these mechanisms to human pathophysiology and how they are harnessed by pathogens for their benefit. We also provide perspectives on targeting autophagosome maturation therapeutically., Following their biogenesis, autophagosomes undergo maturation into degradative autolysosomes by fusing with late endosomes/lysosomes. This process — involving an array of molecular regulators of membrane dynamics — is essential for autophagic degradation, and its deregulation can lead to disease, including neurodegeneration, muscle diseases and cancer, and propagation of pathogens.
Published: 2021

7. The Apertif Radio Transient System (ARTS): Design, commissioning, data release, and detection of the first five fast radio bursts

Author: Joeri van Leeuwen, Eric Kooistra, Leon Oostrum, Liam Connor, Jonathan E. Hargreaves, Yogesh Maan, Inés Pastor-Marazuela, Emily Petroff, Daniel van der Schuur, Alessio Sclocco, Samayra M. Straal, Dany Vohl, Stefan J. Wijnholds, Elizabeth A. K. Adams, Björn Adebahr, Jisk Attema, Cees Bassa, Jeanette E. Bast, Anna Bilous, Willem J. G. de Blok, Oliver M. Boersma, Wim A. van Cappellen, Arthur H. W. M. Coolen, Sieds Damstra, Helga Dénes, Ger N. J. van Diepen, David W. Gardenier, Yan G. Grange, André W. Gunst, Kelley M. Hess, Hanno Holties, Thijs van der Hulst, Boudewijn Hut, Alexander Kutkin, G. Marcel Loose, Danielle M. Lucero, Ágnes Mika, Klim Mikhailov, Raffaella Morganti, Vanessa A. Moss, Henk Mulder, Menno J. Norden, Tom A. Oosterloo, Emaneula Orrú, Zsolt Paragi, Jan-Pieter R. de Reijer, Arno P. Schoenmakers, Klaas J. C. Stuurwold, Sander ter Veen, Yu-Yang Wang, Alwin W. Zanting, and Jacob Ziemke
Subjects: Space and Planetary Science, Astronomy and Astrophysics
Abstract: Fast radio bursts (FRBs) must be powered by uniquely energetic emission mechanisms. This requirement has eliminated a number of possible source types, but several remain. Identifying the physical nature of FRB emitters arguably requires good localisation of more detections, as well as broad-band studies enabled by real-time alerting. In this paper, we present the Apertif Radio Transient System (ARTS), a supercomputing radio-telescope instrument that performs real-time FRB detection and localisation on the Westerbork Synthesis Radio Telescope (WSRT) interferometer. It reaches coherent-addition sensitivity over the entire field of the view of the primary-dish beam. After commissioning results verified that the system performed as planned, we initiated the Apertif FRB survey (ALERT). Over the first 5 weeks we observed at design sensitivity in 2019, we detected five new FRBs, and interferometrically localised each of them to 0.4–10 sq. arcmin. All detections are broad band, very narrow, of the order of 1 ms in duration, and unscattered. Dispersion measures are generally high. Only through the very high time and frequency resolution of ARTS are these hard-to-find FRBs detected, producing an unbiased view of the intrinsic population properties. Most localisation regions are small enough to rule out the presence of associated persistent radio sources. Three FRBs cut through the halos of M31 and M33. We demonstrate that Apertif can localise one-off FRBs with an accuracy that maps magneto-ionic material along well-defined lines of sight. The rate of one every ~7 days ensures a considerable number of new sources are detected for such a study. The combination of the detection rate and localisation accuracy exemplified by the first five ARTS FRBs thus marks a new phase in which a growing number of bursts can be used to probe our Universe.
Published: 2023

8. VMP1 and TMEM41B are essential for DMV formation during β-coronavirus infection

Author: Mingming Ji, Meng Li, Long Sun, Hongyu Zhao, Ying Li, Lulu Zhou, Zhenni Yang, Xin Zhao, Wenyan Qu, Hanbing Xue, Ze Zheng, Yiming Li, Hongyu Deng, and Yan G. Zhao
Subjects: Organelles, SARS-CoV-2, Autophagy, COVID-19, Humans, Membrane Proteins, Phosphatidylserines, Cell Biology, Viral Nonstructural Proteins, Viral Replication Compartments, Virus Replication
Abstract: β-coronaviruses reshape host cell endomembranes to form double-membrane vesicles (DMVs) for genome replication and transcription. Ectopically expressed viral nonstructural proteins nsp3 and nsp4 interact to zipper and bend the ER for DMV biogenesis. Genome-wide screens revealed the autophagy proteins VMP1 and TMEM41B as important host factors for SARS-CoV-2 infection. Here, we demonstrated that DMV biogenesis, induced by virus infection or expression of nsp3/4, is impaired in the VMP1 KO or TMEM41B KO cells. In VMP1 KO cells, the nsp3/4 complex forms normally, but the zippered ER fails to close into DMVs. In TMEM41B KO cells, the nsp3–nsp4 interaction is reduced and DMV formation is suppressed. Thus, VMP1 and TMEM41B function at different steps during DMV formation. VMP1 was shown to regulate cross-membrane phosphatidylserine (PS) distribution. Inhibiting PS synthesis partially rescues the DMV defects in VMP1 KO cells, suggesting that PS participates in DMV formation. We provide molecular insights into the collaboration of host factors with viral proteins to remodel host organelles.
Published: 2022

9. The BADC and BCCP subunits of chloroplast acetyl-CoA carboxylase sense the pH changes of the light–dark cycle

Author: Yan G. Fulcher, Jay J. Thelen, Mizani T. Day, David J. Sliman, Steven R. Van Doren, Rama K. Koppisetti, Yajin Ye, Philip D. Bates, and Mark Schroeder
Subjects: 0301 basic medicine, Biotin carboxylase, Mutant, Arabidopsis, Plant Biology, Biotin carboxyl carrier protein, Biochemistry, Chloroplast Proteins, 03 medical and health sciences, chemistry.chemical_compound, Biotin, Photosynthesis, Molecular Biology, 030102 biochemistry & molecular biology, biology, Arabidopsis Proteins, Acetyl-CoA carboxylase, Cell Biology, Hydrogen-Ion Concentration, Plastid stroma, Pyruvate carboxylase, Chloroplast, 030104 developmental biology, chemistry, biology.protein, Acetyl-CoA Carboxylase
Abstract: Acetyl-CoA carboxylase (ACCase) catalyzes the first committed step in the de novo synthesis of fatty acids. The multisubunit ACCase in the chloroplast is activated by a shift to pH 8 upon light adaptation and is inhibited by a shift to pH 7 upon dark adaptation. Here, titrations with the purified ACCase biotin attachment domain-containing (BADC) and biotin carboxyl carrier protein (BCCP) subunits from Arabidopsis indicated that they can competently and independently bind biotin carboxylase (BC) but differ in responses to pH changes representing those in the plastid stroma during light or dark conditions. At pH 7 in phosphate buffer, BADC1 and BADC2 gain an advantage over BCCP1 and BCCP2 in affinity for BC. At pH 8 in KCl solution, however, BCCP1 and BCCP2 had more than 10-fold higher affinity for BC than did BADC1. The pH-modulated shifts in BC preferences for BCCP and BADC partners suggest they contribute to light-dependent regulation of heteromeric ACCase. Using NMR spectroscopy, we found evidence for increased intrinsic disorder of the BADC and BCCP subunits at pH 7. We propose that this intrinsic disorder potentially promotes fast association with BC through a “fly-casting mechanism.” We hypothesize that the pH effects on the BADC and BCCP subunits attenuate ACCase activity by night and enhance it by day. Consistent with this hypothesis, Arabidopsis badc1 badc3 mutant lines grown in a light–dark cycle synthesized more fatty acids in their seeds. In summary, our findings provide evidence that the BADC and BCCP subunits function as pH sensors required for light-dependent switching of heteromeric ACCase activity.
Published: 2020

10. ANALISIS KEBIJAKAN LUAR NEGERI JOHN HOWARD TERHADAP IMIGRAN ILEGAL DI AUSTRALIA

Author: Dhea T. Lumentut, Johni R.V. Korwa, and Yan G. Pelamonia
Subjects: lcsh:International relations, australia, illegal immigrants, john howard, lcsh:JZ2-6530, policy
Abstract: This paper aims to analyze Australian Prime Minister John Howard’s foreign policy in responding to illegal immigrants who attempt to enter Australian territory by sea. This study employed library research as well as a qualitative approach. In particular, this study used the theory of foreign policy offered by Walter Calsnaes called ‘a logically tripartite approach’ to analyze Howard’s policy in responding to illegal immigrants. This paper found that Howard’s foreign policy in responding to illegal immigrants was not only state-centric in nature focusing on protecting Australian sovereignty, but the policy also had a purpose to maintain power control. Firstly, Howard was willing to show the world that his leadership was different compared to his predecessors, asserting that Australia should not be regarded as a country of easy destination. Secondly, Howard showed that limiting the number of illegal immigrants was in the best interest of the country to protect Australians. Thirdly, Howard proved that his foreign policy towards illegal immigrants could influence the politics of Australia including federal elections. Lastly, Howard demonstrated his ability in the context of institutional settings by issuing new laws to strengthen his foreign policy. Keywords: Australia, John Howard, Illegal Immigrants, Policy Abstrak Tulisan ini bertujuan untuk menganalisis kebijakan luar negeri Perdana Menteri John Howard dalam merespon para imigran ilegal yang datang ke Australia secara khusus melalui jalur laut. Studi ini menggunakan metode studi pustaka dan pendekatan kualitatif. Secara khusus, penulis menggunakan teori kebijakan luar negeri yang ditawarkan oleh Walter Carlsnaes yang disebut „a logically tripartite approach‟ untuk menganalisis kebijakan Howard dalam merespon imigran ilegal. Studi ini menemukan bahwa kebijakan luar negeri Howard dalam merespon imigran ilegal tidak hanya bersifat state-centric yang berfokus pada perlindungan kedaulatan negara, tetapi kebijakan itu juga memiliki motivasi untuk mempertahankan kekuasaan. Pertama, Howard ingin menunjukkan pada dunia bahwa ia adalah pemimpin yang berbeda dari pendahulunya dengan menegaskan bahwa Australia seharusnya tidak dipertimbangkan sebagai negara yang dapat dicapai dengan mudah. Kedua, Howard ingin menunjukkan bahwa pembatasan jumlah imigran ilegal adalah capaian kepentingan nasional untuk melindungi komunitas Australia. Ketiga, Howard menunjukkan bahwa kebijakannya terkait imigran ilegal dapat memengaruhi nuansa perpolitikan di Australia khususnya pada pemilihan umum federal. Keempat, Howard menunjukkan kemampuannya dalam konteks pengelolaan kelembagaan dengan mengeluarkan Undang-Undang baru hasil amandemen untuk memperkuat kebijakan luar negerinya. Kata kunci: Australia, John Howard, Imigran Ilegal, Kebijakan
Published: 2020

11. $K^{*0}$ production in Au+Au collisions at $\sqrt{s_{\rm NN}}$ = 7.7, 11.5, 14.5, 19.6, 27 and 39 GeV from RHIC beam energy scan

Author: STAR Collaboration, Abdallah, M. S., Aboona, B. E., Adam, J., Adamczyk, L., Adams, J. R., Adkins, J. K., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Anderson, D. M., Aschenauer, E. C., Atchison, J., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Bellwied, R., Bhagat, P., Bhasin, A., Bhatta, S., Bielcik, J., Bielcikova, J., Brandenburg, J. D., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Chakaberia, I., Chaloupka, P., Chan, B. K., Chang, Z., Chatterjee, A., Chen, D., Chen, J., Chen, J. H., Chen, X., Chen, Z., Cheng, J., Cheng, Y., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Dale-Gau, G., Daugherity, M., Deppner, I. M., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fawzi, F. M., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Fu, C., Gagliardi, C. A., Galatyuk, T., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Guryn, W., Hamed, A., Han, Y., Harabasz, S., Harasty, M. D., Harris, J. W., Harrison, H., He, S., He, W., He, X. H., He, Y., Heppelmann, S., Herrmann, N., Hoffman, E., Holub, L., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jena, C., Jentsch, A., Ji, Y., Jia, J., Jiang, K., Jin, C., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kagamaster, S., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kelsey, M., Khyzhniak, Y. V., Kikoła, D. P., Kimelman, B., Kincses, D., Kisel, I., Kiselev, A., Knospe, A. G., Ko, H. S., Kosarzewski, L. K., Kramarik, L., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Kwasizur, J. H., Lacey, R., Lan, S., Landgraf, J. M., Lauret, J., Lebedev, A., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Li, Z., Liang, X., Liang, Y., Licenik, R., Lin, T., Lin, Y., Lisa, M. A., Liu, F., Liu, H., Liu, T., Liu, X., Liu, Y., Ljubicic, T., Llope, W. J., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Margetis, S., Markert, C., Matis, H. S., Mazer, J. A., McNamara, G., Mioduszewski, S., Mohanty, B., Mondal, M. M., Mooney, I., Mukherjee, A., Nagy, M. I., Nain, A. S., Nam, J. D., Nasim, Md., Nayak, K., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Niida, T., Nishitani, R., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Pani, T., Paul, A., Pawlik, B., Pawlowska, D., Perkins, C., Pluta, J., Pokhrel, B. R., Porter, J., Posik, M., Protzman, T., Prozorova, V., Pruthi, N. K., Przybycien, M., Putschke, J., Qin, Z., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Reed, R., Ritter, H. G., Robotkova, M., Romero, J. L., Roy, D., Chowdhury, P. Roy, Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Sato, S., Schmidke, W. B., Schmitz, N., Seck, F-J., Seger, J., Seto, R., Seyboth, P., Shah, N., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, R., Sheikh, A. I., Shen, D. Y., Shen, K., Shi, S. S., Shi, Y., Shou, Q. Y., Sichtermann, E. P., Sikora, R., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Smirnov, N., Söhngen, Y., Solyst, W., Song, Y., Srivastava, B., Stanislaus, T. D. S., Stefaniak, M., Stewart, D. J., Stringfellow, B., Suaide, A. A. P., Sumbera, M., Sun, C., Sun, X. M., Sun, X., Sun, Y., Surrow, B., Sweger, Z. W., Szymanski, P., Tang, A. H., Tang, Z., Tarnowsky, T., Thomas, J. H., Timmins, A. R., Tlusty, D., Todoroki, T., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Tripathy, S. K., Truhlar, T., Trzeciak, B. A., Tsai, O. D., Tsang, C. Y., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vanek, J., Vassiliev, I., Verkest, V., Videbæk, F., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, P., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wielanek, D., Wieman, H., Wilks, G., Wissink, S. W., Witt, R., Wu, J., Wu, X., Wu, Y., Xi, B., Xiao, Z. G., Xie, G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yan, Z., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zbroszczyk, H., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, J., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: FOS: Physical sciences, Nuclear Experiment (nucl-ex), Nuclear Experiment
Abstract: We report the measurement of $K^{*0}$ meson at midrapidity ($|y, 17 pages, 12 figures
Published: 2022
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12. Pattern of Global Spin Alignment of $ϕ$ and $K^{*0}$ mesons in Heavy-Ion Collisions

Author: STAR Collaboration, Abdallah, M. S., Aboona, B. E., Adam, J., Adamczyk, L., Adams, J. R., Adkins, J. K., Agakishiev, G., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Aitbaev, A., Alekseev, I., Anderson, D. M., Aparin, A., Aschenauer, E. C., Ashraf, M. U., Atetalla, F. G., Averichev, G. S., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Behera, A., Bellwied, R., Bhagat, P., Bhasin, A., Bielcik, J., Bielcikova, J., Bordyuzhin, I. G., Brandenburg, J. D., Brandin, A. V., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Chakaberia, I., Chaloupka, P., Chan, B. K., Chang, F-H., Chang, Z., Chatterjee, A., Chattopadhyay, S., Chen, D., Chen, J., Chen, J. H., Chen, X., Chen, Z., Cheng, J., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Daugherity, M., Dedovich, T. G., Deppner, I. M., Derevschikov, A. A., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fawzi, F. M., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Francisco, A., Fu, C., Gagliardi, C. A., Galatyuk, T., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Guryn, W., Hamed, A., Han, Y., Harabasz, S., Harasty, M. D., Harris, J. W., Harrison, H., He, S., He, W., He, X. H., He, Y., Heppelmann, S., Herrmann, N., Hoffman, E., Holub, L., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jena, C., Jentsch, A., Ji, Y., Jia, J., Jiang, K., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kagamaster, S., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kechechyan, A., Kelsey, M., Kikoła, D. P., Kimelman, B., Kincses, D., Kisel, I., Kiselev, A., Knospe, A. G., Ko, H. S., Kochenda, L., Korobitsin, A., Kosarzewski, L. K., Kramarik, L., Kravtsov, P., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Kwasizur, J. H., Lacey, R., Lan, S., Landgraf, J. M., Lauret, J., Lebedev, A., Lednicky, R., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Liang, X., Liang, Y., Licenik, R., Lin, T., Lin, Y., Lisa, M. A., Liu, F., Liu, H., Liu, P., Liu, T., Liu, X., Liu, Y., Liu, Z., Ljubicic, T., Llope, W. J., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Manukhov, S. L., Margetis, S., Markert, C., Matis, H. S., Mazer, J. A., Minaev, N. G., Mioduszewski, S., Mohanty, B., Mondal, M. M., Mooney, I., Morozov, D. A., Mukherjee, A., Nagy, M., Nam, J. D., Nasim, Md., Nayak, K., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Nigmatkulov, G., Niida, T., Nishitani, R., Nogach, L. V., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okorokov, V. A., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Panebratsev, Y., Parfenov, P., Paul, A., Pawlik, B., Pawlowska, D., Perkins, C., Pluta, J., Pokhrel, B. R., Porter, J., Posik, M., Prozorova, V., Pruthi, N. K., Przybycien, M., Putschke, J., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Reed, R., Ritter, H. G., Robotkova, M., Romero, J. L., Roy, D., Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Samigullin, E., Sandweiss, J., Sato, S., Schmidke, W. B., Schmitz, N., Schweid, B. R., Seck, F., Seger, J., Seto, R., Seyboth, P., Shah, N., Shahaliev, E., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, R., Sheikh, A. I., Shen, D. Y., Shi, S. S., Shi, Y., Shou, Q. Y., Sichtermann, E. P., Sikora, R., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Smirnov, N., Söhngen, Y., Solyst, W., Song, Y., Spinka, H. M., Srivastava, B., Stanislaus, T. D. S., Stefaniak, M., Stewart, D. J., Strikhanov, M., Stringfellow, B., Suaide, A. A. P., Sumbera, M., Sun, X. M., Sun, X., Sun, Y., Surrow, B., Svirida, D. N., Sweger, Z. W., Szymanski, P., Tang, A. H., Tang, Z., Taranenko, A., Tarnowsky, T., Thomas, J. H., Timmins, A. R., Tlusty, D., Todoroki, T., Tokarev, M., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Tripathy, S. K., Truhlar, T., Trzeciak, B. A., Tsai, O. D., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vanek, J., Vasiliev, A. N., Vassiliev, I., Verkest, V., Videbæk, F., Vokal, S., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, P., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wieman, H., Wissink, S. W., Witt, R., Wu, J., Wu, Y., Xi, B., Xiao, Z. G., Xie, G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zbroszczyk, H., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: High Energy Physics - Phenomenology (hep-ph), High Energy Physics::Phenomenology, FOS: Physical sciences, Nuclear Experiment (nucl-ex)
Abstract: Notwithstanding decades of progress since Yukawa first developed a description of the force between nucleons in terms of meson exchange, a full understanding of the strong interaction remains a major challenge in modern science. One remaining difficulty arises from the non-perturbative nature of the strong force, which leads to the phenomenon of quark confinement at distances on the order of the size of the proton. Here we show that in relativistic heavy-ion collisions, where quarks and gluons are set free over an extended volume, two species of produced vector (spin-1) mesons, namely $ϕ$ and $K^{*0}$, emerge with a surprising pattern of global spin alignment. In particular, the global spin alignment for $ϕ$ is unexpectedly large, while that for $K^{*0}$ is consistent with zero. The observed spin-alignment pattern and magnitude for the $ϕ$ cannot be explained by conventional mechanisms, while a model with a connection to strong force fields, i.e. an effective proxy description within the Standard Model and Quantum Chromodynamics, accommodates the current data. This connection, if fully established, will open a potential new avenue for studying the behaviour of strong force fields.
Published: 2022
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13. Measurement of sequential $Υ$ suppression in Au+Au collisions at $\sqrt{s_{_\mathrm{NN}}}$ = 200 GeV with the STAR experiment

Author: STAR Collaboration, Aboona, B. E., Adam, J., Adamczyk, L., Adams, J. R., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Anderson, D. M., Aschenauer, E. C., Atchison, J., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Bellwied, R., Bhagat, P., Bhasin, A., Bhatta, S., Bielcik, J., Bielcikova, J., Brandenburg, J. D., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Ceska, J., Chakaberia, I., Chaloupka, P., Chan, B. K., Chang, Z., Chen, D., Chen, J., Chen, J. H., Chen, Z., Cheng, J., Cheng, Y., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Dale-Gau, G., Das, A., Daugherity, M., Deppner, I. M., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Flor, F. A., Fu, C., Gagliardi, C. A., Galatyuk, T., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Guryn, W., Hamed, A., Han, Y., Harabasz, S., Harasty, M. D., Harris, J. W., Harrison, H., He, W., He, X. H., He, Y., Heppelmann, S., Herrmann, N., Holub, L., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jalotra, A., Jena, C., Jentsch, A., Ji, Y., Jia, J., Jin, C., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kagamaster, S., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kelsey, M., Khyzhniak, Y. V., Kikoła, D. P., Kimelman, B., Kincses, D., Kisel, I., Kiselev, A., Knospe, A. G., Ko, H. S., Kosarzewski, L. K., Kramarik, L., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Lacey, R., Landgraf, J. M., Lauret, J., Lebedev, A., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Li, Z., Liang, X., Liang, Y., Licenik, R., Lin, T., Lisa, M. A., Liu, C., Liu, F., Liu, H., Liu, L., Liu, T., Liu, X., Liu, Y., Liu, Z., Ljubicic, T., Llope, W. J., Lomicky, O., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Margetis, S., Markert, C., Matis, H. S., Mazer, J. A., McNamara, G., Mi, K., Mioduszewski, S., Mohanty, B., Mooney, I., Mukherjee, A., Nagy, M. I., Nain, A. S., Nam, J. D., Nasim, Md., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Niida, T., Nishitani, R., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Pani, T., Paul, A., Pawlik, B., Pawlowska, D., Perkins, C., Pluta, J., Pokhrel, B. R., Posik, M., Protzman, T., Prozorova, V., Pruthi, N. K., Przybycien, M., Putschke, J., Qin, Z., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Reed, R., Ritter, H. G., Robertson, C. W., Robotkova, M., Romero, J. L., Aguilar, M. A. Rosales, Roy, D., Chowdhury, P. Roy, Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Sato, S., Schmidke, W. B., Schmitz, N., Seck, F-J., Seger, J., Seto, R., Seyboth, P., Shah, N., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, M., Sharma, N., Sharma, R., Sharma, S. R., Sheikh, A. I., Shen, D. Y., Shen, K., Shi, S. S., Shi, Y., Shou, Q. Y., Si, F., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Smirnov, N., Söhngen, Y., Song, Y., Srivastava, B., Stanislaus, T. D. S., Stefaniak, M., Stewart, D. J., Stringfellow, B., Su, Y., Suaide, A. A. P., Sumbera, M., Sun, C., Sun, X., Sun, Y., Surrow, B., Sweger, Z. W., Szymanski, P., Tamis, A., Tang, A. H., Tang, Z., Tarnowsky, T., Thomas, J. H., Timmins, A. R., Tlusty, D., Todoroki, T., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Truhlar, T., Trzeciak, B. A., Tsai, O. D., Tsang, C. Y., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vanek, J., Vassiliev, I., Verkest, V., Videbæk, F., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wielanek, D., Wieman, H., Wilks, G., Wissink, S. W., Witt, R., Wu, J., Wu, X., Wu, Y., Xi, B., Xiao, Z. G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yan, Z., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zbroszczyk, H., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, X., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, J., Zhou, S., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: Nuclear Theory (nucl-th), FOS: Physical sciences, High Energy Physics::Experiment, Nuclear Experiment (nucl-ex), Nuclear Experiment
Abstract: We report on measurements of sequential $Υ$ suppression in Au+Au collisions at $\sqrt{s_{_\mathrm{NN}}}$ = 200 GeV with the STAR detector at the Relativistic Heavy Ion Collider (RHIC) through both the dielectron and dimuon decay channels. In the 0-60% centrality class, the nuclear modification factors ($R_{\mathrm{AA}}$), which quantify the level of yield suppression in heavy-ion collisions compared to $p$+$p$ collisions, for $Υ$(1S) and $Υ$(2S) are $0.40 \pm 0.03~\textrm{(stat.)} \pm 0.03~\textrm{(sys.)} \pm 0.09~\textrm{(norm.)}$ and $0.26 \pm 0.08~\textrm{(stat.)} \pm 0.02~\textrm{(sys.)} \pm 0.06~\textrm{(norm.)}$, respectively, while the upper limit of the $Υ$(3S) $R_{\mathrm{AA}}$ is 0.17 at a 95% confidence level. This provides experimental evidence that the $Υ$(3S) is significantly more suppressed than the $Υ$(1S) at RHIC. The level of suppression for $Υ$(1S) is comparable to that observed at the much higher collision energy at the Large Hadron Collider. These results point to the creation of a medium at RHIC whose temperature is sufficiently high to strongly suppress excited $Υ$ states., 5 pages, 4 figures
Published: 2022
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14. Azimuthal anisotropy measurement of (multi-)strange hadrons in Au+Au collisions at $\sqrt{s_{\text{NN}}}$ = 54.4 GeV

Author: STAR Collaboration, Abdallah, M. S., Aboona, B. E., Adam, J., Adamczyk, L., Adams, J. R., Adkins, J. K., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Anderson, D. M., Aschenauer, E. C., Atchison, J., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Bellwied, R., Bhagat, P., Bhasin, A., Bhatta, S., Bielcik, J., Bielcikova, J., Brandenburg, J. D., Cai, X. Z., Caines, H., Calderón~de~la~Barca~Sánchez, M., Cebra, D., Chakaberia, I., Chaloupka, P., Chan, B. K., Chang, Z., Chatterjee, A., Chattopadhyay, S., Chen, D., Chen, J., Chen, J. H., Chen, X., Chen, Z., Cheng, J., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Daugherity, M., Deppner, I. M., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fawzi, F. M., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Francisco, A., Fu, C., Gagliardi, C. A., Galatyuk, T., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Guryn, W., Hamed, A., Han, Y., Harabasz, S., Harasty, M. D., Harris, J. W., Harrison, H., He, S., He, W., He, X. H., He, Y., Heppelmann, S., Herrmann, N., Hoffman, E., Holub, L., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jena, C., Jentsch, A., Ji, Y., Jia, J., Jiang, K., Jin, C., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kagamaster, S., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kelsey, M., Khyzhniak, Y. V., Kikoła, D. P., Kimelman, B., Kincses, D., Kisel, I., Kiselev, A., Knospe, A. G., Ko, H. S., Kosarzewski, L. K., Kramarik, L., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Kwasizur, J. H., Lacey, R., Lan, S., Landgraf, J. M., Lauret, J., Lebedev, A., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Li, Z., Liang, X., Liang, Y., Licenik, R., Lin, T., Lin, Y., Lisa, M. A., Liu, F., Liu, H., Liu, T., Liu, X., Liu, Y., Ljubicic, T., Llope, W. J., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Margetis, S., Markert, C., Matis, H. S., Mazer, J. A., McNamara, G., Mioduszewski, S., Mohanty, B., Mondal, M. M., Mooney, I., Mukherjee, A., Nagy, M. I., Nain, A. S., Nam, J. D., Nasim, Md., Nayak, K., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Niida, T., Nishitani, R., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Paul, A., Pawlik, B., Pawlowska, D., Perkins, C., Pluta, J., Pokhrel, B. R., Porter, J., Posik, M., Prozorova, V., Pruthi, N. K., Przybycien, M., Putschke, J., Qin, Z., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Reed, R., Ritter, H. G., Robotkova, M., Romero, J. L., Roy, D., Chowdhury, P. Roy, Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Sato, S., Schmidke, W. B., Schmitz, N., Seck, F-J., Seger, J., Sergeeva, M., Seto, R., Seyboth, P., Shah, N., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, R., Sheikh, A. I., Shen, D. Y., Shen, K., Shi, S. S., Shi, Y., Shou, Q. Y., Sichtermann, E. P., Sikora, R., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Smirnov, N., Söhngen, Y., Solyst, W., Song, Y., Srivastava, B., Stanislaus, T. D. S., Stefaniak, M., Stewart, D. J., Stringfellow, B., Suaide, A. A. P., Sumbera, M., Sun, C., Sun, X. M., Sun, X., Sun, Y., Surrow, B., Sweger, Z. W., Szymanski, P., Tang, A. H., Tang, Z., Tarnowsky, T., Thomas, J. H., Timmins, A. R., Tlusty, D., Todoroki, T., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Tripathy, S. K., Truhlar, T., Trzeciak, B. A., Tsai, O. D., Tsang, C. Y., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vanek, J., Vassiliev, I., Verkest, V., Videbæk, F., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, P., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wielanek, D., Wieman, H., Wissink, S. W., Witt, R., Wu, J., Wu, Y., Xi, B., Xiao, Z. G., Xie, G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yan, Z., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zbroszczyk, H., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, J., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: High Energy Physics - Experiment (hep-ex), FOS: Physical sciences, Nuclear Experiment (nucl-ex), Nuclear Experiment, High Energy Physics - Experiment
Abstract: Azimuthal anisotropy of produced particles is one of the most important observables used to access the collective properties of the expanding medium created in relativistic heavy-ion collisions. In this paper, we present second ($v_{2}$) and third ($v_{3}$) order azimuthal anisotropies of $K_{S}^{0}$, $\phi$, $\Lambda$, $\Xi$ and $\Omega$ at mid-rapidity ($|y, Comment: 12 pages, 14 figures
Published: 2022
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15. Azimuthal transverse single-spin asymmetries of inclusive jets and identified hadrons within jets from polarized $pp$ collisions at $\sqrt{s}$ = 200 GeV

Author: STAR Collaboration, Abdallah, M. S., Aboona, B. E., Adam, J., Adamczyk, L., Adams, J. R., Adkins, J. K., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Anderson, D. M., Aschenauer, E. C., Ashraf, M. U., Atchison, J., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Behera, A., Bellwied, R., Bhagat, P., Bhasin, A., Bielcik, J., Bielcikova, J., Brandenburg, J. D., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Chakaberia, I., Chaloupka, P., Chan, B. K., Chang, Z., Chatterjee, A., Chattopadhyay, S., Chen, D., Chen, J., Chen, J. H., Chen, X., Chen, Z., Cheng, J., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Daugherity, M., Deppner, I. M., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fawzi, F. M., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Francisco, A., Fu, C., Gagliardi, C. A., Galatyuk, T., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Guryn, W., Hamed, A., Han, Y., Harabasz, S., Harasty, M. D., Harris, J. W., Harrison, H., He, S., He, W., He, X. H., He, Y., Heppelmann, S., Herrmann, N., Hoffman, E., Holub, L., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jena, C., Jentsch, A., Ji, Y., Jia, J., Jiang, K., Jin, C., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kagamaster, S., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kelsey, M., Khyzhniak, Y. V., Kikoła, D. P., Kimelman, B., Kincses, D., Kisel, I., Kiselev, A., Knospe, A. G., Ko, H. S., Kosarzewski, L. K., Kramarik, L., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Kwasizur, J. H., Lacey, R., Lan, S., Landgraf, J. M., Lauret, J., Lebedev, A., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Li, Z., Liang, X., Liang, Y., Licenik, R., Lin, T., Lin, Y., Lisa, M. A., Liu, F., Liu, H., Liu, P., Liu, T., Liu, X., Liu, Y., Ljubicic, T., Llope, W. J., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Margetis, S., Markert, C., Matis, H. S., Mazer, J. A., Mioduszewski, S., Mohanty, B., Mondal, M. M., Mooney, I., Mukherjee, A., Nagy, M., Nain, A. S., Nam, J. D., Nasim, Md., Nayak, K., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Niida, T., Nishitani, R., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Paul, A., Pawlik, B., Pawlowska, D., Perkins, C., Pinsky, L. S., Pluta, J., Pokhrel, B. R., Porter, J., Posik, M., Prozorova, V., Pruthi, N. K., Przybycien, M., Putschke, J., Qin, Z., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Reed, R., Ritter, H. G., Robotkova, M., Romero, J. L., Roy, D., Chowdhury, P. Roy, Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Sato, S., Schmidke, W. B., Schmitz, N., Schweid, B. R., Seck, F-J., Seger, J., Sergeeva, M., Seto, R., Seyboth, P., Shah, N., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, R., Sheikh, A. I., Shen, D. Y., Shen, K., Shi, S. S., Shi, Y., Shou, Q. Y., Sichtermann, E. P., Sikora, R., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Smirnov, N., Söhngen, Y., Solyst, W., Song, Y., Srivastava, B., Stanislaus, T. D. S., Stefaniak, M., Stewart, D. J., Stringfellow, B., Suaide, A. A. P., Sumbera, M., Sun, X. M., Sun, X., Sun, Y., Surrow, B., Sweger, Z. W., Szymanski, P., Tang, A. H., Tang, Z., Tarnowsky, T., Thomas, J. H., Timmins, A. R., Tlusty, D., Todoroki, T., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Tripathy, S. K., Truhlar, T., Trzeciak, B. A., Tsai, O. D., Tsang, C. Y., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vanek, J., Vassiliev, I., Verkest, V., Videbæk, F., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, P., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wielanek, D., Wieman, H., Wissink, S. W., Witt, R., Wu, J., Wu, Y., Xi, B., Xiao, Z. G., Xie, G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zbroszczyk, H., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, J., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: High Energy Physics - Experiment (hep-ex), Astrophysics::High Energy Astrophysical Phenomena, Nuclear Theory, FOS: Physical sciences, High Energy Physics::Experiment, Nuclear Experiment, High Energy Physics - Experiment
Abstract: The STAR Collaboration reports measurements of the transverse single-spin asymmetries, $A_N$, for inclusive jets and identified `hadrons within jets' production at midrapidity from transversely polarized $pp$ collisions at $\sqrt{s}$ = 200 GeV, based on data recorded in 2012 and 2015. The inclusive jet asymmetry measurements include $A_N$ for inclusive jets and $A_N$ for jets containing a charged pion carrying a momentum fraction $z>0.3$ of the jet momentum. The identified hadron within jet asymmetry measurements include the Collins effect for charged pions, kaons and protons, and the Collins-like effect for charged pions. The measured asymmetries are determined for several distinct kinematic regions, characterized by the jet transverse momentum $p_{T}$ and pseudorapidity $\eta$, as well as the hadron momentum fraction $z$ and momentum transverse to the jet axis $j_{T}$. These results probe higher momentum scales ($Q^{2}$ up to $\sim$\,900 GeV$^{2}$) than current, semi-inclusive deep inelastic scattering measurements, and they provide new constraints on quark transversity in the proton and enable tests of evolution, universality and factorization breaking in the transverse-momentum-dependent formalism., Comment: 24 pages, 24 figures, Accepted by PRD
Published: 2022
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16. Beam energy dependence of the linear and mode-coupled flow harmonics in Au+Au collisions

Author: STAR Collaboration, Aboona, B. E., Adam, J., Adams, J. R., Agakishiev, G., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Aitbaev, A., Alekseev, I., Anderson, D. M., Aparin, A., Atchison, J., Averichev, G. S., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Bhagat, P., Bhasin, A., Bhatta, S., Bordyuzhin, I. G., Brandenburg, J. D., Brandin, A. V., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Ceska, J., Chakaberia, I., Chan, B. K., Chang, Z., Chen, D., Chen, J., Chen, J. H., Chen, Z., Cheng, J., Cheng, Y., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Dale-Gau, G., Das, A., Daugherity, M., Dedovich, T. G., Deppner, I. M., Derevschikov, A. A., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Flor, F. A., Fu, C., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Hamed, A., Han, Y., Harasty, M. D., Harris, J. W., Harrison, H., He, W., He, X. H., He, Y., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jalotra, A., Jena, C., Ji, Y., Jia, J., Jin, C., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kechechyan, A., Kelsey, M., Kimelman, B., Kincses, D., Kiselev, A., Knospe, A. G., Ko, H. S., Kochenda, L., Korobitsin, A. A., Kravtsov, P., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Lacey, R., Landgraf, J. M., Lebedev, A., Lednicky, R., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Li, Z., Liang, X., Liang, Y., Lin, T., Liu, C., Liu, F., Liu, H., Liu, L., Liu, T., Liu, X., Liu, Y., Liu, Z., Ljubicic, T., Llope, W. J., Lomicky, O., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Luong, V. B., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Margetis, S., Matis, H. S., Mazer, J. A., McNamara, G., Mi, K., Minaev, N. G., Mohanty, B., Mooney, I., Morozov, D. A., Mudrokh, A., Mukherjee, A., Nagy, M. I., Nain, A. S., Nam, J. D., Nasim, Md., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Nigmatkulov, G., Niida, T., Nishitani, R., Nogach, L. V., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okorokov, V. A., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Panebratsev, Y., Pani, T., Parfenov, P., Paul, A., Perkins, C., Pokhrel, B. R., Posik, M., Protzman, T., Pruthi, N. K., Putschke, J., Qin, Z., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Ritter, H. G., Robertson, C. W., Rogachevsky, O. V., Aguilar, M. A. Rosales, Roy, D., Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Samigullin, E., Sato, S., Schmidke, W. B., Schmitz, N., Seger, J., Seto, R., Seyboth, P., Shah, N., Shahaliev, E., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, M., Sharma, N., Sharma, R., Sharma, S. R., Sheikh, A. I., Shen, D. Y., Shen, K., Shi, S. S., Shi, Y., Shou, Q. Y., Si, F., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Söhngen, Y., Song, Y., Srivastava, B., Stanislaus, T. D. S., Stewart, D. J., Strikhanov, M., Stringfellow, B., Su, Y., Sun, C., Sun, X., Sun, Y., Surrow, B., Svirida, D. N., Sweger, Z. W., Tamis, A., Tang, A. H., Tang, Z., Taranenko, A., Tarnowsky, T., Thomas, J. H., Tlusty, D., Todoroki, T., Tokarev, M. V., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Tsai, O. D., Tsang, C. Y., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vasiliev, A. N., Verkest, V., Videbæk, F., Vokal, S., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wieman, H., Wilks, G., Wissink, S. W., Wu, J., Wu, X., Wu, Y., Xi, B., Xiao, Z. G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yan, Z., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, X., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, J., Zhou, S., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: Nuclear and High Energy Physics, FOS: Physical sciences, Nuclear Experiment (nucl-ex), Nuclear Experiment
Abstract: The linear and mode-coupled contributions to higher-order anisotropic flow are presented for Au+Au collisions at $\sqrt{s_{\mathrm{NN}}}$ = 27, 39, 54.4, and 200 GeV and compared to similar measurements for Pb+Pb collisions at the Large Hadron Collider (LHC). The coefficients and the flow harmonics' correlations, which characterize the linear and mode-coupled response to the lower-order anisotropies, indicate a beam energy dependence consistent with an influence from the specific shear viscosity ($\eta/s$). In contrast, the dimensionless coefficients, mode-coupled response coefficients, and normalized symmetric cumulants are approximately beam-energy independent, consistent with a significant role from initial-state effects. These measurements could provide unique supplemental constraints to (i) distinguish between different initial-state models and (ii) delineate the temperature ($T$) and baryon chemical potential ($\mu_{B}$) dependence of the specific shear viscosity $\frac{\eta}{s} (T, \mu_B)$., Comment: 11 pages, 4 figures
Published: 2022
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17. Observation of Directed Flow of Hypernuclei $^3_Λ$H and $^4_Λ$H in $\sqrt{s_{\rm NN}}$ = 3 GeV Au+Au Collisions at RHIC

Author: STAR Collaboration, Aboona, B. E., Adam, J., Adams, J. R., Agakishiev, G., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Aitbaev, A., Alekseev, I., Anderson, D. M., Aparin, A., Atchison, J., Averichev, G. S., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Bhagat, P., Bhasin, A., Bhatta, S., Bordyuzhin, I. G., Brandenburg, J. D., Brandin, A. V., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Ceska, J., Chakaberia, I., Chan, B. K., Chang, Z., Chen, D., Chen, J., Chen, J. H., Chen, Z., Cheng, J., Cheng, Y., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Dale-Gau, G., Das, A., Daugherity, M., Dedovich, T. G., Deppner, I. M., Derevschikov, A. A., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Flor, F. A., Fu, C., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Hamed, A., Han, Y., Harasty, M. D., Harris, J. W., Harrison, H., He, W., He, X. H., He, Y., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jalotra, A., Jena, C., Ji, Y., Jia, J., Jin, C., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kechechyan, A., Kelsey, M., Kimelman, B., Kiselev, A., Knospe, A. G., Ko, H. S., Kochenda, L., Korobitsin, A. A., Kravtsov, P., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Lacey, R., Landgraf, J. M., Lebedev, A., Lednicky, R., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Li, Z., Liang, X., Liang, Y., Lin, T., Liu, C., Liu, F., Liu, H., Liu, L., Liu, T., Liu, X., Liu, Y., Liu, Z., Ljubicic, T., Llope, W. J., Lomicky, O., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Luong, V. B., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Margetis, S., Matis, H. S., Mazer, J. A., McNamara, G., Mi, K., Minaev, N. G., Mohanty, B., Mooney, I., Morozov, D. A., Mudrokh, A., Nagy, M. I., Nain, A. S., Nam, J. D., Nasim, Md., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Nigmatkulov, G., Niida, T., Nishitani, R., Nogach, L. V., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okorokov, V. A., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Panebratsev, Y., Pani, T., Parfenov, P., Paul, A., Perkins, C., Pokhrel, B. R., Posik, M., Protzman, T., Pruthi, N. K., Putschke, J., Qin, Z., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Ritter, H. G., Robertson, C. W., Rogachevsky, O. V., Aguilar, M. A. Rosales, Roy, D., Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Samigullin, E., Sato, S., Schmidke, W. B., Schmitz, N., Seger, J., Seto, R., Seyboth, P., Shah, N., Shahaliev, E., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, M., Sharma, N., Sharma, R., Sharma, S. R., Sheikh, A. I., Shen, D. Y., Shen, K., Shi, S. S., Shi, Y., Shou, Q. Y., Si, F., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Söhngen, Y., Song, Y., Srivastava, B., Stanislaus, T. D. S., Stewart, D. J., Strikhanov, M., Stringfellow, B., Su, Y., Sun, C., Sun, X., Sun, Y., Surrow, B., Svirida, D. N., Sweger, Z. W., Tamis, A., Tang, A. H., Tang, Z., Taranenko, A., Tarnowsky, T., Thomas, J. H., Tlusty, D., Todoroki, T., Tokarev, M. V., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Tsai, O. D., Tsang, C. Y., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vasiliev, A. N., Verkest, V., Videbæk, F., Vokal, S., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wieman, H., Wilks, G., Wissink, S. W., Wu, J., Wu, X., Wu, Y., Xi, B., Xiao, Z. G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yan, Z., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, X., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, J., Zhou, S., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: FOS: Physical sciences, Nuclear Experiment (nucl-ex)
Abstract: We report here the first observation of directed flow ($v_1$) of the hypernuclei $^3_Λ$H and $^4_Λ$H in mid-central Au+Au collisions at $\sqrt{s_{\rm NN}}$ = 3 GeV at RHIC. These data are taken as part of the beam energy scan program carried out by the STAR experiment. From 165 $\times$ 10$^{6}$ events in 5%-40% centrality, about 8400 $^3_Λ$H and 5200 $^4_Λ$H candidates are reconstructed through two- and three-body decay channels. We observe that these hypernuclei exhibit significant directed flow. Comparing to that of light nuclei, it is found that the midrapidity $v_1$ slopes of $^3_Λ$H and $^4_Λ$H follow baryon number scaling, implying that the coalescence is the dominant mechanism for these hypernuclei production in such collisions., 5pages, 4 figures. Supplemental material: 6 pages, 5 figures
Published: 2022
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18. Beam Energy Dependence of Fifth and Sixth-Order Net-proton Number Fluctuations in Au+Au Collisions at RHIC

Author: STAR Collaboration, Aboona, B. E., Adam, J., Adamczyk, L., Adams, J. R., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Anderson, D. M., Aschenauer, E. C., Atchison, J., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Bellwied, R., Bhagat, P., Bhasin, A., Bhatta, S., Bielcik, J., Bielcikova, J., Brandenburg, J. D., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Ceska, J., Chakaberia, I., Chaloupka, P., Chan, B. K., Chang, Z., Chen, D., Chen, J., Chen, J. H., Chen, Z., Cheng, J., Cheng, Y., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Dale-Gau, G., Das, A., Daugherity, M., Deppner, I. M., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Flor, F. A., Fu, C., Gagliardi, C. A., Galatyuk, T., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Guryn, W., Hamed, A., Han, Y., Harabasz, S., Harasty, M. D., Harris, J. W., Harrison, H., He, W., He, X. H., He, Y., Heppelmann, S., Herrmann, N., Holub, L., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jalotra, A., Jena, C., Jentsch, A., Ji, Y., Jia, J., Jin, C., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kagamaster, S., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kelsey, M., Khyzhniak, Y. V., Kikoła, D. P., Kimelman, B., Kincses, D., Kisel, I., Kiselev, A., Knospe, A. G., Ko, H. S., Kosarzewski, L. K., Kramarik, L., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Lacey, R., Landgraf, J. M., Lauret, J., Lebedev, A., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Li, Z., Liang, X., Liang, Y., Licenik, R., Lin, T., Lisa, M. A., Liu, C., Liu, F., Liu, H., Liu, L., Liu, T., Liu, X., Liu, Y., Liu, Z., Ljubicic, T., Llope, W. J., Lomicky, O., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Margetis, S., Markert, C., Matis, H. S., Mazer, J. A., McNamara, G., Mi, K., Mioduszewski, S., Mohanty, B., Mooney, I., Mukherjee, A., Nagy, M. I., Nain, A. S., Nam, J. D., Nasim, Md., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Niida, T., Nishitani, R., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Pani, T., Paul, A., Pawlik, B., Pawlowska, D., Perkins, C., Pluta, J., Pokhrel, B. R., Posik, M., Protzman, T., Prozorova, V., Pruthi, N. K., Przybycien, M., Putschke, J., Qin, Z., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Reed, R., Ritter, H. G., Robertson, C. W., Robotkova, M., Romero, J. L., Aguilar, M. A. Rosales, Roy, D., Chowdhury, P. Roy, Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Sato, S., Schmidke, W. B., Schmitz, N., Seck, F-J., Seger, J., Seto, R., Seyboth, P., Shah, N., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, M., Sharma, N., Sharma, R., Sharma, S. R., Sheikh, A. I., Shen, D. Y., Shen, K., Shi, S. S., Shi, Y., Shou, Q. Y., Si, F., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Smirnov, N., Söhngen, Y., Song, Y., Srivastava, B., Stanislaus, T. D. S., Stefaniak, M., Stewart, D. J., Stringfellow, B., Su, Y., Suaide, A. A. P., Sumbera, M., Sun, C., Sun, X., Sun, Y., Surrow, B., Sweger, Z. W., Szymanski, P., Tamis, A., Tang, A. H., Tang, Z., Tarnowsky, T., Thomas, J. H., Timmins, A. R., Tlusty, D., Todoroki, T., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Truhlar, T., Trzeciak, B. A., Tsai, O. D., Tsang, C. Y., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vanek, J., Vassiliev, I., Verkest, V., Videbæk, F., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wielanek, D., Wieman, H., Wilks, G., Wissink, S. W., Witt, R., Wu, J., Wu, X., Wu, Y., Xi, B., Xiao, Z. G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yan, Z., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zbroszczyk, H., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, X., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, J., Zhou, S., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: FOS: Physical sciences, Nuclear Experiment (nucl-ex), nucl-ex, Nuclear Experiment
Abstract: We report the beam energy and collision centrality dependence of fifth and sixth order cumulants ($C_{5}$, $C_{6}$) and factorial cumulants ($\kappa_{5}$, $\kappa_{6}$) of net-proton and proton distributions, from $\sqrt{s_{NN}} = 3 - 200$ GeV Au+Au collisions at RHIC. The net-proton cumulant ratios generally follow the hierarchy expected from QCD thermodynamics, except for the case of collisions at $\sqrt{s_{NN}}$ = 3 GeV. $C_{6}/C_{2}$ for 0-40\% centrality collisions is increasingly negative with decreasing $\sqrt{s_{NN}}$, while it is positive for the lowest $\sqrt{s_{NN}}$ studied. These observed negative signs are consistent with QCD calculations (at baryon chemical potential, $\mu_{B} \leq$ 110 MeV) that include a crossover quark-hadron transition. In addition, for $\sqrt{s_{NN}} \geq$ 11.5 GeV, the measured proton $\kappa_{n}$, within uncertainties, does not support the two-component shape of proton distributions that would be expected from a first-order phase transition. Taken in combination, the hyper-order proton number fluctuations suggest that the structure of QCD matter at high baryon density, $\mu_{B}\sim 750$ MeV ($\sqrt{s_{NN}}$ = 3 GeV) is starkly different from those at vanishing $\mu_{B}\sim 20$MeV ($\sqrt{s_{NN}}$ = 200 GeV and higher)., Comment: 10 pages, 8 figures
Published: 2022
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19. Measurement of $\rm ^4_ΛH$ and $\rm ^4_ΛHe$ binding energy in Au+Au collisions at $\sqrt{s_\mathrm{NN}}$ = 3 GeV

Author: STAR Collaboration, Abdallah, M. S., Aboona, B. E., Adam, J., Adamczyk, L., Adams, J. R., Adkins, J. K., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Anderson, D. M., Aschenauer, E. C., Ashraf, M. U., Atchison, J., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Behera, A., Bellwied, R., Bhagat, P., Bhasin, A., Bielcik, J., Bielcikova, J., Brandenburg, J. D., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Chakaberia, I., Chaloupka, P., Chan, B. K., Chang, Z., Chatterjee, A., Chattopadhyay, S., Chen, D., Chen, J., Chen, J. H., Chen, X., Chen, Z., Cheng, J., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Daugherity, M., Deppner, I. M., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fawzi, F. M., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Francisco, A., Fu, C., Gagliardi, C. A., Galatyuk, T., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Guryn, W., Hamed, A., Han, Y., Harabasz, S., Harasty, M. D., Harris, J. W., Harrison, H., He, S., He, W., He, X. H., He, Y., Heppelmann, S., Herrmann, N., Hoffman, E., Holub, L., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jena, C., Jentsch, A., Ji, Y., Jia, J., Jiang, K., Jin, C., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kagamaster, S., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kelsey, M., Khyzhniak, Y. V., Kikoła, D. P., Kimelman, B., Kincses, D., Kisel, I., Kiselev, A., Knospe, A. G., Ko, H. S., Kosarzewski, L. K., Kramarik, L., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Kwasizur, J. H., Lacey, R., Lan, S., Landgraf, J. M., Lauret, J., Lebedev, A., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Li, Z., Liang, X., Liang, Y., Licenik, R., Lin, T., Lin, Y., Lisa, M. A., Liu, F., Liu, H., Liu, P., Liu, T., Liu, X., Liu, Y., Ljubicic, T., Llope, W. J., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Margetis, S., Markert, C., Matis, H. S., Mazer, J. A., Mioduszewski, S., Mohanty, B., Mondal, M. M., Mooney, I., Mukherjee, A., Nagy, M., Nain, A. S., Nam, J. D., Nasim, Md., Nayak, K., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Niida, T., Nishitani, R., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Paul, A., Pawlik, B., Pawlowska, D., Perkins, C., Pinsky, L. S., Pluta, J., Pokhrel, B. R., Porter, J., Posik, M., Prozorova, V., Pruthi, N. K., Przybycien, M., Putschke, J., Qin, Z., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Reed, R., Ritter, H. G., Robotkova, M., Romero, J. L., Roy, D., Chowdhury, P. Roy, Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Sato, S., Schmidke, W. B., Schmitz, N., Schweid, B. R., Seck, F-J., Seger, J., Sergeeva, M., Seto, R., Seyboth, P., Shah, N., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, R., Sheikh, A. I., Shen, D. Y., Shen, K., Shi, S. S., Shi, Y., Shou, Q. Y., Sichtermann, E. P., Sikora, R., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Smirnov, N., Söhngen, Y., Solyst, W., Song, Y., Srivastava, B., Stanislaus, T. D. S., Stefaniak, M., Stewart, D. J., Stringfellow, B., Suaide, A. A. P., Sumbera, M., Sun, X. M., Sun, X., Sun, Y., Surrow, B., Sweger, Z. W., Szymanski, P., Tang, A. H., Tang, Z., Tarnowsky, T., Thomas, J. H., Timmins, A. R., Tlusty, D., Todoroki, T., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Tripathy, S. K., Truhlar, T., Trzeciak, B. A., Tsai, O. D., Tsang, C. Y., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vanek, J., Vassiliev, I., Verkest, V., Videbæk, F., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, P., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wielanek, D., Wieman, H., Wissink, S. W., Witt, R., Wu, J., Wu, Y., Xi, B., Xiao, Z. G., Xie, G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zbroszczyk, H., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, J., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: FOS: Physical sciences, High Energy Physics::Experiment, Nuclear Experiment (nucl-ex), Nuclear Experiment, Astrophysics::Galaxy Astrophysics
Abstract: Measurements of mass and $Λ$ binding energy of $\rm ^4_ΛH$ and $\rm ^4_ΛHe$ in Au+Au collisions at $\sqrt{s_{_{\rm NN}}}=3$ GeV are presented, with an aim to address the charge symmetry breaking (CSB) problem in hypernuclei systems with atomic number A = 4. The $Λ$ binding energies are measured to be $\rm 2.22\pm0.06(stat.) \pm0.14(syst.)$ MeV and $\rm 2.38\pm0.13(stat.) \pm0.12(syst.)$ MeV for $\rm ^4_ΛH$ and $\rm ^4_ΛHe$, respectively. The measured $Λ$ binding-energy difference is $\rm 0.16\pm0.14(stat.)\pm0.10(syst.)$ MeV for ground states. Combined with the $γ$-ray transition energies, the binding-energy difference for excited states is $\rm -0.16\pm0.14(stat.)\pm0.10(syst.)$ MeV, which is negative and comparable to the value of the ground states within uncertainties. These new measurements on the $Λ$ binding-energy difference in A = 4 hypernuclei systems are consistent with the theoretical calculations that result in $\rm ΔB_Λ^4(1_{exc}^{+})\approx -ΔB_Λ^4(0_{g.s.}^{+}), 8 pages, 5 figures
Published: 2022
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20. Early transgene expression of GALC enzyme in a phase I/II safety, tolerability and efficacy study of PBKR03 in infants with early infantile Krabbe disease (EIKD) (GALax-C)

Author: Samiah A. Al-Zaidy, Nicole I. Wolf, Simon Jones, Eric J. Mallack, Amy Waldman, Jennifer P. Rubin, Joshua L. Bonkowsky, Adi Aran, Yan G. Ni, Pruthvi Nagilla, Dan Donahue, Roberto Giugliani, Mark S. Forman, and Geneviève Bernard
Subjects: Endocrinology, Endocrinology, Diabetes and Metabolism, Genetics, Molecular Biology, Biochemistry
Published: 2023

21. Updated interim safety, biomarker, and efficacy data from Imagine-1: A phase 1/2 open-label, multicenter study to assess the safety, tolerability, and efficacy of a single dose, intra-cisterna magna (ICM) administration of PBGM01 in subjects with type I (early onset) and type IIA (late onset) infantile GM1 gangliosidosis (GM1)

Author: Jeanine R. Jarnes, Caroline A. Hastings, Can H. Ficicioglu, Debra-Lynn Day-Salvatore, Roberto Giugliani, Julien Baruteau, Chester B. Whitley, Michal Inbar-Feigenberg, Geneviève Bernard, Fatih S. Ezgü, Yan G. Ni, Michelle Miller, Michael H. Gelb, Pruthvi Nagilla, Rose Johnstone, Patricia Elsasser, Elizabeth Cunningham, Victoria Ballard, Thomas F. Haws, Mark S. Forman, and David A. Weinstein
Subjects: Endocrinology, Endocrinology, Diabetes and Metabolism, Genetics, Molecular Biology, Biochemistry
Published: 2023

22. DMV biogenesis during β-coronavirus infection requires autophagy proteins VMP1 and TMEM41B

Author: Mingming Ji, Meng Li, Long Sun, Hongyu Deng, and Yan G. Zhao
Subjects: Cell Biology, Molecular Biology
Abstract: Upon entering host cells, β-coronaviruses specifically induce generation of replication organelles (ROs) from the endoplasmic reticulum (ER) through their nonstructural protein 3 (nsp3) and nsp4 for viral genome transcription and replication. The most predominant ROs are double-membrane vesicles (DMVs). The ER-resident proteins VMP1 and TMEM41B, which form a complex to regulate autophagosome and lipid droplet (LD) formation, were recently shown to be essential for β-coronavirus infection. Here we report that VMP1 and TMEM41B contribute to DMV generation but function at different steps. TMEM41B facilitates nsp3-nsp4 interaction and ER zippering, while VMP1 is required for subsequent closing of the paired ER into DMVs. Additionally, inhibition of phosphatidylserine (PS) formation by
Published: 2022

23. Decision letter: Selective sorting of microRNAs into exosomes by phase-separated YBX1 condensates

Author: Yan G Zhao
Subjects: Chemistry, Phase (matter), microRNA, Sorting, Microvesicles, Cell biology
Published: 2021

24. Orexin A peptidergic system: Comparative physiology, morphology and population between brains of nomal and Alzheimer’s disease mice

Author: Wang Q, Yan G, Zhou Y, Jin Z, Zhao P, Yaqian You, Wang Z, Sun H, and Chai G
Subjects: Orexin-A, education.field_of_study, nervous system, Comparative physiology, mental disorders, Population, Morphology (biology), Disease, Biology, education, Neuroscience, psychological phenomena and processes
Abstract: Sleep disturbance is common in patients with Alzheimer’s disease (AD), and orexin A is a pivotal neurotransmitter for bidirectional regulating the amyloid-β (Aβ) deposition of AD brain and poor sleep. In the present study, we examined the characteristic of sleep-wake architecture in APPswe/PSldE9 (APP/PS1) and Aβ-treated mice using electroencephalogram (EEG) and electromyographic (EMG) analysis. We compared the expression of orexin A, distribution, and morphology of the corresponding orexin A neurons using innovative methods including three-dimensional reconstruction and brain tissue clearing between Wild type (WT) and APP/PS1 mice. Results from our study demonstrated that increased wakefulness and reduced NREM sleep were seen in APP/PS1 and Aβ treated mice while the expression of orexin A was significantly upregulated. Higher density and distribution of orexin A activated neurons were seen in APP/PS1 mice, with a location of 1.06 mm to 2.30 mm away from the anterior fontanelle compared to 1.34 mm to 2.18 mm away from the anterior fontanelle in WT mice. These results suggested that the population and distribution of orexin A may play an important role in the progression of AD.
Published: 2021

25. Endomembrane remodeling in SARS-CoV-2 infection

Author: Di Chen, Yan G. Zhao, and Hong Zhang
Published: 2022

26. Autophagosome maturation: An epic journey from the ER to lysosomes

Author: Hong Zhang and Yan G. Zhao
Subjects: Autophagosome, Autophagic Cell Death, ATG8, Autophagosome maturation, Biological Transport, Active, Reviews, Review, GTPase, Biology, Endoplasmic Reticulum, 03 medical and health sciences, 0302 clinical medicine, Animals, Humans, 030304 developmental biology, 0303 health sciences, Vesicle, Autophagy, Autophagosomes, Neurodegenerative Diseases, Cell Biology, Cell biology, Cytoplasm, Rab, Lysosomes, 030217 neurology & neurosurgery
Abstract: Zhao and Zhang summarize recent advances in our molecular understanding of the maturation of nascent autophagosomes into degradative autolysosomes in multicellular organisms., Macroautophagy involves the sequestration of cytoplasmic contents in a double-membrane autophagosome and their delivery to lysosomes for degradation. In multicellular organisms, nascent autophagosomes fuse with vesicles originating from endolysosomal compartments before forming degradative autolysosomes, a process known as autophagosome maturation. ATG8 family members, tethering factors, Rab GTPases, and SNARE proteins act coordinately to mediate fusion of autophagosomes with endolysosomal vesicles. The machinery mediating autophagosome maturation is under spatiotemporal control and provides regulatory nodes to integrate nutrient availability with autophagy activity. Dysfunction of autophagosome maturation is associated with various human diseases, including neurodegenerative diseases, Vici syndrome, cancer, and lysosomal storage disorders. Understanding the molecular mechanisms underlying autophagosome maturation will provide new insights into the pathogenesis and treatment of these diseases.
Published: 2018

27. Improved prime editors enable pathogenic allele correction and cancer modelling in adult mice

Author: Esther Mintzer, Chunwei Zheng, Scot A. Wolfe, Aamir Mir, Erik J. Sontheimer, Wen Xue, Shun-Qing Liang, Guangping Gao, Terence R. Flotte, Yan G. Zhao, Karthikeyan Ponnienselvan, and Pengpeng Liu
Subjects: CRISPR-Cas9 genome editing, 0301 basic medicine, Carcinogenesis, Somatic cell, Science, Genetic enhancement, General Physics and Astronomy, Computational biology, Biology, Transfection, Genome, Article, Virus, General Biochemistry, Genetics and Molecular Biology, Prime (order theory), Mice, 03 medical and health sciences, chemistry.chemical_compound, Gene therapy, 0302 clinical medicine, Genome editing, Neoplasms, Animals, Humans, Guide RNA, Allele, Cancer genetics, Alleles, Gene Editing, Multidisciplinary, RNA, General Chemistry, Dependovirus, Disease Models, Animal, HEK293 Cells, 030104 developmental biology, chemistry, 030220 oncology & carcinogenesis, CRISPR-Cas Systems, DNA, HeLa Cells, RNA, Guide, Kinetoplastida
Abstract: Prime editors (PEs) mediate genome modification without utilizing double-stranded DNA breaks or exogenous donor DNA as a template. PEs facilitate nucleotide substitutions or local insertions or deletions within the genome based on the template sequence encoded within the prime editing guide RNA (pegRNA). However, the efficacy of prime editing in adult mice has not been established. Here we report an NLS-optimized SpCas9-based prime editor that improves genome editing efficiency in both fluorescent reporter cells and at endogenous loci in cultured cell lines. Using this genome modification system, we could also seed tumor formation through somatic cell editing in the adult mouse. Finally, we successfully utilize dual adeno-associated virus (AAVs) for the delivery of a split-intein prime editor and demonstrate that this system enables the correction of a pathogenic mutation in the mouse liver. Our findings further establish the broad potential of this genome editing technology for the directed installation of sequence modifications in vivo, with important implications for disease modeling and correction., Prime editors use a template sequence within their pegRNA to facilitate nucleotide substitutions or local indels. Here the authors use AAVs to deliver a split-intein prime editor in vivo to correct a pathogenic mutation.
Published: 2021

28. Comparative genomics of Chinese and international isolates of Escherichia albertii: population structure and evolution of virulence and antimicrobial resistance

Author: yan G, Lijuan Luo, Li Q, Zou N, Xuzhi Zhang, Haibin Wang, Ruiting Lan, Yanwen Xiong, Li Zhang, Bai L, Chen X, Wan Z, Zhang Z, Michael Payne, Liang C, and Zheng H
Subjects: Comparative genomics, Multiple drug resistance, Genetics, education.field_of_study, Plasmid, biology, Population, Virulence, biology.organism_classification, education, Genome, Prophage, Escherichia albertii
Abstract: Escherichia albertii is a newly recognized species in the genus Escherichia that causes diarrhea. The population structure, genetic diversity and genomic features has not been fully examined. Here, 169 E. albertii isolates from different sources and regions in China were sequenced and combined with 312 publicly available genomes for phylogenetic and genomic analyses. The E. albertii population was divided into 2 clades and 8 lineages, with lineage 3 (L3), L5 and L8 more common in China. Clinical isolates were observed in all clades/lineages. Virulence genes were found to be distributed differently among lineages: subtypes of the intimin encoding gene eae and the cytolethal distending toxin (Cdt) gene cdtB were lineage associated, the second type three secretion system (ETT2) island was truncated in L3 and L6. Seven new eae subtypes and 1 new cdtB subtype (cdtB-VI) were found. Alarmingly, 85.9% of the Chinese E. albertii isolates were predicted to be multidrug resistant (MDR) with 35.9% harboured genes capable of conferring resistance to 10 to 14 different drug classes. By in silico multi-locus sequence typing, majority of the MDR isolates belonged to 4 STs (ST4638, ST4479, ST4633 and ST4488). Thirty-four intact plasmids carrying MDR and virulence genes, and 130 intact prophages were identified from 17 complete E. albertii genomes. Ten plasmid replicon types were found to be significantly associated with MDR. The 130 intact prophages were clustered into 5 groups, with group 5 prophages harbouring more virulence genes. Our findings provided fundamental insights into the population structure, virulence variation and MDR of E. albertii.Impact statementE. albertii is newly recognized foodborne pathogen causing diarrhea. Elucidation of its genomic features is important for surveillance and control of E. albertii infections. In this work, 169 E. albertii genomes from difference sources and regions in China were collected and sequenced, which contributed to the currently limited genomic data pool of E. albertii. In combination with 312 publicly available genomes from 14 additional countries, the population structure of E. albertii was defined. The presence and subtypes of virulence genes in different lineages were significantly different, indicating potential pathogenicity variation. Additionally, the presence of multidrug resistance (MDR) genes was alarmingly high in the Chinese dominated lineages. MDR associated STs and plasmid subtypes were identified, which could be used as sentinels for MDR surveillance. Moreover, the subtypes of plasmids and prophages were distributed differently across lineages, and were found to contribute to the acquisition of virulence and MDR genes of E. albertii. Altogether, this work reveals the diversity of E. albertii and characterized its genomic features in unprecedented detail.Data SummaryAll newly sequenced data in this work were deposited in National Center for Biotechnology Information (NCBI) under the BioProject of PRJNA693666, including 6 complete genomes and raw reads of 164 E. albertii isolates.
Published: 2021

29. Vmp1, Vps13D, and Marf/Mfn2 function in a conserved pathway to regulate mitochondria and ER contact in development and disease

Author: James Shen, Ruoxi Wang, Eric H. Baehrecke, Margit Burmeister, Tina M. Fortier, and Yan G. Zhao
Subjects: 0301 basic medicine, Mutant, MFN2, Biology, Mitochondrion, Mitochondrial Size, Endoplasmic Reticulum, Mitochondrial Dynamics, General Biochemistry, Genetics and Molecular Biology, Article, GTP Phosphohydrolases, Mitochondrial Proteins, 03 medical and health sciences, 0302 clinical medicine, Autophagy, Humans, Endoplasmic reticulum, Membrane Proteins, Proteins, Phenotype, Cell biology, Mitochondria, 030104 developmental biology, mitochondrial fusion, General Agricultural and Biological Sciences, 030217 neurology & neurosurgery
Abstract: Mutations in Vps13D cause defects in autophagy, clearance of mitochondria, and human movement disorders. Here, we discover that Vps13D functions in a pathway downstream of Vmp1 and upstream of Marf/Mfn2. Like vps13d, vmp1 mutant cells exhibit defects in autophagy, mitochondrial size, and clearance. Through the relationship between vmp1 and vps13d, we reveal a novel role for Vps13D in the regulation of mitochondria and endoplasmic reticulum (ER) contact. Significantly, the function of Vps13D in mitochondria and ER contact is conserved between fly and human cells, including fibroblasts derived from patients suffering from VPS13D mutation-associated neurological symptoms. vps13d mutants have increased levels of Marf/MFN2, a regulator of mitochondrial fusion. Importantly, loss of marf/MFN2 suppresses vps13d mutant phenotypes, including mitochondria and ER contact. These findings indicate that Vps13d functions at a regulatory point between mitochondria and ER contact, mitochondrial fusion and autophagy, and help to explain how Vps13D contributes to disease.
Published: 2021

30. Characterization of Intestinal Microbiota and Serum Metabolites in Patients with Mild Hepatic Encephalopathy

Author: Yan G, Feng F, Zhang J, Long F, Wang M, Lin Y, and Peng Z
Subjects: medicine.medical_specialty, business.industry, Internal medicine, medicine, In patient, medicine.disease, business, Hepatic encephalopathy, Gastroenterology
Published: 2021

31. Evidence for Nonlinear Gluon Effects in QCD and their $A$ Dependence at STAR

Author: STAR Collaboration, Abdallah, M. S., Aboona, B. E., Adam, J., Adamczyk, L., Adams, J. R., Adkins, J. K., Agakishiev, G., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Aitbaev, A., Alekseev, I., Anderson, D. M., Aparin, A., Aschenauer, E. C., Ashraf, M. U., Atetalla, F. G., Averichev, G. S., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Behera, A., Bellwied, R., Bhagat, P., Bhasin, A., Bielcik, J., Bielcikova, J., Bordyuzhin, I. G., Brandenburg, J. D., Brandin, A. V., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Chakaberia, I., Chaloupka, P., Chan, B. K., Chang, F-H., Chang, Z., Chatterjee, A., Chattopadhyay, S., Chen, D., Chen, J., Chen, J. H., Chen, X., Chen, Z., Cheng, J., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Daugherity, M., Dedovich, T. G., Deppner, I. M., Derevschikov, A. A., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fawzi, F. M., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Francisco, A., Fu, C., Gagliardi, C. A., Galatyuk, T., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Guryn, W., Hamed, A., Han, Y., Harabasz, S., Harasty, M. D., Harris, J. W., Harrison, H., He, S., He, W., He, X. H., He, Y., Heppelmann, S., Herrmann, N., Hoffman, E., Holub, L., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jena, C., Jentsch, A., Ji, Y., Jia, J., Jiang, K., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kagamaster, S., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kechechyan, A., Kelsey, M., Khyzhniak, Y. V., Kikoła, D. P., Kimelman, B., Kincses, D., Kisel, I., Kiselev, A., Knospe, A. G., Ko, H. S., Kochenda, L., Korobitsin, A., Kosarzewski, L. K., Kramarik, L., Kravtsov, P., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Kwasizur, J. H., Lacey, R., Lan, S., Landgraf, J. M., Lauret, J., Lebedev, A., Lednicky, R., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Liang, X., Liang, Y., Licenik, R., Lin, T., Lin, Y., Lisa, M. A., Liu, F., Liu, H., Liu, P., Liu, T., Liu, X., Liu, Y., Liu, Z., Ljubicic, T., Llope, W. J., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Manukhov, S. L., Margetis, S., Markert, C., Matis, H. S., Mazer, J. A., Minaev, N. G., Mioduszewski, S., Mohanty, B., Mondal, M. M., Mooney, I., Morozov, D. A., Mukherjee, A., Nagy, M., Nam, J. D., Nasim, Md., Nayak, K., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Nigmatkulov, G., Niida, T., Nishitani, R., Nogach, L. V., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okorokov, V. A., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Panebratsev, Y., Parfenov, P., Paul, A., Pawlik, B., Pawlowska, D., Perkins, C., Pluta, J., Pokhrel, B. R., Porter, J., Posik, M., Prozorova, V., Pruthi, N. K., Przybycien, M., Putschke, J., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Reed, R., Ritter, H. G., Robotkova, M., Rogachevskiy, O. V., Romero, J. L., Roy, D., Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Samigullin, E., Sandweiss, J., Sato, S., Schmidke, W. B., Schmitz, N., Schweid, B. R., Seck, F., Seger, J., Seto, R., Seyboth, P., Shah, N., Shahaliev, E., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, R., Sheikh, A. I., Shen, D. Y., Shi, S. S., Shi, Y., Shou, Q. Y., Sichtermann, E. P., Sikora, R., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Smirnov, N., Söhngen, Y., Solyst, W., Song, Y., Spinka, H. M., Srivastava, B., Stanislaus, T. D. S., Stefaniak, M., Stewart, D. J., Strikhanov, M., Stringfellow, B., Suaide, A. A. P., Sumbera, M., Summa, B., Sun, X. M., Sun, X., Sun, Y., Surrow, B., Svirida, D. N., Sweger, Z. W., Szymanski, P., Tang, A. H., Tang, Z., Taranenko, A., Tarnowsky, T., Thomas, J. H., Timmins, A. R., Tlusty, D., Todoroki, T., Tokarev, M., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Tripathy, S. K., Truhlar, T., Trzeciak, B. A., Tsai, O. D., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vanek, J., Vasiliev, A. N., Vassiliev, I., Verkest, V., Videbæk, F., Vokal, S., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, P., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wieman, H., Wissink, S. W., Witt, R., Wu, J., Wu, Y., Xi, B., Xiao, Z. G., Xie, G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zbroszczyk, H., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: High Energy Physics - Theory, Nuclear Theory (nucl-th), High Energy Physics - Experiment (hep-ex), Nuclear Theory, High Energy Physics - Theory (hep-th), FOS: Physical sciences, High Energy Physics::Experiment, Nuclear Experiment (nucl-ex), Nuclear Experiment, High Energy Physics - Experiment
Abstract: The STAR Collaboration reports measurements of back-to-back azimuthal correlations of di-$\pi^0$s produced at forward pseudorapidities ($2.6, Comment: 7 pages,3 figures, 1 supplemental material
Published: 2021
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32. Light Nuclei Collectivity from $\sqrt{s_{\rm NN}}$ = 3 GeV Au+Au Collisions at RHIC

Author: STAR Collaboration, Abdallah, M. S., Aboona, B. E., Adam, J., Adamczyk, L., Adams, J. R., Adkins, J. K., Agakishiev, G., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Aitbaev, A., Alekseev, I., Anderson, D. M., Aparin, A., Aschenauer, E. C., Ashraf, M. U., Atetalla, F. G., Averichev, G. S., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Behera, A., Bellwied, R., Bhagat, P., Bhasin, A., Bielcik, J., Bielcikova, J., Bordyuzhin, I. G., Brandenburg, J. D., Brandin, A. V., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Chakaberia, I., Chaloupka, P., Chan, B. K., Chang, F-H., Chang, Z., Chatterjee, A., Chattopadhyay, S., Chen, D., Chen, J., Chen, J. H., Chen, X., Chen, Z., Cheng, J., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Daugherity, M., Dedovich, T. G., Deppner, I. M., Derevschikov, A. A., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fawzi, F. M., Fazio, S., Feng, C. J., Feng, Y., Finch, E., Fisyak, Y., Francisco, A., Fu, C., Gagliardi, C. A., Galatyuk, T., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Guryn, W., Hamed, A., Han, Y., Harabasz, S., Harasty, M. D., Harris, J. W., Harrison, H., He, S., He, W., He, X. H., He, Y., Heppelmann, S., Herrmann, N., Hoffman, E., Holub, L., Hu, C., Hu, Q., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Isenhower, D., Isshiki, M., Jacobs, W. W., Jena, C., Jentsch, A., Ji, Y., Jia, J., Jiang, K., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kagamaster, S., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kechechyan, A., Kelsey, M., Khyzhniak, Y. V., Kikoła, D. P., Kimelman, B., Kincses, D., Kisel, I., Kiselev, A., Knospe, A. G., Ko, H. S., Kochenda, L., Korobitsin, A., Kosarzewski, L. K., Kramarik, L., Kravtsov, P., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Kwasizur, J. H., Lacey, R., Lan, S., Landgraf, J. M., Lauret, J., Lebedev, A., Lednicky, R., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Liang, X., Liang, Y., Licenik, R., Lin, T., Lin, Y., Lisa, M. A., Liu, F., Liu, H., Liu, P., Liu, T., Liu, X., Liu, Y., Liu, Z., Ljubicic, T., Llope, W. J., Longacre, R. S., Loyd, E., Lu, T., Lukow, N. S., Luo, X. F., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Manukhov, S. L., Margetis, S., Markert, C., Matis, H. S., Mazer, J. A., Minaev, N. G., Mioduszewski, S., Mohanty, B., Mondal, M. M., Mooney, I., Morozov, D. A., Mukherjee, A., Nagy, M., Nam, J. D., Nasim, Md., Nayak, K., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Nigmatkulov, G., Niida, T., Nishitani, R., Nogach, L. V., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okorokov, V. A., Okubo, K., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Panebratsev, Y., Parfenov, P., Paul, A., Pawlik, B., Pawlowska, D., Perkins, C., Pinsky, L. S., Pluta, J., Pokhrel, B. R., Porter, J., Posik, M., Prozorova, V., Pruthi, N. K., Przybycien, M., Putschke, J., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Reed, R., Ritter, H. G., Robotkova, M., Rogachevskiy, O. V., Romero, J. L., Roy, D., Ruan, L., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Samigullin, E., Sandweiss, J., Sato, S., Schmidke, W. B., Schmitz, N., Schweid, B. R., Seck, F., Seger, J., Seto, R., Seyboth, P., Shah, N., Shahaliev, E., Shanmuganathan, P. V., Shao, M., Shao, T., Sharma, R., Sheikh, A. I., Shen, D. Y., Shi, S. S., Shi, Y., Shou, Q. Y., Sichtermann, E. P., Sikora, R., Singh, J., Singha, S., Sinha, P., Skoby, M. J., Smirnov, N., Söhngen, Y., Solyst, W., Song, Y., Spinka, H. M., Srivastava, B., Stanislaus, T. D. S., Stefaniak, M., Stewart, D. J., Strikhanov, M., Stringfellow, B., Suaide, A. A. P., Sumbera, M., Summa, B., Sun, X. M., Sun, X., Sun, Y., Surrow, B., Svirida, D. N., Sweger, Z. W., Szymanski, P., Tang, A. H., Tang, Z., Taranenko, A., Tarnowsky, T., Thomas, J. H., Timmins, A. R., Tlusty, D., Todoroki, T., Tokarev, M., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Tripathy, S. K., Truhlar, T., Trzeciak, B. A., Tsai, O. D., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vanek, J., Vasiliev, A. N., Vassiliev, I., Verkest, V., Videbæk, F., Vokal, S., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, P., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Westfall, G. D., Wieman, H., Wissink, S. W., Witt, R., Wu, J., Wu, Y., Xi, B., Xiao, Z. G., Xie, G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zbroszczyk, H., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, F., Zhao, J., Zhao, M., Zhou, C., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: Nuclear Theory, FOS: Physical sciences, Nuclear Experiment (nucl-ex), Nuclear Experiment
Abstract: In high-energy heavy-ion collisions, partonic collectivity is evidenced by the constituent quark number scaling of elliptic flow anisotropy for identified hadrons. A breaking of this scaling and dominance of baryonic interactions is found for identified hadron collective flow measurements in $\sqrt{s_{\rm NN}}$ = 3 GeV Au+Au collisions. In this paper, we report measurements of the first- and second-order azimuthal anisotropic parameters, $v_1$ and $v_2$, of light nuclei ($d$, $t$, $^{3}$He, $^{4}$He) produced in $\sqrt{s_{\rm NN}}$ = 3 GeV Au+Au collisions at the STAR experiment. An atomic mass number scaling is found in the measured $v_1$ slopes of light nuclei at mid-rapidity. For the measured $v_2$ magnitude, a strong rapidity dependence is observed. Unlike $v_2$ at higher collision energies, the $v_2$ values at mid-rapidity for all light nuclei are negative and no scaling is observed with the atomic mass number. Calculations by the Jet AA Microscopic Transport Model (JAM), with baryonic mean-field plus nucleon coalescence, are in good agreement with our observations, implying baryonic interactions dominate the collective dynamics in 3 GeV Au+Au collisions at RHIC.
Published: 2021
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33. Measurements of ${}^3_Λ\rm{H}$ and ${}^4_Λ\rm{H}$ Lifetimes and Yields in Au+Au Collisions in the High Baryon Density Region

Author: STAR Collaboration, Abdallah, M. S., Aboona, B. E., Adam, J., Adamczyk, L., Adams, J. R., Adkins, J. K., Agakishiev, G., Aggarwal, I., Aggarwal, M. M., Ahammed, Z., Alekseev, I., Anderson, D. M., Aparin, A., Aschenauer, E. C., Ashraf, M. U., Atetalla, F. G., Attri, A., Averichev, G. S., Bairathi, V., Baker, W., Cap, J. G. Ball, Barish, K., Behera, A., Bellwied, R., Bhagat, P., Bhasin, A., Bielcik, J., Bielcikova, J., Bordyuzhin, I. G., Brandenburg, J. D., Brandin, A. V., Bunzarov, I., Cai, X. Z., Caines, H., Sánchez, M. Calderón de la Barca, Cebra, D., Chakaberia, I., Chaloupka, P., Chan, B. K., Chang, F-H., Chang, Z., Chankova-Bunzarova, N., Chatterjee, A., Chattopadhyay, S., Chen, D., Chen, J., Chen, J. H., Chen, X., Chen, Z., Cheng, J., Chevalier, M., Choudhury, S., Christie, W., Chu, X., Crawford, H. J., Csanád, M., Daugherity, M., Dedovich, T. G., Deppner, I. M., Derevschikov, A. A., Dhamija, A., Di Carlo, L., Didenko, L., Dixit, P., Dong, X., Drachenberg, J. L., Duckworth, E., Dunlop, J. C., Elsey, N., Engelage, J., Eppley, G., Esumi, S., Evdokimov, O., Ewigleben, A., Eyser, O., Fatemi, R., Fawzi, F. M., Fazio, S., Federic, P., Fedorisin, J., Feng, C. J., Feng, Y., Filip, P., Finch, E., Fisyak, Y., Francisco, A., Fu, C., Fulek, L., Gagliardi, C. A., Galatyuk, T., Geurts, F., Ghimire, N., Gibson, A., Gopal, K., Gou, X., Grosnick, D., Gupta, A., Guryn, W., Hamad, A. I., Hamed, A., Han, Y., Harabasz, S., Harasty, M. D., Harris, J. W., Harrison, H., He, S., He, W., He, X. H., He, Y., Heppelmann, S., Herrmann, N., Hoffman, E., Holub, L., Hu, Y., Huang, H., Huang, H. Z., Huang, S. L., Huang, T., Huang, X., Huang, Y., Humanic, T. J., Igo, G., Isenhower, D., Jacobs, W. W., Jena, C., Jentsch, A., Ji, Y., Jia, J., Jiang, K., Ju, X., Judd, E. G., Kabana, S., Kabir, M. L., Kagamaster, S., Kalinkin, D., Kang, K., Kapukchyan, D., Kauder, K., Ke, H. W., Keane, D., Kechechyan, A., Kelsey, M., Khyzhniak, Y. V., Kikoła, D. P., Kim, C., Kimelman, B., Kincses, D., Kisel, I., Kiselev, A., Knospe, A. G., Ko, H. S., Kochenda, L., Kosarzewski, L. K., Kramarik, L., Kravtsov, P., Kumar, L., Kumar, S., Elayavalli, R. Kunnawalkam, Kwasizur, J. H., Lacey, R., Lan, S., Landgraf, J. M., Lauret, J., Lebedev, A., Lednicky, R., Lee, J. H., Leung, Y. H., Lewis, N., Li, C., Li, W., Li, X., Li, Y., Liang, X., Liang, Y., Licenik, R., Lin, T., Lin, Y., Lisa, M. A., Liu, F., Liu, H., Liu, P., Liu, T., Liu, X., Liu, Y., Liu, Z., Ljubicic, T., Llope, W. J., Longacre, R. S., Loyd, E., Lukow, N. S., Luo, X. F., Ma, L., Ma, R., Ma, Y. G., Magdy, N., Mallick, D., Margetis, S., Markert, C., Matis, H. S., Mazer, J. A., Minaev, N. G., Mioduszewski, S., Mohanty, B., Mondal, M. M., Mooney, I., Morozov, D. A., Mukherjee, A., Nagy, M., Nam, J. D., Nasim, Md., Nayak, K., Neff, D., Nelson, J. M., Nemes, D. B., Nie, M., Nigmatkulov, G., Niida, T., Nishitani, R., Nogach, L. V., Nonaka, T., Nunes, A. S., Odyniec, G., Ogawa, A., Oh, S., Okorokov, V. A., Page, B. S., Pak, R., Pan, J., Pandav, A., Pandey, A. K., Panebratsev, Y., Parfenov, P., Pawlik, B., Pawlowska, D., Perkins, C., Pinsky, L., Pintér, R. L., Pluta, J., Pokhrel, B. R., Ponimatkin, G., Porter, J., Posik, M., Prozorova, V., Pruthi, N. K., Przybycien, M., Putschke, J., Qiu, H., Quintero, A., Racz, C., Radhakrishnan, S. K., Raha, N., Ray, R. L., Reed, R., Ritter, H. G., Robotkova, M., Rogachevskiy, O. V., Romero, J. L., Roy, D., Ruan, L., Rusnak, J., Sahoo, A. K., Sahoo, N. R., Sako, H., Salur, S., Sandweiss, J., Sato, S., Schmidke, W. B., Schmitz, N., Schweid, B. R., Seck, F., Seger, J., Sergeeva, M., Seto, R., Seyboth, P., Shah, N., Shahaliev, E., Shanmuganathan, P. V., Shao, M., Shao, T., Sheikh, A. I., Shen, D. Y., Shi, S. S., Shi, Y., Shou, Q. Y., Sichtermann, E. P., Sikora, R., Simko, M., Singh, J., Singha, S., Skoby, M. J., Smirnov, N., Söhngen, Y., Solyst, W., Sorensen, P., Spinka, H. M., Srivastava, B., Stanislaus, T. D. S., Stefaniak, M., Stewart, D. J., Strikhanov, M., Stringfellow, B., Suaide, A. A. P., Sumbera, M., Summa, B., Sun, X. M., Sun, X., Sun, Y., Surrow, B., Svirida, D. N., Sweger, Z. W., Szymanski, P., Tang, A. H., Tang, Z., Taranenko, A., Tarnowsky, T., Thomas, J. H., Timmins, A. R., Tlusty, D., Todoroki, T., Tokarev, M., Tomkiel, C. A., Trentalange, S., Tribble, R. E., Tribedy, P., Tripathy, S. K., Truhlar, T., Trzeciak, B. A., Tsai, O. D., Tu, Z., Ullrich, T., Underwood, D. G., Upsal, I., Van Buren, G., Vanek, J., Vasiliev, A. N., Vassiliev, I., Verkest, V., Videbæk, F., Vokal, S., Voloshin, S. A., Wang, F., Wang, G., Wang, J. S., Wang, P., Wang, X., Wang, Y., Wang, Z., Webb, J. C., Weidenkaff, P. C., Wen, L., Westfall, G. D., Wieman, H., Wissink, S. W., Witt, R., Wu, J., Wu, Y., Xi, B., Xiao, Z. G., Xie, G., Xie, W., Xu, H., Xu, N., Xu, Q. H., Xu, Y., Xu, Z., Yan, G., Yang, C., Yang, Q., Yang, S., Yang, Y., Ye, Z., Yi, L., Yip, K., Yu, Y., Zbroszczyk, H., Zha, W., Zhang, C., Zhang, D., Zhang, J., Zhang, S., Zhang, X. P., Zhang, Y., Zhang, Z. J., Zhang, Z., Zhao, J., Zhou, C., Zhou, Y., Zhu, X., Zurek, M., and Zyzak, M.
Subjects: FOS: Physical sciences, Nuclear Experiment (nucl-ex)
Abstract: We report precision measurements of hypernuclei ${}^3_Λ\rm{H}$ and ${}^4_Λ\rm{H}$ lifetimes obtained from Au+Au collisions at \snn = 3.0\,GeV and 7.2\,GeV collected by the STAR experiment at RHIC, and the first measurement of ${}^3_Λ\rm{H}$ and ${}^4_Λ\rm{H}$ mid-rapidity yields in Au+Au collisions at \snn = 3.0\,GeV. ${}^3_Λ\rm{H}$ and ${}^4_Λ\rm{H}$, being the two simplest bound states composed of hyperons and nucleons, are cornerstones in the field of hypernuclear physics. Their lifetimes are measured to be $221\pm15(\rm stat.)\pm19(\rm syst.)$\,ps for ${}^3_Λ\rm{H}$ and $218\pm6(\rm stat.)\pm13(\rm syst.)$\,ps for ${}^4_Λ\rm{H}$. The $p_T$-integrated yields of ${}^3_Λ\rm{H}$ and ${}^4_Λ\rm{H}$ are presented in different centrality and rapidity intervals. It is observed that the shape of the rapidity distribution of ${}^4_Λ\rm{H}$ is different for 0--10\% and 10--50\% centrality collisions. Thermal model calculations, using the canonical ensemble for strangeness, describes the ${}^3_Λ\rm{H}$ yield well, while underestimating the ${}^4_Λ\rm{H}$ yield. Transport models, combining baryonic mean-field and coalescence (JAM) or utilizing dynamical cluster formation via baryonic interactions (PHQMD) for light nuclei and hypernuclei production, approximately describe the measured ${}^3_Λ\rm{H}$ and ${}^4_Λ\rm{H}$ yields. Our measurements provide means to precisely assess our understanding of the fundamental baryonic interactions with strange quarks, which can impact our understanding of more complicated systems involving hyperons, such as the interior of neutron stars or exotic hypernuclei., 8 pages, 4 captioned figures
Published: 2021
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34. Atlastin 2/3 regulate ER targeting of the ULK1 complex to initiate autophagy

Author: Nan Liu, Hongyu Zhao, Junjie Hu, Hong Zhang, and Yan G Zhao
Subjects: Atlastin, Er targeting, Autophagy, Membrane and Lipid Biology, Autophagosomes, Intracellular Signaling Peptides and Proteins, Vesicular Transport Proteins, Biophysics, Tissue membrane, Autophagy-Related Proteins, Cell Biology, Biology, ULK1, Autophagy-related protein 13, Autophagosome formation, Transmembrane protein, Article, Cell biology, GTP Phosphohydrolases, Multiprotein Complexes, Animals, Autophagy-Related Protein-1 Homolog, Humans
Abstract: Atlastin mediates fusion of ER membranes. Liu et al. show that Atlastin 2/3 also contribute to the recruitment and stabilization of ULK1 and ATG101 at the autophagosome formation sites on the ER., Dynamic targeting of the ULK1 complex to the ER is crucial for initiating autophagosome formation and for subsequent formation of ER–isolation membrane (IM; autophagosomal precursor) contact during IM expansion. Little is known about how the ULK1 complex, which comprises FIP200, ULK1, ATG13, and ATG101 and does not exist as a constitutively coassembled complex, is recruited and stabilized on the ER. Here, we demonstrate that the ER-localized transmembrane proteins Atlastin 2 and 3 (ATL2/3) contribute to recruitment and stabilization of ULK1 and ATG101 at the FIP200-ATG13–specified autophagosome formation sites on the ER. In ATL2/3 KO cells, formation of FIP200 and ATG13 puncta is unaffected, while targeting of ULK1 and ATG101 is severely impaired. Consequently, IM initiation is compromised and slowed. ATL2/3 directly interact with ULK1 and ATG13 and facilitate the ATG13-mediated recruitment/stabilization of ULK1 and ATG101. ATL2/3 also participate in forming ER–IM tethering complexes. Our study provides insights into the dynamic assembly of the ULK1 complex on the ER for autophagosome formation.
Published: 2020

35. Perempuan Pedesaan dan Disabilitas di Provinsi Papua dan Papua Barat (Suatu Analisa Hubungan Internasional dalam Pelaksanaan Otsus Papua)

Author: Yan G. Pelamonia, Dhea T. Lumentut, and Melyana R. Pugu
Abstract: Tujuan penelitian ini adalah mendapatkan gambaran dan analisa terkait perempuan pedesaan dan disabilitas di Provinsi Papua dan Papua Barat pada saat pelaksanaan Otonomi Khusus Papua yang dianalisa dengan menggunakan konsep dan teori Feminisme dalam Hubungan Internasional. Penelitian ini menggunakan metode penelitian kualitatif yaitu mencoba memberikan penjelasan melalui berbagai data yang diperoleh kemudian dianalisa dan mendapatkan kesimpulan dari permasalahan ini. Luaran dari penelitian adalah perempuan pedesaan dan disabilitas di Provinsi Papua dan Papua Barat dalam pelaksanaan Otonomi Khusus Papua yang diketahui sebagai salah satu jawaban bagi kesejahteraan orang asli Papua ternyata dalam Analisa hubungan internasional menggunakan pendekatan Femisnime belum mampu mensejajarkan peran dan partisipasi perempuan dan disabilitas di Papua dan Papua Barat. Hal ini mengakibatkan perempuan pedesaan dan disabilitas di wilayah ini masih miskin dan termarginalkan jauh dari pembangunan dan kesejahteraan.
Published: 2022

36. The BPAN and intellectual disability disease proteins WDR45 and WDR45B modulate autophagosome-lysosome fusion

Author: Yan G Zhao and Cuicui Ji
Subjects: Autophagosome, Endosome, Autophagosome maturation, Mutant, Neurodegeneration, Autophagy, Autophagosomes, Cell Biology, Biology, medicine.disease, Cell biology, WDR45, Intellectual Disability, Macroautophagy, medicine, Humans, Carrier Proteins, Lysosomes, Molecular Biology, Biogenesis
Abstract: WDR45 and WDR45B are β-propeller proteins belonging to the WIPI (WD repeat domain, phosphoinositide interacting) family. Mutations in WDR45 and WDR45B are genetically linked with beta-propeller protein-associated neurodegeneration (BPAN) and intellectual disability (ID), respectively. WDR45 and WDR45B are homologs of yeast Atg18. Atg18 forms a complex with Atg2 for autophagosome biogenesis, probably by transferring lipids from the ER to phagophores. We revealed that WDR45 and WDR45B are critical for autophagosome-lysosome fusion in neural cells. WDR45 and WDR45B, but not their disease-related mutants, bind to the tether protein EPG5 and facilitate its targeting to late endosomes/lysosomes. In Wdr45 Wdr45b-deficient cells, the formation of tether-SNARE fusion machinery is compromised. The macroautophagy/autophagy deficiency in wdr45 wdr45b DKO cells is ameliorated by suppression of O-GlcNAcylation, which promotes autophagosome maturation. Thus, our results provide insights into the pathogenesis of WDR45- and WDR45B-related neurological diseases.
Published: 2021

37. Phase Separation in Membrane Biology: The Interplay between Membrane-Bound Organelles and Membraneless Condensates

Author: Yan G. Zhao and Hong Zhang
Subjects: Membrane biology, Biology, General Biochemistry, Genetics and Molecular Biology, Biophysical Phenomena, Cell Physiological Phenomena, 03 medical and health sciences, 0302 clinical medicine, Organelle, Humans, Nuclear pore, Molecular Biology, 030304 developmental biology, Organelles, 0303 health sciences, Membranes, Vesicle, Autophagy, Autophagosomes, Cell Biology, Compartmentalization (psychology), Membrane, Biophysics, 030217 neurology & neurosurgery, Biogenesis, Developmental Biology
Abstract: In eukaryotic cells, various membrane-bound organelles compartmentalize diverse cellular activities in a spatially and temporally controlled manner. Numerous membraneless organelles assembled via liquid-liquid phase separation (LLPS), known as condensates, also facilitate compartmentalization of cellular functions. Emerging evidence shows that these two organelle types interact in many biological processes. Membranes modulate the biogenesis and dynamics of phase-separated condensates by serving as assembly platforms or by forming direct contacts. Phase separation of membrane-associated proteins participates in various trafficking events, such as clustering of vesicles for temporally controlled fusion and storage, and transport of membraneless condensates on membrane-bound organelles. Phase separation also acts in cargo trafficking pathways by sorting and docking cargos for translocon-mediated transport across membranes, by shuttling cargos through the nuclear pore complex, and by triggering the formation of surrounding autophagosomes for delivery to lysosomes. The coordinated actions of membrane-bound and membraneless organelles ensure spatiotemporal control of various cellular functions.
Published: 2020

38. Considerations for Soluble Protein Biomarker Blood Sample Matrix Selection

Author: Jon E. Peterson, Daoyu Duan, Yan G. Ni, Connie Wang, Chad Ray, John Allinson, Martha Hokom, Sara Hamon, Joel A Mathews, Xuemei Zhao, and Greta Wegner
Subjects: Blood Platelets, Analyte, Protein biomarkers, Chemistry, Sample (material), Anticoagulants, Reproducibility of Results, Pharmaceutical Science, Blood Proteins, Computational biology, 030226 pharmacology & pharmacy, Biomarkers, Pharmacological, Protein markers, 03 medical and health sciences, 0302 clinical medicine, Drug development, Predictive Value of Tests, 030220 oncology & carcinogenesis, Immune Cell Activation, Leukocytes, Animals, Humans, Biomarker (medicine), Blood Chemical Analysis, Selection (genetic algorithm)
Abstract: Blood-based soluble protein biomarkers provide invaluable clinical information about patients and are used as diagnostic, prognostic, and pharmacodynamic markers. The most commonly used blood sample matrices are serum and different types of plasma. In drug development research, the impact of sample matrix selection on successful protein biomarker quantification is sometimes overlooked. The sample matrix for a specific analyte is often chosen based on prior experience or literature searches, without good understanding of the possible effects on analyte quantification. Using a data set of 32 different soluble protein markers measured in matched serum and plasma samples, we examined the differences between serum and plasma and discussed how platelet or immune cell activation can change the quantified concentration of the analyte. We have also reviewed the effect of anticoagulant on analyte quantification. Finally, we provide specific recommendations for biomarker sample matrix selection and propose a systematic and data-driven approach for sample matrix selection. This review is intended to raise awareness of the impact and considerations of sample matrix selection on biomarker quantification.
Published: 2020

39. Is there Na I in the atmosphere of HD 209458b?

Author: N. Casasayas-Barris, E. Pallé, F. Yan, G. Chen, R. Luque, M. Stangret, E. Nagel, M. Zechmeister, M. Oshagh, J. Sanz-Forcada, L. Nortmann, F. J. Alonso-Floriano, P. J. Amado, J. A. Caballero, S. Czesla, S. Khalafinejad, M. López-Puertas, J. López-Santiago, K. Molaverdikhani, D. Montes, A. Quirrenbach, A. Reiners, I. Ribas, A. Sánchez-López, M. R. Zapatero Osorio
Published: 2020
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40. Nursing Care of Critically Ill Patient Infected With COVID-19 Virus in China, Shanghai: A Case Report

Author: Yan G
Subjects: Nursing care, medicine.medical_specialty, Coronavirus disease 2019 (COVID-19), business.industry, Critically ill, Medicine, business, China, Intensive care medicine, Virus
Published: 2020

41. Fusion peptide from SARS-2 spike transforms into a wedge inserted in a bilayer leaflet, and thins the opposite leaflet

Author: Steven R. Van Doren, Benjamin Scott, Yan G. Fulcher, and Rama K. Koppisetti
Subjects: Biophysics
Published: 2022

42. Peripheral membrane associations of matrix metalloproteinases

Author: Alexander Jurkevich, Tara C. Marcink, Steven R. Van Doren, Yan G. Fulcher, and Rama K. Koppisetti
Subjects: 0301 basic medicine, Proteolysis, Matrix metalloproteinase, Endocytosis, Article, Extracellular matrix, 03 medical and health sciences, Protein Domains, Matrix Metalloproteinase 12, Matrix Metalloproteinase 14, medicine, Animals, Humans, Lipid bilayer, Nuclear Magnetic Resonance, Biomolecular, Molecular Biology, 030102 biochemistry & molecular biology, medicine.diagnostic_test, Heparin, Chemistry, Cell Membrane, Peripheral membrane protein, Cell Biology, Sheddase, 030104 developmental biology, Biochemistry, Matrix Metalloproteinase 7, Biophysics, Proteoglycans, Intracellular
Abstract: Water soluble matrix metalloproteinases (MMPs) have been regarded as diffusing freely in the extracellular matrix. Yet multiple MMPs are also observed at cell surfaces. Their membrane-proximal activities include sheddase activities, collagenolysis, bacterial killing, and intracellular trafficking reaching as far as the nucleus. The catalytic domains of MMP-7 and MMP-12 bind bilayers peripherally, each in two different orientations, by presenting positive charges and a few hydrophobic groups to the surface. Related peripheral membrane associations are predicted for other soluble MMPs. The peripheral membrane associations may support pericellular proteolysis and endocytosis. The isolated soluble domains of MT1-MMP can also associate with membranes. NMR assays suggest transient association of the hemopexin-like domains of MT1-MMP and MMP-12 with lipid bilayers. Peripheral association of soluble MMP domains with bilayers or heparin sulfate proteoglycans probably concentrates them near the membrane. This could increase the probability of forming complexes with membrane-associated proteins, such as those targeted for proteolysis. This article is part of a Special Issue entitled: Matrix Metalloproteinases edited by Rafael Fridman.
Published: 2017

43. Recommendations for Selection and Characterization of Protein Biomarker Assay Calibrator Material

Author: Medha Kamat, Damien Fink, Yuda Zhu, Yan G. Ni, Mark Cameron, Renee Riffon, Lakshmi Amaravadi, Kyra J. Cowan, Darshana Jani, Robert Neely, Lindsay King, and Paul Rhyne
Subjects: Computer science, 010401 analytical chemistry, Pharmacology toxicology, Proteins, Pharmaceutical Science, Bioinformatics, 030226 pharmacology & pharmacy, 01 natural sciences, 0104 chemical sciences, 03 medical and health sciences, 0302 clinical medicine, Calibration, Biomarker (medicine), Biochemical engineering, Biomarkers, Selection (genetic algorithm)
Abstract: As biomarkers continue to become an integral part of drug development and decision-making, there are increased expectations for reliable and quantitative assays. Protein biomarker assay results are directly influenced by the calibrator material. The selection of calibrator material presents many challenges that impact the relative accuracy and performance of the assay. There is an industry-wide challenge finding reliable and well-characterized calibrator material with good documentation. Several case studies are presented that demonstrate some of the challenges involved in selecting appropriate calibrators along with the resolutions that were ultimately applied. From these experiences, we present here a set of recommendations for selecting and characterizing calibrator material based on the intended purpose of the assay. Finally, we introduce a commutability approach, based on common clinical chemistry practices, which can be used to demonstrate inter-changeability with calibrator materials across multiple lots and technology platforms for all types of protein biomarker assays.
Published: 2017

44. A switch from canonical to noncanonical autophagy shapes B cell responses

Author: Selina Jessica Keppler, Nuria Martinez-Martin, Paula Maldonado, Marie-Charlotte Domart, Francesca Gasparrini, Marianne Burbage, Bruno Frederico, Harold B.J. Jefferies, Beatriz Montaner, Carlson Tsui, Lucy M. Collinson, Shweta Aggarwal, Usha Nair, Facundo D. Batista, Andreas Bruckbauer, Sharon A. Tooze, Mauro Gaya, and Yan G. Zhao
Subjects: 0301 basic medicine, Programmed cell death, WD40 Repeats, Down-Regulation, Stimulation, Mechanistic Target of Rapamycin Complex 1, Lymphocyte Activation, BAG3, Article, Mice, 03 medical and health sciences, Immune system, Autophagy, medicine, Animals, Mechanistic target of rapamycin, B cell, Mice, Knockout, B-Lymphocytes, Multidisciplinary, biology, TOR Serine-Threonine Kinases, Germinal center, Germinal Center, Mitochondria, Cell biology, Mice, Inbred C57BL, 030104 developmental biology, medicine.anatomical_structure, Virus Diseases, Multiprotein Complexes, Immunology, biology.protein, Microtubule-Associated Proteins
Abstract: Autophagy is important in a variety of cellular and pathophysiological situations; however, its role in immune responses remains elusive. Here, we show that among B cells, germinal center (GC) cells exhibited the highest rate of autophagy during viral infection. In contrast to mechanistic target of rapamycin complex 1-dependent canonical autophagy, GC B cell autophagy occurred predominantly through a noncanonical pathway. B cell stimulation was sufficient to down-regulate canonical autophagy transiently while triggering noncanonical autophagy. Genetic ablation of WD repeat domain, phosphoinositide-interacting protein 2 in B cells alone enhanced this noncanonical autophagy, resulting in changes of mitochondrial homeostasis and alterations in GC and antibody-secreting cells. Thus, B cell activation prompts a temporal switch from canonical to noncanonical autophagy that is important in controlling B cell differentiation and fate.
Published: 2017

45. 2016 White Paper on recent issues in bioanalysis: focus on biomarker assay validation (BAV): (Part 3 – LBA, biomarkers and immunogenicity)

Author: Akiko Ishii-Watabe, Albert Torri, Rong Zeng, Daniel Kramer, Steven P. Piccoli, David J. Uhlinger, Stephanie Fraser, Patricia Siguenza, Afshin Safavi, John Smeraglia, Apollon Papadimitriou, Yan G. Ni, Susan M. Richards, Kyra J. Cowan, Alessandra Vitaliti, Lakshmi Amaravadi, Boris Gorovits, Gustavo Mendes Lima Santos, John Kadavil, Sam Haidar, Jan Welink, Yongchang Qiu, João Pedras-Vasconcelos, Chan C. Whiting, Li Xue, Christina Satterwhite, John Kamerud, Swati Gupta, Natasha Savoie, Herbert Birnboeck, Yoshiro Saito, Paul Rhyne, Fabrizio Galliccia, Laurent Cocea, Stephanie Croft, Bonnie Wu, Theingi M. Thway, Virginia Litwin, Corinna Krinos-Fiorotti, Darshana Jani, Charles S Hottenstein, Vinita Gupta, Roland F Staack, Fabio Garofolo, Eginhard Schick, Kara Scheibner, Meena Subramanyam, John Allinson, Renuka Pillutla, Robert Nelson, Flora Berisha, Martin Ullmann, and Giane Sumner
Subjects: Bioanalysis, Macromolecular Substances, Consensus Development Conferences as Topic, Clinical Biochemistry, Validation Studies as Topic, Ligands, 030226 pharmacology & pharmacy, 01 natural sciences, Mass Spectrometry, Analytical Chemistry, 03 medical and health sciences, Government Agencies, 0302 clinical medicine, White paper, Humans, General Pharmacology, Toxicology and Pharmaceutics, Chromatography, High Pressure Liquid, business.industry, Immunogenicity, 010401 analytical chemistry, Scientific excellence, Antibodies, Monoclonal, General Medicine, Data science, 0104 chemical sciences, Biotechnology, Medical Laboratory Technology, Biopharmaceutical, Business, Biomarkers
Abstract: The 2016 10th Workshop on Recent Issues in Bioanalysis (10th WRIB) took place in Orlando, Florida with participation of close to 700 professionals from pharmaceutical/biopharmaceutical companies, biotechnology companies, contract research organizations, and regulatory agencies worldwide. WRIB was once again a weeklong event – A Full Immersion Week of Bioanalysis for PK, Biomarkers and Immunogenicity. As usual, it is specifically designed to facilitate sharing, reviewing, discussing and agreeing on approaches to address the most current issues of interest including both small and large molecules involving LCMS, hybrid LBA/LCMS, and LBA approaches, with the focus on PK, biomarkers and immunogenicity. This 2016 White Paper encompasses recommendations emerging from the extensive discussions held during the workshop, and is aimed to provide the bioanalytical community with key information and practical solutions on topics and issues addressed, in an effort to enable advances in scientific excellence, improved quality and better regulatory compliance. This White Paper is published in 3 parts due to length. This part (Part 3) discusses the recommendations for large molecule bioanalysis using LBA, biomarkers and immunogenicity. Parts 1 (small molecule bioanalysis using LCMS) and Part 2 (Hybrid LBA/LCMS and regulatory inputs from major global health authorities) have been published in the Bioanalysis journal, issues 22 and 23, respectively.
Published: 2016

46. A critical role of VMP1 in lipoprotein secretion

Author: Norito Tamura, Noboru Mizushima, Dongfang Li, Yan G. Zhao, Yuki Kanda, Taki Nishimura, Hideaki Morishita, Mitsuyo Okazaki, and Yuriko Sakamaki
Subjects: Mouse, QH301-705.5, Lipoproteins, Science, autophagy-related gene, Lumen (anatomy), General Biochemistry, Genetics and Molecular Biology, Mice, medicine, Animals, Secretion, VMP1, Biology (General), Lipid bilayer, Zebrafish, General Immunology and Microbiology, Chemistry, General Neuroscience, Endoplasmic reticulum, lipoprotein, Autophagy, Membrane Proteins, Cell Biology, General Medicine, Transmembrane protein, Cell biology, Protein Transport, endoplasmic reticulum, medicine.anatomical_structure, Medicine, lipids (amino acids, peptides, and proteins), Endoderm, Research Article, Human, Lipoprotein
Abstract: Lipoproteins are lipid-protein complexes that are primarily generated and secreted from the intestine, liver, and visceral endoderm and delivered to peripheral tissues. Lipoproteins, which are assembled in the endoplasmic reticulum (ER) membrane, are released into the ER lumen for secretion, but its mechanism remains largely unknown. Here, we show that the release of lipoproteins from the ER membrane requires VMP1, an ER transmembrane protein essential for autophagy and certain types of secretion. Loss of vmp1, but not other autophagy-related genes, in zebrafish causes lipoprotein accumulation in the intestine and liver. Vmp1 deficiency in mice also leads to lipid accumulation in the visceral endoderm and intestine. In VMP1-depleted cells, neutral lipids accumulate within lipid bilayers of the ER membrane, thus affecting lipoprotein secretion. These results suggest that VMP1 is important for the release of lipoproteins from the ER membrane to the ER lumen in addition to its previously known functions.
Published: 2019

47. Author response: A critical role of VMP1 in lipoprotein secretion

Author: Taki Nishimura, Yuki Kanda, Noboru Mizushima, Yan G. Zhao, Mitsuyo Okazaki, Dongfang Li, Norito Tamura, Hideaki Morishita, and Yuriko Sakamaki
Subjects: medicine.medical_specialty, Endocrinology, Chemistry, Internal medicine, medicine, Secretion, Lipoprotein
Published: 2019

48. β-propeller proteins WDR45 and WDR45B regulate autophagosome maturation into autolysosomes in neural cells

Author: Hong Zhang, Yan G. Zhao, Cuicui Ji, Di Chen, and Hongyu Zhao
Subjects: 0301 basic medicine, Autophagosome, Saccharomyces cerevisiae Proteins, Protein family, Endosome, Autophagosome maturation, Autophagy-Related Proteins, Saccharomyces cerevisiae, Biology, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, 0302 clinical medicine, Phosphatidylinositol Phosphates, Macroautophagy, Autophagy, medicine, Humans, Endoplasmic reticulum, Neurodegeneration, Autophagosomes, medicine.disease, Autophagic Punctum, Cell biology, 030104 developmental biology, Carrier Proteins, Lysosomes, SNARE Proteins, General Agricultural and Biological Sciences, SNARE complex, 030217 neurology & neurosurgery
Abstract: Summary Mutations in WDR45 and WDR45B cause the human neurological diseases β-propeller protein-associated neurodegeneration (BPAN) and intellectual disability (ID), respectively. WDR45 and WDR45B, along with WIPI1 and WIPI2, belong to a WD40 repeat-containing phosphatidylinositol-3-phosphate (PI(3)P)-binding protein family. Their yeast homolog Atg18 forms a complex with Atg2 and is required for autophagosome formation in part by tethering isolation membranes (IMs) (autophagosome precursor) to the endoplasmic reticulum (ER) to supply lipid for IM expansion in the autophagy pathway. The exact functions of WDR45/45B are unclear. We show here that WDR45/45B are specifically required for neural autophagy. In Wdr45/45b-depleted cells, the size of autophagosomes is decreased, and this is rescued by overexpression of ATG2A, providing in vivo evidence for the lipid transfer activity of ATG2-WIPI complexes. WDR45/45B are dispensable for the closure of autophagosomes but essential for the progression of autophagosomes into autolysosomes. WDR45/45B interact with the tether protein EPG5 and target it to late endosomes/lysosomes to promote autophagosome maturation. In the absence of Wdr45/45b, formation of the fusion machinery, consisting of SNARE proteins and EPG5, is dampened. BPAN- and ID-related mutations of WDR45/45B fail to rescue the autophagy defects in Wdr45/45b-deficient cells, possibly due to their impaired binding to EPG5. Promoting autophagosome maturation by inhibiting O-GlcNAcylation increases SNARE complex formation and facilitates the fusion of autophagosomes with late endosomes/lysosomes in Wdr45/45b double knockout (DKO) cells. Thus, our results uncover a novel function of WDR45/45B in autophagosome-lysosome fusion and provide molecular insights into the development of WDR45/WDR45B mutation-associated diseases.
Published: 2021

49. The Nobel Prize: an appetizer before the feast

Author: Yan G. Zhao and Hong Zhang
Subjects: 0301 basic medicine, World Wide Web, 03 medical and health sciences, Thesaurus (information retrieval), Engineering, 030104 developmental biology, Multidisciplinary, Operations research, business.industry, business
Published: 2016

50. ULK1 cycling: The ups and downs of the autophagy response

Author: Hong Zhang and Yan G. Zhao
Subjects: 0301 basic medicine, Atg1, Nedd4 Ubiquitin Protein Ligases, Ubiquitin-Protein Ligases, Cell, Cellular homeostasis, Biology, Models, Biological, Mice, 03 medical and health sciences, 0302 clinical medicine, Autophagy, medicine, Protein biosynthesis, Animals, Autophagy-Related Protein-1 Homolog, Humans, Spotlight, Starvation, Endosomal Sorting Complexes Required for Transport, Ubiquitin, Kinase, Ubiquitination, Cell Biology, ULK1, Cell biology, 030104 developmental biology, medicine.anatomical_structure, cardiovascular system, Commentary, medicine.symptom, hormones, hormone substitutes, and hormone antagonists, 030217 neurology & neurosurgery, HeLa Cells
Abstract: Zhao and Zhang discuss a new study by Nazio et al. that demonstrates that NEDD4L and mTOR regulate autophagy via modulation of ULK1 levels., The Ser/Thr kinase ULK1/Atg1 controls autophagy initiation under nutrient starvation conditions. In this issue, Nazio et al. (2016. J. Cell Biol. https://doi.org/10.1083/jcb.201605089) demonstrate that oscillatory modulation of NEDD4L-mediated proteasomal degradation and mTOR-dependent de novo protein synthesis of ULK1 ensures the proper amplitude and duration of the autophagy response during prolonged starvation, thus maintaining cellular homeostasis.
Published: 2016

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