Search

Your search keyword '"Hirata T"' showing total 3,372 results
Start Over Author "Hirata T"
3,372 results on '"Hirata T"'

1. Investigation of chromosome Y loss in men with schizophrenia

Author

Hirata T, Hishimoto A, Otsuka I, Okazaki S, Boku S, Kimura A, Horai T, and Sora I

Subjects
loss of chromosome Y, schizophrenia, disease duration, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Neurology. Diseases of the nervous system, RC346-429
Abstract

Takashi Hirata, Akitoyo Hishimoto, Ikuo Otsuka, Satoshi Okazaki, Shuken Boku, Atsushi Kimura, Tadasu Horai, Ichiro Sora Department of Psychiatry, Kobe University Graduate School of Medicine, Kusunoki-cho, Chuo-ku, Kobe, Japan Background: Life expectancy is 10–20 years lower in patients with schizophrenia than in the general population. In addition, men with schizophrenia have an earlier age at onset, more pronounced deficit symptoms, poorer course, and poorer response to antipsychotic medications than women. Recent studies have indicated that loss of chromosome Y (LOY) in peripheral blood is associated with an increased risk of all-cause mortality. In order to elucidate the pathophysiology of male-specific features, we investigated the association between LOY and schizophrenia. Materials and methods: The present study included 360 Japanese men (146 patients with schizophrenia vs 214 controls). The relative amount of Y chromosome was defined as the ratio of chromosome Y to chromosome X (Y/X ratio) based on the fluorescent signal of co-amplified short sequences from the Y-X homologous amelogenin genes (AMELY and AMELX). Results: There was no significant difference in the frequency of LOY between the schizophrenia and control groups. However, longer duration of illness was associated with LOY after controlling for age and smoking status in the schizophrenia group (P=0.007, OR =1.11 [95% CI =1.03–1.19]). Conclusion: According to our results, schizophrenia may not have a remarkable effect on blood LOY; however, LOY may be associated with disease course in patients with schizophrenia. Keywords: loss of chromosome Y, schizophrenia, disease duration

Published
2018

2. mDia1/3-dependent actin polymerization spatiotemporally controls LAT phosphorylation by Zap70 at the immune synapse

Author

Thumkeo, D, Katsura, Y, Nishimura, Y, Kanchanawong, P, Tohyama, K, Ishizaki, T, Kitajima, S, Takahashi, C, Hirata, T, Watanabe, N, Krummel, MF, and Narumiya, S

Subjects
Biochemistry and Cell Biology, Biomedical and Clinical Sciences, Biological Sciences, Neurosciences, 1.1 Normal biological development and functioning, Underpinning research, Inflammatory and immune system, Actin Cytoskeleton, Actins, Adaptor Proteins, Signal Transducing, Animals, Formins, Gene Expression Regulation, Humans, Immune System, Jurkat Cells, Membrane Proteins, Mice, Mice, Knockout, Phosphorylation, Polymerization, Receptors, Antigen, T-Cell, Signal Transduction, ZAP-70 Protein-Tyrosine Kinase
Abstract

The mechanism by which the cytosolic protein Zap70 physically interacts with and phosphorylates its substrate, the transmembrane protein LAT, upon T cell receptor (TCR) stimulation remains largely obscure. In this study, we found that the pharmacological inhibition of formins, a major class of actin nucleators, suppressed LAT phosphorylation by Zap70, despite TCR stimulation-dependent phosphorylation of Zap70 remaining intact. High-resolution imaging and three-dimensional image reconstruction revealed that localization of phosphorylated Zap70 to the immune synapse (IS) and subsequent LAT phosphorylation are critically dependent on formin-mediated actin polymerization. Using knockout mice, we identify mDia1 and mDia3, which are highly expressed in T cells and which localize to the IS upon TCR activation, as the critical formins mediating this process. Our findings therefore describe previously unsuspected roles for mDia1 and mDia3 in the spatiotemporal control of Zap70-dependent LAT phosphorylation at the IS through regulation of filamentous actin, and underscore their physiological importance in TCR signaling.

Published
2020

7. Wnt7A is a putative prognostic and chemosensitivity marker in human malignant pleural mesothelioma

Author

Jablons, David, Hirata, T, Zheng, Q, Chen, Z, Kinoshita, H, Okamoto, J, Kratz, J, Li, H, Lui, N, Do, H, and Cheng, T

Abstract

Malignant pleural mesothelioma (MPM) is a highly aggressive tumor that has a poor prognosis, limited treatment options, and a worldwide incidence that is expected to increase in the next decade. We evaluated Wnt7A expression in 50 surgically resected tumor

Published
2015

8. A Prospective Cohort Study to Define the Clinical Features and Outcome of Lung Cancers Harboring HER2 Aberration in Japan (HER2-CS STUDY)

Author

Gemba, K., Ikeda, G., Yasugi, M., Kurimoto, E., Nakano, K., Moritaka, T., Inoue, K., Miyoshi, S., Hamaguchi, N., Ito, R., Sano, Y., Takata, I., Mitani, A., Nishisaka, T., Shoda, H., Nishida, A., Tamamoto, S., Fujitaka, K., Masuda, T., Miyamoto, S., Hattori, N., Sugimoto, K., Fujii, S., Ueda, Y., Sakugawa, M., Fukamatsu, N., Ogata, Y., Bandoh, S., Kanaji, N., Takigawa, N., Yamane, H., Ochi, N., Honda, Y., Oka, M., Kittaka, M., Kubota, T., Yokoyama, A., Yokoyama, T., Sato, E., Shiota, Y., Horita, N., Kanematsu, T., Awaya, Y., Nakamasu, A., Murakami, I., Kuyama, S., Kudo, K., Tamura, T., Umeno, T., Morichika, D., Fujiwara, K., Sato, K., Harada, D., Nogami, N., Nishii, K., Fuchimoto, Y., Kishimoto, T., Kawai, H., Watanabe, K., Tokumo, K., Isobe, T., Tsubata, Y., Inoue, M., Ichikawa, H., Nishioka, Y., Hanibuchi, M., Goto, H., Sumikawa, T., Kodani, M., Suyama, H., Makino, H., Kinosita, N., Shimizu, E., Obata, H., Ikegami, H., Chikamori, K., Maeda, T., Kishino, T., Kamei, H., Ueoka, H., Kunihiro, Y., Kobayashi, T., Ueda, K., Hayashi, M., Kamiya, M., Murakami, J., Sato, A., Ichihara, E., Kubo, T., Ninomiya, T., Hirata, T., Minami, D., Kato, Y., Higo, H., Makimoto, G., Toyota, Y., Oda, N., Nakanishi, M., Kayatani, H., Senoo, S., Kano, H., Watanabe, H., Ando, T., Nakasuka, T., Hara, N., Itano, J., Nakashima, H., Tabata, M., Ninomiya, Kiichiro, Hata, Tae, Yoshioka, Hiroshige, Ohashi, Kadoaki, Bessho, Akihiro, Hosokawa, Shinobu, Ishikawa, Nobuhisa, Yamasaki, Masahiro, Shibayama, Takuo, Aoe, Keisuke, Kozuki, Toshiyuki, Harita, Shingo, Ueda, Yutaka, Murakami, Toshi, Fujimoto, Nobukazu, Yanai, Hiroyuki, Toyooka, Shinichi, Takata, Minoru, Hotta, Katsuyuki, and Kiura, Katsuyuki

Published
2019
Full Text
View/download PDF

9. Targeting Gli transcription activation by small molecule suppresses tumor growth.

Author

Bosco-Clément, G, Zhang, F, Chen, Z, Zhou, H-M, Li, H, Mikami, I, Hirata, T, Yagui-Beltran, A, Lui, N, Do, H, Cheng, T, Tseng, H-H, Choi, H, Fang, L-T, Kim, I-J, Yue, D, Wang, C, Zheng, Q, Fujii, N, He, B, Jablons, David, and Mann, Michael

Subjects
Animals, Cell Line, Tumor, Cell Proliferation, Female, HCT116 Cells, HEK293 Cells, HT29 Cells, Hedgehog Proteins, Humans, Immunoblotting, Mice, Mice, Nude, NIH 3T3 Cells, Neoplasms, Oligonucleotide Array Sequence Analysis, Protein Binding, Pyrazoles, RNA Interference, Reverse Transcriptase Polymerase Chain Reaction, Small Molecule Libraries, TATA-Binding Protein Associated Factors, Transcription Factor TFIID, Transcription Factors, Transcriptional Activation, Transcriptome, Tumor Burden, Xenograft Model Antitumor Assays, Zinc Finger Protein GLI1
Abstract

Targeted inhibition of Hedgehog signaling at the cell membrane has been associated with anticancer activity in preclinical and early clinical studies. Hedgehog signaling involves activation of Gli transcription factors that can also be induced by alternative pathways. In this study, we identified an interaction between Gli proteins and a transcription coactivator TBP-associated factor 9 (TAF9), and validated its functional relevance in regulating Gli transactivation. We also describe a novel, synthetic small molecule, FN1-8, that efficiently interferes with Gli/TAF9 interaction and downregulate Gli/TAF9-dependent transcriptional activity. More importantly, FN1-8 suppresses cancer cell proliferation in vitro and inhibits tumor growth in vivo. Our results suggest that blocking Gli transactivation, an important control point of multiple oncogenic pathways, may be an effective anticancer strategy.

Published
2014

10. Targeting Gli transcription activation by small molecule suppresses tumor growth

Author

Jablons, David, Bosco-Clément, G, Zhang, F, Chen, Z, Zhou, HM, Li, H, Mikami, I, Hirata, T, Yagui-Beltran, A, Lui, N, and Do, HT

Abstract

Targeted inhibition of Hedgehog signaling at the cell membrane has been associated with anticancer activity in preclinical and early clinical studies. Hedgehog signaling involves activation of Gli transcription factors that can also be induced by alternati

Published
2014

14. Down-Regulation of SIX3 is Associated with Clinical Outcome in Lung Adenocarcinoma

Author

Jablons, David, Mo, ML, Okamoto, J, Chen, Z, Hirata, T, Mikami, I, Bosco-Clément, G, Li, H, Zhou, HM, Jablons, DM, and He, B

Abstract

Background:Lung cancer is a common cancer and the leading cause of cancer-related death worldwide. SIX3 is a human homologue of the highly conserved sine oculis gene family essential during embryonic development in vertebrates, and encodes a homeo-domain c

Published
2013

16. High-dose-rate mold brachytherapy for mandibular gingival squamous cell carcinoma in outpatient setting – Initial case report

Author

Takeshita, A., Shimamoto, H., Uchimoto, Y., Tsujimoto, T., Miyamoto, T., Kreiborg, S., Mallya, S. M., Oda, M., Hirata, T., Ogawa, K., Shiomi, H., Murakami, S., Takeshita, A., Shimamoto, H., Uchimoto, Y., Tsujimoto, T., Miyamoto, T., Kreiborg, S., Mallya, S. M., Oda, M., Hirata, T., Ogawa, K., Shiomi, H., and Murakami, S.

Abstract

Brachytherapy is often used to treat oral cancer, as it generally yields a good outcome with little oral function loss. In particular, mold brachytherapy is ideally suited for superficial oral cases, such as cancers developing on the gingiva, palate, or buccal mucosa, with little to no bone involvement and thin tissue thickness. Mold brachytherapy including that at a high-dose-rate (HDR) is used to treat gingival cancer, though hospitalization is the typical treatment setting. Reported here are details of HDR mold brachytherapy performed in an outpatient setting for a mandibular gingival case of squamous cell carcinoma (SCC). Mandibular gingival SCC in a 71-year-old man was treated as an outpatient using HDR mold brachytherapy (54 Gy in 9 fractions, 5 days). After receiving mold treatment for thirty months, there was no sign of recurrence or metastasis. To our knowledge, this is the first report of HDR mold brachytherapy in an outpatient setting for treating mandibular gingival cancer.

Published
2023

25. The Origin of the Paleo‐Kuril Arc, NE Japan: Sediment Provenance Change and its Implications for Plate Configuration in the NW Pacific Region since the Late Cretaceous

Author

Harisma, H., Naruse, H., Asanuma, H., Hirata, T., Harisma, H., Naruse, H., Asanuma, H., and Hirata, T.

Abstract

The Nemuro Belt is a tectonic belt in the Paleo-Kuril Arc system, the NW Pacific region. The Paleo-Kuril Arc has been interpreted as an intra-oceanic arc system between the Izanagi and Pacific plates during the Late Cretaceous, suggesting that the boundary between these plates was a trench. However, this study shows it was a volcanic arc that developed atop a continental margin. To determine the nature of this arc during the Late Cretaceous, U-Pb ages of detrital zircons from the Nemuro and Urahoro groups in the Paleo-Kuril Arc were analyzed. Our results identify two distinct types of detrital zircon U-Pb age distributions. The first (Type 1) is characterized by multimodal age distributions with peaks ranging from ca. 1.8 Ga to 78 Ma. The other (Type 2) exhibits a unimodal age distribution with a peak at 60–52 Ma. These different age distributions indicate a provenance transition occurred between the Late Cretaceous and Paleogene. Precambrian zircons in Type 1 sandstones indicate that the Paleo-Kuril Arc was part of a continental plate, presumably the Okhotsk Block, in NE Asia during the Late Cretaceous. In contrast, Type 2 sandstones were supplied only from the magmatic arc region that the Izanagi-Pacific Ridge subduction could have activated. This provenance transition suggests the initially continental arc became separated from its continental source at the beginning of the Paleogene.

Published
2022

26. Topic: Incisional Hernia — “Difficult case” as specialistic case: real loss of substance, multi recurrences, infections, fistulas, lombocel, burst abdomen, reconstruction of the entire wall

Author

Tuveri, M., Tuveri, A., Nicolo, E., Tsuruma, T., Nagayama, M., Nakano, S., Trombetta, F., Moscato, R., Ghiglione, F., Ciamporcero, T., Galasso, E., Morino, M., Tharao, M., Ndungu, B., Saidi, H., Mwige, P., Gichere, J., Skipworth, J., Younis, I., Floyd, D., Shankar, A., Sarangi, Rathindra, Morehead, P., Williams, J., Minamimura, K., Mafune, K., Irie, S., Kobayashi, T., Hirata, T., Matapurkar, B., Bhargave, A., Lopez-Monclus, J., Garcia-Ureña, M. A., Blazquez-Hernando, L. A., Melero-Montes, D. A., Robin, A., Jimenez-Ceinos, C., Becerra-Ortiz, R., Aguilera, A., Moreno, A., González, E., Light, D., Horgan, L., Lambrecht, J., Skauby, M., Trondsen, E., Vaktskjold, A., Øyen, O., Kulic, V., Matkovic, M., Knaapen, L., Lomme, R., Goor van, H., Iudica, F., Cingolani, P., Isemer, F., Sohlbach, D., Gregorczyk, M., Barski, K., Gogia, B., Alyautdinov, R., Forgione, U., Damiano, G., Palumbo, V. D., Spinelli, G., Ficarella, S., Buscemi, S., Sinagra, E., Marrazzo, A., Lo Monte, A. I., Naranjo-Fernandez, J. R., Soriano, A. Cuado, Orta, E. Martin, Valera-Sanchez, Z., Intantes-Ormad, M., Piñan-Diez, J., Dominguez-Amodeo, A., Ruiz-Zafra, A., Navarrete-Carcer, E., Olivia-Mompean, F., Padillo-Ruiz, J., Cijan, V., Scepanovic, M., Bojovic, P., Bustos-Jimenez, M., Tamayo-López, M. J., MartÜn-Cartes, J. A., Rapoport, A., Waksman, I., Efremov, O., Bukin, A., Biswas, S., Birolini, C., Miranda, J. S., Utiyama, E. M., Rasslan, S., Birolini, D., Bertoglio, C., Magistro, C., De Martini, P., Lo Conte, D., Di Lernia, S., Ferrari, G., Pugliese, R., Bendavid, Y., Dépeault, A., Baik, Y., Oh, Mingu, Park, Youngjin, Choi, Wonyoung, Han, Inwoong, Lee, Changhyung, Chen, F. Q., Shen, Y. M., and Chen, J.

Published
2015
Full Text
View/download PDF

27. Topic: Rare and Special Cases, The Real “Strange Cases”

Author

Zarrinkhoo, E., Miller, J., Walker, A., Weisman, M., Towfigh, S., Tushev, R., Petkov, I., Tsutsumi, G., Leija, C., Castillo, E., Moncada, F., Mendoza, M., Morua, A. Garcia, Bravo, R., Azcarate, A., Zavala, H., Coman, I. S., Radu, E. V., David, O. I., Stoian, A. R., Strambu, V. E., Iancu, C., Gheorghiu, L. I., Grigorean, V. T., Sinescu, D. R., Plesa, E., Lupascu, C., Straja, D. N., Iacobini, M. A., Ponten, J., Luyer, M., Nienhuijs, S., Permekerlis, A., Petousis, S., Miroforidis, A., Milias, K., Kouridakis, P., Park, J., Kim, D., Nakata, R., Chihara, N., Suzuki, H., Watanabe, M., Uchida, E., Nakanaga, H., Irie, S., Endo, Y., Sonoda, H., Minamimura, K., Kobayashi, T., Hirata, T., Mafune, K., Milosevic, P., Babovic, M., Sorat, D., Light, D., Aawsaj, Y., Horgan, L., Latham, L., Ceriani, I., Livraghi, L., Berselli, M., Gambitta, B., Galvanin, J., Cotronea, C., Pagano, G., Farassino, L., Ambrosoli, A., Crespi, A., Cocozza, E., Kulic, V., Matkovic, M., Percevic, G., Katayama, T., Kumata, Y., Ogawa, E., Horikawa, M., Yaguchi, Y., Inaba, T., Fukushima, R., Jaroszewski, D., Johnson, K., Harold, K., Mori, M., Kumata, M., Guarnieri, F., Smaldone, W., Gaspard, M., Bomben, F., Ceranto, S., Gamarra, M. Florez, Soria, M. Peña, Olivero, C. Fraile, Martinez, M. Josa, Contin, M. Perez, Gómez, J. Cabeza, Jiménez-Valladolid, D., Torres García, A., Descloux, A., Pohle, S., Schramm, B., Schneider, U., Nocito, A., Navarrete, M. Cesardo, Solis, A., Ortega, N., Bergamini, S., Semeraro, C., Armengol, M., Cano, M. Lopez, Torrecilla, N. Ortega, Cavallaro, G., Iorio, O., Avallone, M., Ruscio, S., Rizzello, M., Silecchia, G., Butron, T., Rubio, E., Passas, J., Sopeña, R., Lagaron, E., Silan, F., Garcia, V., Bernal, J., Ortiz, M., Guadarrama, J., Shirai, K., Lomas, M., Shah, B. Bc, and Degloorkar, S. Sarang

Published
2015
Full Text
View/download PDF

28. ICES-PICES-PAME Working Group on Integrated Ecosystem Assessment (IEA) for the Central Arctic Ocean (WGICA)

Author

Jorgensen, L.L., Saitoh, Sei-Ichi, Bengtson, J., Bluhm, Bodil A., Christensen, T.R., Edelvang, K., Flores, H., Frie, Anne Kirstine, Fukamachi, Y., Gavrilo, M., Gjøsæter, H., Grebmeier, J., Einar, B., Harada, N., Hedges, K., van den Heuvel-Greve, M.J., Hirata, T., Hirawake, T., Hakon Hoel, A., Ingvaldsen, R., Ivanov, V., Lindal Jørgensen, L., Kuletz, K., Larsen, J.R., Snoejis Leonmalm, P., Melnikov, I., Mosbech, A., Mulder, Ingeborg, Niehoff, Barabara, Nishino, S., Ohnishi, F., Otsuka, N., van Pelt, T., von Quillfeldt, C., Chul Shin, Hyoung, Rune Skjoldal, Hein, Speer, L., and Yang, S.

Subjects
Onderz. Form. D, Life Science
Published
2022

43. mDia1/3-dependent actin polymerization spatiotemporally controls LAT phosphorylation by Zap70 at the immune synapse

Author

Thumkeo, D., Katsura, Y., Nishimura, Y., Kanchanawong, P., Tohyama, K., Ishizaki, T., Kitajima, S., Takahashi, C., Hirata, T., Watanabe, N., Krummel, M. F., Narumiya, S., Thumkeo, D., Katsura, Y., Nishimura, Y., Kanchanawong, P., Tohyama, K., Ishizaki, T., Kitajima, S., Takahashi, C., Hirata, T., Watanabe, N., Krummel, M. F., and Narumiya, S.

Abstract

The mechanism by which the cytosolic protein Zap70 physically interacts with and phosphorylates its substrate, the transmembrane protein LAT, upon T cell receptor (TCR) stimulation remains largely obscure. In this study, we found that the pharmacological inhibition of formins, a major class of actin nucleators, suppressed LAT phosphorylation by Zap70, despite TCR stimulation–dependent phosphorylation of Zap70 remaining intact. High-resolution imaging and three-dimensional image reconstruction revealed that localization of phosphorylated Zap70 to the immune synapse (IS) and subsequent LAT phosphorylation are critically dependent on formin-mediated actin polymerization. Using knockout mice, we identify mDia1 and mDia3, which are highly expressed in T cells and which localize to the IS upon TCR activation, as the critical formins mediating this process. Our findings therefore describe previously unsuspected roles for mDia1 and mDia3 in the spatiotemporal control of Zap70-dependent LAT phosphorylation at the IS through regulation of filamentous actin, and underscore their physiological importance in TCR signaling.

Published
2020

44. Chemokine receptor CXCR7 non-cell-autonomously controls pontine neuronal migration and nucleus formation

Author

Zhu, Y, Hirata, T, Mackay, F, Murakami, F, Zhu, Y, Hirata, T, Mackay, F, and Murakami, F

Abstract

Long distance tangential migration transports neurons from their birth places to distant destinations to be incorporated into neuronal circuits. How neuronal migration is guided during these long journeys is still not fully understood. We address this issue by studying the migration of pontine nucleus (PN) neurons in the mouse hindbrain. PN neurons migrate from the lower rhombic lip first anteriorly and then turn ventrally near the trigeminal ganglion root towards the anterior ventral hindbrain. Previously we showed that in mouse depleted of chemokine receptor CXCR4 or its ligand CXCL12, PN neurons make their anterior-to-ventral turn at posteriorized positions. However, the mechanism that spatiotemporally controls the anterior-to-ventral turning is still unclear. Furthermore, the role of CXCR7, the atypical receptor of CXCL12, in pontine migration has yet to be examined. Here, we find that the PN is elongated in Cxcr7 knockout due to a broadened anterior-to-ventral turning positions. Cxcr7 is not expressed in migrating PN neurons en route to their destinations, but is strongly expressed in the pial meninges. Neuroepithelium-specific knockout of Cxcr7 does not recapitulate the PN phenotype in Cxcr7 knockout, suggesting that CXCR7 acts non-cell-autonomously possibly from the pial meninges. We show further that CXCR7 regulates pontine migration by modulating CXCL12 protein levels.

Published
2020

45. ICES/PICES/PAME Working Group on Integrated Ecosystem Assessment (IEA) for the Central Arctic Ocean (WGICA)

Author

Jorgensen, L.L., Saitoh, Sei-Ichi, Bengtson, J., Bluhm, Bodil A., Christensen, T.R., Edelvang, K., Flores, H., Frie, Anne Kirstine, Fukamachi, Y., Gavrilo, M., Gjøsæter, H., Grebmeier, J., Einar, B., Harada, N., Hedges, K., van den Heuvel-Greve, M.J., Hirata, T., Hirawake, T., Hakon Hoel, A., Ingvaldsen, R., Ivanov, V., Lindal Jørgensen, L., Kuletz, K., Larsen, J.R., Snoejis Leonmalm, P., Melnikov, I., Mosbech, A., Mulder, Ingeborg, Niehoff, Barabara, Nishino, S., Ohnishi, F., Otsuka, N., van Pelt, T., von Quillfeldt, C., Chul Shin, Hyoung, Rune Skjoldal, Hein, Speer, L., Yang, S., Jorgensen, L.L., Saitoh, Sei-Ichi, Bengtson, J., Bluhm, Bodil A., Christensen, T.R., Edelvang, K., Flores, H., Frie, Anne Kirstine, Fukamachi, Y., Gavrilo, M., Gjøsæter, H., Grebmeier, J., Einar, B., Harada, N., Hedges, K., van den Heuvel-Greve, M.J., Hirata, T., Hirawake, T., Hakon Hoel, A., Ingvaldsen, R., Ivanov, V., Lindal Jørgensen, L., Kuletz, K., Larsen, J.R., Snoejis Leonmalm, P., Melnikov, I., Mosbech, A., Mulder, Ingeborg, Niehoff, Barabara, Nishino, S., Ohnishi, F., Otsuka, N., van Pelt, T., von Quillfeldt, C., Chul Shin, Hyoung, Rune Skjoldal, Hein, Speer, L., and Yang, S.

Published
2020

Catalog

Books, media, physical & digital resources
See catalog results