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1,141 results on '"Zeng, Xue"'

1. Targeting immune–fibroblast cell communication in heart failure

Author

Amrute, Junedh M., Luo, Xin, Penna, Vinay, Yang, Steven, Yamawaki, Tracy, Hayat, Sikander, Bredemeyer, Andrea, Jung, In-Hyuk, Kadyrov, Farid F., Heo, Gyu Seong, Venkatesan, Rajiu, Shi, Sally Yu, Parvathaneni, Alekhya, Koenig, Andrew L., Kuppe, Christoph, Baker, Candice, Luehmann, Hannah, Jones, Cameran, Kopecky, Benjamin, Zeng, Xue, Bleckwehl, Tore, Ma, Pan, Lee, Paul, Terada, Yuriko, Fu, Angela, Furtado, Milena, Kreisel, Daniel, Kovacs, Atilla, Stitziel, Nathan O., Jackson, Simon, Li, Chi-Ming, Liu, Yongjian, Rosenthal, Nadia A., Kramann, Rafael, Ason, Brandon, and Lavine, Kory J.

Published
2024
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5. Crystal structure of (2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(((4aS,5R,6S)-1-oxo-5-vinyl-4,4a,5,6-tetrahydro-1H,3H-pyrano[3,4-c]pyran-6-yl)oxy)tetrahydro-2H-pyran-3-yl 2,3-dihydroxybenzoate hydrate, C23H26O12·H2O

Author

Zeng Xue, Feng Yuanjiao, Shi Lei, Zhong Wenwu, and Niu Yahui

Subjects
2326684, Physics, QC1-999, Crystallography, QD901-999
Abstract

C23H26O12·H2O, orthorhombic, P212121 (no. 19), a = 6.2630(6) Å, b = 17.5649(18) Å, c = 21.929(2) Å, V = 2412.4(4) Å3, Z = 4, Rgt(F) = 0.0381, wRref(F2) = 0.1017, T = 296 K.

Published
2024
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10. Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations

Author

Zhao, Shujuan, Mekbib, Kedous Y., van der Ent, Martijn A., Allington, Garrett, Prendergast, Andrew, Chau, Jocelyn E., Smith, Hannah, Shohfi, John, Ocken, Jack, Duran, Daniel, Furey, Charuta G., Hao, Le Thi, Duy, Phan Q., Reeves, Benjamin C., Zhang, Junhui, Nelson-Williams, Carol, Chen, Di, Li, Boyang, Nottoli, Timothy, Bai, Suxia, Rolle, Myron, Zeng, Xue, Dong, Weilai, Fu, Po-Ying, Wang, Yung-Chun, Mane, Shrikant, Piwowarczyk, Paulina, Fehnel, Katie Pricola, See, Alfred Pokmeng, Iskandar, Bermans J., Aagaard-Kienitz, Beverly, Moyer, Quentin J., Dennis, Evan, Kiziltug, Emre, Kundishora, Adam J., DeSpenza, Jr., Tyrone, Greenberg, Ana B. W., Kidanemariam, Seblewengel M., Hale, Andrew T., Johnston, James M., Jackson, Eric M., Storm, Phillip B., Lang, Shih-Shan, Butler, William E., Carter, Bob S., Chapman, Paul, Stapleton, Christopher J., Patel, Aman B., Rodesch, Georges, Smajda, Stanislas, Berenstein, Alejandro, Barak, Tanyeri, Erson-Omay, E. Zeynep, Zhao, Hongyu, Moreno-De-Luca, Andres, Proctor, Mark R., Smith, Edward R., Orbach, Darren B., Alper, Seth L., Nicoli, Stefania, Boggon, Titus J., Lifton, Richard P., Gunel, Murat, King, Philip D., Jin, Sheng Chih, and Kahle, Kristopher T.

Published
2023
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12. Solution technology of system side harmonic variable impedance based on minimum norm

Author

XU Fangwei, ZENG Xue, WANG Chuan, and ZHENG Hongru

Subjects
harmonic impedance, amount of impedance change, minimum norm, background harmonics, power quality, non-interventional, Applications of electric power, TK4001-4102
Abstract

To calculate the harmonic impedance on the system side is crucial for the safe and stable operation of the new power system. Existing algorithms for harmonic impedance estimation usually assume that the harmonic impedance on the system side is constant during the measurement period. However, the voltage on the system side always changes according to the working mode of the power grid or access of large power load demand, resulting in fluctuations of the harmonic impedance on the system side. Luckly, the harmonic impedance on the system side does not change much in the adjacent sampling time interval. On this basis, the paper proposes a new non-intervention solution for the variable harmonic impedance on the system side. In this method, the second-order change of the harmonic impedance and the second-order change of voltage in the adjacent sampling time interval are taken as the objective function. The harmonic impedance on the system side is solved by minimizing the target function. The proposed method is proved to be accurate and reliable by simulation and practical analysis, especially in the condition that the strong background harmonic or user-side harmonic impedance is not much stronger than the harmonic impedance on the system side.

Published
2023
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13. Screening of Plant Growth Regulators and Antibiotics in Sprout Vegetables by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry

Author

ZENG Xue-Fang, QI Chun-Yan, XIE Ai-Hua, and LEI Yi

Subjects
ultra performance liquid chromatography-tandem mass spectrometry, screening, sprout vegetables, plant growth regulators, antibiotics, Food processing and manufacture, TP368-456, Nutrition. Foods and food supply, TX341-641
Abstract

In this study, chromatographic and mass spectrometry conditions, sample cleanup and extraction, composition and ratio of salt and purifiers were optimized, which established a high-throughput screening method for 11 plant growth regulators and 79 antibiotic drugs in sprout vegetables by ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Samples were extracted by 1% acetonitrile-EDTA-mcllvaine buffer solution, purified by QuEChERS, and separated by ACQUITY UPLC HSS T3 column with gradient elution. Electrospray positive and negative ion mode was used in multi-reaction monitoring mode, and matrix curve external standard method was used to quantify. The limits of quantitation of 90 compounds were in the range of 0.1~15.4 μg/kg. The average recoveries were in the range of 42.2%~138.6% with relative standard deviations lower than 17.2%. In this study, simultaneous, rapid and high-throughput screening and detection of 90 high-risk substances in sprout vegetables were established, which is conducive to a more full understanding of the quality and safety problems of sprout vegetables.

Published
2023
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18. Rapid Determination of Bucinnazine in Blood by UPLC-MS/MS

Author

Zhang-ming GAO, Jing-yu SHI, Hao ZENG, Xue-jun ZHANG

Subjects
forensic medicine, toxicological analysis, bucinnazine, blood, ultra-high performance liquid chromatography-tandem mass spectrometry （uplc-ms/ms）, Medicine
Abstract

Objective To establish a rapid method for the analysis of bucinnazine in blood by UPLC-MS/MS and to apply the method to the practical case. Methods After the internal standard was added to blood, the protein was precipitated with 900 μL mixed solution （Vacetonitrile∶Vwater=8∶2）. After vortex and centrifugation, the protein was measured through 0.22 μm filter membrane. The separation was performed on C18 chromatography column, with acetonitrile and 5 mmol/L ammonium acetate containing 0.1% formic acid aqueous as mobile phase gradient elution at the flow rate of 0.4 mL/min. Multiple reaction monitoring scan was performed in electrospray positive ion mode, quantitative measurement was performed by internal standard method, and methodological verification was carried out. Results The linear relationship of bucinnazine in blood was good in the range of 0.5-200 μg/L, the correlation coefficient （r） was 0.999 7, the limit of detection was 0.1 μg/L, the limit of quantitation was 0.5 μg/L, and the recovery was 78.3%-83.8% at 1, 10 and 100 μg/L mass concentration levels. The matrix effect was 69.4%-73.8%, the intra-day precision was 1.9%-2.8%, and the inter-day precision was 2.8%-3.2%, the accuracy was 3.1%-3.5%. The stability test results of 1 and 100 μg/L mass concentrations at -25 ℃ showed that the accuracy （bias） of 10 d was less than 4.5%. Conclusion This method has the advantages of simple pre-treatment process, fast sample processing speed, high sensitivity of instrument analysis, good stability of content determination and reliable identification results, and can meet the needs of case identification.

Published
2023
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20. Blood transcriptomic signature in type-2 biomarker-low severe asthma and asthma control

Author

Zeng, Xue, Qing, Jing, Li, Chi-Ming, Lu, Jiamiao, Yamawaki, Tracy, Hsu, Yi-Hsiang, Vander Lugt, Bryan, Hsu, Hailing, Busby, John, McDowell, P.J., Jackson, David J., Djukanovic, Ratko, Matthews, John G., Arron, Joseph R., Bradding, Peter, Brightling, Christopher E., Chaudhuri, Rekha, Choy, David F., Cowan, D., Fowler, S.J., Hardman, Timothy C., Harrison, Tim, Howarth, Peter, Lordan, James, Mansur, A.H., Menzies-Gow, Andrew, Pavord, Ian D., Walker, Samantha, Woodcock, Ashley, and Heaney, Liam G.

Published
2023
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29. De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias

Author

Helbig, Katherine L, Lauerer, Robert J, Bahr, Jacqueline C, Souza, Ivana A, Myers, Candace T, Uysal, Betül, Schwarz, Niklas, Gandini, Maria A, Huang, Sun, Keren, Boris, Mignot, Cyril, Afenjar, Alexandra, de Villemeur, Thierry Billette, Héron, Delphine, Nava, Caroline, Valence, Stéphanie, Buratti, Julien, Fagerberg, Christina R, Soerensen, Kristina P, Kibaek, Maria, Kamsteeg, Erik-Jan, Koolen, David A, Gunning, Boudewijn, Schelhaas, H Jurgen, Kruer, Michael C, Fox, Jordana, Bakhtiari, Somayeh, Jarrar, Randa, Padilla-Lopez, Sergio, Lindstrom, Kristin, Jin, Sheng Chih, Zeng, Xue, Bilguvar, Kaya, Papavasileiou, Antigone, Xing, Qinghe, Zhu, Changlian, Boysen, Katja, Vairo, Filippo, Lanpher, Brendan C, Klee, Eric W, Tillema, Jan-Mendelt, Payne, Eric T, Cousin, Margot A, Kruisselbrink, Teresa M, Wick, Myra J, Baker, Joshua, Haan, Eric, Smith, Nicholas, Sadeghpour, Azita, Davis, Erica E, Katsanis, Nicholas, Genomics, Task Force for Neonatal, Allori, Alexander, Angrist, Misha, Ashley, Patricia, Bidegain, Margarita, Boyd, Brita, Chambers, Eileen, Cope, Heidi, Cotten, C Michael, Curington, Theresa, Ellestad, Sarah, Fisher, Kimberley, French, Amanda, Gallentine, William, Goldberg, Ronald, Hill, Kevin, Kansagra, Sujay, Katsanis, Sara, Kurtzberg, Joanne, Marcus, Jeffrey, McDonald, Marie, Mikati, Mohammed, Miller, Stephen, Murtha, Amy, Perilla, Yezmin, Pizoli, Carolyn, Purves, Todd, Ross, Sherry, Smith, Edward, Wiener, John, Corbett, Mark A, MacLennan, Alastair H, Gecz, Jozef, Biskup, Saskia, Goldmann, Eva, Rodan, Lance H, Kichula, Elizabeth, Segal, Eric, Jackson, Kelly E, Asamoah, Alexander, Dimmock, David, McCarrier, Julie, Botto, Lorenzo D, Filloux, Francis, Tvrdik, Tatiana, and Cascino, Gregory D

Subjects
Medical Physiology, Biomedical and Clinical Sciences, Neurodegenerative, Brain Disorders, Neurosciences, Epilepsy, Pediatric, 2.1 Biological and endogenous factors, Aetiology, Neurological, Adolescent, Adult, Calcium Channels, R-Type, Cation Transport Proteins, Child, Child, Preschool, Contracture, Dyskinesias, Female, Genetic Variation, Humans, Infant, Male, Megalencephaly, Neurodevelopmental Disorders, Spasms, Infantile, Task Force for Neonatal Genomics, Deciphering Developmental Disorders Study, CACNA1E, ion channel, arthrogryposis, calcium channel, epilepsy, Biological Sciences, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences
Abstract

Developmental and epileptic encephalopathies (DEEs) are severe neurodevelopmental disorders often beginning in infancy or early childhood that are characterized by intractable seizures, abundant epileptiform activity on EEG, and developmental impairment or regression. CACNA1E is highly expressed in the central nervous system and encodes the α1-subunit of the voltage-gated CaV2.3 channel, which conducts high voltage-activated R-type calcium currents that initiate synaptic transmission. Using next-generation sequencing techniques, we identified de novo CACNA1E variants in 30 individuals with DEE, characterized by refractory infantile-onset seizures, severe hypotonia, and profound developmental impairment, often with congenital contractures, macrocephaly, hyperkinetic movement disorders, and early death. Most of the 14, partially recurring, variants cluster within the cytoplasmic ends of all four S6 segments, which form the presumed CaV2.3 channel activation gate. Functional analysis of several S6 variants revealed consistent gain-of-function effects comprising facilitated voltage-dependent activation and slowed inactivation. Another variant located in the domain II S4-S5 linker results in facilitated activation and increased current density. Five participants achieved seizure freedom on the anti-epileptic drug topiramate, which blocks R-type calcium channels. We establish pathogenic variants in CACNA1E as a cause of DEEs and suggest facilitated R-type calcium currents as a disease mechanism for human epilepsy and developmental disorders.

Published
2018

30. Thrombectomy for delayed thromboembolism in a recurrent cerebral aneurysm previously treated with coiling: A case report

Author

Shao, Ya, primary, Yang, Yuan, additional, Huang, Haidong, additional, Wang, Ting, additional, Li, Jinglun, additional, Jiang, Yushan, additional, Yuan, Ziwei, additional, Tang, Jiayi, additional, Wang, Dihu, additional, Xiang, Zerui, additional, Zeng, Xue, additional, Yu, Zhou, additional, He, Zhongchun, additional, and Yuan, Zhengzhou, additional

Published
2024
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34. Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

Author

Jin, Sheng Chih, Homsy, Jason, Zaidi, Samir, Lu, Qiongshi, Morton, Sarah, DePalma, Steven R, Zeng, Xue, Qi, Hongjian, Chang, Weni, Sierant, Michael C, Hung, Wei-Chien, Haider, Shozeb, Zhang, Junhui, Knight, James, Bjornson, Robert D, Castaldi, Christopher, Tikhonoa, Irina R, Bilguvar, Kaya, Mane, Shrikant M, Sanders, Stephan J, Mital, Seema, Russell, Mark W, Gaynor, J William, Deanfield, John, Giardini, Alessandro, Porter, George A, Srivastava, Deepak, Lo, Cecelia W, Shen, Yufeng, Watkins, W Scott, Yandell, Mark, Yost, H Joseph, Tristani-Firouzi, Martin, Newburger, Jane W, Roberts, Amy E, Kim, Richard, Zhao, Hongyu, Kaltman, Jonathan R, Goldmuntz, Elizabeth, Chung, Wendy K, Seidman, Jonathan G, Gelb, Bruce D, Seidman, Christine E, Lifton, Richard P, and Brueckner, Martina

Subjects
Biological Sciences, Genetics, Cardiovascular, Pediatric, Congenital Structural Anomalies, Brain Disorders, Heart Disease, Heart Disease - Coronary Heart Disease, 2.1 Biological and endogenous factors, Aetiology, Adult, Autistic Disorder, Cardiac Myosins, Case-Control Studies, Child, Exome, Female, Gene Expression, Genetic Predisposition to Disease, Genome-Wide Association Study, Growth Differentiation Factor 1, Heart Defects, Congenital, Heterozygote, High-Throughput Nucleotide Sequencing, Homozygote, Humans, Male, Mutation, Myosin Heavy Chains, Pedigree, Risk, Vascular Endothelial Growth Factor Receptor-3, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology
Abstract

Congenital heart disease (CHD) is the leading cause of mortality from birth defects. Here, exome sequencing of a single cohort of 2,871 CHD probands, including 2,645 parent-offspring trios, implicated rare inherited mutations in 1.8%, including a recessive founder mutation in GDF1 accounting for ∼5% of severe CHD in Ashkenazim, recessive genotypes in MYH6 accounting for ∼11% of Shone complex, and dominant FLT4 mutations accounting for 2.3% of Tetralogy of Fallot. De novo mutations (DNMs) accounted for 8% of cases, including ∼3% of isolated CHD patients and ∼28% with both neurodevelopmental and extra-cardiac congenital anomalies. Seven genes surpassed thresholds for genome-wide significance, and 12 genes not previously implicated in CHD had >70% probability of being disease related. DNMs in ∼440 genes were inferred to contribute to CHD. Striking overlap between genes with damaging DNMs in probands with CHD and autism was also found.

Published
2017

35. Psoriasis risk SNPs and their association with HIV-1 control

Author

Nititham, Joanne, Gupta, Rashmi, Zeng, Xue, Hartogensis, Wendy, Nixon, Douglas F, Deeks, Steven G, Hecht, Frederick M, and Liao, Wilson

Subjects
Medical Microbiology, Biomedical and Clinical Sciences, Immunology, Infectious Diseases, Genetics, HIV/AIDS, Autoimmune Disease, Psoriasis, Clinical Research, Sexually Transmitted Infections, Aetiology, 2.1 Biological and endogenous factors, Infection, Inflammatory and immune system, Good Health and Well Being, Adult, Asymptomatic Diseases, Cohort Studies, Female, Genetic Predisposition to Disease, Genotype, HIV Infections, HIV-1, HLA Antigens, Humans, Linkage Disequilibrium, Male, Middle Aged, Polymorphism, Single Nucleotide, Risk, Urban Population, Viral Load, HIV, Immunogenetics, MHC, Viral control, Viral load, Primary infection
Abstract

Human evolution has resulted in selection for genetic polymorphisms beneficial in the defense against pathogens. However, such polymorphisms may have the potential to heighten the risk of autoimmune disease. Here, we investigated whether psoriasis-associated single nucleotide polymorphisms influence host control of HIV-1 infection. We studied psoriasis and viral immune response variants in three HIV-positive cohorts: (1) HIV-1 controllers and non-controllers in the Study of the Consequences of the Protease Inhibitor Era (SCOPE) cohort (n=366), (2) Individuals with primary HIV infection in the Options cohort (n=675), and (3) HIV-positive injection drug users from the Urban Health Study (UHS) (n=987). We found a strong association of two psoriasis MHC variants, rs9264942 and rs3021366, with both HIV-1 controller status and viral load, and identified another Class III MHC variant rs9368699 to be strongly associated with viral load. A number of genetic variants outside the MHC (SOX5, TLR9, SDC4, PROX1, IL12B, TLR4, MBL-2, TYK2, IFIH1) demonstrated nominal significance. Overall, our data suggest that several psoriasis variants within the MHC have a robust impact on HIV-1 control, while variants outside the MHC require further investigation.

Published
2017

38. Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal Neuralgia

Author

Dong, Weilai, Jin, Sheng Chih, Allocco, August, Zeng, Xue, Sheth, Amar H., Panchagnula, Shreyas, Castonguay, Annie, Lorenzo, Louis-Étienne, Islam, Barira, Brindle, Geneviève, Bachand, Karine, Hu, Jamie, Sularz, Agata, Gaillard, Jonathan, Choi, Jungmin, Dunbar, Ashley, Nelson-Williams, Carol, Kiziltug, Emre, Furey, Charuta Gavankar, Conine, Sierra, Duy, Phan Q., Kundishora, Adam J., Loring, Erin, Li, Boyang, Lu, Qiongshi, Zhou, Geyu, Liu, Wei, Li, Xinyue, Sierant, Michael C., Mane, Shrikant, Castaldi, Christopher, López-Giráldez, Francesc, Knight, James R., Sekula, Raymond F., Jr., Simard, J. Marc, Eskandar, Emad N., Gottschalk, Christopher, Moliterno, Jennifer, Günel, Murat, Gerrard, Jason L., Dib-Hajj, Sulayman, Waxman, Stephen G., Barker, Fred G., II, Alper, Seth L., Chahine, Mohamed, Haider, Shozeb, De Koninck, Yves, Lifton, Richard P., and Kahle, Kristopher T.

Published
2020
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42. Analysis of self-efficacy and its correlated factors of nursing skill evaluation by nursing interns

Author

ZHANG Qi, ZHANG Yun, FU Chen, ZHANG Wei, ZHAO Xia, ZENG Xue-jun

Subjects
undergraduate nursing interns, nursing assessment, self-efficacy, correlated factor, Medicine
Abstract

Objective To investigate nursing interns' self-efficacy of clinical nursing assessment skills and its influencing factors, both at the middle and the final stages of their internship, so to improve the quality of clinical teaching and students' assessment skills. Methods We used convenience sampling to enroll nursing students who completed their internship in Peking Union Medical College Hospital from January 2016 to December 2017. A self-designed questionnaire was introduced to evaluate their self-efficacy of clinical nursing assessment skills in the middle and the final stages of internship. Differences between the two stages were compared, and influencing factors were analyzed. Results Forty-five students (with junior college diploma or above) were included, with a mean age of (22.0±1.1) years. There were 9 males (18.0%), and the mean interning duration were (6.0±1.4) months in the middle stages of internship and (10.2±1.6) months in the final stage. Scores of self-efficacy at admission were similar between the middle and final stages of internship. However, students at the final stage of internship got significantly higher scores both in total and in therapeutic assessment skills than those in the middle internship stage (77.3±7.9 versus 73.5±11.0, P＜0.05; 38.9±5.9 versus 36.2±7.8,P＜0.05).Gender, age and diploma were related to scores of self-efficacy in the mid-final stage of internship (P＜0.05). Conclusions Clinical teaching played a critical role in the education of nursing students. Targeted teaching measures should be taken to promote their ability of training assessment according to the stages of their internship, their gender, age and diploma, so to further improve the quality of clinical training.

Published
2020

43. A questionnaire on the current situation of patient safety and quality improvement in a tertiary hospital

Author

WANG Yu, ZHANG Yun, ZHAO Dan-qing, CHU Xiao-tian, ZHANG Qi, ZENG Xue-jun

Subjects
patient safety, quality improvement, medical education, job burnout, Medicine
Abstract

Objective To investigate the current situation of improving patient safety and healthcare quality in a tertiary hospital and the understanding of healthcare providers and medical students. Methods A total of 526 valid questionnaires were collected from clinicians, nurses, residents from Peking Union Medical College Hospital(PUMCH) and medical students of Peking Union Medical College(PUMC). Results In the past year, there were 8.2% and 58.8% of the respondents who had experienced medical errors and found potential risks in the clinical process. More than half of respondent's team had reported adverse events, and most of them (75.3%) followed the right way to report. Most people believed hospital authority encouraged reporting medical adverse events, while some of them still worried about potential blame and punishment stemmed from reporting. The results also showed that 88.0% supported development of special curriculum in this field. Some of them had experiences that may have impacts on patient safety in transfer-ring(42.6%)and handover (15.4%), and the majority of people agreed that occupational burnouthas negative impact to patient safety. Almost all the investigation participnts-complained that their emotions and work would be negatively affected if there was a medical error, while 44.5% said that the error also had a positive impact. Conclusions Most of the respondents are relatively satisfied with the current measures of patient safety and quality improvement in PUMCH, but they are still worried about the negative impact on the individuals after the adverse events are reported.

Published
2020

45. Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus

Author

Jin, Sheng Chih, Dong, Weilai, Kundishora, Adam J., Panchagnula, Shreyas, Moreno-De-Luca, Andres, Furey, Charuta G., Allocco, August A., Walker, Rebecca L., Nelson-Williams, Carol, Smith, Hannah, Dunbar, Ashley, Conine, Sierra, Lu, Qiongshi, Zeng, Xue, Sierant, Michael C., Knight, James R., Sullivan, William, Duy, Phan Q., DeSpenza, Tyrone, Reeves, Benjamin C., Karimy, Jason K., Marlier, Arnaud, Castaldi, Christopher, Tikhonova, Irina R., Li, Boyang, Peña, Helena Perez, Broach, James R., Kabachelor, Edith M., Ssenyonga, Peter, Hehnly, Christine, Ge, Li, Keren, Boris, Timberlake, Andrew T., Goto, June, Mangano, Francesco T., Johnston, James M., Butler, William E., Warf, Benjamin C., Smith, Edward R., Schiff, Steven J., Limbrick, Jr, David D., Heuer, Gregory, Jackson, Eric M., Iskandar, Bermans J., Mane, Shrikant, Haider, Shozeb, Guclu, Bulent, Bayri, Yasar, Sahin, Yener, Duncan, Charles C., Apuzzo, Michael L. J., DiLuna, Michael L., Hoffman, Ellen J., Sestan, Nenad, Ment, Laura R., Alper, Seth L., Bilguvar, Kaya, Geschwind, Daniel H., Günel, Murat, Lifton, Richard P., and Kahle, Kristopher T.

Published
2020
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46. Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

Author

Jin, Sheng Chih, Lewis, Sara A., Bakhtiari, Somayeh, Zeng, Xue, Sierant, Michael C., Shetty, Sheetal, Nordlie, Sandra M., Elie, Aureliane, Corbett, Mark A., Norton, Bethany Y., van Eyk, Clare L., Haider, Shozeb, Guida, Brandon S., Magee, Helen, Liu, James, Pastore, Stephen, Vincent, John B., Brunstrom-Hernandez, Janice, Papavasileiou, Antigone, Fahey, Michael C., Berry, Jesia G., Harper, Kelly, Zhou, Chongchen, Zhang, Junhui, Li, Boyang, Zhao, Hongyu, Heim, Jennifer, Webber, Dani L., Frank, Mahalia S. B., Xia, Lei, Xu, Yiran, Zhu, Dengna, Zhang, Bohao, Sheth, Amar H., Knight, James R., Castaldi, Christopher, Tikhonova, Irina R., López-Giráldez, Francesc, Keren, Boris, Whalen, Sandra, Buratti, Julien, Doummar, Diane, Cho, Megan, Retterer, Kyle, Millan, Francisca, Wang, Yangong, Waugh, Jeff L., Rodan, Lance, Cohen, Julie S., Fatemi, Ali, Lin, Angela E., Phillips, John P., Feyma, Timothy, MacLennan, Suzanna C., Vaughan, Spencer, Crompton, Kylie E., Reid, Susan M., Reddihough, Dinah S., Shang, Qing, Gao, Chao, Novak, Iona, Badawi, Nadia, Wilson, Yana A., McIntyre, Sarah J., Mane, Shrikant M., Wang, Xiaoyang, Amor, David J., Zarnescu, Daniela C., Lu, Qiongshi, Xing, Qinghe, Zhu, Changlian, Bilguvar, Kaya, Padilla-Lopez, Sergio, Lifton, Richard P., Gecz, Jozef, MacLennan, Alastair H., and Kruer, Michael C.

Published
2020
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