Resultats de la cerca - Adam Yongxin Ye
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MosaicHunter: accurate detection of postzygotic single-nucleotide mosaicism through next-generation sequencing of unpaired, trio, and paired samples per August Yue Huang, Zheng Zhang, Adam Yongxin Ye, Yanmei Dou, Linlin Yan, Xiaoxu Yang, Yuehua Zhang, Liping Wei
Publicat 2017Artigo -
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Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals per Boxun Zhao, Qixi Wu, Adam Yongxin Ye, Jing Guo, Xianing Zheng, Xiaoxu Yang, Linlin Yan, Qing‐Rong Liu, Thomas M. Hyde, Liping Wei, August Yue Huang
Publicat 2019Artigo -
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Postzygotic single‐nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations per Yanmei Dou, Xiaoxu Yang, Ziyi Li, Sheng Wang, Zheng Zhang, Adam Yongxin Ye, Linlin Yan, Changhong Yang, Qixi Wu, Jiarui Li, Boxun Zhao, August Yue Huang, Liping Wei
Publicat 2017Artigo -
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Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort per Xiaoxu Yang, Aijie Liu, Xiaojing Xu, Xiaoling Yang, Qi Zeng, Adam Yongxin Ye, Zhe Yu, Sheng Wang, August Yue Huang, Xiru Wu, Qixi Wu, Liping Wei, Yuehua Zhang
Publicat 2017Artigo -
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Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “ <i>de novo</i> ” <i>SCN1A</i> Mutations in Children with Dravet Syndrome per Xiaojing Xu, Xiaoxu Yang, Qixi Wu, Aijie Liu, Xiaoling Yang, Adam Yongxin Ye, August Yue Huang, Jiarui Li, Meng Wang, Zhe Yu, Sheng Wang, Zhichao Zhang, Xiru Wu, Liping Wei, Yuehua Zhang
Publicat 2015Artigo -
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Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype–phenotype correlations per Wei‐Zhen Zhou, Jie Zhang, Ziyi Li, Xiaojing Lin, Jiarui Li, Sheng Wang, Changhong Yang, Qixi Wu, Adam Yongxin Ye, Meng Wang, Dandan Wang, Tad Zhengzhang Pu, Yu‐Yu Wu, Liping Wei
Publicat 2019Artigo -
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AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder per Changhong Yang, Jiarui Li, Qixi Wu, Xiaoxu Yang, August Yue Huang, Yuehua Zhang, Adam Yongxin Ye, Yanmei Dou, Linlin Yan, Wei‐Zhen Zhou, Lei Kong, Meng Wang, Ai Chen, De-Chang Yang, Liping Wei
Publicat 2018Artigo -
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Loop extrusion mediates physiological Igh locus contraction for RAG scanning per Hai-Qiang Dai, Hongli Hu, Jiangman Lou, Adam Yongxin Ye, Zhaoqing Ba, Xuefei Zhang, Yiwen Zhang, Lijuan Zhao, Hye Suk Yoon, Aimee Williams, Nia Kyritsis, Huan Chen, Kerstin Johnson, Sherry Lin, A. Conte, Rafael Casellas, Cheng‐Sheng Lee, Frederick W. Alt
Publicat 2021Artigo -
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Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals per August Yue Huang, Xiaojing Xu, Adam Yongxin Ye, Qixi Wu, Linlin Yan, Boxun Zhao, Xiaoxu Yang, Yao He, Sheng Wang, Zheng Zhang, Bowen Gu, Hanqing Zhao, Meng Wang, Hua Gao, Ge Gao, Zhichao Zhang, Xiaoling Yang, Xiru Wu, Yuehua Zhang, Liping Wei
Publicat 2014Artigo -
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Generation of a live attenuated influenza A vaccine by proteolysis targeting per Longlong Si, Quan Shen, Jing Li, Li Chen, Jinying Shen, Xue Xiao, Haiqing Bai, Tang Feng, Adam Yongxin Ye, Le Li, Chunhe Zhang, Zhen Li, Ping Wang, Crystal Yuri Oh, Atiq Nurani, Siwen Niu, Chengxin Zhang, Xiaoqiong Wei, Wanqiong Yuan, Hao Liao, Xiaojie Huang, Ning Wang, Wen‐xia Tian, Hongwei Tian, Li Li, Xiaoheng Liu, Roberto Plebani
Publicat 2022Artigo -
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An antibody from single human V <sub>H</sub> -rearranging mouse neutralizes all SARS-CoV-2 variants through BA.5 by inhibiting membrane fusion per Sai Luo, Jun Zhang, Alex J.B. Kreutzberger, Amanda Eaton, Robert J. Edwards, Changbin Jing, Hai-Qiang Dai, Gregory D. Sempowski, Kenneth Cronin, Robert Parks, Adam Yongxin Ye, Katayoun Mansouri, Maggie Barr, Novalia Pishesha, Aimee Williams, Lucas Vieira Francisco, Anand Saminathan, Hanqin Peng, Himanshu Batra, Lorenza Bellusci, Surender Khurana, S. Munir Alam, David C. Montefiori, Kevin O. Saunders, Ming Tian, Hidde L. Ploegh, Tomas Kirchhausen, Bing Chen, Barton F. Haynes, Frederick W. Alt
Publicat 2022Artigo -
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De Novo Insertions and Deletions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder per Shan Dong, Michael F. Walker, Nicholas Carriero, Michael DiCola, A. Jeremy Willsey, Adam Yongxin Ye, Zainulabedin Waqar, Luis Eduardo González, John D. Overton, Stephanie Frahm, John F. Keaney, Nicole A. Teran, Jeanselle Dea, Jeffrey D. Mandell, Vanessa H. Bal, Catherine Sullivan, Nicholas M. DiLullo, Rehab O. Khalil, Jake Gockley, Zafer Yüksel, Sinem M Sertel, A. Gulhan Ercan‐Sencicek, Abha R. Gupta, Shrikant Mane, Michael Sheldon, Andrew I. Brooks, Kathryn Roeder, Bernie Devlin, Matthew W. State, Liping Wei, Stephan Sanders
Publicat 2014Artigo
Eines de cerca:
Matèries relacionades
Biology
Genetics
Gene
Mutation
Allele
Autism
Autism spectrum disorder
Computational biology
Genome
Genotype
Neuroscience
Proband
Cell biology
Developmental psychology
Dravet syndrome
Epilepsy
Molecular biology
Psychology
Single-nucleotide polymorphism
Antibody
Biochemistry
CTCF
Computer science
DNA
Enhancer
Exome sequencing
Immunoglobulin light chain
Immunology
Indel
Locus (genetics)