Ohcanbohtosat - Adam Yongxin Ye

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  1. 1
    A Guide RNA Sequence Design Platform for the CRISPR/Cas9 System for Model Organism Genomes

    A Guide RNA Sequence Design Platform for the CRISPR/Cas9 System for Model Organism Genomes Dahkki Ming Ma, Adam Yongxin Ye, Weiguo Zheng, Lei Kong

    Almmustuhtton 2013
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  2. 2
    MosaicHunter: accurate detection of postzygotic single-nucleotide mosaicism through next-generation sequencing of unpaired, trio, and paired samples

    MosaicHunter: accurate detection of postzygotic single-nucleotide mosaicism through next-generation sequencing of unpaired, trio, and paired samples Dahkki August Yue Huang, Zheng Zhang, Adam Yongxin Ye, Yanmei Dou, Linlin Yan, Xiaoxu Yang, Yuehua Zhang, Liping Wei

    Almmustuhtton 2017
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  3. 3
    Profiling the RNA editomes of wild-type <i>C. elegans</i> and ADAR mutants

    Profiling the RNA editomes of wild-type <i>C. elegans</i> and ADAR mutants Dahkki Hanqing Zhao, Pan Zhang, Hua Gao, Xiandong He, Yanmei Dou, August Yue Huang, Ximing Liu, Adam Yongxin Ye, Meng‐Qiu Dong, Liping Wei

    Almmustuhtton 2014
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  4. 4
    Molecular basis for differential Igk versus Igh V(D)J joining mechanisms

    Molecular basis for differential Igk versus Igh V(D)J joining mechanisms Dahkki Yiwen Zhang, Xiang Li, Zhaoqing Ba, Jiangman Lou, K. Elyse Gaertner, T N Zhu, Xin Lin, Adam Yongxin Ye, Frederick W. Alt, Hongli Hu

    Almmustuhtton 2024
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  5. 5
    Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals

    Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals Dahkki 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

    Almmustuhtton 2019
    Viečča ollesdeavstta
    Artigo
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  6. 6
    Postzygotic single‐nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations

    Postzygotic single‐nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations Dahkki 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

    Almmustuhtton 2017
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  7. 7
    Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort

    Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort Dahkki 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

    Almmustuhtton 2017
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  8. 8
    CTCF orchestrates long-range cohesin-driven V(D)J recombinational scanning

    CTCF orchestrates long-range cohesin-driven V(D)J recombinational scanning Dahkki Zhaoqing Ba, Jiangman Lou, Adam Yongxin Ye, Hai-Qiang Dai, Edward W. Dring, Sherry Lin, Suvi Jain, Nia Kyritsis, Kyong-Rim Kieffer-Kwon, Rafael Casellas, Frederick W. Alt

    Almmustuhtton 2020
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    Artigo
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  9. 9
    BCR selection and affinity maturation in Peyer’s patch germinal centres

    BCR selection and affinity maturation in Peyer’s patch germinal centres Dahkki Huan Chen, Yuxiang Zhang, Adam Yongxin Ye, Zhou Du, Mo Xu, Cheng‐Sheng Lee, Joyce K. Hwang, Nia Kyritsis, Zhaoqing Ba, Donna Neuberg, Dan R. Littman, Frederick W. Alt

    Almmustuhtton 2020
    Viečča ollesdeavstta
    Artigo
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  10. 10
    Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “ <i>de novo</i> ” <i>SCN1A</i> Mutations in Children with Dravet Syndrome

    Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “ <i>de novo</i> ” <i>SCN1A</i> Mutations in Children with Dravet Syndrome Dahkki 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

    Almmustuhtton 2015
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  11. 11
    Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype–phenotype correlations

    Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype–phenotype correlations Dahkki 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

    Almmustuhtton 2019
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  12. 12
    AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder

    AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder Dahkki 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

    Almmustuhtton 2018
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  13. 13
    Loop extrusion mediates physiological Igh locus contraction for RAG scanning

    Loop extrusion mediates physiological Igh locus contraction for RAG scanning Dahkki 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

    Almmustuhtton 2021
    Viečča ollesdeavstta
    Artigo
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  14. 14
    Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals

    Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals Dahkki 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

    Almmustuhtton 2014
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  15. 15
    Generation of a live attenuated influenza A vaccine by proteolysis targeting

    Generation of a live attenuated influenza A vaccine by proteolysis targeting Dahkki 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

    Almmustuhtton 2022
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  16. 16
    An antibody from single human V <sub>H</sub> -rearranging mouse neutralizes all SARS-CoV-2 variants through BA.5 by inhibiting membrane fusion

    An antibody from single human V <sub>H</sub> -rearranging mouse neutralizes all SARS-CoV-2 variants through BA.5 by inhibiting membrane fusion Dahkki 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

    Almmustuhtton 2022
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  17. 17
    De Novo Insertions and Deletions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder

    De Novo Insertions and Deletions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder Dahkki 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

    Almmustuhtton 2014
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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