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浏览/检索结果: 共9条，第1-9条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations 期刊论文 HUMAN MUTATION, 2017 Dou, Yanmei; Yang, Xiaoxu; Li, Ziyi; Wang, Sheng; Zhang, Zheng; Ye, Adam Yongxin; Yan, Linlin; Yang, Changhong; Wu, Qixi; Li, Jiarui; Zhao, Boxun; Huang, August Yue; Wei, Liping 收藏  |  浏览/下载：121/0  |  提交时间：2017/12/03 autism spectrum disorder  autistic traits  parental mosaicism  single-nucleotide mosaicism  DE-NOVO MUTATIONS  INTERACTION NETWORKS  SOMATIC MOSAICISM  DRAVET SYNDROME  HUMAN-DISEASE  GENETIC RISK  HUMAN BRAIN  EVOLUTION  PATTERNS  GENOME   MosaicHunter: accurate detection of postzygotic single-nucleotide mosaicism through next-generation sequencing of unpaired, trio, and paired samples 期刊论文 NUCLEIC ACIDS RESEARCH, 2017 Huang, August Yue; Zhang, Zheng; Ye, Adam Yongxin; Dou, Yanmei; Yan, Linlin; Yang, Xiaoxu; Zhang, Yuehua; Wei, Liping 收藏  |  浏览/下载：6/0  |  提交时间：2017/12/03 MONOZYGOTIC TWINS DISCORDANT  SOMATIC POINT MUTATIONS  HUMAN CANCER GENOMES  DE-NOVO MUTATIONS  WHOLE-GENOME  COPY NUMBER  CLONAL HEMATOPOIESIS  HUMAN TISSUES  VARIANT  IDENTIFICATION   Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome 期刊论文 HUMAN MUTATION, 2015 Xu, Xiaojing; Yang, Xiaoxu; Wu, Qixi; Liu, Aijie; Yang, Xiaoling; Ye, Adam Yongxin; Huang, August Yue; Li, Jiarui; Wang, Meng; Yu, Zhe; Wang, Sheng; Zhang, Zhichao; Wu, Xiru; Wei, Liping; Zhang, Yuehua 收藏  |  浏览/下载：5/0  |  提交时间：2017/12/03 de novo  mosaic  Dravet syndrome  SCN1A  next-generation sequencing  somatic mutation  SEVERE MYOCLONIC EPILEPSY  AUTISM SPECTRUM DISORDERS  HUMAN GENETIC-DISEASE  SOMATIC MOSAICISM  MISSENSE MUTATION  FEBRILE SEIZURES  POINT MUTATIONS  DENOVO MUTATION  MARFAN-SYNDROME  ALPORT-SYNDROME   Single cell sequencing: technique, application, and future development 期刊论文 science bulletin, 2015 Xue, Ruidong; Li, Ruoyan; Bai, Fan 收藏  |  浏览/下载：3/0  |  提交时间：2015/11/10 Single cell isolation  Genetic heterogeneity  Single cell genome sequencing  Single cell transcriptome sequencing  Single cell methylome sequencing  CIRCULATING TUMOR-CELLS  EMBRYONIC STEM-CELLS  MULTIPLE DISPLACEMENT AMPLIFICATION  COPY NUMBER VARIATION  MESSENGER-RNA-SEQ  GENE-EXPRESSION  MAMMALIAN DEVELOPMENT  DNA  SPERM  SCALE   KRAS G12D mosaic mutation in a Chinese linear nevus sebaceous syndrome infant 期刊论文 BMC MEDICAL GENETICS, 2015, 卷号: 16 作者:  Wang, Huijun;  Qian, Yanyan;  Wu, Bingbing;  Zhang, Ping;  Zhou, Wenhao 收藏  |  浏览/下载：5/0  |  提交时间：2019/12/13 Linear Nevus Sebaceous Syndrome (LNSS)  KRAS  Somatic Mosaicism  Epilepsy   信息推送-NIH院外研究处2014年1月至7月14日发布的基金资助计划 其他 2014-07-28 作者:  王玮 收藏  |  浏览/下载：29/0  |  提交时间：2014/07/28 Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals 期刊论文 细胞研究英文版, 2014 Huang, August Y.; Xu, Xiaojing; Ye, Adam Y.; Wu, Qixi; Yan, Linlin; Zhao, Boxun; Yang, Xiaoxu; He, Yao; Wang, Sheng; Zhang, Zheng; Gu, Bowen; Zhao, Han-Qing; Wang, Meng; Gao, Hua; Gao, Ge; Zhang, Zhichao; Yang, Xiaoling; Wu, Xiru; Zhang, Yuehua; Wei, Liping 收藏  |  浏览/下载：6/0  |  提交时间：2015/11/11 single-nucleotide mutation  postzygotic mosaicism  Dravet syndrome  next-generation sequencing  Bayesian model  DETECTABLE CLONAL MOSAICISM  SOMATIC MUTATIONS  DRAVET SYNDROME  MATERNAL MICROCHIMERISM  SENSITIVE DETECTION  HUMAN TISSUES  PIK3CA CAUSE  HUMAN BRAIN  CANCER  DISEASE   Reevaluation of the safety of induced pluripotent stem cells: a call from somatic mosaicism 期刊论文 PROTEIN & CELL, 2013, 卷号: 4, 期号: 2, 页码: 83-85 Liu, Wensu; Li, Ming; Qu, Jing; Yi, Fei; Liu, Guanghui; 刘光慧 收藏  |  浏览/下载：16/0  |  提交时间：2013/12/24 Embryonic and genetic manipulation in fish 期刊论文 CELL RESEARCH, 2000, 卷号: 10, 期号: 1, 页码: 17-27 作者:  Zhu, ZY;  Sun, YH 收藏  |  浏览/下载：18/0  |  提交时间：2010/10/13 fish  nuclear transplantation  transgenic fish  gene targeting