QQ客服 官方微博 反馈留言

浏览/检索结果: 共15条，第1-10条 帮助 限定条件 专题：北京大学    第一署名单位    第一作者单位    通讯作者单位     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 Cell Culture System for Analysis of Genetic Heterogeneity Within Hepatocellular Carcinomas and Response to Pharmacologic Agents 其他 2017-01-01 Gao, Qiang; Wang, Zhi-Chao; Duan, Meng; Lin, Yi-Hui; Zhou, Xue-Ya; Worthley, Daniel L.; Wang, Xiao-Ying; Niu, Gang; Xia, Yuchao; Deng, Minghua; Liu, Long-Zi; Shi, Jie-Yi; Yang, Liu-Xiao; Zhang, Shu; Ding, Zhen-Bin; Zhou, Jian; Liang, Chun-Min; Cao, Ya; Xiong, Lei; Xi, Ruibin; Shi, Yong-Yong; Fan, Jia 收藏  |  浏览/下载：35/0  |  提交时间：2017/12/04 Liver Cancer  Next-Generation Sequencing  Patient-Derived Cell Lines  Targeted Therapy  INTRATUMOR HETEROGENEITY  GENOMIC HETEROGENEITY  TUMOR HETEROGENEITY  DRUG-SENSITIVITY  SEQUENCING DATA  CANCER-CELLS  LIVER-CANCER  MUTATIONS  EVOLUTION  SORAFENIB   pBACode: a random-barcode-based high-throughput approach for BAC paired-end sequencing and physical clone mapping 期刊论文 NUCLEIC ACIDS RESEARCH, 2017 Wei, Xiaolin; Xu, Zhichao; Wang, Guixing; Hou, Jilun; Ma, Xiaopeng; Liu, Haijin; Liu, Jiadong; Chen, Bo; Luo, Meizhong; Xie, Bingyan; Li, Ruiqiang; Ruan, Jue; Liu, Xiao 收藏  |  浏览/下载：9/0  |  提交时间：2017/12/03 GENOME SEQUENCE  LIBRARY CONSTRUCTION  QUALITY ASSESSMENT  PROVIDES INSIGHTS  IN-VITRO  EVOLUTION  MAP  ILLUMINA  PROJECT  INFORMATION   Gene mutation analysis of 175 Chinese patients with early-onset epileptic encephalopathy 期刊论文 CLINICAL GENETICS, 2017 Zhang, Q.; Li, J.; Zhao, Y.; Bao, X.; Wei, L.; Wang, J. 收藏  |  浏览/下载：4/0  |  提交时间：2017/12/03 CDKL5  early-onset epileptic encephalopathy  KCNQ2  recommending treatment  targeted next-generation sequencing  KCNQ2 ENCEPHALOPATHY  POTASSIUM CHANNEL  CDKL5  SPECTRUM  LOCALIZATION  EPILEPSIES  QUINIDINE  INFANCY  GAIN   Application of Single-cell Sequencing Technologies in Reproductive Medicine 期刊论文 生殖与发育医学（英文）, 2017 Peng Yuan; Li-Ying Yan; Jie Qiao 收藏  |  浏览/下载：2/0  |  提交时间：2017/12/03 Early Embryonic Development Multi-omics Assay Reproductive Medicine Single-cell Sequencing  Early Embryonic Development  Multi-omics Assay  Reproductive Medicine  Single-cell Sequencing   A mutation in ADIPOR1 causes nonsyndromic autosomal dominant retinitis pigmentosa 期刊论文 HUMAN GENETICS, 2016 Zhang, Jinlu; Wang, Changguan; Shen, Yan; Chen, Ningning; Wang, Likun; Liang, Ling; Guo, Tong; Yin, Xiaobei; Ma, Zhizhong; Zhang, Bo; Yang, Liping 收藏  |  浏览/下载：2/0  |  提交时间：2017/12/04 DOCOSAHEXAENOIC ACID  ADIPONECTIN RECEPTOR  MACULAR DEGENERATION  MOLECULAR DIAGNOSIS  DIABETES-MELLITUS  CELL-SURVIVAL  NEOVASCULARIZATION  RETINOPATHY  EXPRESSION  DISEASES   Questions about NgAgo 期刊论文 PROTEIN & CELL, 2016 Burgess, Shawn; Cheng, Linzhao; Gu, Feng; Huang, Junjiu; Huang, Zhiwei; Lin, Shuo; Li, Jinsong; Li, Wei; Qin, Wei; Sun, Yujie; Zhou Songyang; Wei, Wensheng; Wu, Qiang; Wang, Haoyi; Wang, Xiaoqun; Xiong, Jing-Wei; Xi, Jianzhong; Yang, Hui; Zhou, Bin; Zhang, Bo 收藏  |  浏览/下载：4/0  |  提交时间：2017/12/03 2015年中国动物遗传学研究领域若干重要进展 期刊论文 遗传, 2016 张博; 陈晓芳; 黄勋; 杨晓 收藏  |  浏览/下载：5/0  |  提交时间：2017/12/04 中国  动物遗传学  研究进展  2015年  China  animal genetics  research advances  2015   Efficient bi-allelic gene knockout and site-specific knock-in mediated by TALENs in pigs 会议论文 Yao Jing; HUANG Jiao-jiao; HAI Tang; WANG Xian-long; QIN Guo-song; ZHANG Hong-yong; WU Rong; CAO Chun-wei; XI Jian-zhong; ZHOU Qi; YUAN Zeng-qiang; ZHAO Jian-guo 收藏  |  浏览/下载：3/0  |  提交时间：2017/12/03 TALENs  GGTA1  Parkin  DJ-1  Pig  TALENs  GGTA1  Parkin  DJ-1  Pig   A large-scale screen for coding variants predisposing to psoriasis 期刊论文 nature genetics, 2014 Tang, Huayang; Jin, Xin; Li, Yang; Jiang, Hui; Tang, Xianfa; Yang, Xu; Cheng, Hui; Qiu, Ying; Chen, Gang; Mei, Junpu; Zhou, Fusheng; Wu, Renhua; Zuo, Xianbo; Zhang, Yong; Zheng, Xiaodong; Cai, Qi; Yin, Xianyong; Quan, Cheng; Shao, Haojing; Cui, Yong; Tian, Fangzhen; Zhao, Xia; Liu, Hong; Xiao, Fengli; Xu, Fengping; Han, Jianwen; Shi, Dongmei; Zhang, Anping; Zhou, Cheng; Li, Qibin; Fan, Xing; Lin, Liya; Tian, Hongqing; Wang, Zaixing; Fu, Huiling; Wang, Fang; Yang, Baoqi; Huang, Shaowei; Liang, Bo; Xie, Xuefeng; Ren, Yunqing; Gu, Qingquan; Wen, Guang 收藏  |  浏览/下载：9/0  |  提交时间：2015/11/13 GENOME-WIDE ASSOCIATION  INFLAMMATORY-BOWEL-DISEASE  SUSCEPTIBILITY LOCI  COMMON VARIANTS  RARE VARIANTS  MISSING HERITABILITY  SEQUENCING DATA  COMPLEX DISEASES  LOW-FREQUENCY  ARTHRITIS   Mutation of POC1B in a Severe Syndromic Retinal Ciliopathy 期刊论文 human mutation, 2014 Beck, Bodo B.; Phillips, Jennifer B.; Bartram, Melte P.; Wegner, Jeremy; Thoenes, Michaele; Pannes, Andrea; Sampson, Josephina; Heller, Raoul; Goebel, Heike; Koerber, Friederike; Neugebauer, Antje; Hedergott, Andrea; Nuernberg, Gudrun; Nuernberg, Peter; Thiele, Holger; Altmueller, Janine; Toliat, Mohammad R.; Staubach, Simon; Boycott, Kym M.; Valente, Enza Maria; Janecke, Andreas R.; Eisenberger, Tobias; Bergmann, Carsten; Tebbe, Lars; Wang, Yang; Wu, Yundong; Fry, Andrew M.; Westerfield, Monte; Wolfrum, Uwe; Bolz, Hanno J. 收藏  |  浏览/下载：4/0  |  提交时间：2015/11/11 POC1B  LCA  Joubert syndrome  cliopathy  zebrafish  LEBER CONGENITAL AMAUROSIS  SENIOR-LOKEN SYNDROME  JOUBERT-SYNDROME  LINKAGE ANALYSIS  DOMAIN PROTEIN  CILIARY  GENE  DISEASE  CELLS  NEPHRONOPHTHISIS