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浏览/检索结果: 共6条，第1-6条 帮助 限定条件 发表日期：2017    专题：复旦大学上海医学院    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 Hypomethylation and decreased expression of BRG1 in the myocardium of patients with congenital heart disease 期刊论文 BIRTH DEFECTS RESEARCH, 2017, 卷号: 109, 期号: 15 作者:  Qian, Yanyan;  Xiao, Deyong;  Guo, Xiao;  Chen, Hongbo;  Hao, Lili 收藏  |  浏览/下载：5/0  |  提交时间：2019/12/05 congenital heart disease (CHD)  BRG1  DNA methylation  GATA4  gene expression   Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation 期刊论文 JOURNAL OF TRANSLATIONAL MEDICINE, 2017, 卷号: 15 作者:  Qian, Yanyan;  Xiao, Deyong;  Guo, Xiao;  Chen, Hongbo;  Hao, Lili 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/05 Congenital heart disease (CHD)  Next-generation sequencing  Functional study  Multigene disease  Variants   Mutations in Interleukin-10 Receptor and Clinical Phenotypes in Patients with Very Early Onset Inflammatory Bowel Disease: A Chinese VEO-IBD Collaboration Group Survey 期刊论文 INFLAMMATORY BOWEL DISEASES, 2017, 卷号: 23, 期号: 4 作者:  Huang, Zhiheng;  Peng, Kaiyue;  Li, Xiaoqin;  Zhao, Ruiqin;  You, Jieyu 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/05 IL10  IL10 receptor  very early onset inflammatory bowel diseases  Chinese children   A RASSF1A 133 single-nucleotide polymorphism is associated with increased susceptibility and unfavorable prognosis in non-small cell lung cancer 期刊论文 INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2017, 卷号: 10, 期号: 7 作者:  Wang, An;  Hou, Likun;  Huang, Dayu;  Zhang, Huijun;  Wang, Shaohua 收藏  |  浏览/下载：7/0  |  提交时间：2019/12/05 RASSF1A SNP  prognosis  tumor-suppressor gene (TSG)  NSCLC  EGFR mutation   A genome-wide association study identifies six novel risk loci for primary biliary cholangitis 期刊论文 NATURE COMMUNICATIONS, 2017, 卷号: 8 作者:  Huang, Lihua;  Qing, Zhuye;  Wu, Jianfang;  Huang, Qinghai;  Han, Junhai 收藏  |  浏览/下载：29/0  |  提交时间：2019/12/05 Whole genome sequencing identifies a novel ALMS1 gene mutation in two Chinese siblings with Alstrom syndrome 期刊论文 BMC MEDICAL GENETICS, 2017, 卷号: 18 作者:  Yang, Lin;  Li, Zixiu;  Mei, Mei;  Fan, Xiaomei;  Zhan, Guodong 收藏  |  浏览/下载：7/0  |  提交时间：2019/12/05 Alstrom syndrome  Whole genome sequencing  ALMS1 gene  Cone-rod dystrophy