CORC

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CORC

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Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese 期刊论文
NATIONAL SCIENCE REVIEW, 2019, 卷号: 6, 期号: 2, 页码: 257-274
作者:  Zhang, Deng-Feng;  Fan, Yu;  Xu, Min;  Wang, Guihong;  Wang, Dong
收藏  |  浏览/下载：64/0  |  提交时间：2019/07/11
EGFR signaling confers resistance to BET inhibition in hepatocellular carcinoma through stabilizing oncogenic MYC 期刊论文
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2019, 卷号: 38, 页码: 15
作者:  Qin, Jianhua;  Liu, Yang;  Yin, Yalei;  Sun, Mingju;  Zhan, Xi
收藏  |  浏览/下载：107/0  |  提交时间：2019/06/20
Egfr signaling confers resistance to bet inhibition in hepatocellular carcinoma through stabilizing oncogenic myc 期刊论文
Journal of experimental & clinical cancer research, 2019, 卷号: 38, 页码: 15
作者:  Yin, Yalei;  Sun, Mingju;  Zhan, Xi;  Wu, Changqing;  Geng, Pengyu
收藏  |  浏览/下载：137/0  |  提交时间：2019/05/08
Whole-Exome Sequencing Identified a Novel Compound Heterozygous Genotype in ASL in a Chinese Han Patient with Argininosuccinate Lyase Deficiency 期刊论文
BIOMED RESEARCH INTERNATIONAL, 2019, 页码: 7
作者:  Zhao, Mei;  Hou, Lingling;  Teng, Huajing;  Li, Jinchen;  Wang, Jiesi
收藏  |  浏览/下载：59/0  |  提交时间：2019/06/12
[Clinical application of whole exome sequencing in monogenic hereditary disorders in critically ill newborns]. 期刊论文
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2019, 卷号: 21, 期号: 7
作者:  Qi Zhi-Ye;  Duan Jiang;  He Xiang-Ying;  Zhong Qing-Hua;  Zhang Cai-Ying
收藏  |  浏览/下载：21/0  |  提交时间：2019/12/04
PTCH1 alterations are frequent but other genetic alterations are rare in sporadic odontogenic keratocysts. 期刊论文
Oral diseases, 2019
作者:  Qu Jiafei;  Zhang Jianyun;  Zhang Heyu;  Li Xuefen;  Hong Yingying
收藏  |  浏览/下载：22/0  |  提交时间：2019/12/04
Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese 期刊论文
国家科学评论, 2019, 卷号: 6, 期号: 2
作者:  Zhang Dengfeng;  Fan Yu;  Xu Min;  Wang Guihong;  Wang Dong
收藏  |  浏览/下载：34/0  |  提交时间：2019/12/04
A family with Danon disease caused by a splice site mutation in LAMP2 that generates a truncated protein 期刊论文
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 卷号: 7, 期号: 3
作者:  Tang, Lu;  Sun, Minmin;  Pan, Cuizhen;  Shu, Xianhong;  Zhou, Nianwei
收藏  |  浏览/下载：41/0  |  提交时间：2019/12/05
Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype-phenotype correlations 期刊论文
HUMAN GENETICS, 2019, 卷号: 138, 期号: 1
作者:  Wang, Xiuxia;  Wang, Qiqi;  Li, Da;  Cai, Baozhu;  Chen, Qing
收藏  |  浏览/下载：25/0  |  提交时间：2019/12/05
Whole-exome sequencing reveals a novel mutation of MT-ND5 gene in a mitochondrial cardiomyopathy pedigree: Patients who show biventricular hypertrophy, hyperlactacidemia, pulmonary hypertension, and decreased exercise tolerance 期刊论文
ANATOLIAN JOURNAL OF CARDIOLOGY, 2019, 卷号: 21, 期号: 1
作者:  Zhou, Nianwei;  Tang, Lu;  Jiang, Yingying;  Qin, Shengmei;  Cui, Jie
收藏  |  浏览/下载：81/0  |  提交时间：2019/12/05

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