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CORC

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Deregulated Gab2 phosphorylation mediates aberrant AKT and STAT3 signaling upon PIK3R1 loss in ovarian cancer 期刊论文
NATURE COMMUNICATIONS, 2019, 卷号: 10
作者:  Li, Xinran;  Wang, Chao;  Zhou, Yuan;  Mak, Victor C. Y.;  Cheung, Lydia W. T.
收藏  |  浏览/下载：19/0  |  提交时间：2019/12/05
Single-Cell Transcriptomics Uncovers Glial Progenitor Diversity and Cell Fate Determinants during Development and Gliomagenesis 期刊论文
CELL STEM CELL, 2019, 卷号: 24, 期号: 5
作者:  Verma, Ravinder;  Weng, Qinjie;  Wang, Jincheng;  Wang, Jiajia;  He, Danyang
收藏  |  浏览/下载：69/0  |  提交时间：2019/12/05
Novel Strategies Targeting Obesity and Metabolic Diseases 期刊论文
FRONTIERS IN PHYSIOLOGY, 2019, 卷号: 10
作者:  Ma, Xinran;  Feng, Dechun;  Lu, Yan;  Sun, Nuo;  Wang, Jiqiu
收藏  |  浏览/下载：15/0  |  提交时间：2019/12/05
Silver nanoparticles inhibit beige fat function and promote adiposity 期刊论文
MOLECULAR METABOLISM, 2019, 卷号: 22
作者:  Yue, Lishu;  Zhao, Wenjun;  Wang, Dongmei;  Meng, Meiyao;  Zheng, Ying
收藏  |  浏览/下载：28/0  |  提交时间：2019/12/05
Data on mutations and Clinical features in SCN1A or SCN2A gene 期刊论文
DATA IN BRIEF, 2019, 卷号: 22
作者:  Kong, Yanting;  Yan, Kai;  Hu, Liyuan;  Wang, Mingbang;  Dong, Xinran
收藏  |  浏览/下载：29/0  |  提交时间：2019/12/05
Early onset developmental delay and epilepsy in pediatric patients with WDR45 variants 期刊论文
EUROPEAN JOURNAL OF MEDICAL GENETICS, 2019, 卷号: 62, 期号: 2
作者:  Chen, Hongbo;  Qian, Yanyan;  Yu, Sha;  Xiao, Deyong;  Guo, Xiao
收藏  |  浏览/下载：20/0  |  提交时间：2019/12/05
Clinical and genetic spectrum of a large cohort of children with epilepsy in China 期刊论文
GENETICS IN MEDICINE, 2019, 卷号: 21, 期号: 3
作者:  Yang, Lin;  Kong, Yanting;  Dong, Xinran;  Hu, Liyuan;  Lin, Yifeng
收藏  |  浏览/下载：28/0  |  提交时间：2019/12/05
One Novel 2.43Kb Deletion and One Single Nucleotide Mutation of the INSR Gene in a Chinese Neonate with Rabson-Mendenhall Syndrome 期刊论文
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, 2018, 卷号: 10, 期号: 2
作者:  Chen, Xiang;  Wang, Huijun;  Wu, Bingbing;  Dong, Xinran;  Liu, Bo
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05
Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures 期刊论文
CLINICA CHIMICA ACTA, 2018, 卷号: 483
作者:  Kong, Yanting;  Yan, Kai;  Hu, Liyuan;  Wang, Mingbang;  Dong, Xinran
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05
Speech and language delay in a patient with WDR4 mutations 期刊论文
EUROPEAN JOURNAL OF MEDICAL GENETICS, 2018, 卷号: 61, 期号: 8
作者:  Wu, Bingbing;  Chen, Xiang;  Gao, Yanyan;  Yang, Lin;  Dong, Xinran
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/05

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