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CORC

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Identifying phenotype-associated subpopulations by integrating bulk and single-cell sequencing data 期刊论文
NATURE BIOTECHNOLOGY, 2021, 页码: 18
作者:  Sun, Duanchen;  Guan, Xiangnan;  Moran, Amy E.;  Wu, Ling-Yun;  Qian, David Z.
收藏  |  浏览/下载：28/0  |  提交时间：2022/04/02
Small-molecule inhibitor targeting orphan nuclear receptor COUP-TFII for prostate cancer treatment 期刊论文
SCIENCE ADVANCES, 2020, 卷号: 6, 期号: 18, 页码: 11
作者:  Wang, Leiming;  Cheng, Chiang-Min;  Qin, Jun;  Xu, Mafei;  Kao, Chung-Yang
收藏  |  浏览/下载：31/0  |  提交时间：2020/07/01
Missense mutations in LAMA2 causing a new phenotype of mild cognitive impairment proximal myopathy, seizure, and severe leukoencephalopathy: A case report and protein analysis 期刊论文
CLINICAL NEUROPATHOLOGY, 2019, 卷号: 38, 期号: 3
作者:  Ding, Man;  Wang, Xi;  Zeng, Yanping;  Lu, Zuneng;  Cai, Shuang
收藏  |  浏览/下载：36/0  |  提交时间：2019/12/05
Management strategies in facioscapulohumeral muscular dystrophy 期刊论文
INTRACTABLE & RARE DISEASES RESEARCH, 2019, 卷号: 8, 期号: 1
作者:  Lu, Junren;  Yao, Zhenjun;  Yang, Yi;  Zhang, Chi;  Zhang, Jian
收藏  |  浏览/下载：13/0  |  提交时间：2019/12/05
Congenital muscular dystrophies in China 期刊论文
CLINICAL GENETICS, 2019, 卷号: 96, 期号: 3
作者:  Ge, Lin;  Zhang, Cheng;  Wang, Zhaoxia;  Chan, Sophelia H. S.;  Zhu, Wenhua
收藏  |  浏览/下载：36/0  |  提交时间：2019/12/05
Missense mutations in LAMA2 causing a new phenotype of mild cognitive impairment proximal myopathy, seizure, and severe leukoencephalopathy: A case report and protein analysis 期刊论文
CLINICAL NEUROPATHOLOGY, 2019, 卷号: 38, 期号: 3
作者:  Ding, Man;  Wang, Xi;  Zeng, Yanping;  Lu, Zuneng;  Cai, Shuang
收藏  |  浏览/下载：24/0  |  提交时间：2019/12/05
Can urinary titin be used for predicting Duchenne muscular dystrophy? 期刊论文
CLINICA CHIMICA ACTA, 2019, 卷号: 490, 页码: 161-161
作者:  Bai, Shu-Mei;  Guo, Xu-Xiao
收藏  |  浏览/下载：1/0  |  提交时间：2019/12/11
Congenital muscular dystrophies in China 期刊论文
CLINICAL GENETICS, 2019, 卷号: 96, 期号: 3, 页码: 207-215
作者:  Ge, Lin;  Zhang, Cheng;  Wang, Zhaoxia;  Chan, Sophelia H. S.;  Zhu, Wenhua
收藏  |  浏览/下载：13/0  |  提交时间：2019/12/11
Molecular Genetics Analysis of 70 Chinese Families With Muscular Dystrophy Using Multiplex Ligation-Dependent Probe Amplification and Next-Generation Sequencing 期刊论文
FRONTIERS IN PHARMACOLOGY, 2019, 卷号: 10
作者:  Wang, Dong;  Gao, Min;  Zhang, Kaihui;  Jin, Ruifeng;  Lv, Yuqiang
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/11
Limb girdle muscular dystrophy D3 HNRNPDL related in a Chinese family with distal muscle weakness caused by a mutation in the prion-like domain. 期刊论文
Journal of neurology, 2019
作者:  Sun Yanan;  Chen Hai;  Lu Yan;  Duo Jianying;  Lei Lin
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/13

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