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Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders 期刊论文
American Journal of Human Genetics, 2019, 卷号: 105, 期号: 1, 页码: 166-176
作者:  Tian, Yun;  Wang, Jun-Ling;  Huang, Wen;  Zeng, Sheng;  Jiao, Bin
收藏  |  浏览/下载:21/0  |  提交时间:2019/12/27
Fragile X-Associated Tremor/Ataxia Syndrome: From Molecular Pathogenesis to Development of Therapeutics. 期刊论文
FRONTIERS IN CELLULAR NEUROSCIENCE, 2017, 卷号: 11, 页码: 128
作者:  Kong, Ha Eun;  Zhao, Juan;  Xu, Shunliang;  Jin, Peng*;  Jin, Yan*
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/03
CRISPR/Cas9-mediated gene editing ameliorates neurotoxicity in mouse model of Huntington's disease 期刊论文
2017, 卷号: 127, 期号: [db:dc_citation_issue], 页码: 2719
作者:  Yang, Su[1];  Chang, Renbao[1,2,3];  Yang, Huiming[1];  Zhao, Ting[1];  Hong, Yan[1]
收藏  |  浏览/下载:8/0  |  提交时间:2019/12/03
Fragile X-Associated Tremor/Ataxia Syndrome: From Molecular Pathogenesis to Development of Therapeutics 期刊论文
FRONTIERS IN CELLULAR NEUROSCIENCE, 2017, 卷号: 11
作者:  Kong, Ha Eun;  Zhao, Juan;  Xu, Shunliang;  Jin, Peng;  Jin, Yan
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/12


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