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CORC

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Deletion of a flippase subunit Tmem30a in hematopoietic cells impairs mouse fetal liver erythropoiesis 期刊论文
HAEMATOLOGICA, 2019, 卷号: 104, 期号: 10, 页码: 1984-1994
作者:  Yang, Fan;  Huang, Yumin;  Chen, Xianda;  Liu, Lu;  Liao, Dandan
收藏  |  浏览/下载：15/0  |  提交时间：2021/11/04
Lentiviral Vector-Mediated Expression of Exoenzyme C3 Transferase Lowers Intraocular Pressure in Monkeys 期刊论文
MOLECULAR THERAPY, 2019, 卷号: 27, 期号: 7, 页码: 1327-1338
作者:  Tan, Junkai;  Liu, Guo;  Zhu, Xianjun;  Wu, Zhijian;  Wang, Ningli
收藏  |  浏览/下载：11/0  |  提交时间：2021/11/10
Tmem30a Plays Critical Roles in Ensuring the Survival of Hematopoietic Cells and Leukemia Cells in Mice 期刊论文
AMERICAN JOURNAL OF PATHOLOGY, 2018, 卷号: 188, 期号: 6, 页码: 1457-1468
作者:  Li, Ning;  Yang, Yeming;  Liang, Cailing;  Qiu, Qiang;  Pan, Cong
收藏  |  浏览/下载：35/0  |  提交时间：2020/12/24
Targeted Next-Generation Sequencing Reveals a Novel Frameshift Mutation in the MERTK Gene in a Chinese Family with Retinitis Pigmentosa 期刊论文
GENETIC TESTING AND MOLECULAR BIOMARKERS, 2018, 卷号: 22, 期号: 3, 页码: 165-169
作者:  Yang, Mu;  Li, Shujin;  Liu, Wenjing;  Yang, Yeming;  Zhang, Lin
收藏  |  浏览/下载：21/0  |  提交时间：2020/12/24
Targeted Next-Generation Sequencing Reveals Novel RP1 Mutations in Autosomal Recessive Retinitis Pigmentosa 期刊论文
GENETIC TESTING AND MOLECULAR BIOMARKERS, 2018, 卷号: 22, 期号: 2, 页码: 109-114
作者:  Li, Shujin;  Yang, Mu;  Liu, Wenjing;  Liu, Yuqing;  Zhang, Lin
收藏  |  浏览/下载：22/0  |  提交时间：2020/12/24
Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells 期刊论文
CELL DEATH & DISEASE, 2018, 卷号: 9, 页码: 899
作者:  Yang, Yeming;  Sun, Kuanxiang;  Liu, Wenjing;  Zhang, Lin;  Peng, Kun
收藏  |  浏览/下载：5/0  |  提交时间：2021/10/29
Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells 期刊论文
CELL DEATH & DISEASE, 2018, 卷号: 9, 页码: 899
作者:  Yang, Yeming;  Sun, Kuanxiang;  Liu, Wenjing;  Zhang, Lin;  Peng, Kun
收藏  |  浏览/下载：14/0  |  提交时间：2021/10/29
A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosa 期刊论文
HUMAN MOLECULAR GENETICS, 2018, 卷号: 27, 期号: 14, 页码: 2563-2572
作者:  Zhou, Yu;  Li, Shujin;  Huang, Lulin;  Yang, Yeming;  Zhang, Lin
收藏  |  浏览/下载：15/0  |  提交时间：2021/11/01
Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population 期刊论文
JOURNAL OF HUMAN GENETICS, 2015, 卷号: 60, 期号: 10, 页码: 625-630
作者:  Zhou, Yu;  Saikia, Bibhuti B.;  Jiang, Zhilin;  Zhu, Xiong;  Liu, Yuqing
收藏  |  浏览/下载：35/0  |  提交时间：2016/12/22
Exome Sequencing Analysis Identifies Compound Heterozygous Mutation in ABCA4 in a Chinese Family with Stargardt Disease 期刊论文
PLOS ONE, 2014, 卷号: 9, 期号: 3, 页码: e91962(1-8)
Zhou, Yu; Tao, Siyu; Chen, Hui; Huang, Lulin; Zhu, Xiong; Li, Youping; Wang, Zhili; Lin, He; Hao, Fang; Yang, Zhenglin; Wang, Liya; Zhu, Xianjun
收藏  |  浏览/下载：36/0  |  提交时间：2016/01/07

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