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CORC

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RNA methylomes reveal the m(6)A-mediated regulation of DNA demethylase gene SlDML2 in tomato fruit ripening 期刊论文
GENOME BIOLOGY, 2019, 卷号: 20, 期号: 1
作者:  Zhou, Leilei;  Tian, Shiping;  Qin, Guozheng
收藏  |  浏览/下载：9/0  |  提交时间：2022/01/06
Evolution of Darwin's Peloric Gloxinia (Sinningia speciosa) Is Caused by a Null Mutation in a Pleiotropic TCP Gene 期刊论文
MOLECULAR BIOLOGY AND EVOLUTION, 2018, 卷号: 35, 期号: 8, 页码: 1901-1915
作者:  Dong, Yang;  Liu, Jing;  Li, Peng-Wei;  Li, Chao-Qun;  Lu, Tian-Feng
收藏  |  浏览/下载：8/0  |  提交时间：2022/02/25
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：34/0  |  提交时间：2016/12/22
Patient-specific induced-pluripotent stem cells-derived cardiomyocytes recapitulate the pathogenic phenotypes of dilated cardiomyopathy due to a novel DES mutation identified by whole exome sequencing 期刊论文
HUMAN MOLECULAR GENETICS, 2013, 卷号: 22, 期号: 7
Tse, Hung-Fat; Ho, Jenny C. Y.; Choi, Shing-Wan; Lee, Yee-Ki; Butler, Amy W.; Ng, Kwong-Man; Siu, Chung-Wah; Simpson, Michael A.; Lai, Wing-Hon; Chan, Yau-Chi; Au, Ka-Wing; Zhang, Jinqiu; Lay, Kenneth W. J.; Esteban, Miguel A.; Nicholls, John M.; Colman, Alan; Sham, Pak C.
收藏  |  浏览/下载：32/0  |  提交时间：2016/12/16
Patient-specific induced-pluripotent stem cells-derived cardiomyocytes recapitulate the pathogenic phenotypes of dilated cardiomyopathy due to a novel DES mutation identified by whole exome sequencing 期刊论文
HUMAN MOLECULAR GENETICS, 2013, 卷号: 22, 期号: 7
作者:  Sham, Pak C.;  Tse, Hung-Fat;  Ho, Jenny C. Y.;  Choi, Shing-Wan;  Lee, Yee-Ki
收藏  |  浏览/下载：29/0  |  提交时间：2018/12/13
Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndrome 期刊论文
CLINICAL GENETICS, 2010, 卷号: 77, 期号: 2, 页码: 155-162
Yu, Y.; Xu, C.; Pan, X.; Ren, H.; Wang, W.; Meng, X.; Huang, F.; Chen, N.
收藏  |  浏览/下载：26/0  |  提交时间：2012/07/13
Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome 期刊论文
AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 卷号: 80, 期号: 2, 页码: 361-371
作者:  Zhao, XL;  Sun, M;  Zhao, J;  Leyva, JA;  Zhu, HW
收藏  |  浏览/下载：6/0  |  提交时间：2015/12/22
Sequence Variations in the Mu-opioid Receptor Gene (OPRM1) Associated with Human Addiction to Heroin 期刊论文
HUMAN MUTATION, 2002, 卷号: 19, 期号: 4, 页码: 42006
作者:  Shi, JX;  Hui, LJ;  Xu, YH;  Wang, F;  Huang, W
收藏  |  浏览/下载：13/0  |  提交时间：2015/07/22
Identification and characterization of a novel human cDNA encoding a 21 kDa pRb-associated protein 期刊论文
GENE, 2001, 卷号: 263, 期号: 1, 页码: 85-92
作者:  Wen, H;  Ao, SZ
收藏  |  浏览/下载：15/0  |  提交时间：2015/07/22

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