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CORC

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Mechanism of Early Flowering in a Landrace Naked Barley eam8.l Mutant 期刊论文
AGRONOMY-BASEL, 2022, 卷号: 12, 期号: 9
作者:  Mao, CZ;  Xu, JQ;  Wang, HD;  Chen, TR;  Bian, HY
收藏  |  浏览/下载：16/0  |  提交时间：2022/12/02
Somatic synonymous mutations in regulatory elements contribute to the genetic aetiology of melanoma 期刊论文
BMC MEDICAL GENOMICS, 2020, 卷号: 13
作者:  Zhang, Di;  Xia, Junfeng
收藏  |  浏览/下载：6/0  |  提交时间：2021/09/06
Large-scale prediction of ADAR-mediated effective human A-to-I RNA editing 期刊论文
BRIEFINGS IN BIOINFORMATICS, 2019, 卷号: 20, 期号: 1
作者:  Shen, Xizhong;  Song, Guangqi;  Wang, Jinlin;  Zhao, Yicheng;  Zhu, Jimin
收藏  |  浏览/下载：25/0  |  提交时间：2019/12/05
SF3B1 mutation predicts unfavorable treatment-free survival in Chinese chronic lymphocytic leukemia patients 期刊论文
ANNALS OF TRANSLATIONAL MEDICINE, 2019, 卷号: 7, 期号: 8
作者:  Miao, Yi;  Zou, Yi-Xin;  Gu, Dan-Ling;  Zhu, Hong-Cheng;  Zhu, Hua-Yuan
收藏  |  浏览/下载：43/0  |  提交时间：2019/12/05
A splice site mutation causing exon 6 skipping in SLC20A2 gene in a primary familial brain calcification family 期刊论文
Brain Research Bulletin, 2019
作者:  Yuan-Tao Huang;  Li-Hua Zhang;  Mei-Fang Li;  Lin Cheng;  Guo-Ying Zou
收藏  |  浏览/下载：10/0  |  提交时间：2019/12/13
Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia 期刊论文
Archives of Oral Biology, 2019, 卷号: Vol.100, 页码: 49-56
作者:  Tingting Zhang;  Jing Wu;  Xiaoxue Zhao;  Feifei Hou;  Tengfei Ma
收藏  |  浏览/下载：31/0  |  提交时间：2019/12/17
Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia. 期刊论文
Archives of oral biology, 2019, 卷号: Vol.100, 页码: 49-56
作者:  Tingting Zhang;  Jing Wu;  Xiaoxue Zhao;  Feifei Hou;  Tengfei Ma
收藏  |  浏览/下载：15/0  |  提交时间：2019/12/17
A splice site mutation causing exon 6 skipping in SLC20A2 gene in a primary familial brain calcification family. 期刊论文
Brain research bulletin, 2019
作者:  Yuan-Tao Huang;  Li-Hua Zhang;  Mei-Fang Li;  Lin Cheng;  Guo-Ying Zou
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/13
A novel phenotype with splicing mutation identified in a Chinese family with desminopathy 期刊论文
2019, 卷号: 132, 期号: 2, 页码: 127-134
作者:  Fan, Peng;  Lu, Chao-Xia;  Dong, Xue-Qi;  Zhu, Di;  Yang, Kun-Qi
收藏  |  浏览/下载：14/0  |  提交时间：2020/01/03
An exonic splicing enhancer mutation in DUOX2 causes aberrant alternative splicing and severe congenital hypothyroidism in Bama pigs 期刊论文
Disease Models & Mechanisms, 2019, 卷号: 12, 期号: 1, 页码: 1-8
作者:  Cao CW(曹春伟);  Zhang Y(张颖);  Jia QT(贾启涛);  Wang X(王霄);  Zheng QT(郑千涛)
收藏  |  浏览/下载：11/0  |  提交时间：2020/11/17

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