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CORC

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Recurrent somatic mutations of PRKAR1A in isolated cardiac myxoma 期刊论文
ONCOTARGET, 2017, 卷号: 8, 期号: 61, 页码: 103968-103974
作者:  He, Jian;  Sun, Mingju;  Li, Enyou;  Hou, Yingyong;  Shepard, Matthew J.
收藏  |  浏览/下载：21/0  |  提交时间：2019/06/20
Inhibition of MAPK pathway is essential for suppressing Rheb-Y35N driven tumor growth 期刊论文
ONCOGENE, 2017, 卷号: 36, 期号: 6, 页码: 756-765
作者:  Piao, H-I;  Wang, Y.;  Hong, X.;  Wang, J.;  Yin, Y.
收藏  |  浏览/下载：24/0  |  提交时间：2019/06/20
Recurrent somatic mutations of PRKAR1A in isolated cardiac myxoma 期刊论文
ONCOTARGET, 2017, 卷号: 8, 期号: 61
作者:  He, Jian;  Sun, Mingju;  Li, Enyou;  Hou, Yingyong;  Shepard, Matthew J.
收藏  |  浏览/下载：6/0  |  提交时间：2019/12/05
Genomic analysis of oesophageal squamous-cell carcinoma identifies alcohol drinking-related mutation signature and genomic alterations 其他
2017-01-01
Chang, Jiang; Tan, Wenle; Ling, Zhiqiang; Xi, Ruibin; Shao, Mingming; Chen, Mengjie; Luo, Yingying; Zhao, Yanjie; Liu, Yun; Huang, Xiancong; Xia, Yuchao; Hu, Jinlin; Parker, Joel S.; Marron, David; Cui, Qionghua; Peng, Linna; Chu, Jiahui; Li, Hongmin; Du, Zhongli; Han, Yaling; Tan, Wen; Liu, Zhihua; Zhan, Qimin; Li, Yun; Mao, Weimin; Wu, Chen; Lin, Dongxin
收藏  |  浏览/下载：5/0  |  提交时间：2017/12/03
SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures 期刊论文
BMC MEDICAL GENETICS, 2017
Wang, Jiaping; Gao, Hua; Bao, Xinhua; Zhang, Qingping; Li, Jiarui; Wei, Liping; Wu, Xiru; Chen, Yan; Yu, Shujie
收藏  |  浏览/下载：5/0  |  提交时间：2017/12/03
Recurrent c.G1636A (p.G546S) mutation of COL2A1 in a Chinese family with skeletal dysplasia and different metaphyseal changes: a case report 期刊论文
BMC PEDIATRICS, 2017, 卷号: 17
作者:  Chen, Jing;  Ma, Xiaomin;  Zhou, Yulin;  Li, Guimei;  Guo, Qiwei
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/11
A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility 期刊论文
AMERICAN JOURNAL OF HUMAN GENETICS, 2017, 卷号: 101, 期号: 3, 页码: 459-465
作者:  Chen, Tailai;  Bian, Yuehong;  Liu, Xiaoman;  Zhao, Shigang;  Wu, Keliang
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/12
Recurrent mutations in a SERPINC1 hotspot associate with venous thrombosis without apparent antithrombin deficiency 期刊论文
ONCOTARGET, 2017, 卷号: 8, 期号: 48
作者:  Zeng, Wei;  Hu, Bei;  Tang, Liang;  You, Yan-Yan;  Toderici, Mara
收藏  |  浏览/下载：1/0  |  提交时间：2019/12/05
Recurrent and novel mutations in the NTRK1 gene lead to rare congenital insensitivity to pain with anhidrosis in two Chinese patients 期刊论文
2017, 卷号: 468, 页码: 39-45
作者:  Lv Fang;  Xu Xiao-Jie;  Song Yu-Wen;  Li Lu-Jiao;  Wang Ou
收藏  |  浏览/下载：7/0  |  提交时间：2020/01/04

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