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Allosteric Inhibitors of SHP2: An Updated Patent Review (2015-2020) 期刊论文
CURRENT MEDICINAL CHEMISTRY, 2021, 卷号: 28, 期号: 19, 页码: 3825-3842
作者:  Wu, Jingwei;  Zhang, Huan;  Zhao, Guilong;  Wang, Runling
收藏  |  浏览/下载:65/0  |  提交时间:2021/08/17
A novel RIT1 mutation causes deterioration of Noonan syndrome-associated cardiac hypertrophy 其他
2019-01-01
作者:  Cai, Jingjing;  Li, Hongliang
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/05
BRaf signaling principles unveiled by large-scale human mutation analysis with a rapid lentivirus-based gene replacement method 期刊论文
GENES & DEVELOPMENT, 2017
Lim, Chae-Seok; Kang, Xi; Mirabella, Vincent; Zhang, Huaye; Bu, Qian; Araki, Yoichi; Hoang, Elizabeth T.; Wang, Shiqiang; Shen, Ying; Choi, Sukwoo; Kaang, Bong-Kiun; Chang, Qiang; Pang, Zhiping P.; Huganir, Richard L.; Zhu, J. Julius
收藏  |  浏览/下载:10/0  |  提交时间:2017/12/03
Plasiatine, an Unprecedented Indole-Phenylpropanoid Hybrid from Plantago asiatica as a Potent Activator of the Nonreceptor Protein Tyrosine Phosphatase Shp2 期刊论文
SCIENTIFIC REPORTS, 2016, 卷号: 6, 期号: 1, 页码: 24945
作者:  Gao, Zhong-Hua;  Shi, Yi-Ming;  Qiang, Zhe;  Wang, Xia;  Shang, Shan-Zhai
收藏  |  浏览/下载:78/0  |  提交时间:2016/08/22
Braf gene: from human cancers to developmental syndromes 期刊论文
Saudi journal of biological sciences, 2015, 卷号: 22, 期号: 4, 页码: 359-373
作者:  Hussain, Muhammad Ramzan Manwar;  Baig, Mukhtiar;  Mohamoud, Hussein Sheik Ali;  Ulhaq, Zaheer;  Hoessli, Daniel C.
收藏  |  浏览/下载:35/0  |  提交时间:2019/05/10
Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11 期刊论文
Molecular Cytogenetics, 2014, 卷号: 7, 期号: 1, 页码: 28
作者:  Chen, Jin-Lan;  Zhu, Xin;  Zhao, Tian-Li;  Wang, Jian;  Yang, Yi-Feng
收藏  |  浏览/下载:7/0  |  提交时间:2019/12/03
Regulation of the HDM2-p53 pathway by ribosomal protein L6 in response to ribosomal stress 期刊论文
核酸研究, 2014
Bai, Dongmei; Zhang, Jinfang; Xiao, Weichun; Zheng, Xiaofeng
收藏  |  浏览/下载:4/0  |  提交时间:2015/11/13
Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism 期刊论文
cell, 2013
Willsey, A. Jeremy; Sanders, Stephan J.; Li, Mingfeng; Dong, Shan; Tebbenkamp, Andrew T.; Muhle, Rebecca A.; Reilly, Steven K.; Lin, Leon; Fertuzinhos, Sofia; Miller, Jeremy A.; Murtha, Michael T.; Bichsel, Candace; Niu, Wei; Cotney, Justin; Ercan-Sencicek, A. Gulhan; Gockley, Jake; Gupta, Abha R.; Han, Wenqi; He, Xin; Hoffman, Ellen J.; Klei, Lambertus; Lei, Jing; Liu, Wenzhong; Liu, Li; Lu, Cong; Xu, Xuming; Zhu, Ying; Mane, Shrikant M.; Lein, Ed S.; Wei, Liping; Noonan, James P.; Roeder, Kathryn; Devlin, Bernie; Sestan, Nenad; State, Mat
收藏  |  浏览/下载:4/0  |  提交时间:2015/11/11
Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome 期刊论文
American Journal of Medical Genetics Part A, 2012, 卷号: 158A, 期号: 8, 页码: 1918-1923
作者:  Luo, Cheng;  Yang, Yi-Feng;  Yin, Bang-Liang;  Chen, Jin-Lan;  Huang, Can
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/03
无权访问的条目 期刊论文
作者:  Huang, Heng;  Jin, Ting;  He, Jing;  Ding, QiuRong(丁秋蓉);  Xu, Daqian
收藏  |  浏览/下载:8/0  |  提交时间:2015/08/25


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