CORC

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CORC

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Covalent Inhibitors Allosterically Block the Activation of Rho Family Proteins and Suppress Cancer Cell Invasion 期刊论文
ADVANCED SCIENCE, 2020, 页码: 13
作者:  Sun, Zhongya;  Zhang, Hao;  Zhang, Yuanyuan;  Liao, Liping;  Zhou, Wen
收藏  |  浏览/下载：107/0  |  提交时间：2020/07/01
A Novel Subfamily of Endo-beta-1,4-Glucanases in Glycoside Hydrolase Family 10 期刊论文
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2019, 卷号: 85, 期号: 18
作者:  Zhao, Fang;  Cao, Hai-Yan;  Zhao, Long-Sheng;  Zhang, Yi;  Li, Chun-Yang
收藏  |  浏览/下载：23/0  |  提交时间：2019/12/11
A novel subfamily of endo-β-1,4-glucanases in glycoside hydrolase family 10 期刊论文
Applied and Environmental Microbiology, 2019, 卷号: 85, 期号: 18
作者:  Zhao F.;  Cao H.-Y.;  Zhao L.-S.;  Zhang Y.;  Li C.-Y.
收藏  |  浏览/下载：19/0  |  提交时间：2019/12/11
Identification of a novel mutation in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct syndrome 期刊论文
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2016, 卷号: 85, 页码: 75-79
作者:  Zhang, Fengguo;  Bai, Xiaohui;  Xiao, Yun;  Zhang, Xue;  Zhang, Guodong
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/16
An Arabidopsis Transcriptional Regulatory Map Reveals Distinct Functional and Evolutionary Features of Novel Transcription Factors 期刊论文
分子生物学与进化, 2015
Jin Jinpu; He Kun; Tang Xing; Li Zhe; Lv Le; Zhao Yi; Luo Jingchu; Gao Ge
收藏  |  浏览/下载：1/0  |  提交时间：2015/11/11
Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome 期刊论文
2015, 卷号: 128, 期号: 10, 页码: 1336-1339
作者:  Liu, Jia-Wei;  Si, Nuo;  Wang, Lian-Qing;  Shen, Ti;  Zeng, Xue-Jun
收藏  |  浏览/下载：4/0  |  提交时间：2020/01/13
Whole-exome sequencing reveals a novel CHM gene mutation in a family with choroideremia initially diagnosed as retinitis pigmentosa 会议论文
第十四次全国医学遗传学学术会议
作者:  Hui Guo;  Ji-sheng Li;  Fei Gao;  Jiang-xia Li;  Qi-ji Liu
收藏  |  浏览/下载：10/0  |  提交时间：2019/12/31
An Arabidopsis Transcriptional Regulatory Map Reveals Distinct Functional and Evolutionary Features of Novel Transcription Factors 期刊论文
MOLECULAR BIOLOGY AND EVOLUTION, 2015, 卷号: 32, 期号: 7, 页码: 1767-1773
作者:  Jin, Jinpu;  He, Kun;  Tang, Xing;  Li, Zhe;  Lv, Le
收藏  |  浏览/下载：2/0  |  提交时间：2022/09/13
A Chinese family carrying novel mutations in SEC23B and HFE2, the genes responsible for congenital dyserythropoietic anaemia II (CDA II) and primary iron overload, respectively 期刊论文
BRITISH JOURNAL OF HAEMATOLOGY, 2012, 卷号: 158, 期号: 1
作者:  Liu, Gang;  Niu, Shiwen;  Dong, Ailian;  Cai, Hao;  Anderson, Gregory J.
收藏  |  浏览/下载：6/0  |  提交时间：2019/12/05
A Chinese family carrying novel mutations in SEC23B and HFE2, the genes responsible for congenital dyserythropoietic anaemia II (CDA II) and primary iron overload, respectively 期刊论文
2012, 卷号: 158, 期号: 1, 页码: 143-145
作者:  Liu, Gang;  Niu, Shiwen;  Dong, Ailian;  Cai, Hao;  Anderson, Gregory J.
收藏  |  浏览/下载：6/0  |  提交时间：2020/01/13

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