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A Pandas complex adapted for piRNA-guided transcriptional silencing and heterochromatin formation 期刊论文
2019
作者:  Zhao Kang;  Cheng Sha;  Miao Na;  Xu Ping;  Lu Xiaohua
收藏  |  浏览/下载:39/0  |  提交时间:2020/01/03
CFEA: a cell-free epigenome atlas in human diseases 期刊论文
2019
作者:  Yu Fulong;  Li Kai;  Li Shuangquan;  Liu Jiaqi;  Zhang Yan
收藏  |  浏览/下载:22/0  |  提交时间:2020/01/03
TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease 期刊论文
2019
作者:  Chen Weisheng;  Lin Jiachen;  Wang Lianlei;  Li Xiaoxin;  Zhao Sen
收藏  |  浏览/下载:35/0  |  提交时间:2020/01/03
TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice 期刊论文
2019, 卷号: 28, 期号: 4, 页码: 539-547
作者:  Yang, Nan;  Wu, Nan;  Zhang, Ling;  Zhao, Yanxue;  Liu, Jiaqi
收藏  |  浏览/下载:10/0  |  提交时间:2020/01/03
Protein kinase D3 promotes gastric cancer development through p65/6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 activation of glycolysis 期刊论文
2019, 卷号: 380, 期号: 2, 页码: 188-197
作者:  Zhang, Jianwei;  Zhang, Yajing;  Wang, Jiaqi;  Zhang, Shuisheng;  Zhao, Yajie
收藏  |  浏览/下载:30/0  |  提交时间:2020/01/03
A20 as a novel target for the anti-neuroinflammatory effect of chrysin via inhibition of NF-kappa B signaling pathway 期刊论文
2019, 卷号: 79, 页码: 228-235
作者:  Li, Zhipeng;  Chu, Shifeng;  He, Wenbin;  Zhang, Zhao;  Liu, Jiaqi
收藏  |  浏览/下载:2/0  |  提交时间:2020/01/03
Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population 期刊论文
2019, 卷号: 688, 页码: 215-220
作者:  Liu, Gang;  Liu, Sen;  Li, Xiaoxin;  Chen, Jia;  Chen, Weisheng
收藏  |  浏览/下载:5/0  |  提交时间:2020/01/03
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model 期刊论文
2019, 卷号: 21, 期号: 7, 页码: 1548-1558
作者:  Liu, Jiaqi;  Wu, Nan;  Yang, Nan;  Takeda, Kazuki;  Chen, Weisheng
收藏  |  浏览/下载:36/0  |  提交时间:2020/01/03
Perturbations of BMP/TGF-beta and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM) 期刊论文
2018, 卷号: 55, 期号: 10, 页码: 675-684
作者:  Wang, Kun;  Zhao, Sen;  Liu, Bowen;  Zhang, Qianqian;  Li, Yaqi
收藏  |  浏览/下载:6/0  |  提交时间:2020/01/03
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease 期刊论文
2018, 卷号: 137, 期号: 6-7, 页码: 553-567
作者:  Liu, Jiaqi;  Zhou, Yangzhong;  Liu, Sen;  Song, Xiaofei;  Yang, Xin-Zhuang
收藏  |  浏览/下载:9/0  |  提交时间:2020/01/03


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