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CORC

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Controllable spiking dynamics in cascaded VCSEL-SA photonic neurons 期刊论文
NONLINEAR DYNAMICS, 2020, 卷号: 99, 期号: 2, 页码: 1103-1114
作者:  Zhenxue Zhang;   Zhengmao Wu;   Dan Lu;   Guangqiong Xia ;   Tao Deng
收藏  |  浏览/下载：7/0  |  提交时间：2021/12/16
Mutational landscape of gastric cancer and clinical application of genomic profiling based on target next-generation sequencing 期刊论文
JOURNAL OF TRANSLATIONAL MEDICINE, 2019, 卷号: 17, 期号: 1
作者:  Cai, Hui;  Jing, Changqing;  Chang, Xusheng;  Ding, Dan;  Han, Ting
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/11
Novel mutation of EDA causes new asymmetrical X-linked hypohidrotic ectodermal dysplasia phenotypes in a female 期刊论文
JOURNAL OF DERMATOLOGY, 2019, 卷号: 46, 期号: 8, 页码: 731-733
作者:  Shen, Lu;  LIu, Cenying;  Gao, Ming;  Li, Hongmei;  Zhang, Yaowen
收藏  |  浏览/下载：13/0  |  提交时间：2019/12/11
Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort 期刊论文
SCIENTIFIC REPORTS, 2017, 卷号: 7, 页码: 44155
作者:  Guo, Hui;  Peng, Yu;  Hu, Zhengmao;  Li, Ying;  Xun, Guanglei
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/03
Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia 期刊论文
SCIENTIFIC REPORTS, 2016, 卷号: 6, 页码: 24327
作者:  Zhou, Zhifan;  Hu, Zhengmao;  Zhang, Lu;  Hu, Zhaoting;  Liu, Haihong
收藏  |  浏览/下载：6/0  |  提交时间：2019/12/03
De novo genic mutations among a Chinese autism spectrum disorder cohort 期刊论文
Nature Communications, 2016, 卷号: 7, 页码: 13316
作者:  Wang, Tianyun;  Guo, Hui;  Xiong, Bo;  Stessman, Holly A F;  Wu, Huidan
收藏  |  浏览/下载：11/0  |  提交时间：2019/12/03
Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family 期刊论文
Journal of Human Genetics, 2015, 卷号: 60, 期号: 3, 页码: 119-126
作者:  Wang, Honghan;  Wang, Xinwei;  He, Chufeng;  Li, Haibo;  Qing, Jie
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/03
Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia 期刊论文
Genetics in Medicine, 2015, 卷号: 17, 期号: 4, 页码: 300-306
作者:  Guo, Hui;  Tong, Ping;  Liu, Yanling;  Xia, Lu;  Wang, Tianyun
收藏  |  浏览/下载：8/0  |  提交时间：2019/12/03
MSX2 mediates entry of human pluripotent stem cells into mesendoderm by simultaneously suppressing SOX2 and activating NODAL signaling 期刊论文
2015, 卷号: 25, 期号: 12, 页码: 1314-1332
作者:  Wu, Qingqing;  Zhang, Leisheng;  Su, Pei;  Lei, Xiaohua;  Liu, Xin
收藏  |  浏览/下载：2/0  |  提交时间：2020/01/13
MSX2  hPSC  SOX2  NODAL  mesendoderm  
Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients 期刊论文
Molecular Biology Reports, 2014, 卷号: 41, 期号: 6, 页码: 4133-4140
作者:  Xu, Xiaojuan;  Xiong, Zhimin;  Zhang, Lusi;  Liu, Yalan;  Lu, Lina
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/03

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