CORC

浏览/检索结果: 共10条,第1-10条 帮助

已选(0)清除 条数/页:   排序方式:
Human Cytomegalovirus Immediate Early 1 Protein Causes Loss of SOX2 from Neural Progenitor Cells by Trapping Unphosphorylated STAT3 in the Nucleus 期刊论文
JOURNAL OF VIROLOGY, 2018, 卷号: 92, 期号: 17, 页码: 18
作者:  Luo, Min-Hua;  Nevels, Michael;  Paulus, Christina;  Britt, William J.;  Wang, Wei
收藏  |  浏览/下载:58/0  |  提交时间:2018/12/29
Human cytomegalovirus infection dysregulates neural progenitor cell fate by disrupting hes1 rhythm and down-regulating its expression 期刊论文
Virologica sinica, 2017, 卷号: 32, 期号: 3, 页码: 188-198
作者:  Liu, Xi-Juan;  Jiang, Xuan;  Huang, Sheng-Nan;  Sun, Jin-Yan;  Zhao, Fei
收藏  |  浏览/下载:37/0  |  提交时间:2019/05/08
Early-onset hearing loss reorganizes the visual and auditory network in children without cochlear implantation 期刊论文
NeuroReport, 2016, 卷号: 27, 期号: 3
作者:  Shi, Bin/57111333900[0];  Yang, Lizhuang/57104020200[1];  Liu, Ying/56457779400[2];  Zhao, Shuli/57111125500[3];  Wang, Ying/56681858000[4]
收藏  |  浏览/下载:9/0  |  提交时间:2019/12/06
Human cytomegalovirus infection dysregulates the localization and stability of nicd1 and jag1 in neural progenitor cells 期刊论文
Journal of virology, 2015, 卷号: 89, 期号: 13, 页码: 6792-6804
作者:  Li, Xiao-Jun;  Liu, Xi-Juan;  Yang, Bo;  Fu, Ya-Ru;  Zhao, Fei
收藏  |  浏览/下载:28/0  |  提交时间:2019/05/09
Non-manifesting AHI1 truncations indicate localized loss-of-function tolerance in a severe Mendelian disease gene 期刊论文
human molecular genetics, 2015
Elsayed Solaf M; Phillips Jennifer B; Heller Raoul; Thoenes Michaela; Elsobky Ezzat; Nürnberg Gudrun; Nürnberg Peter; Seland Saskia; Ebermann Inga; Altmüller Janine; Thiele Holger; Toliat Mohammad; K?rber Friederike; Hu Xue-Jia; Wu Yun-Dong; Zaki Maha S; Abdel-Salam Ghada; Gleeson Joseph; Boltshauser Eugen; Westerfield Monte; Bolz Hanno J
收藏  |  浏览/下载:4/0  |  提交时间:2015/11/13
First healthy baby born after PGD (preimplantation genetic diagnosis) - noninvasive haplotype screening in couples both carrying deafness gene GJB2 mutation 会议论文
31st Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology (ESHRE), JUN 14-17, 2015
作者:  Chen, Z.;  Gao, Y.;  Huang, S.;  Yan, J.;  Li, J.
收藏  |  浏览/下载:11/0  |  提交时间:2019/12/31
Murine model for congenital CMV infection and hearing impairment 期刊论文
http://dx.doi.org/10.1186/1743-422X-8-70, 2011
Chen Juanjuan; Feng Yan; Chen Li; Liu Haizhi; Wang Ling; Wang Xinrong; Xiao Juan; Liu Tao; Yin Zongzhi; Chen Suhua; 陈亮
收藏  |  浏览/下载:6/0  |  提交时间:2013/12/12
Grhl2 deficiency impairs otic development and hearing ability in a zebrafish model of the progressive dominant hearing loss DFNA28 期刊论文
HUMAN MOLECULAR GENETICS, 2011, 卷号: 20, 期号: 16, 页码: 3213-3226
作者:  Du, Jiulin
收藏  |  浏览/下载:39/0  |  提交时间:2012/07/13
A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family 期刊论文
LARYNGOSCOPE, 2006, 卷号: 116, 期号: 6
作者:  Wang, Qiu-Ju;  Li, Qing-Zhong;  Rao, Shao-Qi;  Zhao, Ya-Li;  Yuan, Hu
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/27


©版权所有 ©2017 CSpace - Powered by CSpace