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CORC

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The influence of genetic and acquired factors on the vulnerability to develop depression: a review 期刊论文
BIOSCIENCE REPORTS, 2023, 卷号: 43, 期号: 5
作者:  Zhang, Xingfang;  Qiao, Yajun;  Wang, Mengyuan;  Liang, Xinxin;  Zhang, Ming
收藏  |  浏览/下载：2/0  |  提交时间：2023/12/01
Impaired face recognition is associated with abnormal gray matter volume in the posterior cingulate cortex in congenital amusia 期刊论文
NEUROPSYCHOLOGIA, 2021, 卷号: 156, 页码: 7
作者:  Jin, Zhishuai;  Lu, Xuejing;  Huyang, Sizhu;  Yan, Yajun;  Jiang, Lichen
收藏  |  浏览/下载：52/0  |  提交时间：2021/06/14
In-vivo efficacy of biodegradable ultrahigh ductility Mg-Li-Zn alloy tracheal stents for pediatric airway obstruction 期刊论文
COMMUNICATIONS BIOLOGY, 2020, 卷号: 3, 期号: 1, 页码: 11
作者:  Wu, Jingyao;  Mady, Leila J.;  Roy, Abhijit;  Aral, Ali Mubin;  Lee, Boeun
收藏  |  浏览/下载：30/0  |  提交时间：2021/03/15
Zika Virus Potentiates the Development of Neurological Defects and Microcephaly: Challenges and Control Strategies 期刊论文
FRONTIERS IN NEUROLOGY, 2019, 卷号: 10, 页码: 9
作者:  Siddique, Rabeea;  Liu, Yang;  Nabi, Ghulam;  Sajjad, Wasim;  Xue, Mengzhou
收藏  |  浏览/下载：70/0  |  提交时间：2019/05/20
Zika Virus Potentiates the Development of Neurological Defects and Microcephaly: Challenges and Control Strategies 期刊论文
FRONTIERS IN NEUROLOGY, 2019, 卷号: 10, 页码: 9
作者:  Siddique, Rabeea;  Liu, Yang;  Nabi, Ghulam;  Sajjad, Wasim;  Xue, Mengzhou
收藏  |  浏览/下载：59/0  |  提交时间：2019/06/10
Deficiency of lrp4 in zebrafish and human LRP4 mutation induce aberrant activation of Jagged-Notch signaling in fin and limb development 期刊论文
CELLULAR AND MOLECULAR LIFE SCIENCES, 2019, 卷号: 76, 期号: 1, 页码: 163-178
作者:  Tian, Jing;  Shao, Jinhui;  Liu, Cong;  Hou, Hsin-Yu;  Chou, Chih-Wei
收藏  |  浏览/下载：66/0  |  提交时间：2019/07/01
TBX6-associated congenital scoliosis as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model 期刊论文
Genetics in Medicine, 2019
作者:  Jiaqi Liu;  Nan Wu;  Deciphering Disorders Involving Scoliosis and COmorbidities study, Nan Yang;  Kazuki Takeda;  Weisheng Chen
收藏  |  浏览/下载：40/0  |  提交时间：2019/12/13
Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review. 期刊论文
Neuromuscular disorders : NMD, 2019, 卷号: 29, 期号: 4
作者:  Tian Wo-Tu;  Luan Xing-Hua;  Zhou Hai-Yan;  Zhang Chao;  Huang Xiao-Jun
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/06
The ribosome biogenesis protein Esf1 is essential for pharyngeal cartilage formation in zebrafish 期刊论文
FEBS JOURNAL, 2018, 卷号: 285, 期号: 18, 页码: 3464-3484
作者:  Chen, Jian-Yang;  Tan, Xungang;  Wang, Zheng-Hua;  Liu, Yun-Zhang;  Zhou, Jian-Feng
收藏  |  浏览/下载：42/0  |  提交时间：2019/08/27
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

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