CORC

在结果中检索

CORC

浏览/检索结果: 共11条，第1-10条 帮助

限定条件                
已选(0)清除 条数/页：   排序方式：
[C5H12N]SnCl3: A Tin Halide Organic-Inorganic Hybrid as an Above-Room-Temperature Solid-State Nonlinear Optical Switch 期刊论文
CHEMISTRY-A EUROPEAN JOURNAL, 2019, 卷号: 25, 期号: 10, 页码: 2610-2615
作者:  Liu, Xitao;  Ji, Chengmin;  Wu, Zhenyue;  Li, Lina;  Han, Shiguo
收藏  |  浏览/下载：14/0  |  提交时间：2019/12/11
The relationship between DNA repair genes (XPA, XPF, XPG) polymorphism and the risk of preeclampsia in Chinese Han Women 期刊论文
PREGNANCY HYPERTENSION-AN INTERNATIONAL JOURNAL OF WOMENS CARDIOVASCULAR HEALTH, 2018, 卷号: 14, 页码: 145-149
作者:  Wang, Haiyan;  Liu, Jingjing;  Zhang, Ru;  Liu, Yun;  Ren, Xiaoyan
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/11
Analysis of osteoblast-specific histone-modifying enzymes Mof reveals novel epigenetic basis of osteoblast differenntiation 会议论文
Annual Meeting of the American-Society-for-Bone-and-Mineral-Research, SEP 28-OCT 01, 2018
作者:  Li, Xiangzhi;  Chen, Jianmei;  Liu, Di;  Li, Minqi;  Yang, Yang
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/31
Hypothalamic Astrocytes Respond to Gastric Mucosa! Damage Induced by Restraint Water-Immersion Stress in Rat 期刊论文
FRONTIERS IN BEHAVIORAL NEUROSCIENCE, 2016, 卷号: 10
作者:  Sun, Haiji;  Li, Ruisheng;  Xu, Shiguo;  Liu, Zhen;  Ma, Xiaoli
收藏  |  浏览/下载：11/0  |  提交时间：2019/12/16
Whole exome sequencing identifies a novel SPG4 mutation in a Chinese family with hereditary spastic paraplegias 期刊论文
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2016, 卷号: 9, 期号: 10, 页码: 10274-10281
作者:  Liu, Shiguo;  Jing, Zhongcui;  Liu, Shien;  Zheng, Xueping;  Wang, Haiyan
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/16
A De novo PAX8 mutation in a Chinese child with congenital thyroid dysgenesis 期刊论文
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2015, 卷号: 8, 期号: 9, 页码: 11434-11439
作者:  Zou, Hui;  Chai, Jian;  Liu, Shiguo;  Zang, Hongwei;  Yu, Xiaoxia
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/17
The role of GRIN2B in Tourette syndrome: Results from a transmission disequilibrium study 期刊论文
JOURNAL OF AFFECTIVE DISORDERS, 2015, 卷号: 187, 页码: 62-65
作者:  Che, Fengyuan;  Zhang, Ying;  Wang, Guiju;  Heng, Xueyuan;  Liu, Shiguo
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/17
TS  Grin2B  TDT  HRR  
A Novel Missense Mutation (I26M) in DUOXA2 Causing Congenital Goiter Hypothyroidism Impairs NADPH Oxidase Activity but Not Protein Expression 期刊论文
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2015, 卷号: 100, 期号: 4, 页码: 1225-1229
作者:  Liu, Shiguo;  Liu, Lu;  Niu, Xiaoyan;  Lu, Deguo;  Xia, Hongfei
收藏  |  浏览/下载：1/0  |  提交时间：2019/12/17
Do obsessive-compulsive disorder and Tourette syndrome share a common susceptibility gene? An association study of the BDNF Val66Met polymorphism in the Chinese Han population 期刊论文
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2015, 卷号: 16, 期号: 8, 页码: 602-609
作者:  Liu, Shiguo;  Cui, Jiajia;  Niu, Zhaoyuan;  Yi, Mingji;  Zhang, Xinhua
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/17
Lack of Association Between Polymorphism-592A/C in the Promoter Region of the IL10 Gene and Tourette's Syndrome in a Family-Based Association Study in the Chinese Han Population 期刊论文
GENETIC TESTING AND MOLECULAR BIOMARKERS, 2011, 卷号: 15, 期号: 10, 页码: 733-735
作者:  Liu, Shiguo;  Yi, Mingji;  Qi, Fengguang;  Che, Fengyuan;  Ma, Xu
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/23

©版权所有 ©2017 CSpace - Powered by CSpace