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科研机构
四川大学 [11]
湖南大学 [9]
山东大学 [6]
南开大学 [5]
昆明动物研究所 [5]
复旦大学上海医学院 [4]
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期刊论文 [59]
发表日期
2016 [59]
学科主题
Genetics &... [2]
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Targeted Genes Sequencing Identified a Novel 15 bp Deletion on GJA8 in a Chinese Family with Autosomal Dominant Congenital Cataracts
期刊论文
CHINESE MEDICAL JOURNAL, 2016, 卷号: 129, 期号: 7, 页码: 860-+
作者:
Min, Han-Yi
;
Qiao, Peng-Peng
;
Asan
;
Yan, Zhi-Hui
;
Jiang, Hui-Feng
收藏
  |  
浏览/下载:20/0
  |  
提交时间:2017/03/13
Congenital Cataract
GJA8
Next Generation Sequencing
Novel In-frame Deletion
Targeted Genes Capture
PI3K AKT and P-AKT levels in thin endometrium
期刊论文
GENETICS AND MOLECULAR RESEARCH, 2016
作者:
Le, A. W.
;
Shan, L. L.
;
Dai, X. Y.
;
Xiao, T. H.
;
Li, X. R.
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2017/01/16
The impact of CACNA1C allelic variation on regional gray matter volume in Chinese population
期刊论文
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2016, 卷号: 171, 期号: 3
作者:
Sun, Xuejin
;
Yu, Hualin
;
Li, Hao
;
Wu, Lichuan
;
Li, Ming
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/04
CACNA1C
rs1006737
voxel-based morphometry
gray matter
Han Chinese
Genetic polymorphisms in the DNA repair gene, XRCC1 associate with non-Hodgkin lymphoma susceptibility: A systematic review and meta-analysis
期刊论文
EUROPEAN JOURNAL OF MEDICAL GENETICS, 2016, 卷号: 59, 期号: 2
作者:
Li, Yuying
;
Bai, Ou
;
Cui, Jiuwei
;
Li, Wei
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
XRCC1
SNPs
Non-Hodgkin lymphoma
Meta-analysis
Meta-analysis of the clinical value of oxymatrine on sustained virological response in chronic hepatitis B
期刊论文
Annals of Hepatology, 2016, 卷号: 15, 期号: 4
作者:
He, M., Wu, Y., Wang, M., Chen, W., Jiang, J.
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
alanine aminotransferase
hepatitis B(e) antigen
interferon
oxymatrine
alkaloid
antivirus agent
hepatitis B(e) antigen
interferon
macrogol derivative
oxymatrine
quinolizine derivative
virus DNA
Article
China
chronic hepatitis B
combination chemotherapy
drug efficacy
human
infection risk
medical literature
meta analysis
monotherapy
publication
randomized controlled trial (topic)
seroconversion
systematic review
treatment indication
treatment response
virology
blood
combination drug therapy
genetics
Hepatitis B virus
Hepatitis B, Chronic
immunology
sustained virologic response
A Novel Functional Missense Mutation p.T219A in Type 1 Gauchers Disease
期刊论文
CHINESE MEDICAL JOURNAL, 2016, 卷号: 129, 期号: 9
作者:
Liu, Lin-Yu
;
Liu, Fei
;
Du, Si-Chen
;
Jiang, Sha-Yi
;
Wang, Hui-Jun
收藏
  |  
浏览/下载:8/0
  |  
提交时间:2019/12/05
Gaucher's Disease
GCase
Genetics
Novel Missense Mutation
CRISPR-Cas9 for medical genetic screens: applications and future perspectives
期刊论文
JOURNAL OF MEDICAL GENETICS, 2016, 卷号: 53, 期号: 2
作者:
Xue, Hui-Ying
;
Ji, Li-Juan
;
Gao, Ai-Mei
;
Liu, Ping
;
He, Jing-Dong
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
AKAP2 identified as a novel gene mutated in a Chinese family with adolescent idiopathic scoliosis
期刊论文
Journal of Medical Genetics, 2016, 卷号: 53, 期号: 7, 页码: 488-493
作者:
Li, Wei
;
Li, YaWei
;
Zhang, Lusi
;
Guo, Hui
;
Tian, Di
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/03
*AKAP2
*adolescent idiopathic scoliosis
*whole-exome sequencing
Association of AIRE gene polymorphisms with susceptibility to rheumatoid arthritis among ethnic Han Chinese from Shaanxi].
期刊论文
Chinese journal of medical genetics, 2016, 卷号: 33, 期号: [db:dc_citation_issue], 页码: 373-7
作者:
Li Xiaobo
;
Li Ting
;
Chen Miao
;
Chai Yang
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/02
Two-Stage Additional Evidence Support Association of Common Variants in the HDAC3 With the Increasing Risk of Schizophrenia Susceptibility
期刊论文
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2016, 卷号: 171, 期号: [db:dc_citation_issue], 页码: 1105-1111
作者:
Jia, Xiaodi
;
Zhang, Tianxiao
;
Li, Lu
;
Fu, Dongke
;
Lin, Huali
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/02
common variants
susceptibility
schizophrenia
Han Chinese
HDAC3
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