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期刊论文 [50]
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Genetic variant in the promoter region of microRNA-137 reduces the warfarin maintenance dose in patients with atrial fibrillation
期刊论文
MOLECULAR MEDICINE REPORTS, 2019, 卷号: 19, 期号: 6
作者:
Wu, Donghui
;
Tian, Zhen
;
Yang, Yushuang
;
Liu, Dongna
;
Feng, Zhaohui
收藏
  |  
浏览/下载:38/0
  |  
提交时间:2019/12/05
genetic variant
VKORC1
promoter region
microRNA-137
warfarin maintenance dose
atrial fibrillation
Genetic polymorphisms in complement receptor 1 gene and its association with HBV-related liver disease: A case-control study
期刊论文
Gene, 2019, 卷号: Vol.688, 页码: 107-118
作者:
Jingrong Luo
;
Siyuan Chen
;
Jin Wang
;
Shan Ou
;
Wei Zhang
收藏
  |  
浏览/下载:14/0
  |  
提交时间:2019/12/13
Complement
receptor
1
HBV-related
liver
disease
Genetic
variant
Single
nucleotide
polymorphism
Association of SMUG1 SNPs in Intron Region and Linkage Disequilibrium with Occurrence of Cervical Carcinoma and HPV Infection in Chinese Population.
期刊论文
Journal of Cancer, 2019, 卷号: Vol.10 No.1, 页码: 238-248
作者:
Feng Ye
;
Hanzhi Wang
;
Jia Liu
;
Qi Cheng
;
Xiaojing Chen
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2019/12/13
CIN
III
SMUG1
cervical
squamous
cell
carcinoma
genetic
variant
intron
linkage
disequilibrium
Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China
期刊论文
2019, 卷号: 105, 期号: 4, 页码: 803-812
作者:
Dai Pu
;
Huang Li-Hui
;
Wang Guo-Jian
;
Gao Xue
;
Qu Chun-Yan
收藏
  |  
浏览/下载:37/0
  |  
提交时间:2020/01/03
aminoglycoside antibiotics
deafness genes
genetic deafness
habilitation
late-onset hearing loss
microarray
newborn genetic screening
newborn hearing screening
ototoxicity
pathogenic variant
Insights into genetics, human biology and disease gleaned from family based genomic studies
期刊论文
2019, 卷号: 21, 期号: 4, 页码: 798-812
作者:
Posey, Jennifer E.
;
O'Donnell-Luria, Anne H.
;
Chong, Jessica X.
;
Harel, Tamar
;
Jhangiani, Shalini N.
收藏
  |  
浏览/下载:28/0
  |  
提交时间:2020/01/03
rare variant phenotypes
Mendelian conditions
Centers for Mendelian Genomics (CMG)
genetic models for disease
disease traits
Marie Unna hereditary hypotrichosis accompanied by multiple familial trichoepithelioma in a Chinese family
期刊论文
2019, 卷号: 46, 期号: 5, 页码: 413-417
作者:
Huang, Ye
;
Cai, Chuan
;
Ren, Li
;
Cui, Caijuan
;
Zhang, Xue
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2020/01/03
HR
fatty acid-binding protein 12
genetic variant
Marie Unna hereditary hypotrichosis
multiple familial trichoepithelioma
Cumulative evidence for relationships between multiple variants in 8q24 and colorectal cancer incidence
期刊论文
MEDICINE, 2018, 卷号: Vol.97 No.35
作者:
Tong, Yu
;
Wang, Huiqing
;
Li, Shiping
;
Zhao, Fengyan
;
Ying, Junjie
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2019/02/25
8q24
colorectal cancer
genetic variant
susceptibility
The Functional MDM4 Genetic Polymorphsim as Prognostic Biomarker for Advanced Lung Adenocarcinoma Patients' Survival to EGFR-TKIs Therapy
期刊论文
JOURNAL OF THORACIC ONCOLOGY, 2018, 卷号: 13, 期号: 10, 页码: S593-S593
作者:
Yang, M.
;
Zhang, N.
;
Xing, H.
;
Liu, J.
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/11
functional MDM4 genetic variant
EGFR-TKIs treatment
Prognostic
Biomarker
Clinical Implications of the BIM Deletion Polymorphism in Advanced Lung Adenocarcinoma Treated With Gefitinib
期刊论文
CLINICAL LUNG CANCER, 2018, 卷号: 19, 期号: 4, 页码: E431-E438
作者:
Yuan, Jupeng
;
Li, Bo
;
Zhang, Nasha
;
Zhu, Hui
;
Zhou, Liqing
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/11
Apoptosis
Drug resistance
EGFR-TKI
Genetic variant
Survival
Genetic polymorphisms in complement receptor 1 gene and its association with HBV-related liver disease: A case-control study.
期刊论文
Gene, 2018
作者:
Luo Jingrong
;
Chen Siyuan
;
Wang Jin
;
Ou Shan
;
Zhang Wei
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/26
Complement
receptor
1
Genetic
variant
HBV-related
liver
disease
Single
nucleotide
polymorphism
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