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心理研究所 [2]
武汉大学 [1]
复旦大学上海医学院 [1]
上海中医药大学 [1]
湖南大学 [1]
中国医学科学院 北京... [1]
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期刊论文 [9]
发表日期
2019 [9]
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An epistasis between dopaminergic and oxytocinergic systems confers risk of post-traumatic stress disorder in a traumatized Chinese cohort
期刊论文
SCIENTIFIC REPORTS, 2019, 卷号: 9, 页码: 8
作者:
Zhang, Kunlin
;
Li, Gen
;
Wang, Li
;
Cao, Chengqi
;
Fang, Ruojiao
收藏
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浏览/下载:28/0
  |  
提交时间:2020/02/29
Genome-Wide Comparisons of Mutations Induced by Carbon-Ion Beam and Gamma-Rays Irradiation in Rice via Resequencing Multiple Mutants
期刊论文
FRONTIERS IN PLANT SCIENCE, 2019, 卷号: 10, 页码: 13
作者:
Yang, Guili
;
Luo, Wenlong
;
Zhang, Jian
;
Yan, Xiancheng
;
Du, Yan
收藏
  |  
浏览/下载:13/0
  |  
提交时间:2022/01/19
Oryza sativa L
carbon-ion beams (CIBs) irradiation
gamma rays (GRs)
resequencing
single base substitution (SBS)
InDels
multiple nucleotide variant (MNV)
structural variant (SV)
The TNF-Alpha Gene-1031T > C Polymorphism Is Associated With Onset Age but Not With Risk of Schizophrenia in a Chinese Population
期刊论文
NEUROPSYCHOLOGY, 2019, 卷号: 33, 期号: 4, 页码: 482-489
作者:
Xiu, Meihong
;
Zhang, Guangya
;
Chen, Nan
;
Chen, Song
;
Tan, Yunlong
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  |  
浏览/下载:73/0
  |  
提交时间:2019/06/03
schizophrenia
tumor necrosis factor
genotype
association
immune
onset age
A regulatory variant in TBX2 promoter is related to the decreased susceptibility of congenital heart disease in the Han Chinese population
期刊论文
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 卷号: 7, 期号: 2
作者:
Zhang, Ran-ran
;
Cai, Ke
;
Liu, Lian
;
Yang, Qian
;
Zhang, Ping
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  |  
浏览/下载:0/0
  |  
提交时间:2019/12/05
congenital heart disease
promoter
single-nucleotide polymorphism
TBX2
Schizophrenia Patient Shows a Rare Interleukin 15 Receptor alpha Variant Disrupting Signal Transduction
期刊论文
CURRENT MOLECULAR MEDICINE, 2019, 卷号: 19, 期号: 8
作者:
Pan, Yanli
;
Wang, Zhimin
;
Zhang, Guangping
;
Guo, Junhua
;
Zhu, Xuequan
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  |  
浏览/下载:24/0
  |  
提交时间:2019/12/05
Interleukin 15 receptor alpha
interleukin 15
single nucleotide polymorphism
schizophrenia
IL-15RA
STAT3 phosphorylation
Significant association of rare variant p.Gly8Ser in cardiac sodium channel beta 4-subunit SCN4B with atrial fibrillation
期刊论文
ANNALS OF HUMAN GENETICS, 2019, 卷号: 83, 期号: 4
作者:
Xiong, Hongbo
;
Yang, Qin
;
Zhang, Xiaoping
;
Wang, Pengxia
;
Chen, Feifei
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  |  
浏览/下载:43/0
  |  
提交时间:2019/12/05
atrial fibrillation
case-control association study
genetics
single-nucleotide polymorphism (SNP)
sodium channel beta 4-subunit (SCN4B)
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
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  |  
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
Minor alleles of genetic variants in second heart field increase the risk of hypoplastic right heart syndrome
期刊论文
2019, 卷号: 98, 期号: 2
作者:
Wang, Enshi
;
Nie, Yu
;
Fan, Xuesong
;
Zheng, Zhe
;
Gu, Haiyong
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  |  
浏览/下载:28/0
  |  
提交时间:2020/01/03
hypoplastic right heart syndrome
single-nucleotide variant
second heart field
transcription factor
congenital heart disease
Genetic polymorphism analysis of mitochondrial DNA from Chinese Xinjiang Kazak ethnic group by a novel mitochondrial DNA genotyping panel
期刊论文
MOLECULAR BIOLOGY REPORTS, 2019, 卷号: 46, 期号: 1, 页码: 17-25
作者:
Xie, T
;
Hu, L
;
Guo, YX
;
Li, YC
;
Chen, F
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  |  
浏览/下载:36/0
  |  
提交时间:2019/09/10
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