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科研机构
中国医学科学院 北... [37]
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期刊论文 [37]
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2019 [9]
2018 [6]
2017 [5]
2016 [9]
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专题:中国医学科学院 北京协和医学院
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Combined therapy with atorvastatin and atorvastatin-pretreated mesenchymal stem cells enhances cardiac performance after acute myocardial infarction by activating SDF-1/CXCR4 axis
期刊论文
2019, 卷号: 11, 期号: 7, 页码: 4214-+
作者:
Tian, Xia-Qiu
;
Yang, Yue-Jin
;
Li, Qing
;
Xu, Jun
;
Huang, Pei-Sen
收藏
  |  
浏览/下载:20/0
  |  
提交时间:2020/01/03
Mesenchymal stem cells
atorvastatin
acute myocardial infarction
SDF-1/CXCR4
Optimization of Timing and Times for Administration of Atorvastatin-Pretreated Mesenchymal Stem Cells in a Preclinical Model of Acute Myocardial Infarction
期刊论文
2019, 卷号: 8, 期号: 10, 页码: 1068-1083
作者:
Xu Jun
;
Xiong Yu-Yan
;
Li Qing
;
Hu Meng-Jin
;
Huang Pei-Sen
收藏
  |  
浏览/下载:13/0
  |  
提交时间:2020/01/03
Acute myocardial infarction
Atorvastatin
Mesenchymal stem cells
Multiple administrations
Timing
A Recurrent Rare SOX9 Variant (M469V) is Associated with Congenital Vertebral Malformations
期刊论文
2019
作者:
Wu Nan
;
Wang Lianlei
;
Hu Jianhua
;
Zhao Sen
;
Liu Bowen
收藏
  |  
浏览/下载:12/0
  |  
提交时间:2020/01/03
Acampomelic campomelic dysplasia
Campomelic dysplasia
Congenital scoliosis
Congenital vertebral malformations
Exome sequencing
SOX9 gene
The Progress of CRISPR/Cas9-Mediated Gene Editing in Generating Mouse/Zebrafish Models of Human Skeletal Diseases
期刊论文
2019, 卷号: 17, 页码: 954-962
作者:
Wu Nan
;
Liu Bowen
;
Du Huakang
;
Zhao Sen
;
Li Yaqi
收藏
  |  
浏览/下载:11/0
  |  
提交时间:2020/01/03
TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease
期刊论文
2019
作者:
Chen Weisheng
;
Lin Jiachen
;
Wang Lianlei
;
Li Xiaoxin
;
Zhao Sen
收藏
  |  
浏览/下载:32/0
  |  
提交时间:2020/01/03
TBX6 gene
compound inheritance model
congenital scoliosis (CS)
gene dosage
genotype-phenotype correlation
TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice
期刊论文
2019, 卷号: 28, 期号: 4, 页码: 539-547
作者:
Yang, Nan
;
Wu, Nan
;
Zhang, Ling
;
Zhao, Yanxue
;
Liu, Jiaqi
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2020/01/03
Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population
期刊论文
2019, 卷号: 688, 页码: 215-220
作者:
Liu, Gang
;
Liu, Sen
;
Li, Xiaoxin
;
Chen, Jia
;
Chen, Weisheng
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2020/01/03
Adolescent idiopathic scoliosis (AIS)
PAX1
Northern Han Chinese
Single nucleotide polymorphism (SNP)
PUMC classification system
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model
期刊论文
2019, 卷号: 21, 期号: 7, 页码: 1548-1558
作者:
Liu, Jiaqi
;
Wu, Nan
;
Yang, Nan
;
Takeda, Kazuki
;
Chen, Weisheng
收藏
  |  
浏览/下载:34/0
  |  
提交时间:2020/01/03
congenital scoliosis (CS)
16p11.2/TBX6
compound inheritance model
genotype-phenotype correlation
gene dosage
Efficacy of bisphosphonates in patients with synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome: a prospective open study
期刊论文
2019
作者:
Li Chen
;
Zhao Yanxue
;
Zuo Yuzhi
;
Zhou Yangzhong
;
Zhang Fa
收藏
  |  
浏览/下载:66/0
  |  
提交时间:2020/01/03
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease
期刊论文
2018, 卷号: 137, 期号: 6-7, 页码: 553-567
作者:
Liu, Jiaqi
;
Zhou, Yangzhong
;
Liu, Sen
;
Song, Xiaofei
;
Yang, Xin-Zhuang
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2020/01/03
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