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Journal of Molecular and Cellular Cardiology
|
February 18, 2019
UBC9 regulates cardiac sodium channel Na<sub>v</sub>1.5 ubiquitination, degradation and sodium current density
Bo Tang, Yushuang Hu, Zhijie Wang, et al.
Journal of the American Heart Association
|
April 3, 2020
Statistical and Functional Studies Identify Epistasis of Cardiovascular Risk Genomic Variants From Genome-Wide Association Studies
Yabo Li, Hyosuk Cho, Fan Wang, et al.
The Journal of Biological Chemistry
|
June 27, 2009
Novel roles of GATA1 in regulation of angiogenic factor AGGF1 and endothelial cell function
Chun Fan, Ping Ouyang, Ayse A Timur, et al.
Molecular Vision
|
October 30, 2008
Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese family
Shirong Zhang, Mugen Liu, Jia Mei Dong, et al.
European Journal of Human Genetics : EJHG
|
January 14, 2018
De novo BK channel variant causes epilepsy by affecting voltage gating but not Ca<sup>2+</sup> sensitivity
Xia Li, Sibylle Poschmann, Qiuyun Chen, et al.
Journal of the American Heart Association
|
August 5, 2017
De Novo <i>FGF12</i> (Fibroblast Growth Factor 12) Functional Variation Is Potentially Associated With Idiopathic Ventricular Tachycardia
Qianqian Li, Yuanyuan Zhao, Gang Wu, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
June 25, 2017
Androgen inhibits key atherosclerotic processes by directly activating ADTRP transcription
Chunyan Luo, Elisabeth Pook, Bo Tang, et al.
Human Molecular Genetics
|
August 15, 2016
Haploinsufficiency of Klippel-Trenaunay syndrome gene Aggf1 inhibits developmental and pathological angiogenesis by inactivating PI3K and AKT and disrupts vascular integrity by activating VE-cadherin
Teng Zhang, Yufeng Yao, Jingjing Wang, et al.
Human Mutation
|
November 30, 2018
Lamin A mutation impairs interaction with nucleoporin NUP155 and disrupts nucleocytoplasmic transport in atrial fibrillation
Meng Han, Miao Zhao, Chen Cheng, et al.
BMC Medical Genetics
|
May 15, 2009
Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study
Nicola Martinelli, Oliviero Olivieri, Gong-Qing Shen, et al.
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Search research articles
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Showing results (31-40 of 51) with videos related to
Sort By:
Page
of 6
Journal of Molecular and Cellular Cardiology
|
February 18, 2019
UBC9 regulates cardiac sodium channel Na<sub>v</sub>1.5 ubiquitination, degradation and sodium current density
Bo Tang, Yushuang Hu, Zhijie Wang, et al.
Journal of the American Heart Association
|
April 3, 2020
Statistical and Functional Studies Identify Epistasis of Cardiovascular Risk Genomic Variants From Genome-Wide Association Studies
Yabo Li, Hyosuk Cho, Fan Wang, et al.
The Journal of Biological Chemistry
|
June 27, 2009
Novel roles of GATA1 in regulation of angiogenic factor AGGF1 and endothelial cell function
Chun Fan, Ping Ouyang, Ayse A Timur, et al.
Molecular Vision
|
October 30, 2008
Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese family
Shirong Zhang, Mugen Liu, Jia Mei Dong, et al.
European Journal of Human Genetics : EJHG
|
January 14, 2018
De novo BK channel variant causes epilepsy by affecting voltage gating but not Ca<sup>2+</sup> sensitivity
Xia Li, Sibylle Poschmann, Qiuyun Chen, et al.
Journal of the American Heart Association
|
August 5, 2017
De Novo <i>FGF12</i> (Fibroblast Growth Factor 12) Functional Variation Is Potentially Associated With Idiopathic Ventricular Tachycardia
Qianqian Li, Yuanyuan Zhao, Gang Wu, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
June 25, 2017
Androgen inhibits key atherosclerotic processes by directly activating ADTRP transcription
Chunyan Luo, Elisabeth Pook, Bo Tang, et al.
Human Molecular Genetics
|
August 15, 2016
Haploinsufficiency of Klippel-Trenaunay syndrome gene Aggf1 inhibits developmental and pathological angiogenesis by inactivating PI3K and AKT and disrupts vascular integrity by activating VE-cadherin
Teng Zhang, Yufeng Yao, Jingjing Wang, et al.
Human Mutation
|
November 30, 2018
Lamin A mutation impairs interaction with nucleoporin NUP155 and disrupts nucleocytoplasmic transport in atrial fibrillation
Meng Han, Miao Zhao, Chen Cheng, et al.
BMC Medical Genetics
|
May 15, 2009
Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study
Nicola Martinelli, Oliviero Olivieri, Gong-Qing Shen, et al.
Page
of 6