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Qing Kenneth Wang

Showing results (11-20 of 51) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 12, 2018
Angiotensin II increases angiogenesis by NF-κB-mediated transcriptional activation of angiogenic factor AGGF1Wenxia Si, Wen Xie, Wenbing Deng, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|May 3, 2011
Identification and molecular characterization of two novel mutations in COL1A2 in two Chinese families with osteogenesis imperfectaZhenping Xu, Yulei Li, Xiangyang Zhang, et al.
International Journal of Dermatology|January 8, 2009
A novel mutation in the ATP2C1 gene is associated with Hailey-Hailey disease in a Chinese familyJiang Zhou Liu, Zhou Jiang Liu, Tao Yang, et al.
International Journal of Cardiology|September 19, 2009
LQTS mutation N1325S in cardiac sodium channel gene SCN5A causes cardiomyocyte apoptosis, cardiac fibrosis and contractile dysfunction in miceTeng Zhang, Sandro L Yong, Jeanne K Drinko, et al.
RNA Biology|July 1, 2020
Splice variants of lncRNA RNA ANRIL exert opposing effects on endothelial cell activities associated with coronary artery diseaseHyosuk Cho, Yabo Li, Stephen Archacki, et al.
Heart Rhythm|May 16, 2024
14-3-3ε/YWHAE regulates the transcriptional expression of cardiac sodium channel Na<sub>V</sub>1.5Yushuang Hu, Chi Zhang, Shun Wang, et al.
Cytokine|February 22, 2023
Gene polymorphism in IL17A and gene-gene interaction in the IL23R/IL17A axis are associated with susceptibility to coronary artery diseaseHongsong Zhang, Shaofang Nie, Qianwen Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 26, 2011
Family-based and population-based association studies validate PTPRD as a risk factor for restless legs syndromeQinbo Yang, Lin Li, Rong Yang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 11, 2008
[A Novel mutation of F189L in CASQ2 in families with catecholaminergic polymorphic ventricular tachycardia]Qian-qian Liu, Carlos Oberti, Xian-qin Zhang, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 26, 2017
Identification of a molecular signaling gene-gene regulatory network between GWAS susceptibility genes ADTRP and MIA3/TANGO1 for coronary artery diseaseChunyan Luo, Fan Wang, Xiang Ren, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

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Pageof 6
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 12, 2018
Angiotensin II increases angiogenesis by NF-κB-mediated transcriptional activation of angiogenic factor AGGF1Wenxia Si, Wen Xie, Wenbing Deng, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|May 3, 2011
Identification and molecular characterization of two novel mutations in COL1A2 in two Chinese families with osteogenesis imperfectaZhenping Xu, Yulei Li, Xiangyang Zhang, et al.
International Journal of Dermatology|January 8, 2009
A novel mutation in the ATP2C1 gene is associated with Hailey-Hailey disease in a Chinese familyJiang Zhou Liu, Zhou Jiang Liu, Tao Yang, et al.
International Journal of Cardiology|September 19, 2009
LQTS mutation N1325S in cardiac sodium channel gene SCN5A causes cardiomyocyte apoptosis, cardiac fibrosis and contractile dysfunction in miceTeng Zhang, Sandro L Yong, Jeanne K Drinko, et al.
RNA Biology|July 1, 2020
Splice variants of lncRNA RNA ANRIL exert opposing effects on endothelial cell activities associated with coronary artery diseaseHyosuk Cho, Yabo Li, Stephen Archacki, et al.
Heart Rhythm|May 16, 2024
14-3-3ε/YWHAE regulates the transcriptional expression of cardiac sodium channel Na<sub>V</sub>1.5Yushuang Hu, Chi Zhang, Shun Wang, et al.
Cytokine|February 22, 2023
Gene polymorphism in IL17A and gene-gene interaction in the IL23R/IL17A axis are associated with susceptibility to coronary artery diseaseHongsong Zhang, Shaofang Nie, Qianwen Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 26, 2011
Family-based and population-based association studies validate PTPRD as a risk factor for restless legs syndromeQinbo Yang, Lin Li, Rong Yang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 11, 2008
[A Novel mutation of F189L in CASQ2 in families with catecholaminergic polymorphic ventricular tachycardia]Qian-qian Liu, Carlos Oberti, Xian-qin Zhang, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 26, 2017
Identification of a molecular signaling gene-gene regulatory network between GWAS susceptibility genes ADTRP and MIA3/TANGO1 for coronary artery diseaseChunyan Luo, Fan Wang, Xiang Ren, et al.
Pageof 6