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Chengqi Xu

Showing results (71-80 of 94) with videos related to

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Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 15, 2024
A novel HOIP frameshift variant alleviates NF-kappaB signalling and sensitizes cells to TNF-induced deathMengru Wang, Ying Bai, Dan Jiang, et al.
Biochemical and Biophysical Research Communications|June 19, 2010
Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID populationPengyun Wang, Qinbo Yang, Xiaofen Wu, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 26, 2018
Small GTPases SAR1A and SAR1B regulate the trafficking of the cardiac sodium channel Na<sub>v</sub>1.5Zhijie Wang, Gang Yu, Yinan Liu, et al.
Atherosclerosis|January 18, 2016
Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarctionShanshan Chen, Xiaojing Wang, Junhan Wang, et al.
Acta Physiologica (Oxford, England)|October 8, 2020
Mog1 knockout causes cardiac hypertrophy and heart failure by downregulating tbx5-cryab-hspb2 signalling in zebrafishDongzhi Gou, Juan Zhou, Qixue Song, et al.
Molecular Genetics and Genomics : MGG|April 26, 2019
Identification of rare variants in cardiac sodium channel β4-subunit gene SCN4B associated with ventricular tachycardiaQin Yang, Hongbo Xiong, Chengqi Xu, et al.
Gene|May 24, 2020
ADTRP regulates TFPI expression via transcription factor POU1F1 involved in coronary artery diseaseChunyan Luo, Elisabeth Pook, Fan Wang, et al.
Clinical and Translational Medicine|May 28, 2021
A genome-wide association study identifies novel association between genetic variants in GGT7 and LINC00944 and hypertensionChengcheng Tan, Hongfu Zhang, Dong Yu, et al.
Scientific Reports|February 10, 2017
Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery DiseaseDan Yin, Duraid Hamied Naji, Yunlong Xia, et al.
Human Genetics|August 27, 2009
Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han populationLisong Shi, Cong Li, Chuchu Wang, et al.
Pageof 10

Showing results (71-80 of 94) with videos related to

Sort By:
Pageof 10
Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 15, 2024
A novel HOIP frameshift variant alleviates NF-kappaB signalling and sensitizes cells to TNF-induced deathMengru Wang, Ying Bai, Dan Jiang, et al.
Biochemical and Biophysical Research Communications|June 19, 2010
Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID populationPengyun Wang, Qinbo Yang, Xiaofen Wu, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 26, 2018
Small GTPases SAR1A and SAR1B regulate the trafficking of the cardiac sodium channel Na<sub>v</sub>1.5Zhijie Wang, Gang Yu, Yinan Liu, et al.
Atherosclerosis|January 18, 2016
Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarctionShanshan Chen, Xiaojing Wang, Junhan Wang, et al.
Acta Physiologica (Oxford, England)|October 8, 2020
Mog1 knockout causes cardiac hypertrophy and heart failure by downregulating tbx5-cryab-hspb2 signalling in zebrafishDongzhi Gou, Juan Zhou, Qixue Song, et al.
Molecular Genetics and Genomics : MGG|April 26, 2019
Identification of rare variants in cardiac sodium channel β4-subunit gene SCN4B associated with ventricular tachycardiaQin Yang, Hongbo Xiong, Chengqi Xu, et al.
Gene|May 24, 2020
ADTRP regulates TFPI expression via transcription factor POU1F1 involved in coronary artery diseaseChunyan Luo, Elisabeth Pook, Fan Wang, et al.
Clinical and Translational Medicine|May 28, 2021
A genome-wide association study identifies novel association between genetic variants in GGT7 and LINC00944 and hypertensionChengcheng Tan, Hongfu Zhang, Dong Yu, et al.
Scientific Reports|February 10, 2017
Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery DiseaseDan Yin, Duraid Hamied Naji, Yunlong Xia, et al.
Human Genetics|August 27, 2009
Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han populationLisong Shi, Cong Li, Chuchu Wang, et al.
Pageof 10