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Yanxia Wu

Showing results (91-100 of 102) with videos related to

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Scientific Reports|May 14, 2016
Analysis of the genetic association between IL27 variants and coronary artery disease in a Chinese Han populationQian Fan, Shaofang Nie, Sihui Li, et al.
Diabetes|January 29, 2011
The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han populationXiang Cheng, Lisong Shi, Shaofang Nie, et al.
American Journal of Human Genetics|October 1, 2013
The IL-33-ST2L pathway is associated with coronary artery disease in a Chinese Han populationXin Tu, Shaofang Nie, Yuhua Liao, et al.
Scientific Reports|February 21, 2018
Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial FibrillationPengxia Wang, Weixi Qin, Pengyun Wang, et al.
Annals of Human Genetics|March 2, 2019
Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4-subunit SCN4B with atrial fibrillationHongbo Xiong, Qin Yang, Xiaoping Zhang, et al.
Stroke|January 4, 2014
Regulation of CARD8 expression by ANRIL and association of CARD8 single nucleotide polymorphism rs2043211 (p.C10X) with ischemic strokeYing Bai, Shaofang Nie, Guiqing Jiang, et al.
Human Genetics|November 6, 2013
BRG1 variant rs1122608 on chromosome 19p13.2 confers protection against stroke and regulates expression of pre-mRNA-splicing factor SFRS3Xin Xiong, Chengqi Xu, Yuting Zhang, et al.
Scientific Reports|February 17, 2025
Whole genome sequencing of hepatitis B virus using tiled amplicon (HEPTILE) and probe based enrichment on Illumina and Nanopore platformsSheila F Lumley, Chris Kent, Daisy Jennings, et al.
Circulation. Cardiovascular Genetics|September 25, 2014
Candidate pathway-based genome-wide association studies identify novel associations of genomic variants in the complement system associated with coronary artery diseaseChengqi Xu, Qin Yang, Hongbo Xiong, et al.
Cancer Communications (London, England)|June 1, 2022
Transcriptome-wide association analysis identified candidate susceptibility genes for nasopharyngeal carcinomaYong-Qiao He, Wen-Qiong Xue, Dan-Hua Li, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
Scientific Reports|May 14, 2016
Analysis of the genetic association between IL27 variants and coronary artery disease in a Chinese Han populationQian Fan, Shaofang Nie, Sihui Li, et al.
Diabetes|January 29, 2011
The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han populationXiang Cheng, Lisong Shi, Shaofang Nie, et al.
American Journal of Human Genetics|October 1, 2013
The IL-33-ST2L pathway is associated with coronary artery disease in a Chinese Han populationXin Tu, Shaofang Nie, Yuhua Liao, et al.
Scientific Reports|February 21, 2018
Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial FibrillationPengxia Wang, Weixi Qin, Pengyun Wang, et al.
Annals of Human Genetics|March 2, 2019
Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4-subunit SCN4B with atrial fibrillationHongbo Xiong, Qin Yang, Xiaoping Zhang, et al.
Stroke|January 4, 2014
Regulation of CARD8 expression by ANRIL and association of CARD8 single nucleotide polymorphism rs2043211 (p.C10X) with ischemic strokeYing Bai, Shaofang Nie, Guiqing Jiang, et al.
Human Genetics|November 6, 2013
BRG1 variant rs1122608 on chromosome 19p13.2 confers protection against stroke and regulates expression of pre-mRNA-splicing factor SFRS3Xin Xiong, Chengqi Xu, Yuting Zhang, et al.
Scientific Reports|February 17, 2025
Whole genome sequencing of hepatitis B virus using tiled amplicon (HEPTILE) and probe based enrichment on Illumina and Nanopore platformsSheila F Lumley, Chris Kent, Daisy Jennings, et al.
Circulation. Cardiovascular Genetics|September 25, 2014
Candidate pathway-based genome-wide association studies identify novel associations of genomic variants in the complement system associated with coronary artery diseaseChengqi Xu, Qin Yang, Hongbo Xiong, et al.
Cancer Communications (London, England)|June 1, 2022
Transcriptome-wide association analysis identified candidate susceptibility genes for nasopharyngeal carcinomaYong-Qiao He, Wen-Qiong Xue, Dan-Hua Li, et al.
Pageof 11