Search Results - "Wang, Qing K."
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A non-canonical pathway regulates ER stress signaling and blocks ER stress-induced apoptosis and heart failure
Published in Nature communications (25-07-2017)“…Endoplasmic reticulum stress is an evolutionarily conserved cell stress response associated with numerous diseases, including cardiac hypertrophy and heart…”
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2
AGGF1 therapy inhibits thoracic aortic aneurysms by enhancing integrin α7-mediated inhibition of TGF-β1 maturation and ERK1/2 signaling
Published in Nature communications (20-04-2023)“…Thoracic aortic aneurysm (TAA) is a localized or diffuse dilatation of the thoracic aortas, and causes many sudden deaths each year worldwide. However, there…”
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Genome-Wide Analysis of DNA Methylation and Acute Coronary Syndrome
Published in Circulation research (26-05-2017)“…RATIONALE:Acute coronary syndrome (ACS) is a leading cause of death worldwide. Immune functions play a vital role in ACS development, however, whether…”
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TAGAP instructs Th17 differentiation by bridging Dectin activation to EPHB2 signaling in innate antifungal response
Published in Nature communications (20-04-2020)“…The TAGAP gene locus has been linked to several infectious diseases or autoimmune diseases, including candidemia and multiple sclerosis. While previous studies…”
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Post-transcriptional regulation of cardiac sodium channel gene SCN5A expression and function by miR-192-5p
Published in Biochimica et biophysica acta. Molecular basis of disease (01-10-2015)“…The SCN5A gene encodes cardiac sodium channel Nav1.5 and causes lethal ventricular arrhythmias/sudden death and atrial fibrillation (AF) when mutated…”
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Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation
Published in PLoS genetics (01-08-2015)“…Atrial fibrillation (AF) is the most common cardiac arrhythmia at the clinic. Recent GWAS identified several variants associated with AF, but they account for…”
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Protein therapy of skeletal muscle atrophy and mechanism by angiogenic factor AGGF1
Published in Journal of cachexia, sarcopenia and muscle (01-04-2023)“…Background Skeletal muscle atrophy is a common condition without a pharmacologic therapy. AGGF1 encodes an angiogenic factor that regulates cell…”
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The IL-33-ST2L Pathway Is Associated with Coronary Artery Disease in a Chinese Han Population
Published in American journal of human genetics (03-10-2013)“…The effects of interleukin-33 (IL-33) on the immune system have been clearly demonstrated; however, in cardiovascular diseases, especially in coronary artery…”
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Genetic susceptibility to myocardial infarction and coronary artery disease
Published in Human molecular genetics (15-10-2006)“…Atherosclerotic involvement in the coronary arteries, which can result in heart attack and sudden death, is a common disease and prototypic of a complex human…”
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10
Analysis of causal effect of APOA5 variants on premature coronary artery disease
Published in Annals of human genetics (01-11-2018)“…Apolipoprotein A5 (APOA5) regulates the metabolisms of triglyceride and HDL. APOA5 variants have been linked to coronary artery disease (CAD), but their causal…”
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Integrative Analysis of miRNA and mRNA Expression Profiles Associated With Human Atrial Aging
Published in Frontiers in physiology (19-09-2019)“…Limited findings have been reported to systematically study miRNA and mRNA expression profiles in aged human atria. In this study, we aimed to identify miRNAs,…”
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Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease
Published in Scientific reports (14-07-2017)“…Coronary artery disease (CAD) is the leading cause of death, and genetic factors contribute significantly to risk of CAD. This study aims to identify new CAD…”
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13
Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population
Published in PloS one (19-05-2015)“…Heart failure affects 1-2% of the adult population worldwide and coronary artery disease (CAD) is the underlying etiology of heart failure in 70% of the…”
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14
Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population
Published in Journal of human genetics (01-02-2008)“…Genome-wide single nucleotide polymorphism (SNP) association studies recently identified four SNPs (rs10757274, rs2383206, rs2383207, and rs10757278) on…”
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Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population
Published in Journal of the American Heart Association (01-05-2015)“…Background Recent genome‐wide association studies (GWAS) in European ancestry populations revealed several genomic loci for atrial fibrillation (AF). We…”
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16
Genetic variants at newly identified lipid loci are associated with coronary heart disease in a Chinese Han population
Published in PloS one (14-11-2011)“…Recent genome-wide association studies (GWAS) have mapped several novel loci influencing blood lipid levels in Caucasians. We sought to explore whether the…”
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Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01-10-2010)“…Idiopathic basal ganglia calcification (IBGC) is a neurodegenerative disorder that is characterized by basal ganglia and extrabasal ganglia calcification, and…”
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Loss of heterozygosity detected at three short tandem repeat locus commonly used for human DNA identification in a case of paternity testing
Published in Legal medicine (Tokyo, Japan) (01-01-2017)“…Graphical abstract…”
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Genetic Regulation of the Thymic Stromal Lymphopoietin (TSLP)/TSLP Receptor (TSLPR) Gene Expression and Influence of Epistatic Interactions Between IL-33 and the TSLP/TSLPR Axis on Risk of Coronary Artery Disease
Published in Frontiers in immunology (03-08-2018)“…The thymic stromal lymphopoietin (TSLP)/TSLP receptor (TSLPR) axis is involved in multiple inflammatory immune diseases, including coronary artery disease…”
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Genome-wide linkage scan identifies two novel genetic loci for coronary artery disease: in GeneQuest families
Published in PloS one (08-12-2014)“…Coronary artery disease (CAD) is the leading cause of death worldwide. Recent genome-wide association studies (GWAS) identified >50 common variants associated…”
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