Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Val109Asp polymorphism in Intelectin 1 gene is associated with coronary artery disease severity in women.

Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir - 1 Jan 2022

Güçlü-Geyik Filiz, Erkan Aycan Fahri, Özuynuk Aybike Sena, Ekici Berkay, Çoban Neslihan

Abstract excerpt

OBJECTIVE: Intelectin-1 is an anti-inflammatory adipokine encoded by the Intelectin 1 (ITLN1) gene. Genetic variations in the ITLN1 gene affect the risk of coronary artery disease (CAD) and related CAD risk factors. In this study, we aimed to investigate whether the ITLN1 gene Val109Asp polymorphism has an effect on the severity of CAD and serum lipid levels in both men and women. METHODS: A total of 493 subjects...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Case-Control Studies
Share to Coronary Angiography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Coronary Artery Disease

Share to Coronary Stenosis

Share to Cytokines

Share to Gene Frequency

Share to GPI-Linked Proteins

Share to Lectins

Source

Identifiers

PMID: 35197231
DOI: 10.5543/tkda.2022.21003

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Val109Asp polymorphism in Intelectin 1 gene is associated with coronary artery disease severity in women.PMID 35197231Read ↗

Omentin-1 Val109Asp polymorphism and increased coronary artery disease risk in smokers with type 2 diabetes.Semantic proximity Read ↗

Omentin Val109Asp polymorphism and risk of coronary artery disease.Semantic proximity Read ↗

Association of omentin Val109Asp polymorphism with coronary artery disease.Semantic proximity Read ↗

An oxidized low‐density lipoprotein receptor gene variant is inversely associated with the severity of coronary artery diseaseSemantic proximity Read ↗

LOX-1 variants modulate the severity of cardiovascular disease: state of the art and future directions.Semantic proximity Read ↗

Genetic variation in lectin-like oxidized low-density lipoprotein receptor 1 (LOX1) gene and the risk of coronary artery disease.Semantic proximity Read ↗

The association of Val109Asp polymorphic marker of intelectin 1 gene with abdominal obesity in Kyrgyz population.Semantic proximity Read ↗

Association of Angio-LncRNAs MIAT rs1061540/MALAT1 rs3200401 Molecular Variants with Gensini Score in Coronary Artery Disease Patients Undergoing Angiography.Semantic proximity Read ↗

Genetic variants of PEAR1 and ischemic clinical outcomes in coronary artery disease patients: a systematic review and meta-analysis.Semantic proximity Read ↗

Role of the fractalkine receptor CX3CR1 polymorphisms V249I and T280M as risk factors for early-onset coronary artery disease in patients with no classic risk factors.Semantic proximity Read ↗

Association of anti-oxidized LDL and candidate genes with severity of coronary stenosis in the Women's Ischemia Syndrome Evaluation study.Semantic proximity Read ↗

Association between the severity of angiographic coronary artery disease and paraoxonase gene polymorphisms in the National Heart, Lung, and Blood Institute-sponsored Women's Ischemia Syndrome Evaluation (WISE) study.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.