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

The influence of apolipoprotein A5 T-1131C and apolipoprotein E common genetic variants on the levels of hemostatic markers in dyslipidemic patients.

Clinica chimica acta; international journal of clinical chemistry - 25 Sept 2014

Novotny Dalibor, Karasek David, Vaverkova Helena, Slavik Ludek

Abstract excerpt

OBJECTIVES: The aim of this study was to evaluate the relationships of the T-1131C (rs662799) polymorphism variants of apolipoprotein A5 (Apo A5) gene and variants of apolipoprotein E (Apo E) gene common polymorphism (rs429358, rs7412) to selected hemostatic markers. STUDY DESIGN AND METHODS: We examined 590 asymptomatic dyslipidemic patients, subsequently divided into MetS+ (n=146) and MetS- (n=444) groups...

Read the complete abstract on PubMed

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Topics

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

Share to Apolipoproteins A
Share to Apolipoproteins E
Share to Asymptomatic Diseases
Share to Biomarkers
Share to Dyslipidemias
Share to Hemostasis
Share to Polymorphism, Single Nucleotide
Share to Tissue Plasminogen Activator

Source

Identifiers

PMID: 24815086
DOI: 10.1016/j.cca.2014.04.029

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The influence of apolipoprotein A5 T-1131C and apolipoprotein E common genetic variants on the levels of hemostatic markers in dyslipidemic patients.PMID 24815086Read ↗

APOA5 Variant rs662799, Role in Cardiovascular Traits and Serum Adipokine Levels in Caucasian Obese Subjects.Semantic proximity Read ↗

The polymorphism -1131T>C in apolipoprotein A5 gene is associated with dyslipidemia in Brazilian subjects.Semantic proximity Read ↗

Association of Apolipoprotein A5 Gene Polymorphisms with Metabolic Syndrome in the Korean Population.Semantic proximity Read ↗

APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia.Semantic proximity Read ↗

Apolipoprotein A5 T-1131C variant confers risk for metabolic syndrome.Semantic proximity Read ↗

Effects of APOA5 -1131T>C (rs662799) on fasting plasma lipids and risk of metabolic syndrome: evidence from a case-control study in China and a meta-analysis.Semantic proximity Read ↗

APOA5 variants and metabolic syndrome in Caucasians.Semantic proximity Read ↗

Interaction between APOA5 -1131T>C and APOE polymorphisms and their association with severe hypertriglyceridemia.Semantic proximity Read ↗

Association of APOA5 -1131T>C and S19W gene polymorphisms with both mild hypertriglyceridemia and hyperchylomicronemia in type 2 diabetic patients.Semantic proximity Read ↗

Contribution of APOA5 gene variants to plasma triglyceride determination and to the response to both fat and glucose tolerance challenges.Semantic proximity Read ↗

Genetic association analysis of rs662799 ( − 1131A > G) polymorphism of APOA5 gene with morphometric and physio-metric traits using multiplex PCRSemantic proximity Read ↗

Common functional variants of APOA5 and GCKR accumulate gradually in association with triglyceride increase in metabolic syndrome patients.Semantic proximity Read ↗

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