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

Association of apelin genetic variants with type 2 diabetes and related clinical features in Chinese Hans.

Chinese medical journal - 5 Jun 2009

Zhang Rong, Hu Cheng, Wang Cong-rong, Ma Xiao-jing, Bao Yu-qian, Xu Jing, Lu Jing-yi, Qin Wen, Xiang Kun-san, Jia Wei-ping

Abstract excerpt

BACKGROUND: Apelin is an adipokine that contributes to the pathogenesis of type 2 diabetes. The plasma levels of apelin increased in obese patients and diabetic subjects. This study aimed to investigate the effects of apelin genetic variants on type 2 diabetes and related quantitative traits. MET...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Asian People
Share to Diabetes Mellitus, Type 2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Genotype

Share to Intercellular Signaling Peptides and Proteins

Share to Linkage Disequilibrium

Source

Identifiers

PMID: 19567136

Genes

APLN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19567136-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of apelin genetic variants with type 2 diabetes and related clinical features in Chinese Hans.PMID 19567136Read ↗

The association between single nucleotide polymorphisms of the Apelin gene and diabetes mellitus in a Chinese population.Semantic proximity Read ↗

Search for Genetic Variant in the Apelin Gene by Resequencing and Association Study in European Subjects.Semantic proximity Read ↗

Associations of common variants at APLN and hypertension in Chinese subjects with and without diabetes.Semantic proximity Read ↗

Genotype screening of APLN rs3115757 variant in Egyptian women population reveals an association with obesity and insulin resistance.Semantic proximity Read ↗

Apelin gene polymorphism influences apelin expression and obesity phenotypes in Chinese women.Semantic proximity Read ↗

Association between the apelin rs2235306 gene polymorphism and metabolic syndrome.Semantic proximity Read ↗

[Association of SNP276 in adiponectin gene with type 2 diabetes mellitus and insulin sensitivity].Semantic proximity Read ↗

Heritability and genome-wide association analyses of fasting plasma glucose in Chinese adult twins.Semantic proximity Read ↗

Family-based analysis of apelin and AGTRL1 gene polymorphisms with hypertension in Han Chinese.Semantic proximity Read ↗

Associations between gene polymorphisms of the apelin-APJ system and the risk of hypertension.Semantic proximity Read ↗

Genetic variants of LPIN1 indicate an association with Type 2 diabetes mellitus in a Chinese population.Semantic proximity Read ↗

Association of ADIPOQ variants with type 2 diabetes mellitus susceptibility in ethnic Han Chinese from northeast China.Semantic proximity Read ↗

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