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

eNOS gene Glu298Asp and 4b/a polymorphisms are associated with renal function parameters in Mexican patients with Fabry disease.

Genetics and molecular research : GMR - 24 Oct 2016

Marin-Medina A, Brambila-Tapia A J L, Picos-Cárdenas V J, Gallegos-Arreola M P, Figuera L E

Abstract excerpt

Fabry disease (FD) is an inherited X-linked lysosomal disease that causes renal failure in a high percentage of affected individuals. The eNOS gene encodes for endothelial nitric oxide synthase, which plays an important role in glomerular hemodynamics. This gene has two main polymorphisms (Glu298Asp and 4b/a) that have been studied in the context of many different diseases, including those involving...

Read the complete abstract on PubMed

Topics

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

Share to Creatinine
Share to Fabry Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glomerular Filtration Rate

Share to Guanine Nucleotide Exchange Factors

Share to Mexico

Share to Nitric Oxide Synthase Type III

Share to Renal Insufficiency

Source

Identifiers

PMID: 27813552
DOI: 10.4238/gmr15047802

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

eNOS gene Glu298Asp and 4b/a polymorphisms are associated with renal function parameters in Mexican patients with Fabry disease.PMID 27813552Read ↗

Endothelial nitric oxide synthase gene polymorphisms in Fabry's disease.Semantic proximity Read ↗

Association of endothelial nitric oxide synthase gene polymorphisms with end-stage renal disease: a systematic review and meta-analysis.Semantic proximity Read ↗

Association of eNOS gene polymorphisms with renal disease in Caucasians with type 2 diabetes.Semantic proximity Read ↗

Association of ecNOS gene polymorphisms with end stage renal diseases.Semantic proximity Read ↗

The Endothelial Nitric Oxide Synthase Gene Polymorphism is Associated with the Susceptibility to Immunoglobulin a Nephropathy in Chinese Population.Semantic proximity Read ↗

Endothelial nitric oxide synthase gene polymorphism in intron 4 affects the progression of renal failure in non-diabetic renal diseasesSemantic proximity Read ↗

Endothelial nitric oxide synthetase, methylenetetrahydrofolate reductase polymorphisms, and cardiovascular complications in Tunisian patients with nondiabetic renal disease.Semantic proximity Read ↗

Genetic and phenotypic profile of Fabry disease in the population of Vale do Paraiba and Eastern São Paulo.Semantic proximity Read ↗

Endothelial nitric oxide synthase gene intron 4 a/b VNTR polymorphism in children with APSGN.Semantic proximity Read ↗

Association of the nitric oxide synthase (eNOS) gene polymorphism with increased risk for both lupus glomerulonephritis and rheumatoid arthritis in a single genetically homogeneous population.Semantic proximity Read ↗

Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism with the risk of end-stage renal disease.Semantic proximity Read ↗

Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon.Semantic proximity Read ↗

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