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 between SRBD1 and ELOVL5 gene polymorphisms and primary open-angle glaucoma.

Investigative ophthalmology & visual science - 28 Jun 2011

Mabuchi Fumihiko, Sakurada Yoichi, Kashiwagi Kenji, Yamagata Zentaro, Iijima Hiroyuki, Tsukahara Shigeo

Abstract excerpt

PURPOSE: The S1 RNA binding domain 1 (SRBD1) and elongation of long-chain fatty acids family member 5 (ELOVL5) have been reported to be susceptibility genes for early-onset normal-tension glaucoma (NTG). The present study we conducted to assess whether these genes were associated with primary open-angle glaucoma (POAG), including late-onset NTG and high-tension glaucoma (HTG). METHODS: Three hundred seventy...

Read the complete abstract on PubMed

Topics

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

Share to Acetyltransferases
Share to Fatty Acid Elongases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Glaucoma, Open-Angle

Share to Polymerase Chain Reaction

Share to Polymorphism, Genetic

Share to Ribonucleoproteins

Source

Identifiers

PMID: 21508110
DOI: 10.1167/iovs.11-7382

Genes

ELOVL5
SRBD1

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

Association between SRBD1 and ELOVL5 gene polymorphisms and primary open-angle glaucoma.PMID 21508110Read ↗

Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility.Semantic proximity Read ↗

Involvement of genetic variants associated with primary open-angle glaucoma in pathogenic mechanisms and family history of glaucoma.Semantic proximity Read ↗

Clinical and Genetic Characteristics Analysis of Korean Patients with Stargardt Disease Using Targeted Exome Sequencing.Semantic proximity Read ↗

Association of Gene Polymorphisms with Normal Tension Glaucoma: A Systematic Review and Meta-Analysis.Semantic proximity Read ↗

Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis?Semantic proximity Read ↗

Identification of lncRNA–miRNA–mRNA regulatory network associated with primary open angle glaucomaSemantic proximity Read ↗

Association of Long Non-coding RNA C1RL-AS1 and PTPN6 Gene Polymorphisms with Ocular Behcet's Disease in Han Chinese.Semantic proximity Read ↗

Dogs and humans share a common susceptibility gene SRBD1 for glaucoma risk.Semantic proximity Read ↗

Evaluation of the ELOVL4, PRPH2 and ABCA4 genes in patients with Stargardt macular degeneration.Semantic proximity Read ↗

Identification of lncRNA–miRNA–mRNA regulatory network associated with Primary Open Angle GlaucomaSemantic proximity Read ↗

Exploring the role of apolipoprotein E gene promoter polymorphisms in susceptibility to normal-tension glaucoma in a Korean population.Semantic proximity Read ↗

LOXL1 variants in elderly Japanese patients with exfoliation syndrome/glaucoma, primary open-angle glaucoma, normal tension glaucoma, and cataract.Semantic proximity Read ↗

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