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

Analysis of phosducin as a candidate gene for retinopathies.

Ophthalmic genetics - 1 Mar 1996

Ara-Iwata F, Jacobson S G, Gass J D, Hotta Y, Fujiki K, Hayakawa M, Inana G

Abstract excerpt

Phosducin, a retina-expressed gene mapped to chromosome 1q25-32.1, was analyzed as a candidate gene for retinopathies. The phosducin gene was cloned and characterized, and PCR primers were designed. Eighty-three patients with various retinopathies and 45 control subjects (24 American, 21 Japanese) were analyzed for mutations in the phosducin gene by PCR, denaturing gradient gel electrophoresis (DGGE), and...

Read the complete abstract on PubMed

Topics

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

Share to Base Sequence
Share to Chromosome Mapping
Share to Cloning, Molecular

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to DNA Primers

Share to Molecular Sequence Data

Share to Mutation

Share to Phosphoproteins

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 8740692
DOI: 10.3109/13816819609057863

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Analysis of phosducin as a candidate gene for retinopathies.PMID 8740692Read ↗

Mutation screening of the phosducin gene PDC in patients with retinitis pigmentosa and allied diseases.Semantic proximity Read ↗

Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy.Semantic proximity Read ↗

Protocadherin-21 (PCDH21), a candidate gene for human retinal dystrophies.Semantic proximity Read ↗

USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids.Semantic proximity Read ↗

Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa.Semantic proximity Read ↗

A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants.Semantic proximity Read ↗

Seven novel mutations in the long isoform of the USH2A gene in Chinese families with nonsyndromic retinitis pigmentosa and Usher syndrome Type II.Semantic proximity Read ↗

Targeted exon sequencing in Usher syndrome type I.Semantic proximity Read ↗

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