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

A tool set to allow rapid screening of dog families with PRA for association with candidate genes.

Veterinary ophthalmology - 1 Jul 2017

Winkler Paige A, Davis Jennifer A, Petersen-Jones Simon M, Venta Patrick J, Bartoe Joshua T

Abstract excerpt

OBJECTIVE: To develop a method to rapidly screen candidate genes for association with recessively inherited progressive retinal atrophy (PRA) in pedigrees of dog in which a causative mutation has not been identified. ANIMAL STUDIED: Thirteen PRA-affected dogs were used in this study. PROCEDURES: Two microsatellite markers (MS) were designed flanking 45 candidate genes. MS markers were analyzed for heterozygosity...

Read the complete abstract on PubMed

Topics

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

Share to Dog Diseases
Share to Dogs
Share to Genes, Recessive

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to Mutation

Share to Pedigree

Share to Retinal Degeneration

Share to Species Specificity

Source

Identifiers

PMID: 27317651
DOI: 10.1111/vop.12401

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

A tool set to allow rapid screening of dog families with PRA for association with candidate genes.PMID 27317651Read ↗

A novel mutation in PDE6B in Spanish Water Dogs with early-onset progressive retinal atrophy.Semantic proximity Read ↗

Gene Panel Screening Across Canine Eye Disorders Highlights Genetic Heterogeneity and the Need for Molecular DiscoveriesSemantic proximity Read ↗

Elucidating the genetic basis of canine progressive retinal atrophies in several breeds of dogSemantic proximity Read ↗

Genetic screening for PRA-associated mutations in multiple dog breeds shows that PRA is heterogeneous within and between breeds.Semantic proximity Read ↗

Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogsSemantic proximity Read ↗

Identification of the mutation causing progressive retinal atrophy in Old Danish Pointing Dog.Semantic proximity Read ↗

The challenges of pedigree dog health: approaches to combating inherited diseaseSemantic proximity Read ↗

Progressive retinal atrophy in Shetland sheepdog is associated with a mutation in the CNGA1 gene.Semantic proximity Read ↗

Identification of putative SNPs in progressive retinal atrophy affected Canis lupus familiaris using exome sequencing.Semantic proximity Read ↗

Late-onset progressive retinal atrophy in the Gordon and Irish Setter breeds is associated with a frameshift mutation in C2orf71.Semantic proximity Read ↗

Haplotype-defined linkage region for gPRA in Schapendoes dogs.Semantic proximity Read ↗

Analysis of PDE6D and PDE6G genes for generalised progressive retinal atrophy (gPRA) mutations in dogs.Semantic proximity Read ↗

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