Progressive retinal atrophy in the Border Collie: a new XLPRA. (Q33322223)

25 July 2017

title

Progressive retinal atrophy in the Border Collie: a new XLPRA. (English)

1 reference

25 July 2017

8

0 references

Catherine Bourgain

object named as

Catherine Bourgain

6

0 references

author name string

Thierry Vilboux

1

1 reference

25 July 2017

Gilles Chaudieu

2

1 reference

25 July 2017

Patricia Jeannin

3

1 reference

25 July 2017

Delphine Delattre

4

1 reference

25 July 2017

Benoit Hedan

5

1 reference

25 July 2017

Guillaume Queney

7

1 reference

25 July 2017

Anne Thomas

9

1 reference

25 July 2017

Catherine André

10

1 reference

25 July 2017

publication date

3 March 2008

1 reference

25 July 2017

published in

BMC Veterinary Research

1 reference

25 July 2017

volume

4

1 reference

25 July 2017

page(s)

10

1 reference

Bestrophin gene mutations cause canine multifocal retinopathy: a novel animal model for best disease

25 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Linkage disequilibrium mapping in domestic dog breeds narrows the progressive rod-cone degeneration interval and identifies ancestral disease-transmitting chromosome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindness

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Advances in the molecular understanding of canine retinal diseases.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Dog star rising: the canine genetic system

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Breed distribution and history of canine mdr1-1Delta, a pharmacogenetic mutation that marks the emergence of breeds from the collie lineage

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Degenerations of the dog retina. VI. Central progressive atrophy with pigment epithelial dystrophy

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Linkage mapping of the primary disease locus for collie eye anomaly

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Different RPGR exon ORF15 mutations in Canids provide insights into photoreceptor cell degeneration

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosa

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Generalized progressive retinal atrophy of Sloughi dogs is due to an 8-bp insertion in exon 21 of the PDE6B gene

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Retinal dystrophy of Swedish briard/briard-beagle dogs is due to a 4-bp deletion in RPE65.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Characterization of canine photoreceptor phosducin cDNA and identification of a sequence variant in dogs with photoreceptor dysplasia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Positional cloning of the gene for X-linked retinitis pigmentosa 2

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit gene

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2324077

Restoration of vision in RPE65-deficient Briard dogs using an AAV serotype 4 vector that specifically targets the retinal pigmented epithelium

14 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1746-6148-4-10

Genetics of retinitis pigmentosa: metabolic classification and phenotype/genotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1746-6148-4-10

Mapping a new genetic locus for X linked retinitis pigmentosa to Xq28.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1746-6148-4-10

Canine Models of Ocular Disease: Outcross Breedings Define a Dominant Disorder Present in the English Mastiff and Bull Mastiff Dog Breeds

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1746-6148-4-10

Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1746-6148-4-10

Canine RPGRIP1 mutation establishes cone-rod dystrophy in miniature longhaired dachshunds as a homologue of human Leber congenital amaurosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1746-6148-4-10

cGMP phosphodiesterase-alpha mutation causes progressive retinal atrophy in the Cardigan Welsh corgi dog

21 January 2018

1 reference

12 December 2020

Companion animal medicine in the age of medical genetics

1 reference

12 December 2020

Evidence for a new locus for X-linked retinitis pigmentosa (RP23)

1 reference

12 December 2020

[Dog as a mammalian genetic model]

1 reference

12 December 2020

Vitamin E deficiency retinopathy in dogs

1 reference

12 December 2020

Collie eye anomaly in the border collie

1 reference

12 December 2020

A novel locus for X-linked retinitis pigmentosa

1 reference

12 December 2020

Identifiers

DOI

10.1186/1746-6148-4-10

1 reference

Dimensions Publication ID

25 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1746-6148-4-10

9 September 2019

1 reference

25 July 2017

1 reference