A novel form of progressive retinal atrophy in Swedish vallhund dogs - sprookjes - yvandenbroek - TriplyDB

A novel form of progressive retinal atrophy in Swedish vallhund dogs

A novel form of progressive retinal atrophy in Swedish vallhund dogs

http://www.wikidata.org/entity/Q34149777

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Canine CNGA3 Gene Mutations Provide Novel Insights into Human Achromatopsia-Associated Channelopathies and Treatment Increased expression of MERTK is associated with a unique form of canine retinopathy Whole-genome sequence, SNP chips and pedigree structure: building demographic profiles in domestic dog breeds to optimize genetic-trait mapping An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs.Identification of putative SNPs in progressive retinal atrophy affected Canis lupus familiaris using exome sequencing.Clinical studies on progressive retinal atrophy in 31 dogs.Characterization of a novel form of progressive retinal atrophy in Whippet dogs: a clinical, electroretinographic, and breeding study.The genetics of inherited retinal disorders in dogs: implications for diagnosis and management

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P2860

A novel form of progressive retinal atrophy in Swedish vallhund dogs

http://www.wikidata.org/entity/Q34149777

description

2014 nî lūn-bûn

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2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

A novel form of progressive retinal atrophy in Swedish vallhund dogs

@ast

A novel form of progressive retinal atrophy in Swedish vallhund dogs

@en

A novel form of progressive retinal atrophy in Swedish vallhund dogs

@nl

type

label

A novel form of progressive retinal atrophy in Swedish vallhund dogs

@ast

A novel form of progressive retinal atrophy in Swedish vallhund dogs

@en

A novel form of progressive retinal atrophy in Swedish vallhund dogs

@nl

prefLabel

A novel form of progressive retinal atrophy in Swedish vallhund dogs

@ast

A novel form of progressive retinal atrophy in Swedish vallhund dogs

@en

A novel form of progressive retinal atrophy in Swedish vallhund dogs

@nl

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A novel form of progressive retinal atrophy in Swedish vallhund dogs

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Alison Duncan

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András M Komáromy

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Ann E Cooper

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Eija H Seppälä

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Jessica S Rowlan

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Päivi Vanhapelto

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P2860

Gene therapy rescues cone function in congenital achromatopsia.

The prevalence of age-related eye diseases and visual impairment in aging: current estimates

Canine retina has a primate fovea-like bouquet of cone photoreceptors which is affected by inherited macular degenerations

Restoration of vision in the pde6β-deficient dog, a large animal model of rod-cone dystrophy

Retinal degeneration associated with vitamin E deficiency in hunting dogs

Genetic and phenotypic variations of inherited retinal diseases in dogs: the power of within- and across-breed studies

Successful gene therapy in the RPGRIP1-deficient dog: a large model of cone-rod dystrophy.

In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosa

Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect.

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

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