| scholarly article | Q13442814 |
| P2093 | author name string | Anna Palanova | |
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| Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans | Q33255648 | ||
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| Retinal dystrophy of Swedish briard/briard-beagle dogs is due to a 4-bp deletion in RPE65. | Q33857732 | ||
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| COL9A2 and COL9A3 mutations in canine autosomal recessive oculoskeletal dysplasia | Q34198153 | ||
| Degenerations of the dog retina. II. Generalized progressive atrophy of hereditary origin | Q34246871 | ||
| Assessment of canine BEST1 variations identifies new mutations and establishes an independent bestrophinopathy model (cmr3). | Q34434212 | ||
| Genomic deletion of CNGB3 is identical by descent in multiple canine breeds and causes achromatopsia | Q34678016 | ||
| A large animal model for CNGB1 autosomal recessive retinitis pigmentosa | Q34973721 | ||
| A CNGB1 frameshift mutation in Papillon and Phalène dogs with progressive retinal atrophy | Q34981371 | ||
| Altered miRNA expression in canine retinas during normal development and in models of retinal degeneration. | Q35104863 | ||
| An Intronic SINE insertion in FAM161A that causes exon-skipping is associated with progressive retinal atrophy in Tibetan Spaniels and Tibetan Terriers | Q35140451 | ||
| Molecular consequences of BEST1 gene mutations in canine multifocal retinopathy predict functional implications for human bestrophinopathies. | Q35220933 | ||
| Canine RPGRIP1 mutation establishes cone-rod dystrophy in miniature longhaired dachshunds as a homologue of human Leber congenital amaurosis. | Q53594146 | ||
| Exclusion of thePDE6Agene for generalised progressive retinal atrophy in 11 breeds of dog | Q60689209 | ||
| Variation in retinal degeneration phenotype inherited at the prcd locus | Q67921992 | ||
| Retinal degenerations in the dog: IV. Early retinal degeneration (erd) in Norwegian elkhounds | Q68822731 | ||
| An improved diagnostic test for rod cone dysplasia 1 (rcd1) using allele-specific polymerase chain reaction | Q71161069 | ||
| Secondary retinoschisis in a dog | Q71565727 | ||
| Molecular diagnostic tests for ascertainment of genotype at the rod cone dysplasia 1 (rcd1) locus in Irish setters | Q72348048 | ||
| Confirmation of the rod cGMP phosphodiesterase beta subunit (PDE beta) nonsense mutation in affected rcd-1 Irish setters in the UK and development of a diagnostic test | Q72658484 | ||
| Pathogenesis of progressive rod-cone degeneration in miniature poodles | Q72767545 | ||
| XLPRA: a canine retinal degeneration inherited as an X-linked trait | Q72849441 | ||
| Development and use of a polymerase chain reaction-based diagnostic test for the causal mutation of progressive retinal atrophy in Cardigan Welsh Corgis | Q74004818 | ||
| cGMP phosphodiesterase-alpha mutation causes progressive retinal atrophy in the Cardigan Welsh corgi dog | Q77958620 | ||
| Clinical findings in early onset cone-rod dystrophy in the Standard Wire-haired Dachshund | Q79835083 | ||
| Pathological and electrophysiological features of a canine cone-rod dystrophy in the miniature longhaired dachshund | Q80853950 | ||
| The cone dysfunction syndromes | Q35635184 | ||
| DNA testing and domestic dogs | Q35745619 | ||
| Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa | Q35751018 | ||
| Bestrophin gene mutations cause canine multifocal retinopathy: a novel animal model for best disease | Q35910846 | ||
| Exclusion of RPGRIP1 ins44 from primary causal association with early-onset cone-rod dystrophy in dogs. | Q36173074 | ||
| Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit gene | Q36274060 | ||
| 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 | Q36825024 | ||
| Haplotype-defined linkage region for gPRA in Schapendoes dogs | Q36869324 | ||
| Canine RD3 mutation establishes rod-cone dysplasia type 2 (rcd2) as ortholog of human and murine rd3. | Q37119492 | ||
| A non-stop S-antigen gene mutation is associated with late onset hereditary retinal degeneration in dogs | Q37146160 | ||
| Canine multifocal retinopathy in the Australian Shepherd: a case report | Q37207542 | ||
| Intravitreal injection of ciliary neurotrophic factor (CNTF) causes peripheral remodeling and does not prevent photoreceptor loss in canine RPGR mutant retina | Q37259762 | ||
| IQCB1 and PDE6B mutations cause similar early onset retinal degenerations in two closely related terrier dog breeds | Q37259774 | ||
| Photoreceptor cell death mechanisms in inherited retinal degeneration. | Q37316717 | ||
| Genome-wide association study in RPGRIP1(-/-) dogs identifies a modifier locus that determines the onset of retinal degeneration. | Q37626843 | ||
| Epigenetic regulatory mechanisms in vertebrate eye development and disease. | Q37697504 | ||
| Retinal degeneration in the dog and cat. | Q37937795 | ||
| In vivo gene therapy in young and adult RPE65-/- dogs produces long-term visual improvement. | Q40594379 | ||
| Evaluation of cGMP-phosphodiesterase (PDE) subunits for causal association with rod-cone dysplasia 2 (rcd2), a canine model of abnormal retinal cGMP metabolism. | Q40925985 | ||
| Exonic SINE insertion in STK38L causes canine early retinal degeneration (erd) | Q41234566 | ||
| A deletion in nephronophthisis 4 (NPHP4) is associated with recessive cone-rod dystrophy in standard wire-haired dachshund | Q41954216 | ||
| An ADAM9 mutation in canine cone-rod dystrophy 3 establishes homology with human cone-rod dystrophy 9 | Q42522157 | ||
| Structure and analysis of the transducin beta3-subunit gene, a candidate for inherited cone degeneration (cd) in the dog. | Q42662242 | ||
| Different RPGR exon ORF15 mutations in Canids provide insights into photoreceptor cell degeneration | Q42675161 | ||
| Screening for a canine model of choroideremia exclusively identifies nonpathogenic CHM variants | Q42676285 | ||
| Investigation of fellow eye of unilateral retinal detachment in Shih-Tzu | Q42907762 | ||
| Generalized progressive retinal atrophy in the Irish Glen of Imaal Terrier is associated with a deletion in the ADAM9 gene | Q42944117 | ||
| Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene | Q43272208 | ||
| An improved DNA-based test for detection of the codon 616 mutation in the alpha cyclic GMP phosphodiesterase gene that causes progressive retinal atrophy in the Cardigan Welsh Corgi. | Q44033041 | ||
| Segregation distortion in inheritance of progressive rod cone degeneration (prcd) in miniature poodle dogs | Q44046730 | ||
| Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3. | Q44078571 | ||
| Gene transfer in the RPE65 null mutation dog: relationship between construct volume, visual behavior and electroretinographic (ERG) results | Q44185833 | ||
| Functional and structural recovery of the retina after gene therapy in the RPE65 null mutation dog. | Q44376450 | ||
| Canine Models of Ocular Disease: Outcross Breedings Define a Dominant Disorder Present in the English Mastiff and Bull Mastiff Dog Breeds | Q44401222 | ||
| Cloning of the canine ABCA4 gene and evaluation in canine cone-rod dystrophies and progressive retinal atrophies. | Q44830407 | ||
| Inherited retinal dysplasia and persistent hyperplastic primary vitreous in Miniature Schnauzer dogs | Q44848670 | ||
| Best's disease. Overview of pathology and its causes | Q45229288 | ||
| Restoration of vision in RPE65-deficient Briard dogs using an AAV serotype 4 vector that specifically targets the retinal pigmented epithelium | Q45863029 | ||
| Canine cone transducin-gamma gene and cone degeneration in the cd dog. | Q45931114 | ||
| The beta subunit of cyclic GMP phosphodiesterase mRNA is deficient in canine rod-cone dysplasia 1 | Q46168845 | ||
| Late-onset progressive retinal atrophy in the Gordon and Irish Setter breeds is associated with a frameshift mutation in C2orf71. | Q46331334 | ||
| Canine multifocal retinopathy caused by a BEST1 mutation in a Boerboel. | Q46425472 | ||
| Linkage mapping of canine rod cone dysplasia type 2 (rcd2) to CFA7, the canine orthologue of human 1q32. | Q46966342 | ||
| Nonallelism of erd and prcd and exclusion of the canine RDS/peripherin gene as a candidate for both retinal degeneration loci | Q48065444 | ||
| P275 | copyright license | Creative Commons Attribution-NonCommercial 3.0 Unported | Q18810331 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | diagnosis | Q16644043 |
| P304 | page(s) | 41-51 | |
| P577 | publication date | 2016-01-01 | |
| P1433 | published in | Veterinary Medicine: Research and Reports | Q15817527 |
| P1476 | title | The genetics of inherited retinal disorders in dogs: implications for diagnosis and management | |
| P478 | volume | 7 |
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