Detalles de la búsqueda
1.
Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs.
PLoS Genet
; 19(2): e1010651, 2023 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-36848397
2.
Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats.
PLoS Genet
; 18(6): e1009804, 2022 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-35709088
3.
A new Finnish flavor of feline coat coloration, "salmiak," is associated with a 95-kb deletion downstream of the KIT gene.
Anim Genet
; 2024 May 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-38721753
4.
A loss-of-function variant in canine GLRA1 associates with a neurological disorder resembling human hyperekplexia.
Hum Genet
; 142(8): 1221-1230, 2023 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-37222814
5.
Correction: Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs.
PLoS Genet
; 15(1): e1007938, 2019 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30657768
6.
Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs.
PLoS Genet
; 14(4): e1007361, 2018 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-29708978
7.
Defining the ABC of gene essentiality in streptococci.
BMC Genomics
; 18(1): 426, 2017 05 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-28569133
8.
Canine genome assembly correction facilitates identification of a MAP9 deletion as a potential age of onset modifier for RPGRIP1-associated canine retinal degeneration.
Mamm Genome
; 27(5-6): 237-45, 2016 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-27017229
9.
Genome sequencing reveals a splice donor site mutation in the SNX14 gene associated with a novel cerebellar cortical degeneration in the Hungarian Vizsla dog breed.
BMC Genet
; 17(1): 123, 2016 08 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-27566131
10.
Spinocerebellar ataxia in the Italian Spinone dog is associated with an intronic GAA repeat expansion in ITPR1.
Mamm Genome
; 26(1-2): 108-17, 2015 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-25354648
11.
Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed.
PLoS Genet
; 8(1): e1002462, 2012 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-22253609
12.
Association of FGF4L1 Retrogene Insertion with Prolapsed Gland of the Nictitans (Cherry Eye) in Dogs.
Genes (Basel)
; 15(2)2024 02 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-38397188
13.
Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation.
BMC Genet
; 13: 55, 2012 Jul 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-22781464
14.
Congenital keratoconjunctivitis sicca and ichthyosiform dermatosis in Cavalier King Charles spaniel dogs. Part II: candidate gene study.
Vet Ophthalmol
; 15(5): 327-32, 2012 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-22339941
15.
Large scale across-breed genome-wide association study reveals a variant in HMGA2 associated with inguinal cryptorchidism risk in dogs.
PLoS One
; 17(5): e0267604, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35617214
16.
Environmental risk factors in puppies and kittens for developing chronic disorders in adulthood: A call for research on developmental programming.
Front Vet Sci
; 9: 944821, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36619947
17.
ADAMTS17 mutation associated with primary lens luxation is widespread among breeds.
Vet Ophthalmol
; 14(6): 378-84, 2011 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-22050825
18.
Charcot-Marie-Tooth type 4B2 demyelinating neuropathy in miniature Schnauzer dogs caused by a novel splicing SBF2 (MTMR13) genetic variant: a new spontaneous clinical model.
PeerJ
; 7: e7983, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31772832
19.
Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration.
Genes (Basel)
; 10(5)2019 05 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-31117272
20.
Hereditary ataxia in four related Norwegian Buhunds.
J Am Vet Med Assoc
; 253(6): 774-780, 2018 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-30179085