Detalhe da pesquisa
1.
A frameshift-deletion mutation in Reelin causes cerebellar hypoplasia in White Swiss Shepherd dogs.
Anim Genet;
54(5): 632-636, 2023 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37334487
2.
An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome.
PLoS Genet;
15(5): e1008102, 2019 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31095560
3.
Inflammatory pattern of the infrapatellar fat pad in dogs with canine cruciate ligament disease.
BMC Vet Res;
14(1): 161, 2018 May 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29769086
4.
A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease.
PLoS Genet;
11(4): e1005169, 2015 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25875846
5.
A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH).
PLoS Genet;
10(5): e1004370, 2014.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24832243
6.
A mutation in the SUV39H2 gene in Labrador Retrievers with hereditary nasal parakeratosis (HNPK) provides insights into the epigenetics of keratinocyte differentiation.
PLoS Genet;
9(10): e1003848, 2013.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24098150
7.
A frameshift mutation in the cubilin gene (CUBN) in Beagles with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption).
Anim Genet;
45(1): 148-50, 2014 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24164695
8.
Magnetic resonance imaging and genetic investigation of a case of Rottweiler leukoencephalomyelopathy.
BMC Vet Res;
9: 57, 2013 Mar 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23531239
9.
PKD1 Nonsense Variant in a Lagotto Romagnolo Family with Polycystic Kidney Disease.
Genes (Basel);
14(6)2023 06 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37372390
10.
SGCD Missense Variant in a Lagotto Romagnolo Dog with Autosomal Recessively Inherited Limb-Girdle Muscular Dystrophy.
Genes (Basel);
14(8)2023 08 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37628692
11.
Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human.
Genome Med;
15(1): 73, 2023 09 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37723491
12.
Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture.
Genome Biol;
24(1): 187, 2023 08 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37582787
13.
The Effects of FGF4 Retrogenes on Canine Morphology.
Genes (Basel);
13(2)2022 02 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35205370
14.
Genome-Wide Analyses for Osteosarcoma in Leonberger Dogs Reveal the CDKN2A/B Gene Locus as a Major Risk Locus.
Genes (Basel);
12(12)2021 12 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34946912
15.
A single codon insertion in the PICALM gene is not associated with subvalvular aortic stenosis in Newfoundland dogs.
Hum Genet;
134(1): 127-9, 2015 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25391634
16.
SLC19A3 Loss-of-Function Variant in Yorkshire Terriers with Leigh-Like Subacute Necrotizing Encephalopathy.
Genes (Basel);
11(10)2020 10 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33081289
17.
Abnormal keratinocyte differentiation in the nasal planum of Labrador Retrievers with hereditary nasal parakeratosis (HNPK).
PLoS One;
15(3): e0225901, 2020.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32119674
18.
A whole-genome scan for recurrent airway obstruction in Warmblood sport horses indicates two positional candidate regions.
Mamm Genome;
20(8): 504-15, 2009 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19760324
19.
Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease.
Genomics;
92(6): 474-7, 2008 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18786632
20.
A large deletion in the GP9 gene in Cocker Spaniel dogs with Bernard-Soulier syndrome.
PLoS One;
14(9): e0220625, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31484196