Detalhe da pesquisa
1.
Recent, full-length gene retrocopies are common in canids.
Genome Res;
2022 Aug 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35961775
2.
Genetic Variants Affecting Skeletal Morphology in Domestic Dogs.
Trends Genet;
36(8): 598-609, 2020 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32487495
3.
NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia.
PLoS Genet;
15(9): e1008378, 2019 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31479451
4.
Canine DVL2 variant contributes to brachycephalic phenotype and caudal vertebral anomalies.
Hum Genet;
140(11): 1535-1545, 2021 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33599851
5.
Variants at the ASIP locus contribute to coat color darkening in Nellore cattle.
Genet Sel Evol;
53(1): 40, 2021 Apr 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33910501
6.
Whole genome variant association across 100 dogs identifies a frame shift mutation in DISHEVELLED 2 which contributes to Robinow-like syndrome in Bulldogs and related screw tail dog breeds.
PLoS Genet;
14(12): e1007850, 2018 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30521570
7.
FGF4 retrogene on CFA12 is responsible for chondrodystrophy and intervertebral disc disease in dogs.
Proc Natl Acad Sci U S A;
114(43): 11476-11481, 2017 10 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29073074
8.
Pathologic Features of the Intervertebral Disc in Young Nova Scotia Duck Tolling Retrievers Confirms Chondrodystrophy Degenerative Phenotype Associated With Genotype.
Vet Pathol;
56(6): 895-902, 2019 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31526126
9.
Utilizing the Dog Genome in the Search for Novel Candidate Genes Involved in Glioma Development-Genome Wide Association Mapping followed by Targeted Massive Parallel Sequencing Identifies a Strongly Associated Locus.
PLoS Genet;
12(5): e1006000, 2016 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27171399
10.
Evaluation of the major histocompatibility complex (MHC) class II as a candidate for sudden acquired retinal degeneration syndrome (SARDS) in Dachshunds.
Vet Ophthalmol;
22(6): 751-759, 2019 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30791205
11.
Identification of a Candidate Mutation in the COL1A2 Gene of a Chow Chow With Osteogenesis Imperfecta.
J Hered;
109(3): 308-314, 2018 03 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29036614
12.
SERPINB11 frameshift variant associated with novel hoof specific phenotype in Connemara ponies.
PLoS Genet;
11(4): e1005122, 2015 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25875171
13.
Early Developmental and Evolutionary Origins of Gene Body DNA Methylation Patterns in Mammalian Placentas.
PLoS Genet;
11(8): e1005442, 2015 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26241857
14.
Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate.
PLoS Genet;
11(3): e1005059, 2015 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25798845
15.
Genetic analysis of optic nerve head coloboma in the Nova Scotia Duck Tolling Retriever identifies discordance with the NHEJ1 intronic deletion (collie eye anomaly mutation).
Vet Ophthalmol;
21(2): 144-150, 2018 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28702949
16.
Developing a 670k genotyping array to tag ~2M SNPs across 24 horse breeds.
BMC Genomics;
18(1): 565, 2017 07 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28750625
17.
A LINE-1 insertion in DLX6 is responsible for cleft palate and mandibular abnormalities in a canine model of Pierre Robin sequence.
PLoS Genet;
10(4): e1004257, 2014 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24699068
18.
Genome-wide SNP and haplotype analyses reveal a rich history underlying dog domestication.
Nature;
464(7290): 898-902, 2010 Apr 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20237475
19.
Gonadectomy effects on the risk of immune disorders in the dog: a retrospective study.
BMC Vet Res;
12(1): 278, 2016 Dec 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27931211
20.
Genome-wide association mapping in dogs enables identification of the homeobox gene, NKX2-8, as a genetic component of neural tube defects in humans.
PLoS Genet;
9(7): e1003646, 2013.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23874236