Detalhe da pesquisa
1.
Generation of a de novo transcriptome from equine lamellar tissue.
BMC Genomics
; 16: 739, 2015 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26432030
2.
Detection of two equine trisomies using SNP-CGH.
Mamm Genome
; 24(5-6): 252-6, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23515943
3.
Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes.
Anim Genet
; 44(6): 763-5, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23659293
4.
A novel splice mutation within equine KIT and the W15 allele in the homozygous state lead to all white coat color phenotypes.
Anim Genet
; 48(4): 497-498, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28378922
5.
Transcriptome diversity and differential expression in supporting limb laminitis.
Vet Immunol Immunopathol
; 243: 110353, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34839133
6.
Whole genome detection of sequence and structural polymorphism in six diverse horses.
PLoS One
; 15(4): e0230899, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32271776
7.
Genome Diversity and the Origin of the Arabian Horse.
Sci Rep
; 10(1): 9702, 2020 06 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-32546689
8.
Use of principle component analysis to quantitatively score the equine metabolic syndrome phenotype in an Arabian horse population.
PLoS One
; 13(7): e0200583, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30001422
9.
Construction of two whole genome radiation hybrid panels for dromedary (Camelus dromedarius): 5000RAD and 15000RAD.
Sci Rep
; 8(1): 1982, 2018 01 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-29386528
10.
A Frameshift Mutation in KIT is Associated with White Spotting in the Arabian Camel.
Genes (Basel)
; 8(3)2017 Mar 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28282952
11.
Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse.
PLoS One
; 8(10): e78280, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24167615