Detalhe da pesquisa
1.
Redundant contribution of a Transient Receptor Potential cation channel Member 1 exon 11 single nucleotide polymorphism to equine congenital stationary night blindness.
BMC Vet Res
; 12(1): 121, 2016 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-27329127
2.
Congenital stationary night blindness is associated with the leopard complex in the Miniature Horse.
Vet Ophthalmol
; 15(1): 18-22, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22051042
3.
Relative quantification of white blood cell mitochondrial DNA and assessment of mitochondria by use of transmission electron microscopy in English Springer Spaniels with and without retinal dysplasia.
Am J Vet Res
; 71(4): 454-9, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20367054
4.
Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus).
Genetics
; 179(4): 1861-70, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18660533
5.
Congenital ocular anomalies in purebred and crossbred Rocky and Kentucky Mountain horses in Canada.
Can Vet J
; 49(7): 675-81, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18827844
6.
Differential mitochondrial DNA and gene expression in inherited retinal dysplasia in miniature Schnauzer dogs.
Invest Ophthalmol Vis Sci
; 47(5): 1810-6, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16638985
7.
Development of a murine ocular posterior segment explant culture for the study of intravitreous vector delivery.
Can J Vet Res
; 79(1): 31-8, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25673906
8.
Differences in expression of retinal pigment epithelium mRNA between normal canines.
Can J Vet Res
; 68(3): 201-7, 2004 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15352545
9.
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
10.
Mitochondrial transcription factor A (Tfam) gene sequencing and mitochondrial evaluation in inherited retinal dysplasia in miniature schnauzer dogs.
Can J Vet Res
; 75(2): 134-40, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21731185
11.
Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses.
Brief Funct Genomics
; 9(3): 193-207, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20353955
12.
Structure and function of CLCA proteins.
Physiol Rev
; 85(3): 1061-92, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15987802
13.
Complex expression and localization of inactivating Kv channels in cultured hippocampal astrocytes.
J Neurophysiol
; 93(3): 1699-709, 2005 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15738276
14.
The calcium-dependent chloride conductance mediator pCLCA1.
Am J Physiol Cell Physiol
; 283(2): C412-21, 2002 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12107050
15.
pCLCA1 lacks inherent chloride channel activity in an epithelial colon carcinoma cell line.
Am J Physiol Gastrointest Liver Physiol
; 287(1): G33-41, 2004 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-14988065
16.
pCLCA1 becomes a cAMP-dependent chloride conductance mediator in Caco-2 cells.
Biochem Biophys Res Commun
; 298(4): 531-6, 2002 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-12408984
17.
CLCA protein and chloride transport in canine retinal pigment epithelium.
Am J Physiol Cell Physiol
; 285(5): C1314-21, 2003 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-12867361