Identical mutation in a novel retinal gene causes progressive rod–cone degeneration in dogs and retinitis pigmentosa in humans
Top Cited Papers
- 30 August 2006
- Vol. 88 (5), 551-563
- https://doi.org/10.1016/j.ygeno.2006.07.007
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Linkage disequilibrium mapping in domestic dog breeds narrows the progressive rod–cone degeneration interval and identifies ancestral disease-transmitting chromosomeGenomics, 2006
- Development and Characterization of a Normalized Canine Retinal cDNA Library for Genomic and Expression StudiesInvestigative Opthalmology & Visual Science, 2006
- Genome sequence, comparative analysis and haplotype structure of the domestic dogNature, 2005
- Analysis of prevalence of presumed inherited eye diseases in Entlebucher Mountain DogsVeterinary Ophthalmology, 2005
- SOX7 and SOX17 Regulate the Parietal Endoderm-specific Enhancer Activity of Mouse Laminin α1 GenePublished by Elsevier ,2004
- Sox17 and β-catenin cooperate to regulate the transcription of endodermal genesDevelopment, 2004
- Radiation hybrid map, physical map, and low-pass genomic sequence of the canine prcd region on CFA9 and comparative mapping with the syntenic region on human chromosome 17Genomics, 2003
- Physical and Linkage Mapping of Human Chromosome 17 Loci to Dog Chromosomes 9 and 5Genomics, 1997
- Comparative Protein Modelling by Satisfaction of Spatial RestraintsJournal of Molecular Biology, 1993
- Interphotoreceptor retinoid-binding protein (IRBP) in progressive rod-cone degeneration (prcd)—Biochemical, immunocytochemical and immunologic studiesExperimental Eye Research, 1991