Characterization of Human and Mouse Rod cGMP Phosphodiesterase δ Subunit (PDE6D) and Chromosomal Localization of the Human Gene
- 1 April 1998
- journal article
- Published by Elsevier BV in Genomics
- Vol. 49 (1), 76-82
- https://doi.org/10.1006/geno.1998.5210
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Conservation of function and expression of unc-119 from two Caenorhabditis species despite divergence of non-coding DNAGene, 1996
- Solubilization of Membrane-bound Rod Phosphodiesterase by the Rod Phosphodiesterase Recombinant δ SubunitOnline Journal of Public Health Informatics, 1996
- Cloning of the cDNA for a Novel Photoreceptor ProteinOnline Journal of Public Health Informatics, 1996
- Autosomal recessive retinitis pigmentosa caused by mutations in the α subunit of rod cGMP phosphodiesteraseNature Genetics, 1995
- Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa.Proceedings of the National Academy of Sciences of the United States of America, 1995
- Fluorescence in Situ Hybridization Mapping of 25 Markers on Distal Human Chromosome 2q Surrounding the Human Waardenburg Syndrome, Type I (WS1) Locus (PAX3 Gene)Genomics, 1993
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Retinal degeneration in the rd mouse is caused by a defect in the β subunit of rod cGMP-phosphodiesteraseNature, 1990
- Subunit stoichiometry of retinal rod cGMP phosphodiesteraseBiochemistry, 1990
- cGMP phosphodiesterase of retinal rods is regulated by two inhibitory subunits.Proceedings of the National Academy of Sciences of the United States of America, 1988