terminal modifications / N Medical Center / University of Utah / terminal P23H / University of Utah School / /
IndustryTerm
Mammalian systems / signal processing attributes / potent tools / spatial processing / transgenic mouse systems / tandem device / transcriptional networks / retinoid processing pathway elements / recent media / rodent model systems / selective detection technologies / /
MedicalCondition
primary rod diseases / retinal degenerations / dominant diseases / Retinitis pigmentosa / direct photoreceptor phototoxicity / isolated photopic dysfunction / CORD adRP adRP adRP Knockout Gene Cellular phenotype Human disease / aside human diseases / congenital amaurosis / diverse diseases / fast human diseases / human autosomal dominant disease / apparent retinal degeneration / yet retinal degenerations / debris-initiated diseases / Debris-initiated retinal degenerations / neural remodeling Natural Gene rd1 Cellular phenotype Human disease / different disease / Leber Congenital Amaurosis / human recessive disease / Rod diseases / former ganglion / Cone-initiated diseases / Stargardt’s Disease / Human retinal degenerations / cone death Diseases / II Transgenic Gene Cellular phenotype Human disease / disease / phototoxicity RP / experimental retinal detachment / cone diseases / CORD-like diseases / phototoxicity / dominant disease / total blindness / retinal degeneration Robert E. Marca / ganglion / retinal degeneration / retinal disease / rod-initiated disease / diseases / severe blindness / clinical entity retinitis pigmentosa / LCA Induced Gene Cellular phenotype Human disease / oligogenic disease / focal injury / human disease / disorders / /
NaturalFeature
Ca channel / /
Organization
University of Utah School of Medicine / Department of Ophthalmology / University of Utah / John A. Moran Eye Center / Medical Center / /
Person
Carl B. Watta / Bryan W. Jonesa / Gene Cellular / Enrica Strettoib / Blair / Mata / Robert E. Marca / /