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Histology / Visual system / Photoreceptor cells / Vision / Retina / Visual phototransduction / Retinitis pigmentosa / Rod cell / Muller glia / Biology / Anatomy / Neurons


ARTICLE IN PRESS Progress in Retinal and Eye Research–655 Neural remodeling in retinal degeneration Robert E. Marca,*, Bryan W. Jonesa, Carl B. Watta, Enrica Strettoib
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Document Date: 2014-07-26 20:25:36


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File Size: 2,97 MB

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Pisa / Salt Lake City / /

Company

ARTICLE IN PRESS / Elsevier Ltd. / Medline / AMD / /

Country

United States / /

Event

Product Issues / /

Facility

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 / /

Position

Retina *Corresponding author / Representative / Usher / /

Product

soma / iRiver E30 Portable Audio Device / Nokia E55 Smartphone / rhodopsin / /

ProvinceOrState

Utah / /

Technology

selective detection technologies / transplantation / apoptosis / gene expression / /

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