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Volumn 277, Issue 37, 2002, Pages 34150-34160

A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system

(4) Illing, Michelle E a,b Rajan, Rahul S a,b Bence, Neil F a,b Kopito, Ron R a,b

a Department of Biological Sciences ^* (United States)

b STANFORD UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PHOTO-RECEPTOR CELLS;

DISEASES; GENES; MOLECULAR WEIGHT; NEUROLOGY;

BIOCHEMISTRY;

MUTANT PROTEIN; PROTEASOME; PROTEASOME INHIBITOR; PROTEIN P23H; RHODOPSIN; UBIQUITIN; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BLINDNESS; CELL DESTRUCTION; CELL INCLUSION; CHOROID; CYTOPLASM; CYTOSKELETON; DEGENERATIVE DISEASE; FLUORESCENCE; FLUORESCENCE RESONANCE ENERGY TRANSFER; GENE MUTATION; GENETIC TRANSFECTION; HIGH RISK POPULATION; HUMAN; HUMAN CELL; MISSENSE MUTATION; MOLECULAR WEIGHT; PHOTORECEPTOR CELL; PIGMENT EPITHELIUM; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN INTERACTION; RETINITIS PIGMENTOSA;

CYSTEINE ENDOPEPTIDASES; HUMANS; MULTIENZYME COMPLEXES; MUTATION; PROTEASOME ENDOPEPTIDASE COMPLEX; PROTEIN FOLDING; RETINITIS PIGMENTOSA; RHODOPSIN; UBIQUITIN;

EID: 0037072934 PISSN: 00219258 EISSN: None Source Type: Journal
DOI: 10.1074/jbc.M204955200 Document Type: Article

Times cited : (266)

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