Mice with a D190N mutation in the gene encoding rhodopsin: A model for human autosomal-dominant retinitis pigmentosa

Molecular Medicine

Volumn 18, Issue 4, 2012, Pages 549-555

  Sancho Pelluz, Javier ^a,b   Tosi, Joaquin ^a,b,c   Hsu, Chun Wei ^a,b   Lee, Frances ^d   Wolpert, Kyle ^a,b   Refidaff, Cref ^a,b   Greenberg, Jonathan P ^b   Tsang, Stephen H ^a,b   Lin, Chyuan Sheng ^a,d  

^a Columbia University ^*  (United States)

^b New York Presbyterian Hospital   (United States)

^c WAYNE STATE UNIVERSITY   (United States)

^d Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

G PROTEIN COUPLED RECEPTOR; RHODOPSIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CONTROLLED STUDY; DISEASE MODEL; ELECTROPHYSIOLOGY; FLUORESCENCE; GENE TARGETING; GENETIC ENGINEERING; HISTOLOGY; HUMAN; MISSENSE MUTATION; MOUSE; NONHUMAN; PATHOGENESIS; PHOTON; PHOTORECEPTOR CELL; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; SIGNAL TRANSDUCTION;

ANIMALS; DISEASE MODELS, ANIMAL; GENE ORDER; GENE TARGETING; GENES, DOMINANT; HUMANS; MICE; MICE, TRANSGENIC; MUTATION; PROTEIN TRANSPORT; RETINAL ROD PHOTORECEPTOR CELLS; RETINITIS PIGMENTOSA; RHODOPSIN;

EID: 84862225379     PISSN: 10761551     EISSN: None     Source Type: Journal    
DOI: 10.2119/molmed.2011.00475     Document Type: Article

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