Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration

Human molecular genetics

Volumn 23, Issue 19, 2014, Pages 5197-5210

  Karlstetter, Marcus ^a   Sorusch, Nasrin ^a   Caramoy, Albert ^a   Dannhausen, Katharina ^a   Aslanidis, Alexander ^a   Fauser, Sascha ^a   Boesl, Michael R ^b   Nagel Wolfrum, Kerstin ^a   Tamm, Ernst R ^a   Jägle, Herbert ^a   Stoehr, Heidi ^a   Wolfrum, Uwe ^a   Langmann, Thomas ^a  

^a UNIVERSITY OF COLOGNE   (Germany)

^b JOHANNES GUTENBERG UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; EYE PROTEIN; FAM161A PROTEIN, MOUSE; PROTEIN BINDING;

ACTION POTENTIAL; ANIMAL; FEMALE; GENE EXPRESSION; GENE LOCUS; GENE TARGETING; GENETICS; GENOTYPE; HUMAN; MALE; METABOLISM; MICROGLIA; MOUSE; MUTATION; PATHOLOGY; PATHOPHYSIOLOGY; PHOTORECEPTOR CELL; PIGMENT EPITHELIUM; PROTEIN TRANSPORT; RETINA; RETINA DEGENERATION; TRANSGENIC MOUSE; ULTRASTRUCTURE; VISUAL DISORDER;

ACTION POTENTIALS; ANIMALS; CARRIER PROTEINS; EYE PROTEINS; FEMALE; GENE EXPRESSION; GENE TARGETING; GENETIC LOCI; GENOTYPE; HUMANS; MALE; MICE; MICE, TRANSGENIC; MICROGLIA; MUTATION; PHOTORECEPTOR CELLS; PROTEIN BINDING; PROTEIN TRANSPORT; RETINA; RETINAL DEGENERATION; RETINAL PIGMENT EPITHELIUM; VISION DISORDERS;

EID: 84908684087     PISSN: None     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddu242     Document Type: Article

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