A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity

Proceedings of the National Academy of Sciences of the United States of America

Volumn 104, Issue 49, 2007, Pages 19422-19427

  Davis, Roger E ^a,b   Swiderski, Ruth E ^a,b   Rahmouni, Kamal ^a   Nishimura, Darryl Y ^a,b   Mullins, Robert F ^a   Agassandian, Khristofor ^a   Philp, Alisdair R ^a,b   Searby, Charles C ^a,b   Andrews, Michael P ^a,b   Thompson, Stewart ^a,b   Berry, Christopher J ^a   Thedens, Daniel R ^a   Yang, Baoli ^a   Weiss, Robert M ^a   Cassell, Martin D ^a   Stone, Edwin M ^a,b   Sheffield, Val C ^a,b  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF IOWA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTERIAL PRESSURE; ARTICLE; BARDET BIEDL SYNDROME; BRAIN REGION; BRAIN VENTRICLE DILATATION; CONTROLLED STUDY; EUKARYOTIC FLAGELLUM; HYPERLEPTINEMIA; HYPERPHAGIA; LOCOMOTION; MALE INFERTILITY; MISSENSE MUTATION; MOUSE; NONHUMAN; OBESITY; PHENOTYPE; PRIORITY JOURNAL; RETINA DEGENERATION; RETINOPATHY; VENTRICULOMEGALY;

ANIMALS; BARDET-BIEDL SYNDROME; CEREBRAL VENTRICLES; CILIA; DISEASE MODELS, ANIMAL; MALE; MICE; MICROTUBULE-ASSOCIATED PROTEINS; MUTATION; OBESITY; RETINAL DISEASES; SPERM TAIL;

MUS;

EID: 37649020306     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.0708571104     Document Type: Article

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