Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quakingviable mutant mouse

Human Molecular Genetics

Volumn 19, Issue 8, 2010, Pages 1593-1602

  Wilson, Gabrielle R ^a,b   Wang, Hong X ^b   Egan, Gary F ^b   Robinson, Philip J ^c   Delatycki, Martin B ^a,b   O'Bryan, Moira K ^d   Lockhart, Paul J ^a,b  

^a MURDOCH CHILDREN'S RESEARCH INSTITUTE   (Australia)

^b UNIVERSITY OF MELBOURNE   (Australia)

^c ROYAL CHILDREN'S HOSPITAL   (Australia)

^d MONASH UNIVERSITY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME PROTEIN; PARKIN; PARKIN COREGULATED PROTEIN; QUAKING PROTEIN; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL FUNCTION; CHROMOSOME 17; CILIARY DYSKINESIA; CILIARY MOTILITY; CONTROLLED STUDY; EMBRYO; EPENDYMA CELL; GENE DELETION; GENE EXPRESSION; GENE LOSS; HISTOPATHOLOGY; HYDROCEPHALUS; MALE STERILITY; MOUSE; MOUSE MUTANT; MYELIN DEFICIENCY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; QUANTITATIVE ANALYSIS;

ANIMALS; CILIA; DISEASE MODELS, ANIMAL; EPENDYMA; FEMALE; GENE DELETION; HUMANS; HYDROCEPHALUS; MALE; MICE; MICE, QUAKING; PROTEINS;

MUS; VERTEBRATA;

EID: 77952313773     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddq031     Document Type: Article

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