Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells

Development

Volumn 125, Issue 4, 1998, Pages 557-566

  Self, Tim ^a   Mahony, Mary ^a   Fleming, Jane ^a   Walsh, James ^b   Brown, Steve D M ^b   Steel, Karen P ^a  

^a MRC INSTITUTE OF HEARING RESEARCH   (United Kingdom)

^b MRC MAMMALIAN GENETICS UNIT   (United Kingdom)

Author keywords

Cochlea; Hair cell; Hearing; Mouse mutant; Myosin VIIA; shaker 1; Stereocilia; Usher syndrome

Indexed keywords

MYOSIN;

ANIMAL CELL; ARTICLE; COCHLEA; CONTROLLED STUDY; DEPOLARIZATION; DEVELOPMENTAL GENETICS; ELECTROPHYSIOLOGY; GENE MUTATION; HAIR CELL; HEARING IMPAIRMENT; MOUSE; NONHUMAN; PRIORITY JOURNAL; STEREOCILIUM; USHER SYNDROME;

ANIMALS; ANIMALS, NEWBORN; BASE SEQUENCE; CILIA; DNA PRIMERS; DYNEIN ATPASE; ELECTROPHYSIOLOGY; HAIR CELLS; HUMANS; IN SITU HYBRIDIZATION; MICE; MICE, MUTANT STRAINS; MICROSCOPY, ELECTRON; MICROSCOPY, ELECTRON, SCANNING; MUTATION; MYOSINS;

ANIMALIA;

EID: 0031884319     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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