Otoconin-90 deletion leads to imbalance but normal hearing: A comparison with other otoconia mutants

Neuroscience

Volumn 153, Issue 1, 2008, Pages 289-299

  Zhao, X ^a   Jones, S M ^b   Yamoah, E N ^c   Lundberg, Y Wang ^a  

^a BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

^b EAST CAROLINA UNIVERSITY   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

adaptation; balance; compensation; hearing; otoconia; vestibule

Indexed keywords

GLYCOPROTEIN; OTOCONIN 90; UNCLASSIFIED DRUG;

ANIMAL BEHAVIOR; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BALANCE IMPAIRMENT; CONTROLLED STUDY; DISTORTION PRODUCT OTOACOUSTIC EMISSION; EVOKED BRAIN STEM AUDITORY RESPONSE; EVOKED RESPONSE; GAIT; GENE DELETION; HEARING; HISTOPATHOLOGY; MORBIDITY; MOUSE; NONHUMAN; OTOLITH; PRIORITY JOURNAL; SENSORY STIMULATION; SWIMMING; VESTIBULAR DISORDER; VESTIBULOOCULAR REFLEX;

ADAPTATION, PHYSIOLOGICAL; ANIMALS; EVOKED POTENTIALS; EXTRACELLULAR MATRIX PROTEINS; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MICE, MUTANT STRAINS; MUSCULOSKELETAL EQUILIBRIUM; OTOLITHIC MEMBRANE; VESTIBULAR DISEASES; VESTIBULE, LABYRINTH;

EID: 41949116366     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2008.01.055     Document Type: Article

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