Null mutation of α1D Ca2+ channel gene results in deafness but no vestibular defect in mice

JARO - Journal of the Association for Research in Otolaryngology

Volumn 5, Issue 2, 2004, Pages 215-226

  Dou, Hongwei ^a   Vazquez, Ana E ^b   Namkung, Yoon ^c   Chu, Hanqi ^b   Cardell, Emma Lou ^a   Nie, Liping ^b   Parson, Susan ^b   Shin, Hee Sup ^c   Yamoah, Ebenezer N ^a,d  

^a CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c Pohang University of Science and Technology (POSTECH)   (South Korea)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Balancing; Ca2+ channels; Hair cells; Hearing; Inner ear; Voltage clamp

Indexed keywords

CALCIUM CHANNEL; CALCIUM ION; BARIUM; CACNA1D PROTEIN, MOUSE; CALCIUM CHANNEL L TYPE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUDITORY THRESHOLD; COCHLEA; CONTROLLED STUDY; DISTORTION PRODUCT OTOACOUSTIC EMISSION; EVOKED BRAIN STEM AUDITORY RESPONSE; GENE MUTATION; HAIR CELL; HEARING IMPAIRMENT; HISTOPATHOLOGY; MOUSE; NONHUMAN; NULL ALLELE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SCANNING ELECTRON MICROSCOPY; UTRICLE; ANIMAL; BODY EQUILIBRIUM; C57BL MOUSE; CYTOLOGY; GENETICS; METABOLISM; MOUSE MUTANT; PATCH CLAMP; PATHOLOGY; PATHOPHYSIOLOGY; PHENOTYPE; PHYSIOLOGY; ULTRASTRUCTURE; VESTIBULE;

ANIMALS; AUDITORY THRESHOLD; BARIUM; CALCIUM CHANNELS, L-TYPE; COCHLEA; DEAFNESS; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; HAIR CELLS, OUTER; MICE; MICE, INBRED C57BL; MICE, MUTANT STRAINS; MICROSCOPY, ELECTRON, SCANNING; MUSCULOSKELETAL EQUILIBRIUM; PATCH-CLAMP TECHNIQUES; PHENOTYPE; SACCULE AND UTRICLE; VESTIBULE;

EID: 3042543371     PISSN: 15253961     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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