Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants

Journal of Neuroscience

Volumn 29, Issue 4, 2009, Pages 1212-1223

  Mustapha, Mirna ^a   Fang, Qing ^a   Gong, Tzy Wen ^a   Dolan, David F ^a   Raphael, Yehoash ^a   Camper, Sally A ^a   Duncan, R Keith ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

KCNJ10; KCNQ1; KCNQ4; POU1F1; Prestin; Secondary hypothyroidism; Tectorial membrane

Indexed keywords

POTASSIUM CHANNEL; POTASSIUM CHANNEL KCNJ10; POTASSIUM CHANNEL KCNQ4; THYROID HORMONE; TRANSCRIPTION FACTOR PIT 1; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL STRESS; COCHLEA DUCT; COCHLEA POTENTIAL; CONTROLLED STUDY; GENE EXPRESSION; HAIR CELL; HEARING IMPAIRMENT; HYPOTHYROIDISM; INNER EAR DISEASE; MOUSE; MUTANT; NONHUMAN; OTOACOUSTIC EMISSION; PRIORITY JOURNAL; STRIA VASCULARIS;

AGE FACTORS; ANIMALS; ANIMALS, NEWBORN; DEAFNESS; DISEASE MODELS, ANIMAL; GENE EXPRESSION REGULATION; HAIR CELLS, AUDITORY, OUTER; HYPOTHYROIDISM; KCNQ POTASSIUM CHANNELS; MICE; MICE, MUTANT STRAINS; MICROSCOPY, ELECTRON, TRANSMISSION; MOLECULAR MOTOR PROTEINS; OTOACOUSTIC EMISSIONS, SPONTANEOUS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; STRIA VASCULARIS; SYNAPTOPHYSIN; TECTORIAL MEMBRANE; TRANSCRIPTION FACTOR PIT-1;

EID: 59649088581     PISSN: 02706474     EISSN: 02706474     Source Type: Journal    
DOI: 10.1523/JNEUROSCI.4957-08.2009     Document Type: Article

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