Prevention of auditory dysfunction in hypothyroid Tshr mutant mice by thyroxin treatment during development

JARO - Journal of the Association for Research in Otolaryngology

Volumn 2, Issue 4, 2001, Pages 348-361

  Sprenkle, Pamela M ^a,b   McGee, JoAnn ^a,c   Bertoni, John M ^b   Walsh, Edward J ^a,c  

^a BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

^b CREIGHTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c CREIGHTON UNIVERSITY   (United States)

Author keywords

Deafness; Development; Hearing; Hypothyroidism; Maturation; Thyrotropin

Indexed keywords

THYROXINE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; AUDITORY THRESHOLD; CONTROLLED STUDY; EUTHYROIDISM; FEMALE; GENE; HEARING; HEARING DISORDER; HORMONE SUBSTITUTION; HYPOTHYROIDISM; HYT GENE; LATENT PERIOD; MALE; MOUSE; NONHUMAN; ONTOGENY; POSTNATAL DEVELOPMENT; PRENATAL DEVELOPMENT; PRIORITY JOURNAL; TSHR GENE;

AGING; ANIMALS; AUDITORY THRESHOLD; BEHAVIOR, ANIMAL; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; FEMALE; FETUS; HEARING DISORDERS; HYPOTHYROIDISM; MICE; MICE, MUTANT STRAINS; MUTATION; PREGNANCY; REACTION TIME; RECEPTORS, THYROTROPIN; THYROXINE;

EID: 0035685948     PISSN: 15253961     EISSN: None     Source Type: Journal    
DOI: 10.1007/s101620010078     Document Type: Article

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