A modifier gene alleviates hypothyroidism-induced hearing impairment in Pou1f1 dw Dwarf mice

Genetics

Volumn 189, Issue 2, 2011, Pages 665-673

  Fang, Qing ^a   Longo Guess, Chantal ^b   Gagnon, Leona H ^b   Mortensen, Amanda H ^a   Dolan, David F ^a   Camper, Sally A ^a   Johnson, Kenneth R ^b  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b JACKSON LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MICROTUBULE ASSOCIATED PROTEIN 1; THYROID HORMONE; THYROTROPIN; TRANSCRIPTION FACTOR PIT 1;

ARTICLE; CHROMOSOME 2; DISEASE SEVERITY; GENETIC VARIABILITY; GENOME ANALYSIS; HEARING IMPAIRMENT; HORMONE DEFICIENCY; HYPOTHYROIDISM; INBREEDING; MOUSE; NONHUMAN; PRIORITY JOURNAL;

ALLELES; ANIMALS; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, MAMMALIAN; CROSSES, GENETIC; FEMALE; GENES, MODIFIER; GENETIC PREDISPOSITION TO DISEASE; HEARING LOSS; HYPOTHYROIDISM; MALE; MICE; MICE, INBRED AKR; MICE, INBRED C3H; MICE, INBRED C57BL; MICE, INBRED STRAINS; MICE, KNOCKOUT; MICE, MUTANT STRAINS; MICROTUBULE-ASSOCIATED PROTEINS; MOLECULAR SEQUENCE DATA; POLYMORPHISM, SINGLE NUCLEOTIDE; QUANTITATIVE TRAIT LOCI; TRANSCRIPTION FACTOR PIT-1;

MUS; MUS MUSCULUS CASTANEUS;

EID: 80053945833     PISSN: 00166731     EISSN: 19432631     Source Type: Journal    
DOI: 10.1534/genetics.111.130633     Document Type: Article

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