Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression

American Journal of Physiology - Renal Physiology

Volumn 297, Issue 5, 2009, Pages

  Wangemann, Philine ^a   Kim, Hyoung Mi ^a   Billings, Sara ^a   Nakaya, Kazuhiro ^a,b   Li, Xiangming ^a   Singh, Ruchira ^a   Sharlin, David S ^c   Forrest, Douglas ^c   Marcus, Daniel C ^a   Fong, Peying ^a  

^a KANSAS STATE UNIVERSITY   (United States)

^b TOHOKU UNIVERSITY   (Japan)

^c NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

Author keywords

Bicarbonate; DFNB4; Pendred syndrome; Tectb; Thyroid

Indexed keywords

PENDRIN; THYROXINE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; COCHLEA; GENE; GENE EXPRESSION; HEARING IMPAIRMENT; HYPOTHYROIDISM; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PH MEASUREMENT; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SLC26A4 GENE; THYROID FOLLICLE;

EID: 70350705957     PISSN: 1931857X     EISSN: 15221466     Source Type: Journal    
DOI: 10.1152/ajprenal.00011.2009     Document Type: Article

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