Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice

Development

Volumn 130, Issue 9, 2003, Pages 2013-2025

  Hulander, Malin ^a   Kiernan, Amy E ^b   Blomqvist, Sandra Rodrigo ^a   Carlsson, Peter ^a   Samuelsson, Emma Johanna ^a   Johansson, Bengt R ^a   Steel, Karen P ^b   Enerbäck, Sven ^a  

^a UNIVERSITY OF GOTHENBURG   (Sweden)

^b MRC INSTITUTE OF HEARING RESEARCH   (United Kingdom)

Author keywords

Deafness; Forkhead; Foxi1; Inner ear; Mouse; Pendrin

Indexed keywords

CHLORIDE ION; IODIDE; PENDRIN; PROTEIN FOXI1; REGULATOR PROTEIN; UNCLASSIFIED DRUG;

ANIMAL TISSUE; BALANCE DISORDER; CELL TYPE; CEREBELLUM; CONTROLLED STUDY; EMBRYO; EMBRYO DEVELOPMENT; ENDOLYMPHATIC SAC; GENE MUTATION; GENETIC CODE; GENETIC TRANSCRIPTION; HEARING IMPAIRMENT; HISTOLOGY; IN SITU HYBRIDIZATION; INNER EAR; MOUSE; NONHUMAN; PENDRED SYNDROME; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVIEW; THREE DIMENSIONAL IMAGING; WILD TYPE;

ANIMALS; CALCIUM-BINDING PROTEINS; CARRIER PROTEINS; DEAFNESS; EPITHELIUM; FORKHEAD TRANSCRIPTION FACTORS; GENETIC MARKERS; INTERCELLULAR SIGNALING PEPTIDES AND PROTEINS; MEMBRANE PROTEINS; MEMBRANE TRANSPORT PROTEINS; MICE; NUCLEAR PROTEINS; PROTEINS; TRANSCRIPTION FACTORS; VESTIBULAR AQUEDUCT;

ANIMALIA; MAMMALIA;

EID: 0037959640     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: 10.1242/dev.00376     Document Type: Review

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