A compendium of mouse knockouts with inner ear defects
AV Anagnostopoulos - Trends Genet, 2002 - tbase.jax.org
... Foxi1 (Fkh10) Forkhead box I1 (forkhead homolog 10, Unknown 5437, 5438 [42] ...
Gata3 GATA-binding protein 3 2 (7.0) 7108, 7109, 7113 [63] ...
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Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner … - Full text - MIT Libraries
M Hulander, AE Kiernan, SR Blomqvist, P Carlsson, … - Development, 2003 - dev.biologists.org
... DEVELOPMENT AND DISEASE. Lack of pendrin expression leads to deafness and expansion
of the endolymphatic compartment in inner ears of Foxi1 null mutant mice. ...
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Keeping Sensory Cells and Evolving Neurons to Connect Them to the Brain: Molecular Conservation and … - Full text - MIT Libraries
BFKW Beisel - Brain Behav Evol, 2004 - content.karger.com
... Another gene of the zinc-finger transcription family, Gata3, is involved in
hearing-related disorders in humans [Van Esch and Dev- riendt, 2001], and Gata3 ...
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