Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31-Reference-Cited by-同舟云学术

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

Published:2003-06-29 Issue:4 Volume:34 Page:421-428
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Mburu Philomena,Mustapha Mirna,Varela Anabel,Weil Dominique,El-Amraoui Aziz,Holme Ralph H,Rump Andreas,Hardisty Rachel E,Blanchard Stéphane,Coimbra Roney S,Perfettini Isabelle,Parkinson Nick,Mallon Ann-Marie,Glenister Pete,Rogers Mike J,Paige Adam J,Moir Lee,Clay Jo,Rosenthal Andre,Liu Xue Zhong,Blanco Gonzalo,Steel Karen P,Petit Christine,Brown Steve D M

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1208.pdf

Reference45 articles.

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3. Kaltenbach, J.A. & Falzarano, P.R. Postnatal development of the hamster cochlea. I. Growth of hair cells and the organ of Corti. J. Comp. Neurol. 340, 87–97 (1994).

4. Kollmar, R. Who does the hair cell's 'do? Rho GTPases and hair-bundle morphogenesis. Curr. Opin. Neurobiol. 9, 394–398 (1999).

5. Muller, U. & Littlewood-Evans, A. Mechanisms that regulate mechanosensory hair cell differentiation. Trends Cell Biol. 11, 334–342 (2001).

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