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Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 20, 2011
Temporal expression pattern of Fkbp8 in rodent cochleaMagdalena Zak, Andreas Bress, Markus Pfister, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|May 23, 2012
Ergic2, a brain specific interacting partner of OtoferlinMagdalena Żak, Andreas Bress, Niels Brandt, et al.
Human Molecular Genetics|September 6, 2008
Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness formPaulina Heidrych, Ulrike Zimmermann, Andreas Bress, et al.
Journal of Applied Genetics|January 7, 2015
A TMC1 (transmembrane channel-like 1) mutation (p.S320R) in a Polish family with hearing impairmentMohamed Ahamed Hassan, Aftab Ali Shah, Elzbieta Szmida, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 5, 2014
Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signalingMegan Ealy, Nicole C Meyer, Johnny Cruz Corchado, et al.
Disease Models & Mechanisms|February 10, 2010
Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutationAnping Xia, Simon S Gao, Tao Yuan, et al.
Molecular and Cellular Endocrinology|September 10, 2013
Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cellsJuliane Dettling, Christoph Franz, Ulrike Zimmermann, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|January 12, 2011
Functional analysis of a novel I71N mutation in the GJB2 gene among Southern Egyptians causing autosomal recessive hearing lossMostafa R Mohamed, Ioana Alesutan, Michael Föller, et al.
Histochemistry and Cell Biology|April 2, 2013
Generation of somatic electromechanical force by outer hair cells may be influenced by prestin-CASK interaction at the basal junction with the Deiter's cellJelka Cimerman, Jörg Waldhaus, Csaba Harasztosi, et al.
The Journal of Biological Chemistry|May 1, 2012
Loss of mammal-specific tectorial membrane component carcinoembryonic antigen cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequenciesRobert Kammerer, Lukas Rüttiger, Rainer Riesenberg, et al.
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