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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 12, 2007
Estrogen and the inner ear: megalin knockout mice suffer progressive hearing lossOvidiu König, Lukas Rüttiger, Marcus Müller, 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.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 2002
Thyroid hormone is a critical determinant for the regulation of the cochlear motor protein prestinThomas Weber, Ulrike Zimmermann, Harald Winter, et al.
Development (Cambridge, England)|August 20, 2003
Lack of Bdnf and TrkB signalling in the postnatal cochlea leads to a spatial reshaping of innervation along the tonotopic axis and hearing lossThomas Schimmang, Justin Tan, Marcus Müller, et al.
Histochemistry and Cell Biology|January 31, 2008
Expression of glycine receptors and gephyrin in the rat cochleaJulia Dlugaiczyk, Wibke Singer, Bernhard Schick, et al.
The European Journal of Neuroscience|January 19, 2007
Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the ratNicola Schug, Claudia Braig, Ulrike Zimmermann, et al.
The Journal of Physiology|August 12, 2006
Deafness in LIMP2-deficient mice due to early loss of the potassium channel KCNQ1/KCNE1 in marginal cells of the stria vascularisMarlies Knipper, Cathrin Claussen, Lukas Rüttiger, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 5, 2003
Expression of prestin-homologous solute carrier (SLC26) in auditory organs of nonmammalian vertebrates and insectsThomas Weber, Martin C Gopfert, Harald Winter, et al.
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