The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1

By van Wijk Erwin   van der Zwaag Bert   Peters Theo   Zimmermann Ulrike   te Brinke Heleen   Kersten Ferry F.J.   Märker Tina   Aller Elena   Hoefsloot Lies H.   Cremers Cor W.R.J.   Cremers Frans P.M.   Wolfrum Uwe   Knipper Marlies   Roepman Ronald  

Human Molecular Genetics, Vol. 15, Iss. 5, 2006-03 ,pp. : 751-765

Oxford University Press

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Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2

By Reiners Jan   van Wijk Erwin   Zimmermann Ulrike   Jürgens Karin   te Brinke Heleen   Overlack Nora   Roepman Ronald   Knipper Marlies   Kremer Hannie   Wolfrum Uwe  

Human Molecular Genetics, Vol. 14, Iss. 24, 2005-12 ,pp. : 3933-3943

Oxford University Press

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Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells

By Adato Avital   Lefèvre Gaëlle   Delprat Benjamin   Michel Vincent   Michalski Nicolas   Chardenoux Sébastien   Weil Dominique   El-Amraoui Aziz   Petit Christine  

Human Molecular Genetics, Vol. 14, Iss. 24, 2005-12 ,pp. : 3921-3932

Oxford University Press

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A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells

By Maerker Tina   van Wijk Erwin   Overlack Nora   Kersten Ferry F.J.   McGee JoAnn   Goldmann Tobias   Sehn Elisabeth   Roepman Ronald   Walsh Edward J.   Kremer Hannie   Wolfrum Uwe  

Human Molecular Genetics, Vol. 17, Iss. 1, 2008-01 ,pp. : 71-86

Oxford University Press

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Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

By Weil Dominique  

Human Molecular Genetics, Vol. 12, Iss. 5, 2003-03 ,pp. : 463-471

Oxford University Press

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