Myosin VI is required for the proper maturation and function of inner hair cell ribbon synapses

By Roux Isabelle   Hosie Suzanne   Johnson Stuart L.   Bahloul Amel   Cayet Nadge   Nouaille Sylvie   Kros Corn J.   Petit Christine   Safieddine Saaid  

Human Molecular Genetics, Vol. 18, Iss. 23, 2009-12 ,pp. : 4615-4628

Oxford University Press

Access to resources Recommend Favorite

Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium

By Kikkawa Yoshiaki  

Human Molecular Genetics, Vol. 14, Iss. 3, 2005-02 ,pp. : 391-400

Oxford University Press

Access to resources Recommend Favorite

Spinocerebellar Ataxia Type-1 and Spinobulbar Muscular Atrophy Gene Products Interact with Glyceraldehyde-3-Phosphate Dehydrogenase

By Koshy Beena   Matilla Toni   Burright Eric N.   Merry Diane E.   Fischbeck Kenneth H.   Orr Harry T.   Zoghbi Huda Y.  

Human Molecular Genetics, Vol. 5, Iss. 9, 1996-01 ,pp. : 1311-1318

Oxford University Press

Access to resources Recommend Favorite

Mariner is defective in myosin VIIA : a zebrafish model for human hereditary deafness

By Ernest Sylvain   Rauch Gerd-Jörg  

Human Molecular Genetics, Vol. 9, Iss. 14, 2000-09 ,pp. : 2189-2196

Oxford University Press

Access to resources Recommend Favorite

A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

By Ebermann Inga   Scholl Hendrik   Charbel Issa Peter   Becirovic Elvir   Lamprecht Jürgen   Jurklies Bernhard   Millán José   Aller Elena   Mitter Diana   Bolz Hanno  

Human Genetics, Vol. 121, Iss. 2, 2007-04 ,pp. : 203-211

Springer Publishing Company

Access to resources Recommend Favorite