Role for a Novel Usher Protein Complex in Hair Cell Synaptic Maturation

Regulation of PCDH15 function in mechanosensory hair cells by alternative splicing of the cytoplasmic domain

(2011) S. W. Webb et al.   DEVELOPMENT

Harmonin inhibits presynaptic Cav1.3 Ca2+ channels in mouse inner hair cells

(2011) Frederick D Gregory et al.   NATURE NEUROSCIENCE

Mutations in Protocadherin 15 and Cadherin 23 Affect Tip Links and Mechanotransduction in Mammalian Sensory Hair Cells

(2011) Kumar N. Alagramam et al.   PLoS One

Biochemical Characterization of Native Usher Protein Complexes from a Vesicular Subfraction of Tracheal Epithelial Cells

(2010) Marisa Zallocchi et al.   BIOCHEMISTRY

Control of Exocytosis by Synaptotagmins and Otoferlin in Auditory Hair Cells

(2010) M. Beurg et al.   JOURNAL OF NEUROSCIENCE

Type III intermediate filament peripherin inhibits neuritogenesis in type II spiral ganglion neurons in vitro

(2010) Meagan Barclay et al.   NEUROSCIENCE LETTERS

Localization and expression of clarin-1, the Clrn1 gene product, in auditory hair cells and photoreceptors

(2009) Marisa Zallocchi et al.   HEARING RESEARCH

Clarin-1 protein expression in photoreceptors

(2009) Dominic Cosgrove et al.   HEARING RESEARCH

Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation

(2009) R. Geng et al.   HUMAN MOLECULAR GENETICS

Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell

(2009) P. Heidrych et al.   HUMAN MOLECULAR GENETICS

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

(2009) Isabelle Roux et al.   HUMAN MOLECULAR GENETICS

The Molecular Architecture of Ribbon Presynaptic Terminals

(2009) George Zanazzi et al.   MOLECULAR NEUROBIOLOGY

CLRN1 Is Nonessential in the Mouse Retina but Is Required for Cochlear Hair Cell Development

(2009) Scott F. Geller et al.   PLoS Genetics

A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth

(2008) G. Lefevre et al.   DEVELOPMENT

Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome

(2008) Zubair M. Ahmed et al.   HUMAN GENETICS

Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness form

(2008) P. Heidrych et al.   HUMAN MOLECULAR GENETICS

 II- V spectrin bridges the plasma membrane and cortical lattice in the lateral wall of the auditory outer hair cells

(2008) K. Legendre et al.   JOURNAL OF CELL SCIENCE