Direct Interaction of Otoferlin with Syntaxin 1A, SNAP-25, and the L-type Voltage-gated Calcium Channel CaV1.3
Open Access
- 1 January 2009
- journal article
- Published by Elsevier
- Vol. 284 (3) , 1364-1372
- https://doi.org/10.1074/jbc.m803605200
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Surface Plasmon Resonance (SPR) Analysis of Binding Interactions of Proteins in Inner-Ear Sensory EpitheliaPublished by Springer Nature ,2009
- Regulation of Escherichia coli SOS mutagenesis by dimeric intrinsically disordered umuD gene productsProceedings of the National Academy of Sciences, 2008
- A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9Hearing Research, 2007
- Synaptotagmin C2A Loop 2 Mediates Ca2+-dependent SNARE Interactions Essential for Ca2+-triggered Vesicle ExocytosisMolecular Biology of the Cell, 2007
- Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the ratEuropean Journal of Neuroscience, 2006
- Few CaV1.3 Channels Regulate the Exocytosis of a Synaptic Vesicle at the Hair Cell Ribbon SynapseJournal of Neuroscience, 2005
- A novel missense mutation in a C2 domain ofOTOF results in autosomal recessive auditory neuropathyAmerican Journal of Medical Genetics Part A, 2005
- The C2A Domain of Synaptotagmin Alters the Kinetics of Voltage-gated Ca2+ Channels Cav1.2 (Lc-type) and Cav2.3 (R-type)Published by Elsevier ,2003
- Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing lossJournal of Medical Genetics, 2002
- Voltage- and ion-dependent conductances in solitary vertebrate hair cellsNature, 1983