Molecular basis of human Usher syndrome: Deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease
Authors:
- Kerstin Nagel-WolfrumKNKerstin Nagel-Wolfrum
- Karin JürgensKJKarin Jürgens
- Tina MärkerTMTina Märker
- Uwe WolfrumUWUwe Wolfrum
- 1 July 2006
- journal article
- review article
- Published by Elsevier in Experimental Eye Research
- Vol. 83 (1) , 97-119
Abstract
No abstract availableKeywords
This publication has 174 references indexed in Scilit:
- Recent progress towards understanding the synaptic ribbonCurrent Opinion in Neurobiology, 2005
- Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cellsDevelopmental Biology, 2005
- Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell developmentDevelopmental Biology, 2005
- Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafnessHuman Genetics, 2002
- A human homologue of Drosophila kelch associates with myosin‐VIIa in specialized adhesion junctionsCell Motility, 2002
- A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24–25Human Genetics, 2002
- Regulators of G-Protein signalling as new central nervous system drug targetsNature Reviews Drug Discovery, 2002
- Myosin VIIA is specifically associated with calmodulin and microtubule-associated protein-2B (MAP-2B)Biochemical Journal, 2001
- Presynaptic bodies (”ribbons"): from ultrastructural observations to molecular perspectivesCell and tissue research, 1997
- The kinocilium of auditory hair cells and evidence for its morphogenetic role during the regeneration of stereocilia and cuticular platesJournal of Neurocytology, 1995