Myosin VIIA is specifically associated with calmodulin and microtubule-associated protein-2B (MAP-2B)
- 1 March 2001
- journal article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 354 (2)
- https://doi.org/10.1042/0264-6021:3540267
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Unconventional Myosins in Cell Movement, Membrane Traffic, and Signal TransductionScience, 1998
- Plasma Membrane Ca2+-ATPase Extrudes Ca2+from Hair Cell StereociliaJournal of Neuroscience, 1998
- Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA geneNature Genetics, 1997
- Mutation Profile of All 49 Exons of the Human Myosin VIIA Gene, and Haplotype Analysis, in Usher 1B Families from Diverse OriginsAmerican Journal of Human Genetics, 1997
- Unconventional Myosins in Inner-Ear Sensory EpitheliaThe Journal of cell biology, 1997
- Mutations in the myosin VIIA gene cause non-syndromic recessive deafnessNature Genetics, 1997
- Phosphatidic acid formation by phospholipase D is required for transport from the endoplasmic reticulum to the Golgi complexCurrent Biology, 1997
- Myosin VIIa, the product of the Usher 1B syndrome gene, is concentrated in the connecting cilia of photoreceptor cellsCell Motility, 1997
- Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expressionCell Motility, 1997
- Molecular Cloning and Domain Structure of Human Myosin-VIIa, the Gene Product Defective in Usher Syndrome 1BGenomics, 1996