Mouse Myosin X: Molecular Architecture and Tissue Expression as Revealed by Northern Blot and in Situ Hybridization Analyses
- 10 May 2000
- journal article
- Published by Elsevier BV in Biochemical and Biophysical Research Communications
- Vol. 271 (2), 526-533
- https://doi.org/10.1006/bbrc.2000.2669
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 35 references indexed in Scilit:
- Unconventional Myosins in Cell Movement, Membrane Traffic, and Signal TransductionScience, 1998
- Unconventional Myosins, the Basis for Deafness in Mouse and ManAmerican Journal of Human Genetics, 1997
- Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va geneNature Genetics, 1997
- Mutations in the myosin VIIA gene cause non-syndromic recessive deafnessNature Genetics, 1997
- Myosin diversity and diseaseTrends in Genetics, 1996
- The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cellsNature Genetics, 1995
- Unconventional MyosinsAnnual Review of Cell and Developmental Biology, 1995
- Defective myosin VIIA gene responsible for Usher syndrome type IBNature, 1995
- Novel myosin heavy chain encoded by murine dilute coat colour locusNature, 1991
- A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutationCell, 1990