Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia
- 1 April 2003
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 72 (4), 839-849
- https://doi.org/10.1086/373883
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Altered Trafficking of Membrane Proteins in Purkinje Cells of SCA1 Transgenic MiceThe American Journal of Pathology, 2001
- The C1 Domain of Protein Kinase C as a Lipid Bilayer Surface Sensing ModuleBiochemistry, 2001
- No Mutations in the Coding Region of the PRKCG Gene in Three Families with Retinitis Pigmentosa Linked to the RP11 Locus on Chromosome 19qAmerican Journal of Human Genetics, 1999
- Segregation of a PRKCG Mutation in Two RP11 FamiliesAmerican Journal of Human Genetics, 1998
- Impaired motor coordination correlates with persistent multiple climbing fiber innervation in PKCγ mutant miceCell, 1995
- AMBER, a package of computer programs for applying molecular mechanics, normal mode analysis, molecular dynamics and free energy calculations to simulate the structural and energetic properties of moleculesComputer Physics Communications, 1995
- Crystal structure of the Cys2 activator-binding domain of protein kinase Cδ in complex with phorbol esterCell, 1995
- A Second Generation Force Field for the Simulation of Proteins, Nucleic Acids, and Organic MoleculesJournal of the American Chemical Society, 1995
- Multiple, Distinct Forms of Bovine and Human Protein Kinase C Suggest Diversity in Cellular Signaling PathwaysScience, 1986
- Cloning and expression of multiple protein kinase C cDNAsCell, 1986