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PRKCG wt Allele

Known as: MGC57564, PKCC, Protein Kinase C, Gamma wt Allele 
Human PRKCG wild-type allele is located in the vicinity of 19q13.4 and is approximately 28 kb in length. This allele, which encodes Protein kinase C… 
National Institutes of Health

Related topics

Related topics

3 relations
PhosphorylationSerine/Threonine PhosphorylationSignal Transduction

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
A novel mutation in the C2 domain of protein kinase C gamma associated with spinocerebellar ataxia type 14
Spinocerebellar ataxia type 14 (SCA14; Online Mendelian Inheritance in Man, OMIM #605361) is an autosomal dominant… 
2012
2012
Genomic medicine enters the neurology clinic
Extraordinary advances in genetics and genomics are revolutionizing the practice of medicine. In this issue of Neurology ®, 3… 
2010
2010
Mutant protein kinase C gamma that causes spinocerebellar ataxia type 14 (SCA14) is selectively degraded by autophagy
Several causal missense mutations in the protein kinase Cγ (γPKC) gene have been found in spinocerebellar ataxia type 14 (SCA14… 
Review
2008
Review
2008
[Molecular epidemiology of cerebrovascular diseases; the Hisayama study and the Fukuoka Stroke Registry (FSR)].
The underlying pathogenesis of stroke is mediated by a variety of environmental risk factors as well as genetic ones. Thus, we… 
2007
2007
Benign SCA14 phenotype in a German patient associated with a missense mutation in exon 3 of the PRKCG gene
instrumental musicians. Muscle Nerve 2003;27:549-561. 3. Cersosimo MG, Koller WC. Essential tremor. In: Watts RL, Koller WC… 
2004
2004
Mutations in the FGF14 gene are not a major cause of spinocerebellar ataxia in Caucasians
Spinocerebellar ataxias (SCAs) are heterogeneous dominantly inherited neurodegenerative disorders, clinically characterized by… 
Highly Cited
2003
Highly Cited
2003
Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma.
BACKGROUND We previously discovered spinocerebellar ataxia type 14 (SCA14) in a single Japanese family with an autosomal dominant… 
Highly Cited
2003
Highly Cited
2003
A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.
The autosomal dominant cerebellar ataxias (ADCA) are a clinically, pathologically and genetically heterogeneous group of… 
2000
2000
Ca 2 1-Evoked Serotonin Secretion by Parafollicular Cells : Roles in Signal Transduction of Phosphatidylinositol 3 *-kinase , and the g and z Isoforms of Protein Kinase C
Parafollicular (PF) cells secrete 5-HT in response to stimulation of a G-protein-coupled Ca receptor (CaR) by increased… 
1998
1998
Alzheimer’s-specific effects of soluble b -amyloid on protein kinase C- a and - g degradation in human fibroblasts
Alzheimer’s disease (AD) is a multifactorial disease in which b -amyloid peptide ( b AP) plays a critical role. We report here… 
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