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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

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Related topics

3 relations
PhosphorylationSerine/Threonine PhosphorylationSignal Transduction

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
A brain proteomic investigation of rapamycin effects in the Tsc1+/− mouse model
BackgroundTuberous sclerosis complex (TSC) is a rare monogenic disorder characterized by benign tumors in multiple organs as well… 
Review
2011
Review
2011
[Lysophosphatidic acid as initiator of neuropathic pain].
  • H. Ueda
  • Nihon yakurigaku zasshi. Folia pharmacologica…
  • 2011
  • Corpus ID: 8434568
The injury-induced intense stimulation of spinal cord neurons causes lysophosphatidic acid (LPA) biosynthesis. LPA(1) receptor… 
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… 
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… 
2006
2006
Identification of a new family of spinocerebellar ataxia type 14 in the japanese spinocerebellar ataxia population by the screening of PRKCG exon 4
Spinocerebellar ataxia type 14 (SCA14) is an autosomal dominant neurodegenerative disorder characterized by cerebellar ataxia and… 
2005
2005
Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population
Missense mutations in the PRKCG gene have recently been identified in spinocerebellar ataxia 14 (SCA14) patients; these include… 
Highly Cited
2004
Highly Cited
2004
Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.
BACKGROUND Autosomal dominant cerebellar ataxias comprise a clinically, neuropathologically, and genetically heterogeneous group… 
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… 
Highly Cited
1999
Highly Cited
1999
Protein kinase C reduces the KCa current of rat tail artery smooth muscle cells.
The hypothesis that protein kinase C (PKC) is able to regulate the whole cell Ca-activated K (KCa) current independently of PKC… 
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