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PARK2 gene

Known as: AR-JP, Parkinson Disease (Autosomal Recessive, Juvenile) 2, Parkin Gene, PRKN 
This gene may play a role in the mediation of proteasomal targeting.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Recent consensus on the definition, phenomenology and classification of dystonia centres around phenomenology and guides our… 
Review
2011
Review
2011
Macroautophagy and chaperone-mediated autophagy (CMA) are the two main mammalian lysosomal proteolytic systems. In macroautophagy… 
Review
2008
Review
2008
Overactivation of N-methyl-D-aspartate (NMDA)-type glutamate receptors accounts, at least in part, for excitotoxic neuronal… 
Highly Cited
2006
Highly Cited
2006
Mouse embryonic stem cells (mESCs) represent a unique tool for many researchers; however, the process of ESC derivation is often… 
Highly Cited
2005
Highly Cited
2005
Mutations in parkin are currently recognized as the most common cause of familial Parkinsonism. Emerging evidence also suggests… 
Highly Cited
2004
Highly Cited
2004
To investigate striatal and cortical pre- and postsynaptic dopaminergic function in parkin-linked parkinsonism, 13 unrelated… 
Highly Cited
2003
Highly Cited
2003
Parkin, a RING-type ubiquitin ligase, is the product of the gene responsible for autosomal recessive juvenile parkinsonism. A… 
Highly Cited
2002
Highly Cited
2002
The Parkin gene on 6q25.2–27 is responsible for about 50% of autosomal recessive juvenile parkinsonism and less than 20% of… 
Highly Cited
2002
Highly Cited
2002
Loss-of-function mutations in the parkin gene were first identified in autosomal recessive juvenile parkinsonism (AR-JP…