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PARK2 wt Allele

Known as: Parkinson Disease (Autosomal Recessive, Juvenile) 2, Parkin wt Allele, PDJ, AR-JP 
Human PARK2 wild-type allele is located within 6q25.2-q27 and is approximately 1459 kb in length. This allele, which encodes E3 ubiquitin-protein… 
National Institutes of Health

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Related topics

7 relations
Cell DeathPARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILEParkinson DiseasePolyubiquitination

Broader (1)

PARK2 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
A common leucine‐rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia
A PARK8 form of Parkinson's disease (PD) is caused by a novel gene, leucine‐rich repeat kinase 2 (LRRK2), and a single mutation… 
2006
2006
Detection of compound heterozygous deletions in the parkin gene of fibroblasts in patients with autosomal recessive hereditary parkinsonism (PARK2)
2005
2005
Prevalence of parkin gene mutations and variations in idiopathic Parkinson's disease.
2003
2003
Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism
Autosomal recessive juvenile parkinsonism (AR‐JP) is a form of hereditary parkinsonism characterized by variable clinical… 
Highly Cited
2002
Highly Cited
2002
Functional association of the parkin gene promoter with idiopathic Parkinson's disease.
Loss-of-function mutations in the parkin gene were first identified in autosomal recessive juvenile parkinsonism (AR-JP… 
2002
2002
Progressive supranuclear palsy and tau hyperphosphorylation in a patient with a C212Y parkin mutation.
Autosomal recessive-juvenile parkinsonism (AR-JP) is one of the most common forms of familial Parkinson's disease (PD) and is… 
2002
2002
Distribution of parkin in the adult rat brain
2002
2002
Striatal dopaminergic denervation in early and late onset Parkinson's disease assessed by PET and the tracer [11C]FECIT: preliminary findings in one patient with autosomal recessive parkinsonism…
Abstract. Neuroimaging studies of striatal dopamine transporters (DAT) have shown that this measurement is a specific marker of… 
2000
2000
Regional and cellular expression of the parkin gene in the rat cerebral cortex
A mutation in the parkin gene has been identified as the cause for an autosomal recessively inherited form of early onset… 
Highly Cited
1998
Highly Cited
1998
Differential expression of the parkin gene in the human brain and peripheral leukocytes
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