SummaryParkin is an E3 ubiquitin ligase, mutations in which are responsible for autosomal recessive juvenile parkinsonism. Recently, several structures of Parkin have been solved, revealing its serpentine shape and modes of auto-inhibition
Autosomal recessive juvenile parkinsonism (ARJP) is an early onset familial form of Parkinson\u27s d...
Parkin is an RBR E3 ubiquitin ligase that has been implicated in both sporadic and familial Parkinso...
Mutations in the Parkin gene cause a juvenile-onset form of Parkinson's disease (PD) that is transm...
SummaryParkin is an E3 ubiquitin ligase, mutations in which are responsible for autosomal recessive ...
Mutations in the park2 gene, encoding the RING-inBetweenRING-RING E3 ubiquitin ligase parkin, cause ...
Parkin is an E3-ubiquitin ligase belonging to the RBR (RING–InBetweenRING–RING family), and is invol...
Missense mutations in park2, encoding the parkin protein, account for approximately 50% of autosomal...
Parkinson’s disease (PD), the second most common neurodegenerative disease in men. Parkin is an E3 u...
Parkin is a ubiquitin-protein isopeptide ligase (E3) involved in ubiquitin/proteasome-mediated prote...
The PARK2 gene is mutated in 50 % of autosomal recessive juvenile parkinsonism (ARJP) cases. It enco...
Mutations in the park2 gene, encoding the RING-inBetweenRING-RING E3 ubiquitin ligase parkin, cause ...
Autosomal recessive juvenile parkinsonism (ARJP) is an early onset familial form of Parkinson’s dise...
Summary. Parkinson's Disease (PD) is a common neurodegenerative disorder that is characterized ...
The PARK2 gene is mutated in 50% of autosomal recessive juvenile parkinsonism (ARJP) cases. It encod...
AbstractParkinson's disease (PD) is a neurodegenerative disease characterized by the selective demis...
Autosomal recessive juvenile parkinsonism (ARJP) is an early onset familial form of Parkinson\u27s d...
Parkin is an RBR E3 ubiquitin ligase that has been implicated in both sporadic and familial Parkinso...
Mutations in the Parkin gene cause a juvenile-onset form of Parkinson's disease (PD) that is transm...
SummaryParkin is an E3 ubiquitin ligase, mutations in which are responsible for autosomal recessive ...
Mutations in the park2 gene, encoding the RING-inBetweenRING-RING E3 ubiquitin ligase parkin, cause ...
Parkin is an E3-ubiquitin ligase belonging to the RBR (RING–InBetweenRING–RING family), and is invol...
Missense mutations in park2, encoding the parkin protein, account for approximately 50% of autosomal...
Parkinson’s disease (PD), the second most common neurodegenerative disease in men. Parkin is an E3 u...
Parkin is a ubiquitin-protein isopeptide ligase (E3) involved in ubiquitin/proteasome-mediated prote...
The PARK2 gene is mutated in 50 % of autosomal recessive juvenile parkinsonism (ARJP) cases. It enco...
Mutations in the park2 gene, encoding the RING-inBetweenRING-RING E3 ubiquitin ligase parkin, cause ...
Autosomal recessive juvenile parkinsonism (ARJP) is an early onset familial form of Parkinson’s dise...
Summary. Parkinson's Disease (PD) is a common neurodegenerative disorder that is characterized ...
The PARK2 gene is mutated in 50% of autosomal recessive juvenile parkinsonism (ARJP) cases. It encod...
AbstractParkinson's disease (PD) is a neurodegenerative disease characterized by the selective demis...
Autosomal recessive juvenile parkinsonism (ARJP) is an early onset familial form of Parkinson\u27s d...
Parkin is an RBR E3 ubiquitin ligase that has been implicated in both sporadic and familial Parkinso...
Mutations in the Parkin gene cause a juvenile-onset form of Parkinson's disease (PD) that is transm...
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