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PARK2 gene
Known as:
AR-JP
, Parkinson Disease (Autosomal Recessive, Juvenile) 2, Parkin Gene
, PRKN
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This gene may play a role in the mediation of proteasomal targeting.
National Institutes of Health
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Related topics
Related topics
9 relations
Cell Death
PARK2 protein, human
PARK3 gene
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
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PARK2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Isolated and combined dystonia syndromes – an update on new genes and their phenotypes
B. Balint
,
K. Bhatia
European Journal of Neurology
2015
Corpus ID: 31312448
Recent consensus on the definition, phenomenology and classification of dystonia centres around phenomenology and guides our…
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Review
2011
Review
2011
Autophagic pathways in Parkinson disease and related disorders
M. Xilouri
,
L. Stefanis
Expert Reviews in Molecular Medicine
2011
Corpus ID: 41852563
Macroautophagy and chaperone-mediated autophagy (CMA) are the two main mammalian lysosomal proteolytic systems. In macroautophagy…
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Review
2008
Review
2008
Emerging roles of S-nitrosylation in protein misfolding and neurodegenerative diseases.
Tomohiro Nakamura
,
S. Lipton
Antioxidants and Redox Signaling
2008
Corpus ID: 40944820
Overactivation of N-methyl-D-aspartate (NMDA)-type glutamate receptors accounts, at least in part, for excitotoxic neuronal…
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Highly Cited
2006
Highly Cited
2006
An Efficient Method for the Derivation of Mouse Embryonic Stem Cells
Vítezlav Bryja
,
S. Bonilla
,
+5 authors
E. Arenas
Stem Cells
2006
Corpus ID: 22757180
Mouse embryonic stem cells (mESCs) represent a unique tool for many researchers; however, the process of ESC derivation is often…
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Highly Cited
2005
Highly Cited
2005
Stress-induced alterations in parkin solubility promote parkin aggregation and compromise parkin's protective function.
Cheng Wang
,
H. Ko
,
+11 authors
K. Lim
Human Molecular Genetics
2005
Corpus ID: 25220711
Mutations in parkin are currently recognized as the most common cause of familial Parkinsonism. Emerging evidence also suggests…
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Highly Cited
2004
Highly Cited
2004
Striatal and cortical pre- and postsynaptic dopaminergic dysfunction in sporadic parkin-linked parkinsonism.
C. Scherfler
,
N. Khan
,
+7 authors
P. Piccini
Brain : a journal of neurology
2004
Corpus ID: 18022972
To investigate striatal and cortical pre- and postsynaptic dopaminergic function in parkin-linked parkinsonism, 13 unrelated…
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Highly Cited
2003
Highly Cited
2003
A Product of the Human Gene Adjacent to parkin Is a Component of Lewy Bodies and Suppresses Pael Receptor-induced Cell Death*
Y. Imai
,
Mariko Soda
,
T. Murakami
,
M. Shoji
,
K. Abe
,
R. Takahashi
Journal of Biological Chemistry
2003
Corpus ID: 33442264
Parkin, a RING-type ubiquitin ligase, is the product of the gene responsible for autosomal recessive juvenile parkinsonism. A…
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Review
2002
Review
2002
MPTP: insights into parkinsonian neurodegeneration.
S. Speciale
Neurotoxicology and Teratology
2002
Corpus ID: 22820181
Highly Cited
2002
Highly Cited
2002
Park6‐linked parkinsonism occurs in several european families
E. Valente
,
F. Brancati
,
+20 authors
N. Wood
Annals of Neurology
2002
Corpus ID: 30608433
The Parkin gene on 6q25.2–27 is responsible for about 50% of autosomal recessive juvenile parkinsonism and less than 20% of…
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Highly Cited
2002
Highly Cited
2002
Functional association of the parkin gene promoter with idiopathic Parkinson's disease.
A. West
,
D. Maraganore
,
+6 authors
M. Farrer
Human Molecular Genetics
2002
Corpus ID: 16728663
Loss-of-function mutations in the parkin gene were first identified in autosomal recessive juvenile parkinsonism (AR-JP…
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