×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
Biomarker
group
HPO
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
CausalMutation
group
CLINVAR
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
BEFREE
Parkinsonism due to mutations in PINK1 , parkin, and DJ-1 and oxidative stress and mitochondrial pathways.
22951446
2012
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
Biomarker
group
BEFREE
PARK6 is a common cause of familial parkinsonism .
12548371
2002
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
LHGDN
PARK6 is a common cause of familial parkinsonism .
12548371
2002
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
Biomarker
group
BEFREE
PINK1 , Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism .
15970950
2005
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
BEFREE
PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonism .
16700027
2006
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
BEFREE
PINK1 mutation in Taiwanese early-onset parkinsonism : clinical, genetic, and dopamine transporter studies.
17960343
2007
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
Biomarker
group
BEFREE
PINK1 -linked parkinsonism is associated with Lewy body pathology.
20356854
2010
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
Biomarker
group
BEFREE
PINK1 parkinsonism and Parkinson disease: distinguishable brain mitochondrial function and metabolomics.
23063710
2013
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
BEFREE
PINK1 and Parkin, the products of two genes responsible for autosomal recessive Parkinsonian syndromes with early onset, act as a quality control system on the outer mitochondrial membrane to preserve mitochondrial integrity.
23206589
2013
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
Biomarker
group
BEFREE
PINK1 (PTEN induced putative kinase 1 ) and PARKIN (also known as PARK2) have been identified as the causal genes responsible for hereditary recessive early-onset Parkinsonism .
24784582
2014
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
Biomarker
group
BEFREE
PINK1 -type of early-onset parkinsonism can occur in very young patients, and phenotypic expression of PINK1 mutations may depend on age of onset and ethnicity.
28062148
2017
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
BEFREE
A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism .
27413743
2016
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
LHGDN
All sites of mutations were novel, suggesting that PINK1 may be the second most common causative gene next to parkin in parkinsonism with the recessive mode of inheritance.
15349870
2004
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
Biomarker
group
BEFREE
All sites of mutations were novel, suggesting that PINK1 may be the second most common causative gene next to parkin in parkinsonism with the recessive mode of inheritance.
15349870
2004
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
BEFREE
Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan.
16257123
2006
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
Biomarker
group
BEFREE
Bilateral subthalamic stimulation in Parkin and PINK1 parkinsonism .
18378882
2008
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
BEFREE
Deficits in temporal processing might be considered as subclinical signs of alteration at least in PINK1 -related parkinsonism .
18584234
2008
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
Biomarker
group
CTD_human
Downregulation of Pink1 influences mitochondrial fusion-fission machinery and sensitizes to neurotoxins in dopaminergic cells.
24792327
2014
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
BEFREE
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.
16009891
2005
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
LHGDN
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.
16009891
2005
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
Biomarker
group
CTD_human
Enhancing nucleotide metabolism protects against mitochondrial dysfunction and neurodegeneration in a PINK1 model of Parkinson's disease.
24441527
2014
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
BEFREE
Familial Parkinsonism with digenic parkin and PINK1 mutations.
18546294
2008
×
Entrez Id:
65018
Gene Symbol:
PINK1
PINK1
0.700
GeneticVariation
group
BEFREE
Familial Parkinsonism is associated with loss-of-function mutations in PINK1 and Parkin.
27593930
2017