Familial Juvenile Parkinsonism
|
0.300 |
Biomarker
|
disease |
CTD_human |
Methylmercury can induce Parkinson's-like neurotoxicity similar to 1-methyl-4- phenylpyridinium: a genomic and proteomic analysis on MN9D dopaminergic neuron cells.
|
26558463 |
2015 |
Familial Juvenile Parkinsonism
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Methylmercury can induce Parkinson's-like neurotoxicity similar to 1-methyl-4- phenylpyridinium: a genomic and proteomic analysis on MN9D dopaminergic neuron cells.
|
26558463 |
2015 |
Familial Juvenile Parkinsonism
|
0.300 |
Therapeutic
|
disease |
CTD_human |
A recurrent mutation in PARK2 is associated with familial lung cancer.
|
25640678 |
2015 |
Familial Juvenile Parkinsonism
|
0.300 |
Biomarker
|
disease |
CTD_human |
A recurrent mutation in PARK2 is associated with familial lung cancer.
|
25640678 |
2015 |
Familial Juvenile Parkinsonism
|
0.300 |
Biomarker
|
disease |
CTD_human |
Low doses of paraquat and polyphenols prolong life span and locomotor activity in knock-down parkin Drosophila melanogaster exposed to oxidative stress stimuli: implication in autosomal recessive juvenile parkinsonism.
|
23046578 |
2013 |
Familial Juvenile Parkinsonism
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Low doses of paraquat and polyphenols prolong life span and locomotor activity in knock-down parkin Drosophila melanogaster exposed to oxidative stress stimuli: implication in autosomal recessive juvenile parkinsonism.
|
23046578 |
2013 |
Familial Juvenile Parkinsonism
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Parkin protects against neurotoxicity in the 6-hydroxydopamine rat model for Parkinson's disease.
|
16914382 |
2006 |
Familial Juvenile Parkinsonism
|
0.300 |
Biomarker
|
disease |
CTD_human |
Parkin protects against neurotoxicity in the 6-hydroxydopamine rat model for Parkinson's disease.
|
16914382 |
2006 |
Familial Juvenile Parkinsonism
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Parkin disease: a phenotypic study of a large case series.
|
12764051 |
2003 |
Familial Juvenile Parkinsonism
|
0.300 |
Biomarker
|
disease |
CTD_human |
Parkin disease: a phenotypic study of a large case series.
|
12764051 |
2003 |
Familial Juvenile Parkinsonism
|
0.300 |
Biomarker
|
disease |
CTD_human |
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36.
|
11254447 |
2001 |
Familial Juvenile Parkinsonism
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36.
|
11254447 |
2001 |
Familial Juvenile Parkinsonism
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.
|
10894217 |
2000 |
Familial Juvenile Parkinsonism
|
0.300 |
Biomarker
|
disease |
CTD_human |
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.
|
10894217 |
2000 |
Familial Juvenile Parkinsonism
|
0.300 |
Therapeutic
|
disease |
CTD_human |
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
|
10072423 |
1999 |
Familial Juvenile Parkinsonism
|
0.300 |
Biomarker
|
disease |
CTD_human |
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
|
10072423 |
1999 |