Autosomal Dominant 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 |
Autosomal Dominant Parkinsonism
|
0.300 |
Therapeutic
|
disease |
CTD_human |
A recurrent mutation in PARK2 is associated with familial lung cancer.
|
25640678 |
2015 |
Autosomal Dominant Parkinsonism
|
0.300 |
Biomarker
|
disease |
CTD_human |
A recurrent mutation in PARK2 is associated with familial lung cancer.
|
25640678 |
2015 |
Autosomal Dominant 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 |
Autosomal Dominant 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 |
Autosomal Dominant 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 |
Autosomal Dominant Parkinsonism
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Parkin protects against neurotoxicity in the 6-hydroxydopamine rat model for Parkinson's disease.
|
16914382 |
2006 |
Autosomal Dominant Parkinsonism
|
0.300 |
Biomarker
|
disease |
CTD_human |
Parkin protects against neurotoxicity in the 6-hydroxydopamine rat model for Parkinson's disease.
|
16914382 |
2006 |
Autosomal Dominant Parkinsonism
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Parkin disease: a phenotypic study of a large case series.
|
12764051 |
2003 |
Autosomal Dominant Parkinsonism
|
0.300 |
Biomarker
|
disease |
CTD_human |
Parkin disease: a phenotypic study of a large case series.
|
12764051 |
2003 |
Autosomal Dominant 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 |
Autosomal Dominant 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 |
Autosomal Dominant Parkinsonism
|
0.300 |
Biomarker
|
disease |
CTD_human |
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.
|
10894217 |
2000 |
Autosomal Dominant Parkinsonism
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.
|
10894217 |
2000 |
Autosomal Dominant 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 |
Autosomal Dominant 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 |