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Nobutaka Hattori Selected Research
Parkinson Disease (Parkinson's Disease)
08/2008
Calbindin 1, fibroblast growth factor 20, and alpha-synuclein in sporadic Parkinson's disease.
01/2008
Visual impairment in Parkinson's disease treated with amantadine: case report and review of the literature.
08/2007
[Relationship between alpha-synuclein and Parkinson's disease]
08/2007
Correlation between levels of pigment epithelium-derived factor and vascular endothelial growth factor in the striatum of patients with Parkinson's disease.
06/2007
Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population.
02/2007
Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population.
10/2006
Nuclear localization of the 20S proteasome subunit in Parkinson's disease.
09/2006
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.
08/2006
Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.
08/2006
Up-regulation of hMUTYH, a DNA repair enzyme, in the mitochondria of substantia nigra in Parkinson's disease.
04/2006
Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease.
02/2006
Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease.
11/2005
[Pathogenesis of Parkinson's disease: a common pathway between alpha-synuclein and parkin and the mechanism of Lewy bodies formation]
05/2005
Phosphorylated IkappaBalpha is a component of Lewy body of Parkinson's disease.
03/2005
Urinary 8-hydroxydeoxyguanosine levels as a biomarker for progression of Parkinson disease.
03/2005
Expression of 8-oxoguanine DNA glycosylase (OGG1) in Parkinson's disease and related neurodegenerative disorders.
12/2003
Appropriate dosing of pergolide in monotherapy and adjunctive therapy in Parkinson's disease.
01/2003
Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.
11/2002
Golden mean to longevity: rareness of mitochondrial cytochrome b variants in centenarians but not in patients with Parkinson's disease.
Articles by Research Topic
Disease
19
Parkinson Disease (Parkinson's Disease)
08/2008 - 11/2002
1
Ischemia
07/2008
1
Parkinsonian Disorders (Parkinsonism)
06/2008
1
Neurodegenerative Diseases (Neurodegenerative Disease)
03/2005
1
Atherosclerosis (Atheroma)
04/2004
1
Progressive Supranuclear Palsy (Steele Richardson Olszewski Syndrome)
08/2002
Drug/Important Bio-Agent (IBA)
8
alpha-Synuclein
IBA
08/2008 - 01/2003
2
Fibroblast Growth Factors (Fibroblast Growth Factor)
IBA
08/2008 - 06/2007
2
Leucine (L-Leucine)
FDA Link
02/2007 - 09/2006
2
Phosphotransferases (Kinase)
IBA
02/2007 - 09/2006
1
calbindin
IBA
08/2008
1
Type 2 Angiotensin Receptor
IBA
07/2008
1
Amantadine (Aman)
FDA Link
Generic
01/2008
1
Vascular Endothelial Growth Factor A (Vascular Endothelial Growth Factor)
IBA
08/2007
1
pigment epithelium-derived factor
IBA
08/2007
1
Proteasome Endopeptidase Complex (Proteasome)
IBA
10/2006
1
A-Form DNA (A-DNA)
IBA
08/2006
1
NF-kappaB inhibitor alpha
IBA
05/2005
1
8-hydroxy-2'-deoxyguanosine
IBA
03/2005
1
8-hydroxyguanine
IBA
03/2005
1
DNA Glycosylases (DNA Glycosylase)
IBA
03/2005
1
Mitochondrial DNA (mtDNA)
IBA
04/2004
1
Pergolide (Permax)
FDA Link
12/2003
1
Cytochromes b (Cytochrome b)
IBA
11/2002
1
Messenger RNA (mRNA)
IBA
08/2002
1
Protein Isoforms (Isoforms)
IBA
08/2002