Genetic association between α-synuclein and idiopathic parkinson's disease
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α-Synuclein genetic variants predict faster motor symptom progression in idiopathic Parkinson diseaseGenetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation updateGenetics of Parkinson's disease - a clinical perspectiveCommon genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.Visualizing disease associations: graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's diseaseSNCA variant associated with Parkinson disease and plasma alpha-synuclein level.A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2Compounds from an unbiased chemical screen reverse both ER-to-Golgi trafficking defects and mitochondrial dysfunction in Parkinson's disease modelsLRRK2 mutations and risk variants in Japanese patients with Parkinson's diseaseLipid classes and fatty acid patterns are altered in the brain of γ-synuclein null mutant mice.Postural instability/gait disturbance in Parkinson's disease has distinct subtypes: an exploratory analysis.α-Synuclein gene may interact with environmental factors in increasing risk of Parkinson's diseaseThe heritability of risk and age at onset of Parkinson's disease after accounting for known genetic risk factorsDisease-related and genetic correlates of psychotic symptoms in Parkinson's disease.The genetics of Parkinson disease.Genome-wide association study confirms extant PD risk loci among the Dutch.Head injury, α-synuclein genetic variability and Parkinson's disease.Head injury, α-synuclein Rep1, and Parkinson's disease.A novel resource for studying function and dysfunction of α-synuclein: mouse lines for modulation of endogenous Snca gene expression.Alpha-synuclein and familial Parkinson's diseaseGeneration of mouse lines with conditionally or constitutively inactivated Snca gene and Rosa26-stop-lacZ reporter located in cis on the mouse chromosome 6.Traumatic brain injury, paraquat exposure, and their relationship to Parkinson disease.Up-regulation of SNCA gene expression: implications to synucleinopathiesControlling the mass action of alpha-synuclein in Parkinson's disease.Genetic insights into sporadic Parkinson's disease pathogenesis.First-in-human assessment of PRX002, an anti-α-synuclein monoclonal antibody, in healthy volunteersGenetic variability in SNCA and Parkinson's disease.Genetic Variants in SNCA and the Risk of Sporadic Parkinson's Disease and Clinical Outcomes: A ReviewStructural variants in SNCA gene and the implication to synucleinopathies.Combinational losses of synucleins reveal their differential requirements for compensating age-dependent alterations in motor behavior and dopamine metabolism.Mutations in PRKN and SNCA Genes Important for the Progress of Parkinson's Disease.The genetic architecture of mitochondrial dysfunction in Parkinson's disease.
P2860
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P2860
Genetic association between α-synuclein and idiopathic parkinson's disease
description
article
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в жовтні 2008
@uk
name
Genetic association between α-synuclein and idiopathic parkinson's disease
@en
Genetic association between α-synuclein and idiopathic parkinson's disease
@nl
type
label
Genetic association between α-synuclein and idiopathic parkinson's disease
@en
Genetic association between α-synuclein and idiopathic parkinson's disease
@nl
prefLabel
Genetic association between α-synuclein and idiopathic parkinson's disease
@en
Genetic association between α-synuclein and idiopathic parkinson's disease
@nl
P2093
P356
P1476
Genetic association between α-synuclein and idiopathic parkinson's disease
@en
P2093
Alida Griffith
April J. Atkins
Berta C. Leis
Cyrus P. Zabetian
Denise M. Kay
Donald S. Higgins
Dora Yearout
Haydeh Payami
Jennifer S. Montimurro
P2860
P304
P356
10.1002/AJMG.B.30758
P577
2008-10-05T00:00:00Z