Complete genomic screen in Parkinson disease: evidence for multiple genes.
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The genetic epidemiology of neurodegenerative disease.Parkin mono-ubiquitinates Bcl-2 and regulates autophagyIdentification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.Genetics of Parkinson diseaseGenome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson diseaseMutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson diseaseLack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patientsTAU haplotype and the Saitohin Q7R gene polymorphism do not influence CSF Tau in Alzheimer's disease and are not associated with frontotemporal dementia or Parkinson's diseaseParkin binds to alpha/beta tubulin and increases their ubiquitination and degradationGenome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's diseaseParkinson disease loci in the mid-western AmishQuantitative assessment of the effect of FGF20 rs12720208 variant on the risk of Parkinson's disease: a meta-analysis.Genomewide association study for susceptibility genes contributing to familial Parkinson diseaseHaplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD StudyPARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study.Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease.Effects of gender on nigral gene expression and parkinson disease.An evaluation of the performance of HapMap SNP data in a Shanghai Chinese population: analyses of allele frequency, linkage disequilibrium pattern and tagging SNPs transferability on chromosome 1q21-q25SLEPR: a sample-level enrichment-based pathway ranking method -- seeking biological themes through pathway-level consistencyParkinson's disease.Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease.Seeking unique and common biological themes in multiple gene lists or datasets: pathway pattern extraction pipeline for pathway-level comparative analysis.Brain mitochondria from DJ-1 knockout mice show increased respiration-dependent hydrogen peroxide consumption.Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP dataFGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expression.Accounting for linkage in family-based tests of association with missing parental genotypesThe PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval.Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease.Genetic variation in FGF20 modulates hippocampal biologyMutations in NR4A2 associated with familial Parkinson disease.Single nucleotide polymorphism seeking long term association with complex diseaseResistance of alpha -synuclein null mice to the parkinsonian neurotoxin MPTP.Current concepts in the diagnosis and management of Parkinson's diseaseInvestigation of the PARK10 gene in Parkinson disease.Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes.Genetics of parkinsonism.The genetic basis of Parkinson's diseaseRare genetic mutations shed light on the pathogenesis of Parkinson diseaseLearning about the X from our parents
P2860
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P2860
Complete genomic screen in Parkinson disease: evidence for multiple genes.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
Complete genomic screen in Parkinson disease: evidence for multiple genes.
@en
Complete genomic screen in Parkinson disease: evidence for multiple genes.
@nl
type
label
Complete genomic screen in Parkinson disease: evidence for multiple genes.
@en
Complete genomic screen in Parkinson disease: evidence for multiple genes.
@nl
prefLabel
Complete genomic screen in Parkinson disease: evidence for multiple genes.
@en
Complete genomic screen in Parkinson disease: evidence for multiple genes.
@nl
P2093
P356
P1476
Complete genomic screen in Parkinson disease: evidence for multiple genes.
@en
P2093
B Slotterbeck
D Masterman
E Rampersaud
F Mastaglia
P304
P356
10.1001/JAMA.286.18.2239
P407
P577
2001-11-01T00:00:00Z