Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease. - Wikidata - awgldk - TriplyDB

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.

http://www.wikidata.org/entity/Q30493604

about

Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease Recurrent inversion events at 17q21.31 microdeletion locus are linked to the MAPT H2 haplotype Genetics of Parkinson's disease - a clinical perspective Parkinson's disease dementia: convergence of α-synuclein, tau and amyloid-β pathologies.Alpha-synuclein and tau: teammates in neurodegeneration?Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.Loss of vesicular dopamine release precedes tauopathy in degenerative dopaminergic neurons in a Drosophila model expressing human tau.Genetic susceptibility in Parkinson's disease Genomewide association study for susceptibility genes contributing to familial Parkinson disease Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study 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 disease Tau isoform regulation is region- and cell-specific in mouse brain.A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2 Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease.Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease.Caenorhabditis elegans: a model to investigate oxidative stress and metal dyshomeostasis in Parkinson's disease Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders.LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease Physiological transgene regulation and functional complementation of a neurological disease gene deficiency in neurons The neurobiological basis of cognitive impairment in Parkinson's disease.Tau levels do not influence human ALS or motor neuron degeneration in the SOD1G93A mouse.Analysis of GWAS-linked loci in Parkinson disease reaffirms PARK16 as a susceptibility locus.Postural instability/gait disturbance in Parkinson's disease has distinct subtypes: an exploratory analysis.The heritability of risk and age at onset of Parkinson's disease after accounting for known genetic risk factors Disease-related and genetic correlates of psychotic symptoms in Parkinson's disease.APOE, MAPT, and SNCA genes and cognitive performance in Parkinson disease.A robust and efficient statistical method for genetic association studies using case and control samples from multiple cohorts.The genetics of Parkinson disease.Genome-wide association study confirms extant PD risk loci among the Dutch.Neuropathologically defined subtypes of Alzheimer's disease with distinct clinical characteristics: a retrospective study.SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population A novel Alzheimer disease locus located near the gene encoding tau protein.The Role of MAPT Haplotype H2 and Isoform 1N/4R in Parkinsonism of Older Adults.Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.Association of the MAPT locus with Parkinson's disease.Back to the tubule: microtubule dynamics in Parkinson's disease.Cognitive impairment and dementia in patients with Parkinson disease.Development of Parkinson's disease biomarkers.Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis.

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P2860

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.

http://www.wikidata.org/entity/Q30493604

description

2007 nî lūn-bûn

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2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի օգոստոսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.

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Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.

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type

label

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.

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Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.

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prefLabel

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.

@ast

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.

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P1433

Annals of Neurology

P1476

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.

@en

P2093

Ali Samii

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Alida Griffith

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Berta C Leis

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Carolyn M Hutter

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Donald S Higgins

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Dora Yearout

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Haydeh Payami

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Jennifer S Montimurro

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John W Roberts

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Karen L Edwards

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P2860

Interface between tauopathies and synucleinopathies: A tale of two proteins

A haplotype map of the human genome

Haploview: analysis and visualization of LD and haplotype maps

Strong association between Saitohin gene polymorphism and tau haplotype in the Polish population

TAU 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 disease

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

A common inversion under selection in Europeans

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

Neurodegenerative tauopathies

Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study.

P304

137-144

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scholarly article

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10.1002/ANA.21157

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2

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62

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Cyrus P Zabetian

Stewart A Factor

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2007-08-01T00:00:00Z

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6317318

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17514749

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P921

Parkinson's disease

P932

2836920

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