Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study - Test2 - elhamkhani - TriplyDB

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study

http://www.wikidata.org/entity/Q30439341

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The Genetic Basis of Cognitive Impairment and Dementia in Parkinson's Disease The role of tau in neurodegenerative diseases and its potential as a therapeutic target Linking the genetic architecture of cytosine modifications with human complex traits Genetic susceptibility in Parkinson's disease Genomewide association study for susceptibility genes contributing to familial Parkinson disease Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease.Physiological transgene regulation and functional complementation of a neurological disease gene deficiency in neurons Mutant LRRK2(R1441G) BAC transgenic mice recapitulate cardinal features of Parkinson's disease.DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E in vitro POLG1 polyglutamine tract variants associated with Parkinson's disease.Genome-wide association study confirms extant PD risk loci among the Dutch.Variation in MAPT is not a contributing factor to the incomplete penetrance in LHON.Association between MAPT haplotype and memory function in patients with Parkinson's disease and healthy aging individuals.Tau splicing and the intricacies of dementia.Regulation of human MAPT gene expression.SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain.Human inversions and their functional consequences Structural diversity and African origin of the 17q21.31 inversion polymorphism.Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31.Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants.Commonalities in the genetics of Alzheimer's disease and Parkinson's disease.Association of the MAPT locus with Parkinson's disease.Back to the tubule: microtubule dynamics in Parkinson's disease.Development of Parkinson's disease biomarkers.A tangled web - tau and sporadic Parkinson's disease FUS-mediated alternative splicing in the nervous system: consequences for ALS and FTLD.The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohort.Identification of Parkinson's disease candidate genes using CAESAR and screening of MAPT and SNCAIP in South African Parkinson's disease patients.Leucine-Rich Repeat Kinase (LRRK2) Genetics and Parkinson's Disease.Meta-analysis of the association between variants in MAPT and neurodegenerative diseases.Secondary RNA structure and nucleotide specificity contribute to internal initiation mediated by the human tau 5' leader.Genetic Architecture of MAPT Gene Region in Parkinson Disease Subtypes.Tau as a biomarker of neurodegenerative diseases.Fractalkine signaling and Tau hyper-phosphorylation are associated with autophagic alterations in lentiviral Tau and Aβ1-42 gene transfer models.MAPT Genetic Variation and Neuronal Maturity Alter Isoform Expression Affecting Axonal Transport in iPSC-Derived Dopamine Neurons.Loss of fused in sarcoma (FUS) promotes pathological Tau splicing.Roles of the tau gene short tandem repeats in late-onset Alzheimer's disease.Association of rs62063857 variant of the saitohin gene with Parkinson's disease.Atypical tauopathy in a patient with LRRK2-G2019S mutation and tremor-dominant Parkinsonism.

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Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study

http://www.wikidata.org/entity/Q30439341

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2008年の論文

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2008年論文

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Haplotypes and gene expression ...... nson disease: the GenePD Study

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Haplotypes and gene expression ...... nson disease: the GenePD Study

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Haplotypes and gene expression ...... nson disease: the GenePD Study

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Haplotypes and gene expression ...... nson disease: the GenePD Study

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Haplotypes and gene expression ...... nson disease: the GenePD Study

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Haplotypes and gene expression ...... nson disease: the GenePD Study

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Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human brain

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

A polymorphic gene nested within an intron of the tau gene: implications for Alzheimer's disease.

Sepiapterin reductase expression is increased in Parkinson's disease brain tissue

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

Haploview: analysis and visualization of LD and haplotype maps

Tauopathies: classification and clinical update on neurodegenerative diseases associated with microtubule-associated protein tau

Saitohin, which is nested in the tau locus and confers allele-specific susceptibility to several neurodegenerative diseases, interacts with peroxiredoxin 6

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

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scholarly article

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1

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James F. Gusella

Richard H Myers

Stefano Goldwurm

Anita L DeStefano

Richard H. Roxburgh

Jeanne C Latourelle

Audrey E Hendricks

Marie-Helene Saint-Hilaire

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2008-05-28T00:00:00Z

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5342091

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Parkinson's disease

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2654275

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