Functional MAPT haplotypes: bridging the gap between genotype and neuropathology - Test2 - elhamkhani - TriplyDB

Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

http://www.wikidata.org/entity/Q24651392

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The regulation and deregulation of Wnt signaling by PARK genes in health and disease Genetic studies in human prion diseases.Physiological transgene regulation and functional complementation of a neurological disease gene deficiency in neurons DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E in vitro 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.The cardiotonic steroid digitoxin regulates alternative splicing through depletion of the splicing factors SRSF3 and TRA2B The role of tau in neurodegeneration Splicing factor TRA2B is required for neural progenitor survival.Increased 4R tau expression and behavioural changes in a novel MAPT-N296H genomic mouse model of tauopathy Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.Impaired intracellular trafficking defines early Parkinson's disease Tau mis-splicing in the pathogenesis of neurodegenerative disorders.Tau as a biomarker of neurodegenerative diseases.Tau pathology: predictive diagnostics, targeted preventive and personalized medicine and application of advanced research in medical practice.Commentary: Genome-wide association study identifies 74 loci associated with educational attainment.Unilateral retinitis pigmentosa and cone-rod dystrophy.Haplotype-specific MAPT exon 3 expression regulated by common intronic polymorphisms associated with Parkinsonian disorders.Cardiac CRFR1 Expression Is Elevated in Human Heart Failure and Modulated by Genetic Variation and Alternative Splicing.The role of MAPT sequence variation in mechanisms of disease susceptibility.Family-based association analysis of the MAPT gene in Parkinson disease.

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P2860

Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

http://www.wikidata.org/entity/Q24651392

description

2007 nî lūn-bûn

@nan

2007 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի հուլիսին 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

Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

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Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

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Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

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type

label

Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

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Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

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Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

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prefLabel

Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

@ast

Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

@en

Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

@nl

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J.NBD.2007.04.006

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Neurobiology of Disease

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Functional MAPT haplotypes: bridging the gap between genotype and neuropathology

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Tara M Caffrey

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P2860

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

Interaction of tau with the neural plasma membrane mediated by tau's amino-terminal projection domain

Global prevalence of dementia: a Delphi consensus study

Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease: identification as the microtubule-associated protein tau

Global variation in copy number in the human genome

Mutations in tau gene exon 10 associated with FTDP-17 alter the activity of an exonic splicing enhancer to interact with Tra2 beta

Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17

Intracellular processing of aggregated tau differs between corticobasal degeneration and progressive supranuclear palsy.

Tra2 beta, SF2/ASF and SRp30c modulate the function of an exonic splicing enhancer in exon 10 of tau pre-mRNA

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

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1-10

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10.1016/J.NBD.2007.04.006

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1

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27

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