Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments - Wikidata - wikimedia - TriplyDB

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments

http://www.wikidata.org/entity/Q24684804

about

Mutations in tau gene exon 10 associated with FTDP-17 alter the activity of an exonic splicing enhancer to interact with Tra2 beta Ubiquitin C-terminal hydrolase L1 (UCH-L1): structure, distribution and roles in brain function and dysfunction Molecular Mechanisms in the Pathogenesis of Alzheimer's disease and Tauopathies-Prion-Like Seeded Aggregation and Phosphorylation Tau Protein Hyperphosphorylation and Aggregation in Alzheimer's Disease and Other Tauopathies, and Possible Neuroprotective Strategies Therapeutic and diagnostic challenges for frontotemporal dementia Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17 The role of α-synuclein and tau hyperphosphorylation-mediated autophagy and apoptosis in lead-induced learning and memory injury Comprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathways Reduced binding of protein phosphatase 2A to tau protein with frontotemporal dementia and parkinsonism linked to chromosome 17 mutations Neurodegeneration and defective neurotransmission in a Caenorhabditis elegans model of tauopathy.Pseudomonas aeruginosa exotoxin Y is a promiscuous cyclase that increases endothelial tau phosphorylation and permeability Severe amygdala dysfunction in a MAPT transgenic mouse model of frontotemporal dementia A new family with frontotemporal dementia with intronic 10+3 splice site mutation in the tau gene: neuropathology and molecular effects.Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.In vivo and postmortem clinicoanatomical correlations in frontotemporal dementia and parkinsonism linked to chromosome 17.REVIEW: tau protein pathology in Alzheimer's disease and related disorders.Filamentous nerve cell inclusions in neurodegenerative diseases: tauopathies and alpha-synucleinopathies.Neurofibrillary tangle parkinsonian disorders--tau pathology and tau genetics.TDP-43 suppresses tau expression via promoting its mRNA instability.Fibrillogenesis of tau: insights from tau missense mutations in FTDP-17.Tau-directed drug discovery for Alzheimer's disease and related tauopathies: a focus on tau assembly inhibitors.The oligodendroglia cytoskeleton in health and disease.Aberrant splicing of tau pre-mRNA caused by intronic mutations associated with the inherited dementia frontotemporal dementia with parkinsonism linked to chromosome 17.Diagnosis, classification and natural history of degenerative dementias.Organization and functional roles of the cytoskeleton in oligodendrocytes.High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers.Hereditary frontotemporal dementia caused by Tau gene mutations.Cerebral hypometabolism and grey matter density in MAPT intron 10 +3 mutation carriers A network of RNA and protein interactions in Fronto Temporal Dementia.Familial behavioral variant frontotemporal dementia associated with astrocyte-predominant tauopathy Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17 Transgenic expression of the shortest human tau affects its compartmentalization and its phosphorylation as in the pretangle stage of Alzheimer's disease Tau isoform composition influences rate and extent of filament formation Selective neurodegeneration, without neurofibrillary tangles, in a mouse model of Niemann-Pick C disease.Tau Aggregation Propensity Engrained in Its Solution State.Tau alternative splicing and frontotemporal dementia.Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements Mutation in the tau gene in familial multiple system tauopathy with presenile dementia.

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Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments

http://www.wikidata.org/entity/Q24684804

description

1997 nî lūn-bûn

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1997 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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1997 թվականի ապրիլին հրատարակված գիտական հոդված

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1997年の論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年论文

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name

Familial multiple system tauop ...... uronal and glial tau filaments

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Familial multiple system tauop ...... uronal and glial tau filaments

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Familial multiple system tauop ...... uronal and glial tau filaments

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type

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Familial multiple system tauop ...... uronal and glial tau filaments

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Familial multiple system tauop ...... uronal and glial tau filaments

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Familial multiple system tauop ...... uronal and glial tau filaments

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prefLabel

Familial multiple system tauop ...... uronal and glial tau filaments

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Familial multiple system tauop ...... uronal and glial tau filaments

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Familial multiple system tauop ...... uronal and glial tau filaments

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Familial multiple system tauop ...... uronal and glial tau filaments

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P2093

B Ghetti

http://www.w3.org/2001/XMLSchema#string

J R Murrell

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M G Spillantini

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M Goedert

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M R Farlow

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R A Crowther

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P2860

Ultrastructure and biochemical composition of paired helical filaments in corticobasal degeneration

Amyotrophic lateral sclerosis/parkinsonism-dementia complex of Guam: quantitative neuropathology, immunohistochemical analysis of neuronal vulnerability, and comparison with related neurodegenerative disorders

Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

Topographical relationship between beta-amyloid and tau protein epitopes in tangle-bearing cells in Alzheimer disease.

A preparation of Alzheimer paired helical filaments that displays distinct tau proteins by polyacrylamide gel electrophoresis.

Identification of cDNA clones for the human microtubule-associated protein tau and chromosomal localization of the genes for tau and microtubule-associated protein 2.

Neuropathologic overlap of progressive supranuclear palsy, Pick's disease and corticobasal degeneration.

Neurofibrillary degeneration in amyotrophic lateral sclerosis/parkinsonism-dementia complex of Guam. Immunochemical characterization of tau proteins.

Ultrastructural instability of paired helical filaments from corticobasal degeneration as examined by scanning transmission electron microscopy.

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4113-8

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2011217

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10.1073/PNAS.94.8.4113

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8

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94

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9108114

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