Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17 - Wikidata - wikimedia - TriplyDB

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

http://www.wikidata.org/entity/Q35249974

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Tau Protein Hyperphosphorylation and Aggregation in Alzheimer's Disease and Other Tauopathies, and Possible Neuroprotective Strategies Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging Tau physiology and pathomechanisms in frontotemporal lobar degeneration A new family with frontotemporal dementia with intronic 10+3 splice site mutation in the tau gene: neuropathology and molecular effects.Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.Alternative splicing of exon 10 in the tau gene as a target for treatment of tauopathies.High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands Cerebral hypometabolism and grey matter density in MAPT intron 10 +3 mutation carriers Mutation in the tau gene in familial multiple system tauopathy with presenile dementia.Update on recent molecular and genetic advances in frontotemporal lobar degeneration.The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family.Inheritance of frontotemporal dementia.Frontotemporal dementia genetics.Antibody Therapeutics Targeting Aβ and Tau.Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.Frontal lobe dementia with novel tauopathy: sporadic multiple system tauopathy with dementia.

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P2860

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

http://www.wikidata.org/entity/Q35249974

description

1997 nî lūn-bûn

@nan

1997 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

1997 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

1997年の論文

@ja

1997年論文

@yue

1997年論文

@zh-hant

1997年論文

@zh-hk

1997年論文

@zh-mo

1997年論文

@zh-tw

1997年论文

@wuu

name

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

@ast

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

@en

type

label

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

@ast

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

@en

prefLabel

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

@ast

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

@en

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P1433

American Journal of Human Genetics

P1476

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

@en

P2093

B Ghetti

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

D Koller

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

J R Murrell

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

M G Spillantini

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

M Goedert

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

M R Farlow

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

T Foroud

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

P2860

A Gene Map of the Human Genome

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

Familial non-specific dementia maps to chromosome 3

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

Human glial fibrillary acidic protein: complementary DNA cloning, chromosome localization, and messenger RNA expression in human glioma cell lines of various phenotypes.

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

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance.

Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype

Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.

Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration.

P304

1131-1138

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scholarly article

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10.1086/301594

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P433

5

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P478

61

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Howard J Edenberg

P577

1997-11-01T00:00:00Z

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P5875

13883862

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9345089

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P932

1716034

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