(Q34348115)

1 August 2017

1 reference

title

The role of tau (MAPT) in frontotemporal dementia and related tauopathies (English)

1 reference

1 August 2017

frontotemporal dementia

1 reference

1 reference

Rademakers R

1

1 reference

PubMed ID

15365985

1 August 2017

Cruts M

series ordinal

2

1 reference

PubMed ID

15365985

1 August 2017

van Broeckhoven C

series ordinal

3

1 reference

1 August 2017

1 October 2004

1 reference

1 August 2017

1 reference

1 August 2017

24

1 reference

1 August 2017

277-295

1 reference

1 August 2017

4

1 reference

Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD.

1 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Early and pre-symptomatic neuropsychological dysfunction in the PPND family with the N279K tau mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

The tau gene A0 allele and progressive supranuclear palsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Missense and splice site mutations in tau associated with FTDP-17: multiple pathogenic mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Neuropathologic variation in frontotemporal dementia due to the intronic tau 10(+16) mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Filamentous tau in oligodendrocytes and astrocytes of transgenic mice expressing the human tau isoform with the P301L mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Analysis of tau haplotypes in Pick's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Tau gene mutation K257T causes a tauopathy similar to Pick's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Early-onset, rapidly progressive familial tauopathy with R406W mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Argyrophilic grain disease is a sporadic 4-repeat tauopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Domains of tau protein, differential phosphorylation, and dynamic instability of microtubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Distinct FTDP-17 missense mutations in tau produce tau aggregates and other pathological phenotypes in transfected CHO cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Tau protein in frontotemporal dementia linked to chromosome 3 (FTD-3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

Abundant tau filaments and nonapoptotic neurodegeneration in transgenic mice expressing human P301S tau protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Hyperphosphorylation and aggregation of tau in mice expressing normal human tau isoforms.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Structure and novel exons of the human tau gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

NACP/alpha-synuclein and tau constitute two distinctive subsets of filaments in the same neuronal inclusions in brains from a family of parkinsonism and dementia with Lewy bodies: double-immunolabeling fluorescence and electron microscopic studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Association of an extended haplotype in the tau gene with progressive supranuclear palsy.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Direct genetic evidence for involvement of tau in progressive supranuclear palsy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The distribution of tau in the mammalian central nervous system

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Prevalence of TAU mutations in an Italian clinical series of familial frontotemporal patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Familial non-specific dementia maps to chromosome 3

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

FTDP-17: phenotypical heterogeneity within P301S

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

A polymorphism in the tau gene associated with risk for Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau protein binds to microtubules through a flexible array of distributed weak sites

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Projection domains of MAP2 and tau determine spacings between microtubules in dendrites and axons

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Expression of tau exon 8 in different species

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Physical and chemical properties of purified tau factor and the role of tau in microtubule assembly

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Purification of tau, a microtubule-associated protein that induces assembly of microtubules from purified tubulin

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Age-dependent association between the Q7R polymorphism in the Saitohin gene and sporadic Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Genetic evidence for the involvement of tau in progressive supranuclear palsy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Primary structure of high molecular weight tau present in the peripheral nervous system

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

A large Calabrian kindred segregating frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

A family with autosomal dominant, non-Alzheimer's presenile dementia.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Mutations in tau reduce its microtubule binding properties in intact cells and affect its phosphorylation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The tau locus is not significantly associated with pathologically confirmed sporadic Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Missense tau mutations identified in FTDP-17 have a small effect on tau-microtubule interactions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

tau Exon 10 expression involves a bipartite intron 10 regulatory sequence and weak 5' and 3' splice sites

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Characterization of pathology in transgenic mice over-expressing human genomic and cDNA tau transgenes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Overexpression of tau protein inhibits kinesin-dependent trafficking of vesicles, mitochondria, and endoplasmic reticulum: implications for Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Identification of a novel polymorphism in the promoter region of the tau gene highly associated to progressive supranuclear palsy in humans.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Clinic-based cases with frontotemporal dementia show increased cerebrospinal fluid tau and high apolipoprotein E epsilon4 frequency, but no tau gene mutations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The Tau H1 Haplotype is associated with Parkinson's disease in the Norwegian population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The structure of divalent cation-induced aggregates of PIP2 and their alteration by gelsolin and tau

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

tau Regulation of microtubule-microtubule spacing and bundling

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Extended investigation of tau and mutation screening of other candidate genes on chromosome 17q21 in a Swedish FTDP-17 family

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

In vitro polymerization of tau protein monitored by laser light scattering: method and application to the study of FTDP-17 mutants

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The apolipoprotein E epsilon4 allele is not a significant risk factor for frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Cloning of a big tau microtubule-associated protein characteristic of the peripheral nervous system

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Neurofibrillary pathology of Alzheimer's disease and other tauopathies.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau mutations cause frontotemporal dementias.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Effects of frontotemporal dementia FTDP-17 mutations on heparin-induced assembly of tau filaments

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The tau A0 allele in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Identification of a novel microtubule binding and assembly domain in the developmentally regulated inter-repeat region of tau.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Structural and functional differences between 3-repeat and 4-repeat tau isoforms. Implications for normal tau function and the onset of neurodegenetative disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau and transgenic animal models

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau filament formation in transgenic mice expressing P301L tau.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Formation of neurofibrillary tangles in P301l tau transgenic mice induced by Abeta 42 fibrils

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Oligodendroglial tau filament formation in transgenic mice expressing G272V tau.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

5' splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Effects on splicing and protein function of three mutations in codon N296 of tau in vitro

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

A novel tau mutation in exon 9 (1260V) causes a four-repeat tauopathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau is widely expressed in rat tissues

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Domains of tau protein and interactions with microtubules

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Late-onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Hereditary frontotemporal dementia is linked to chromosome 17q21?q22: A genetic and clinicopathological study of three dutch families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

An extended 5'-tau susceptibility haplotype in progressive supranuclear palsy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Microtubule organization and dynamics dependent on microtubule-associated proteins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Frequency oftau mutations in three series of non-Alzheimer's degenerative dementia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau haplotype frequency in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Analysis of tauopathies with transgenic mice

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Activation of phospholipase C-gamma by the concerted action of tau proteins and arachidonic acid

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Muscle weakness, hyperactivity, and impairment in fear conditioning in tau-deficient mice.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Increased risk for frontotemporal dementia through interaction between tau polymorphisms and apolipoprotein E epsilon4.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau gene mutations: dissecting the pathogenesis of FTDP-17.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau complexes with phospholipase C-gamma in situ

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Aberrant splicing of tau pre-mRNA caused by intronic mutations associated with the inherited dementia frontotemporal dementia with parkinsonism linked to chromosome 17.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Fetal-type phosphorylation of the tau in paired helical filaments

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

A novel L266V mutation of the tau gene causes frontotemporal dementia with a unique tau pathology.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Genetic analysis in patients with familial and sporadic frontotemporal dementia: two tau mutations in only familial cases and no association with apolipoprotein epsilon4

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Neurodegeneration and defective neurotransmission in a Caenorhabditis elegans model of tauopathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Mutant (R406W) human tau is hyperphosphorylated and does not efficiently bind microtubules in a neuronal cortical cell model

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The primary structure and heterogeneity of tau protein from mouse brain.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The microtubule binding domain of tau protein.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Enhanced neurofibrillary degeneration in transgenic mice expressing mutant tau and APP.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau gene polymorphisms and apolipoprotein E epsilon4 may interact to increase risk for Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Frontotemporal dementia with novel tau pathology and a Glu342Valtau mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Functional implications for the microtubule-associated protein tau: localization in oligodendrocytes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Molecular classification of the dementias

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Case-control study of the extended tau gene haplotype in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Interest in genetic testing in pallido-ponto-nigral degeneration (PPND): a family with frontotemporal dementia with Parkinsonism linked to chromosome 17.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Argyrophilic grain disease: molecular genetic difference to other four-repeat tauopathies.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Familial frontotemporal dementia and parkinsonism with a novel mutation at an intron 10+11-splice site in the tau gene.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The genetic and pathological classification of familial frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Accelerated filament formation from tau protein with specific FTDP-17 missense mutations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Molecular evolution of tau protein: implications for Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

An English kindred with a novel recessive tauopathy and respiratory failure.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

PAR-1 kinase plays an initiator role in a temporally ordered phosphorylation process that confers tau toxicity in Drosophila.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Significant Changes in the Tau A0 and A3 Alleles in Progressive Supranuclear Palsy and Improved Genotyping by Silver Detection

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Kinetic stabilization of microtubule dynamics at steady state by tau and microtubule-binding domains of tau.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Co-localization of alpha-synuclein and phosphorylated tau in neuronal and glial cytoplasmic inclusions in a patient with multiple system atrophy of long duration.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Frontotemporal dementia with Pick-type histology associated with Q336R mutation in the tau gene.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau is a candidate gene for chromosome 17 frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in Western Europe

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Autosomal dominant dementia with widespread neurofibrillary tangles.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Mutation screening of the tau gene in patients with early-onset Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Progressive supranuclear palsy and Parkinson's disease in a family with a new mutation in the tau gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The extended haplotype of the microtubule associated protein tau gene is not associated with Pick's disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The microtubule associated protein Tau gene and Alzheimer's disease--an association study and meta-analysis.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Missense point mutations of tau to segregate with FTDP-17 exhibit site-specific effects on microtubule structure in COS cells: a novel action of R406W mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Microtubule-associated proteins regulate microtubule function as the track for intracellular membrane organelle transports

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Search for a mutation in the tau gene in a Swiss family with frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau and neurofilaments in a family with frontotemporal dementia unlinked to chromosome 17q21-22.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Convergence of Lewy bodies and neurofibrillary tangles in amygdala neurons of Alzheimer's disease and Lewy body disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Differences in tau and apolipoprotein E polymorphism frequencies in sporadic frontotemporal lobar degeneration syndromes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Possible association of the tau H1/H1 genotype with primary progressive aphasia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Novel tau polymorphisms, tau haplotypes, and splicing in familial and sporadic frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

A Case of Dementia Parkinsonism Resembling Progressive Supranuclear Palsy Due to Mutation in the Tau Protein Gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The alpha-synucleinopathies: Parkinson's disease, dementia with Lewy bodies, and multiple system atrophy.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Mutations in the tau gene that cause an increase in three repeat tau and frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Impact of DNA testing for early-onset familial Alzheimer disease and frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Neurodegeneration with tau accumulation in a transgenic mouse expressing V337M human tau.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tau filament formation and associative memory deficit in aged mice expressing mutant (R406W) human tau.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

REVIEW: tau protein pathology in Alzheimer's disease and related disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The slow axonal transport of the microtubule-associated protein tau and the transport rates of different isoforms and mutants in cultured neurons.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Familial Frontotemporal Dementia: From Gene Discovery to Clinical Molecular Diagnostics

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315R.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Phenotypic variation in hereditary frontotemporal dementia with tau mutations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Association between the extended tau haplotype and frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Mutations of tau protein in frontotemporal dementia promote aggregation of paired helical filaments by enhancing local beta-structure

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Splicing of a regulated exon reveals additional complexity in the axonal microtubule-associated protein tau

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

The splicing determinants of a regulated exon in the axonal MAP tau reside within the exon and in its upstream intron

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

A protein factor essential for microtubule assembly

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Tauopathy in Drosophila: neurodegeneration without neurofibrillary tangles

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

A Japanese patient with frontotemporal dementia and parkinsonism by a tau P301S mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Functional effects of tau gene mutations deltaN296 and N296H

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Loss of brain tau defines novel sporadic and familial tauopathies with frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Selective reduction of soluble tau proteins in sporadic and familial frontotemporal dementias: an international follow-up study.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20086

7 January 2021

Identifiers

DOI

10.1002/HUMU.20086

1 reference

1 August 2017

1 reference

PubMed ID

15365985