(Q27020981)

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Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging

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29 April 2021

Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging (English)

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frontotemporal dementia

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6 November 2020

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12 September 2019

genetic variation

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14 September 2019

cytoskeletal proteins

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11 December 2019

nerve tissue proteins

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19 December 2019

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6 November 2020

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29 April 2021

Adrian L. Oblak

2

object named as

Adrian L. Oblak

1 reference

Bradley F Boeve

3

object named as

Bradley F. Boeve

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Bernardino F. Ghetti

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object named as

Bernardino Ghetti

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author name string

Keith A. Johnson

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Bradford C. Dickerson

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Michel Goedert

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publication date

February 2015

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1 February 2015

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25 April 2019

20 June 2019

30 June 2019

12 September 2019

14 September 2019

11 December 2019

19 December 2019

6 November 2020

29 April 2021

Neuropathology and Applied Neurobiology

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20 June 2019

30 June 2019

12 September 2019

14 September 2019

11 December 2019

19 December 2019

6 November 2020

29 April 2021

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copyright license

Creative Commons Attribution 4.0 International

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Europe PubMed Central

25 April 2019

Europe PubMed Central

20 June 2019

Europe PubMed Central

30 June 2019

Europe PubMed Central

12 September 2019

Europe PubMed Central

14 September 2019

Europe PubMed Central

11 December 2019

Europe PubMed Central

19 December 2019

Europe PubMed Central

6 November 2020

Europe PubMed Central

29 April 2021

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Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

21 March 2017

Selective interaction of lansoprazole and astemizole with tau polymers: potential new clinical use in diagnosis of Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

21 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

21 March 2017

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

21 March 2017

A protein factor essential for microtubule assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

21 March 2017

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

21 March 2017

Tau imaging: early progress and future directions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

21 March 2017

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

21 March 2017

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

21 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

21 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

21 March 2017

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

7 April 2017

Abnormal phosphorylation of the microtubule-associated protein tau (tau) in Alzheimer cytoskeletal pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

7 April 2017

Cerebral hypometabolism and grey matter density in MAPT intron 10 +3 mutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Tau, amyloid, and hypometabolism in a patient with posterior cortical atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Lower motor neuron disease with respiratory failure caused by a novel MAPT mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Imaging of tau pathology in a tauopathy mouse model and in Alzheimer patients compared to normal controls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Frontotemporal dementia: implications for understanding Alzheimer disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Altered functional connectivity in asymptomatic MAPT subjects: a comparison to bvFTD

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Trajectories of brain and hippocampal atrophy in FTD with mutations in MAPT or GRN.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Semantic dementia associated with mutation V363I in the tau gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Three repeat isoforms of tau inhibit assembly of four repeat tau filaments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Refining frontotemporal dementia with parkinsonism linked to chromosome 17: introducing FTDP-17 (MAPT) and FTDP-17 (PGRN).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Clinical and pathological features of an Alzheimer's disease patient with the MAPT Delta K280 mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

A century of Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Stabilization of the tau exon 10 stem loop alters pre-mRNA splicing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Phenotypic heterogeneity within a new family with the MAPT p301s mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

A new family with frontotemporal dementia with intronic 10+3 splice site mutation in the tau gene: neuropathology and molecular effects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Frontotemporal dementia: impact of P301L tau mutation on a healthy carrier

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Genotype-phenotype correlations in FTDP-17: does form follow function?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Hereditary tauopathies and parkinsonism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Phenotypic correlations in FTDP-17.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Abnormal tau-containing filaments in neurodegenerative diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Isolation of a fragment of tau derived from the core of the paired helical filament of Alzheimer disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Structural characterization of the core of the paired helical filament of Alzheimer disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

Expression of separate isoforms of human tau protein: correlation with the tau pattern in brain and effects on tubulin polymerization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 September 2017

[(18)F]T807, a novel tau positron emission tomography imaging agent for Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

Molecular analysis of mutant and wild-type tau deposited in the brain affected by the FTDP-17 R406W mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

Tau pathology in a family with dementia and a P301L mutation in tau.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

A distinct familial presenile dementia with a novel missense mutation in the tau gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

Frontotemporal dementia and Parkinsonism linked to chromosome 17: a new group of tauopathies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

Autosomal dominant dementia with widespread neurofibrillary tangles.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

Pick's disease: hyperphosphorylated tau protein segregates to the somatoaxonal compartment.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

Filamentous aggregates in Pick's disease, progressive supranuclear palsy, and Alzheimer's disease share antigenic determinants with microtubule-associated protein, tau.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

Familial presenile dementia with psychosis associated with cortical neurofibrillary tangles and degeneration of the amygdala

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

31 May 2018

Re-examination of a family with Pick's disease

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Hereditary Pick's disease: second re-examination of the large family and discussion of other hereditary cases, with particular reference to electroencephalography, a computerized tomography.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Tau is a candidate gene for chromosome 17 frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Clinical and genetic studies of families with the tau N279K mutation (FTDP-17).

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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/10.1111%2FNAN.12213

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathology.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Biochemical and pathological characterization of frontotemporal dementia due to a Leu266Val mutation in microtubule-associated protein tau in an African American individual.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

The neuropathology of a chromosome 17-linked autosomal dominant parkinsonism and dementia ("pallido-ponto-nigral degeneration").

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

The DeltaK280 mutation in MAP tau favors exon 10 skipping in vivo.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Tau phosphorylation and kinase activation in familial tauopathy linked to deln296 mutation.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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/10.1111%2FNAN.12213

21 January 2018

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/10.1111%2FNAN.12213

21 January 2018

A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Phenotypic variation in hereditary frontotemporal dementia with tau mutations.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Phenotypic presentation of frontotemporal dementia with Parkinsonism‐chromosome 17 type P301S in a patient of Jewish‐Algerian origin

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Familial autosomal dominant cortico-basal degeneration with the P301S mutation in the tau gene: an example of phenotype variability.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

A novel MAPT mutation (P301T) associated with familial frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Selective deposition of mutant tau in the FTDP-17 brain affected by the P301L mutation.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Mutation-dependent aggregation of tau protein and its selective depletion from the soluble fraction in brain of P301L FTDP-17 patients.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsy.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Another phenotype of frontotemporal dementia and parkinsonism linked to chromosome-17 (FTDP-17) with a missense mutation of S305N closely resembling Pick's disease

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Neuropathology in the S305S tau gene mutation.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Tau gene mutation in familial progressive subcortical gliosis.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke Family 1684.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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/10.1111%2FNAN.12213

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

The novel Tau mutation G335S: clinical, neuropathological and molecular characterization.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Pick's disease associated with the novel Tau gene mutation K369I.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Familial frontotemporal dementia associated with the novel MAPT mutation T427M.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

New mutations in MAPT gene causing frontotemporal lobar degeneration: biochemical and structural characterization.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Promotion of hyperphosphorylation by frontotemporal dementia tau mutations

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Distinctive MRI findings in pallidopontonigral degeneration (PPND).

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Validating FDG-PET as a biomarker for frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

In vivo detection of neuropathologic changes in presymptomatic MAPT mutation carriers: a PET and MRI study

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Advances in molecular imaging for the diagnosis of dementia.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Novel 18F-labeled arylquinoline derivatives for noninvasive imaging of tau pathology in Alzheimer disease

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

PET of brain amyloid and tau in mild cognitive impairment.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

MAPT S305I mutation: implications for argyrophilic grain disease

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

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/10.1111%2FNAN.12213

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

A family with a tau P301L mutation presenting with parkinsonism

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

18F-THK523: a novel in vivo tau imaging ligand for Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12213

21 January 2018

Early clinical PET imaging results with the novel PHF-tau radioligand [F-18]-T807.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 November 2018

Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 November 2018

A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 November 2018

Pick's disease is associated with mutations in the tau gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 November 2018

Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4329416

28 November 2018

A case of frontotemporal dementia with tau P301L mutation in the Far East

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive nonfluent aphasia associated with a new mutation V363I in tau gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new case of frontotemporal dementia and parkinsonism resulting from an intron 10 +3-splice site mutation in the tau gene: clinical and pathological features

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto)

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical genetics of Pick's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel G335V mutation in the tau gene associated with early onset familial frontotemporal dementia

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frontotemporal dementia and Parkinsonism linked to chromosome 17 in a young Australian patient with the G389R Tau mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial frontotemporal dementia with a P301L tau mutation in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/25556536

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/NAN.12213

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

release_hpuyhsume5e45ah7scq3czatqi

0 references

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

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