(Q48568406)

12 February 2018

title

FTDP-17 with Pick body-like inclusions associated with a novel tau mutation, p.E372G. (English)

1 reference

12 February 2018

12

Leonard Petrucelli

1 reference

12 February 2018

9

Zbigniew K Wszolek

1 reference

12 February 2018

13

Rosa Rademakers

1 reference

12 February 2018

16

Ronald C Petersen

1 reference

12 February 2018

8

Bradley F Boeve

1 reference

12 February 2018

Neill R Graff-Radford

10

Neill R Graff-Radford

1 reference

12 February 2018

Keith A Josephs

7

Keith A Josephs

1 reference

12 February 2018

Melissa E. Murray

5

Melissa E Murray

1 reference

12 February 2018

Dennis W. Dickson

17

Dennis W Dickson

1 reference

12 February 2018

Joseph E Parisi

11

Joseph E Parisi

1 reference

12 February 2018

N Kouri

18

Naomi Kouri

1 reference

12 February 2018

Michael A DeTure

2

Michael A DeTure

1 reference

12 February 2018

Yari Carlomagno

3

Yari Carlomagno

1 reference

12 February 2018

author name string

Pawel Tacik

1

1 reference

12 February 2018

Wen-Lang Lin

4

1 reference

12 February 2018

Matthew C Baker

6

1 reference

12 February 2018

Richard S Isaacson

14

1 reference

12 February 2018

Kenneth M Heilman

15

1 reference

12 February 2018

publication date

16 August 2016

1 reference

12 February 2018

published in

Brain Pathology

1 reference

12 February 2018

volume

27

1 reference

12 February 2018

page(s)

612-626

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12 February 2018

issue

5

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12 February 2018

A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease

cites work

1 reference

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Slowly progressive behavioural presentation in two UK cases with the R406W MAPT mutation.

26 August 2018

1 reference

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A novel tau mutation, p.K317N, causes globular glial tauopathy

26 August 2018

1 reference

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

Invited review: Neuropathology of tauopathies: principles and practice.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

Juvenile frontotemporal dementia with parkinsonism associated with tau mutation G389R.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

Tau pathology and neurodegeneration

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

An integrated map of genetic variation from 1,092 human genomes

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

Mutational analysis in early-onset familial dementia in the Japanese population. The role of PSEN1 and MAPT R406W mutations.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

Familial frontotemporal dementia associated with the novel MAPT mutation T427M.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

Progress in hereditary tauopathies: a mutation in the Tau gene (G389R) causes a Pick disease-like syndrome.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

Phenotypic variation in hereditary frontotemporal dementia with tau mutations.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

Tau is a candidate gene for chromosome 17 frontotemporal dementia

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

Autosomal dominant dementia with widespread neurofibrillary tangles.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5380645

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

26 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27529406

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27529406

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27529406

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/BPA.12428

1 reference

12 February 2018

0 references

1 reference

12 February 2018