(Q39034334)

8 September 2017

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

1 reference

8 September 2017

6

Brian Granger

1 reference

8 September 2017

Andrew Grover

1

1 reference

8 September 2017

Elisabet England

2

1 reference

8 September 2017

Mathew Baker

3

1 reference

8 September 2017

Naruhiko Sahara

4

1 reference

8 September 2017

Jennifer Adamson

5

1 reference

8 September 2017

Henry Houlden

7

1 reference

8 September 2017

Ulla Passant

8

1 reference

8 September 2017

Shu-Hui Yen

9

1 reference

8 September 2017

Michael DeTure

10

1 reference

8 September 2017

Michael Hutton

11

1 reference

8 September 2017

language of work or name

English

0 references

publication date

1 November 2003

1 reference

8 September 2017

Experimental Neurology

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8 September 2017

184

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8 September 2017

1

1 reference

8 September 2017

131-140

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Distinct isoforms of tau aggregated in neurons and glial cells in brains of patients with Pick's disease, corticobasal degeneration and progressive supranuclear palsy.

8 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

Effects of brain microtubule-associated proteins on microtubule dynamics and the nucleating activity of centrosomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

Specific pathological Tau protein variants characterize Pick's disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

Vulnerable neuronal subsets in Alzheimer's and Pick's disease are distinguished by their tau isoform distribution and phosphorylation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

In vitro assembly of Alzheimer-like filaments. How a small cluster of charged residues in Tau and MAP2 controls filament morphology.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

Rapid assembly of Alzheimer-like paired helical filaments from microtubule-associated protein tau monitored by fluorescence in solution.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

Assembly of microtubule-associated protein tau into Alzheimer-like filaments induced by sulphated glycosaminoglycans.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

Neurodegenerative tauopathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

Tau is a candidate gene for chromosome 17 frontotemporal dementia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

Tau blocks traffic of organelles, neurofilaments, and APP vesicles in neurons and enhances oxidative stress

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

Argyrophilic grain disease is a sporadic 4-repeat tauopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

Phenotypic variation in hereditary frontotemporal dementia with tau mutations.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

A protein factor essential for microtubule assembly

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

Sporadic Pick's disease: a tauopathy characterized by a spectrum of pathological tau isoforms in gray and white matter

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900393-5

10.1016/S0014-4886(03)00393-5

7 January 2021

Identifiers

DOI

1 reference

8 September 2017

1 reference