(Q50482315)

14 March 2018

title

Glial and neuronal tau pathology in tauopathies: characterization of disease-specific phenotypes and tau pathology progression. (English)

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14 March 2018

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8

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Esther Dalfó

object named as

Esther Dalfó

5

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Isidro Ferrer

1

object named as

Isidre Ferrer

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14 March 2018

author name string

Irene López-González

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14 March 2018

Margarita Carmona

3

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14 March 2018

Laura Arregui

4

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14 March 2018

Benjamin Torrejón-Escribano

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14 March 2018

Roberta Diehl

7

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14 March 2018

publication date

1 January 2014

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14 March 2018

Journal of Neuropathology & Experimental Neurology

published in

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14 March 2018

volume

73

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14 March 2018

issue

1

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14 March 2018

page(s)

81-97

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14 March 2018

Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's disease

cites work

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Argyrophilic grain disease is a sporadic 4-repeat tauopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Neuropathology of variants of progressive supranuclear palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Corticobasal degeneration: a pathologically distinct 4R tauopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Neuropathology of frontotemporal lobar degeneration-tau (FTLD-tau).

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Ballooned neurons in progressive supranuclear palsy are usually due to concurrent argyrophilic grain disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Distribution of tuft-shaped astrocytes in the cerebral cortex in progressive supranuclear palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

High prevalence of thorn-shaped astrocytes in the aged human medial temporal lobe.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Ultrastructural characteristics of tau filaments in tauopathies: immuno-electron microscopic demonstration of tau filaments in tauopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Frontal lobe dementia with novel tauopathy: sporadic multiple system tauopathy with dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Globular glial tauopathies (GGT) presenting with motor neuron disease or frontotemporal dementia: an emerging group of 4-repeat tauopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Cleavage and conformational changes of tau protein follow phosphorylation during Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Stepwise proteolysis liberates tau fragments that nucleate the Alzheimer-like aggregation of full-length tau in a neuronal cell model

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Proteolytic processing of tau.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Tau truncation is a productive posttranslational modification of neurofibrillary degeneration in Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Phosphorylation and cleavage of tau in non-AD tauopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Characterization of thorn-shaped astrocytes in white matter of temporal lobe in Alzheimer's disease brains

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Brain banks: benefits, limitations and cautions concerning the use of post-mortem brain tissue for molecular studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Neuropathology of the hippocampus in FTLD-Tau with Pick bodies: a study of the BrainNet Europe Consortium.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Cellular tau pathology and immunohistochemical study of tau isoforms in sporadic tauopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Ubiquitin is associated with early truncation of tau protein at aspartic acid(421) during the maturation of neurofibrillary tangles in Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Heterogeneity in astrocyte morphology and physiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Astrocyte heterogeneity: an underappreciated topic in neurobiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

Hyperphosphorylated tau proteins differentiate corticobasal degeneration and Pick's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0000000000000030

10.1097/NEN.0000000000000030

21 January 2018

Identifiers

DOI

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14 March 2018

PubMed ID

24335532

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14 March 2018