Distinct pathological subtypes of FTLD-FUS. (Q34024578)

30 July 2017

title

Distinct pathological subtypes of FTLD-FUS. (English)

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30 July 2017

9

Manuela Neumann

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30 July 2017

8

Nigel J Cairns

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30 July 2017

Ian R A Mackenzie

1

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30 July 2017

David G Munoz

2

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30 July 2017

Hirofumi Kusaka

3

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30 July 2017

Osamu Yokota

4

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30 July 2017

Kenji Ishihara

5

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30 July 2017

Sigrun Roeber

6

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30 July 2017

Hans A Kretzschmar

7

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30 July 2017

publication date

30 October 2010

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30 July 2017

published in

Acta Neuropathologica

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30 July 2017

volume

121

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30 July 2017

issue

2

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30 July 2017

page(s)

207-218

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The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Progressive dementia with parkinsonism in corticobasal and brainstem degeneration with neuronal inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Frontotemporal and motor neurone degeneration with neurofilament inclusion bodies: additional evidence for overlap between FTD and ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

alpha-internexin is present in the pathological inclusions of neuronal intermediate filament inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

The RNA binding protein TLS is translocated to dendritic spines by mGluR5 activation and regulates spine morphology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

TLS facilitates transport of mRNA encoding an actin-stabilizing protein to dendritic spines

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Novel FUS/TLS mutations and pathology in familial and sporadic amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Extensive FUS-immunoreactive pathology in juvenile amyotrophic lateral sclerosis with basophilic inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

An autopsy case of frontotemporal dementia with severe dysarthria and motor neuron disease showing numerous basophilic inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Neurofilament inclusion body disease: a new proteinopathy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Extending the clinicopathological spectrum of neurofilament inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Occurrence of basophilic inclusions and FUS-immunoreactive neuronal and glial inclusions in a case of familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Rethinking ALS: the FUS about TDP-43.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Classic and generalized variants of Pick's disease: A clinicopathological, ultrastructural, and immunocytochemical comparative study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

FUS pathology in basophilic inclusion body disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

A new subtype of frontotemporal lobar degeneration with FUS pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

The molecular basis of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Sarcomas: genetics, signalling, and cellular origins. Part 1: The fellowship of TET.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Neurodegeneration with features of NIFID and ALS--extended clinical and neuropathological spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Screening for neurofilament inclusion disease using alpha-internexin immunohistochemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Genetic contribution of FUS to frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

A Japanese ALS6 family with mutation R521C in the FUS/TLS gene: a clinical, pathological and genetic report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Fused in sarcoma/translocated in liposarcoma: a multifunctional DNA/RNA binding protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Basophilic inclusion body disease and neuronal intermediate filament inclusion disease: a comparative clinicopathological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Frontotemporal lobar degeneration with ubiquitin-positive, but TDP-43-negative inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

Clinical and Pathological Heterogeneity of Neuronal Intermediate Filament Inclusion Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00401-010-0764-0

10.1007/S00401-010-0764-0

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

30 July 2017

1023615004

0 references

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