(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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https://scigraph.springernature.com/pub.10.1007/s00401-010-0764-0

30 July 2017

exact match

0 references

cites work

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

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

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

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

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Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease

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Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions.

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

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

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

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

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

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FUS pathology in basophilic inclusion body disease

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Screening for neurofilament inclusion disease using alpha-internexin immunohistochemistry

21 January 2018

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

21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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10.1007/S00401-010-0764-0

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

30 July 2017

1023615004

0 references

1 reference