Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutations (Q46624207)

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scientific article published on 28 July 2012

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English	Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutations	scientific article published on 28 July 2012

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scholarly article

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutations (English)

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

amyotrophic lateral sclerosis

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based on heuristic

inferred from title

5

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

Manuela Neumann

1

object named as

Manuela Neumann

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Europe PubMed Central

23 December 2017

author name string

Chiara F Valori

2

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

Olaf Ansorge

3

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

Hans A Kretzschmar

4

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

Hirofumi Kusaka

6

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

Osamu Yokota

7

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

Kenji Ishihara

8

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

Lee-Cyn Ang

9

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

Juan M Bilbao

10

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

Ian R A Mackenzie

11

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23 December 2017

http://europepmc.org/abstract/MED/22842875

publication date

28 July 2012

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23 December 2017

http://europepmc.org/abstract/MED/22842875

Acta Neuropathologica

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23 December 2017

http://europepmc.org/abstract/MED/22842875

124

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http://europepmc.org/abstract/MED/22842875

5

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23 December 2017

http://europepmc.org/abstract/MED/22842875

705-716

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23 December 2017

http://europepmc.org/abstract/MED/22842875

https://scigraph.springernature.com/pub.10.1007/s00401-012-1020-6

0 references

Exposure on cell surface and extensive arginine methylation of ewing sarcoma (EWS) protein

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Expression and subcellular localization of Ewing sarcoma (EWS) protein is affected by the methylation process

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Transportin1: a marker of FTLD-FUS

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

The RNA-binding protein FUS/TLS is a common aggregate-interacting protein in polyglutamine diseases

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Arginine methylation of the nuclear poly(a) binding protein weakens the interaction with its nuclear import receptor, transportin.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Nuclear transport impairment of amyotrophic lateral sclerosis-linked mutations in FUS/TLS.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

PRMT1 mediated methylation of TAF15 is required for its positive gene regulatory function

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Intracellular localization and splicing regulation of FUS/TLS are variably affected by amyotrophic lateral sclerosis-linked mutations

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

TLS, EWS and TAF15: a model for transcriptional integration of gene expression

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Rules for nuclear localization sequence recognition by karyopherin beta 2

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Distinct pathological subtypes of FTLD-FUS.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

A harmonized classification system for FTLD-TDP pathology

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

FUS pathology in basophilic inclusion body disease

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

A new subtype of frontotemporal lobar degeneration with FUS pathology

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

FUS immunogold labeling TEM analysis of the neuronal cytoplasmic inclusions of neuronal intermediate filament inclusion disease: a frontotemporal lobar degeneration with FUS proteinopathy

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Detection of arginine dimethylated peptides by parallel precursor ion scanning mass spectrometry in positive ion mode

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Modular organization and combinatorial energetics of proline-tyrosine nuclear localization signals

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

The TET family of proteins: functions and roles in disease

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Arginine methylation by PRMT1 regulates nuclear-cytoplasmic localization and toxicity of FUS/TLS harbouring ALS-linked mutations

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

FUS-immunoreactive intranuclear inclusions in neurodegenerative disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Identification and characterization of the nuclear localization/retention signal in the EWS proto-oncoprotein

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

The clinical and neuroanatomical phenotype of FUS associated frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1020-6

21 January 2018

Identifiers

10.1007/S00401-012-1020-6

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/22842875

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