FUS/TLS-immunoreactive neuronal and glial cell inclusions increase with disease duration in familial amyotrophic lateral sclerosis with an R521C FUS/TLS mutation (Q48414675)

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scientific article published in September 2012

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English	FUS/TLS-immunoreactive neuronal and glial cell inclusions increase with disease duration in familial amyotrophic lateral sclerosis with an R521C FUS/TLS mutation	scientific article published in September 2012

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scholarly article

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Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

FUS/TLS-immunoreactive neuronal and glial cell inclusions increase with disease duration in familial amyotrophic lateral sclerosis with an R521C FUS/TLS mutation (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

amyotrophic lateral sclerosis

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PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

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PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

author name string

Shinsuke Kato

2

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Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

Masako Kato

3

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Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

Hideki Mizuno

5

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Europe PubMed Central

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11 February 2018

http://europepmc.org/abstract/MED/22878663

Masaaki Kato

6

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11 February 2018

http://europepmc.org/abstract/MED/22878663

Naoko Shimakura

7

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11 February 2018

http://europepmc.org/abstract/MED/22878663

Haruhiko Akiyama

8

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Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

Zen Kobayashi

9

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Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

Hidehiko Konno

10

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11 February 2018

http://europepmc.org/abstract/MED/22878663

Masashi Aoki

11

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11 February 2018

http://europepmc.org/abstract/MED/22878663

publication date

1 September 2012

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PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

Journal of Neuropathology & Experimental Neurology

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11 February 2018

http://europepmc.org/abstract/MED/22878663

71

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http://europepmc.org/abstract/MED/22878663

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PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

779-788

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PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

Molecular biology of amyotrophic lateral sclerosis: insights from genetics

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

Mutations in FUS cause FALS and SALS in French and French Canadian populations

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

Induced ncRNAs allosterically modify RNA-binding proteins in cis to inhibit transcription

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

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/10.1097%2FNEN.0B013E318264F164

21 January 2018

FUS pathology in basophilic inclusion body disease

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

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/10.1097%2FNEN.0B013E318264F164

21 January 2018

Basophilic inclusions in sporadic juvenile amyotrophic lateral sclerosis: an immunocytochemical and ultrastructural study

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

Diminution of dopaminergic neurons in the substantia nigra of sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

Non-cell autonomous effect of glia on motor neurons in an embryonic stem cell-based ALS model

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

Astrocytic protection of spinal motor neurons but not cortical neurons against loss of Als2/alsin function.

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

A new subtype of frontotemporal lobar degeneration with FUS pathology

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

FUS transgenic rats develop the phenotypes of amyotrophic lateral sclerosis and frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E318264F164

21 January 2018

Identifiers

10.1097/NEN.0B013E318264F164

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22878663

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