(Q35869162)

English

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

scientific article published on 21 May 2011

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

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

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

amyotrophic lateral sclerosis

0 references

Manuela Neumann

11

object named as

Manuela Neumann

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Rosa Rademakers

10

object named as

Rosa Rademakers

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

author name string

Ian R A Mackenzie

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Olaf Ansorge

2

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Michael Strong

3

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Juan Bilbao

4

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Lorne Zinman

5

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Lee-Cyn Ang

6

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Matt Baker

7

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Heather Stewart

8

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Andrew Eisen

9

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

publication date

21 May 2011

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Acta Neuropathologica

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

122

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

87-98

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

Distinct pathological subtypes of FTLD-FUS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

An autopsied case of sporadic adult-onset amyotrophic lateral sclerosis with FUS-positive basophilic inclusions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

FUS pathology in basophilic inclusion body disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

A new subtype of frontotemporal lobar degeneration with FUS pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

Familial amyotrophic lateral sclerosis with posterior column degeneration and basophilic inclusion bodies: a clinical, genetic and pathological study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

TLS (FUS) binds RNA in vivo and engages in nucleo-cytoplasmic shuttling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

Sporadic juvenile amyotrophic lateral sclerosis. A clinicopathological study of a case with neuronal cytoplasmic inclusions containing RNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

A novel double mutation in FUS gene causing sporadic ALS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

Immunohistochemical identification of messenger RNA-related proteins in basophilic inclusions of adult-onset atypical motor neuron disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

Immunohistochemical and ultrastructural study of basophilic inclusions in adult-onset motor neuron disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

24 September 2018

The clinical and neuroanatomical phenotype of FUS associated frontotemporal lobar degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3319073

14 November 2018

Numerous FUS-positive inclusions in an elderly woman with motor neuron disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21604077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Basophilic cytoplasmic inclusions in a case of sporadic juvenile amyotrophic lateral sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21604077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An adult-onset case of sporadic motor neuron disease with basophilic inclusions

1 reference

https://pubmed.ncbi.nlm.nih.gov/21604077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adult-onset motor neuron disease with basophilic intraneuronal inclusion bodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/21604077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dementia with ALS features and diffuse Pick body-like inclusions (atypical Pick's disease?)

1 reference

https://pubmed.ncbi.nlm.nih.gov/21604077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD

1 reference

https://pubmed.ncbi.nlm.nih.gov/21604077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00401-011-0838-7

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

ResearchGate publication ID

0 references

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