FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis (Q34118590)

31 July 2017

title

FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis (English)

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amyotrophic lateral sclerosis

31 July 2017

main subject

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Eileen H Bigio

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31 July 2017

Han-Xiang Deng

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31 July 2017

Hong Zhai

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31 July 2017

Jianhua Yan

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31 July 2017

Faisal Fecto

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31 July 2017

Kaouther Ajroud

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31 July 2017

Manjari Mishra

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31 July 2017

Senda Ajroud-Driss

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31 July 2017

Scott Heller

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31 July 2017

Robert Sufit

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31 July 2017

Nailah Siddique

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31 July 2017

Enrico Mugnaini

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31 July 2017

Teepu Siddique

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31 July 2017

publication date

1 June 2010

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31 July 2017

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31 July 2017

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31 July 2017

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31 July 2017

page(s)

739-748

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FUS mutations in sporadic amyotrophic lateral sclerosis

31 July 2017

cites work

1 reference

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FUS pathology in basophilic inclusion body disease

28 July 2018

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

28 July 2018

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A new subtype of frontotemporal lobar degeneration with FUS pathology

28 July 2018

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Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

28 July 2018

1 reference

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Rethinking ALS: the FUS about TDP-43.

28 July 2018

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

28 July 2018

1 reference

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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

28 July 2018

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Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approach.

28 July 2018

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TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

28 July 2018

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TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

28 July 2018

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TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

28 July 2018

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Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease.

28 July 2018

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A century-old debate on protein aggregation and neurodegeneration enters the clinic

28 July 2018

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

28 July 2018

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Molecular biology of amyotrophic lateral sclerosis: insights from genetics

28 July 2018

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Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria

28 July 2018

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

28 July 2018

1 reference

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Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

28 July 2018

1 reference

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New pathological findings in amyotrophic lateral sclerosis

28 July 2018

1 reference

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Ubiquitin-immunoreactive intraneuronal inclusions in amyotrophic lateral sclerosis. Morphology, distribution, and specificity

28 July 2018

1 reference

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FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.

28 July 2018

1 reference

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

28 October 2018

1 reference

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

28 October 2018

1 reference

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

28 October 2018

1 reference

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Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4376270

Fus deficiency in mice results in defective B-lymphocyte development and activation, high levels of chromosomal instability and perinatal death.

28 October 2018

1 reference

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Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvement

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4376270

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4376270

Expression of ubiquitin-binding protein p62 in ubiquitin-immunoreactive intraneuronal inclusions in amyotrophic lateral sclerosis with dementia: analysis of five autopsy cases with broad clinicopathological spectrum

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20517935

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mutations of FUS gene in sporadic amyotrophic lateral sclerosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20517935

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1001/ARCHNEUROL.2010.101

1 reference

31 July 2017

1 reference

31 July 2017

1 reference