FUS immunogold labeling TEM analysis of the neuronal cytoplasmic inclusions of neuronal intermediate filament inclusion disease: a frontotemporal lobar degeneration with FUS proteinopathy (Q33908722)

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

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scholarly article

1 reference

Europe PubMed Central

29 July 2017

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

1 reference

Europe PubMed Central

29 July 2017

frontotemporal lobar degeneration

1 reference

based on heuristic

inferred from title

neuronal intermediate filament inclusion disease

1 reference

based on heuristic

inferred from title

Julian R Thorpe

object named as

Julian R Thorpe

12

0 references

object named as

Alison M Goate

10

0 references

11

object named as

Nigel J Cairns

1 reference

Europe PubMed Central

29 July 2017

9

object named as

Isidre Ferrer

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Europe PubMed Central

29 July 2017

7

object named as

Eileen H Bigio

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Europe PubMed Central

29 July 2017

author name string

Tristan Page

1

1 reference

Europe PubMed Central

29 July 2017

Michael A Gitcho

2

1 reference

Europe PubMed Central

29 July 2017

Sabrina Mosaheb

3

1 reference

Europe PubMed Central

29 July 2017

Deborah Carter

4

1 reference

Europe PubMed Central

29 July 2017

Sumi Chakraverty

5

1 reference

Europe PubMed Central

29 July 2017

Robert H Perry

6

1 reference

Europe PubMed Central

29 July 2017

Marla Gearing

8

1 reference

Europe PubMed Central

29 July 2017

publication date

21 May 2011

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Europe PubMed Central

29 July 2017

Journal of Molecular Neuroscience

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Europe PubMed Central

29 July 2017

45

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Europe PubMed Central

29 July 2017

409-421

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Europe PubMed Central

29 July 2017

3

1 reference

Europe PubMed Central

29 July 2017

https://scigraph.springernature.com/pub.10.1007/s12031-011-9549-8

0 references

The spectrum and severity of FUS-immunoreactive inclusions in the frontal and temporal lobes of ten cases of 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=3374931

5 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=3374931

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 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=3374931

5 July 2018

Gigaxonin mutation analysis in patients with NIFID.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Paraspeckles: nuclear bodies built on long noncoding RNA

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

A new subtype of frontotemporal lobar degeneration with FUS pathology

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 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=3374931

5 July 2018

TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Rethinking ALS: the FUS about TDP-43.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 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=3374931

5 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=3374931

5 July 2018

VCP mutations causing frontotemporal lobar degeneration disrupt localization of TDP-43 and induce cell death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Fine structural analysis of the neuronal inclusions of frontotemporal lobar degeneration with TDP-43 proteinopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 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=3374931

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

TARDBP mutations in individuals with sporadic and 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=3374931

5 July 2018

TDP-43 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=3374931

5 July 2018

TDP-43 A315T mutation in familial motor neuron disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

The two faces of protein misfolding: gain- and loss-of-function in neurodegenerative diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Splicing speckles are not reservoirs of RNA polymerase II, but contain an inactive form, phosphorylated on serine2 residues of the C-terminal domain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Neuronal intranuclear inclusions are ultrastructurally and immunologically distinct from cytoplasmic inclusions of 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=3374931

5 July 2018

Extending the clinicopathological spectrum of neurofilament inclusion disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Clinical and neuropathologic variation 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=3374931

5 July 2018

Shortfalls in the peptidyl-prolyl cis-trans isomerase protein Pin1 in neurons are associated with frontotemporal dementias.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Neurodegenerative diseases: a decade of discoveries paves the way for therapeutic breakthroughs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

alpha-Internexin aggregates are abundant in neuronal intermediate filament inclusion disease (NIFID) but rare in other neurodegenerative diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

alpha-internexin is present in the pathological inclusions of 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=3374931

5 July 2018

PSF acts through the human immunodeficiency virus type 1 mRNA instability elements to regulate virus expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Neurofilament inclusion body disease: a new proteinopathy?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

The fate of dsRNA in the nucleus: a p54(nrb)-containing complex mediates the nuclear retention of promiscuously A-to-I edited RNAs

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping

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5 July 2018

Binding of a putative and a known chaperone protein revealed by immunogold labeling transmission electron microscopy: A suggested use of chaperones as probes for the distribution of their target proteins.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Human 75-kDa DNA-pairing protein is identical to the pro-oncoprotein TLS/FUS and is able to promote D-loop formation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Human POMp75 is identified as the pro-oncoprotein TLS/FUS: both POMp75 and POMp100 DNA homologous pairing activities are associated to cell proliferation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

The application of LR gold resin for immunogold labeling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

Oncoprotein TLS interacts with serine-arginine proteins involved in RNA splicing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 July 2018

TLS/FUS, a pro-oncogene involved in multiple chromosomal translocations, is a novel regulator of BCR/ABL-mediated leukemogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374931

5 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=3374931

5 July 2018

Fusion of CHOP to a novel RNA-binding protein in human myxoid liposarcoma

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5 July 2018

Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions.

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https://api.crossref.org/works/10.1007%2FS12031-011-9549-8

21 January 2018

Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID).

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https://api.crossref.org/works/10.1007%2FS12031-011-9549-8

21 January 2018

Heterogeneous inclusions in neurofilament inclusion disease.

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9549-8

21 January 2018

Genetic contribution of FUS to frontotemporal lobar degeneration

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https://api.crossref.org/works/10.1007%2FS12031-011-9549-8

21 January 2018

FUS-immunoreactive intranuclear inclusions in neurodegenerative disease.

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9549-8

21 January 2018

Clinical and Pathological Heterogeneity of Neuronal Intermediate Filament Inclusion Disease

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9549-8

21 January 2018

Neurofilament inclusion body disease with early onset frontotemporal dementia and primary lateral sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21603978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paraspeckles: a novel nuclear domain

1 reference

https://pubmed.ncbi.nlm.nih.gov/21603978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1007/S12031-011-9549-8

1 reference

Europe PubMed Central

29 July 2017

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1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

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