Familial behavioral variant frontotemporal dementia associated with astrocyte-predominant tauopathy (Q35196395)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25756587%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

title

Familial behavioral variant frontotemporal dementia associated with astrocyte-predominant tauopathy (English)

1 reference

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2 March 2020

main subject

astrocyte

0 references

frontotemporal dementia

1 reference

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25756587%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

William W Seeley

1 reference

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2 March 2020

Isidre Ferrer

1 reference

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2 March 2020

author name string

J Carlos García-Monco

1 reference

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2 March 2020

Marian Gomez-Beldarrain

1 reference

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2 March 2020

Margarita Carmona

1 reference

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2 March 2020

Rosa Blanco

1 reference

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2 March 2020

Giovanni Coppola

1 reference

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2 March 2020

publication date

1 April 2015

1 reference

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Journal of Neuropathology & Experimental Neurology

2 March 2020

published in

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2 March 2020

volume

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2 March 2020

issue

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2 March 2020

page(s)

370-379

1 reference

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The role of FUS gene variants in neurodegenerative diseases

2 March 2020

cites work

1 reference

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Globular glial tauopathies (GGT): consensus recommendations

13 July 2018

1 reference

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FUS-mediated alternative splicing in the nervous system: consequences for ALS and FTLD.

13 July 2018

1 reference

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FUS-regulated region- and cell-type-specific transcriptome is associated with cell selectivity in ALS/FTLD.

13 July 2018

1 reference

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TARDBP and FUS mutations associated with amyotrophic lateral sclerosis: summary and update

13 July 2018

1 reference

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Familial dementia with frontotemporal features associated with M146V presenilin-1 mutation

13 July 2018

1 reference

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Position-dependent FUS-RNA interactions regulate alternative splicing events and transcriptions

13 July 2018

1 reference

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Loss of fused in sarcoma (FUS) promotes pathological Tau splicing

13 July 2018

1 reference

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Selective tau tyrosine nitration in non-AD tauopathies

13 July 2018

1 reference

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Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

13 July 2018

1 reference

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Neuropathology of frontotemporal lobar degeneration-tau (FTLD-tau).

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

The spectrum and severity of FUS-immunoreactive inclusions in the frontal and temporal lobes of ten cases of neuronal intermediate filament inclusion disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

FUS mutations in sporadic amyotrophic lateral sclerosis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

FUS pathology in basophilic inclusion body disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

A new subtype of frontotemporal lobar degeneration with FUS pathology

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Argyrophilic grain disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Corticobasal degeneration with focal, massive tau accumulation in the subcortical white matter astrocytes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Tau proteins of Alzheimer paired helical filaments: abnormal phosphorylation of all six brain isoforms

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Glial and neuronal tau pathology in tauopathies: characterization of disease-specific phenotypes and tau pathology progression

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Aprosodic speech with insular hyperintensities and 4R Tau pathology on autopsy

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Impaired glutamate transport in a mouse model of tau pathology in astrocytes.

26 September 2018

1 reference

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Transgenic mouse model of tau pathology in astrocytes leading to nervous system degeneration.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Pick bodies in a family with presenilin-1 Alzheimer's disease

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Specific pathological Tau protein variants characterize Pick's disease.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Phenotypic variability within the inclusion body spectrum of basophilic inclusion body disease and neuronal intermediate filament inclusion disease in frontotemporal lobar degenerations with FUS-positive inclusions

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4366320

Progressive Supranuclear Palsy and Corticobasal Degeneration

24 October 2018

1 reference

Crossref

https://api.crossref.org/works/10.1097%2FNEN.0000000000000180

Hyperphosphorylated tau proteins differentiate corticobasal degeneration and Pick's disease

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1097%2FNEN.0000000000000180

Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis

21 January 2018

1 reference

12 December 2020

A peculiar constellation of tau pathology defines a subset of dementia in the elderly

1 reference

12 December 2020

Pathogenesis of the Tauopathies

1 reference

12 December 2020

FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis

1 reference

12 December 2020

10.1097/NEN.0000000000000180

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25756587%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25756587%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

PubMed publication ID

25756587

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25756587%20AND%20SRC:MED&resulttype=core&format=json