(Q58477808)

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p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS

scientific article published on 19 November 2011

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scholarly article

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17 January 2020

p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS (English)

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17 January 2020

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amyotrophic lateral sclerosis

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inferred from title

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Bradley N. Smith

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Ammar Al-Chalabi

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Christopher Shaw

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Safa Al-Sarraj

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Satomi Maekawa

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Andrew King

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Tibor Hortobágyi

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19 November 2011

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Acta Neuropathologica

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691-702

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17 January 2020

https://scigraph.springernature.com/pub.10.1007/s00401-011-0911-2

0 references

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Motor neurone disease-inclusion dementia.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Exome sequencing reveals VCP mutations as a cause of familial ALS

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Frontotemporal lobar degeneration with ubiquitinated tau-negative inclusions and additional alpha-synuclein pathology but also unusual cerebellar ubiquitinated p62-positive, TDP-43-negative inclusions

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Ubiquitin deposits in anterior horn cells in motor neurone disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

The neuropathology and clinical phenotype of FTD with progranulin mutations

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Mutations of optineurin in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

RNA-mediated neurodegeneration in repeat expansion disorders

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Signaling, polyubiquitination, trafficking, and inclusions: sequestosome 1/p62's role in neurodegenerative disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0911-2

21 January 2018

Identifiers

10.1007/S00401-011-0911-2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22101323%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1 reference

Europe PubMed Central

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17 January 2020

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