C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci. (Q37316053)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24170096%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

title

C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci (English)

1 reference

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frontotemporal lobar degeneration

28 February 2020

main subject

1 reference

4

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28 February 2020

Pietro Fratta

6

1 reference

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28 February 2020

2

Tammaryn Lashley

1 reference

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28 February 2020

author name string

Sarah Mizielinska

1

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28 February 2020

Frances E Norona

3

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28 February 2020

Charlotte E Ridler

5

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28 February 2020

Adrian M Isaacs

8

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28 February 2020

language of work or name

1 reference

30 October 2013

1 reference

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28 February 2020

published in

Acta Neuropathologica

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28 February 2020

volume

126

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28 February 2020

issue

6

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28 February 2020

page(s)

845-857

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Creative Commons Attribution 2.0 Generic

28 February 2020

copyright license

start time

30 October 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.

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Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.

6 September 2017

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Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS

6 September 2017

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The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS.

6 September 2017

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Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

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

6 September 2017

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

6 September 2017

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6 September 2017

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6 September 2017

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

6 September 2017

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Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

6 September 2017

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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

6 September 2017

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The prevalence and causes of dementia in people under the age of 65 years

6 September 2017

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The prevalence of frontotemporal dementia

6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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26 June 2018

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Crossref

https://api.crossref.org/works/10.1007%2FS00401-013-1200-Z

The i-motif in nucleic acids

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24170096

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00401-013-1200-Z

1 reference

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28 February 2020

1 reference

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28 February 2020

PubMed publication ID

24170096

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24170096%20AND%20SRC:MED&resulttype=core&format=json