(Q46797980)

25 December 2017

title

Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins (English)

1 reference

25 December 2017

14

Christian Haass

0 references

Kohji Mori

Kohji Mori

1

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Dieter Edbauer

15

Dieter Edbauer

1 reference

Christine Van Broeckhoven

25 December 2017

11

Christine Van Broeckhoven

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25 December 2017

9

Julie van der Zee

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25 December 2017

Thomas Arzberger

2

Thomas Arzberger

1 reference

25 December 2017

Friedrich Grässer

3

Friedrich A Grässer

1 reference

25 December 2017

Marc Cruts

10

Marc Cruts

1 reference

25 December 2017

Hans Kretzschmar

13

Hans A Kretzschmar

1 reference

25 December 2017

Ilse Gijselinck

4

Ilse Gijselinck

1 reference

25 December 2017

Kristin Rentzsch

6

Kristin Rentzsch

1 reference

25 December 2017

Martin H Schludi

8

Martin H Schludi

1 reference

25 December 2017

author name string

Stephanie May

5

1 reference

25 December 2017

Shih-Ming Weng

7

1 reference

25 December 2017

Elisabeth Kremmer

12

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25 December 2017

publication date

17 October 2013

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25 December 2017

published in

Acta Neuropathologica

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25 December 2017

volume

126

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25 December 2017

issue

6

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25 December 2017

page(s)

881-893

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25 December 2017

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

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion in C9ORF72: clinicopathologic correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Current insights into the C9orf72 repeat expansion diseases of the FTLD/ALS spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

The amyloid state of proteins in human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Asymmetric Arginine dimethylation of Epstein-Barr virus nuclear antigen 2 promotes DNA targeting

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Abnormal phosphorylation of Ser409/410 of TDP-43 in FTLD-U and ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Neuropathological background of phenotypical variability in frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

C9orf72 repeat expansions are a rare genetic cause of parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Repeat Associated Non-ATG Translation Initiation: One DNA, Two Transcripts, Seven Reading Frames, Potentially Nine Toxic Entities!

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Ubiquitinated p62-positive, TDP-43-negative inclusions in cerebellum in frontotemporal lobar degeneration with TAR DNA binding protein 43.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

CGG repeat-associated translation mediates neurodegeneration in fragile X tremor ataxia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Invited article: the Alzheimer disease-frontotemporal lobar degeneration spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

The molecular basis of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Cross-seeding and cross-competition in mouse apolipoprotein A-II amyloid fibrils and protein A amyloid fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

Non-ATG-initiated translation directed by microsatellite expansions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1189-3

10.1007/S00401-013-1189-3

21 January 2018

Identifiers

DOI

1 reference

25 December 2017

1 reference

25 December 2017