Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins (Q46797980)

25 December 2017

title

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

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25 December 2017

14

Christian Haass

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Kohji Mori

Kohji Mori

1

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Dieter Edbauer

15

Dieter Edbauer

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PubMed ID

24132570

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

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25 December 2017

Friedrich Grässer

3

Friedrich A Grässer

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25 December 2017

Marc Cruts

10

Marc Cruts

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25 December 2017

Hans Kretzschmar

13

Hans A Kretzschmar

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25 December 2017

Ilse Gijselinck

4

Ilse Gijselinck

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25 December 2017

Kristin Rentzsch

6

Kristin Rentzsch

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25 December 2017

Martin H Schludi

8

Martin H Schludi

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25 December 2017

author name string

Stephanie May

5

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25 December 2017

Shih-Ming Weng

7

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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

page(s)

881-893

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25 December 2017

issue

6

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25 December 2017

https://scigraph.springernature.com/pub.10.1007/s00401-013-1189-3

exact match

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cites work

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

1 reference

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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.

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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The amyloid state of proteins in human diseases

21 January 2018

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Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.

21 January 2018

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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

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

21 January 2018

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

21 January 2018

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Neuropathological background of phenotypical variability in frontotemporal dementia

21 January 2018

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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

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C9orf72 repeat expansions are a rare genetic cause of parkinsonism

21 January 2018

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

21 January 2018

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

21 January 2018

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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

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

21 January 2018

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

21 January 2018

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Repeat associated non-ATG translation initiation: one DNA, two transcripts, seven reading frames, potentially nine toxic entities!

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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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

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

21 January 2018

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21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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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

PubMed ID

24132570

1 reference

25 December 2017