The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS. (Q34326849)

1 August 2017

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

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amyotrophic lateral sclerosis

1 August 2017

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based on heuristic

inferred from title

author

Christine Van Broeckhoven

10

Christine Van Broeckhoven

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Christian Haass

11

Christian Haass

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Kohji Mori

Kohji Mori

1

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Dieter Edbauer

12

Dieter Edbauer

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1 August 2017

3

Thomas Arzberger

1 reference

1 August 2017

Shih-Ming Weng

2

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1 August 2017

Stephanie May

4

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1 August 2017

Kristin Rentzsch

5

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1 August 2017

Elisabeth Kremmer

6

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1 August 2017

Bettina Schmid

7

1 reference

1 August 2017

Hans A Kretzschmar

8

1 reference

1 August 2017

Marc Cruts

9

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1 August 2017

language of work or name

English

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publication date

7 February 2013

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1 August 2017

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1 August 2017

339

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1 August 2017

1335-1338

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1 August 2017

6125

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Neuropathological background of phenotypical variability in frontotemporal dementia

1 August 2017

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https://api.crossref.org/works/10.1126%2FSCIENCE.1232927

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1232927

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/10.1126%2FSCIENCE.1232927

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/10.1126%2FSCIENCE.1232927

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/10.1126%2FSCIENCE.1232927

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/10.1126%2FSCIENCE.1232927

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1232927

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1232927

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1232927

Identification of evolutionarily conserved non-AUG-initiated N-terminal extensions in human coding sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1232927

Generation of protein isoform diversity by alternative initiation of translation at non-AUG codons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1232927

Non-ATG-initiated translation directed by microsatellite expansions

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1232927

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/10.1126%2FSCIENCE.1232927

Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1232927

Rat monoclonal antibodies differentiating between the Epstein-Barr virus nuclear antigens 2A (EBNA2A) and 2B (EBNA2B).

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1232927

Abnormal association of mutant huntingtin with synaptic vesicles inhibits glutamate release

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1232927

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/10.1126%2FSCIENCE.1232927

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/10.1126%2FSCIENCE.1232927

21 January 2018

Identifiers

DOI

10.1126/SCIENCE.1232927

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1 August 2017

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1 reference