Deletion of C9ORF72 results in motor neuron degeneration and stress sensitivity in C. elegans (Q35070967)

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Language	Label	Description	Also known as
English	Deletion of C9ORF72 results in motor neuron degeneration and stress sensitivity in C. elegans	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

6 August 2017

Deletion of C9ORF72 results in motor neuron degeneration and stress sensitivity in C. elegans (English)

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Europe PubMed Central

PubMed publication ID

6 August 2017

Caenorhabditis elegans

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2

object named as

Guy A Rouleau

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3

object named as

Patrick A Dion

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Martine Therrien

1

object named as

Martine Therrien

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

author name string

J Alex Parker

4

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Europe PubMed Central

PubMed publication ID

6 August 2017

language of work or name

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publication date

12 December 2013

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Europe PubMed Central

PubMed publication ID

6 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

e83450

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

copyright license

Creative Commons Attribution 4.0 International

12 December 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Rab35: GEFs, GAPs and effectors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

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An imbalance between excitatory and inhibitory neurotransmitters in amyotrophic lateral sclerosis revealed by use of 3-T proton magnetic resonance spectroscopy.

1 reference

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8 July 2018

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

1 reference

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8 July 2018

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

1 reference

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8 July 2018

Stress granules as crucibles of ALS pathogenesis.

1 reference

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8 July 2018

FUS/TLS assembles into stress granules and is a prosurvival factor during hyperosmolar stress

1 reference

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Expanded GGGGCC repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration

1 reference

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Controversies and priorities in amyotrophic lateral sclerosis

1 reference

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8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

8 July 2018

The product of C9orf72, a gene strongly implicated in neurodegeneration, is structurally related to DENN Rab-GEFs

1 reference

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8 July 2018

Loss and gain of Drosophila TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration by loss-of-function phenotypes

1 reference

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Discovery of Novel DENN Proteins: Implications for the Evolution of Eukaryotic Intracellular Membrane Structures and Human Disease

1 reference

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8 July 2018

Methylene blue protects against TDP-43 and FUS neuronal toxicity in C. elegans and D. rerio

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

8 July 2018

TDP-1/TDP-43 regulates stress signaling and age-dependent proteotoxicity in Caenorhabditis elegans

1 reference

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8 July 2018

Mutant TDP-43 and FUS cause age-dependent paralysis and neurodegeneration in C. elegans

1 reference

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8 July 2018

Caenorhabditis elegans RNA-processing protein TDP-1 regulates protein homeostasis and life span

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

8 July 2018

The seeds of neurodegeneration: prion-like spreading in ALS

1 reference

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8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

8 July 2018

The ALS-associated proteins FUS and TDP-43 function together to affect Drosophila locomotion and life span.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

8 July 2018

FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

8 July 2018

Hypertonic stress induces rapid and widespread protein damage in C. elegans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

8 July 2018

The genetics of ageing

1 reference

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8 July 2018

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

8 July 2018

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

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TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

1 reference

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TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

1 reference

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Maintenance of C. elegans

1 reference

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8 July 2018

1 reference

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Multiple sequence alignment with the Clustal series of programs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3861484

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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

1 reference

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RNA binding mediates neurotoxicity in the transgenic Drosophila model of TDP-43 proteinopathy

1 reference

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27 September 2018

Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis.

1 reference

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Pharmacological reduction of ER stress protects against TDP-43 neuronal toxicity in vivo.

1 reference

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An RNAi screen identifies genes that regulate GABA synapses

1 reference

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Analysis of synaptic transmission in Caenorhabditis elegans using an aldicarb-sensitivity assay.

1 reference

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Too salty for worms: hypertonic stress challenges proteostasis networks. Focus on “Hypertonic stress induces rapid and widespread protein damage in C. elegans”

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0083450

21 January 2018

Identifiers

10.1371/JOURNAL.PONE.0083450

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

2013PLoSO...883450T

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

ResearchGate publication ID

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