Mutant FUS causes DNA ligation defects to inhibit oxidative damage repair in Amyotrophic Lateral Sclerosis (Q58751835)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30206235%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

title

Mutant FUS causes DNA ligation defects to inhibit oxidative damage repair in Amyotrophic Lateral Sclerosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30206235%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

22 April 2020

main subject

general chemistry

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author

Haibo Wang

1

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22 April 2020

Wenting Guo

2

1 reference

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22 April 2020

Pavana M. Hegde

4

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22 April 2020

Tijs Vandoorne

5

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22 April 2020

Sankar Mitra

7

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22 April 2020

Ludo Van Den Bosch

9

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22 April 2020

Muralidhar L. Hegde

10

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22 April 2020

author name string

Joy Mitra

3

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22 April 2020

Bradley J Eckelmann

6

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22 April 2020

Alan E Tomkinson

8

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22 April 2020

language of work or name

English

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publication date

11 September 2018

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22 April 2020

published in

Nature Communications

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22 April 2020

volume

9

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22 April 2020

issue

1

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22 April 2020

page(s)

3683

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Creative Commons Attribution 4.0 International

22 April 2020

copyright license

start time

11 September 2018

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Chronic oxidative damage together with genome repair deficiency in the neurons is a double whammy for neurodegeneration: Is damage response signaling a potential therapeutic target?

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Human DNA Ligase I Interacts with and Is Targeted for Degradation by the DCAF7 Specificity Factor of the Cul4-DDB1 Ubiquitin Ligase Complex

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R521C and R521H mutations in FUS result in weak binding with Karyopherinβ2 leading to Amyotrophic lateral sclerosis: a molecular docking and dynamics study.

30 November 2018

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Deficient RNA-editing enzyme ADAR2 in an amyotrophic lateral sclerosis patient with a FUS(P525L) mutation.

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The C-terminal Domain (CTD) of Human DNA Glycosylase NEIL1 Is Required for Forming BERosome Repair Complex with DNA Replication Proteins at the Replicating Genome: DOMINANT NEGATIVE FUNCTION OF THE CTD.

30 November 2018

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FUS/TLS deficiency causes behavioral and pathological abnormalities distinct from amyotrophic lateral sclerosis

30 November 2018

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30 November 2018

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FUS is phosphorylated by DNA-PK and accumulates in the cytoplasm after DNA damage

30 November 2018

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30 November 2018

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30 November 2018

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PARP-1 dependent recruitment of the amyotrophic lateral sclerosis-associated protein FUS/TLS to sites of oxidative DNA damage.

30 November 2018

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Interaction of FUS and HDAC1 regulates DNA damage response and repair in neurons.

30 November 2018

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30 November 2018

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Prereplicative repair of oxidized bases in the human genome is mediated by NEIL1 DNA glycosylase together with replication proteins

30 November 2018

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Activation of cellular signaling by 8-oxoguanine DNA glycosylase-1-initiated DNA base excision repair

30 November 2018

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The RNA-binding protein fused in sarcoma (FUS) functions downstream of poly(ADP-ribose) polymerase (PARP) in response to DNA damage

30 November 2018

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30 November 2018

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Fused in sarcoma (FUS): an oncogene goes awry in neurodegeneration

30 November 2018

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ALS mutant FUS disrupts nuclear localization and sequesters wild-type FUS within cytoplasmic stress granules

30 November 2018

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The interaction between polynucleotide kinase phosphatase and the DNA repair protein XRCC1 is critical for repair of DNA alkylation damage and stable association at DNA damage sites

30 November 2018

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30 November 2018

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P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis.

30 November 2018

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Human Mre11/human Rad50/Nbs1 and DNA ligase IIIalpha/XRCC1 protein complexes act together in an alternative nonhomologous end joining pathway

30 November 2018

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Oxidatively Generated Damage to DNA by UVA Radiation in Cells and Human Skin

30 November 2018

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30 November 2018

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30 November 2018

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30 November 2018

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FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis

30 November 2018

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FUS mutations in sporadic amyotrophic lateral sclerosis

30 November 2018

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Oxidative stress and neurodegenerative diseases: a review of upstream and downstream antioxidant therapeutic options

30 November 2018

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Analysis of oxidative damage by gene-specific quantitative PCR.

30 November 2018

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30 November 2018

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Sensitized formation of oxidatively generated damage to cellular DNA by UVA radiation.

30 November 2018

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Human RIF1 encodes an anti-apoptotic factor required for DNA repair

30 November 2018

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

30 November 2018

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

30 November 2018

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Physical and functional interaction between human oxidized base-specific DNA glycosylase NEIL1 and flap endonuclease 1

30 November 2018

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Single-strand break repair and genetic disease

30 November 2018

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Identification and characterization of FUS/TLS as a new target of ATM.

30 November 2018

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Increased mitochondrial oxidative damage and oxidative DNA damage contributes to the neurodegenerative process in sporadic amyotrophic lateral sclerosis

30 November 2018

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Early steps in the DNA base excision/single-strand interruption repair pathway in mammalian cells

30 November 2018

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30 November 2018

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30 November 2018

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Poly(ADP-ribosyl)ation by PARP-1: 'PAR-laying' NAD+ into a nuclear signal

30 November 2018

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A requirement for PARP-1 for the assembly or stability of XRCC1 nuclear foci at sites of oxidative DNA damage

30 November 2018

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DNA single-strand break repair and spinocerebellar ataxia

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30 November 2018

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XRCC1 is specifically associated with poly(ADP-ribose) polymerase and negatively regulates its activity following DNA damage

30 November 2018

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A new hypothesis of the etiology of amyotrophic lateral sclerosis. The DNA hypothesis

30 November 2018

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Crossref

https://api.crossref.org/works/10.1038%2FS41467-018-06111-6

inferred from DOI database lookup

7 January 2021

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Identifiers

DOI

10.1038/S41467-018-06111-6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30206235%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30206235%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

PubMed publication ID

30206235

1 reference