(Q24309516)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17562789%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

title

Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage (English)

1 reference

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31 December 2019

0 references

0 references

1 reference

GOA release 2020-03-11

cellular response to hydrogen peroxide

1 reference

GOA release 2020-03-11

1 reference

1

1 reference

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31 December 2019

author name string

Olivier J Becherel

2

1 reference

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31 December 2019

Philip Chen

3

1 reference

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31 December 2019

Natalie Rundle

4

1 reference

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31 December 2019

Rick Woods

5

1 reference

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31 December 2019

Jun Nakamura

6

1 reference

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31 December 2019

Magtouf Gatei

7

1 reference

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31 December 2019

Chiara Criscuolo

8

1 reference

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31 December 2019

Alessandro Filla

9

1 reference

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31 December 2019

Luciana Chessa

10

1 reference

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31 December 2019

Markus Fusser

11

1 reference

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31 December 2019

Bernd Epe

12

1 reference

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31 December 2019

Nuri Gueven

13

1 reference

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31 December 2019

Martin F Lavin

14

1 reference

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31 December 2019

language of work or name

English

0 references

publication date

11 June 2007

1 reference

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31 December 2019

published in

Journal of Cell Biology

1 reference

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31 December 2019

volume

177

1 reference

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31 December 2019

issue

6

1 reference

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31 December 2019

page(s)

969-979

1 reference

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describes a project that uses

31 December 2019

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2064358/fullTextXML

inferred from PubMed Central ID database lookup

cites work

The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates

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Nucleolar localization of aprataxin is dependent on interaction with nucleolin and on active ribosomal DNA transcription

19 March 2017

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ATM activation by DNA double-strand breaks through the Mre11-Rad50-Nbs1 complex

19 March 2017

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The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4

19 March 2017

1 reference

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DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

19 March 2017

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Aprataxin, a novel protein that protects against genotoxic stress

19 March 2017

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Evidence for a lack of DNA double-strand break repair in human cells exposed to very low x-ray doses

19 March 2017

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19 March 2017

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Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34

19 March 2017

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19 March 2017

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Genome-wide distribution of yeast RNA polymerase II and its control by Sen1 helicase

19 March 2017

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A pathway of double-strand break rejoining dependent upon ATM, Artemis, and proteins locating to gamma-H2AX foci.

19 March 2017

1 reference

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Multiple protein/protein and protein/RNA interactions suggest roles for yeast DNA/RNA helicase Sen1p in transcription, transcription-coupled DNA repair and RNA processing

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2064358

The yeast SEN1 gene is required for the processing of diverse RNA classes

19 March 2017

1 reference

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Genetic and biochemical characterization of mutations in the ATPase and helicase regions of the Upf1 protein

19 March 2017

1 reference

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The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder

19 March 2017

1 reference

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Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies

19 March 2017

1 reference

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DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation

19 March 2017

1 reference

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The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin

19 March 2017

1 reference

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Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

19 March 2017

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Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1

19 March 2017

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Ataxia-ocular motor apraxia: a syndrome mimicking ataxia-telangiectasia

19 March 2017

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RecQ helicases: caretakers of the genome

19 March 2017

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A subgroup of spinocerebellar ataxias defective in DNA damage responses

7 April 2017

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Involvement of novel autophosphorylation sites in ATM activation

27 September 2017

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Senataxin, the yeast Sen1p orthologue: characterization of a unique protein in which recessive mutations cause ataxia and dominant mutations cause motor neuron disease

27 September 2017

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27 September 2017

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Phosphorylated histone H2AX foci persist on rejoined mitotic chromosomes in normal human diploid cells exposed to ionizing radiation

27 September 2017

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Werner protein protects nonproliferating cells from oxidative DNA damage

27 September 2017

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27 September 2017

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27 September 2017

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Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy

27 September 2017

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27 September 2017

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27 September 2017

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Independent roles for nibrin and Mre11-Rad50 in the activation and function of Atm.

27 September 2017

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Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2.

27 September 2017

1 reference

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Requirement of the MRN complex for ATM activation by DNA damage

27 September 2017

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Quantitation of intracellular NAD(P)H can monitor an imbalance of DNA single strand break repair in base excision repair deficient cells in real time

27 September 2017

1 reference

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ATM deficiency and oxidative stress: a new dimension of defective response to DNA damage

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2064358

Biological consequences of free radical-damaged DNA bases.

27 September 2017

1 reference

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The response of L5178Y lymphoma sublines to oxidative stress: antioxidant defence, iron content and nuclear translocation of the p65 subunit of NF-kappaB.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2064358

Oxidative stress and disturbed glutamate transport in hereditary nucleotide repair disorders

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2064358

Immunochemical quantitation of UV-induced oxidative and dimeric DNA damage to human keratinocytes.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2064358

Isolation of full-length ATM cDNA and correction of the ataxia-telangiectasia cellular phenotype

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2064358

A family showing no evidence of linkage between the ataxia telangiectasia gene and chromosome 11q22-23.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2064358

The genetic defect in ataxia-telangiectasia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2064358

Activation of p53 by oxidative stress involves platelet-derived growth factor-beta receptor-mediated ataxia telangiectasia mutated (ATM) kinase activation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2064358

Identification of ataxia telangiectasia heterozygotes, a cancer prone population

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2064358

Heterogeneity in premature senescence by oxidative stress correlates with differential DNA damage during the cell cycle.

30 May 2018

1 reference

https://api.crossref.org/works/10.1083%2FJCB.200701042

Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1083%2FJCB.200701042

In vivo misregulation of genes involved in apoptosis, development and oxidative stress in mice lacking both functional Werner syndrome protein and poly(ADP-ribose) polymerase-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1083%2FJCB.200701042

Reactive oxygen species derived from the mitochondrial respiratory chain are not responsible for the basal levels of oxidative base modifications observed in nuclear DNA of Mammalian cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1083%2FJCB.200701042

Relative contribution of homologous recombination and non-homologous end-joining to DNA double-strand break repair after oxidative stress in Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1083%2FJCB.200701042

The novel human gene aprataxin is directly involved in DNA single-strand-break repair.

21 January 2018

1 reference

https://api.crossref.org/works/10.1083%2FJCB.200701042

RECQL4-deficient cells are hypersensitive to oxidative stress/damage: Insights for osteosarcoma prevalence and heterogeneity in Rothmund-Thomson syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1083%2FJCB.200701042

Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1083%2FJCB.200701042

Comparison of biological effects of DNA damage induced by ionizing radiation and hydrogen peroxide in CHO cells

21 January 2018

1 reference

12 December 2020

Vanillin (3-methoxy-4-hydroxybenzaldehyde) inhibits mutation induced by hydrogen peroxide, N-methyl-N-nitrosoguanidine and mitomycin C but not (137)Cs gamma-radiation at the CD59 locus in human-hamster hybrid A(L) cells

1 reference

12 December 2020

Identification of 4 ataxia telangiectasia cell lines hypersensitive to γ-irradiation but not to hydrogen peroxide

1 reference

12 December 2020

Oxidative DNA damage: endonuclease fingerprinting

1 reference

12 December 2020

Cell cycle constraints on peroxide- and radiation-induced inhibitory checkpoints

1 reference

12 December 2020

A method for isolation and purification of specific antibodies to a protein fused to the GST

1 reference

12 December 2020

Detection of mitochondria-derived reactive oxygen species production by the chemilumigenic probes lucigenin and luminol

1 reference

12 December 2020

Activation of ataxia telangiectasia mutated by DNA strand break-inducing agents correlates closely with the number of DNA double strand breaks

1 reference

12 December 2020

Multiple involvement of oxidative stress in Werner syndrome phenotype

1 reference

12 December 2020

Identifiers

DOI

10.1083/JCB.200701042

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17562789%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17562789%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

PubMed publication ID

17562789

2 references