XRCC1 haploinsufficiency in mice has little effect on aging, but adversely modifies exposure-dependent susceptibility (Q35259040)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21737425 AND SRC:MED&resulttype=core&format=json

7 February 2020

title

XRCC1 haploinsufficiency in mice has little effect on aging, but adversely modifies exposure-dependent susceptibility (English)

1 reference

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7 February 2020

0 references

2

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7 February 2020

Marshall Miller

3

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7 February 2020

Kenneth W. Fishbein

6

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7 February 2020

author name string

Daniel R McNeill

1

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7 February 2020

Paul J Pistell

4

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7 February 2020

Nadja C de Souza-Pinto

5

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7 February 2020

Richard G Spencer

7

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7 February 2020

Yie Liu

8

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7 February 2020

Christina Pettan-Brewer

9

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7 February 2020

Warren C Ladiges

10

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7 February 2020

David M Wilson

11

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7 February 2020

language of work or name

English

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publication date

6 July 2011

1 reference

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7 February 2020

published in

Nucleic Acids Research

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7 February 2020

volume

39

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7 February 2020

issue

18

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7 February 2020

page(s)

7992-8004

1 reference

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Creative Commons Attribution-NonCommercial 3.0 Unported

7 February 2020

copyright license

start time

4 October 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3185405/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

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XRCC1 protects against the lethality of induced oxidative DNA damage in nondividing neural cells

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Ischemic preconditioning induces XRCC1, DNA polymerase-beta, and DNA ligase III and correlates with enhanced base excision repair

27 July 2018

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Analysis of the XRCC1 gene as a modifier of the cerebral response in ischemic stroke

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Mouse models of XRCC1 DNA repair polymorphisms and cancer

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XRCC1 and DNA strand break repair

27 July 2018

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Mutation of TDP1, encoding a topoisomerase I-dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy

27 July 2018

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

27 July 2018

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

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1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21737425

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/GKR280

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21737425 AND SRC:MED&resulttype=core&format=json

7 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21737425 AND SRC:MED&resulttype=core&format=json

7 February 2020

PubMed publication ID

21737425

1 reference