Polymorphisms of the DNA repair gene XRCC1 and the frequency of somatic mutations at the glycophorin A locus in newborns (Q33183668)

23 July 2017

title

Polymorphisms of the DNA repair gene XRCC1 and the frequency of somatic mutations at the glycophorin A locus in newborns (English)

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23 July 2017

5

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Diana S Chase

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author name string

Caroline L Relton

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23 July 2017

C Paul Daniel

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Ann Fisher

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E Janet Tawn

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23 July 2017

language of work or name

English

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publication date

1 May 2002

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23 July 2017

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23 July 2017

volume

502

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23 July 2017

issue

1-2

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23 July 2017

page(s)

61-68

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Alterations in expression and structure of the DNA repair gene XRCC1

23 July 2017

cites work

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Involvement of XRCC1 and DNA ligase III gene products in DNA base excision repair.

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Mutations in hamster single-strand break repair gene XRCC1 causing defective DNA repair

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Holding damaged DNA together

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Life without DNA repair

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XRCC1 polypeptide interacts with DNA polymerase beta and possibly poly (ADP-ribose) polymerase, and DNA ligase III is a novel molecular 'nick-sensor' in vitro

7 January 2021

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XRCC1 keeps DNA from getting stranded

7 January 2021

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Rare microsatellite polymorphisms in the DNA repair genes XRCC1, XRCC3 and XRCC5 associated with cancer in patients of varying radiosensitivity

7 January 2021

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Polymorphisms of DNA repair gene XRCC1 in squamous cell carcinoma of the head and neck

7 January 2021

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Polymorphisms of the DNA repair gene XRCC1 and risk of gastric cancer in a Chinese population

7 January 2021

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Inheritance of the 194Trp and the 399Gln variant alleles of the DNA repair gene XRCC1 are associated with increased risk of early-onset colorectal carcinoma in Egypt

7 January 2021

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The 399Gln polymorphism in the DNA repair gene XRCC1 modulates the genotoxic response induced in human lymphocytes by the tobacco-specific nitrosamine NNK

7 January 2021

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The XRCC1 399 glutamine allele is a risk factor for adenocarcinoma of the lung

7 January 2021

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Diagnosis of ataxia telangiectasia with the glycophorin A somatic mutation assay

7 January 2021

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Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome

7 January 2021

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Frequency of variant erythrocytes at the glycophorin-A locus in two Bloom's syndrome patients

7 January 2021

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In vivo somatic mutations in Werner's syndrome

7 January 2021

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Glycophorin A mutations and risk of secondary leukaemia in patients treated for childhood acute lymphoblastic leukaemia

7 January 2021

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Somatic mutation detection in human biomonitoring

7 January 2021

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In vivo somatic mutation and segregation at the human glycophorin A (GPA) locus: phenotypic variation encompassing both gene-specific and chromosomal mechanisms.

7 January 2021

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Individual variation in somatic mutations of the glycophorin-A gene in neonates in relation to pre-natal factors

7 January 2021

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The North Cumbria Community Genetics Project

7 January 2021

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Human in vivo somatic mutation measured at two loci: individuals with stably elevated background erythrocyte glycophorin A (gpa) variant frequencies exhibit normal T-lymphocyte hprt mutant frequencies

7 January 2021

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Polymorphisms in the DNA repair genes XRCC1 and ERCC2 and biomarkers of DNA damage in human blood mononuclear cells

7 January 2021

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Mutation frequency in human blood cells increases with age

7 January 2021

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Mutation of a BRCT domain selectively disrupts DNA single-strand break repair in noncycling Chinese hamster ovary cells

7 January 2021

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10.1016/S0027-5107(02)00030-1

7 January 2021

Identifiers

DOI

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23 July 2017

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