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Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma.

Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma. Research Abstract Details 

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  • Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma. Abstract Text:

    patrick j haydenPatrick J Hayden,prerna tewariPrerna Tewari,derek w morrisDerek W Morris,anthony stainesAnthony Staines,dominique crowleyDominique Crowley,alexandra nietersAlexandra Nieters,nikolaus beckerNikolaus Becker,silvia Silvia ,lenka foretovaLenka Foretova,marc Marc ,pier luigi coccoPier Luigi Cocco,paolo boffettaPaolo Boffetta,paul brennanPaul Brennan,stephen j chanockStephen J Chanock,paul v brownePaul V Browne,mark lawlerMark Lawler,patrick j haydenPatrick J Hayden,prerna tewariPrerna Tewari,derek w morrisDerek W Morris,anthony stainesAnthony Staines,dominique crowleyDominique Crowley,alexandra nietersAlexandra Nieters,nikolaus beckerNikolaus Becker,silvia Silvia ,lenka foretovaLenka Foretova,marc Marc ,pier luigi coccoPier Luigi Cocco,paolo boffettaPaolo Boffetta,paul brennanPaul Brennan,stephen j chanockStephen J Chanock,paul v brownePaul V Browne,mark lawlerMark Lawler,

    Cytogenetic analysis in myeloma reveals marked chromosomal instability. Both widespread genomic alterations and evidence of aberrant class switch recombination, the physiological process that regulates maturation of the antibody response, implicate the DNA repair pathway in disease pathogenesis. We therefore assessed 27 SNPs in three genes (XRCC3, XRCC4 and XRCC5) central to DNA repair in patients with myeloma and controls from the EpiLymph study and from an Irish hospital registry (n = 306 cases, 263 controls). For the haplotype-tagging SNP (htSNP) rs963248 in XRCC4, Allele A was significantly more frequent in cases than in controls (86.4 versus 80.8%; odds ratio 1.51; 95% confidence interval 1.10-2.08; P = 0.0133), as was the AA genotype (74 versus 65%) (P = 0.026). Haplotype analysis was performed using Unphased for rs963248 in combination with additional SNPs in XRCC4. The strongest evidence of association came from the A-T haplotype from rs963248-rs2891980 (P = 0.008). For XRCC5, the genotype GG from rs1051685 was detected in 10 cases from different national populations but in only one control (P = 0.015). This SNP is located in the 3'-UTR of XRCC5. Overall, these data provide support for the hypothesis that common variation in the genes encoding DNA repair proteins contributes to susceptibility to myeloma.

    Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma. Publishing Authors By Initials

    pj haydenPJ Hayden,p tewariP Tewari,dw morrisDW Morris,a stainesA Staines,d crowleyD Crowley,a nietersA Nieters,n beckerN Becker,s S ,l foretovaL Foretova,m M ,pl coccoPL Cocco,p boffettaP Boffetta,p brennanP Brennan,sj chanockSJ Chanock,pv brownePV Browne,m lawlerM Lawler,pj haydenPJ Hayden,p tewariP Tewari,dw morrisDW Morris,a stainesA Staines,d crowleyD Crowley,a nietersA Nieters,n beckerN Becker,s S ,l foretovaL Foretova,m M ,pl coccoPL Cocco,p boffettaP Boffetta,p brennanP Brennan,sj chanockSJ Chanock,pv brownePV Browne,m lawlerM Lawler,

    For similar abstracts research abstracts see: abstracts research

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    Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Human molecular genetics

    VOLUME: 16

    Page Numbers: 3117-27

    Journal Abbreviation: Hum. Mol. Genet.

    ISSN: 0964-6906

    DAY: 26

    MONTH: 09

    YEAR: 2007

    Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma. Information

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    LANGUAGE: eng

    NlmUniqueID: 9208958

    Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma. Keywords Mesh Terms:

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    Grant and Affiliation Information for Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma.

    AFFILIATION: The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Hum Mol Genet

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