메뉴 건너뛰기




Volumn 545, Issue 1-2, 2004, Pages 49-57

DNA repair gene polymorphisms, pre-natal factors and the frequency of somatic mutations in the glycophorin-A gene among healthy newborns

Author keywords

DNA repair; Glycophorin A; XRCC1; XRCC3; XRCC4

Indexed keywords

ARGININE; GLUTAMINE; GLYCOPHORIN A; THREONINE;

EID: 0346156079     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mrfmmm.2003.09.007     Document Type: Article
Times cited : (25)

References (41)
  • 1
    • 0035150912 scopus 로고    scopus 로고
    • The molecular biology of cancer
    • Bertram J.S. The molecular biology of cancer. Mol. Aspects Med. 21:2000;167-223.
    • (2000) Mol. Aspects Med. , vol.21 , pp. 167-223
    • Bertram, J.S.1
  • 2
    • 0031987280 scopus 로고    scopus 로고
    • Estimation of mutation frequencies in normal mammalian cells and the development of cancer
    • Turker M.S. Estimation of mutation frequencies in normal mammalian cells and the development of cancer. Cancer Biol. 8:1998;407-419.
    • (1998) Cancer Biol. , vol.8 , pp. 407-419
    • Turker, M.S.1
  • 3
    • 0034089945 scopus 로고    scopus 로고
    • Cancer risk and low-penetrance susceptibility genes in gene-environment interactions
    • Shields P.G., Harris C.C. Cancer risk and low-penetrance susceptibility genes in gene-environment interactions. J. Clin. Oncol. 18:2000;2309-2315.
    • (2000) J. Clin. Oncol. , vol.18 , pp. 2309-2315
    • Shields, P.G.1    Harris, C.C.2
  • 4
    • 0037037790 scopus 로고    scopus 로고
    • Molecular epidemiology of smoking and lung cancer
    • Shields P.G. Molecular epidemiology of smoking and lung cancer. Oncogene. 21:2001;6870-6876.
    • (2001) Oncogene , vol.21 , pp. 6870-6876
    • Shields, P.G.1
  • 6
    • 0032565543 scopus 로고    scopus 로고
    • Variation in DNA repair is a factor in cancer susceptibility: A paradigm for the promises and perils of individual and population risk estimation
    • Mohrenweiser H.W., Jones I.M. Variation in DNA repair is a factor in cancer susceptibility: a paradigm for the promises and perils of individual and population risk estimation. Mutat. Res. 400:1998;15-24.
    • (1998) Mutat. Res. , vol.400 , pp. 15-24
    • Mohrenweiser, H.W.1    Jones, I.M.2
  • 9
    • 0027177311 scopus 로고
    • In vivo somatic mutation and segregation at the human glycophorin a (GPA) locus: Phenotypic variation encompassing both gene-specific and chromosomal mechanisms
    • Grant S.G., Bigbee W.L. In vivo somatic mutation and segregation at the human glycophorin A (GPA) locus: phenotypic variation encompassing both gene-specific and chromosomal mechanisms. Mutat. Res. 288:1993;163-172.
    • (1993) Mutat. Res. , vol.288 , pp. 163-172
    • Grant, S.G.1    Bigbee, W.L.2
  • 10
    • 0024590169 scopus 로고
    • Evidence for an elevated frequency of in vivo somatic cell mutations in ataxia telangiectasia
    • Bigbee W.L., Langlois R.G., Swift M., Jensen R.H. Evidence for an elevated frequency of in vivo somatic cell mutations in ataxia telangiectasia. Am. J. Hum. Genet. 44:1989;402-408.
    • (1989) Am. J. Hum. Genet. , vol.44 , pp. 402-408
    • Bigbee, W.L.1    Langlois, R.G.2    Swift, M.3    Jensen, R.H.4
  • 11
    • 0031292790 scopus 로고    scopus 로고
    • Diagnosis of ataxia telangiectasia with the glycophorin a somatic mutation assay
    • Grant S.G., Reeger W., Wenger S.L. Diagnosis of ataxia telangiectasia with the glycophorin A somatic mutation assay. Genet. Test. 1:1997-98;261-267.
    • (1997) Genet. Test. , vol.1 , pp. 261-267
    • Grant, S.G.1    Reeger, W.2    Wenger, S.L.3
  • 12
    • 3142544243 scopus 로고
    • Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome
    • Langlois R.G., Bigbee W.L., Jensen R.H., German J. Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome. Proc. Natl. Acad. Sci. U.S.A. 86:1989;670-674.
    • (1989) Proc. Natl. Acad. Sci. U.S.A. , vol.86 , pp. 670-674
    • Langlois, R.G.1    Bigbee, W.L.2    Jensen, R.H.3    German, J.4
  • 13
    • 0024325920 scopus 로고
    • Frequency of variant erythrocytes at the glycophorin a locus in two Bloom's syndrome patients
    • Kyoizumi S., Nakamura N., Takebe H., Tatsumi K., German J., Akiyama M. Frequency of variant erythrocytes at the glycophorin A locus in two Bloom's syndrome patients. Mutat. Res. 214:1989;215-222.
    • (1989) Mutat. Res. , vol.214 , pp. 215-222
    • Kyoizumi, S.1    Nakamura, N.2    Takebe, H.3    Tatsumi, K.4    German, J.5    Akiyama, M.6
  • 16
    • 0029032680 scopus 로고    scopus 로고
    • Biomarkers of styrene exposure in lamination workers: Levels of O6-guanine DNA adducts, DNA strand breaks and mutant frequencies in the hypoxanthine guanine phosphoribosyltransferase gene in T-lymphocytes
    • Vodicka P., Bastlova T., Vodickova L., Peterokova K., Lavgert B., Hemminiki K. Biomarkers of styrene exposure in lamination workers: levels of O6-guanine DNA adducts, DNA strand breaks and mutant frequencies in the hypoxanthine guanine phosphoribosyltransferase gene in T-lymphocytes. Carcinogenesis. 16:1996;1473-1481.
    • (1996) Carcinogenesis , vol.16 , pp. 1473-1481
    • Vodicka, P.1    Bastlova, T.2    Vodickova, L.3    Peterokova, K.4    Lavgert, B.5    Hemminiki, K.6
  • 19
    • 0033955346 scopus 로고    scopus 로고
    • XRCC1 keeps DNA from getting stranded
    • Thompson L.H., West M.G. XRCC1 keeps DNA from getting stranded. Mutat. Res. 459:2000;1-18.
    • (2000) Mutat. Res. , vol.459 , pp. 1-18
    • Thompson, L.H.1    West, M.G.2
  • 20
    • 0035796042 scopus 로고    scopus 로고
    • Homologous recombinational repair of DNA ensures mammalian chromosome stability
    • Thompson L.H., Schild D. Homologous recombinational repair of DNA ensures mammalian chromosome stability. Mutat. Res. 477:2001;131-153.
    • (2001) Mutat. Res. , vol.477 , pp. 131-153
    • Thompson, L.H.1    Schild, D.2
  • 21
    • 0032904693 scopus 로고    scopus 로고
    • The biochemistry and biological significance of nonhomologous DNA end joining: An essential repair process in multicellular eukaryotes
    • Lieber M.R. The biochemistry and biological significance of nonhomologous DNA end joining: an essential repair process in multicellular eukaryotes. Genes Cells. 4:1999;77-85.
    • (1999) Genes Cells , vol.4 , pp. 77-85
    • Lieber, M.R.1
  • 23
    • 0033065174 scopus 로고    scopus 로고
    • The XRCC2 and XRCC3 repair genes are required for chromosome stability in mammalian cells
    • Cui X., Brenneman M., Meyne J., Oshimura M., Goodwin E.H., Chen D.J. The XRCC2 and XRCC3 repair genes are required for chromosome stability in mammalian cells. Mutat. Res. 434:1999;75-88.
    • (1999) Mutat. Res. , vol.434 , pp. 75-88
    • Cui, X.1    Brenneman, M.2    Meyne, J.3    Oshimura, M.4    Goodwin, E.H.5    Chen, D.J.6
  • 25
    • 0034621670 scopus 로고    scopus 로고
    • Individual variation in somatic mutations of the glycophorin-A gene in neonates in relation to pre-natal factors
    • Daniel C.P., Fisher A., Parker L., Burn J., Tawn E.J. Individual variation in somatic mutations of the glycophorin-A gene in neonates in relation to pre-natal factors. Mutat. Res. 467:2000;153-159.
    • (2000) Mutat. Res. , vol.467 , pp. 153-159
    • Daniel, C.P.1    Fisher, A.2    Parker, L.3    Burn, J.4    Tawn, E.J.5
  • 26
    • 0037157221 scopus 로고    scopus 로고
    • Polymorphisms of the DNA repair gene XRCCI and the frequency of somatic mutations at the glycophorin a locus in newborns
    • Relton C.L., P Daniel C., Fisher A., Chase D.S., Burn J., Tawn E.J. Polymorphisms of the DNA repair gene XRCCI and the frequency of somatic mutations at the glycophorin A locus in newborns. Mutat. Res. 502:2002;61-68.
    • (2002) Mutat. Res. , vol.502 , pp. 61-68
    • Relton, C.L.1    Daniel, C.P.2    Fisher, A.3    Chase, D.S.4    Burn, J.5    Tawn, E.J.6
  • 28
    • 0033152748 scopus 로고    scopus 로고
    • XRCC1 polymorphisms: Effects on aflatoxin B1-DNA adducts and glycophorin a variant frequency
    • Lunn R.M., Langlois R.G., Hsieh L.L., Thompson C.L., Bell D.A. XRCC1 polymorphisms: effects on aflatoxin B1-DNA adducts and glycophorin A variant frequency. Cancer Res. 59:1999;2557-2561.
    • (1999) Cancer Res. , vol.59 , pp. 2557-2561
    • Lunn, R.M.1    Langlois, R.G.2    Hsieh, L.L.3    Thompson, C.L.4    Bell, D.A.5
  • 29
    • 0031756760 scopus 로고    scopus 로고
    • Spontaneous mutation during fetal development and post-natal growth
    • Paashuis-Lew Y.R., Heddle J.A. Spontaneous mutation during fetal development and post-natal growth. Mutagenesis. 13:1998;613-617.
    • (1998) Mutagenesis , vol.13 , pp. 613-617
    • Paashuis-Lew, Y.R.1    Heddle, J.A.2
  • 31
    • 0025308229 scopus 로고
    • An improved flow cytometric assay for somatic mutations at the glycophorin a locus in humans
    • Langlois R.G., Nisbet B.A., Bigbee W.L., Ridinger D.N., Jensen R.H. An improved flow cytometric assay for somatic mutations at the glycophorin A locus in humans. Cytometry. 11:1990;513-521.
    • (1990) Cytometry , vol.11 , pp. 513-521
    • Langlois, R.G.1    Nisbet, B.A.2    Bigbee, W.L.3    Ridinger, D.N.4    Jensen, R.H.5
  • 32
  • 35
    • 0037179177 scopus 로고    scopus 로고
    • Effects on sister chromatid exchange frequency of polymorphisms in DNA repair gene XRCC1 in smokers
    • Lei Y.-C., Hwang S.-J., Chang C.-C., Kuo H.-W., Luo J.-C., Chang M.J.W., Cheng T.-J. Effects on sister chromatid exchange frequency of polymorphisms in DNA repair gene XRCC1 in smokers. Mutat. Res. 519:2002;93-101.
    • (2002) Mutat. Res. , vol.519 , pp. 93-101
    • Lei, Y.-C.1    Hwang, S.-J.2    Chang, C.-C.3    Kuo, H.-W.4    Luo, J.-C.5    Chang, M.J.W.6    Cheng, T.-J.7
  • 36
    • 0034676239 scopus 로고    scopus 로고
    • The 399Gln polymorphism in the DNA repair gene XRCC1 modulates the genotoxic response induced in human lymphocytes by the tobacco-specific nitrosamine NNK
    • Abdel-Rahman S.Z., El-Zein R.A. The 399Gln polymorphism in the DNA repair gene XRCC1 modulates the genotoxic response induced in human lymphocytes by the tobacco-specific nitrosamine NNK. Cancer Lett. 159:2000;63-71.
    • (2000) Cancer Lett. , vol.159 , pp. 63-71
    • Abdel-Rahman, S.Z.1    El-Zein, R.A.2
  • 37
    • 0037202597 scopus 로고    scopus 로고
    • Coding variants in human double-strand break repair genes
    • Ruttan C.C., Glickman B.N. Coding variants in human double-strand break repair genes. Mutat. Res. 509:2002;175-200.
    • (2002) Mutat. Res. , vol.509 , pp. 175-200
    • Ruttan, C.C.1    Glickman, B.N.2
  • 38
    • 0033569684 scopus 로고    scopus 로고
    • XRCC3 promotes homology-directed repair of DNA damage in mammalian cells
    • Pierce A.J., Johnson R.D., Thompson L.H., Jasin M. XRCC3 promotes homology-directed repair of DNA damage in mammalian cells. Genes Dev. 13:1999;2633-2638.
    • (1999) Genes Dev. , vol.13 , pp. 2633-2638
    • Pierce, A.J.1    Johnson, R.D.2    Thompson, L.H.3    Jasin, M.4
  • 39
    • 0033728524 scopus 로고    scopus 로고
    • Identification of single nucleotide polymorphisms in human DNA repair genes
    • Ford B.N., Ruttan C.C., Kyle V.L., Brackley M.E., Glickman B.W. Identification of single nucleotide polymorphisms in human DNA repair genes. Carcinogenesis. 21:2000;1977-1981.
    • (2000) Carcinogenesis , vol.21 , pp. 1977-1981
    • Ford, B.N.1    Ruttan, C.C.2    Kyle, V.L.3    Brackley, M.E.4    Glickman, B.W.5
  • 41
    • 0242501504 scopus 로고    scopus 로고
    • Challenges and complexities in estimating both the functional impact and the disease risk associated with the extensive genetic variation in human DNA repair genes
    • Mohrenweiser H.W., Wilson D.M. III, Jones I.M. Challenges and complexities in estimating both the functional impact and the disease risk associated with the extensive genetic variation in human DNA repair genes. Mutat. Res. 526:2003;93-125.
    • (2003) Mutat. Res. , vol.526 , pp. 93-125
    • Mohrenweiser, H.W.1    Wilson III, D.M.2    Jones, I.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.