-
1
-
-
0035150912
-
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
-
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
-
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
-
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
-
5
-
-
0036754891
-
Genetic polymorphisms and lung cancer susceptibility: A review
-
Kiyohara C., Otsu A., Shirakawa T., Fukuda S., Hopkin J.M. Genetic polymorphisms and lung cancer susceptibility: a review. Lung Cancer. 37:2002;241-256.
-
(2002)
Lung Cancer
, vol.37
, pp. 241-256
-
-
Kiyohara, C.1
Otsu, A.2
Shirakawa, T.3
Fukuda, S.4
Hopkin, J.M.5
-
6
-
-
0032565543
-
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
-
7
-
-
0034739688
-
Cancer chemotherapy and somatic cell mutation
-
Kubota M., Lin Y.-W., Hamahata K., Sawada M., Koishi S., Hirota H., Wakazono Y. Cancer chemotherapy and somatic cell mutation. Mutat. Res. 470:2000;93-102.
-
(2000)
Mutat. Res.
, vol.470
, pp. 93-102
-
-
Kubota, M.1
Lin, Y.-W.2
Hamahata, K.3
Sawada, M.4
Koishi, S.5
Hirota, H.6
Wakazono, Y.7
-
8
-
-
18644370941
-
Three somatic genetic biomarkers and covariates in radiation-exposed Russian cleanup workers of the Chernobyl nuclear reactor 6-13 years after exposure
-
Jones I.M., Galick H., Kato P., Langlois R.G., Mendelsohn M.L., Murphy G.A., Pleshanov P., Ramsey M.J., Thomas C.B., Tucker J.D., Tureva L., Vorobtsova I., Nelson D.O. Three somatic genetic biomarkers and covariates in radiation-exposed Russian cleanup workers of the Chernobyl nuclear reactor 6-13 years after exposure. Radiat. Res. 158:2002;424-442.
-
(2002)
Radiat. Res.
, vol.158
, pp. 424-442
-
-
Jones, I.M.1
Galick, H.2
Kato, P.3
Langlois, R.G.4
Mendelsohn, M.L.5
Murphy, G.A.6
Pleshanov, P.7
Ramsey, M.J.8
Thomas, C.B.9
Tucker, J.D.10
Tureva, L.11
Vorobtsova, I.12
Nelson, D.O.13
-
9
-
-
0027177311
-
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
-
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
-
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
-
13
-
-
0024325920
-
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
-
14
-
-
0031751941
-
In vivo somatic mutations in Werner's syndrome
-
Kyoizumi S., Kusunoki Y., Seyama T., Hatamochi A., Goto M. In vivo somatic mutations in Werner's syndrome. Hum. Genet. 103:1998;405-410.
-
(1998)
Hum. Genet.
, vol.103
, pp. 405-410
-
-
Kyoizumi, S.1
Kusunoki, Y.2
Seyama, T.3
Hatamochi, A.4
Goto, M.5
-
15
-
-
0034194139
-
Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes
-
Moser M.J., Bigbee W.L., Grant S.G., Emond M.J., Langlois R.G., Jensen R.H., Oshima J., Monnat R.J. Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes. Cancer Res. 60:2000;2492-2496.
-
(2000)
Cancer Res.
, vol.60
, pp. 2492-2496
-
-
Moser, M.J.1
Bigbee, W.L.2
Grant, S.G.3
Emond, M.J.4
Langlois, R.G.5
Jensen, R.H.6
Oshima, J.7
Monnat, R.J.8
-
16
-
-
0029032680
-
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
-
17
-
-
0028970067
-
Elevated frequency of glycophorin a mutations in erythrocytes from Chemobyl accident victims
-
Jensen R.H., Langlois R.G., Bigbee W.L., Grant S.G., Moore D. II, Pilinskaya M., Vorobtsova I., Pleshanov P. Elevated frequency of glycophorin A mutations in erythrocytes from Chemobyl accident victims. Radiat. Res. 141:1995;129-135.
-
(1995)
Radiat. Res.
, vol.141
, pp. 129-135
-
-
Jensen, R.H.1
Langlois, R.G.2
Bigbee, W.L.3
Grant, S.G.4
Moore II, D.5
Pilinskaya, M.6
Vorobtsova, I.7
Pleshanov, P.8
-
18
-
-
0029102338
-
Mutation frequency in human blood cells increases with age
-
Akiyama M., Kyoizumi S., Hirai Y., Kusunoki Y., Iwamoto K.S., Nakamura N. Mutation frequency in human blood cells increases with age. Mutat. Res. 338:1995;141-149.
-
(1995)
Mutat. Res.
, vol.338
, pp. 141-149
-
-
Akiyama, M.1
Kyoizumi, S.2
Hirai, Y.3
Kusunoki, Y.4
Iwamoto, K.S.5
Nakamura, N.6
-
19
-
-
0033955346
-
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
-
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
-
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
-
22
-
-
0035902528
-
Complex formation by the human RAD51C and XRCC3 recombination repair proteins
-
Masson J.Y., Stasiak A.Z., Stasiak A., Benson F.E., West S.C. Complex formation by the human RAD51C and XRCC3 recombination repair proteins. Proc. Natl. Acad. Sci. U.S.A. 98:2001;8440-8446.
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 8440-8446
-
-
Masson, J.Y.1
Stasiak, A.Z.2
Stasiak, A.3
Benson, F.E.4
West, S.C.5
-
23
-
-
0033065174
-
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
-
24
-
-
0034690249
-
Interplay of p53 and DNA-repair protein XRCC4 in tumorigenesis, genomic stability and development
-
Gao Y., Ferguson D.O., Xie W., Manis J.P., Sekiguchi J., Frank K.M., Chaudhuri J., Horner J., DePinho R.A., Alt F.W. Interplay of p53 and DNA-repair protein XRCC4 in tumorigenesis, genomic stability and development. Nature. 404:2000;897-900.
-
(2000)
Nature
, vol.404
, pp. 897-900
-
-
Gao, Y.1
Ferguson, D.O.2
Xie, W.3
Manis, J.P.4
Sekiguchi, J.5
Frank, K.M.6
Chaudhuri, J.7
Horner, J.8
Depinho, R.A.9
Alt, F.W.10
-
25
-
-
0034621670
-
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
-
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
-
27
-
-
0031945194
-
The North Cumbria Community Genetics Project
-
Chase D.S., Tawn E.J., Parker L., Jonas P., Parker C.O., Burn J. The North Cumbria Community Genetics Project. J. Med. Genet. 35:1998;413-416.
-
(1998)
J. Med. Genet.
, vol.35
, pp. 413-416
-
-
Chase, D.S.1
Tawn, E.J.2
Parker, L.3
Jonas, P.4
Parker, C.O.5
Burn, J.6
-
28
-
-
0033152748
-
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
-
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
-
30
-
-
0028827391
-
Sensitivity to somatic mutations in human umbilical cord blood to maternal environments
-
Manchester D.K., Nicklas J.A., O'Neill J.P., Lippert M.J., Grant S.G., Langlois R.G., Moore D.H. III, Jensen R.H., Albertini R.J., Bigbee W.L. Sensitivity to somatic mutations in human umbilical cord blood to maternal environments. Environ. Mol. Mutagen. 26:1995;203-212.
-
(1995)
Environ. Mol. Mutagen.
, vol.26
, pp. 203-212
-
-
Manchester, D.K.1
Nicklas, J.A.2
O'Neill, J.P.3
Lippert, M.J.4
Grant, S.G.5
Langlois, R.G.6
Moore III, D.H.7
Jensen, R.H.8
Albertini, R.J.9
Bigbee, W.L.10
-
31
-
-
0025308229
-
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
-
33
-
-
0035808719
-
The XRCC1 399 glutamine allele is a risk factor for adenocarcinoma of the lung
-
Divine K.K., Gilliland F.D., Crowell R.E., Stidley C.A., Bocklage T.J., Cook D.L., Belinsky S.A. The XRCC1 399 glutamine allele is a risk factor for adenocarcinoma of the lung. Mutat. Res. 461:2001;273-278.
-
(2001)
Mutat. Res.
, vol.461
, pp. 273-278
-
-
Divine, K.K.1
Gilliland, F.D.2
Crowell, R.E.3
Stidley, C.A.4
Bocklage, T.J.5
Cook, D.L.6
Belinsky, S.A.7
-
34
-
-
0034098801
-
Polymorphisms in the DNA repair genes XRCC1 and ERCC2 and biomarkers of DNA damage in human blood mononuclear cells
-
Duell E.J., Wiencke J.K., Cheng T.-J., Varkonyi A., Zuo Z.F., Ashok T.D.S., Mark E.J., Wain J.C., Christiani D.C., Kelsey K.T. Polymorphisms in the DNA repair genes XRCC1 and ERCC2 and biomarkers of DNA damage in human blood mononuclear cells. Carcinogenesis. 21:2000;965-971.
-
(2000)
Carcinogenesis
, vol.21
, pp. 965-971
-
-
Duell, E.J.1
Wiencke, J.K.2
Cheng, T.-J.3
Varkonyi, A.4
Zuo, Z.F.5
Ashok, T.D.S.6
Mark, E.J.7
Wain, J.C.8
Christiani, D.C.9
Kelsey, K.T.10
-
35
-
-
0037179177
-
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
-
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
-
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
-
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
-
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
-
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
|