메뉴 건너뛰기




Volumn 13, Issue 1, 2003, Pages 61-69

DNA repair defects in colon cancer

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; POLYDEOXYRIBONUCLEOTIDE SYNTHASE;

EID: 0037307925     PISSN: 0959437X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0959-437X(03)00004-2     Document Type: Review
Times cited : (74)

References (80)
  • 3
    • 0035060081 scopus 로고    scopus 로고
    • Mismatch repair in correction of replication errors and processing of DNA damage
    • Aquilina G., Bignami M. Mismatch repair in correction of replication errors and processing of DNA damage. J. Cell Physiol. 187:2001;145-154.
    • (2001) J. Cell Physiol. , vol.187 , pp. 145-154
    • Aquilina, G.1    Bignami, M.2
  • 4
    • 0035886816 scopus 로고    scopus 로고
    • The selection for mismatch repair defects in hereditary nonpolyposis colorectal cancer: Revising the mutator hypothesis
    • Fishel R. The selection for mismatch repair defects in hereditary nonpolyposis colorectal cancer: revising the mutator hypothesis. Cancer Res. 61:2001;7369-7374.
    • (2001) Cancer Res. , vol.61 , pp. 7369-7374
    • Fishel, R.1
  • 5
    • 0035101436 scopus 로고    scopus 로고
    • DNA mismatch repair and cancer
    • Peltomaki P. DNA mismatch repair and cancer. Mutat. Res. 488:2001;77-85.
    • (2001) Mutat. Res. , vol.488 , pp. 77-85
    • Peltomaki, P.1
  • 8
    • 0037115934 scopus 로고    scopus 로고
    • Recent progress on the Ada response for inducible repair of DNA alkylation damage
    • Sedgwick B., Lindahl T. Recent progress on the Ada response for inducible repair of DNA alkylation damage. Oncogene. 21:2002;8886-8894.
    • (2002) Oncogene , vol.21 , pp. 8886-8894
    • Sedgwick, B.1    Lindahl, T.2
  • 9
    • 0037068312 scopus 로고    scopus 로고
    • CpG island hypermethylation and tumor suppressor genes: A booming present, a brighter future
    • Esteller M. CpG island hypermethylation and tumor suppressor genes: a booming present, a brighter future. Oncogene. 21:2002;5427-5440.
    • (2002) Oncogene , vol.21 , pp. 5427-5440
    • Esteller, M.1
  • 10
    • 0030004207 scopus 로고    scopus 로고
    • Cloning and sequencing a human homolog (hMYH) of the Escherichia coli mutY gene whose function is required for the repair of oxidative DNA damage
    • Slupska M.M., Baikalov C., Luther W.M., Chiang J.H., Wei Y.F., Miller J.H. Cloning and sequencing a human homolog (hMYH) of the Escherichia coli mutY gene whose function is required for the repair of oxidative DNA damage. J. Bacteriol. 178:1996;3885-3892.
    • (1996) J. Bacteriol. , vol.178 , pp. 3885-3892
    • Slupska, M.M.1    Baikalov, C.2    Luther, W.M.3    Chiang, J.H.4    Wei, Y.F.5    Miller, J.H.6
  • 11
    • 0036478899 scopus 로고    scopus 로고
    • Inherited variants of MYH associated with somatic G: C→T: A mutations in colorectal tumors
    • Describes the identification of a compound heterozygous mutation in the MYH gene in three affected members of a multiple colorectal adenoma syndrome family
    • Al-Tassan N., Chmiel N.H., Maynard J., Fleming N., Livingston A.L., Williams G.T., Hodges A.K., Davies D.R., David S.S., Sampson J.R.et al. Inherited variants of MYH associated with somatic G: C→T: A mutations in colorectal tumors Nat. Genet. 30:2002;227-232 Describes the identification of a compound heterozygous mutation in the MYH gene in three affected members of a multiple colorectal adenoma syndrome family.
    • (2002) Nat. Genet. , vol.30 , pp. 227-232
    • Al-Tassan, N.1    Chmiel, N.H.2    Maynard, J.3    Fleming, N.4    Livingston, A.L.5    Williams, G.T.6    Hodges, A.K.7    Davies, D.R.8    David, S.S.9    Sampson, J.R.10
  • 12
    • 0036848267 scopus 로고    scopus 로고
    • Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G: C→T: A mutations
    • ••], the authors identified seven further unrelated patients with >100 colorectal adenomas with biallelic germline mutations in MYH. The colorectal tumours from affected individuals displayed a significant excess of somatic G: C→T: A mutations in the APC gene. These findings confirm the role of MYH in colorectal adenoma and carcinoma predisposition
    • ••], the authors identified seven further unrelated patients with >100 colorectal adenomas with biallelic germline mutations in MYH. The colorectal tumours from affected individuals displayed a significant excess of somatic G: C→T: A mutations in the APC gene. These findings confirm the role of MYH in colorectal adenoma and carcinoma predisposition.
    • (2002) Hum Mol. Genet , vol.11 , pp. 2961-2967
    • Jones, S.1    Emmerson, P.2    Maynard, J.3    Best, J.M.4    Jordan, S.5    Williams, G.T.6    Sampson, J.R.7    Cheadle, J.P.8
  • 13
    • 0033575886 scopus 로고    scopus 로고
    • The thymine glycosylase MBD4 can bind to the product of deamination at methylated CpG sites
    • Hendrich B., Hardeland U., Ng H.H., Jiricny J., Bird A. The thymine glycosylase MBD4 can bind to the product of deamination at methylated CpG sites. Nature. 401:1999;301-304.
    • (1999) Nature , vol.401 , pp. 301-304
    • Hendrich, B.1    Hardeland, U.2    Ng, H.H.3    Jiricny, J.4    Bird, A.5
  • 14
    • 0033777253 scopus 로고    scopus 로고
    • Investigation of the substrate spectrum of the human mismatch-specific DNA N-glycosylase MED1 (MBD4): Fundamental role of the catalytic domain
    • •] describe the identification of the thymine/uracil DNA-glycosylase activity of MBD4 (MED1). These studies showed that the enzyme consisted of two domains, methylated DNA binding domain and an endonuclease domain, both of which are functional. These findings implicated MBD4 (MED1) in the processing of G/T mispairs arising through the deamination of 5-methylcytosine
    • •] describe the identification of the thymine/uracil DNA-glycosylase activity of MBD4 (MED1). These studies showed that the enzyme consisted of two domains, methylated DNA binding domain and an endonuclease domain, both of which are functional. These findings implicated MBD4 (MED1) in the processing of G/T mispairs arising through the deamination of 5-methylcytosine.
    • (2000) J. Cell Physiol. , vol.185 , pp. 473-480
    • Petronzelli, F.1    Riccio, A.2    Markham, G.D.3    Seeholzer, S.H.4    Genuardi, M.5    Karbowski, M.6    Yeung, A.T.7    Matsumoto, Y.8    Bellacosa, A.9
  • 15
    • 0037135130 scopus 로고    scopus 로고
    • Enhanced CpG mutability and tumorigenesis in MBD4-deficient mice
    • Min/- mouse) leads to a substantial increase in the frequency of polyps that is linked to an increase in C to T transition mutations in the Apc gene. This confirms that MBD4 is indeed responsible for the repair of G/T mispairs arising through 5-methylcytosine deamination and links these events to polyp formation through the mutation of the Apc tumor suppressor gene
    • Min/- mouse) leads to a substantial increase in the frequency of polyps that is linked to an increase in C to T transition mutations in the Apc gene. This confirms that MBD4 is indeed responsible for the repair of G/T mispairs arising through 5-methylcytosine deamination and links these events to polyp formation through the mutation of the Apc tumor suppressor gene.
    • (2002) Science , vol.297 , pp. 403-405
    • Millar, C.B.1    Guy, J.2    Sansom, O.J.3    Selfridge, J.4    MacDougall, E.5    Hendrich, B.6    Keightley, P.D.7    Bishop, S.M.8    Clarke, A.R.9    Bird, A.10
  • 17
    • 0035850251 scopus 로고    scopus 로고
    • Molecular mechanisms of DNA mismatch repair
    • Hsieh P. Molecular mechanisms of DNA mismatch repair. Mutat. Res. 486:2001;71-87.
    • (2001) Mutat. Res. , vol.486 , pp. 71-87
    • Hsieh, P.1
  • 19
    • 0035503172 scopus 로고    scopus 로고
    • The distinct spectra of tumor-associated Apc mutations in mismatch repair-deficient Apc1638N mice define the roles of MSH3 and MSH6 in DNA repair and intestinal tumorigenesis
    • Shows that the wt copy of the Apc gene in MMR-deficient animals is inactivated by mutations rather than the usual LOH. This work demonstrates that the mode of inactivation of the Apc tumor suppressor gene in MMR-deficient tumors is different from the mode observed in sporadic tumors
    • Kuraguchi M., Yang K., Wong E., Avdievich E., Fan K., Kolodner R.D., Lipkin M., Brown A.M., Kucherlapati R., Edelmann W. The distinct spectra of tumor-associated Apc mutations in mismatch repair-deficient Apc1638N mice define the roles of MSH3 and MSH6 in DNA repair and intestinal tumorigenesis. Cancer Res. 61:2001;7934-7942 Shows that the wt copy of the Apc gene in MMR-deficient animals is inactivated by mutations rather than the usual LOH. This work demonstrates that the mode of inactivation of the Apc tumor suppressor gene in MMR-deficient tumors is different from the mode observed in sporadic tumors.
    • (2001) Cancer Res. , vol.61 , pp. 7934-7942
    • Kuraguchi, M.1    Yang, K.2    Wong, E.3    Avdievich, E.4    Fan, K.5    Kolodner, R.D.6    Lipkin, M.7    Brown, A.M.8    Kucherlapati, R.9    Edelmann, W.10
  • 23
    • 0032514709 scopus 로고    scopus 로고
    • The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations
    • Flores-Rozas H., Kolodner R.D. The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations. Proc. Natl. Acad. Sci. U.S.A. 95:1998;12404-12409.
    • (1998) Proc. Natl. Acad. Sci. U.S.A. , vol.95 , pp. 12404-12409
    • Flores-Rozas, H.1    Kolodner, R.D.2
  • 25
    • 0035039417 scopus 로고    scopus 로고
    • Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers
    • Lipkin S.M., Wang V., Stoler D.L., Anderson G.R., Kirsch I., Hadley D., Lynch H.T., Collins F.S. Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers. Hum. Mutat. 17:2001;389-396.
    • (2001) Hum. Mutat. , vol.17 , pp. 389-396
    • Lipkin, S.M.1    Wang, V.2    Stoler, D.L.3    Anderson, G.R.4    Kirsch, I.5    Hadley, D.6    Lynch, H.T.7    Collins, F.S.8
  • 27
    • 0037066720 scopus 로고    scopus 로고
    • Human exonuclease I is required for 5′ and 3′ mismatch repair
    • Demonstration of the requirement for EXO1 in human cell-free MMR. Interestingly, the polypeptide, rather than its enzymatic activity, appeared to be required for 3′ to 5′ repair
    • Genschel J., Bazemore L.R., Modrich P. Human exonuclease I is required for 5′ and 3′ mismatch repair. J. Biol. Chem. 277:2002;13302-13311 Demonstration of the requirement for EXO1 in human cell-free MMR. Interestingly, the polypeptide, rather than its enzymatic activity, appeared to be required for 3′ to 5′ repair.
    • (2002) J. Biol. Chem. , vol.277 , pp. 13302-13311
    • Genschel, J.1    Bazemore, L.R.2    Modrich, P.3
  • 29
    • 0037099602 scopus 로고    scopus 로고
    • A hereditary nonpolyposis colorectal carcinoma case associated with hypermethylation of the MLH1 gene in normal tissue and loss of heterozygosity of the unmethylated allele in the resulting microsatellite instability-high tumor
    • Gazzoli I., Loda M., Garber J., Syngal S., Kolodner R.D. A hereditary nonpolyposis colorectal carcinoma case associated with hypermethylation of the MLH1 gene in normal tissue and loss of heterozygosity of the unmethylated allele in the resulting microsatellite instability-high tumor. Cancer Res. 62:2002;3925-3928 The authors describe the identification of an HNPCC patient who appeared to be free of mutations in the MMR genes. However, one allele of hMLH1 was shown to be silenced by methylation in his lymphocytes, and the tumor appeared to have lost the wild type hMLH1 allele.
    • (2002) Cancer Res. , vol.62 , pp. 3925-3928
    • Gazzoli, I.1    Loda, M.2    Garber, J.3    Syngal, S.4    Kolodner, R.D.5
  • 31
    • 0033065150 scopus 로고    scopus 로고
    • Effect of hMSH6 cDNA expression on the phenotype of mismatch repair-deficient colon cancer cell line HCT15
    • Lettieri T., Marra G., Aquilina G., Bignami M., Crompton N.E., Palombo F., Jiricny J. Effect of hMSH6 cDNA expression on the phenotype of mismatch repair-deficient colon cancer cell line HCT15. Carcinogenesis. 20:1999;373-382.
    • (1999) Carcinogenesis , vol.20 , pp. 373-382
    • Lettieri, T.1    Marra, G.2    Aquilina, G.3    Bignami, M.4    Crompton, N.E.5    Palombo, F.6    Jiricny, J.7
  • 32
    • 0037171943 scopus 로고    scopus 로고
    • Methylation tolerance in mismatch repair proficient cells with low MSH2 protein level
    • 2/M checkpoint triggered by DNA damage requires more MMR protein molecules to signal to the apoptotic machinery
    • 2/M checkpoint triggered by DNA damage requires more MMR protein molecules to signal to the apoptotic machinery.
    • (2002) Oncogene , vol.21 , pp. 2873-2879
    • Claij, N.1    Te Riele, H.2
  • 33
    • 0034007120 scopus 로고    scopus 로고
    • Heterozygous DNA mismatch repair gene PMS2-knockout mice are susceptible to intestinal tumor induction with N-methyl-N-nitrosourea
    • Qin X., Shibata D., Gerson S.L. Heterozygous DNA mismatch repair gene PMS2-knockout mice are susceptible to intestinal tumor induction with N-methyl-N-nitrosourea. Carcinogenesis. 21:2000;833-838.
    • (2000) Carcinogenesis , vol.21 , pp. 833-838
    • Qin, X.1    Shibata, D.2    Gerson, S.L.3
  • 34
    • 0032723363 scopus 로고    scopus 로고
    • Signaling mismatch repair in cancer
    • Fishel R. Signaling mismatch repair in cancer. Nat. Med. 5:1999;1239-1241.
    • (1999) Nat. Med. , vol.5 , pp. 1239-1241
    • Fishel, R.1
  • 36
    • 0037064053 scopus 로고    scopus 로고
    • ATM is activated in response to N-methyl-N′-nitro-N-nitrosoguanidine-induced DNA alkylation
    • Adamson A.W., Kim W.J., Shangary S., Baskaran R., Brown K.D. ATM is activated in response to N-methyl-N′-nitro-N-nitrosoguanidine-induced DNA alkylation. J. Biol. Chem. 277:2002;38222-38229.
    • (2002) J. Biol. Chem. , vol.277 , pp. 38222-38229
    • Adamson, A.W.1    Kim, W.J.2    Shangary, S.3    Baskaran, R.4    Brown, K.D.5
  • 40
    • 0030294633 scopus 로고    scopus 로고
    • Drug-related killings: A case of mistaken identity
    • Karran P., Bignami M. Drug-related killings: a case of mistaken identity. Chem. Biol. 3:1996;875-879.
    • (1996) Chem. Biol. , vol.3 , pp. 875-879
    • Karran, P.1    Bignami, M.2
  • 43
    • 19244370208 scopus 로고    scopus 로고
    • Inactivation of the DNA repair gene O6-methylguanine-DNA methyltransferase by promoter hypermethylation is associated with G to A mutations in K-ras in colorectal tumorigenesis
    • Esteller M., Toyota M., Sanchez-Cespedes M., Capella G., Peinado M.A., Watkins D.N., Issa J.P., Sidransky D., Baylin S.B., Herman J.G. Inactivation of the DNA repair gene O6-methylguanine-DNA methyltransferase by promoter hypermethylation is associated with G to A mutations in K-ras in colorectal tumorigenesis. Cancer Res. 60:2000;2368-2371.
    • (2000) Cancer Res. , vol.60 , pp. 2368-2371
    • Esteller, M.1    Toyota, M.2    Sanchez-Cespedes, M.3    Capella, G.4    Peinado, M.A.5    Watkins, D.N.6    Issa, J.P.7    Sidransky, D.8    Baylin, S.B.9    Herman, J.G.10
  • 44
    • 0035874892 scopus 로고    scopus 로고
    • Promoter hypermethylation of the DNA repair gene O(6)-methylguanine-DNA methyltransferase is associated with the presence of G:C to A:T transition mutations in p53 in human colorectal tumorigenesis
    • •] describe cytosine methylation-induced silencing of the MGMT promoter in human malignancy and demonstrate the mutagenic effects of this event on two important genes, p53 and K-ras
    • •] describe cytosine methylation-induced silencing of the MGMT promoter in human malignancy and demonstrate the mutagenic effects of this event on two important genes, p53 and K-ras.
    • (2001) Cancer Res. , vol.61 , pp. 4689-4692
    • Esteller, M.1    Risques, R.A.2    Toyota, M.3    Capella, G.4    Moreno, V.5    Peinado, M.A.6    Baylin, S.B.7    Herman, J.G.8
  • 45
    • 0033955906 scopus 로고    scopus 로고
    • A defect in a single allele of the Mlh1 gene causes dissociation of the killing and tumorigenic actions of an alkylating carcinogen in methyltransferase-deficient mice
    • Kawate H., Itoh R., Sakumi K., Nakabeppu Y., Tsuzuki T., Ide F., Ishikawa T., Noda T., Nawata H., Sekiguchi M. A defect in a single allele of the Mlh1 gene causes dissociation of the killing and tumorigenic actions of an alkylating carcinogen in methyltransferase-deficient mice. Carcinogenesis. 21:2000;301-305.
    • (2000) Carcinogenesis , vol.21 , pp. 301-305
    • Kawate, H.1    Itoh, R.2    Sakumi, K.3    Nakabeppu, Y.4    Tsuzuki, T.5    Ide, F.6    Ishikawa, T.7    Noda, T.8    Nawata, H.9    Sekiguchi, M.10
  • 47
    • 0032100860 scopus 로고    scopus 로고
    • Mammalian base excision repair and DNA polymerase β
    • Wilson S.H. Mammalian base excision repair and DNA polymerase β Mutat. Res. 407:1998;203-215.
    • (1998) Mutat. Res. , vol.407 , pp. 203-215
    • Wilson, S.H.1
  • 50
    • 0035421186 scopus 로고    scopus 로고
    • Excision of deaminated cytosine from the vertebrate genome: Role of the SMUG1 uracil-DNA glycosylase
    • Nilsen H., Haushalter K.A., Robins P., Barnes D.E., Verdine G.L., Lindahl T. Excision of deaminated cytosine from the vertebrate genome: role of the SMUG1 uracil-DNA glycosylase. EMBO J. 20:2001;4278-4286.
    • (2001) EMBO J. , vol.20 , pp. 4278-4286
    • Nilsen, H.1    Haushalter, K.A.2    Robins, P.3    Barnes, D.E.4    Verdine, G.L.5    Lindahl, T.6
  • 51
    • 0037112668 scopus 로고    scopus 로고
    • Human DNA glycosylases of the bacterial Fpg/MutM superfamily: An alternative pathway for the repair of 8-oxoguanine and other oxidation products in DNA
    • Morland I., Rolseth V., Luna L., Rognes T., Bjoras M., Seeberg E. Human DNA glycosylases of the bacterial Fpg/MutM superfamily: an alternative pathway for the repair of 8-oxoguanine and other oxidation products in DNA. Nucleic Acids Res. 30:2002;4926-4936.
    • (2002) Nucleic Acids Res. , vol.30 , pp. 4926-4936
    • Morland, I.1    Rolseth, V.2    Luna, L.3    Rognes, T.4    Bjoras, M.5    Seeberg, E.6
  • 52
    • 0025314841 scopus 로고
    • Mismatch-specific thymine DNA glycosylase and DNA polymerase β mediate the correction of G.T mispairs in nuclear extracts from human cells
    • Wiebauer K., Jiricny J. Mismatch-specific thymine DNA glycosylase and DNA polymerase β mediate the correction of G.T mispairs in nuclear extracts from human cells. Proc. Natl. Acad. Sci. U.S.A. 87:1990;5842-5845.
    • (1990) Proc. Natl. Acad. Sci. U.S.A. , vol.87 , pp. 5842-5845
    • Wiebauer, K.1    Jiricny, J.2
  • 56
    • 0035111895 scopus 로고    scopus 로고
    • Recent progress in the biology, chemistry and structural biology of DNA glycosylases
    • Scharer O.D., Jiricny J. Recent progress in the biology, chemistry and structural biology of DNA glycosylases. Bioessays. 23:2001;270-281.
    • (2001) Bioessays , vol.23 , pp. 270-281
    • Scharer, O.D.1    Jiricny, J.2
  • 57
    • 0035393812 scopus 로고    scopus 로고
    • HMYH cell cycle-dependent expression, subcellular localization and association with replication foci: Evidence suggesting replication- coupled repair of adenine: 8-oxoguanine mispairs
    • Boldogh I., Milligan D., Lee M.S., Bassett H., Lloyd R.S., McCullough A.K. hMYH cell cycle-dependent expression, subcellular localization and association with replication foci: evidence suggesting replication- coupled repair of adenine: 8-oxoguanine mispairs. Nucleic Acids Res. 29:2001;2802-2809.
    • (2001) Nucleic Acids Res. , vol.29 , pp. 2802-2809
    • Boldogh, I.1    Milligan, D.2    Lee, M.S.3    Bassett, H.4    Lloyd, R.S.5    McCullough, A.K.6
  • 58
    • 0037192812 scopus 로고    scopus 로고
    • Human MutY homolog, a DNA glycosylase involved in base excision repair, physically and functionally interacts with mismatch repair proteins human MutS homolog 2/human MutS homolog 6
    • Gu Y., Parker A., Wilson T.M., Bai H., Chang D.Y., Lu A.L. Human MutY homolog, a DNA glycosylase involved in base excision repair, physically and functionally interacts with mismatch repair proteins human MutS homolog 2/human MutS homolog 6. J. Biol. Chem. 277:2002;11135-11142.
    • (2002) J. Biol. Chem. , vol.277 , pp. 11135-11142
    • Gu, Y.1    Parker, A.2    Wilson, T.M.3    Bai, H.4    Chang, D.Y.5    Lu, A.L.6
  • 59
    • 0035899332 scopus 로고    scopus 로고
    • Extensive characterization of genetic alterations in a series of human colorectal cancer cell lines
    • Gayet J., Zhou X.P., Duval A., Rolland S., Hoang J.M., Cottu P., Hamelin R. Extensive characterization of genetic alterations in a series of human colorectal cancer cell lines. Oncogene. 20:2001;5025-5032.
    • (2001) Oncogene , vol.20 , pp. 5025-5032
    • Gayet, J.1    Zhou, X.P.2    Duval, A.3    Rolland, S.4    Hoang, J.M.5    Cottu, P.6    Hamelin, R.7
  • 62
    • 0029101616 scopus 로고
    • Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer
    • de Wind N., Dekker M., Berns A., Radman M., te Riele H. Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer. Cell. 82:1995;321-330.
    • (1995) Cell , vol.82 , pp. 321-330
    • De Wind, N.1    Dekker, M.2    Berns, A.3    Radman, M.4    Te Riele, H.5
  • 79
    • 0031600949 scopus 로고    scopus 로고
    • No female embryonic lethality in mice nullizygous for Msh2 and p53, [letter; Comment]
    • Toft N.J., Arends M.J., Wyllie A.H., Clarke A.R. No female embryonic lethality in mice nullizygous for Msh2 and p53, [letter; comment]. Nat. Genet. 18:1998;17.
    • (1998) Nat. Genet. , vol.18 , pp. 17
    • Toft, N.J.1    Arends, M.J.2    Wyllie, A.H.3    Clarke, A.R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.