메뉴 건너뛰기




Volumn 41, Issue 4, 2003, Pages 452-461

The use of denaturing high-performance liquid chromatography (DHPLC) for the analysis of genetic variations: Impact for diagnostics and pharmacogenetics

Author keywords

Denaturing high performance liquid chromatography (DHPLC); Genotyping; Mutation detection; Mutation screening; Pharmacogenetics; Single nucleotide polymorphism (SNP)

Indexed keywords

DIHYDROPYRIDINE; DNA; FLUOROURACIL; IMMUNOSUPPRESSIVE AGENT; MITOCHONDRIAL DNA; RNA; THIOPURINE METHYLTRANSFERASE;

EID: 0038059078     PISSN: 14346621     EISSN: None     Source Type: Journal    
DOI: 10.1515/CCLM.2003.068     Document Type: Review
Times cited : (56)

References (82)
  • 4
    • 0035816183 scopus 로고    scopus 로고
    • Use of cDNA microarrays to analyze dioxin-induced changes in human liver gene expression
    • Frueh FW, Hayashibara KC, Brown PO, Whitlock JP Jr. Use of cDNA microarrays to analyze dioxin-induced changes in human liver gene expression. Toxicol Lett 2001; 122:189-203.
    • (2001) Toxicol. Lett. , vol.122 , pp. 189-203
    • Frueh, F.W.1    Hayashibara, K.C.2    Brown, P.O.3    Whitlock J.P., Jr.4
  • 5
    • 0035865322 scopus 로고    scopus 로고
    • A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
    • Sachidanandam R, Weissman D, Schmidt SC, Kakol JM, Stein LD, Marth G, et al. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 2001; 409:928-33.
    • (2001) Nature , vol.409 , pp. 928-933
    • Sachidanandam, R.1    Weissman, D.2    Schmidt, S.C.3    Kakol, J.M.4    Stein, L.D.5    Marth, G.6
  • 6
    • 0035654137 scopus 로고    scopus 로고
    • Accessing genetic variation: Genotyping single nucleotide polymorphisms
    • Syvanen AC. Accessing genetic variation: genotyping single nucleotide polymorphisms. Nat Rev Genet 2001; 2: 930-42.
    • (2001) Nat. Rev. Genet. , vol.2 , pp. 930-942
    • Syvanen, A.C.1
  • 7
    • 0027980442 scopus 로고
    • Human immunodeficiency virus type 1 evolution in vivo tracked by DNA heteroduplex mobility assays
    • Delwart EL, Sheppard HW, Walker BD, Goudsmit J, Mullins JI. Human immunodeficiency virus type 1 evolution in vivo tracked by DNA heteroduplex mobility assays. J Virol 1994; 68:6672-83.
    • (1994) J. Virol. , vol.68 , pp. 6672-6683
    • Delwart, E.L.1    Sheppard, H.W.2    Walker, B.D.3    Goudsmit, J.4    Mullins, J.I.5
  • 8
    • 0031214224 scopus 로고    scopus 로고
    • Tracking changes in HIV-1 envelope quasispecies using DNA heteroduplex analysis
    • Delwart EL, Gordon CJ. Tracking changes in HIV-1 envelope quasispecies using DNA heteroduplex analysis. Methods 1997; 12:348-54.
    • (1997) Methods , vol.12 , pp. 348-354
    • Delwart, E.L.1    Gordon, C.J.2
  • 10
    • 0011926452 scopus 로고    scopus 로고
    • Nucleic acid separation on alkylated nonporous polymer beads
    • US patent 5,585,236
    • Bonn G, Huber C, Oefner R Nucleic acid separation on alkylated nonporous polymer beads. US patent 5,585,236. 1996.
    • (1996)
    • Bonn, G.1    Huber, C.2    Oefner, R.3
  • 11
    • 0034999807 scopus 로고    scopus 로고
    • Denaturing high-performance liquid chromatography: A review
    • Xiao W, Oefner PJ. Denaturing high-performance liquid chromatography: a review. Hum Mutat 2001; 17:439-74.
    • (2001) Hum. Mutat. , vol.17 , pp. 439-474
    • Xiao, W.1    Oefner, P.J.2
  • 13
    • 0032496188 scopus 로고    scopus 로고
    • Quantitative analysis of gene expression by ion-pair high-performance liquid chromatography
    • Doris PA, Oefner PJ, Chilton BS, Hayward-Lester A. Quantitative analysis of gene expression by ion-pair high-performance liquid chromatography. J Chromatogr A 1998; 806:47-60.
    • (1998) J. Chromatogr. A , vol.806 , pp. 47-60
    • Doris, P.A.1    Oefner, P.J.2    Chilton, B.S.3    Hayward-Lester, A.4
  • 14
    • 0035220156 scopus 로고    scopus 로고
    • Purification methods for preparing polymerase chain reaction products for capillary electrophoresis analysis
    • Devaney JM, Marino MA. Purification methods for preparing polymerase chain reaction products for capillary electrophoresis analysis. Methods Mol Biol 2001; 162:43-9.
    • (2001) Methods Mol. Biol. , vol.162 , pp. 43-49
    • Devaney, J.M.1    Marino, M.A.2
  • 15
    • 16044370232 scopus 로고    scopus 로고
    • Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2 + channel gene CACNL1A4
    • Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SM, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2 + channel gene CACNL1A4. Cell 1996; 87:543-52.
    • (1996) Cell , vol.87 , pp. 543-552
    • Ophoff, R.A.1    Terwindt, G.M.2    Vergouwe, M.N.3    van Eijk, R.4    Oefner, P.J.5    Hoffman, S.M.6
  • 16
    • 0030660620 scopus 로고    scopus 로고
    • Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography
    • Underhill PA, Jin L, Lin AA, Mehdi SQ, Jenkins T, Vollrath D, et al. Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography. Genome Res 1997; 7:996-1005.
    • (1997) Genome Res. , vol.7 , pp. 996-1005
    • Underhill, P.A.1    Jin, L.2    Lin, A.A.3    Mehdi, S.Q.4    Jenkins, T.5    Vollrath, D.6
  • 18
    • 0035209825 scopus 로고    scopus 로고
    • Denaturing high pressure liquid chromatography (DHPLC) for the analysis of somatic p53 mutations
    • Keller G, Hartmann A, Mueller J, Hofler H. Denaturing high pressure liquid chromatography (DHPLC) for the analysis of somatic p53 mutations. Lab Invest 2001; 81:1735-7.
    • (2001) Lab. Invest. , vol.81 , pp. 1735-1737
    • Keller, G.1    Hartmann, A.2    Mueller, J.3    Hofler, H.4
  • 20
    • 0033572622 scopus 로고    scopus 로고
    • Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations
    • Wagner T, Stoppa-Lyonnet D, Fleischmann E, Muhr D, Pages S, Sandberg T, et al. Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations. Genomics 1999; 62:369-76.
    • (1999) Genomics , vol.62 , pp. 369-376
    • Wagner, T.1    Stoppa-Lyonnet, D.2    Fleischmann, E.3    Muhr, D.4    Pages, S.5    Sandberg, T.6
  • 21
    • 0032764964 scopus 로고    scopus 로고
    • A comparison of BRCA1 mutation analysis by direct sequencing, SSCP and DHPLC
    • Gross E, Arnold N, Goette J, Schwarz-Boeger U, Kiechle M. A comparison of BRCA1 mutation analysis by direct sequencing, SSCP and DHPLC. Hum Genet 1999; 105:72-8.
    • (1999) Hum. Genet. , vol.105 , pp. 72-78
    • Gross, E.1    Arnold, N.2    Goette, J.3    Schwarz-Boeger, U.4    Kiechle, M.5
  • 22
    • 0035726850 scopus 로고    scopus 로고
    • Detection of sequence variations in the adenomatous polyposis coli (APC) gene using denaturing high-performance liquid chromatography
    • Wu G, Wu W, Hegde M, Fawkner M, Chong B, Love D, et al. Detection of sequence variations in the adenomatous polyposis coli (APC) gene using denaturing high-performance liquid chromatography. Genet Test 2001; 5:281-90.
    • (2001) Genet. Test , vol.5 , pp. 281-290
    • Wu, G.1    Wu, W.2    Hegde, M.3    Fawkner, M.4    Chong, B.5    Love, D.6
  • 23
    • 0036671928 scopus 로고    scopus 로고
    • Sequence variation and haplotype structure at the human HFE locus
    • Toomajian C, Kreitman M. Sequence variation and haplotype structure at the human HFE locus. Genetics 2002; 161:1609-23.
    • (2002) Genetics , vol.161 , pp. 1609-1623
    • Toomajian, C.1    Kreitman, M.2
  • 24
    • 0034859463 scopus 로고    scopus 로고
    • Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC
    • Le Gac G, Mura C, Ferec C. Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC. Clin Chem 2001; 47:1633-40.
    • (2001) Clin. Chem. , vol.47 , pp. 1633-1640
    • Le Gac, G.1    Mura, C.2    Ferec, C.3
  • 25
    • 2942523954 scopus 로고    scopus 로고
    • Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing
    • Bennett RR, Dunnen J, O'Brien KF, Darras BT, Kunkel LM. Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing. BMC Genet 2001; 2:17.
    • (2001) BMC Genet. , vol.2 , pp. 17
    • Bennett, R.R.1    Dunnen, J.2    O'Brien, K.F.3    Darras, B.T.4    Kunkel, L.M.5
  • 27
    • 0035020939 scopus 로고    scopus 로고
    • Complete and rapid scanning of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by denaturing high-performance liquid chromatography (D-HPLC): Major implications for genetic counselling
    • Le Marechal C, Audrezet MP, Quere I, Raguenes O, Langonne S, Ferec C. Complete and rapid scanning of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by denaturing high-performance liquid chromatography (D-HPLC): major implications for genetic counselling. Hum Genet 2001; 108:290-8.
    • (2001) Hum. Genet. , vol.108 , pp. 290-298
    • Le Marechal, C.1    Audrezet, M.P.2    Quere, I.3    Raguenes, O.4    Langonne, S.5    Ferec, C.6
  • 28
    • 0033646567 scopus 로고    scopus 로고
    • Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: Identification of several novel mutations and polymorphisms
    • Buyse IM, Fang P, Hoon KT, Amir RE, Zoghbi HY, Roa BB. Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms. Am J Hum Genet 2000; 67:1428-36.
    • (2000) Am. J. Hum. Genet. , vol.67 , pp. 1428-1436
    • Buyse, I.M.1    Fang, P.2    Hoon, K.T.3    Amir, R.E.4    Zoghbi, H.Y.5    Roa, B.B.6
  • 32
    • 0036387074 scopus 로고    scopus 로고
    • Rapid identification of Wilson's disease carriers by denaturing high-performance liquid chromatography
    • Weirich G, Cabras AD, Serra S, Coni PP, Nurchi AM, Faa G, et al. Rapid identification of Wilson's disease carriers by denaturing high-performance liquid chromatography. Prev Med 2002; 35:278-84.
    • (2002) Prev. Med. , vol.35 , pp. 278-284
    • Weirich, G.1    Cabras, A.D.2    Serra, S.3    Coni, P.P.4    Nurchi, A.M.5    Faa, G.6
  • 33
    • 0036341187 scopus 로고    scopus 로고
    • Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practice
    • Halliday DJ, Hutchinson S, Lonie L, Hurst JA, Firth H, Handford PA, et al. Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practice. J Med Genet 2002; 39:589-93.
    • (2002) J. Med. Genet. , vol.39 , pp. 589-593
    • Halliday, D.J.1    Hutchinson, S.2    Lonie, L.3    Hurst, J.A.4    Firth, H.5    Handford, P.A.6
  • 34
    • 0033501118 scopus 로고    scopus 로고
    • Superiority of denaturing high performance liquid chromatography over single-stranded conformation and conformation-sensitive gel electrophoresis for mutation detection in TSC2
    • Choy YS, Dabora SL, Hall F, Ramesh V, Niida Y, Franz D, et al. Superiority of denaturing high performance liquid chromatography over single-stranded conformation and conformation-sensitive gel electrophoresis for mutation detection in TSC2. Ann Hum Genet 1999; 63(Pt 5):383-91.
    • (1999) Ann. Hum. Genet. , vol.63 , Issue.PART 5 , pp. 383-391
    • Choy, Y.S.1    Dabora, S.L.2    Hall, F.3    Ramesh, V.4    Niida, Y.5    Franz, D.6
  • 35
    • 0036511614 scopus 로고    scopus 로고
    • Comparison of SSCP and DHPLC for the detection of LDLR mutations in a New Zealand cohort
    • Bunn CF, Lintott CJ, Scott RS, George PM. Comparison of SSCP and DHPLC for the detection of LDLR mutations in a New Zealand cohort. Hum Mutat 2002; 19:311.
    • (2002) Hum. Mutat. , vol.19 , pp. 311
    • Bunn, C.F.1    Lintott, C.J.2    Scott, R.S.3    George, P.M.4
  • 36
    • 18244377693 scopus 로고    scopus 로고
    • Interpreting epidemiological research: Blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1
    • Eng C, Brody LC, Wagner TM, Devilee P, Vijg J, Szabo C, et al. Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1. J Med Genet 2001; 38:824-33.
    • (2001) J. Med. Genet. , vol.38 , pp. 824-833
    • Eng, C.1    Brody, L.C.2    Wagner, T.M.3    Devilee, P.4    Vijg, J.5    Szabo, C.6
  • 37
    • 0036043220 scopus 로고    scopus 로고
    • The genetic basis of variability in drug responses
    • Roden DM, George AL Jr. The genetic basis of variability in drug responses. Nat Rev Drug Discov 2002; 1:37-44.
    • (2002) Nat. Rev. Drug Discov. , vol.1 , pp. 37-44
    • Roden, D.M.1    George A.L., Jr.2
  • 38
    • 33947223647 scopus 로고    scopus 로고
    • Pharmacogenomics: The promise of personalized medicine
    • [review]
    • Mancinelli L, Cronin M, Sadee W. Pharmacogenomics: the promise of personalized medicine [review]. AAPS Pharm-Sci 2000; 2:E4.
    • (2000) AAPS Pharm-Sci. , vol.2
    • Mancinelli, L.1    Cronin, M.2    Sadee, W.3
  • 39
    • 0033569516 scopus 로고    scopus 로고
    • Pharmacogenomics: Translating functional genomics into rational therapeutics
    • Evans WE, Relling MV. Pharmacogenomics: translating functional genomics into rational therapeutics. Science 1999; 286:487-91.
    • (1999) Science , vol.286 , pp. 487-491
    • Evans, W.E.1    Relling, M.V.2
  • 40
    • 0034638766 scopus 로고    scopus 로고
    • Pharmacogenetics and adverse drug reactions
    • Meyer UA. Pharmacogenetics and adverse drug reactions. Lancet 2000; 356:1667-71.
    • (2000) Lancet , vol.356 , pp. 1667-1671
    • Meyer, U.A.1
  • 42
    • 0034745462 scopus 로고    scopus 로고
    • High-throughput genotyping of thiopurine S-methyltransferase by denaturing HPLC
    • Schaeffeler E, Lang T, Zanger UM, Eichelbaum M, Schwab M. High-throughput genotyping of thiopurine S-methyltransferase by denaturing HPLC. Clin Chem 2001; 47: 548-55.
    • (2001) Clin. Chem. , vol.47 , pp. 548-555
    • Schaeffeler, E.1    Lang, T.2    Zanger, U.M.3    Eichelbaum, M.4    Schwab, M.5
  • 43
    • 0035969941 scopus 로고    scopus 로고
    • The use of denaturing high-pressure liquid chromatography for the detection of mutations in thiopurine methyltransferase
    • Hall AG, Hamilton P, Minto L, Coulthard SA. The use of denaturing high-pressure liquid chromatography for the detection of mutations in thiopurine methyltransferase. J Biochem Biophys Methods 2001; 47:65-71.
    • (2001) J. Biochem. Biophys. Methods , vol.47 , pp. 65-71
    • Hall, A.G.1    Hamilton, P.2    Minto, L.3    Coulthard, S.A.4
  • 44
    • 0036629198 scopus 로고    scopus 로고
    • A high-throughput denaturing high-performance liquid chromatography method for the identification of variant alleles associated with dihydropyrimidine dehydrogenase deficiency
    • Ezzeldin H, Okamoto Y, Johnson MR, Diasio RB. A high-throughput denaturing high-performance liquid chromatography method for the identification of variant alleles associated with dihydropyrimidine dehydrogenase deficiency. Anal Biochem 2002; 306:63-73.
    • (2002) Anal. Biochem. , vol.306 , pp. 63-73
    • Ezzeldin, H.1    Okamoto, Y.2    Johnson, M.R.3    Diasio, R.B.4
  • 45
    • 0035040834 scopus 로고    scopus 로고
    • Pharmacogenetics and drug-induced arrhythmias
    • Roden DM. Pharmacogenetics and drug-induced arrhythmias. Cardiovasc Res 2001; 50:224-31.
    • (2001) Cardiovasc. Res. , vol.50 , pp. 224-231
    • Roden, D.M.1
  • 46
    • 0002853488 scopus 로고    scopus 로고
    • Pharmacogenomics, biomarkers, and the promise of personalized medicine
    • Kalow W, Meyer UA, Tyndale RF, editors. New York and Basel: Marcel Dekker, Inc
    • Silber MB, Pharmacogenomics, biomarkers, and the promise of personalized medicine. Kalow W, Meyer UA, Tyndale RF, editors. Pharmacogenomics. New York and Basel: Marcel Dekker, Inc., 2001:11-31.
    • (2001) Pharmacogenomics , pp. 11-31
    • Silber, M.B.1
  • 49
    • 0036353041 scopus 로고    scopus 로고
    • Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome
    • Wang Z, Li H, Moss AJ, Robinson J, Zareba W, Knilans T, et al. Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome. Mol Genet Metab 2002; 75:308-16.
    • (2002) Mol. Genet. Metab. , vol.75 , pp. 308-316
    • Wang, Z.1    Li, H.2    Moss, A.J.3    Robinson, J.4    Zareba, W.5    Knilans, T.6
  • 51
    • 0029383211 scopus 로고
    • Principles and methods for the analysis and purification of synthetic deoxyribonucleotides by high-performance liquid chromatography
    • Warren WJ, Vella G. Principles and methods for the analysis and purification of synthetic deoxyribonucleotides by high-performance liquid chromatography. Mol Biotechnol 1995; 4:179-99.
    • (1995) Mol. Biotechnol. , vol.4 , pp. 179-199
    • Warren, W.J.1    Vella, G.2
  • 52
    • 0035253584 scopus 로고    scopus 로고
    • Genotyping of two mutations in the HFE gene using single-base extension and high-performance liquid chromatography
    • Devaney JM, Pettit EL, Kaler SG, Vallone PM, Butler JM, Marino MA. Genotyping of two mutations in the HFE gene using single-base extension and high-performance liquid chromatography. Anal Chem 2001; 73:620-4.
    • (2001) Anal. Chem. , vol.73 , pp. 620-624
    • Devaney, J.M.1    Pettit, E.L.2    Kaler, S.G.3    Vallone, P.M.4    Butler, J.M.5    Marino, M.A.6
  • 53
    • 0035969948 scopus 로고    scopus 로고
    • Determination of SNP allele frequencies in pooled DNAs by primer extension genotyping and denaturing high-performance liquid chromatography
    • Giordano M, Mellai M, Hoogendoorn B, Momigliano-Richiardi P. Determination of SNP allele frequencies in pooled DNAs by primer extension genotyping and denaturing high-performance liquid chromatography. J Biochem Biophys Methods 2001; 47:101-10.
    • (2001) J. Biochem. Biophys. Methods , vol.47 , pp. 101-110
    • Giordano, M.1    Mellai, M.2    Hoogendoorn, B.3    Momigliano-Richiardi, P.4
  • 54
    • 17744380449 scopus 로고    scopus 로고
    • Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools
    • Hoogendoorn B, Norton N, Kirov G, Williams N, Hamshere ML, Spurlock G, et al. Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools. Hum Genet 2000; 107:488-93.
    • (2000) Hum. Genet. , vol.107 , pp. 488-493
    • Hoogendoorn, B.1    Norton, N.2    Kirov, G.3    Williams, N.4    Hamshere, M.L.5    Spurlock, G.6
  • 55
    • 0034011878 scopus 로고    scopus 로고
    • Comparative sequencing of the proneurotensin gene and association studies in schizophrenia
    • Austin J, Hoogendoorn B, Buckland P, Speight G, Cardno A, Bowen T, et al. Comparative sequencing of the proneurotensin gene and association studies in schizophrenia. Mol Psychiatry 2000; 5:208-12.
    • (2000) Mol. Psychiatry , vol.5 , pp. 208-212
    • Austin, J.1    Hoogendoorn, B.2    Buckland, P.3    Speight, G.4    Cardno, A.5    Bowen, T.6
  • 56
    • 0033016069 scopus 로고    scopus 로고
    • Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography
    • Hoogendoorn B, Owen MJ, Oefner PJ, Williams N, Austin J, O'Donovan MC. Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography. Hum Genet 1999; 104:89-93.
    • (1999) Hum. Genet. , vol.104 , pp. 89-93
    • Hoogendoorn, B.1    Owen, M.J.2    Oefner, P.J.3    Williams, N.4    Austin, J.5    O'Donovan, M.C.6
  • 57
    • 0037092985 scopus 로고    scopus 로고
    • A strategy for examining complex mixtures of deoxyoligonucleotides using ion-pair-reverse-phase high-performance liquid chromatography, matrix-assisted laser desorption ionization time-of-flight mass spectrometry, and informatics
    • Vallone PM, Devaney JM, Marino MA, Butler JM. A strategy for examining complex mixtures of deoxyoligonucleotides using ion-pair-reverse-phase high-performance liquid chromatography, matrix-assisted laser desorption ionization time-of-flight mass spectrometry, and informatics. Anal Biochem 2002; 304:257-65.
    • (2002) Anal. Biochem. , vol.304 , pp. 257-265
    • Vallone, P.M.1    Devaney, J.M.2    Marino, M.A.3    Butler, J.M.4
  • 58
    • 0036597653 scopus 로고    scopus 로고
    • Genetic detection and clinical applications in patients with hepatocellular carcinoma
    • Takeda S, Nakao A. Genetic detection and clinical applications in patients with hepatocellular carcinoma. Nippon Geka Gakkai Zasshi 2002; 103:472-5.
    • (2002) Nippon Geka Gakkai Zasshi , vol.103 , pp. 472-475
    • Takeda, S.1    Nakao, A.2
  • 59
    • 0036132775 scopus 로고    scopus 로고
    • Stool screening for colorectal cancer: Evolution from occult blood to molecular markers
    • Ahlquist DA, Shuber AP. Stool screening for colorectal cancer: evolution from occult blood to molecular markers. Clin Chim Acta 2002; 315:157-68.
    • (2002) Clin. Chim. Acta , vol.315 , pp. 157-168
    • Ahlquist, D.A.1    Shuber, A.P.2
  • 61
    • 0034537609 scopus 로고    scopus 로고
    • High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC)
    • Wolford JK, Blunt D, Ballecer C, Prochazka M. High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC). Hum Genet 2000; 107:483-7.
    • (2000) Hum. Genet. , vol.107 , pp. 483-487
    • Wolford, J.K.1    Blunt, D.2    Ballecer, C.3    Prochazka, M.4
  • 63
    • 0003635039 scopus 로고    scopus 로고
    • DNA chromatography
    • Weinheim, Germany: Wiley-VCH Verlag GmbH
    • Gjerde DT, Hanna CP, Hornby DP. DNA chromatography. Weinheim, Germany: Wiley-VCH Verlag GmbH, 2002.
    • (2002)
    • Gjerde, D.T.1    Hanna, C.P.2    Hornby, D.P.3
  • 64
    • 0038450528 scopus 로고    scopus 로고
    • Detection of low-level mutations using fluorescent heteroduplex DHPLC analysis
    • 93rd Annual Meeting of the American Association for Cancer Research, San Francisco, CA: AACR
    • Marino MA, Rudolph JG, McAndrew P, Legendre B, Breen JJ. Detection of low-level mutations using fluorescent heteroduplex DHPLC analysis. In: 93rd Annual Meeting of the American Association for Cancer Research, 2001. San Francisco, CA: AACR.
    • (2001)
    • Marino, M.A.1    Rudolph, J.G.2    McAndrew, P.3    Legendre, B.4    Breen, J.J.5
  • 65
    • 0033525773 scopus 로고    scopus 로고
    • Mitochondrial diseases in man and mouse
    • Wallace DC. Mitochondrial diseases in man and mouse. Science 1999; 283:1482-8.
    • (1999) Science , vol.283 , pp. 1482-1488
    • Wallace, D.C.1
  • 68
    • 0036280575 scopus 로고    scopus 로고
    • Rapid screening mitochondrial DNA mutation by using denaturing high-performance liquid chromatography
    • Liu MR, Pan KF, Li ZF, Wang Y, Deng DJ, Zhang L, et al. Rapid screening mitochondrial DNA mutation by using denaturing high-performance liquid chromatography. World J Gastroenterol 2002; 8:426-30.
    • (2002) World J. Gastroenterol. , vol.8 , pp. 426-430
    • Liu, M.R.1    Pan, K.F.2    Li, Z.F.3    Wang, Y.4    Deng, D.J.5    Zhang, L.6
  • 69
    • 0026708177 scopus 로고
    • Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
    • Li E, Bestor TH, Jaenisch R. Targeted mutation of the DNA methyltransferase gene results in embryonic lethality. Cell 1992; 69:915-26.
    • (1992) Cell , vol.69 , pp. 915-926
    • Li, E.1    Bestor, T.H.2    Jaenisch, R.3
  • 70
    • 0033615717 scopus 로고    scopus 로고
    • DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development
    • Okano M, Bell DW, Haber DA, Li E. DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. Cell 1999; 99: 247-57.
    • (1999) Cell , vol.99 , pp. 247-257
    • Okano, M.1    Bell, D.W.2    Haber, D.A.3    Li, E.4
  • 71
    • 0035839057 scopus 로고    scopus 로고
    • The role of DNA methylation in mammalian epigenetics
    • Jones PA, Takai D. The role of DNA methylation in mammalian epigenetics. Science 2001; 293:1068-70.
    • (2001) Science , vol.293 , pp. 1068-1070
    • Jones, P.A.1    Takai, D.2
  • 72
    • 0035977204 scopus 로고    scopus 로고
    • Epigenetics: Unforeseen regulators in cancer
    • 1552
    • Muyrers-Chen I, Paro R. Epigenetics: unforeseen regulators in cancer. Biochim Biophys Acta 2001; 1552:15-26.
    • (2001) Biochim. Biophys. Acta , pp. 15-26
    • Muyrers-Chen, I.1    Paro, R.2
  • 73
    • 0037068378 scopus 로고    scopus 로고
    • DNA methylation and cancer
    • Jones PA. DNA methylation and cancer. Oncogene 2002; 21:5358-60.
    • (2002) Oncogene , vol.21 , pp. 5358-5360
    • Jones, P.A.1
  • 75
    • 0035654288 scopus 로고    scopus 로고
    • Methylation profiling of human cancers in blood: Molecular monitoring and prognostication
    • [review]
    • Wong IH. Methylation profiling of human cancers in blood: molecular monitoring and prognostication [review]. Int J Oncol 2001; 19:1319-24.
    • (2001) Int. J. Oncol. , vol.19 , pp. 1319-1324
    • Wong, I.H.1
  • 76
    • 0034807280 scopus 로고    scopus 로고
    • Methylation and colorectal cancer
    • Jubb AM, Bell SM, Quirke P. Methylation and colorectal cancer. J Pathol 2001; 195:111-34.
    • (2001) J. Pathol. , vol.195 , pp. 111-134
    • Jubb, A.M.1    Bell, S.M.2    Quirke, P.3
  • 77
    • 0032585866 scopus 로고    scopus 로고
    • DNA methylation analysis: A review of current methodologies
    • Oakeley EJ. DNA methylation analysis: a review of current methodologies. Pharmacol Ther 1999; 84:389-400.
    • (1999) Pharmacol. Ther. , vol.84 , pp. 389-400
    • Oakeley, E.J.1
  • 78
    • 0036753290 scopus 로고    scopus 로고
    • DNA methylation: A profile of methods and applications
    • 632,634
    • Fraga MF, Esteller M. DNA methylation: a profile of methods and applications. Biotechniques 2002; 33:632, 634, 636-49.
    • (2002) Biotechniques , vol.33 , pp. 636-649
    • Fraga, M.F.1    Esteller, M.2
  • 79
    • 0041719983 scopus 로고    scopus 로고
    • A rapid, quantitative, non-radioactive bisulfite-SNuPE-IP RP HPLC assay for methylation analysis at specific CpG sites
    • El-Maarri O, Herbiniaux U, Walter J, Oldenburg J. A rapid, quantitative, non-radioactive bisulfite-SNuPE-IP RP HPLC assay for methylation analysis at specific CpG sites. Nucleic Acids Res 2002; 30:e25.
    • (2002) Nucleic Acids Res. , vol.30
    • El-Maarri, O.1    Herbiniaux, U.2    Walter, J.3    Oldenburg, J.4
  • 80
    • 17544402963 scopus 로고    scopus 로고
    • Simultaneous detection of CpG methylation and single nucleotide polymorphism by denaturing high performance liquid chromatography
    • Deng D, Deng G, Smith MF, Zhou J, Xin H, Powell SM, et al. Simultaneous detection of CpG methylation and single nucleotide polymorphism by denaturing high performance liquid chromatography. Nucleic Acids Res 2002; 30:E13.
    • (2002) Nucleic Acids Res. , vol.30
    • Deng, D.1    Deng, G.2    Smith, M.F.3    Zhou, J.4    Xin, H.5    Powell, S.M.6
  • 81
    • 0036311281 scopus 로고    scopus 로고
    • Analysis of the methylation status of imprinted genes based on methylation-specific polymerase chain reaction combined with denaturing high-performance liquid chromatography
    • Baumer A. Analysis of the methylation status of imprinted genes based on methylation-specific polymerase chain reaction combined with denaturing high-performance liquid chromatography. Methods 2002; 27:139-43.
    • (2002) Methods , vol.27 , pp. 139-143
    • Baumer, A.1
  • 82
    • 0035041886 scopus 로고    scopus 로고
    • A novel MSP/DHPLC method for the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicisms
    • Baumer A, Wiedemann U, Hergersberg M, Schinzel A. A novel MSP/DHPLC method for the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicisms. Hum Mutat 2001; 17:423-30.
    • (2001) Hum. Mutat. , vol.17 , pp. 423-430
    • Baumer, A.1    Wiedemann, U.2    Hergersberg, M.3    Schinzel, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.