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Volumn 36, Issue 20, 2008, Pages

Hot Start PCR with heat-activatable primers: A novel approach for improved PCR performance

Author keywords

[No Author keywords available]

Indexed keywords

4 OXO 1PENTYLOLIGONUCLEOTIDE; DNA POLYMERASE; OLIGONUCLEOTIDE; PHOSPHODIESTER OLIGONUCLEOTIDE; PHOSPHOTRIESTER OLIGONUCLEOTIDE; POLYNUCLEOTIDE; PRIMER DNA; RECOMBINANT DNA; UNCLASSIFIED DRUG; DNA DIRECTED DNA POLYMERASE; FLUORESCENT DYE; ORGANIC COMPOUND; ORGANOPHOSPHORUS COMPOUND; PHOSPHORAMIDOUS ACID; SYBR GREEN I; VIRUS DNA;

EID: 56649100796     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkn575     Document Type: Article
Times cited : (45)

References (95)
  • 1
    • 0011686552 scopus 로고
    • Process for amplifying nucleic acid sequences
    • U.S. Patent No. US4683202 28 July
    • Mullis,K.B. (1987) Process for amplifying nucleic acid sequences. U.S. Patent No. US4683202 (28 July 1987).
    • (1987)
    • Mullis, K.B.1
  • 4
    • 0031938641 scopus 로고    scopus 로고
    • A novel p53 mutation hotspot at codon 132 (AAG→AGG) in human renal cancer
    • Dahiya,R., Deng,G., Selph,C., Carroll,P. and Presti,J. Jr. (1998) A novel p53 mutation hotspot at codon 132 (AAG→AGG) in human renal cancer. Biochem. Mol. Biol. Int., 44, 407-415.
    • (1998) Biochem. Mol. Biol. Int , vol.44 , pp. 407-415
    • Dahiya, R.1    Deng, G.2    Selph, C.3    Carroll, P.4    Presti Jr., J.5
  • 6
    • 0030640989 scopus 로고    scopus 로고
    • PCR. Basic principles and routine practice
    • Kolmodin,L.A. and Williams,J.F. (1997) PCR. Basic principles and routine practice. Methods Mol. Biol., 67, 3-15.
    • (1997) Methods Mol. Biol , vol.67 , pp. 3-15
    • Kolmodin, L.A.1    Williams, J.F.2
  • 7
    • 0028210787 scopus 로고
    • A sensitive PCR method for detecting HCV RNA in plasma pools, blood products, and single donations
    • Saldanha,J. and Minor,P. (1994) A sensitive PCR method for detecting HCV RNA in plasma pools, blood products, and single donations. J. Med. Virol., 43, 72-76.
    • (1994) J. Med. Virol , vol.43 , pp. 72-76
    • Saldanha, J.1    Minor, P.2
  • 8
    • 0038077505 scopus 로고    scopus 로고
    • HLA typing of aortic tissues from unidentified bodies using hot start polymerase chain reaction-sequence specific primers
    • Sato,Y., Hayakawa,M., Nakajima,T., Motani,H. and Kiuchi,M. (2003) HLA typing of aortic tissues from unidentified bodies using hot start polymerase chain reaction-sequence specific primers. Leg. Med., 5 (Suppl. 1), S191-S193.
    • (2003) Leg. Med , vol.5 , Issue.SUPPL. 1
    • Sato, Y.1    Hayakawa, M.2    Nakajima, T.3    Motani, H.4    Kiuchi, M.5
  • 9
    • 0034982308 scopus 로고    scopus 로고
    • PCR amplification and sequencing of single copy DNA molecules
    • Wabuyele,M.B. and Soper,S.A. (2001) PCR amplification and sequencing of single copy DNA molecules. Single Mol., 2, 13-21.
    • (2001) Single Mol , vol.2 , pp. 13-21
    • Wabuyele, M.B.1    Soper, S.A.2
  • 10
    • 0037974735 scopus 로고    scopus 로고
    • Single nucleotide polymorphism genotyping: Biochemistry, protocol, cost and throughput
    • Chen,X. and Sullivan,P.F. (2003) Single nucleotide polymorphism genotyping: Biochemistry, protocol, cost and throughput. Pharmacogenomics J., 3, 77-96.
    • (2003) Pharmacogenomics J , vol.3 , pp. 77-96
    • Chen, X.1    Sullivan, P.F.2
  • 11
    • 0036360439 scopus 로고    scopus 로고
    • Progress in high throughput SNP genotyping methods
    • Tsuchihashi,Z. and Dracopoli,N.C. (2002) Progress in high throughput SNP genotyping methods. Pharmacogenomics J., 2, 103-110.
    • (2002) Pharmacogenomics J , vol.2 , pp. 103-110
    • Tsuchihashi, Z.1    Dracopoli, N.C.2
  • 13
    • 29144445330 scopus 로고    scopus 로고
    • PCR-induced sequence artifacts and bias: Insights from comparison of two 16S rRNA clone libraries constructed from the same sample
    • Acinas,S.G., Sarma-Rupavtarm,R., Klepac-Ceraj,V. and Polz,M.F. (2005) PCR-induced sequence artifacts and bias: Insights from comparison of two 16S rRNA clone libraries constructed from the same sample. Appl. Environ. Microbiol., 71, 8966-8969.
    • (2005) Appl. Environ. Microbiol , vol.71 , pp. 8966-8969
    • Acinas, S.G.1    Sarma-Rupavtarm, R.2    Klepac-Ceraj, V.3    Polz, M.F.4
  • 14
    • 0026603267 scopus 로고
    • Prevention of pre-PCR mis-priming and primer dimerization improves low-copy-number amplifications
    • Chou,Q., Russell,M., Birch,D.E., Raymond,J. and Bloch,W. (1992) Prevention of pre-PCR mis-priming and primer dimerization improves low-copy-number amplifications. Nucleic Acids Res., 20, 1717-1723.
    • (1992) Nucleic Acids Res , vol.20 , pp. 1717-1723
    • Chou, Q.1    Russell, M.2    Birch, D.E.3    Raymond, J.4    Bloch, W.5
  • 16
    • 0027257505 scopus 로고
    • An alternative hot start technique for PCR in small volumes using beads of wax-embedded reaction components dried in trehalose
    • Kaijalainen,S., Karhunen,P.J., Lalu,K. and Lindstrom,K. (1993) An alternative hot start technique for PCR in small volumes using beads of wax-embedded reaction components dried in trehalose. Nucleic Acids Res., 21, 2959-2960.
    • (1993) Nucleic Acids Res , vol.21 , pp. 2959-2960
    • Kaijalainen, S.1    Karhunen, P.J.2    Lalu, K.3    Lindstrom, K.4
  • 17
    • 0033543716 scopus 로고    scopus 로고
    • A hot-start reverse transcription-polymerase chain reaction protocol that initiates multiple analyses simultaneously
    • Tanzer,L.R., Hu,Y., Cripe,L. and Moore,R.E. (1999) A hot-start reverse transcription-polymerase chain reaction protocol that initiates multiple analyses simultaneously. Anal. Biochem., 273, 307-310.
    • (1999) Anal. Biochem , vol.273 , pp. 307-310
    • Tanzer, L.R.1    Hu, Y.2    Cripe, L.3    Moore, R.E.4
  • 18
    • 56649110567 scopus 로고    scopus 로고
    • Nucleic acid amplification using a reversibly inactivated thermostable enzyme
    • U.S. Patent No. US5773258 30 June
    • Birch,D.E., Laird,W.J. and Zoccoli,A. (1998) Nucleic acid amplification using a reversibly inactivated thermostable enzyme. U.S. Patent No. US5773258 (30 June 1998).
    • (1998)
    • Birch, D.E.1    Laird, W.J.2    Zoccoli, A.3
  • 19
    • 0030606308 scopus 로고    scopus 로고
    • Oligonucleotide inhibitors of Taq DNA polymerase facilitate detection of low copy number targets by PCR
    • Dang,C. and Jayasena,S.D. (1996) Oligonucleotide inhibitors of Taq DNA polymerase facilitate detection of low copy number targets by PCR. J. Mol. Biol., 264, 268-278.
    • (1996) J. Mol. Biol , vol.264 , pp. 268-278
    • Dang, C.1    Jayasena, S.D.2
  • 20
    • 56649107309 scopus 로고    scopus 로고
    • Hot Start RT-PCR results in improved performance of the enhanced avian RT-PCR system
    • Eastlund,E. and Mueller,E. (2001) Hot Start RT-PCR results in improved performance of the enhanced avian RT-PCR system. Life Sci. Q., 2, 2-5.
    • (2001) Life Sci. Q , vol.2 , pp. 2-5
    • Eastlund, E.1    Mueller, E.2
  • 21
    • 0028182432 scopus 로고
    • TaqStart antibody™: 'hot start' PCR Facilitated by a neutralizing monoclonal antibody directed against Taq DNA polymerase
    • Kellogg,D.E., Rybalkin,I., Chen,S., Mukhamedova,N., Vlasik,T., Siebert,P.D. and Chemchik,A. (1994) TaqStart antibody™: 'hot start' PCR Facilitated by a neutralizing monoclonal antibody directed against Taq DNA polymerase. Biotechniques, 16, 1134-1137.
    • (1994) Biotechniques , vol.16 , pp. 1134-1137
    • Kellogg, D.E.1    Rybalkin, I.2    Chen, S.3    Mukhamedova, N.4    Vlasik, T.5    Siebert, P.D.6    Chemchik, A.7
  • 22
    • 0344011118 scopus 로고    scopus 로고
    • Cold-sensitive mutants of Taq DNA polymerase provide a hot start for PCR
    • Kermekchiev,M.B., Tzekov,A. and Barnes,W.M. (2003) Cold-sensitive mutants of Taq DNA polymerase provide a hot start for PCR. Nucleic Acids Res., 31, 6139-6147.
    • (2003) Nucleic Acids Res , vol.31 , pp. 6139-6147
    • Kermekchiev, M.B.1    Tzekov, A.2    Barnes, W.M.3
  • 23
    • 0032750109 scopus 로고    scopus 로고
    • Characterization and application to hot start PCR of neutralizing monoclonal antibodies against KOD DNA polymerase
    • Mizuguchi,H., Nakatsuji,M., Fujiwara,S., Takagi,M. and Imanaka,T. (1999) Characterization and application to hot start PCR of neutralizing monoclonal antibodies against KOD DNA polymerase. J. Biochem., 126, 762-768.
    • (1999) J. Biochem , vol.126 , pp. 762-768
    • Mizuguchi, H.1    Nakatsuji, M.2    Fujiwara, S.3    Takagi, M.4    Imanaka, T.5
  • 24
    • 0031719262 scopus 로고    scopus 로고
    • Enhancement of PCR amplification yield and specificity using AmpliTaq Gold DNA polymerase
    • Moretti,T., Koons,B. and Budowle,B. (1998) Enhancement of PCR amplification yield and specificity using AmpliTaq Gold DNA polymerase. Biotechniques, 25, 716-722.
    • (1998) Biotechniques , vol.25 , pp. 716-722
    • Moretti, T.1    Koons, B.2    Budowle, B.3
  • 25
    • 56649122760 scopus 로고    scopus 로고
    • Amplification process
    • U.S. Patent No. US2006057617 16 March
    • Clark,D.R. and Vincent,S.P. (2006) Amplification process. U.S. Patent No. US2006057617 (16 March 2006).
    • (2006)
    • Clark, D.R.1    Vincent, S.P.2
  • 26
    • 15944410321 scopus 로고    scopus 로고
    • Application of SSB-like protein from Thermus aquaticus in multiplex PCR of human Y-STR markers identification
    • Olszewskia,M., Rebałab,K., Szczerkowskab,Z. and Kur,J. (2005) Application of SSB-like protein from Thermus aquaticus in multiplex PCR of human Y-STR markers identification. Mol. Cell Probes, 19, 203-205.
    • (2005) Mol. Cell Probes , vol.19 , pp. 203-205
    • Olszewskia, M.1    Rebałab, K.2    Szczerkowskab, Z.3    Kur, J.4
  • 27
    • 24044439503 scopus 로고    scopus 로고
    • Multiplex PCR: Use of heat-stable Thermus thermophilus RecA protein to minimize non-specific PCR products
    • Shigemori,Y., Mikawa,T., Shibata,T. and Oishi,M. (2005) Multiplex PCR: use of heat-stable Thermus thermophilus RecA protein to minimize non-specific PCR products. Nucleic Acids Res., 33, e126.
    • (2005) Nucleic Acids Res , vol.33
    • Shigemori, Y.1    Mikawa, T.2    Shibata, T.3    Oishi, M.4
  • 28
    • 0033729713 scopus 로고    scopus 로고
    • Controlled hot start and improved specificity in carrying out PCR utilizing touch-up and loop incorporated primers (TULIPS)
    • 1018-1020
    • Ailenberg,M. and Silverman,M. (2000) Controlled hot start and improved specificity in carrying out PCR utilizing touch-up and loop incorporated primers (TULIPS). Biotechniques, 29, 1018-1020, 1022-1014.
    • (2000) Biotechniques , vol.29 , pp. 1022-1014
    • Ailenberg, M.1    Silverman, M.2
  • 29
    • 70349182585 scopus 로고    scopus 로고
    • Composition and method for Hot Start nucleic acid amplification
    • U.S. Patent No. US2003119150 26 June
    • Ankenbauer,W., Heindl,D., Laue,F. and Huber,N. (2003) Composition and method for Hot Start nucleic acid amplification. U.S. Patent No. US2003119150 (26 June 2003).
    • (2003)
    • Ankenbauer, W.1    Heindl, D.2    Laue, F.3    Huber, N.4
  • 30
    • 56649119799 scopus 로고    scopus 로고
    • Reversible chemical modification of nucleic acids and improved method for nucleic acid hybridization
    • U.S. Patent No. US2003162199 28 August
    • Bonner,A.G. (2003) Reversible chemical modification of nucleic acids and improved method for nucleic acid hybridization. U.S. Patent No. US2003162199 (28 August 2003).
    • (2003)
    • Bonner, A.G.1
  • 31
    • 0034320328 scopus 로고    scopus 로고
    • PCR hot start using primers with the structure of molecular beacons (hairpin-like structure)
    • Kaboev,O.K., Luchkina,L.A., Tret'iakov,A.N. and Bahrmand,A.R. (2000) PCR hot start using primers with the structure of molecular beacons (hairpin-like structure). Nucleic Acids Res., 28, E94.
    • (2000) Nucleic Acids Res , vol.28
    • Kaboev, O.K.1    Luchkina, L.A.2    Tret'iakov, A.N.3    Bahrmand, A.R.4
  • 32
    • 70349173481 scopus 로고    scopus 로고
    • Amplification using modified primers
    • U.S. Patent No. US2003044817 6 March
    • Laird,W.J. and Niemiec,J.T. (2004) Amplification using modified primers. U.S. Patent No. US2003044817 (6 March 2003).
    • (2003)
    • Laird, W.J.1    Niemiec, J.T.2
  • 33
    • 0028809660 scopus 로고
    • Reduction of mispriming in amplification reactions with restricted PCR
    • Puskas,L.G. and Bottka,S. (1995) Reduction of mispriming in amplification reactions with restricted PCR. Genome Res., 5, 309-311.
    • (1995) Genome Res , vol.5 , pp. 309-311
    • Puskas, L.G.1    Bottka, S.2
  • 34
    • 56649088990 scopus 로고    scopus 로고
    • Method for polynucleotide amplification
    • U.S. Patent No. US6482590 19 November
    • Ullman,E.F., Lishanski,A. and Kurn,N. (2002) Method for polynucleotide amplification. U.S. Patent No. US6482590 (19 November 2002).
    • (2002)
    • Ullman, E.F.1    Lishanski, A.2    Kurn, N.3
  • 35
    • 56649099884 scopus 로고    scopus 로고
    • Modified nucleic acid amplification primers
    • U.S. Patent No. US6001611 14 December
    • Will,S.G. (1999) Modified nucleic acid amplification primers. U.S. Patent No. US6001611 (14 December 1999).
    • (1999)
    • Will, S.G.1
  • 37
    • 49749128451 scopus 로고    scopus 로고
    • Blocking primers to enhance PCR amplification of rare sequences in mixed samples - a case study on prey DNA in Antarctic krill stomachs
    • Vestheim,H. and Jarman,S.N. (2008) Blocking primers to enhance PCR amplification of rare sequences in mixed samples - a case study on prey DNA in Antarctic krill stomachs. Front Zool., 5, 12.
    • (2008) Front Zool , vol.5 , pp. 12
    • Vestheim, H.1    Jarman, S.N.2
  • 38
    • 0023057004 scopus 로고
    • Alkyl phosphotriester modi.ed oligodeoxyribonucleotides. V. Synthesis and absolute configuration of Rp and Sp diastereomers of an ethyl phosphotriester (Et) modified EcoRI recognition sequence, d[GGAA(Et)TTCC]. A synthetic approach to regio- and stereospecific ethylation-interference studies
    • Gallo,K.A., Shao,K.L., Phillips,L.R., Regan,J.B., Koziolkiewicz,M., Uznanski,B., Stec,W.J. and Zon,G. (1986) Alkyl phosphotriester modi.ed oligodeoxyribonucleotides. V. Synthesis and absolute configuration of Rp and Sp diastereomers of an ethyl phosphotriester (Et) modified EcoRI recognition sequence, d[GGAA(Et)TTCC]. A synthetic approach to regio- and stereospecific ethylation-interference studies. Nucleic Acids Res., 14, 7405-7420.
    • (1986) Nucleic Acids Res , vol.14 , pp. 7405-7420
    • Gallo, K.A.1    Shao, K.L.2    Phillips, L.R.3    Regan, J.B.4    Koziolkiewicz, M.5    Uznanski, B.6    Stec, W.J.7    Zon, G.8
  • 39
    • 0023057178 scopus 로고
    • Phosphorothioate-modified oligodeoxyribonucleotides. III. NMR and UV spectroscopic studies of the Rp-Rp, Sp-Sp, and Rp-Sp duplexes, [d(GGSAATTCC)]2, derived from diastereomeric O-ethyl phosphorothioates
    • LaPlanche,L.A., James,T.L., Powell,C., Wilson,W.D., Uznanski,B., Stec,W.J., Summers,M.F. and Zon,G. (1986) Phosphorothioate-modified oligodeoxyribonucleotides. III. NMR and UV spectroscopic studies of the Rp-Rp, Sp-Sp, and Rp-Sp duplexes, [d(GGSAATTCC)]2, derived from diastereomeric O-ethyl phosphorothioates. Nucleic Acids Res., 14, 9081-9093.
    • (1986) Nucleic Acids Res , vol.14 , pp. 9081-9093
    • LaPlanche, L.A.1    James, T.L.2    Powell, C.3    Wilson, W.D.4    Uznanski, B.5    Stec, W.J.6    Summers, M.F.7    Zon, G.8
  • 40
    • 0011248958 scopus 로고
    • A convenient method to stepwise synthesis of oligothymidylate derivatives in large scale quantities
    • Letsinger,R.L. and Ogilvie,K.K. (1967) A convenient method to stepwise synthesis of oligothymidylate derivatives in large scale quantities. J. Am. Chem. Soc., 89, 4801-4808.
    • (1967) J. Am. Chem. Soc , vol.89 , pp. 4801-4808
    • Letsinger, R.L.1    Ogilvie, K.K.2
  • 41
    • 27844555547 scopus 로고
    • Nucleotides part XXXII. Synthesis of a dithymidine dinucleotide containing a 3: 5-internucleotidic linkage
    • Michelson,A.M. and Todd,A.R. (1955) Nucleotides part XXXII. Synthesis of a dithymidine dinucleotide containing a 3: 5-internucleotidic linkage. J. Chem. Soc., 2632-2638.
    • (1955) J. Chem. Soc , pp. 2632-2638
    • Michelson, A.M.1    Todd, A.R.2
  • 42
    • 0011912896 scopus 로고
    • Synthesis and absolute con.guration of P-chiral O-isopropyl oligonucleotide triesters
    • Stec,W.J., Zon,G., Gallo,K.A., Byrd,R.A., UznanskiI,B. and Guga,P. (1985) Synthesis and absolute con.guration of P-chiral O-isopropyl oligonucleotide triesters. Tetrahedron Lett., 26, 2191-2194.
    • (1985) Tetrahedron Lett , vol.26 , pp. 2191-2194
    • Stec, W.J.1    Zon, G.2    Gallo, K.A.3    Byrd, R.A.4    UznanskiI, B.5    Guga, P.6
  • 43
    • 0001756945 scopus 로고
    • P-Chiral analogues of oligodeoxyribonucleotides: Synthesis, stereochemistry and enzyme studies
    • Koziolkiewicz,M., Uznanski,B., Stec,W.J. and Zon,G. (1986) P-Chiral analogues of oligodeoxyribonucleotides: Synthesis, stereochemistry and enzyme studies. Chem. Scr., 26, 251-260.
    • (1986) Chem. Scr , vol.26 , pp. 251-260
    • Koziolkiewicz, M.1    Uznanski, B.2    Stec, W.J.3    Zon, G.4
  • 44
    • 0002094968 scopus 로고    scopus 로고
    • Chirality problem in P-substituted oligonucleotides
    • Lebedev,A.L. and Wickstrom,E. (1996) Chirality problem in P-substituted oligonucleotides. Perspect. Drug Discov., 4, 17-36.
    • (1996) Perspect. Drug Discov , vol.4 , pp. 17-36
    • Lebedev, A.L.1    Wickstrom, E.2
  • 45
    • 33748216395 scopus 로고
    • Stereocontrolled synthesis of oligo (nucleoside phosphorothioate) s
    • Stec,W.J. and Wilk,A. (1994) Stereocontrolled synthesis of oligo (nucleoside phosphorothioate) s. Angew. Chem. Int. Ed Engl., 33 709-722.
    • (1994) Angew. Chem. Int. Ed Engl , vol.33 , pp. 709-722
    • Stec, W.J.1    Wilk, A.2
  • 46
    • 0017131968 scopus 로고
    • Nucleoside-3′-phosphotriesters as key intermediates for the oligoribonucleotide synthesis. III. An improved preparation of nucleoside 3′-phosphotriesters, their 1H NMR characterization and new conditions for removal of 2-cyanoethyl group
    • Adamiak,R.W., Barciszewska,M.Z., Biala,E., Grzeskowiak,K., Kierzek,R., Kraszewski,A., Markiewicz,W.T. and Wiewiorowski,M. (1976) Nucleoside-3′-phosphotriesters as key intermediates for the oligoribonucleotide synthesis. III. An improved preparation of nucleoside 3′-phosphotriesters, their 1H NMR characterization and new conditions for removal of 2-cyanoethyl group. Nucleic Acids Res., 3, 3397-3408.
    • (1976) Nucleic Acids Res , vol.3 , pp. 3397-3408
    • Adamiak, R.W.1    Barciszewska, M.Z.2    Biala, E.3    Grzeskowiak, K.4    Kierzek, R.5    Kraszewski, A.6    Markiewicz, W.T.7    Wiewiorowski, M.8
  • 47
    • 0025906104 scopus 로고
    • Oxalyl-CPG: A labile support for synthesis of sensitive oligonucleotide derivatives
    • Alul,R.H., Singman,C.N., Zhang,G.R. and Letsinger,R.L. (1991) Oxalyl-CPG: A labile support for synthesis of sensitive oligonucleotide derivatives. Nucleic Acids Res., 19, 1527-1532.
    • (1991) Nucleic Acids Res , vol.19 , pp. 1527-1532
    • Alul, R.H.1    Singman, C.N.2    Zhang, G.R.3    Letsinger, R.L.4
  • 48
    • 37049073520 scopus 로고
    • Synthesis of the 3-terminal half of yeast alanine transfer ribonucleic acid (tRNAAla) by the phosphotriester approach in solution. Part 1. Preparation of the nucleoside building blocks
    • Brown,J.M., Christodoulou,C., Jones,S.S., Modak,A.S., Reese,C.B., Sibanda,S. and Ubasawa,A. (1989) Synthesis of the 3-terminal half of yeast alanine transfer ribonucleic acid (tRNAAla) by the phosphotriester approach in solution. Part 1. Preparation of the nucleoside building blocks. J. Chem. Soc., Perkin Trans., 1, 1735-1750.
    • (1989) J. Chem. Soc., Perkin Trans , vol.1 , pp. 1735-1750
    • Brown, J.M.1    Christodoulou, C.2    Jones, S.S.3    Modak, A.S.4    Reese, C.B.5    Sibanda, S.6    Ubasawa, A.7
  • 49
    • 37049083349 scopus 로고
    • Synthesis of the 3-terminal half of yeast alanine transfer ribonucleic acid (tRNAAla) by the phosphotriester approach in solution. Part 2
    • Brown,J.M., Christodoulou,C., Modak,A.S., Reese,C.B. and Serafinowska,H.T. (1989) Synthesis of the 3-terminal half of yeast alanine transfer ribonucleic acid (tRNAAla) by the phosphotriester approach in solution. Part 2. J. Chem. Soc., Perkin Trans., 1 1751-1767.
    • (1989) J. Chem. Soc., Perkin Trans , vol.1 , pp. 1751-1767
    • Brown, J.M.1    Christodoulou, C.2    Modak, A.S.3    Reese, C.B.4    Serafinowska, H.T.5
  • 50
    • 0017772372 scopus 로고
    • Synthesis of oligoribonucleotides based on the facile cleavage of methyl phosphotriester intermediates
    • Daub,G.W. and Tamelen,E.E. (1977) Synthesis of oligoribonucleotides based on the facile cleavage of methyl phosphotriester intermediates. J. Am. Chem. Soc., 99, 3526-3528.
    • (1977) J. Am. Chem. Soc , vol.99 , pp. 3526-3528
    • Daub, G.W.1    Tamelen, E.E.2
  • 51
    • 0019322156 scopus 로고
    • Chromatography on Sephadex LH20 as an efficient purification step after removal of internucleotide 2,2,2-trichloroethyl protective groups from oligoribonucleotide phosphotriesters
    • Grzeskowiak,K., Adamiak,R.W. and Wiewiorowski,M. (1980) Chromatography on Sephadex LH20 as an efficient purification step after removal of internucleotide 2,2,2-trichloroethyl protective groups from oligoribonucleotide phosphotriesters. Nucleic Acids Res., 8, 1097-1105.
    • (1980) Nucleic Acids Res , vol.8 , pp. 1097-1105
    • Grzeskowiak, K.1    Adamiak, R.W.2    Wiewiorowski, M.3
  • 52
    • 0016848749 scopus 로고
    • Use of arylsulfonyltriazoles for the synthesis of oligonucleotides by the triester approach
    • Katagiri,N., Itakura,K. and Narang,S.A. (1975) Use of arylsulfonyltriazoles for the synthesis of oligonucleotides by the triester approach. J. Am. Chem. Soc., 97, 7332-7337.
    • (1975) J. Am. Chem. Soc , vol.97 , pp. 7332-7337
    • Katagiri, N.1    Itakura, K.2    Narang, S.A.3
  • 53
    • 0025044905 scopus 로고
    • Synthesis of well-defined phosphate-methylated DNA fragments: The application of potassium carbonate in methanol as deprotecting reagent
    • Kuijpers,W.H., Huskens,J., Koole,L.H. and van Boeckel,C.A. (1990) Synthesis of well-defined phosphate-methylated DNA fragments: The application of potassium carbonate in methanol as deprotecting reagent. Nucleic Acids Res., 18, 5197-5205.
    • (1990) Nucleic Acids Res , vol.18 , pp. 5197-5205
    • Kuijpers, W.H.1    Huskens, J.2    Koole, L.H.3    van Boeckel, C.A.4
  • 54
    • 0005607143 scopus 로고
    • Synthesis of oligothymidylates via phosphotriester intermediates
    • Letsinger,R.L. and Ogilvie,K.K. (1969) Synthesis of oligothymidylates via phosphotriester intermediates. J. Am. Chem. Soc., 91, 3350-3355.
    • (1969) J. Am. Chem. Soc , vol.91 , pp. 3350-3355
    • Letsinger, R.L.1    Ogilvie, K.K.2
  • 55
    • 0011231518 scopus 로고
    • Developments in synthesis of oligodeoxyribonucleotides and their organic derivatives
    • Letsinger,R.L., Ogilvie,K.K. and Miller,P.S. (1969) Developments in synthesis of oligodeoxyribonucleotides and their organic derivatives. J. Am. Chem. Soc., 91, 3360-3365.
    • (1969) J. Am. Chem. Soc , vol.91 , pp. 3360-3365
    • Letsinger, R.L.1    Ogilvie, K.K.2    Miller, P.S.3
  • 56
    • 2442745187 scopus 로고
    • Solid phase synthesis of oligodeoxyribonucleotides utilizing the phenylthio group as a phosphate protecting group
    • Matsuzaki,J., Kohno,K., Tahara,S., Sekine,M. and Hata,T. (1987) Solid phase synthesis of oligodeoxyribonucleotides utilizing the phenylthio group as a phosphate protecting group. Bull. Chem. Soc. Jpn., 60, 1407-1413.
    • (1987) Bull. Chem. Soc. Jpn , vol.60 , pp. 1407-1413
    • Matsuzaki, J.1    Kohno, K.2    Tahara, S.3    Sekine, M.4    Hata, T.5
  • 57
    • 0024327154 scopus 로고
    • Regiospecific inhibition of DNA duplication by antisense phosphate-methylated oligodeoxynucleotides
    • Moody,H.M., van Genderen,M.H., Koole,L.H., Kocken,H.J., Meijer,E.M. and Buck,H.M. (1989) Regiospecific inhibition of DNA duplication by antisense phosphate-methylated oligodeoxynucleotides. Nucleic Acids Res., 17, 4769-4782.
    • (1989) Nucleic Acids Res , vol.17 , pp. 4769-4782
    • Moody, H.M.1    van Genderen, M.H.2    Koole, L.H.3    Kocken, H.J.4    Meijer, E.M.5    Buck, H.M.6
  • 58
    • 33744769207 scopus 로고
    • Chemical synthesis of the 5′-half molecule of E. coli tRNA2GLY
    • Ohtsuka,E., Yamane,A. and Doi,T. (1984) Chemical synthesis of the 5′-half molecule of E. coli tRNA2GLY. Tetrahedron, 40, 47-57.
    • (1984) Tetrahedron , vol.40 , pp. 47-57
    • Ohtsuka, E.1    Yamane, A.2    Doi, T.3
  • 59
    • 0011225588 scopus 로고
    • Reaction between 4-nitrobenaldoximate ion and phosphotriesters
    • Reese,C.B. and Yau,L. (1978) Reaction between 4-nitrobenaldoximate ion and phosphotriesters. Tetrahedron Lett., 19, 4443-4446.
    • (1978) Tetrahedron Lett , vol.19 , pp. 4443-4446
    • Reese, C.B.1    Yau, L.2
  • 60
    • 0019888453 scopus 로고
    • Some observations relating to the oximate ion promoted unblocking of oligonucleotide aryl esters
    • Reese,C.B. and Zard,L. (1981) Some observations relating to the oximate ion promoted unblocking of oligonucleotide aryl esters. Nucleic Acids Res., 9, 4611-4626.
    • (1981) Nucleic Acids Res , vol.9 , pp. 4611-4626
    • Reese, C.B.1    Zard, L.2
  • 61
    • 0010068559 scopus 로고
    • Oligodeoxyribonucleotide synthesis by the use of S,S-diphenyl deoxyribonucleoside 3′-phosphorodithioates and bifunctional condensing reagents in the phosphotriester approach
    • Sekine,M., Matsuzaki,J. and Hata,T. (1985) Oligodeoxyribonucleotide synthesis by the use of S,S-diphenyl deoxyribonucleoside 3′-phosphorodithioates and bifunctional condensing reagents in the phosphotriester approach. Tetrahedron, 41, 5279-5288.
    • (1985) Tetrahedron , vol.41 , pp. 5279-5288
    • Sekine, M.1    Matsuzaki, J.2    Hata, T.3
  • 62
    • 1542432561 scopus 로고
    • An effective method for removal of the internucleotide phenylthio group from fully protected oligonucleotides by use of bis(tributyltin) oxide
    • Sekine,M., Tanimura,H. and Hata,T. (1985) An effective method for removal of the internucleotide phenylthio group from fully protected oligonucleotides by use of bis(tributyltin) oxide. Tetrahedron Lett. 26, 4621-4624.
    • (1985) Tetrahedron Lett , vol.26 , pp. 4621-4624
    • Sekine, M.1    Tanimura, H.2    Hata, T.3
  • 63
    • 84996295995 scopus 로고
    • Oligonucleotidic compounds. XLIV. Protection of the internucleotidic bond after its synthesis as approach to the synthesis of an oligonucleotidic chain
    • Smrt,J. (1973) Oligonucleotidic compounds. XLIV. Protection of the internucleotidic bond after its synthesis as approach to the synthesis of an oligonucleotidic chain. Collect. Czech. Chem. Commun., 38 3189-3197.
    • (1973) Collect. Czech. Chem. Commun , vol.38 , pp. 3189-3197
    • Smrt, J.1
  • 64
    • 0017374411 scopus 로고
    • A Rapid and convenient synthesis of poly-thymidylic acid by the modified triester approach
    • Sood,A.K. and Narang,S.A. (1976) A Rapid and convenient synthesis of poly-thymidylic acid by the modified triester approach. Nucl. Acids Res., 4, 2757-2765.
    • (1976) Nucl. Acids Res , vol.4 , pp. 2757-2765
    • Sood, A.K.1    Narang, S.A.2
  • 65
    • 26844499501 scopus 로고
    • 1,1,1,3,3,3-Hexafluoro-2-propyl protecting group in the synthesis of DNA fragments via phosphoramidite intermediates
    • Takaku,H., Watanabe,T. and Hamamoto,S. (1988) 1,1,1,3,3,3-Hexafluoro-2-propyl protecting group in the synthesis of DNA fragments via phosphoramidite intermediates. Tetrahedron Lett., 29, 81-84.
    • (1988) Tetrahedron Lett , vol.29 , pp. 81-84
    • Takaku, H.1    Watanabe, T.2    Hamamoto, S.3
  • 66
    • 9644292443 scopus 로고
    • 5-Chloro-8-quinolyl group as high efficient phosphate protecting group for the synthesis of oligoribonucleotides
    • Takaku,H., Yamaguchi,R. and Nomoto,T. (1979) 5-Chloro-8-quinolyl group as high efficient phosphate protecting group for the synthesis of oligoribonucleotides. Tetrahedron Lett., 20, 3857-3860.
    • (1979) Tetrahedron Lett , vol.20 , pp. 3857-3860
    • Takaku, H.1    Yamaguchi, R.2    Nomoto, T.3
  • 67
    • 45249129119 scopus 로고
    • 1,1,1,3,3,3-Hexafluoro-2-propyl group as a new phosphate protecting group for oligoribonucleotide synthesis in the phosphotriester approach
    • Yamakage,S., Fujii,M., Takaku,H. and Uemura,M. (1989) 1,1,1,3,3,3-Hexafluoro-2-propyl group as a new phosphate protecting group for oligoribonucleotide synthesis in the phosphotriester approach. Tetrahedron, 45, 5459-5468.
    • (1989) Tetrahedron , vol.45 , pp. 5459-5468
    • Yamakage, S.1    Fujii, M.2    Takaku, H.3    Uemura, M.4
  • 68
    • 56649105995 scopus 로고    scopus 로고
    • Thermolabile phosphorus protecting groups, associated intermediates and methods of use
    • U.S. Patent No. US2001044529 22 November
    • Beaucage,S.L., Wilk,A. and Grajkowski,A. (2001) Thermolabile phosphorus protecting groups, associated intermediates and methods of use. U.S. Patent No. US2001044529 (22 November 2001).
    • (2001)
    • Beaucage, S.L.1    Wilk, A.2    Grajkowski, A.3
  • 69
    • 0346992398 scopus 로고    scopus 로고
    • Thermolytic properties of 3-(2-Pyridyl)-1-Propyl and 2-[N-Methyl-N-(2-Pyridyl)]Aminoethyl Phosphate/Thiophosphate protecting groups in solid-phase synthesis of oligonucleotides
    • Cieslak,J. and Beaucage,S.L. (2003) Thermolytic properties of 3-(2-Pyridyl)-1-Propyl and 2-[N-Methyl-N-(2-Pyridyl)]Aminoethyl Phosphate/Thiophosphate protecting groups in solid-phase synthesis of oligonucleotides. J. Org. Chem., 68, 10123-10129.
    • (2003) J. Org. Chem , vol.68 , pp. 10123-10129
    • Cieslak, J.1    Beaucage, S.L.2
  • 70
    • 12144287950 scopus 로고    scopus 로고
    • Thermolytic 4-methylthio-1-butyl group for phosphate/thiophosphate protection in solid-phase synthesis of DNA oligonucleotides
    • Cieslak,J., Grajkowski,A., Livengood,V. and Beaucage,S.L. (2004) Thermolytic 4-methylthio-1-butyl group for phosphate/thiophosphate protection in solid-phase synthesis of DNA oligonucleotides. J. Org. Chem., 69, 2509-2515.
    • (2004) J. Org. Chem , vol.69 , pp. 2509-2515
    • Cieslak, J.1    Grajkowski, A.2    Livengood, V.3    Beaucage, S.L.4
  • 72
    • 0035799851 scopus 로고    scopus 로고
    • The 2-(N-formyl-N-methyl)aminoethyl group as a potential phosphate/thiophosphate protecting group in solid-phase oligodeoxyribonucleotides synthesis
    • Grajkowski,A., Wilk,A., Chmielewski,M.K., Phillips,L.R. and Beaucage,S.L. (2001) The 2-(N-formyl-N-methyl)aminoethyl group as a potential phosphate/thiophosphate protecting group in solid-phase oligodeoxyribonucleotides synthesis. Org. Lett., 3, 1287-1290.
    • (2001) Org. Lett , vol.3 , pp. 1287-1290
    • Grajkowski, A.1    Wilk, A.2    Chmielewski, M.K.3    Phillips, L.R.4    Beaucage, S.L.5
  • 73
    • 0035819625 scopus 로고    scopus 로고
    • 2-Benzamidoethyl group - a novel type of phosphate protecting group for oligonucleotide synthesis
    • Guzaev,A.P. and Manoharan,M. (2001) 2-Benzamidoethyl group - a novel type of phosphate protecting group for oligonucleotide synthesis. J. Am. Chem. Soc., 123, 783-793.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 783-793
    • Guzaev, A.P.1    Manoharan, M.2
  • 74
    • 0035855342 scopus 로고    scopus 로고
    • The 4-oxopentyl group as a labile phosphate/ thiophosphate protecting group for synthetic oligodeoxyribonucleotides
    • Wilk,A., Chmielewski,M.K., Grajkowski,A., Phillips,L.R. and Beaucage,S.L. (2001) The 4-oxopentyl group as a labile phosphate/ thiophosphate protecting group for synthetic oligodeoxyribonucleotides. Tetrahedron Lett., 42, 5635-5639.
    • (2001) Tetrahedron Lett , vol.42 , pp. 5635-5639
    • Wilk, A.1    Chmielewski, M.K.2    Grajkowski, A.3    Phillips, L.R.4    Beaucage, S.L.5
  • 75
    • 0037031670 scopus 로고    scopus 로고
    • The 3-(N-tert-butylcarboxamido)-1-propyl group as an attractive phosphate/thiophosphate protecting group for solid-phase oligodeoxyribonucleotide synthesis
    • Wilk,A., Chmielewski,M.K., Grajkowski,A., Phillips,L.R. and Beaucage,S.L. (2002) The 3-(N-tert-butylcarboxamido)-1-propyl group as an attractive phosphate/thiophosphate protecting group for solid-phase oligodeoxyribonucleotide synthesis. J. Org. Chem., 67, 6430-6438.
    • (2002) J. Org. Chem , vol.67 , pp. 6430-6438
    • Wilk, A.1    Chmielewski, M.K.2    Grajkowski, A.3    Phillips, L.R.4    Beaucage, S.L.5
  • 76
    • 0022038229 scopus 로고    scopus 로고
    • Levina,A.S., Nevinskii,G.A. and Lavrik,O.I. (1985) E. coli DNA polymerase. A study of the mechanism of primer binding using oligothymidylate analogs with ethylated internucleotide phosphate groups. Bioorg. Khim., 11, 358-369.
    • Levina,A.S., Nevinskii,G.A. and Lavrik,O.I. (1985) E. coli DNA polymerase. A study of the mechanism of primer binding using oligothymidylate analogs with ethylated internucleotide phosphate groups. Bioorg. Khim., 11, 358-369.
  • 77
    • 0023079026 scopus 로고
    • Prokaryotic and eukaryotic DNA-polymerase. I. The role of internucleotide phosphate groups in the binding of a primer with the enzyme
    • Nevinskii,G.A., Frolova,E.I., Levina,A.S., Podust,V.N. and Lebedev,A.V. (1987) Prokaryotic and eukaryotic DNA-polymerase. I. The role of internucleotide phosphate groups in the binding of a primer with the enzyme. Bioorg. Khim., 13, 45-57.
    • (1987) Bioorg. Khim , vol.13 , pp. 45-57
    • Nevinskii, G.A.1    Frolova, E.I.2    Levina, A.S.3    Podust, V.N.4    Lebedev, A.V.5
  • 78
    • 0022898356 scopus 로고
    • Synthesis and properties of oligodeoxyribonucleotides containing an ethylated internucleotide phosphate
    • Weinfeld,M. and Livingston,D.C. (1986) Synthesis and properties of oligodeoxyribonucleotides containing an ethylated internucleotide phosphate. Biochemistry, 25, 5083-5091.
    • (1986) Biochemistry , vol.25 , pp. 5083-5091
    • Weinfeld, M.1    Livingston, D.C.2
  • 79
    • 0035202091 scopus 로고    scopus 로고
    • Rapid quantification of human ABCA1 mRNA in various cell types and tissues by real-time reverse transcription-PCR
    • Kielar,D., Dietmaier,W., Langmann,T., Aslanidis,C., Probst,M., Naruszewicz,M. and Schmitz,G. (2001) Rapid quantification of human ABCA1 mRNA in various cell types and tissues by real-time reverse transcription-PCR. Clin. Chem., 47, 2089-2097.
    • (2001) Clin. Chem , vol.47 , pp. 2089-2097
    • Kielar, D.1    Dietmaier, W.2    Langmann, T.3    Aslanidis, C.4    Probst, M.5    Naruszewicz, M.6    Schmitz, G.7
  • 80
    • 17844389602 scopus 로고    scopus 로고
    • Thermally reversible inactivation of Taq polymerase in an organic solvent for application in hot start PCR
    • Louwrier,A. and van der Valk,A. (2005) Thermally reversible inactivation of Taq polymerase in an organic solvent for application in hot start PCR. Enzyme Microb. Technol., 36, 947-952.
    • (2005) Enzyme Microb. Technol , vol.36 , pp. 947-952
    • Louwrier, A.1    van der Valk, A.2
  • 81
    • 0027382929 scopus 로고
    • Degradation of DNA during the denaturation step of PCR
    • Douglas,A. and Atchison,B. (1993) Degradation of DNA during the denaturation step of PCR. PCR Methods Appl., 3, 133-134.
    • (1993) PCR Methods Appl , vol.3 , pp. 133-134
    • Douglas, A.1    Atchison, B.2
  • 82
    • 0031568919 scopus 로고    scopus 로고
    • Product differentiation by analysis of DNA melting curves during the polymerase chain reaction
    • Ririea,K.M., Rasmussenb,R.P. and Wittwer,C.T. (1997) Product differentiation by analysis of DNA melting curves during the polymerase chain reaction. Anal. Biochem., 245, 154-160.
    • (1997) Anal. Biochem , vol.245 , pp. 154-160
    • Ririea, K.M.1    Rasmussenb, R.P.2    Wittwer, C.T.3
  • 83
    • 0031022694 scopus 로고    scopus 로고
    • Continuous fluorescence monitoring of rapid cycle DNA amplification
    • Wittwer,C.T., Herrmann,M.G., Moss,A.A. and Rasmussen,R.P. (1997) Continuous fluorescence monitoring of rapid cycle DNA amplification. BioTechniques, 22, 130-131, 134-138.
    • (1997) BioTechniques , vol.22 , Issue.130-131 , pp. 134-138
    • Wittwer, C.T.1    Herrmann, M.G.2    Moss, A.A.3    Rasmussen, R.P.4
  • 84
    • 0037435395 scopus 로고    scopus 로고
    • Assumption-free analysis of quantitative real-time polymerase chain reaction (PCR) data
    • Ramakers,C., Ruijter,J.M., Deprez,R.H. and Moorman,A.F. (2003) Assumption-free analysis of quantitative real-time polymerase chain reaction (PCR) data. Neurosci. Lett., 339, 62-66.
    • (2003) Neurosci. Lett , vol.339 , pp. 62-66
    • Ramakers, C.1    Ruijter, J.M.2    Deprez, R.H.3    Moorman, A.F.4
  • 85
    • 0020480279 scopus 로고
    • Oligothymidylate analogues having stereoregular, alternating methylphosphonate/phosphodiester backbones as primers for DNA polymerase
    • Miller,P.S., Annan,N.D., McParland,K.B. and Pulford,S.M. (1982) Oligothymidylate analogues having stereoregular, alternating methylphosphonate/phosphodiester backbones as primers for DNA polymerase. Biochemistry, 21, 2507-2512.
    • (1982) Biochemistry , vol.21 , pp. 2507-2512
    • Miller, P.S.1    Annan, N.D.2    McParland, K.B.3    Pulford, S.M.4
  • 86
    • 0017600059 scopus 로고
    • Duplex formation of a nonionic oligo(deoxythymidylate) analogue (heptadeoxythymidylyl-(3′-5′)-deoxythymidine heptaethyl ester (d-(Tp(Et))7T)) with poly(deoxyadenylate). Evaluation of the electrostatic interaction
    • Pless,R.C. and Ts'o,P.O. (1977) Duplex formation of a nonionic oligo(deoxythymidylate) analogue (heptadeoxythymidylyl-(3′-5′)-deoxythymidine heptaethyl ester (d-(Tp(Et))7T)) with poly(deoxyadenylate). Evaluation of the electrostatic interaction. Biochemistry, 16, 1239-1250.
    • (1977) Biochemistry , vol.16 , pp. 1239-1250
    • Pless, R.C.1    Ts'o, P.O.2
  • 88
    • 33644868717 scopus 로고    scopus 로고
    • Analysis of one-step and two-step real-time RT-PCR using Superscript III
    • Wacker,M.J. and Godard,M.P. (2005) Analysis of one-step and two-step real-time RT-PCR using Superscript III. J. Biomol. Tech., 16 266-271.
    • (2005) J. Biomol. Tech , vol.16 , pp. 266-271
    • Wacker, M.J.1    Godard, M.P.2
  • 89
    • 0036667911 scopus 로고    scopus 로고
    • Sensitivity and accuracy of quantitative real-time polymerase chain reaction using SYBR green I depends on cDNA synthesis conditions
    • Lekanne Deprez,R.H., Fijnvandraat,A.C., Ruijter,J.M. and Moorman,A.F.M. (2002) Sensitivity and accuracy of quantitative real-time polymerase chain reaction using SYBR green I depends on cDNA synthesis conditions. Anal. Biochem., 307, 63-69.
    • (2002) Anal. Biochem , vol.307 , pp. 63-69
    • Lekanne Deprez, R.H.1    Fijnvandraat, A.C.2    Ruijter, J.M.3    Moorman, A.F.M.4
  • 90
    • 29144495882 scopus 로고    scopus 로고
    • PCR inhibition by reverse transcriptase leads to an overestimation of amplification efficiency
    • Suslov,O. and Steindler,D.A. (2005) PCR inhibition by reverse transcriptase leads to an overestimation of amplification efficiency. Nucleic Acids Res., 33, e181.
    • (2005) Nucleic Acids Res , vol.33
    • Suslov, O.1    Steindler, D.A.2
  • 91
    • 1842829051 scopus 로고    scopus 로고
    • Real-time RT-PCR: Considerations for efficient and sensitive assay design
    • Peters,I.R., Helps,C.R., Hall,E.J. and Day,M.J. (2004) Real-time RT-PCR: considerations for efficient and sensitive assay design. J. Immunol. Methods, 286, 203-217.
    • (2004) J. Immunol. Methods , vol.286 , pp. 203-217
    • Peters, I.R.1    Helps, C.R.2    Hall, E.J.3    Day, M.J.4
  • 92
    • 33747130345 scopus 로고    scopus 로고
    • Miniaturising the laboratory in emulsion droplets
    • Griffiths,A.D. and Tawfik,D.S. (2006) Miniaturising the laboratory in emulsion droplets. Trends Biotechnol., 24, 395-402.
    • (2006) Trends Biotechnol , vol.24 , pp. 395-402
    • Griffiths, A.D.1    Tawfik, D.S.2
  • 93
    • 0034982308 scopus 로고    scopus 로고
    • PCR amplification and sequencing of single copy DNA molecules
    • Musundi,B. and Soper,S.A. (2001) PCR amplification and sequencing of single copy DNA molecules. Single Mol., 2, 13-21.
    • (2001) Single Mol , vol.2 , pp. 13-21
    • Musundi, B.1    Soper, S.A.2
  • 94
    • 32044461294 scopus 로고    scopus 로고
    • Multiplexed profiling of candidate genes for CpG island methylation status using a flexible PCR/LDR/Universal Array assay
    • Cheng,Y.W., Shawber,C., Notterman,D., Paty,P. and Barany,F. (2006) Multiplexed profiling of candidate genes for CpG island methylation status using a flexible PCR/LDR/Universal Array assay. Genome Res. 16, 282-289.
    • (2006) Genome Res , vol.16 , pp. 282-289
    • Cheng, Y.W.1    Shawber, C.2    Notterman, D.3    Paty, P.4    Barany, F.5


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