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Volumn 31, Issue 5, 2012, Pages 389-400

Synthesis and properties of rnas that contain a PNA-RNA dimer

Author keywords

Nucleotide sugars; PNA; RNA synthesis; Solid phase synthesis

Indexed keywords

DIMER; PEPTIDE NUCLEIC ACID; PHOSPHORAMIDOUS ACID; RNA;

EID: 84859806767     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1080/15257770.2012.666609     Document Type: Article
Times cited : (4)

References (22)
  • 1
    • 84990238662 scopus 로고
    • Peptide nucleic-acids (PNA) - Oligonucleotide analogs with an achiral peptide backbone
    • Egholm, M.; Buchardt, O.; Nielsen, P.E.; Berg, R.H. Peptide nucleic-acids (PNA) - oligonucleotide analogs with an achiral peptide backbone. J. Am. Chem. Soc. 1992, 114, 1895-1897.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 1895-1897
    • Egholm, M.1    Buchardt, O.2    Nielsen, P.E.3    Berg, R.H.4
  • 2
    • 0029986009 scopus 로고    scopus 로고
    • Peptide nucleic acids (PNA): Synthesis, properties and potential applications
    • Hyrup, B.;Nielsen, P.E. Peptide nucleic acids (PNA): synthesis, properties and potential applications. Bioorg. Med. Chem. 1996, 4, 5-23.
    • (1996) Bioorg. Med. Chem. , vol.4 , pp. 5-23
    • Hyrup, B.1    Nielsen, P.E.2
  • 3
    • 0037414320 scopus 로고    scopus 로고
    • PNA for one-base differentiating protection of DNA from nuclease and its use for SNPs detection
    • Komiyama, M.; Ye, S.; Liang, X.G.; Yamamoto, Y.; Tomita, T.; Zhou, J.M.; Aburatani, H. PNA for one-base differentiating protection of DNA from nuclease and its use for SNPs detection. J. Am. Chem. Soc. 2003, 125, 3758-3762.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 3758-3762
    • Komiyama, M.1    Ye, S.2    Liang, X.G.3    Yamamoto, Y.4    Tomita, T.5    Zhou, J.M.6    Aburatani, H.7
  • 5
    • 77953879561 scopus 로고    scopus 로고
    • Short peptide nucleic acids bind strongly to homopurine tract of double helical RNA at pH 5.5
    • Li, M.; Zengeya, T.; Rozners, E. Short peptide nucleic acids bind strongly to homopurine tract of double helical RNA at pH 5.5. J. Am. Chem. Soc. 2010, 132, 17052-17052.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 17052-17052
    • Li, M.1    Zengeya, T.2    Rozners, E.3
  • 7
    • 0142043367 scopus 로고    scopus 로고
    • PNA-DNA chimeras containing 5-alkynyl-pyrimidine PNA units. Synthesis, binding properties, and enzymatic stability
    • Bajor, Z.; Sagi, G.; Tegyey, Z.; Kraicsovits, F. PNA-DNA chimeras containing 5-alkynyl-pyrimidine PNA units. Synthesis, binding properties, and enzymatic stability. Nucleosides Nucleotides Nucleic Acids 2003, 22, 1963-1983.
    • (2003) Nucleosides Nucleotides Nucleic Acids , vol.22 , pp. 1963-1983
    • Bajor, Z.1    Sagi, G.2    Tegyey, Z.3    Kraicsovits, F.4
  • 8
    • 33947625050 scopus 로고    scopus 로고
    • Induction of RNase H activity by arabinose-peptide nucleic acid chimeras
    • Patureau, B.M.; Hudson, R.H.E.; Damha, M.J. Induction of RNase H activity by arabinose-peptide nucleic acid chimeras. Bioconjug. Chem. 2007, 18, 421-430.
    • (2007) Bioconjug. Chem. , vol.18 , pp. 421-430
    • Patureau, B.M.1    Hudson, R.H.E.2    Damha, M.J.3
  • 11
    • 0032545933 scopus 로고    scopus 로고
    • Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans
    • Fire, A.; Xu, S.Q.; Montgomery, M.K.; Kostas, S.A.; Driver, S.E.; Mello, C.C. Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans. Nature 1998, 391, 806-811.
    • (1998) Nature , vol.391 , pp. 806-811
    • Fire, A.1    Xu, S.Q.2    Montgomery, M.K.3    Kostas, S.A.4    Driver, S.E.5    Mello, C.C.6
  • 12
    • 52049090811 scopus 로고    scopus 로고
    • Chemically modified siRNA: Tools and applications
    • Watts, J.K.; Deleavey, G.F.; Damha, M.J. Chemically modified siRNA: tools and applications. Drug Discov. Today 2008, 13, 842-855.
    • (2008) Drug Discov. Today , vol.13 , pp. 842-855
    • Watts, J.K.1    Deleavey, G.F.2    Damha, M.J.3
  • 13
    • 84856683514 scopus 로고    scopus 로고
    • Efficient synthesis and cell-based activities of siRNAs that contain triazole backbone modifications
    • Efthymiou, T.C.; Huynh, V.; Oentoro, J.; Peel, J.; Desaulniers, J.-P. Efficient synthesis and cell-based activities of siRNAs that contain triazole backbone modifications. Bioorg. Med. Chem. Lett. 2012, 3, 1722-1726.
    • Bioorg. Med. Chem. Lett. , vol.2012 , Issue.3 , pp. 1722-1726
    • Efthymiou, T.C.1    Huynh, V.2    Oentoro, J.3    Peel, J.4    Desaulniers, J.-P.5
  • 15
    • 0024581185 scopus 로고
    • The stereoselective syntheses of substituted furo 2,3B furans
    • Vader, J.; Sengers, H.; Degroot, A. The stereoselective syntheses of substituted furo 2,3B furans. Tetrahedron 1989, 45, 2131-2142.
    • (1989) Tetrahedron , vol.45 , pp. 2131-2142
    • Vader, J.1    Sengers, H.2    Degroot, A.3
  • 16
    • 0033693577 scopus 로고    scopus 로고
    • Synthesis and structure of novel phosphonodipeptides containing a uracil or thymine group
    • Liu, X.J.; Chen, R.Y.; Weng, L.H.; Leng, X.B. Synthesis and structure of novel phosphonodipeptides containing a uracil or thymine group. Heteroatom Chem. 2000, 11, 422-427.
    • (2000) Heteroatom Chem. , vol.11 , pp. 422-427
    • Liu, X.J.1    Chen, R.Y.2    Weng, L.H.3    Leng, X.B.4
  • 17
    • 0036008125 scopus 로고    scopus 로고
    • An inhibitor of the human UDP-GlcNAc 4-epimerase identified from a uridine-based library: A strategy to inhibit O-linked glycosylation
    • Winans, K.A.; Bertozzi, C.R. An inhibitor of the human UDP-GlcNAc 4-epimerase identified from a uridine-based library: a strategy to inhibit O-linked glycosylation. Chem. Biol. 2002, 9, 113-129.
    • (2002) Chem. Biol. , vol.9 , pp. 113-129
    • Winans, K.A.1    Bertozzi, C.R.2
  • 18
    • 0042869554 scopus 로고
    • The triisopropylsilyl group in organic chemistry - Just a protective group, or more
    • Rucker, C. The triisopropylsilyl group in organic chemistry - just a protective group, or more. Chem. Rev. 1995, 95, 1009-1064.
    • (1995) Chem. Rev. , vol.95 , pp. 1009-1064
    • Rucker, C.1
  • 19
    • 79954569229 scopus 로고    scopus 로고
    • RNA synthesis via dimer and trimer phosphoramidite block coupling
    • Hassler, M.; Wu, Y.Q.; Reddy, N.M.; Chan, T.H.; Damha, M.J. RNA synthesis via dimer and trimer phosphoramidite block coupling. Tet. Lett. 2011, 52, 2575-2578.
    • (2011) Tet. Lett. , vol.52 , pp. 2575-2578
    • Hassler, M.1    Wu, Y.Q.2    Reddy, N.M.3    Chan, T.H.4    Damha, M.J.5
  • 20
    • 0030833028 scopus 로고    scopus 로고
    • Synthesis and hybridization properties of modified oligonucleotides with PNA-DNA dimer blocks
    • Wenninger, D.; Seliger, H. Synthesis and hybridization properties of modified oligonucleotides with PNA-DNA dimer blocks. Nucleosides Nucleotides 1997, 16, 977-980.
    • (1997) Nucleosides Nucleotides , vol.16 , pp. 977-980
    • Wenninger, D.1    Seliger, H.2
  • 21
    • 0023055352 scopus 로고
    • CD of homopolymer DNA·RNA hybrid duplexes and triplexes containing A·T or A·U base-pairs
    • Steely, H.T.; Gray, D.M.; Ratliff, R.L. CD of homopolymer DNA·RNA hybrid duplexes and triplexes containing A·T or A·U base-pairs. Nucleic Acids Res. 1986, 14, 10071-10090.
    • (1986) Nucleic Acids Res. , vol.14 , pp. 10071-10090
    • Steely, H.T.1    Gray, D.M.2    Ratliff, R.L.3
  • 22
    • 0002714675 scopus 로고
    • Rapid chromatographic technique for preparative separations with moderate resolution
    • Still, W.C.; Kahn, M.; Mitra, A. Rapid chromatographic technique for preparative separations with moderate resolution. J. Org. Chem. 1978, 43, 2923-2925.
    • (1978) J. Org. Chem. , vol.43 , pp. 2923-2925
    • Still, W.C.1    Kahn, M.2    Mitra, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.