BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

96 related articles for article (PubMed ID: 18029683)

  • 1. Effective strand invasion ODN incorporating a new bicyclic nucleoside analogue (WNA).
    Aoki E; Taniguchi Y; Sasaki S
    Nucleic Acids Symp Ser (Oxf); 2007; (51):255-6. PubMed ID: 18029683
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Efficient DNA strand displacement by a W-shaped nucleoside analogue (WNA-βT) containing an ortho-methyl-substituted phenyl ring.
    Aoki E; Taniguchi Y; Wada Y; Sasaki S
    Chembiochem; 2012 May; 13(8):1152-60. PubMed ID: 22549913
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Effects of the modified aromatic ring of WNA on stability of triplex DNA.
    Aoki E; Taniguchi Y; Togo M; Sasaki S
    Nucleic Acids Symp Ser (Oxf); 2006; (50):185-6. PubMed ID: 17150879
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Selective formation of stable triplexes including a TA or a CG interrupting site with new bicyclic nucleoside analogues (WNA).
    Sasaki S; Taniguchi Y; Takahashi R; Senko Y; Kodama K; Nagatsugi F; Maeda M
    J Am Chem Soc; 2004 Jan; 126(2):516-28. PubMed ID: 14719949
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Modification of the aromatic ring of the WNA analogues for expansion of the triplex recognition codes.
    Taniguchi Y; Nakamura A; Aoki E; Sasaki S
    Nucleic Acids Symp Ser (Oxf); 2005; (49):173-4. PubMed ID: 17150689
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Formation of a stable triplex incorporating a CG interrupting site by a new WNA derivative containing 3-aminopyrazole as a nucleobase.
    Uchida Y; Taniguchi Y; Aoki E; Togo M; Sasaki S
    Nucleic Acids Symp Ser (Oxf); 2008; (52):137-8. PubMed ID: 18776291
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Effects of halogenated WNA derivatives on sequence dependency for expansion of recognition sequences in non-natural-type triplexes.
    Taniguchi Y; Nakamura A; Senko Y; Nagatsugi F; Sasaki S
    J Org Chem; 2006 Mar; 71(5):2115-22. PubMed ID: 16497000
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Effects of 5-substituted pyrimidine nucleoside bases of WNA on stability of triplex DNA.
    Taniguchi Y; Nakamura A; Senko Y; Sasaki S
    Nucleic Acids Symp Ser (Oxf); 2004; (48):69-70. PubMed ID: 17150482
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An efficient antigene activity and antiproliferative effect by targeting the Bcl-2 or survivin gene with triplex forming oligonucleotides containing a W-shaped nucleoside analogue (WNA-βT).
    Taniguchi Y; Sasaki S
    Org Biomol Chem; 2012 Oct; 10(41):8336-41. PubMed ID: 22987068
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recognition of CG interrupting site by W-shaped nucleoside analogs (WNA) having the pyrazole ring in an anti-parallel triplex DNA.
    Taniguchi Y; Uchida Y; Takaki T; Aoki E; Sasaki S
    Bioorg Med Chem; 2009 Oct; 17(19):6803-10. PubMed ID: 19736014
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expansion of triplex recognition codes by the use of novel bicyclic nucleoside derivatives (WNA).
    Taniguchi Y; Nakamura A; Senko Y; Kodama K; Nagatsugi F; Sasaki S
    Nucleosides Nucleotides Nucleic Acids; 2005; 24(5-7):823-7. PubMed ID: 16250103
    [TBL] [Abstract][Full Text] [Related]  

  • 12. New base analogs for the formation of non-natural triplexes.
    Sasaki S; Yamauchi H; Takahasi R; Taniguchi Y; Maeda M
    Nucleic Acids Res Suppl; 2001; (1):23-4. PubMed ID: 12836245
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Design and evaluation of novel nucleoside analogs (WNA) for specific formation of non-natural type triplexes containing a TA or CG interrupting site.
    Taniguchi Y; Senko Y; Kodama K; Nakamura A; Sasaki S
    Nucleic Acids Res Suppl; 2003; (3):113-4. PubMed ID: 14510406
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Selective formation of non-natural type triplexes containing TA interrupting sites with the TFO incorporating W-shape nucleic acid (WNA) analogs.
    Taniguchi Y; Takahashi R; Kodama K; Senko Y; Maeda M; Sasaki S
    Nucleic Acids Res Suppl; 2002; (2):35-6. PubMed ID: 12903092
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synthesis and evaluation of oligonucleotides incorporating novel artificial nucleobases for the selective formation of non-natural type triplexes.
    Nakashima S; Matsuura N; Nagatsugi F; Maeda M; Sasaki S
    Nucleic Acids Symp Ser; 1997; (37):33-4. PubMed ID: 9585985
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Stable oligonucleotide-directed triplex formation at target sites with CG interruptions: strong sequence-specific recognition by 2',4'-bridged nucleic-acid-containing 2-pyridones under physiological conditions.
    Obika S; Hari Y; Sekiguchi M; Imanishi T
    Chemistry; 2002 Oct; 8(20):4796-802. PubMed ID: 12561120
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Nucleosides and nucleotides. 218. Alternate-strand triple-helix formation by the 3'-3'-linked oligodeoxynucleotides using a purine motif.
    Hoshika S; Ueno Y; Matsuda A
    Bioconjug Chem; 2003; 14(3):607-13. PubMed ID: 12757386
    [TBL] [Abstract][Full Text] [Related]  

  • 18. DNA duplexes and triplex-forming oligodeoxynucleotides incorporating modified nucleosides forming stable and selective triplexes.
    Kanamori T; Masaki Y; Mizuta M; Tsunoda H; Ohkubo A; Sekine M; Seio K
    Org Biomol Chem; 2012 Feb; 10(5):1007-13. PubMed ID: 22146807
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Triplex formation involving 2'-O,4'-C-methylene bridged nucleic acid (2',4'-BNA) with 1-isoquinolone base analogue: efficient and selective recognition of C:G interruption.
    Torigoe H; Hari Y; Obika S; Imanishi T
    Nucleosides Nucleotides Nucleic Acids; 2003; 22(5-8):1571-3. PubMed ID: 14565468
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Promotion of duplex and triplex DNA formation by polycation comb-type copolymers.
    Torigoe H; Maruyama A
    Methods Mol Med; 2001; 65():209-24. PubMed ID: 21318757
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.