BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 32115336)

  • 1. The ability of a triplex-forming oligonucleotide to recognize T-A and C-G base pairs in a DNA duplex is enhanced by incorporating N-acetyl-2,7-diaminoquinoline.
    Ohkubo A; Ohnishi T; Nishizawa S; Nishimura Y; Hisamatsu S
    Bioorg Med Chem; 2020 Apr; 28(7):115350. PubMed ID: 32115336
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Development of antiparallel-type triplex-forming oligonucleotides containing quinoline derivatives capable of recognizing a T-A base pair in a DNA duplex.
    Nishizawa S; Tu G; Ogata D; Miyauchi K; Ohkubo A
    Bioorg Med Chem; 2022 Oct; 71():116934. PubMed ID: 35921784
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis and triplex-forming properties of oligonucleotides capable of recognizing corresponding DNA duplexes containing four base pairs.
    Ohkubo A; Yamada K; Ito Y; Yoshimura K; Miyauchi K; Kanamori T; Masaki Y; Seio K; Yuasa H; Sekine M
    Nucleic Acids Res; 2015 Jul; 43(12):5675-86. PubMed ID: 26013815
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Evidence for a DNA triplex in a recombination-like motif: I. Recognition of Watson-Crick base pairs by natural bases in a high-stability triplex.
    Walter A; Schütz H; Simon H; Birch-Hirschfeld E
    J Mol Recognit; 2001; 14(2):122-39. PubMed ID: 11301482
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 2',4'-BNA derivatives bearing an unnatural nucleobase: synthesis and application to triplex-forming oligonucleotides.
    Inohara H; Obika S; Imanishi T
    Nucleic Acids Symp Ser (Oxf); 2004; (48):63-4. PubMed ID: 17150479
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Recognition of base pair inversions in duplex by chimeric (alpha,beta) triplex-forming oligonucleotides.
    Timofeev EN; Goryaeva BV; Florentiev VL
    J Biomol Struct Dyn; 2006 Oct; 24(2):183-8. PubMed ID: 16928141
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Transcription of DNA duplex containing deoxypseudouridine and deoxypseudoisocytidine, and inhibition of transcription by triplex forming oligonucleotide that recognizes the modified duplex.
    Seio K; Yamaguchi K; Yamazaki A; Kanamori T; Masaki Y
    Nucleosides Nucleotides Nucleic Acids; 2020; 39(6):892-904. PubMed ID: 32126878
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthesis and triplex forming ability of conformationally locked oligonucleotides containing unnatural nucleobases: efficient recognition of a C.G interruption.
    Obika S; Hari Y; Sekiguchi M; Imanishi T
    Nucleic Acids Symp Ser; 2000; (44):131-2. PubMed ID: 12903303
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chemical modification of triplex-forming oligonucleotide to promote pyrimidine motif triplex formation at physiological pH.
    Torigoe H; Nakagawa O; Imanishi T; Obika S; Sasaki K
    Biochimie; 2012 Apr; 94(4):1032-40. PubMed ID: 22245184
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Oligonucleotides Containing Phenoxazine Artificial Nucleobases: Triplex-Forming Abilities and Fluorescence Properties.
    Fujii A; Nakagawa O; Kishimoto Y; Nakatsuji Y; Nozaki N; Obika S
    Chembiochem; 2020 Mar; 21(6):860-864. PubMed ID: 31568630
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An isocytidine derivative with a 2-amino-6-methylpyridine unit for selective recognition of the CG interrupting site in an antiparallel triplex DNA.
    Okamura H; Taniguchi Y; Sasaki S
    Chembiochem; 2014 Nov; 15(16):2374-8. PubMed ID: 25186222
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Highly stable DNA triplexes formed with cationic phosphoramidate pyrimidine alpha-oligonucleotides.
    Michel T; Debart F; Heitz F; Vasseur JJ
    Chembiochem; 2005 Jul; 6(7):1254-62. PubMed ID: 15912553
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Interactions of cytosine derivatives with T.A interruptions in pyrimidine.purine.pyrimidine DNA triplexes.
    Verma S; Miller PS
    Bioconjug Chem; 1996; 7(5):600-5. PubMed ID: 8889023
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Purine- and pyrimidine-triple-helix-forming oligonucleotides recognize qualitatively different target sites at the ribosomal DNA locus.
    Maldonado R; Filarsky M; Grummt I; Längst G
    RNA; 2018 Mar; 24(3):371-380. PubMed ID: 29222118
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Modulation of Cm/T, G/A, and G/T triplex stability by conjugate groups in the presence and absence of KCl.
    Gamper HB; Kutyavin IV; Rhinehart RL; Lokhov SG; Reed MW; Meyer RB
    Biochemistry; 1997 Dec; 36(48):14816-26. PubMed ID: 9398203
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Nuclear magnetic resonance structural studies of intramolecular purine.purine.pyrimidine DNA triplexes in solution. Base triple pairing alignments and strand direction.
    Radhakrishnan I; de los Santos C; Patel DJ
    J Mol Biol; 1991 Oct; 221(4):1403-18. PubMed ID: 1942059
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.