85 related articles for article (PubMed ID: 23660599)
1. N-(guanidinoethyl)-2'-deoxy-5-methylisocytidine exhibits selective recognition of a CG interrupting site for the formation of anti-parallel triplexes.
Okamura H; Taniguchi Y; Sasaki S
Org Biomol Chem; 2013 Jun; 11(23):3918-24. PubMed ID: 23660599
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Effect of the 3-halo substitution of the 2'-deoxy aminopyridinyl-pseudocytidine derivatives on the selectivity and stability of antiparallel triplex DNA with a CG inversion site.
Wang L; Taniguchi Y; Okamura H; Sasaki S
Bioorg Med Chem; 2017 Jul; 25(14):3853-3860. PubMed ID: 28571974
[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. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. Modification of the aminopyridine unit of 2'-deoxyaminopyridinyl-pseudocytidine allowing triplex formation at CG interruptions in homopurine sequences.
Wang L; Taniguchi Y; Okamura H; Sasaki S
Nucleic Acids Res; 2018 Sep; 46(17):8679-8688. PubMed ID: 30102410
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Aminopyridinyl-Pseudodeoxycytidine Derivatives Selectively Stabilize Antiparallel Triplex DNA with Multiple CG Inversion Sites.
Okamura H; Taniguchi Y; Sasaki S
Angew Chem Int Ed Engl; 2016 Sep; 55(40):12445-9. PubMed ID: 27576703
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Synthesis of C-nucleoside analogues based on the pyrimidine skeleton for the formation of anti-parallel-type triplex DNA with a CG mismatch site.
Notomi R; Wang L; Osuki T; Okamura H; Sasaki S; Taniguchi Y
Bioorg Med Chem; 2020 Dec; 28(23):115782. PubMed ID: 32992254
[TBL] [Abstract][Full Text] [Related]
15. Synthesis and duplex DNA recognition studies of oligonucleotides containing a ureido isoindolin-1-one homo-N-nucleoside. A comparison of host-guest and DNA recognition studies.
Mertz E; Mattei S; Zimmerman SC
Bioorg Med Chem; 2004 Mar; 12(6):1517-26. PubMed ID: 15018925
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Synthesis of 2'-deoxy-4-aminopyridinylpseudocytidine Derivatives for Incorporation Into Triplex Forming Oligonucleotides.
Taniguchi Y; Wang L; Okamura H; Sasaki S
Curr Protoc Nucleic Acid Chem; 2019 Jun; 77(1):e80. PubMed ID: 30884181
[TBL] [Abstract][Full Text] [Related]
18. Recognition of 5-methyl-CG and CG base pairs in duplex DNA with high stability using antiparallel-type triplex-forming oligonucleotides with 2-guanidinoethyl-2'-deoxynebularine.
Notomi R; Sasaki S; Taniguchi Y
Nucleic Acids Res; 2022 Nov; 50(21):12071-12081. PubMed ID: 36454012
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]