834 related articles for article (PubMed ID: 12914460)
1. New base pairing motifs. The synthesis and thermal stability of oligodeoxynucleotides containing imidazopyridopyrimidine nucleosides with the ability to form four hydrogen bonds.
Minakawa N; Kojima N; Hikishima S; Sasaki T; Kiyosue A; Atsumi N; Ueno Y; Matsuda A
J Am Chem Soc; 2003 Aug; 125(33):9970-82. PubMed ID: 12914460
[TBL] [Abstract][Full Text] [Related]
2. Synthesis and characterization of oligodeoxynucleotides containing naphthyridine:imidazopyridopyrimidine base pairs at their sticky ends. Application as thermally stabilized decoy molecules.
Hikishima S; Minakawa N; Kuramoto K; Ogata S; Matsuda A
Chembiochem; 2006 Dec; 7(12):1970-5. PubMed ID: 17031887
[TBL] [Abstract][Full Text] [Related]
3. Properties and application of oligodeoxynucleotides containing the naphthyridine:imidazopyridopyrimidine base pairs with the ability to form four hydrogen bonds.
Hikishima S; Kuramoto K; Minakawa N; Matsuda A
Nucleic Acids Symp Ser (Oxf); 2004; (48):295-6. PubMed ID: 17150595
[TBL] [Abstract][Full Text] [Related]
4. Synthesis and incorporation of tricyclic-imidazo[5',4':4,5]pyrido[2,3-d]pyrimidine nucleosides into oligonucleotides and their thermal stability.
Kojima N; Ueno Y; Minakawa N; Matsuda A
Nucleic Acids Symp Ser; 1997; (37):23-4. PubMed ID: 9585980
[TBL] [Abstract][Full Text] [Related]
5. Synthesis and characterization of oligodeoxynucleotides containing a novel tetraazabenzo[cd]azulene:naphthyridine base pair.
Hirama Y; Minakawa N; Matsuda A
Bioorg Med Chem; 2011 Jan; 19(1):352-8. PubMed ID: 21129979
[TBL] [Abstract][Full Text] [Related]
6. New imidazopyridopyrimidine:naphthyridine base-pairing motif, ImN(N):NaO(O), consisting of a DAAD:ADDA hydrogen bonding pattern, markedly stabilize DNA duplexes.
Kuramoto K; Tarashima N; Hirama Y; Kikuchi Y; Minakawa N; Matsuda A
Chem Commun (Camb); 2011 Oct; 47(38):10818-20. PubMed ID: 21863185
[TBL] [Abstract][Full Text] [Related]
7. Hybridization properties and enzymatic recognitions of naphthyridine:imidazopyridopyrimidine base pairs.
Ogata S; Kuramoto K; Inoue N; Minakawa N; Matsuda A
Nucleic Acids Symp Ser (Oxf); 2006; (50):153-4. PubMed ID: 17150863
[TBL] [Abstract][Full Text] [Related]
8. 2'-Deoxyimmunosine: stereoselective synthesis, base pairing and duplex stability of oligonucleotides containing 8-oxo-7-thiaguanine.
Seela F; Ming X
Org Biomol Chem; 2008 Apr; 6(8):1450-61. PubMed ID: 18385852
[TBL] [Abstract][Full Text] [Related]
9. Selective recognition of unnatural imidazopyridopyrimidine:naphthyridine base pairs consisting of four hydrogen bonds by the Klenow fragment.
Minakawa N; Ogata S; Takahashi M; Matsuda A
J Am Chem Soc; 2009 Feb; 131(5):1644-5. PubMed ID: 19146369
[TBL] [Abstract][Full Text] [Related]
10. Chemical synthesis and thermodynamic characterization of oxanine-containing oligodeoxynucleotides.
Pack SP; Nonogawa M; Kodaki T; Makino K
Nucleic Acids Res; 2005; 33(18):5771-80. PubMed ID: 16219806
[TBL] [Abstract][Full Text] [Related]
11. A new four-base genetic helix, yDNA, composed of widened benzopyrimidine-purine pairs.
Lee AH; Kool ET
J Am Chem Soc; 2005 Mar; 127(10):3332-8. PubMed ID: 15755149
[TBL] [Abstract][Full Text] [Related]
12. Bipyridyl- and biphenyl-DNA: a recognition motif based on interstrand aromatic stacking.
Brotschi C; Mathis G; Leumann CJ
Chemistry; 2005 Mar; 11(6):1911-23. PubMed ID: 15685710
[TBL] [Abstract][Full Text] [Related]
13. Synthesis and properties of oligonucleotides with iodo-substituted aromatic aglycons: investigation of possible halogen bonding base pairs.
Tawarada R; Seio K; Sekine M
J Org Chem; 2008 Jan; 73(2):383-90. PubMed ID: 18081343
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Nuclear magnetic resonance spectroscopy and molecular modeling reveal that different hydrogen bonding patterns are possible for G.U pairs: one hydrogen bond for each G.U pair in r(GGCGUGCC)(2) and two for each G.U pair in r(GAGUGCUC)(2).
Chen X; McDowell JA; Kierzek R; Krugh TR; Turner DH
Biochemistry; 2000 Aug; 39(30):8970-82. PubMed ID: 10913310
[TBL] [Abstract][Full Text] [Related]
16. Synthesis and properties of the simplified nucleic acid glycol nucleic acid.
Meggers E; Zhang L
Acc Chem Res; 2010 Aug; 43(8):1092-102. PubMed ID: 20405911
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Effects of the minor groove pyrimidine nucleobase functional groups on the stability of duplex DNA: the impact of uncompensated minor groove amino groups.
Sun Z; McLaughlin LW
Biopolymers; 2007 Oct 5-15; 87(2-3):183-95. PubMed ID: 17657710
[TBL] [Abstract][Full Text] [Related]
19. Synthesis and properties of oligodeoxynucleotides containing 5-carboxy-2'-deoxycytidines.
Sumino M; Ohkubo A; Taguchi H; Seio K; Sekine M
Bioorg Med Chem Lett; 2008 Jan; 18(1):274-7. PubMed ID: 18023346
[TBL] [Abstract][Full Text] [Related]
20. Oligodeoxynucleotides having a loop consisting of 3'-deoxy-4'-C-(2-hydroxyethyl)thymidines form stable hairpins.
Yamamoto Y; Shuto S; Tamura Y; Kodama T; Hoshika S; Ichikawa S; Ueno Y; Ohtsuka E; Komatsu Y; Matsuda A
Biochemistry; 2004 Jul; 43(27):8690-9. PubMed ID: 15236577
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]