174 related articles for article (PubMed ID: 19146369)
1. 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]
2. Unnatural imidazopyridopyrimidine:naphthyridine base pairs: selective incorporation and extension reaction by DNA polymerases.
Minakawa N; Ogata S; Takahashi M; Matsuda A
Nucleic Acids Symp Ser (Oxf); 2009; (53):125-6. PubMed ID: 19749292
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Unnatural imidazopyridopyrimidine:naphthyridine base pairs: selective incorporation and extension reaction by Deep Vent (exo- ) DNA polymerase.
Ogata S; Takahashi M; Minakawa N; Matsuda A
Nucleic Acids Res; 2009 Sep; 37(17):5602-9. PubMed ID: 19628664
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Faithful PCR Amplification of an Unnatural Base-Pair Analogue with Four Hydrogen Bonds.
Tarashima N; Komatsu Y; Furukawa K; Minakawa N
Chemistry; 2015 Jul; 21(30):10688-95. PubMed ID: 26177045
[TBL] [Abstract][Full Text] [Related]
7. Selective transcription of an unnatural naphthyridine:imidazopyridopyrimidine base pair containing four hydrogen bonds with T7 RNA polymerase.
Nomura Y; Kashiwagi S; Sato K; Matsuda A
Angew Chem Int Ed Engl; 2014 Nov; 53(47):12844-8. PubMed ID: 25251031
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Unnatural Base Pairs for Synthetic Biology.
Saito-Tarashima N; Minakawa N
Chem Pharm Bull (Tokyo); 2018; 66(2):132-138. PubMed ID: 29386463
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Evidence for Watson-Crick and not Hoogsteen or wobble base pairing in the selection of nucleotides for insertion opposite pyrimidines and a thymine dimer by yeast DNA pol eta.
Hwang H; Taylor JS
Biochemistry; 2005 Mar; 44(12):4850-60. PubMed ID: 15779911
[TBL] [Abstract][Full Text] [Related]
13. Efficient replication between non-hydrogen-bonded nucleoside shape analogs.
Morales JC; Kool ET
Nat Struct Biol; 1998 Nov; 5(11):950-4. PubMed ID: 9808038
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Fluorous base-pairing effects in a DNA polymerase active site.
Lai JS; Kool ET
Chemistry; 2005 May; 11(10):2966-71. PubMed ID: 15744767
[TBL] [Abstract][Full Text] [Related]
16. Natural versus artificial creation of base pairs in DNA: origin of nucleobases from the perspectives of unnatural base pair studies.
Hirao I; Kimoto M; Yamashige R
Acc Chem Res; 2012 Dec; 45(12):2055-65. PubMed ID: 22263525
[TBL] [Abstract][Full Text] [Related]
17. The effect of minor-groove hydrogen-bond acceptors and donors on the stability and replication of four unnatural base pairs.
Matsuda S; Henry AA; Schultz PG; Romesberg FE
J Am Chem Soc; 2003 May; 125(20):6134-9. PubMed ID: 12785844
[TBL] [Abstract][Full Text] [Related]
18. [Affinity modification of DNA polymerase I from Escherichia coli and its Klenow fragment with nucleotide imidazolides].
Doronin SV; Nevinskiĭ GA; Khomov VV; Lavrik OI
Mol Biol (Mosk); 1991; 25(2):358-67. PubMed ID: 1881393
[TBL] [Abstract][Full Text] [Related]
19. DNA polymerase catalysis in the absence of Watson-Crick hydrogen bonds: analysis by single-turnover kinetics.
Potapova O; Chan C; DeLucia AM; Helquist SA; Kool ET; Grindley ND; Joyce CM
Biochemistry; 2006 Jan; 45(3):890-8. PubMed ID: 16411765
[TBL] [Abstract][Full Text] [Related]
20. [Structural and Dipole Structure Peculiarities of Hoogsteen Base Pairs Formed in Complementary Nucleobases according to ab initio Quantum Mechanics Studies].
Petrenko YM
Biofizika; 2015; 60(5):853-60. PubMed ID: 26591595
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
