Published in Curr Opin Chem Biol on November 09, 2007
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Efforts toward expansion of the genetic alphabet: structure and replication of unnatural base pairs. J Am Chem Soc (2007) 1.25
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Evidence for a Watson-Crick hydrogen bonding requirement in DNA synthesis by human DNA polymerase kappa. Mol Cell Biol (2005) 1.19
The use of nonnatural nucleotides to probe the contributions of shape complementarity and pi-electron surface area during DNA polymerization. Biochemistry (2005) 1.19
Human DNA polymerase alpha uses a combination of positive and negative selectivity to polymerize purine dNTPs with high fidelity. Biochemistry (2007) 1.18
Hydrophobicity, shape, and pi-electron contributions during translesion DNA synthesis. J Am Chem Soc (2006) 1.17
Remarkable sensitivity to DNA base shape in the DNA polymerase active site. Angew Chem Int Ed Engl (2006) 1.15
Efforts towards expansion of the genetic alphabet: pyridone and methyl pyridone nucleobases. Angew Chem Int Ed Engl (2006) 1.15
Optimization of unnatural base pair packing for polymerase recognition. J Am Chem Soc (2006) 1.11
Stability and polymerase recognition of pyridine nucleobase analogues: role of minor-groove H-bond acceptors. Angew Chem Int Ed Engl (2006) 1.10
New base pairing motifs. The synthesis and thermal stability of oligodeoxynucleotides containing imidazopyridopyrimidine nucleosides with the ability to form four hydrogen bonds. J Am Chem Soc (2003) 1.08
An efficient unnatural base pair for a base-pair-expanded transcription system. J Am Chem Soc (2005) 1.06
Human DNA primase uses Watson-Crick hydrogen bonds to distinguish between correct and incorrect nucleoside triphosphates. Biochemistry (2004) 1.06
A series of nonpolar thymidine analogues of increasing size: DNA base pairing and stacking properties. J Org Chem (2005) 1.06
Substituent effects on the pairing and polymerase recognition of simple unnatural base pairs. Nucleic Acids Res (2006) 1.04
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The roles of hydrogen bonding and sterics in RNA interference. Angew Chem Int Ed Engl (2006) 1.00
DNA polymerase template interactions probed by degenerate isosteric nucleobase analogs. Chem Biol (2003) 0.99
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An efficiently extended class of unnatural base pairs. J Am Chem Soc (2006) 0.97
pentafluorophenyl-phenyl interactions in biphenyl-DNA. Chemistry (2005) 0.95
Selective pairing of polyfluorinated DNA bases. J Am Chem Soc (2004) 0.92
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Stable, specific, and reversible base pairing via Schiff base. J Am Chem Soc (2005) 0.88
A synthetic nucleoside probe that discerns a DNA adduct from unmodified DNA. J Am Chem Soc (2007) 0.86
Solution structure and dynamics of DNA duplexes containing the universal base analogues 5-nitroindole and 5-nitroindole 3-carboxamide. Nucleic Acids Res (2007) 0.84
Nonpolar isosteres of damaged DNA bases: effective mimicry of mutagenic properties of 8-oxopurines. J Am Chem Soc (2007) 0.82
Base pair stability of 8-chloro- and 8-iodo-2'-deoxyguanosine opposite 2'-deoxycytidine: implications regarding the bioactivity of 8-oxo-2'-deoxyguanosine. J Am Chem Soc (2005) 0.82
The role of minor groove functional groups in DNA hydration. Nucleic Acids Res (2003) 0.80
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Toward a new genetic system with expanded dimensions: size-expanded analogues of deoxyadenosine and thymidine. J Am Chem Soc (2004) 1.35
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Detecting RNA and DNA with templated chemical reactions. Chem Rev (2006) 1.31
Functional evidence for a small and rigid active site in a high fidelity DNA polymerase: probing T7 DNA polymerase with variably sized base pairs. J Biol Chem (2005) 1.29
Modified DNA analogues that sense light exposure with color changes. J Am Chem Soc (2004) 1.28
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Exploring the limits of DNA size: naphtho-homologated DNA bases and pairs. J Am Chem Soc (2006) 1.04
Quenched probes for highly specific detection of cellular RNAs. Trends Biotechnol (2005) 1.04
Probing the requirements for recognition and catalysis in Fpg and MutY with nonpolar adenine isosteres. J Am Chem Soc (2003) 1.04
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Oligodeoxyfluorosides: Strong Sequence Dependence of Fluorescence Emission. Tetrahedron (2007) 0.99
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