-
A branched DNA signal amplification assay for quantification of nucleic acid targets below 100 molecules/ml.
Nucleic Acids Res. 1997 Aug 1;25(15):2979-84
PMID: 9224596
-
High-fidelity in vivo replication of DNA base shape mimics without Watson-Crick hydrogen bonds.
Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4469-73
PMID: 12676985
-
Defined dimensional changes in enzyme substrates and cofactors. Synthesis of lin-benzoadenosine and enzymatic evaluation of derivatives of the benzopurines.
J Am Chem Soc. 1976 Jun 23;98(13):3987-94
PMID: 819479
-
Synthetic biology: Act natural.
Nature. 2003 Jan 9;421(6919):118
PMID: 12520282
-
Enzymatic incorporation of a third nucleobase pair.
Nucleic Acids Res. 2007;35(13):4238-49
PMID: 17576683
-
Synthesis and properties of size-expanded DNAs: toward designed, functional genetic systems.
Acc Chem Res. 2007 Feb;40(2):141-50
PMID: 17309194
-
Chemical etiology of nucleic acid structure.
Science. 1999 Jun 25;284(5423):2118-24
PMID: 10381870
-
DNA polymerase template interactions probed by degenerate isosteric nucleobase analogs.
Chem Biol. 2003 Sep;10(9):815-25
PMID: 14522052
-
Fluorescent probing for RNA molecules by an unnatural base-pair system.
Nucleic Acids Res. 2007;35(16):5360-9
PMID: 17693436
-
Artificial DNA made exclusively of nonnatural C-nucleosides with four types of nonnatural bases.
J Am Chem Soc. 2008 Jul 9;130(27):8762-8
PMID: 18543918
-
Fluorous base-pairing effects in a DNA polymerase active site.
Chemistry. 2005 May 6;11(10):2966-71
PMID: 15744767
-
Recognition of the nonpolar base 4-methylindole in DNA by the DNA repair adenine glycosylase MutY.
Org Lett. 2000 May 4;2(9):1341-4
PMID: 10810743
-
Functional hydrogen-bonding map of the minor groove binding tracks of six DNA polymerases.
Biochemistry. 2000 Oct 24;39(42):12979-88
PMID: 11041863
-
Gene silencing activity of siRNAs with a ribo-difluorotoluyl nucleotide.
ACS Chem Biol. 2006 Apr 25;1(3):176-83
PMID: 17163665
-
Importance of hydrogen bonding for efficiency and specificity of the human mitochondrial DNA polymerase.
J Biol Chem. 2008 May 23;283(21):14402-10
PMID: 17650502
-
Hydrophobicity, shape, and pi-electron contributions during translesion DNA synthesis.
J Am Chem Soc. 2006 Jan 11;128(1):143-9
PMID: 16390141
-
Difluorotoluene, a Nonpolar Isostere for Thymine, Codes Specifically and Efficiently for Adenine in DNA Replication.
J Am Chem Soc. 1997 Feb 26;119(8):2056-2057
PMID: 20737028
-
Enzymatic incorporation of a new base pair into DNA and RNA extends the genetic alphabet.
Nature. 1990 Jan 4;343(6253):33-7
PMID: 1688644
-
A four-base paired genetic helix with expanded size.
Science. 2003 Oct 31;302(5646):868-71
PMID: 14593180
-
DNA polymerase catalysis in the absence of Watson-Crick hydrogen bonds: analysis by single-turnover kinetics.
Biochemistry. 2006 Jan 24;45(3):890-8
PMID: 16411765
-
A new four-base genetic helix, yDNA, composed of widened benzopyrimidine-purine pairs.
J Am Chem Soc. 2005 Mar 16;127(10):3332-8
PMID: 15755149
-
Remarkable sensitivity to DNA base shape in the DNA polymerase active site.
Angew Chem Int Ed Engl. 2006 Mar 13;45(12):1974-9
PMID: 16506248
-
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. 2006 Jan 27;281(4):2289-95
PMID: 16311403
-
A series of nonpolar thymidine analogues of increasing size: DNA base pairing and stacking properties.
J Org Chem. 2005 Mar 18;70(6):2048-53
PMID: 15760186
-
Probing the active site tightness of DNA polymerase in subangstrom increments.
Proc Natl Acad Sci U S A. 2005 Nov 1;102(44):15803-8
PMID: 16249340
-
An efficiently extended class of unnatural base pairs.
J Am Chem Soc. 2006 May 31;128(21):6780-1
PMID: 16719445
-
Optimization of unnatural base pair packing for polymerase recognition.
J Am Chem Soc. 2006 May 17;128(19):6369-75
PMID: 16683801
-
Toward a new genetic system with expanded dimensions: size-expanded analogues of deoxyadenosine and thymidine.
J Am Chem Soc. 2004 Feb 4;126(4):1102-9
PMID: 14746479
-
Discovery, characterization, and optimization of an unnatural base pair for expansion of the genetic alphabet.
J Am Chem Soc. 2008 Feb 20;130(7):2336-43
PMID: 18217762
-
The use of nonnatural nucleotides to probe the contributions of shape complementarity and pi-electron surface area during DNA polymerization.
Biochemistry. 2005 Oct 4;44(39):13101-10
PMID: 16185078
-
The use of thymidine analogs to improve the replication of an extra DNA base pair: a synthetic biological system.
Nucleic Acids Res. 2005 Sep 28;33(17):5640-6
PMID: 16192575
-
Assembly of the complete eight-base artificial genetic helix, xDNA, and its interaction with the natural genetic system.
Angew Chem Int Ed Engl. 2005 May 13;44(20):3118-22
PMID: 15834852
-
Enzymatic recognition of the base pair between isocytidine and isoguanosine.
Biochemistry. 1993 Oct 5;32(39):10489-96
PMID: 7691174
-
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 Aug 20;125(33):9970-82
PMID: 12914460
-
Helix-forming properties of size-expanded DNA, an alternative four-base genetic form.
J Am Chem Soc. 2005 Feb 9;127(5):1396-402
PMID: 15686371
-
Selective and Stable DNA Base Pairing without Hydrogen Bonds.
J Am Chem Soc. 1998;120(24):6191-6192
PMID: 20852721
-
An unusual mode of DNA duplex association: Watson-Crick interaction of all-purine deoxyribonucleic acids.
Chem Biol. 2007 May;14(5):525-31
PMID: 17524983
-
Size-expanded analogues of dG and dC: synthesis and pairing properties in DNA.
J Org Chem. 2005 Jan 21;70(2):639-47
PMID: 15651812
-
Hydrophobic, Non-Hydrogen-Bonding Bases and Base Pairs in DNA.
J Am Chem Soc. 1995 Feb 22;117(7):1863-1872
PMID: 20882111
-
Aromatic Nonpolar Nucleosides as Hydrophobic Isosteres of Pyrimidine and Purine Nucleosides.
J Org Chem. 1994 Dec 1;59(24):7238-7242
PMID: 20882116
-
A thymine isostere in the templating position disrupts assembly of the closed DNA polymerase beta ternary complex.
Biochemistry. 2005 Nov 22;44(46):15230-7
PMID: 16285726
-
Fluorescence of size-expanded DNA bases: reporting on DNA sequence and structure with an unnatural genetic set.
J Am Chem Soc. 2008 Mar 26;130(12):3989-99
PMID: 18311973
-
Evolving a thermostable DNA polymerase that amplifies from highly damaged templates.
Angew Chem Int Ed Engl. 2007;46(17):3115-7
PMID: 17366498
-
An unnatural hydrophobic base pair system: site-specific incorporation of nucleotide analogs into DNA and RNA.
Nat Methods. 2006 Sep;3(9):729-35
PMID: 16929319
-
Efficient PCR amplification by an unnatural base pair system.
Nucleic Acids Symp Ser (Oxf). 2008;(52):469-70
PMID: 18776457
-
Probing the requirements for recognition and catalysis in Fpg and MutY with nonpolar adenine isosteres.
J Am Chem Soc. 2003 Dec 31;125(52):16235-42
PMID: 14692765
-
Nonpolar nucleobase analogs illuminate requirements for site-specific DNA cleavage by vaccinia topoisomerase.
J Biol Chem. 2006 Nov 24;281(47):35914-21
PMID: 17005552
-
The role of minor groove functional groups in DNA hydration.
Nucleic Acids Res. 2003 Mar 1;31(5):1536-40
PMID: 12595562
-
Directed evolution of novel polymerase activities: mutation of a DNA polymerase into an efficient RNA polymerase.
Proc Natl Acad Sci U S A. 2002 May 14;99(10):6597-602
PMID: 12011423
-
Efficient replication between non-hydrogen-bonded nucleoside shape analogs.
Nat Struct Biol. 1998 Nov;5(11):950-4
PMID: 9808038
-
Exploring the limits of DNA size: naphtho-homologated DNA bases and pairs.
J Am Chem Soc. 2006 Jul 19;128(28):9219-30
PMID: 16834396
-
Exploration of factors driving incorporation of unnatural dNTPS into DNA by Klenow fragment (DNA polymerase I) and DNA polymerase alpha.
Nucleic Acids Res. 2005 May 06;33(8):2620-8
PMID: 15879351
-
Varying DNA base-pair size in subangstrom increments: evidence for a loose, not large, active site in low-fidelity Dpo4 polymerase.
Biochemistry. 2006 Mar 7;45(9):2772-8
PMID: 16503632
-
Selective pairing of polyfluorinated DNA bases.
J Am Chem Soc. 2004 Mar 17;126(10):3040-1
PMID: 15012120
-
yDNA: a new geometry for size-expanded base pairs.
Angew Chem Int Ed Engl. 2004 Nov 5;43(43):5834-6
PMID: 15523708
-
A third base pair for the polymerase chain reaction: inserting isoC and isoG.
Nucleic Acids Res. 2004 Mar 29;32(6):1937-41
PMID: 15051811
-
Synthesis of 1,8-naphthyridine C-nucleosides and their base-pairing properties in oligodeoxynucleotides: thermally stable naphthyridine:imidazopyridopyrimidine base-pairing motifs.
Angew Chem Int Ed Engl. 2005 Jan 14;44(4):596-8
PMID: 15612071
-
Exploiting the enzymatic recognition of an unnatural base pair to develop a universal genetic analysis system.
Clin Chem. 2003 Mar;49(3):407-14
PMID: 12600952
-
The roles of hydrogen bonding and sterics in RNA interference.
Angew Chem Int Ed Engl. 2006 Jul 24;45(30):4994-7
PMID: 16802393
-
A specific partner for abasic damage in DNA.
Nature. 1999 Jun 17;399(6737):704-8
PMID: 10385125