Prof. Keith Fox
Keith is Professor of Biochemistry in the Centre for Biological Sciences in Southampton University. His research concerns the sequence specific recognition of DNA by small molecules, oligonucleotides and proteins, and the formation of unusual DNA structures (triplexes and quadruplexes).
50 Papers
Coralyne has a preference for intercalation between TA.T triplets in intramolecular DNA triple helices
Nucleic Acids Res. 25 (10), 1890-1896, 1997.
5-(1-propargylamino)-2'-deoxyuridine (U-P): a novel thymidine analogue for generating DNA triplexes with increased stability
Nucleic Acids Res. 27 (8), 1802-1809, 1999.
DNA triple helix formation at target sites containing several pyrimidine interruptions: Stabilization by protonated cytosine or 5-(1-propargylamino)dU
Biochemistry 38 (41), 13747-13758, 1999.
DNA triple helix stabilisation by covalent attachment of a triplex-specific ligand
Biochim. Biophys. Acta Gene Struct. Expression 1447 (2-3), 137-145, 1999.
Recognition of GT mismatches by Vsr mismatch endonuclease
Nucleic Acids Res. 28 (13), 2535-2540, 2000.
Synthesis of a novel bis-amino-modified thymidine monomer for use in DNA triplex stabilisation
Phys. Chem. Chem. Phys. 2 (23), 2315-2316, 2000.
Affinity of mismatch-binding protein MutS for heteroduplexes containing different mismatches
Biochem. J 354, 627-633, 2001.
High throughput measurement of duplex, triplex and quadruplex melting curves using molecular beacons and a LightCycler
Nucleic Acids Res. 30 (9), e39, 2002.
Stable DNA triple helix formation using oligonucleotides containing 2'-aminoethoxy,5-propargylamino-U
Biochemistry 41 (23), 7224-7231, 2002.
First synthesis of 1-deazacytidine, the C-nucleoside analogue of cytidine
Tetrahedron Lett. 43 (17), 3121-3123, 2002.
Cleavage of fragments containing DNA mismatches by enzymic and chemical probes
Biochem. J 371, 697-708, 2003.
Thermodynamic and kinetic stability of intermolecular triple helices containing different proportions of C+.GC and T.AT triplets
Nucleic Acids Res. 31 (19), 5598-5606, 2003.
DNA sequence specificity of triplex-binding ligands
Eur. J. Biochem. 270 (24), 4982-4992, 2003.
Effects of a hairpin polyamide on DNA melting: comparison with distamycin and Hoechst 33258
Biophys. Chem. 111 (3), 205-212, 2004.
DNA sequence recognition by an isopropyl substituted thiazole polyamide
Nucleic Acids Res. 32 (11), 3410-3417, 2004.
Selectivity and affinity of triplex-forming oligonucleotides containing 2'-aminoethoxy-5-(3-aminoprop-1-ynyl)uridine for recognizing AT base pairs in duplex DNA
Nucleic Acids Res. 32 (15), 4439-4447, 2004.
Exceptionally slow kinetics of the intramolecular quadruplex formed by the Oxytricha telomeric repeat
Org. Biomol. Chem. 3 (22), 4153-4157, 2005.
An extra dimension in nucleic acid sequence recognition
Q. Rev. Biophys 38 (4), 311-320, 2005.
Recognition of CG inversions in DNA triple helices by methylated 3H-pyrrolo[2,3-d] pyrimidin-2(7H)-one nucleoside analogues
Chem. Commun. 2555-2557, 2005.
Combining nucleoside analogues to achieve recognition of oligopurine tracts by triplex-forming oligonucleotides at physiological pH
FEBS Lett. 579 (29), 6616-6620, 2005.
Four base recognition by triplex-forming oligonucleotides at physiological pH
Nucleic Acids Res. 33 (9), 3025-3032, 2005.
Stable recognition of TA interruptions by triplex forming oligonucleotides containing a novel nucleoside
Biochemistry 44 (15), 5884-5892, 2005.
DNA sequence recognition by an imidazole-containing isopropyl-substituted thiazole polyamide (thiazotropsin B)
Bioorg. Med. Chem. Lett. 16 (13), 3469-3474, 2006.
Triplex staples: DNA double-strand cross-linking at internal and terminal sites using psoralen-containing triplex-forming oligonucleotides
Bioconjugate Chem. 17 (6), 1561-1567, 2006.
DNA triple-helix formation at target sites containing duplex mismatches
Biophys. Chem. 123 (2-3), 134-140, 2006.
2'-O-dimethylaminoethoxyuridine and 5-dimethylaminopropargyl deoxyuridine for at base pair recognition in triple helices
Nucleosides Nucleotides Nucl. Acids 26 (10-12), 1283-1286, 2007.
CG base pair recognition within DNA triple helices using N-methyl-3H-pyrrolo 2,3-d pyrimidin-2(7H)-one nucleoside analogues
Nucleosides Nucleotides Nucl. Acids 26 (10-12), 1363-1367, 2007.
Photoinduced crosslinking of double-helical DNA by psoralen covalently linked to a triple helix-forming oligonucleotide under near-physiological conditions
Nucleosides Nucleotides Nucl. Acids 26 (8-9), 1005-1009, 2007.
Sequence effects of single base loops in intramolecular quadruplex DNA
FEBS Lett. 581 (8), 1657-1660, 2007.
Effect of G-tract length on the topology and stability of intramolecular DNA quadruplexes
Biochemistry 46 (11), 3036-3044, 2007.
Intramolecular DNA quadruplexes with different arrangements of short and long loops
Nucleic Acids Res. 35 (12), 4214-4222, 2007.
Synthesis of anthraquinone oligonucleotides for triplex stabilization
Nucleosides Nucleotides Nucl. Acids 26 (8-9), 921-925, 2007.
Kinetic studies on the formation of DNA triplexes containing the nucleoside analogue 2'-O-(2-aminoethyl)-5-(3-amino-1-propynyl)uridine
Org. Biomol. Chem. 6 (1), 122-129, 2008.
Potent Triple Helix Stabilization by 5',3'-Modified Triplex-Forming Oligonucleotides
ChemBioChem 10 (11), 1839-1851, 2009.
DNA triplex formation with 5-dimethylaminopropargyl deoxyuridine
Nucleic Acids Res. 37 (4), 1288-1296, 2009.
The stability of triplex DNA is affected by the stability of the underlying duplex
Biophys. Chem. 145 (2-3), 105-110, 2009.
Synthesis and properties of triplex-forming oligonucleotides containing 2'-O-(2-methoxyethyl)-5-(3-aminoprop-1-ynyl)-uridine
Bioorg. Med. Chem. 18 (17), 6389-6397, 2010.
CG base pair recognition within DNA triple helices by modified N-methylpyrrolo-dC nucleosides
Org. Biomol. Chem. 8 (22), 5087-5096, 2010.
2’-Substituted 2-Amino-3-Methylpyridine Ribonucleosides in Triplex-Forming Oligonucleotides: Triplex Stability is Determined by Chemical Environment
Med. Chem. Comm. 2, 550-558, 2011.
Formation of stable DNA triplexes
Biochem. Soc. Trans. 39 (2), 629-634, 2011.
2'-Aminoethoxy-2-amino-3-methylpyridine in Triplex-Forming Oligonucleotides: High Affinity, Selectivity and Resistance to Enzymatic Degradation
Chem. Eur. J. 17 (52), 14851-14856, 2011.
Towards the Targeted Modulation of Gene Expression by Modified Triplex-Forming Oligonucleotides
Curr. Chem. Biol. 2, 1-10, 2008.
Stable DNA triple helix formation
Nucleic Acids Sym. Ser. 53 (1), 71, 2009.
Secondary binding sites for heavily modified triplex forming oligonucleotides
Nucleic Acids Res. 40 (8), 3753-3762, 2012.
Triplex-Directed Recognition of a DNA Nanostructure Assembled by Crossover Strand Exchange
ACS Nano 6 (4), 3604-3613, 2012.
Triplex-Directed Covalent Cross-Linking of a DNA Nanostructure
Chem. Commun. 48, 9592-9594, 2012.
Functionalizing Designer DNA Crystals with a Triple-Helical Veneer
Angew. Chem. Int. Ed. 53 (15), 3979-3982, 2014.
A Mutant of Uracil DNA Glycosylase That Distinguishes between Cytosine and 5-Methylcytosine
PLOS ONE 2014.
The effect of sequence context on the activity of cytosine DNA glycosylases
Mol. Biosyst. 106, 353-358, 2015.
Stabilisation of self-assembled DNA crystals by triplex-directed photo-cross-linking
Chem. Commun. 2016.
