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Variations in the constituent sugars of the polysaccharides from New Zealand species of Pachymenia (Halymeniaceae), Miller, I. J., Falshaw R., Furneaux R. H., and Hemmingson J. A. , Botanica Marina, Volume 40, p.119-127, (1997) Abstract
Variation of native agar gel strength in light deprived Gracilaria chilensis Bird, McLachlan et Oliveira, Hemmingson, J. A., and Furneaux R. H. , Botanica Marina, Volume 46, p.307-314, (2003) Abstract
Validation of an LC-MS/MS assay for detecting relevant disaccharides from keratan sulfate as a biomarker for Morquio A syndrome, Martell, L. A., Cunico R. L., Ohh J., Fulkerson W., Furneaux R. H., and Foehr E. D. , Bioanalysis, Volume 3, Number 16, p.1855-1866, (2011) Abstract
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Using gigartinine to track the distribution of an alien species of Gracilaria in New Zealand, Wilcox, S. J., Barr N., Broom J., Furneaux R. H., and Nelson W. A. , Journal of Applied Phycology, Volume 19, p.313-323, (2007) Abstract
Use of enzyme technology to convert waste lactose into valuable products, Stevenson, D. E., Stanley R. A., and Furneaux R. H. , Annals of the New York Academy of Sciences, Volume 799, p.555-558, (1996)
Unusual glycosylation of 9-O-benzylallosamizoline, Blattner, R., Furneaux R. H., Gainsford G. J., and Wong H. , Australian Journal of Chemistry, Volume 57, p.799-802, (2004) Abstract
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Trichomonas vaginalis: Detection of nucleoside hydrolase activity as a potential screening procedure, Gero, A. M., Kang E. W., Harvey J. E., Schofield P. J., Clinch K., and Furneaux R. H. , Experimental Parasitology, Volume 94, p.125-128, (2000)
Transition-state analogs as inhibitors of human and malarial hypoxanthine-guanine phosphoribosyltransferases, Li, C. M., Tyler P. C., Furneaux R. H., Kicska G., Xu Y., Grubmeyer C., Girvin M. E., and Schramm V. L. , Nature Structural Biology, Volume 6, p.582-587, (1999) Abstract
Transition state structure of purine nucleoside phosphorylase and principles of atomic motion in enzymatic catalysis, Fedorov, A., Shi W., Kicska G., Schramm V. L., Almo S. C., Fedorov E., Tyler P. C., Furneaux R. H., Hanson J. C., Gainsford G. J., et al. , Biochemistry, Volume 40, p.853-860, (2001) Abstract
Transition state analogue inhibitors of purine nucleoside phosphorylase from Plasmodium falciparum, Kicska, G. A., Tyler P. C., Evans G. B., Furneaux R. H., Kim K., and Schramm V. L. , Journal of Biological Chemistry, Volume 277, p.3219-3225, (2002) Abstract
Transition state analogue inhibitors of protozoan nucleoside hydrolases, Furneaux, R. H., Schramm V. L., and Tyler P. C. , Bioorganic and Medicinal Chemistry, Volume 7, p.2599-2606, (1999) Abstract
Transition state analogue inhibitors of N-ribosyltransferases: new drugs by targeting nucleoside processing enzymes., Evans, G. B., Furneaux R. H., Kelly P. M., Schramm V. L., and Tyler P. C. , Nucleic acids symposium series (2004), p.63-64, (2007) Abstract
Transition state analogue discrimination by related purine nucleoside phosphorylases, Taylor Ringia, E. A., Tyler P. C., Evans G. B., Furneaux R. H., Murkin A. S., and Schramm V. L. , Journal of the American Chemical Society, Volume 128, p.7126-7127, (2006) Abstract
Third-generation immucillins: Syntheses and bioactivities of acyclic immucillin inhibitors of human purine nucleoside phosphorylase, Clinch, K., Evans G. B., Frohlich R. F. G., Furneaux R. H., Kelly P. M., Legentil L., Murkin A. S., Li L., Schramm V. L., Tyler P. C., et al. , Journal of Medicinal Chemistry, Volume 52, p.1126-1143, (2009) Abstract
Targeting the polyamine pathway with transition-state analogue inhibitors of 5′-methylthioadenosine phosphorylase, Evans, G. B., Furneaux R. H., Schramm V. L., Singh V., and Tyler P. C. , Journal of Medicinal Chemistry, Volume 47, p.3275-3281, (2004) Abstract
Targeting a novel Plasmodium falciparum purine recycling pathway with specific immucillins, Ting, L. - M., Shi W., Lewandowicz A., Singh V., Mwakingwe A., Birck M. R., Taylor Ringia E. A., Bench G., Madrid D. C., Tyler P. C., et al. , Journal of Biological Chemistry, Volume 280, p.9547-9554, (2005) Abstract
S
Synthesis studies of structural analogues of tagetitoxin: 4-O-acetyl-3- amino-1,6-anhydro-3-deoxy-D-gulose 2-phosphate, Dent, B. R., Furneaux R. H., Gainsford G. J., and Lynch G. P. , Tetrahedron, Volume 55, p.6977-6996, (1999) Abstract
Synthesis of transition state inhibitors for N-riboside hydrolases and transferases, Furneaux, R. H., Limberg G., Tyler P. C., and Schramm V. L. , Tetrahedron, Volume 53, p.2915-2930, (1997) Abstract
Synthesis of transition state analogue inhibitors for purine nucleoside phosphorylase and N-riboside hydrolases, Evans, G. B., Furneaux R. H., Gainsford G. J., Schramm V. L., and Tyler P. C. , Tetrahedron, Volume 56, p.3053-3062, (2000) Abstract
Synthesis of the enantiomers of hexahydrodibenz[d,f]azecines, Furneaux, R. H., Gainsford G. J., and Mason J. M. , Journal of Organic Chemistry, Volume 69, p.7665-7671, (2004) Abstract
Synthesis of Second-Generation Transition State Analogues of Human Purine Nucleoside Phosphorylase, Evans, G. B., Furneaux R. H., Lewandowicz A., Schramm V. L., and Tyler P. C. , Journal of Medicinal Chemistry, Volume 46, p.5271-5276, (2003) Abstract
Synthesis of allyl β-D-galactopyranoside from lactose using Streptococcus thermophilus β-D-galactosidase, Stevenson, D. E., and Furneaux R. H. , Carbohydrate Research, Volume 284, p.279-283, (1996)
Synthesis of allosamidin analogues, Blattner, R., Furneaux R. H., and Lynch G. P. , Carbohydrate Research, Volume 294, p.29-40, (1996) Abstract
Synthesis of a transition state analogue inhibitor of purine nucleoside phosphorylase via the Mannich reaction, Evans, G. B., Furneaux R. H., Tyler P. C., and Schramm V. L. , Organic Letters, Volume 5, p.3639-3640, (2003) Abstract
Synthesis of a new spiroacetal based herbicide, Brimble, M. A., Johnston A. D., and Furneaux R. H. , Tetrahedron Letters, Volume 38, p.3591-3594, (1997) Abstract
Synthesis of 2-fluoroethyl β-D-galactopyranoside and 2-fluoroethyl 6-O-β-D-galactopyranosyl-β-D-galactopyranoside from lactose using β-D-galactosidase, Stevenson, D. E., Woolhouse A. D., Furneaux R. H., Batcheler D., and Eason C. T. , Carbohydrate Research, Volume 256, p.185-188, (1994) Abstract
Synthesis of 2-acetamido-1,2,4-trideoxy-1,4-imino-D-galactitol, a new hexosaminidase inhibitor, Furneaux, R. H., Lynch G. P., Way G., and Winchester B. , Tetrahedron Letters, Volume 34, p.3477-3480, (1993) Abstract
Synthesis of 2-acetamido-1,2,4-trideoxy-1,4-imino-D-galactitol and -D-glucitol for evaluation as glycosidase inhibitors, Croucher, P. D., Furneaux R. H., and Lynch G. P. , Tetrahedron, Volume 50, p.13299-13312, (1994) Abstract
Synthesis of 1,5-dideoxy-1,5-imino-D-galactitol from L-sorbose, Furneaux, R. H., Tyler P. C., and Whitehouse L. A. , Tetrahedron Letters, Volume 34, p.3609-3612, (1993) Abstract
Synthesis and utility of sulfated chromogenic carbohydrate model substrates for measuring activities of mucin-desulfating enzymes, Clinch, K., Evans G. B., Furneaux R. H., Rendle P. M., Rhodes P. L., Roberton A. M., Rosendale D. I., Tyler P. C., and Wright D. P. , Carbohydrate Research, Volume 337, p.1095-1111, (2002) Abstract
The synthesis and immune stimulating action of mannose-capped lysine-based dendrimers, Greatrex, B. W., Brodie S. J., Furneaux R. H., Hook S. M., McBurney W. T., Painter G. F., Rades T., and Rendle P. M. , Tetrahedron, Volume 65, p.2939-2950, (2009) Abstract
Synthesis and Herbicidal Activity of [3R*, 5S*, 6S*]-3-Benzyloxy-5-methoxy-1,7-dioxaspiro[5.5]undecane and [3R*, 5S*, 6S*]-3-Methoxy-5-benzyloxy-1,7-dioxaspiro[5.5]undecane, Brimble, M. A., Johnston A. D., and Furneaux R. H. , Journal of Organic Chemistry, Volume 63, p.471-479, (1998) Abstract
The synthesis and antibacterial activity of totarol derivatives. Part 3: modification of ring-B, Evans, G. B., Furneaux R. H., Gainsford G. J., and Murphy M. P. , Bioorganic and Medicinal Chemistry, Volume 8, p.1663-1675, (2000) Abstract
The synthesis and antibacterial activity of totarol derivatives. Part 2: Modifications at C-12 and O-13, Evans, G. B., and Furneaux R. H. , Bioorganic and Medicinal Chemistry, Volume 8, p.1653-1662, (2000) Abstract
The synthesis and antibacterial activity of totarol derivatives. Part 1: Modifications of ring-C and pro-drugs, Evans, G. B., Furneaux R. H., Gravestock M. B., Lynch G. P., and Scott G. K. , Bioorganic and Medicinal Chemistry, Volume 7, p.1953-1964, (1999) Abstract
Syntheses of the fungicide/insecticide allosamidin and a structural isomer, Blattner, R., Furneaux R. H., Kemmitt T., Tyler P. C., Ferrier R. J., and Tidén A. - K. , Journal of the Chemical Society, Perkin Transactions 1, p.3411-3421, (1994) Abstract
Syntheses of oligomannosides in solution and on a soluble polymer support: A comparison, Blattner, R., Furneaux R. H., and Ludewig M. , Carbohydrate Research, Volume 341, p.299-321, (2006) Abstract
Syntheses and bio-activities of the l-enantiomers of two potent transition state analogue inhibitors of purine nucleoside phosphorylases, Clinch, K., Evans G. B., Fleet G. W. J., Furneaux R. H., Johnson S. W., Lenz D. H., Mee S. P. H., Rands P. R., Schramm V. L., Taylor Ringia E. A., et al. , Organic and Biomolecular Chemistry, Volume 4, p.1131-1139, (2006) Abstract
A synchrotron radiation study of the one-dimensional complex of sodium with (1S)-N-carboxylato-1-(9-deazaadenin-9-yl)-1,4-dideoxy-1,4-imino-D-ribitol, a member of the 'immucillin' family, Gainsford, G. J., Furneaux R. H., Tyler P. C., Sauve A., and Shramm V. L. , Acta Crystallographica Section C: Crystal Structure Communications, Volume 66, p.m65-m68, (2010) Abstract
Structures of purine nucleoside phosphorylase from Mycobacterium tuberculosis in complexes with immucillin-H and its pieces, Shi, W., Basso L. A., Santos D. S., Tyler P. C., Furneaux R. H., Blanchard J. S., Almo S. C., and Schramm V. L. , Biochemistry, Volume 40, p.8204-8215, (2001) Abstract
Structure of the exudate gum from Meryta sinclairii, Sims, I. M., and Furneaux R. H. , Carbohydrate Polymers, Volume 52, p.423-431, (2003) Abstract
Structure of fructans from excised leaves of New Zealand flax, Sims, I. M., Cairns A. J., and Furneaux R. H. , Phytochemistry, Volume 57, p.661-668, (2001) Abstract
Structure and inhibition of a quorum sensing target from Streptococcus pneumoniae, Singh, V., Shi W., Almo S. C., Evans G. B., Furneaux R. H., Tyler P. C., Painter G. F., Lenz D. H., Mee S., Zheng R., et al. , Biochemistry, Volume 45, p.12929-12941, (2006) Abstract
Structure and antiviral activity of the galactofucan sulfates extracted from Undaria pinnatifida (Phaeophyta), Hemmingson, J. A., Falshaw R., Furneaux R. H., and Thompson K. , Journal of Applied Phycology, Volume 18, p.185-193, (2006) Abstract
Structural rationale for the affinity of pico- and femtomolar transition state analogues of Escherichia coli 5′-methylthioadenosine/S- adenosylhomocysteine nucleosidase, Lee, J. E., Singh V., Evans G. B., Tyler P. C., Furneaux R. H., Cornell K. A., Riscoe M. K., Schramm V. L., and Howell P. L. , Journal of Biological Chemistry, Volume 280, p.18274-18282, (2005) Abstract
The structural determination of the agaroid polysaccharides from four New Zealand algae in the order ceramiales by means of 13C NMR spectroscopy, Miller, I. J., and Furneaux R. H. , Botanica Marina, Volume 40, p.333-339, (1997)
Structural analysis of the polysaccharide from Pachymenia lusoria (Cryptonemiaceae, Rhodophyta), Miller, I. J., Falshaw R., and Furneaux R. H. , Carbohydrate Research, Volume 268, p.219-232, (1995) Abstract
A structural analysis of the polysaccharide from Kallymenia berggrenii J. Ag, Miller, I. J., and Furneaux R. H. , Botanica Marina, Volume 39, p.141-147, (1996) Abstract
The structural analysis of disaccharides from red algal galactans by methylation and reductive partial-hydrolysis, Falshaw, R., and Furneaux R. H. , Carbohydrate Research, Volume 269, p.183-189, (1995)
Structural analysis of carrageenans from the tetrasporic stages of the red algae, Gigartina lanceata and Gigartina chapmanii (Gigartinaceae, Rhodophyta), Falshaw, R., and Furneaux R. H. , Carbohydrate Research, Volume 307, p.325-331, (1998) Abstract