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Hall RA and Gow NAR. (2013) Mannosylation in Candida albicans: role in cell wall function and immune recognition. Mol. Microbiol. 90, 1147-61 Bates S, Hall RA, Cheetham J, Netea MG, MacCallum DM, Brown AJ, Odds FC, Gow NA. (2013) Role of the Candida albicans MNN1 gene family in cell wall structure and virulence. BMC Res Notes. 6, 294. Hall RA, Bates S, Lenardon MD, Maccallum DM, Wagener J, Lowman DW, Kruppa MD, Williams DL, Odds FC, Brown AJ, Gow NA. (2013), The Mnn2 mannosyltransferase family modulates mannoprotein fibril length, immune recognition and virulence of Candida albicans. PLoS Pathog. 9(4):e1003276. Davis RA, Hofmann A, Osman A, Hall RA, Mühlschlegel FA, Vullo D, Innocenti A, Supuran CT, Poulsen SA. (2011) Natural product-based phenols as novel probes for mycobacterial and fungal carbonic anhydrases. J Med Chem. 54, 1682-92. Hall RA, Turner KJ, Chaloupka J, Cottier F, De Sordi L, Sanglard D, Levin LR, Buck J, Mühlschlegel FA (2011). The quorum-sensing molecules farnesol/homoserine lactone and dodecanol operate via distinct modes of action in Candida albicans. Eukaryotic Cell, 10, 1034-42. Carta F, Innocenti A, Hall RA, Mühlschlegel FA, Scozzafava A, Supuran CT (2011). Carbonic anhydrase inhibitors. Inhibition of the β-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with branched aliphatic/aromatic carboxylates and their derivatives. Bioorg. Med. Chem. Lett., 21, 2521-2526. Davis RA, Hofmann A, Osman A, Hall RA, Mühlschlegel FA, Vullo D, Innocenti A, Supuran CT, Poulsen SA (2011). Natural product-based phenols as novel probes for mycobacterial and fungal carbonic anhydrases. J. Med. Chem. 54, 1682-1692. Sheth CC, Hall R, Lewis L, Brown AJ, Odds FC, Erwig LP, Gow NA (2011). Glycosylation status of the C. albicans cell wall affects the efficiency of neutrophil phagocytosis and killing but not cytokine signaling. Med. Mycol., 49, 513-524. Hall RA, De Sordi L, Eaton R, Bloor JW, Steegborn C, and Mühlschlegel FA (2010). CO(2) acts as a signalling molecule in populations of the fungal pathogen Candida albicans. PLoS Pathog., 6 :e1001193. Hall RA, Mühlschlegel FA (2010). A multi-protein complex controls cAMP signalling and filamentation in the fungal pathogen Candida albicans. Mol. Microbiol., 75, 579-591. Güzel O, Maresca A, Hall RA, Scozzafava A, Mastrolorenzo A, Mühlschlegel FA, Supuran CT (2010). Carbonic anhydrase inhibitors. The beta-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides. Bioorg. Med. Chem. Lett., 20, 2508-2511 Innocenti A, Hall RA, Scozzafava A, Mühlschlegel FA, Supuran CT (2010). Carbonic anhydrase activators: activation of the beta-carbonic anhydrases from the pathogenic fungi Candida albicans and Cryptococcus neoformans with amines and amino acids. Bioorg. Med. Chem., 18, 1034-1037. Hall RA, Cottier F, Mühlschlegel FA (2009). Molecular networks in the pathogen Candida albicans. Advances in Applied Microbiology, 67, 191-212 Schlicker C, Hall RA, Vullo D., Middelhaufe S, Gertz M, Supuran CT, Mühlschlegel FA, Steegborn C (2009). Structure and inhibition of the CO2-sensing carbonic anhydrase Can2 from the pathogenic fungus Cryptococcus neoformans. J. Mol. Biol., 385, 1207–1220 Innocenti A, Hall RA, Schlicker C, Scozzafava A, Steegborn C, Mühlschlegel FA, Supuran CT (2009). Carbonic anhydrase inhibitors. Inhibition and homology modeling studies of the fungal beta-carbonic anhydrase from Candida albicans with sulfonamides. Bioorg. Med. Chem., 17, 4503-4509. Innocenti A, Hall RA, Schlicker C, Mühlschlegel FA, Supuran CT (2009). Carbonic anhydrase inhibitors. Inhibition of the beta-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with aliphatic and aromatic carboxylates. Bioorg. Med. Chem., 17, 2654-2657. Güzel O, Innocenti A, Hall RA, Scozzafava A, Mühlschlegel FA, Supuran CT (2009). Carbonic anhydrase inhibitors. The nematode alpha-carbonic anhydrase of Caenorhabditis elegans CAH-4b is highly inhibited by 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides. Bioorg. Med. Chem., 17, 3212-3215. Innocenti A, Winum JY, Hall RA, Mühlschlegel FA, Scozzafava A, Supuran CT (2009). Carbonic anhydrase inhibitors. Inhibition of the fungal beta-carbonic anhydrases from Candida albicans and Cryptococcus neoformans with boronic acids. Bioorg. Med. Chem. Lett., 19, 2642-2645. Crocetti L, Maresca A, Temperini C, Hall RA, Scozzafava A, Mühlschlegel FA, Supuran CT (2009). A thiabendazole sulfonamide shows potent inhibitory activity against mammalian and nematode alpha-carbonic anhydrases. Bioorg. Med. Chem. Lett., 19, 1371-1375. Innocenti A, Mühlschlegel FA, Hall RA, Steegborn C, Scozzafava A, Supuran CT (2008). Carbonic anhydrase inhibitors: inhibition of the beta-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with simple anions. Bioorg. Med. Chem. Lett., 18, 5066-5070. Hall RA, Vullo D, Innocenti A, Scozzafava A, Supuran CT, Klappa P, Mühlschlegel FA (2008). External pH influences the transcriptional profile of the carbonic anhydrase, CAH-4b in Caenorhabditis elegans. Mol. Biochem. Parasitol., 161, 140-149.