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Number of items: 10.

Article

Hall, R.A. and Turner, K.J. and Chaloupka, J. and Cottier, F. and De Sordi, L. and Sanglard, D. and Levin, L.R. and Buck, J. and Muhlschlegel, F.A. (2011) The Quorum-Sensing Molecules Farnesol/Homoserine Lactone and Dodecanol Operate via Distinct Modes of Action in Candida albicans. Eukaryotic Cell, 10 (8). pp. 1034-1042. ISSN 1535-9778. The full text of this publication is not available from this repository.

Carta, F. and Innocenti, A. and Hall, R.A. and Muhlschlegel, F.A. and Scozzafava, A. and Supuran, C.T. (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. Bioorganic & Medicinal Chemistry Letters, 21 (8). pp. 2521-2526. ISSN 0960-894X. The full text of this publication is not available from this repository.

Hall, R.A. and De Sordi, L. and Maccallum, D.M. and Topal, H. and Eaton, R. and Bloor, J.W. and Robinson, Gary K and Levin, L.R. and Buck, J. and Wang, Y. and Gow, N.A.R. and Steegborn, C. and Muhlschlegel, F.A. (2010) CO(2) acts as a signalling molecule in populations of the fungal pathogen Candida albicans. PLoS pathogens, 6 (11). e1001193. ISSN 1553-7374.

Preview

Güzel, O. and Maresca, A. and Hall, R.A. and Scozzafava, A. and Mastrolorenzo, A. and Muhlschlegel, F.A. and Supuran, C.T. (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. Bioorganic & medicinal chemistry letters, 20 (8). pp. 2508-11. ISSN 1464-3405. The full text of this publication is not available from this repository.

Hall, R.A. and Muhlschlegel, F.A. (2010) A multi-protein complex controls cAMP signalling and filamentation in the fungal pathogen Candida albicans. Molecular microbiology, 75 (3). pp. 534-537. ISSN 1365-2958. The full text of this publication is not available from this repository.

Innocenti, A. and Hall, R.A. and Scozzafava, A. and Muhlschlegel, F.A. and Supuran, C.T. (2010) Carbonic anhydrase activators: activation of the beta-carbonic anhydrases from the pathogenic fungi Candida albicans and Cryptococcus neoformans with amines and amino acids. Bioorganic & medicinal chemistry, 18 (3). pp. 1034-1037. ISSN 1464-3391. The full text of this publication is not available from this repository.

Hall, R.A. and Vullo, D. and Innocenti, A. and Scozzafava, A. and Supuran, C.T. and Klappa, P. and Muhlschlegel, F.A. (2008) External pH influences the transcriptional profile of the carbonic anhydrase, CAH-4b in Caenorhabditis elegans. Molecular and Biochemical Parasitology, 161 (2). pp. 140-149. ISSN 0166-6851. The full text of this publication is not available from this repository.

Innocenti, A. and Muhlschlegel, F.A. and Hall, R.A. and Steegborn, C. and Scozzafava, A. and Supuran, C.T. (2008) Carbonic anhydrase inhibitors: Inhibition of the beta-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with simple anions. Bioorganic & Medicinal Chemistry Letters, 18 (18). pp. 5066-5070. ISSN 0960-894X. The full text of this publication is not available from this repository.

Hall, R.A. and Muhlschlegel, F.A. (2008) Linking interkingdom communication with host sensing. Mycoses, 51 (5). p. 373. ISSN 0933-7407. The full text of this publication is not available from this repository.

Book section

Hall, R.A. and Muhlschlegel, F.A. (2009) Fungal and Nematode Carbonic Anhydrases: Their Inhibition in Drug Design. In: Supuran, C.T. and Winum, J.-Y., eds. Drug Design of Zinc-Enzyme Inhibitors. John Wiley & Sons, Inc., pp. 301-322. ISBN 978-0-470-27500-9. The full text of this publication is not available from this repository.

This list was generated on Mon May 20 16:56:37 2013 BST.