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Results: 1-8 |
Results: 8
Iron-free pyoverdin binds to its outer membrane receptor FpvA in Pseudomonas aeruginosa: a new mechanism for membrane iron transport
Authors: Schalk, IJ Hennard, C Dugave, C Poole, K Abdallah, MA Pattus, F
Citation: Ij. Schalk et al., Iron-free pyoverdin binds to its outer membrane receptor FpvA in Pseudomonas aeruginosa: a new mechanism for membrane iron transport, MOL MICROB, 39(2), 2001, pp. 351-360
Synthesis of optically pure N-Boc-protected (2R,3R)- and (2R,3S)-3-fluoroprolines
Authors: Demange, L Cluzeau, J Menez, A Dugave, C
Citation: L. Demange et al., Synthesis of optically pure N-Boc-protected (2R,3R)- and (2R,3S)-3-fluoroprolines, TETRAHEDR L, 42(4), 2001, pp. 651-653
Synthesis of phosphinic alanyl-proline surrogates Ala psi(PO2R-CH)Pro as potential inhibitors of the human cyclophilin hCyp-18
Authors: Demange, L Dugave, C
Citation: L. Demange et C. Dugave, Synthesis of phosphinic alanyl-proline surrogates Ala psi(PO2R-CH)Pro as potential inhibitors of the human cyclophilin hCyp-18, TETRAHEDR L, 42(36), 2001, pp. 6295-6297
The synthetic peptide Trp-Lys-Tyr-Met-Val-Met-NH2 specifically activates neutrophils through FPRL1/lipoxin A(4) receptors and is an agonist for the orphan monocyte-expressed chemoattractant receptor FPRL2
Authors: Christophe, T Karlsson, A Dugave, C Rabiet, MJ Boulay, F Dahlgren, C
Citation: T. Christophe et al., The synthetic peptide Trp-Lys-Tyr-Met-Val-Met-NH2 specifically activates neutrophils through FPRL1/lipoxin A(4) receptors and is an agonist for the orphan monocyte-expressed chemoattractant receptor FPRL2, J BIOL CHEM, 276(24), 2001, pp. 21585-21593
Interaction of human cyclophilin hCyp-18 with short peptides suggests the existence of two functionally independent subsites
Authors: Demange, L Moutiez, M Vaudry, K Dugave, C
Citation: L. Demange et al., Interaction of human cyclophilin hCyp-18 with short peptides suggests the existence of two functionally independent subsites, FEBS LETTER, 505(1), 2001, pp. 191-195
Design of a Gag pentapeptide analogue that binds human cyclophilin A more efficiently than the entire capsid protein: New insights for the development of novel anti-HIV-1 drugs
Authors: Li, Q Moutiez, M Charbonnier, JB Vaudry, K Menez, A Quemeneur, E Dugave, C
Citation: Q. Li et al., Design of a Gag pentapeptide analogue that binds human cyclophilin A more efficiently than the entire capsid protein: New insights for the development of novel anti-HIV-1 drugs, J MED CHEM, 43(9), 2000, pp. 1770-1779
Cellular uptake and interaction with purified membranes of rebeccamycin derivatives
Authors: Goossens, JF Henichart, JP Anizon, F Prudhomme, M Dugave, C Riou, JF Bailly, C
Citation: Jf. Goossens et al., Cellular uptake and interaction with purified membranes of rebeccamycin derivatives, EUR J PHARM, 389(2-3), 2000, pp. 141-146
Investigation of the DsbA mechanism through the synthesis and analysis of an irreversible enzyme-ligand complex
Authors: Couprie, J Vinci, F Dugave, C Quemeneur, E Moutiez, M
Citation: J. Couprie et al., Investigation of the DsbA mechanism through the synthesis and analysis of an irreversible enzyme-ligand complex, BIOCHEM, 39(22), 2000, pp. 6732-6742
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