Authors:
Spisani, S
Fabbri, E
Muccinelli, M
Cariani, A
Barbin, L
Trotta, F
Dovigo, L
Citation: S. Spisani et al., Inhibition of neutrophil responses by cyclosporin A. An insight into molecular mechanisms, RHEUMATOLOG, 40(7), 2001, pp. 794-800
Citation: G. Cavicchioni et S. Spisani, A hydrophilic residue at position 2 can improve specific biological responses in fMLP-OMe analogs, J PEPT RES, 58(3), 2001, pp. 257-262
Authors:
Torrini, I
Nalli, M
Paradisi, MP
Zecchini, GP
Lucente, G
Spisani, S
Citation: I. Torrini et al., Pseudopeptides containing the 2-hydrazonoacyl fragment: analogs of the chemotactic agent HCO-Met-Leu-Phe-OMe, J PEPT RES, 58(1), 2001, pp. 56-66
Citation: G. Cavicchioni et al., Biological activity in human neutrophils of di-tripeptides, analogues of the chemotactic fMLP, BIOORG MED, 11(24), 2001, pp. 3157-3159
Authors:
Ferretti, ME
Nalli, M
Biondi, C
Colamussi, ML
Pavan, B
Traniello, S
Spisani, S
Citation: Me. Ferretti et al., Modulation of neutrophil phospholipase C activity and cyclic AMP levels byfMLP-OMe analogues, CELL SIGNAL, 13(4), 2001, pp. 233-240
Authors:
Dalpiaz, A
Scatturin, A
Vertuani, G
Pecoraro, R
Borea, PA
Varani, K
Traniello, S
Spisani, S
Citation: A. Dalpiaz et al., Met-Ile-Phe-Leu derivatives: full and partial agonists of human neutrophilformylpeptide receptors, EUR J PHARM, 411(3), 2001, pp. 327-333
Authors:
Bisaccia, F
Castiglione-Morelli, MA
Spisani, S
Serafini-Fracassini, A
Tamburro, AM
Citation: F. Bisaccia et al., Solution structure of the amino acid sequence coded by the rarely expressed exon 26A of human elastin: the N-terminal region, J PEPT RES, 56(4), 2000, pp. 201-209
Authors:
Torrini, I
Paradisi, MP
Zecchini, GP
Lucente, G
Mastropietro, G
Spisani, S
Citation: I. Torrini et al., Bioactive fMLF-OMe analogs containing a N-terminal oximic or formylhydrazonic moiety, J PEPT RES, 55(2), 2000, pp. 102-109
Authors:
Boschi, A
Uccelli, L
Bolzati, C
Marastoni, M
Tomatis, R
Spisani, S
Traniello, S
Piffanelli, A
Citation: A. Boschi et al., A CD4/T-4 receptor peptide ligand labeled with technetium-99m: Synthesis and biological activity, NUCL MED BI, 27(8), 2000, pp. 791-795
Authors:
Manfredini, S
Marastoni, M
Tomatis, R
Durini, E
Spisani, S
Pani, A
Marceddu, T
Musiu, C
Marongiu, ME
La Colla, P
Citation: S. Manfredini et al., Peptide T-araC conjugates: Solid-phase synthesis and biological activity of N-4-(acylpeptidyl)-araC, BIO MED CH, 8(3), 2000, pp. 539-547
Authors:
Fabbri, E
Spisani, S
Barbin, L
Biondi, C
Buzzi, M
Traniello, S
Zecchini, GP
Ferretti, ME
Citation: E. Fabbri et al., Studies on fMLP-receptor interaction and signal transduction pathway by means of fMLP-OMe selective analogues, CELL SIGNAL, 12(6), 2000, pp. 391-398
Citation: S. Spisani et G. Cavicchioni, Differences arising in human neutrophil activation passing from N-formyl to N-acetyl-oligopeptides, BIOORG CHEM, 28(4), 2000, pp. 252-259
Citation: S. Spisani et G. Cavicchioni, The importance of the methionine configuration in for-Met-Leu-Phe-OMe biological activities, BIOORG CHEM, 28(1), 2000, pp. 39-44
Authors:
Andreani, A
Rambaldi, M
Leoni, A
Locatelli, A
Morigi, R
Traniello, S
Cariani, A
Rizzuti, O
Spisani, S
Citation: A. Andreani et al., 6-(hydroxyphenyl)imidazo[2,1-b]thiazoles as potential antiinflammatory agents: Effects on human neutrophil functions, COLL CZECH, 65(2), 2000, pp. 267-279
Authors:
Dalpiaz, A
Ferretti, ME
Pecoraro, R
Fabbri, E
Traniello, S
Scatturin, A
Spisani, S
Citation: A. Dalpiaz et al., Phe-D-Leu-Phe-D-Leu-Phe derivatives as formylpeptide receptor antagonists in human neutrophils: cellular and conformational aspects, BBA-PROT ST, 1432(1), 1999, pp. 27-39
Authors:
Cavicchioni, G
Monesi, LG
Ferretti, ME
Fabbri, E
Rizzuti, O
Spisani, S
Citation: G. Cavicchioni et al., fMLP-OMe analogs substituted at the methionine residue: An insight into the receptor properties, ARCH PHARM, 331(11), 1998, pp. 368-370