Works by Spisani, Susanna
Results: 23
CD16 and CR3 receptors distinguish between the two mechanisms of tumour cytotoxicity in neutrophils.
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- British Journal of Haematology, 1991, v. 79, n. 2, p. 170, doi. 10.1111/j.1365-2141.1991.tb04518.x
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- Article
Evaluation of CR1 expression in neutrophils from chronic myeloid leukaemia: relationship between prognosis and cellular activity.
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- British Journal of Haematology, 1991, v. 77, n. 1, p. 66, doi. 10.1111/j.1365-2141.1991.tb07950.x
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- Article
fMLP-OMe Analogs Substituted at the Methionine Residue: An Insight into the Receptor Properties.
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- Archiv der Pharmazie, 1998, v. 331, n. 11, p. 368, doi. 10.1002/(SICI)1521-4184(199811)331:11<368::AID-ARDP368>3.0.CO;2-B
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New fMLF-OMe Analogues Containing Constrained Mimics of Phenylalanine Residue.
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- Archiv der Pharmazie, 1998, v. 331, n. 5, p. 170, doi. 10.1002/(SICI)1521-4184(199805)331:5<170::AID-ARDP170>3.0.CO;2-B
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Chemotactic Peptide Analogues Centrally Constrained Chemotactic N-Formyltripeptides: Synthesis, Conformation, and Activity of Two New Analogues.
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- Archiv der Pharmazie, 1996, v. 329, n. 12, p. 517, doi. 10.1002/ardp.19963291202
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Chemotactic Peptide Analogues The Role of ( Z)-2,3-Didehydrophenylalanine and Phenylalanine C-Terminal Residues in Determining the Chemotactic Activity of Formylpeptides.
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- Archiv der Pharmazie, 1996, v. 329, n. 3, p. 143, doi. 10.1002/ardp.19963290306
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- Article
Chemotactic Peptide Analogues. Synthesis and Chemotactic Activity of N-Formyl-Met-Leu-Phe Analogues Containing ( S)-Phenylalaninol Derivatives.
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- Archiv der Pharmazie, 1995, v. 328, n. 9, p. 673, doi. 10.1002/ardp.19953280908
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Cyclic Analogs of Chemotactic Formylpeptides, I.: Synthesis and Biological Activity of For-Cys-Leu-Phe-Cys-OMe.
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- Archiv der Pharmazie, 1993, v. 326, n. 12, p. 955, doi. 10.1002/ardp.19933261208
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Synthesis and Chemotactic Activity of the fMLP Analog HCO-Hmb-Leu-Phe-OMe.
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- Archiv der Pharmazie, 1993, v. 326, n. 8, p. 461, doi. 10.1002/ardp.19933260807
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Synthesis and biological evaluation of new active For-Met-Leu-Phe-OMe analogues containing para-substituted Phe residues.
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- Journal of Peptide Science, 2012, v. 18, n. 6, p. 418, doi. 10.1002/psc.2414
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Conformation-activity relationship of peptide T and new pseudocyclic hexapeptide analogs.
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- Journal of Peptide Science, 2007, v. 13, n. 6, p. 413, doi. 10.1002/psc.865
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Hybrid α/β<sup>3</sup>-peptides with proteinogenic side chains. monosubstituted analogues of the chemotactic tripeptide For-Met-Leu-Phe-OMe.
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- Journal of Peptide Science, 2004, v. 10, n. 8, p. 510, doi. 10.1002/psc.562
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Synthetic formyl tripeptide chemoattractants: a C<sup>α, α</sup>-dialkylated, amphiphilic glycyl residue at position 1.
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- Journal of Peptide Science, 2003, v. 9, n. 6, p. 354, doi. 10.1002/psc.461
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Probing structural requirements of fMLP receptor: On the size of the hydrophobic pocket corresponding to residue 2 of the tripeptide.
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- Journal of Peptide Science, 2002, v. 8, n. 2, p. 56, doi. 10.1002/psc.369
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Peptide T revisited: conformational mimicry of epitopes of anti-HIV proteins.
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- Journal of Peptide Science, 2001, v. 7, n. 4, p. 197, doi. 10.1002/psc.320
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The Importance of the Peptide Bond at Position 2 in HCO-Met-Leu-Phe-OMe Analogues as shown by Studies on Human Neutrophils.
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- Journal of Peptide Science, 1996, v. 2, n. 3, p. 135, doi. 10.1002/psc.55
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Anti-inflammatory and analgesic effects displayed by peptides derived from PKI55 protein, an endogenous protein kinase C inhibitor.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2010, v. 382, n. 3, p. 193, doi. 10.1007/s00210-010-0536-3
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Differential Effects of Angelicin Analogues on NF-κB Activity and IL-8 Gene Expression in Cystic Fibrosis IB3-1 Cells.
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- Mediators of Inflammation, 2017, p. 1, doi. 10.1155/2017/2389487
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Study of synthetic peptides derived from the PKI55 protein, a protein kinase C modulator, in human neutrophils stimulated by the methyl ester derivative of the hydrophobic N-formyl tripeptide for-Met-Leu-Phe-OH.
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- FEBS Journal, 2008, v. 275, n. 3, p. 449, doi. 10.1111/j.1742-4658.2007.06212.x
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A‘pure’ chemoattractant formylpeptide analogue triggers a specific signalling pathway in human neutrophil chemotaxis.
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- FEBS Journal, 2005, v. 272, n. 4, p. 883, doi. 10.1111/j.1742-4658.2004.04497.x
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IL-8 enhances antibody-dependent cellular cytotoxicity in human neutrophils.
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- Immunology & Cell Biology, 1995, v. 73, n. 3, p. 234, doi. 10.1038/icb.1995.38
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Effect of low frequency electromagnetic fields on A[sub2A] adenosine receptors in human neutrphils.
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- British Journal of Pharmacology, 2002, v. 136, n. 1, p. 57, doi. 10.1038/sj.bjp.0704695
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Neutrophils from Patients with Myelodysplastic Syndromes: Relationship between Impairment of Granular Contents, Complement Receptors, Functional Activities and Disease Status.
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- Leukemia & Lymphoma, 1994, v. 13, n. 5/6, p. 471, doi. 10.3109/10428199409049637
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