Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Stefania Viganò"'
Autor:
Claudia Galoppini, Laura Quartara, Mariella Tancredi, Stefania Meini, Stefania Viganò, Paolo Rovero, Antonio Triolo, Riccardo Patacchini, Carlo Alberto Maggi
Publikováno v:
Letters in Peptide Science. 6:123-127
It has recently been shown that the biological activity of the second generation kinin B1 receptor selective antagonist, desArg10 HOE 140, can be improved by specific amino acid substitutions. Starting from this observation, we undertook a systematic
Autor:
Paolo Rovero, Leopoldo Laricchia-Robbio, Stefania Moscato, Stefania Viganò, Alessandra Guidi, Roberto P. Revoltella
Publikováno v:
Biosensors and Bioelectronics. 12:765-778
A surface plasmon resonance-based biosensor (BIA technology) and enzyme-linked immunosorbent assays (ELISA) have been used for detecting and characterizing human endothelin (ET), a potent vasoactive 21 amino acid polypeptide. Antibodies produced agai
Publikováno v:
Rapid Communications in Mass Spectrometry. 10:1128-1132
A series of newly synthesized peptides (M(r) = 1600-2250 Da), corresponding to portions of the extracellular domain of human granulocyte-macrophage colony stimulating factor receptor alpha subunit have been examined by capillary zone electrophoresis/
Publikováno v:
Letters in Peptide Science. 2:319-323
This paper describes the synthesis of the bradykinin B1 antagonist [desArg10]HOE 140 (d-Arg-Arg-Pro-Hyp-Gly-Thi-Ser-d-Tic-Oic-OH) by the solid-phase method. This synthesis is predicted to be a difficult one because the C-terminal sequence d-Tic-Oic,
Autor:
Ettore Balestreri, Cristina Amato, Lucia Vaccari, Paolo Rovero, Romano Felicioli, Stefania Viganò, S. Pegoraro
Publikováno v:
Letters in Peptide Science. 2:27-32
The synthesis and biological activity of a photochromic compound, in which two Lys2 dipeptides are linked through their N-terminal amino groups by an azobenzene moiety, are reported. The synthesis was achieved by a novel solid-phase dimerization stra
Autor:
Giulia Greco, S. Pegoraro, Richard H. Butler, Paolo Rovero, Doriana Fruci, Stefania Viganò, Nobuyuki Tanigaki, Roberto P. Revoltella, Daniela Riganelli
Publikováno v:
Scopus-Elsevier
A direct binding assay has been used to investigate the effect of the secondary anchor residues on peptide binding to class I proteins of the major histocompatibility complex. Based on predictions from a previous chemometric approach, synthetic pepti
Publikováno v:
Letters in Peptide Science. 1:149-155
Several side reactions can be encountered in the synthesis of Trp-containing peptides, due to molecular species originating from side chain-protecting groups or from the linker during acidolytic cleavage of the peptide from the resin. The linker can
Autor:
Richard H. Butler, Paolo Rovero, Stefania Viganò, S. Pegoraro, Sergio Clementi, Doriana Fruci, Tanigaki Nobuyuki, Daniela Riganelli, Roberto P. Revoltella, Giulia Greco
Publikováno v:
Molecular Immunology. 31:549-554
In this paper we report a chemometric approach to Quantitative Structure-Activity Relationship (QSAR) analysis applied to a study of the binding of peptides to Major Histocompatibility Complex (MHC) class I proteins. Peptides which possess the known
Autor:
D. Verniani, E. Chiello, P Beffy, S. Pegoraro, Ersilia Cassano, Mahmoud Hamdan, Paolo Rovero, V. Di Bartolo, Stefania Viganò, A. Danè, R. P. Revoltella
Publikováno v:
Scopus-Elsevier
We have synthesized a series of peptides corresponding to portions of the extracellular domain of human granulocyte-macrophage colony stimulating factor receptor alpha subunit (hGM-CSFR alpha). The sequences were chosen according to the homology betw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edf1928de12b40dad803655a4bc84c19
http://www.scopus.com/inward/record.url?eid=2-s2.0-9344251652&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-9344251652&partnerID=MN8TOARS