Establishment and genomic characterization of the new chordoma cell line Chor-IN-1 von Bosotti, Roberta, Magnaghi, Paola, Di Bella, Sebastiano, Cozzi, Liviana, Cusi, Carlo, Bozzi, Fabio, Beltrami, Nicola, Carapezza, Giovanni, Ballinari, Dario, Amboldi, Nadia, Lupi, Rosita, Somaschini, Alessio, Raddrizzani, Laura, Salom, Barbara, Galvani, Arturo, Stacchiotti, Silvia, Tamborini, Elena, Isacchi, Antonella

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Afatinib Is a New Therapeutic Approach in Chordoma with a Unique Ability to Target EGFR and Brachyury von Magnaghi, Paola, Salom, Barbara, Cozzi, Liviana, Amboldi, Nadia, Ballinari, Dario, Tamborini, Elena, Gasparri, Fabio, Montagnoli, Alessia, Raddrizzani, Laura, Somaschini, Alessio, Bosotti, Roberta, Orrenius, Christian, Bozzi, Fabio, Pilotti, Silvana, Galvani, Arturo, Sommer, Josh, Stacchiotti, Silvia, Isacchi, Antonella

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Stereoselective synthesis of 3,4‐dihydropyrrolo[1,2‐a]pyrazin‐1(2H)‐one derivatives as PIM kinase inhibitors inspired from marine alkaloids von Casuscelli, Francesco, Ardini, Elena, Avanzi, Nilla, Badari, Alessandra, Casale, Elena, Disingrini, Teresa, Donati, Daniele, Ermoli, Antonella, Felder, Eduard R., Galvani, Arturo, Isacchi, Antonella, Menichincheri, Maria, Montemartini, Marisa, Orrenius, Christian, Piutti, Claudia, Salom, Barbara, Papeo, Gianluca

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Stereoselective synthesis of 3,4‐dihydropyrrolopyrazin‐1(2H)‐one derivatives as PIM kinase inhibitors inspired from marine alkaloids von Casuscelli, Francesco, Ardini, Elena, Avanzi, Nilla, Badari, Alessandra, Casale, Elena, Disingrini, Teresa, Donati, Daniele, Ermoli, Antonella, Felder, Eduard R, Galvani, Arturo, Isacchi, Antonella, Menichincheri, Maria, Montemartini, Marisa, Orrenius, Christian, Piutti, Claudia, Salom, Barbara, Papeo, Gianluca

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Discovery of 2‑(Cyclohexylmethylamino)pyrimidines as a New Class of Reversible Valosine Containing Protein Inhibitors von Cervi, Giovanni, Magnaghi, Paola, Asa, Daniela, Avanzi, Nilla, Badari, Alessandra, Borghi, Daniela, Caruso, Michele, Cirla, Alessandra, Cozzi, Liviana, Felder, Eduard, Galvani, Arturo, Gasparri, Fabio, Lomolino, Antonio, Magnuson, Steven, Malgesini, Beatrice, Motto, Ilaria, Pasi, Maurizio, Rizzi, Simona, Salom, Barbara, Sorrentino, Graziella, Troiani, Sonia, Valsasina, Barbara, O’Brien, Thomas, Isacchi, Antonella, Donati, Daniele, D’Alessio, Roberto

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Discovery and optimization of pyrrolo[1,2-a]pyrazinones leads to novel and selective inhibitors of PIM kinases von Casuscelli, Francesco, Ardini, Elena, Avanzi, Nilla, Casale, Elena, Cervi, Giovanni, D’Anello, Matteo, Donati, Daniele, Faiardi, Daniela, Ferguson, Ronald D., Fogliatto, Gianpaolo, Galvani, Arturo, Marsiglio, Aurelio, Mirizzi, Danilo G., Montemartini, Marisa, Orrenius, Christian, Papeo, Gianluca, Piutti, Claudia, Salom, Barbara, Felder, Eduard R.

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Abstract 74: Establishment and characterization of the new sacral chordoma cell line Chor-IN-1 von Magnaghi, Paola, Bosotti, Roberta, Amboldi, Nadia, Cozzi, Liviana, Somaschini, Alessio, Stacchiotti, Silvia, Bozzi, Fabio, Tamborini, Elena, Conca, Elena, Pilotti, Silvana, Pierotti, Marco A., Di Bella, Sebastiano, Cusi, Carlo, Ballinari, Dario, Galvani, Arturo, Salom, Barbara, Isacchi, Antonella

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The generation of purinome-targeted libraries as a means to diversify ATP-mimetic chemical classes for lead finding von Felder, Eduard R., Badari, Alessandra, Disingrini, Teresa, Mantegani, Sergio, Orrenius, Christian, Avanzi, Nilla, Isacchi, Antonella, Salom, Barbara

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Hotel housekeepers and occupational health: experiences and perceived risks von Chela-Alvarez, Xènia, Bulilete, Oana, Garcia-Illan, Encarna, Vidal-Thomàs, MClara, Llobera, Joan

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A new method for the solution and solid phase synthesis of chiral β-sulfonopeptides under mild conditions von Gude, Markus, Piarulli, Umberto, Potenza, Donatella, Salom, Barbara, Gennari, Cesare

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Conformational Studies of Chiral Vinylogous Sulfonamidopeptides von Gennari, Cesare, Salom, Barbara, Potenza, Donatella, Longari, Chiara, Fioravanzo, Elena, Carugo, Oliviero, Sardone, Nicola

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Synthesis of Sulfonamido-Pseudopeptides: New Chiral Unnatural Oligomers von Gennari, Cesare, Salom, Barbara, Potenza, Donatella, Williams, Anthony

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Synthesis of Combinatorial Libraries of Vinylogous Sulfonamidopeptides (vs-Peptides) von Gennari, Cesare, Longari, Chiara, Ressel, Stefano, Salom, Barbara, Piarulli, Umberto, Ceccarelli, Simona, Mielgo, Antonia

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Synthesis of Chiral Vinylogous Sulfonamidopeptides (vs-Peptides) von Gennari, Cesare, Longari, Chiara, Ressel, Stefano, Salom, Barbara, Mielgo, Antonia

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Combinatorial Libraries: Studies in Molecular Recognition and the Quest for New Catalysts von Gennari, Cesare, Nestler, H. Peter, Piarulli, Umberto, Salom, Barbara

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Synthetic Receptors Based on Vinylogous Sulfonyl Peptides von Gennari, Cesare, Nestler, H. Peter, Salom, Barbara, Still, W. Clark

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SUBSTITUTED PYRIMIDINYL AND PYRIDINYL-PYRROLOPYRIDINONES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS KINASE INHIBITORS von QUARTIERI, Francesca, POLUCCI, Paolo, SALSA, Matteo, ANGIOLINI, Mauro, SALOM, Barbara, MENICHINCHERI, Maria, CARUSO, Michele, ZUCCOTTO, Fabio, BERTRAND, Jay Aaron

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3,4-DIHYDRO-2H-PYRAZINO[1,2-A]INDOL-1-ONE DERIVATIVES ACTIVE AS KINASE INHIBITORS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM von PAPEO, GIANLUCA MARIANO ENRICO, D'ANELLO, MATTEO, CERVI, GIOVANNI, SALOM, BARBARA

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Stereoselective radical-mediated cyclization of norephdrine derived α-iodoamides: synthesis of enantiopure pyrrolidines and trandition state modelling1 von Belvisi, Laura, Gennari, Cesare, Poli, Giovanni, Scolastico, Carlo, Salom, Barbara, Vassallo, Marco

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Stereoselective radical-mediated cyclization of norephedrine derived o-bromobenzamides: Enantioselective synthesis of 4-substituted 1,2,3,4-tetrahydroisoquinolines von Belvisi, Laura, Gennari, Cesare, Poli, Giovanni, Scolastico, Carlo, Salom, Barbara

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