Zobrazeno 1 - 10
of 288
pro vyhledávání: '"L. Rausa"'
First Published in 1988. This is a collection of the Proceedings of a course held at the International School of Medical Sciences Ettore Majorana Centre for Scientific Culture, Italy 5-13 September 1986.
Autor:
S. Palmeri, M. Meli, M. Danova, G. Bernardo, V. Leonardi, G. Dastoli, L. Rausa, A. Russo, G. Filippelli, G. Palmieri, M. Della Vittoria Scarpati, V. Lo Russo, L. Di Lauro, G. Colucci, G. Bruni, M. Piazzi, N. Gebbia, S. Spada
Publikováno v:
Journal of Cancer Research and Clinical Oncology. 124:191-198
Biochemical modulation is one of the most interesting fields in cancer chemotherapy. Interferon-alpha (IFNalpha) is a cytokine that is able to influence the pharmacodynamics of 5-fluorouracil (5FU) through a number of mechanisms. With the aim of conf
Autor:
V. Leonardi, Maria Meli, Sergio Palmeri, L. Rausa, G. Failla, Marco Danova, P. Ferrara, Marco Benazzo, Silvia Brugnatelli, Antonio Russo
Publikováno v:
Oncology reports. 1(6)
Treatment of advanced head and neck cancer is still a matter of controversy. Although current chemotherapy regimens are able to induce high response rates, they have not shown improved survival. We employed a combination of cisplatin (CDDP), 5-fluoro
Autor:
C. Presot, M. S. Dionisi, A. Lucenti, M. Minelli, M. Antimi, P. Manente, Massimo Federico, E. Sansoni, C. M. Foggi, T. Buniva, D. Negri, Giovanni Quarta, Albano Del Favero, Maurizio Tonato, D. Amadori, C. Epifani, M. Maltoni, G. Gorzegno, M. Giordano, C. Milandri, R. Casaretti, G. Ciccarese, P. Marchei, F. De Vita, I. Carreca, V. Fosser, D. Donati, G. Cruciani, S. Della Gaspera, F. M. Gioffré, L. De Sio, B. Agostara, Verena De Angelis, Roberto Sabbatini, Fausto Roila, R. Sabbioni, R. Maccaferri, G. Villani, G. Bernardo, M. R. Strada, A. Contu, G. Amunni, A. Villanucci, S. Schiavon, S. Tumolo, A. Pazzola, C. Caroti, L. Merlini, A. Amodio, M. Marzi, G. Garofolo, G. Catalano, L. Dogliotti, P. Alessadroni, P. Malacarne, M. Ceccolini, F. Conti, F. Di Costanzo, L. Rausa, M. A. Palladino, M. Lopez, L. Montanari, L. Gallo, G. Iodice, G. L. Cetto, A. Venuti, S. Mazzotta, M. T. Cattaneo, C. Pacilio, G. Palmiotti, R. Nortilli, R. Forcignanò, G. Troccoli, A. Giglio, G. Comella, G. Rosati, Enzo Ballatori, S. Amici, Roberta Depenni, Vittorio Silingardi, S. Porrozzi, L. Meneghetti, G. Muran, B. Orlandini
Publikováno v:
Scopus-Elsevier
Aims and Background The necessity of an antiemetic prophylaxis in patients treated with chemotherapy of low emetogenic potential, such as 5-fluorouracil ± folinic acid fractionated over several consecutive days, is controversial. The aim of the stud
Autor:
R, Sanguedolce, R, Alessandro, G, De Leo, L, Gullotti, F, Sanguedolce, G, Vultaggio, G, Diana, B, Cirello, L, Rausa
Publikováno v:
Anticancer research. 20(6B)
Structural changes in the macromolecular targets of pharmacological agents can result in alterations in the efficacy of these agents. In previous studies Berger et al. (1) identified a variant structural form of thymidylate synthase (TS) that is asso
Autor:
Maria Grazia Cusi, Sp Prete, Pierpaolo Correale, L Rausa, Roberto Petrioli, M Sabatino, Giorgio Giorgi, Guido Francini, A. Aquino, Mario Turriziani, Cristina Nencini, R Sanguedolce, L De Vecchis, Daniele Pozzessere, Lucia Micheli
Publikováno v:
Europe PubMed Central
Università degli Studi di Siena-IRIS
Scopus-Elsevier
Università degli Studi di Siena-IRIS
Scopus-Elsevier
5-Fluorouracil (5-FU) is a pyrimidine antimetabolite active against colorectal carcinoma and other malignancies of the digestive tract. Over-expression or mutation of thymidylate synthase (TS), the target enzyme of the 5-FU metabolite, 5-fluorodeoxyu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68b513e3d09d9308b191a89c52952e5f
http://hdl.handle.net/11365/35667
http://hdl.handle.net/11365/35667
Autor:
R, Sanguedolce, G, Vultaggio, F, Sanguedolce, G, Modica, F, Li Volsi, G, Diana, G, Guereio, L, Bellanca, L, Rausa
Publikováno v:
Anticancer research. 18(3A)
Inhibition of Thymidylate Synthase (TS) by the 5-Fluorouracil (5Fu) active metabolite Fluoro-deoxy-uridine-monophosphate (FdUMP) is considered to be the main mechanism of action of 5Fu. TS level from tumors and normal mucosa of 62 untreated patients
Publikováno v:
Oncology Reports.
The role of chemotherapy in refractory metastatic breast cancer is still debated. We employed a schedule of cisplatin, mitomycin and vindesine in twenty-one anthracycline- or anthraquinone-pretreated breast cancer patients. The most relevant characte
Publikováno v:
Anticancer research. 15(3)
5-Fluorouracil is the drug chosen for the treatment of patients with advanced colorectal carcinoma; its major site of action is thymidylate synthase (TS), resulting in pronounced and prolonged inhibition of DNA synthesis. The aim of this study was to