Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Alberto Garbin"'
Autor:
Maria Gabriella Brasca, Claudia Covaciu, Marina Ciomei, Ester Alvino, Enzo Bonmassar, Daniele Castiglia, Lauretta Levati, Giuseppe Starace, Stefania D'Atri, Alberto Garbin, Simona Caporali
Publikováno v:
Pharmacological research
61(5) (2010): 437–448.
info:cnr-pdr/source/autori:(a)Simona Caporali; (b)Ester Alvino; (b, c)Giuseppe Starace; (d)Marina Ciomei; (d)Maria Gabriella Brasca; (a)Lauretta Levati; (a)Alberto Garbin; (e)Daniele Castiglia; (e)Claudia Covaciu; (b,f)Enzo Bonmassar; (a)Stefania D'Atri/titolo:The cyclin-dependent kinase inhibitor PHA-848125 suppresses the in vitro growth of human melanomas sensitive or resistant to temozolomide, and shows synergistic effects in combination with this triazene compound/doi:/rivista:Pharmacological research (Print)/anno:2010/pagina_da:437/pagina_a:448/intervallo_pagine:437–448/volume:61(5)
61(5) (2010): 437–448.
info:cnr-pdr/source/autori:(a)Simona Caporali; (b)Ester Alvino; (b, c)Giuseppe Starace; (d)Marina Ciomei; (d)Maria Gabriella Brasca; (a)Lauretta Levati; (a)Alberto Garbin; (e)Daniele Castiglia; (e)Claudia Covaciu; (b,f)Enzo Bonmassar; (a)Stefania D'Atri/titolo:The cyclin-dependent kinase inhibitor PHA-848125 suppresses the in vitro growth of human melanomas sensitive or resistant to temozolomide, and shows synergistic effects in combination with this triazene compound/doi:/rivista:Pharmacological research (Print)/anno:2010/pagina_da:437/pagina_a:448/intervallo_pagine:437–448/volume:61(5)
PHA-848125 is a novel cyclin-dependent kinase inhibitor under Phase I/II clinical investigation. In this study, we describe, for the first time, the effect of PHA-848125 on human melanoma cells in vitro. Seven melanoma cell lines with different sensi
Autor:
Ester Alvino, Patrizia Caporaso, Stefania D'Atri, Francesco Buccisano, Francesco Marchesi, Adriano Venditti, Grazia Tortorelli, Sergio Amadori, Maria Cristina Tirindelli, Alberto Garbin, Laura Toppo, Mario Turriziani, Enzo Bonmassar
Previous studies indicated that dacarbazine and Temozolomide could be highly effective against refractory acute leukaemia. Their activity relies mainly on the generation of methyl adducts at the O 6 -position of guanine in DNA. High levels of O 6 -me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6a871afa0319675491570b5df97487e
https://hdl.handle.net/2108/45834
https://hdl.handle.net/2108/45834