Sfoglia per Autore
Apoptosis induced by N-hexanoylsphingosine in CHP-100 cells associates with accumulation of endogenous ceramide and is potentiated by inhibition of glucocerebroside synthesis
1998-01-01 Spinedi, A; DI BARTOLOMEO, S; Piacentini, M
Ceramide-induced apoptosis is mediated by caspase activation independently from retinoblastoma protein post-translational modification
1998-01-01 Spinedi, A; Amendola, A; DI BARTOLOMEO, S; Piacentini, M
N-oleoylethanolamine inhibits glucosylation of natural ceramides in CHP-100 neuroepithelioma cells: Possible implications for apoptosis
1999-01-01 Spinedi, A; DI BARTOLOMEO, S; Piacentini, M
Ceramide accumulation precedes caspase-dependent apoptosis in CHP-100 neuroepithelioma cells exposed to the protein phosphatase inhibitor okadaic acid
1999-07-01 Spinedi, A; DI BARTOLOMEO, S; DI SANO, F; Rodolfo, C; Ambrosino, A; Piacentini, M
Apoptosis induced by doxorubicin in neurotumor cells is divorced from drug effects on ceramide accumulation and may involve cell cycle-dependent caspase activation
2000-08-01 DI BARTOLOMEO, S; DI SANO, F; Piacentini, M; Spinedi, A
Potentiation of okadaic acid-induced ceramide elevation but not apoptosis by inhibition of glucosylceramide synthase in human neuroepithelioma cells
2001-01-01 DI BARTOLOMEO, S; Spinedi, A
Differential chemosensitizing effect of two glucosylceramide synthase inhibitors in hepatoma cells
2001-01-01 DI BARTOLOMEO, S; Spinedi, A
Ordering ceramide-induced cell detachment and apoptosis in human neuroepithelioma
2002-01-01 DI BARTOLOMEO, S; Spinedi, A
Antisense to glucosylceramide synthase in human neuroepithelioma affects cell growth but not apoptosis
2002-06-01 DI SANO, F; DI BARTOLOMEO, S; Fazi, B; Fiorentini, C; Matarrese, P; Spinedi, A; Piacentini, M
Caspase inhibition shifts neuroepithelioma cell response to okadaic acid from apoptosis to an apoptotic-like form of death
2003-01-01 Romano, E; Cannata, S; DI BARTOLOMEO, S; Spinedi, A
Two glucosylceramide synthase inhibitors attenuate doxorubicin-induced p21Cip1/Waf1 upregulation in HepG2 cells, irrespective of their differential chemosensitizing properties
2005-01-01 DI BARTOLOMEO, S; Spinedi, A
A novel role for autophagy in neurodevelopment
2007-01-01 Cecconi, F; DI BARTOLOMEO, S; Nardacci, R; Fuoco, C; Corazzari, M; Giunta, L; Romagnoli, A; Stoykova, A; Chowdhury, K; Fimia, G; Piacentini, M
Ambra1 regulates autophagy and development of the nervous system
2007-06-28 Fimia, G; Stoykova, A; Romagnoli, A; Giunta, L; DI BARTOLOMEO, S; Nardacci, R; Corazzari, M; Fuoco, C; Ucar, A; Schwartz, P; Gruss, P; Piacentini, M; Chowdhury, K; Cecconi, F
Long-chain ceramide produced in response to N-hexanoylsphingosine does not induce apoptosis in CHP-100 cells.
2009-01-01 Mancinetti, A; DI BARTOLOMEO, S; Spinedi, A
P-Glycoprotein is not a key target for the chemosensitizing effect of 1-phenyl-2-decanoylamino-3-morpholino-1-propanol in HepG2 cells exposed to doxorubicin
2010-01-01 DI BARTOLOMEO, S; Luly, P; Spinedi, A
The role of autophagy during development in higher eukaryotes
2010-10-01 DI BARTOLOMEO, S; Nazio, F; Cecconi, F
The dynamic interaction of AMBRA1 with the dynein motor complex regulates mammalian autophagy
2010-10-04 DI BARTOLOMEO, S; Corazzari, M; Nazio, F; Oliverio, S; Lisi, G; Antonioli, M; Pagliarini, V; Matteoni, S; Fuoco, C; Giunta, L; D'Amelio, M; Nardacci, R; Romagnoli, A; Piacentini, M; Cecconi, F; Fimia, G
Unleashing the Ambra1-Beclin 1 complex from dynein chains: Ulk1 sets Ambra1 free to induce autophagy
2011-01-01 Fimia, G; DI BARTOLOMEO, S; Piacentini, M; Cecconi, F
Reduced cathepsins B and D cause impaired autophagic degradation that can be almost completely restored by overexpression of these two proteases in Sap C-deficient fibroblasts
2012-12-01 Tatti, M; Motta, M; DI BARTOLOMEO, S; Scarpa, S; Cianfanelli, V; Cecconi, F; Salvioli, R
Zebrafish ambra1a and ambra1b knockdown impairs skeletal muscle development
2014-01-01 Skobo, T; Benato, F; Grumati, P; Meneghetti, G; Cianfanelli, V; Castagnaro, S; Chrisam, M; DI BARTOLOMEO, S; Bonaldo, P; Cecconi, F; Dalla Valle, L
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