Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Agata Desantis"'
Autor:
Elisabetta Mattei, Nicoletta Corbi, Maria Grazia Di Certo, Georgios Strimpakos, Cinzia Severini, Annalisa Onori, Agata Desantis, Valentina Libri, Serena Buontempo, Aristide Floridi, Maurizio Fanciulli, Dilair Baban, Kay E Davies, Claudio Passananti
Publikováno v:
PLoS ONE, Vol 2, Iss 8, p e774 (2007)
Duchenne Muscular Dystrophy (DMD) is a severe muscle degenerative disease, due to absence of dystrophin. There is currently no effective treatment for DMD. Our aim is to up-regulate the expression level of the dystrophin related gene utrophin in DMD,
Externí odkaz:
https://doaj.org/article/048d05e732e0409cba8e9153bd4c3701
Autor:
Marta Chesi, Francesca La Rosa, Francesca De Nicola, P. Leif Bergsagel, Giovanni Tonon, Aristide Floridi, Elena Lesma, Tiziana Bruno, Frauke Goeman, Claudio Passananti, Gianluca Bossi, Vincenzo Federico, Maurizio Fanciulli, Valeria Catena, Maria Teresa Petrucci, Maria Rosaria Ricciardi, Cristina Sorino, Tiziana Castrignanò, Paolo D'Onorio De Meo, Maurilio Ponzoni, Giovanni Blandino, Francesco Pisani, Simona Iezzi, Agata Desantis
Publikováno v:
The EMBO Journal. 34:1214-1230
Mammalian target of rapamycin (mTOR) is a key protein kinase that regulates cell growth, metabolism, and autophagy to maintain cellular homeostasis. Its activity is inhibited by adverse conditions, including nutrient limitation, hypoxia, and DNA dama
Autor:
Aristide Floridi, Cesare Manetti, Matteo Pallocca, Valeria Catena, Luca Casadei, Francesca De Nicola, Maurizio Fanciulli, Mariacristina Valerio, Tiziana Bruno, Giovanni Blandino, Agata Desantis, Cristina Sorino, Simona Iezzi, Frauke Goeman
Publikováno v:
Journal of Experimental & Clinical Cancer Research : CR
Background Solid tumours are less oxygenated than normal tissues. Consequently, cancer cells acquire to be adapted to a hypoxic environment. The poor oxygenation of solid tumours is also a major indicator of an adverse cancer prognosis and leads to r
Autor:
Claudio Passananti, Agata Desantis, Simona Iezzi, Francesca La Rosa, Maurizio Fanciulli, Alfonso Bellacosa, Gianluca Bossi, Giovanni Blandino, Aristide Floridi, Annapaola Franchitto, Silvia Di Agostino, Sergio Galanti, Barbara Benassi, Cristina Sorino, Francesca De Nicola, Tiziana Bruno
Publikováno v:
Cancer cell
18 (2010): 122–134. doi:10.1016/j.ccr.2010.05.027
info:cnr-pdr/source/autori:Bruno T; Desantis A; Bossi G; Di Agostino S; Sorino C; De Nicola F; Iezzi S; Franchitto A; Benassi B; Galanti S; La Rosa F; Floridi A; Bellacosa A; Passananti C; Blandino G; Fanciulli M./titolo:Che-1 promotes tumor cell survival by sustaining mutant p53 transcription and inhibiting DNA damage response activation/doi:10.1016%2Fj.ccr.2010.05.027/rivista:Cancer cell (Print)/anno:2010/pagina_da:122/pagina_a:134/intervallo_pagine:122–134/volume:18
18 (2010): 122–134. doi:10.1016/j.ccr.2010.05.027
info:cnr-pdr/source/autori:Bruno T; Desantis A; Bossi G; Di Agostino S; Sorino C; De Nicola F; Iezzi S; Franchitto A; Benassi B; Galanti S; La Rosa F; Floridi A; Bellacosa A; Passananti C; Blandino G; Fanciulli M./titolo:Che-1 promotes tumor cell survival by sustaining mutant p53 transcription and inhibiting DNA damage response activation/doi:10.1016%2Fj.ccr.2010.05.027/rivista:Cancer cell (Print)/anno:2010/pagina_da:122/pagina_a:134/intervallo_pagine:122–134/volume:18
Summary Che-1 is a RNA polymerase II binding protein involved in the regulation of gene transcription and, in response to DNA damage, promotes p53 transcription. In this study, we investigated whether Che-1 regulates mutant p53 expression. We found t
Autor:
Agata Desantis, Francesca De Nicola, Claudio Passananti, Maria Grazia Di Certo, Tiziana Bruno, Simona Iezzi, Maria Teresa Ciotti, Elisabetta Mattei, Maurizio Fanciulli, Aristide Floridi, Nicoletta Corbi
Publikováno v:
Journal of Cell Science. 120:1852-1858
Neurotrophin receptor-interacting MAGE homolog (NRAGE) has been recently identified as a cell-death inducer, involved in molecular events driving cells through apoptotic networks during neuronal development. Recently, we have focused on the functiona
Autor:
Cinzia Rinaldo, F De Nicola, Silvia Soddu, Maurizio Fanciulli, Maurizio De Crescenzi, Valeria Catena, Aristide Floridi, Claudio Passananti, Tommaso Bruno, Cristina Sorino, Serena Camerini, Simona Iezzi, Agata Desantis
Publikováno v:
Cell Death & Disease
Cell death and disease 5 (2014). doi:10.1038/cddis.2014.381
info:cnr-pdr/source/autori:De Nicola, F.; Catena, V.; Rinaldo, C.; Bruno, T.; Iezzi, S.; Sorino, C.; Desantis, A.; Camerini, S.; Crescenzi, M.; Floridi, A.; Passananti, C.; Soddu, S.; Fanciulli, M./titolo:HIPK2 sustains apoptotic response by phosphorylating Che-1%2FAATF and promoting its degradation/doi:10.1038%2Fcddis.2014.381/rivista:Cell death and disease/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume:5
Cell death and disease 5 (2014). doi:10.1038/cddis.2014.381
info:cnr-pdr/source/autori:De Nicola, F.; Catena, V.; Rinaldo, C.; Bruno, T.; Iezzi, S.; Sorino, C.; Desantis, A.; Camerini, S.; Crescenzi, M.; Floridi, A.; Passananti, C.; Soddu, S.; Fanciulli, M./titolo:HIPK2 sustains apoptotic response by phosphorylating Che-1%2FAATF and promoting its degradation/doi:10.1038%2Fcddis.2014.381/rivista:Cell death and disease/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume:5
Che-1/AATF is an RNA polymerase II-binding protein that is involved in the regulation of gene transcription, which undergoes stabilization and accumulation in response to DNA damage. We have previously demonstrated that following apoptotic induction,
Autor:
Enrico Cundari, Claudio Passananti, Simona Iezzi, Agata Desantis, Francesca De Nicola, Maria Grazia Di Certo, Maurizio Fanciulli, Valeria Catena, Aristide Floridi, Luciana Chessa, Cristina Sorino, Tiziana Bruno
Publikováno v:
The Journal of biological chemistry
288 (2013): 23348–23357.
info:cnr-pdr/source/autori:Sorino C, Bruno T, Desantis A, Di Certo MG, Iezzi S, De Nicola F, Catena V, Floridi A, Chessa L, Passananti C, Cundari E, Fanciulli M./titolo:) Centrosomal Che-1 protein is involved in the regulation of mitosis and DNA damage response by mediating pericentrin (PCNT)-dependent Chk1 protein localization./doi:/rivista:The Journal of biological chemistry (Print)/anno:2013/pagina_da:23348/pagina_a:23357/intervallo_pagine:23348–23357/volume:288
288 (2013): 23348–23357.
info:cnr-pdr/source/autori:Sorino C, Bruno T, Desantis A, Di Certo MG, Iezzi S, De Nicola F, Catena V, Floridi A, Chessa L, Passananti C, Cundari E, Fanciulli M./titolo:) Centrosomal Che-1 protein is involved in the regulation of mitosis and DNA damage response by mediating pericentrin (PCNT)-dependent Chk1 protein localization./doi:/rivista:The Journal of biological chemistry (Print)/anno:2013/pagina_da:23348/pagina_a:23357/intervallo_pagine:23348–23357/volume:288
To combat threats posed by DNA damage, cells have evolved mechanisms, collectively termed DNA damage response (DDR). These mechanisms detect DNA lesions, signal their presence, and promote their repair. Centrosomes integrate G2/M checkpoint control a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdac02d7d29a7e1cd608884cd3d73ac1
http://hdl.handle.net/11573/673237
http://hdl.handle.net/11573/673237
Autor:
Agata Desantis, Elisabetta Mattei, Annalisa Onori, Claudio Passananti, Maurizio Fanciulli, Maria Grazia Di Certo, Nicoletta Corbi
Publikováno v:
Neuromuscular disorders : NMD. 19(2)
Our aim is to upregulate the expression level of the dystrophin related gene utrophin in Duchenne muscular dystrophy, thus complementing the lack of dystrophin functions. To this end, we have engineered synthetic zinc finger based transcription facto
Autor:
M G Di Certo, M. Di Padova, F De Nicola, Agata Desantis, Simona Iezzi, M Scarsella, Carlo Leonetti, Claudio Passananti, Tommaso Bruno, Aristide Floridi, Maurizio Fanciulli
Publikováno v:
Cell death and differentiation 15 (2008): 515–520. doi:10.1038/sj.cdd.4402284
info:cnr-pdr/source/autori:T Bruno; S Iezzi; F De Nicola; M Di Padova; A Desantis; M Scarsella; M G Di Certo; C Leonetti; A Floridi; C Passananti; M Fanciulli/titolo:Che-1 activates XIAP expression in response to DNA damage/doi:10.1038%2Fsj.cdd.4402284/rivista:Cell death and differentiation/anno:2008/pagina_da:515/pagina_a:520/intervallo_pagine:515–520/volume:15
info:cnr-pdr/source/autori:T Bruno; S Iezzi; F De Nicola; M Di Padova; A Desantis; M Scarsella; M G Di Certo; C Leonetti; A Floridi; C Passananti; M Fanciulli/titolo:Che-1 activates XIAP expression in response to DNA damage/doi:10.1038%2Fsj.cdd.4402284/rivista:Cell death and differentiation/anno:2008/pagina_da:515/pagina_a:520/intervallo_pagine:515–520/volume:15
X-linked inhibitor of apoptosis protein (XIAP) is a member of the inhibitor of apoptosis proteins family that selectively binds and inhibits caspase-3, -7 and -9. As such, XIAP is an extremely potent suppressor of apoptosis and an attractive target f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16fd959b3b8080bcc6a6fc643e81a2e3
http://www.cnr.it/prodotto/i/167457
http://www.cnr.it/prodotto/i/167457