Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Leonardo Manzoni"'
Autor:
Luca Muzio, Riccardo Sirtori, Davide Gornati, Simona Eleuteri, Andrea Fossaghi, Diego Brancaccio, Leonardo Manzoni, Linda Ottoboni, Luca De Feo, Angelo Quattrini, Eloise Mastrangelo, Luca Sorrentino, Emanuele Scalone, Giancarlo Comi, Luciana Marinelli, Nilo Riva, Mario Milani, Pierfausto Seneci, Gianvito Martino
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-17 (2020)
ALS is a neurodegenerative disease characterized by loss of motor neurons. Here, the authors showed that reduced levels of the VSP35 subunit in the retromer complex is a conserved ALS feature and identified a new lead compound increasing retromer sta
Externí odkaz:
https://doaj.org/article/2a79c2c4685b4d2598d773092d995d7b
Publikováno v:
ARKIVOC, Vol 2013, Iss 2, Pp 185-200 (2012)
Externí odkaz:
https://doaj.org/article/5174042eaede4542811280f6b2a03160
Publikováno v:
Recent patents on anti-cancer drug discovery
(2017): 148–168. doi:10.2174/1574892812666170203151930
info:cnr-pdr/source/autori:Arosio, Daniela; Manzoni, Leonardo; Corno, Cristina; Perego, Paola/titolo:Integrin-targeted peptide-and peptidomimetic-drug conjugates for the treatment of tumors./doi:10.2174%2F1574892812666170203151930/rivista:Recent patents on anti-cancer drug discovery (Print)/anno:2017/pagina_da:148/pagina_a:168/intervallo_pagine:148–168/volume
(2017): 148–168. doi:10.2174/1574892812666170203151930
info:cnr-pdr/source/autori:Arosio, Daniela; Manzoni, Leonardo; Corno, Cristina; Perego, Paola/titolo:Integrin-targeted peptide-and peptidomimetic-drug conjugates for the treatment of tumors./doi:10.2174%2F1574892812666170203151930/rivista:Recent patents on anti-cancer drug discovery (Print)/anno:2017/pagina_da:148/pagina_a:168/intervallo_pagine:148–168/volume
Background: Integrins are heterodimeric cell surface receptors that mediate cell-cell and cellextracellular matrix adhesion. These molecules play a role in processes such as cell growth and proliferation, differentiation, migration, cell trafficking,
Autor:
Daniela Arosio, Alessandro Samela, Silvia Cairati, Pierfausto Seneci, Stefano Barbini, Marta Penconi, Daniele Lecis, Leonardo Manzoni
Publikováno v:
Bioorganic & medicinal chemistry letters
27 (2017): 2336–2344. doi:10.1016/j.bmcl.2017.04.032
info:cnr-pdr/source/autori:Manzoni, Leonardo; Samela, Alessandro; Barbini, Stefano; Cairati, Silvia; Penconi, Marta; Arosio, Daniela; Lecis, Daniele; Seneci, Pierfausto/titolo:4-Connected azabicyclo[5.3.0]decane Smac mimetics-Zn2+ chelators as dual action antitumoral agents/doi:10.1016%2Fj.bmcl.2017.04.032/rivista:Bioorganic & medicinal chemistry letters (Print)/anno:2017/pagina_da:2336/pagina_a:2344/intervallo_pagine:2336–2344/volume:27
27 (2017): 2336–2344. doi:10.1016/j.bmcl.2017.04.032
info:cnr-pdr/source/autori:Manzoni, Leonardo; Samela, Alessandro; Barbini, Stefano; Cairati, Silvia; Penconi, Marta; Arosio, Daniela; Lecis, Daniele; Seneci, Pierfausto/titolo:4-Connected azabicyclo[5.3.0]decane Smac mimetics-Zn2+ chelators as dual action antitumoral agents/doi:10.1016%2Fj.bmcl.2017.04.032/rivista:Bioorganic & medicinal chemistry letters (Print)/anno:2017/pagina_da:2336/pagina_a:2344/intervallo_pagine:2336–2344/volume:27
Putative dual action compounds (DACs 3a d) based on azabicyclo[5.3.0]decane (ABD) Smac mimetic scaffolds linked to Zn2+-chelating 2,2'-dipicolylamine (DPA) through their 4 position are reported and characterized. Their synthesis, their target affinit
Autor:
Luciana Marinelli, Preet Lal, Emiliano Biasini, Chiara Zucal, Alessandro Provenzani, Vito Giuseppe D'Agostino, Pierfausto Seneci, Vanessa Baj, Natthakan Thongon, Saioa R. Elezgarai, Danilo Di Maio, Linda Cerofolini, Claudio Luchinat, Leonardo Manzoni, Ettore Novellino, Marta Brambilla, Marco Fragai, Marco Miceli, Isabelle Bonomo
Publikováno v:
Journal of medicinal chemistry 61 (2018): 1483–1498. doi:10.1021/acs.jmedchem.7b01176
info:cnr-pdr/source/autori:Manzoni L.; Zucal C.; Maio D.D.; D'Agostino V.G.; Thongon N.; Bonomo I.; Lal P.; Miceli M.; Baj V.; Brambilla M.; Cerofolini L.; Elezgarai S.; Biasini E.; Luchinat C.; Novellino E.; Fragai M.; Marinelli L.; Provenzani A.; Seneci P./titolo:Interfering with HuR-RNA Interaction: Design, Synthesis and Biological Characterization of Tanshinone Mimics as Novel, Effective HuR Inhibitors/doi:10.1021%2Facs.jmedchem.7b01176/rivista:Journal of medicinal chemistry/anno:2018/pagina_da:1483/pagina_a:1498/intervallo_pagine:1483–1498/volume:61
info:cnr-pdr/source/autori:Manzoni L.; Zucal C.; Maio D.D.; D'Agostino V.G.; Thongon N.; Bonomo I.; Lal P.; Miceli M.; Baj V.; Brambilla M.; Cerofolini L.; Elezgarai S.; Biasini E.; Luchinat C.; Novellino E.; Fragai M.; Marinelli L.; Provenzani A.; Seneci P./titolo:Interfering with HuR-RNA Interaction: Design, Synthesis and Biological Characterization of Tanshinone Mimics as Novel, Effective HuR Inhibitors/doi:10.1021%2Facs.jmedchem.7b01176/rivista:Journal of medicinal chemistry/anno:2018/pagina_da:1483/pagina_a:1498/intervallo_pagine:1483–1498/volume:61
The human antigen R (HuR) is an RNA-binding protein known to modulate the expression of target mRNA coding for proteins involved in inflammation, tumorigenesis, and stress responses and is a valuable drug target. We previously found that dihydrotansh
Autor:
Monica Civera, Fabio Doro, Emilio Parisini, Umberto Piarulli, Roberto Fanelli, Leonardo Manzoni, Chiara Alberti, Elena Luison, Daniela Arosio, Cinzia Colombo, Antonella Tomassetti, Mariangela Figini, Laura Belvisi, Cesare Casagrande
Publikováno v:
Organic & biomolecular chemistry 13 (2015): 2570–2573. doi:10.1039/C4OB02538E
info:cnr-pdr/source/autori:F. Doro, C. Colombo, C. Alberti, D. Arosio, L. Belvisi, C. Casagrande, R. Fanelli, L. Manzoni, E. Parisini, U. Piarulli, E. Luison, M. Figini, A. Tomassetti, M. Civera/titolo:Computational design of novel peptidomimetic inhibitors of cadherin homophilic interactions/doi:10.1039%2FC4OB02538E/rivista:Organic & biomolecular chemistry/anno:2015/pagina_da:2570/pagina_a:2573/intervallo_pagine:2570–2573/volume:13
info:cnr-pdr/source/autori:F. Doro, C. Colombo, C. Alberti, D. Arosio, L. Belvisi, C. Casagrande, R. Fanelli, L. Manzoni, E. Parisini, U. Piarulli, E. Luison, M. Figini, A. Tomassetti, M. Civera/titolo:Computational design of novel peptidomimetic inhibitors of cadherin homophilic interactions/doi:10.1039%2FC4OB02538E/rivista:Organic & biomolecular chemistry/anno:2015/pagina_da:2570/pagina_a:2573/intervallo_pagine:2570–2573/volume:13
We report a first set of peptidomimetic ligands mimicking the adhesive interface identified by recent crystallographic structures of E- and N-cadherin. Compounds 2 and 3 inhibit adhesion of epithelial ovarian cancer (EOC) cells with improved efficacy
Autor:
Daniela Arosio, Umberto Piarulli, Laura Belvisi, Simone Zanella, Luca Pignataro, Cesare Gennari, Leonardo Manzoni, Francesca Bonato, Monica Civera
Publikováno v:
Cancers, Vol 9, Iss 10, p 128 (2017)
Cancers (Basel) 9 (2017). doi:10.3390/cancers9100128
info:cnr-pdr/source/autori:Civera, Monica; Arosio, Daniela; Bonato, Francesca; Manzoni, Leonardo; Pignataro, Luca; Zanella, Simone; Gennari, Cesare; Piarulli, Umberto; Belvisi, Laura/titolo:Investigating the Interaction of Cyclic RGD Peptidomimetics with alphaVbeta6 Integrin by Biochemical and Molecular Docking Studies./doi:10.3390%2Fcancers9100128/rivista:Cancers (Basel)/anno:2017/pagina_da:/pagina_a:/intervallo_pagine:/volume:9
Cancers
Cancers; Volume 9; Issue 10; Pages: 128
Cancers (Basel) 9 (2017). doi:10.3390/cancers9100128
info:cnr-pdr/source/autori:Civera, Monica; Arosio, Daniela; Bonato, Francesca; Manzoni, Leonardo; Pignataro, Luca; Zanella, Simone; Gennari, Cesare; Piarulli, Umberto; Belvisi, Laura/titolo:Investigating the Interaction of Cyclic RGD Peptidomimetics with alphaVbeta6 Integrin by Biochemical and Molecular Docking Studies./doi:10.3390%2Fcancers9100128/rivista:Cancers (Basel)/anno:2017/pagina_da:/pagina_a:/intervallo_pagine:/volume:9
Cancers
Cancers; Volume 9; Issue 10; Pages: 128
The interaction of a small library of cyclic RGD (Arg-Gly-Asp) peptidomimetics with alphaVbeta6 integrin has been investigated by means of competitive solid phase binding assays to the isolated receptor and docking calculations in the crystal structu
Autor:
Leonardo, Manzoni, Alessandro, Samela, Stefano, Barbini, Silvia, Cairati, Marta, Penconi, Daniela, Arosio, Daniele, Lecis, Pierfausto, Seneci
Publikováno v:
Bioorganicmedicinal chemistry letters. 27(11)
Putative dual action compounds (DACs 3a-d) based on azabicyclo[5.3.0]decane (ABD) Smac mimetic scaffolds linked to Zn
Autor:
Ranjan Preet, Luciana Marinelli, Pierfausto Seneci, Emiliano Biasini, Linda Cerofolini, Ettore Novellino, Vito Giuseppe D'Agostino, Dan A. Dixon, Vikalp Vishwakarma, Isabelle Bonomo, Carmelo Fuccio, Max S. Fairlamb, Sha Neisha Williams, Marco Fragai, Preet Lal, Saioa R. Elezgarai, Rachel Munk, Alessandro Provenzani, Kotb Abdelmohsen, Chiara Zucal, Myriam Gorospe, Erik Dassi, Danilo Di Maio, Claudio Luchinat, Elin Lehrmann, Stefano Giuntini, Leonardo Manzoni, Alessandro Quattrone
Publikováno v:
Nucleic Acids Research
Nucleic acids research 45 (2017): 9514–9527. doi:10.1093/nar/gkx623
info:cnr-pdr/source/autori:Lal, Preet; Cerofolini, Linda; D'Agostino, Vito Giuseppe; Zucal, Chiara; Fuccio, Carmelo; Bonomo, Isabelle; Dassi, Erik; Giuntini, Stefano; Di Maio, Danilo; Vishwakarma, Vikalp; Preet, Ranjan; Williams, Sha Neisha; Fairlamb, Max S.; Munk, Rachel; Lehrmann, Elin; Abdelmohsen, Kotb; Elezgarai, Saioa R.; Luchinat, Claudio; Novellino, Ettore; Quattrone, Alessandro; Biasini, Emiliano; Manzoni, Leonardo; Gorospe, Myriam; Dixon, Dan A.; Seneci, Pierfausto; Marinelli, Luciana; Fragai, Marco; Provenzani, Alessandro/titolo:Regulation of HuR structure and function by dihydrotanshinone-I/doi:10.1093%2Fnar%2Fgkx623/rivista:Nucleic acids research/anno:2017/pagina_da:9514/pagina_a:9527/intervallo_pagine:9514–9527/volume:45
Nucleic acids research 45 (2017): 9514–9527. doi:10.1093/nar/gkx623
info:cnr-pdr/source/autori:Lal, Preet; Cerofolini, Linda; D'Agostino, Vito Giuseppe; Zucal, Chiara; Fuccio, Carmelo; Bonomo, Isabelle; Dassi, Erik; Giuntini, Stefano; Di Maio, Danilo; Vishwakarma, Vikalp; Preet, Ranjan; Williams, Sha Neisha; Fairlamb, Max S.; Munk, Rachel; Lehrmann, Elin; Abdelmohsen, Kotb; Elezgarai, Saioa R.; Luchinat, Claudio; Novellino, Ettore; Quattrone, Alessandro; Biasini, Emiliano; Manzoni, Leonardo; Gorospe, Myriam; Dixon, Dan A.; Seneci, Pierfausto; Marinelli, Luciana; Fragai, Marco; Provenzani, Alessandro/titolo:Regulation of HuR structure and function by dihydrotanshinone-I/doi:10.1093%2Fnar%2Fgkx623/rivista:Nucleic acids research/anno:2017/pagina_da:9514/pagina_a:9527/intervallo_pagine:9514–9527/volume:45
The Human antigen R protein (HuR) is an RNA-binding protein that recognizes U/AU-rich elements in diverse RNAs through two RNA-recognition motifs, RRM1 and RRM2, and post-transcriptionally regulates the fate of target RNAs. The natural product dihydr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0536c8768e996bb44932195f81ad5642
http://hdl.handle.net/11588/700351
http://hdl.handle.net/11588/700351
Autor:
Leonardo Manzoni, Claudia Kusmic, Antonio L'Abbate, Piero Salvadori, Debora Petroni, Daniela Arosio, Marco Matteucci, Daniele Panetta, Luca Menichetti, Cesare Casagrande
Publikováno v:
European journal of nuclear medicine and molecular imaging
40 (2013): 1265–1274. doi:10.1007/s00259-013-2432-9
info:cnr-pdr/source/autori:Luca Menichetti, Claudia Kusmic, Daniele Panetta, Daniela Arosio, Debora Petroni, Marco Matteucci, Piero A. Salvadori, Cesare Casagrande, Antonio L'Abbate, Leonardo Manzoni/titolo:MicroPET%2FCT imaging of alphavbeta3 integrin via a novel 68Ga-NOTA-RGD peptidomimetic conjugate in rat myocardial infarction/doi:10.1007%2Fs00259-013-2432-9/rivista:European journal of nuclear medicine and molecular imaging (Print)/anno:2013/pagina_da:1265/pagina_a:1274/intervallo_pagine:1265–1274/volume:40
40 (2013): 1265–1274. doi:10.1007/s00259-013-2432-9
info:cnr-pdr/source/autori:Luca Menichetti, Claudia Kusmic, Daniele Panetta, Daniela Arosio, Debora Petroni, Marco Matteucci, Piero A. Salvadori, Cesare Casagrande, Antonio L'Abbate, Leonardo Manzoni/titolo:MicroPET%2FCT imaging of alphavbeta3 integrin via a novel 68Ga-NOTA-RGD peptidomimetic conjugate in rat myocardial infarction/doi:10.1007%2Fs00259-013-2432-9/rivista:European journal of nuclear medicine and molecular imaging (Print)/anno:2013/pagina_da:1265/pagina_a:1274/intervallo_pagine:1265–1274/volume:40
Purpose: The alphavbeta3 integrin is expressed in angiogenic vessels and is a potential target for molecular imaging of evolving pathological processes. Its expression is upregulated in cancer lesions and metastases as well as in acute myocardial inf