BOCCHINFUSO, GIANFRANCO

BOCCHINFUSO, GIANFRANCO  

Dipartimento di Scienze e Tecnologie Chimiche  

Mostra records
Risultati 1 - 20 di 106 (tempo di esecuzione: 0.028 secondi).
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-2013 3D Structure, Dynamics, and Activity of Synthetic Analog of the Peptaibiotic Trichodecenin I Gatto, E; Bocchinfuso, G; Palleschi, A; Oncea, S; De Zotti, M; Formaggio, F; Toniolo, C; Venanzi, M Articolo su rivista
1-gen-2005 A new polysaccharidic gel matrix for drug delivery: Preparation and mechanical properties Coviello, T; Alhaique, F; Parisi, C; Matricardi, P; Bocchinfuso, G; Grassi, M Articolo su rivista
1-gen-2005 A new scleroglucan/borax hydrogel: Swelling and drug release studies Coviello, T; Grassi, M; Palleschi, A; Bocchinfuso, G; Coluzzi, G; Banishoeib, F; Alhaique, F Articolo su rivista
1-gen-2012 A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre Syndrome Caputo, V; Cianetti, L; Niceta, M; Carta, C; Ciolfi, A; Bocchinfuso, G; Carrani, E; Dentici, M; Biamino, E; Belligni, E; Garavelli, L; Boccone, L; Melis, D; Andria, G; Gelb, B; Stella, L; Silengo, M; Dallapiccola, B; Tartaglia, M Articolo su rivista
1-gen-2005 A selective chemoreceptor for Aflatoxin B1. Bocchinfuso, G; Micheli, L; Palleschi, A; Palleschi, G; Capodilupo, Al; Venanzi, M Intervento a convegno
1-gen-2006 A Time Resolved Spectroscopic Study On Peptide Folding Pispisa, B; Gatto, E; Bocchinfuso, G; Palleschi, A; Stella, L; Venanzi, M; Formaggio, F; Toniolo, C Contributo in libro
1-gen-2015 Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome Cordeddu, V; Yin, J; Gunnarsson, C; Virtanen, C; Drunat, S; Lepri, F; De Luca, A; Rossi, C; Ciolfi, A; Pugh, T; Bruselles, A; Priest, J; Pennacchio, L; Lu, Z; Danesh, A; Quevedo, R; Hamid, A; Martinelli, S; Pantaleoni, F; Gnazzo, M; Daniele, P; Lissewski, C; Bocchinfuso, G; Stella, L; Odent, S; Philip, N; Faivre, L; Vlckova, M; Seemanova, E; Digilio, C; Zenker, M; Zampino, G; Verloes, A; Dallapiccola, B; Roberts, A; Cave, H; Gelb, B; Neel, B; Tartaglia, M Articolo su rivista
1-gen-2014 Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis Flex, E; Jaiswal, M; Pantaleoni, F; Martinelli, S; Strullu, M; Fansa, E; Caye, A; De Luca, A; Lepri, F; Dvorsky, R; Pannone, L; Paolacci, S; Zhang, S; Fodale, V; Bocchinfuso, G; Rossi, C; Burkitt Wright, E; Farrotti, A; Stellacci, E; Cecchetti, S; Ferese, R; Bottero, L; Castro, S; Fenneteau, O; Brethon, B; Sanchez, M; Roberts, A; Yntema, H; Van Der Burgt, I; Cianci, P; Bondeson, M; Cristina Digilio, M; Zampino, G; Kerr, B; Aoki, Y; Loh, M; Palleschi, A; Di Schiavi, E; Care, A; Selicorni, A; Dallapiccola, B; Cirstea, I; Stella, L; Zenker, M; Gelb, B; Cave, H; Ahmadian, M; Tartaglia, M Articolo su rivista
1-gen-2016 ACTIVITY AND SELECTIVITY OF HOST DEFENSE PEPTIDES: A COMPLEX INTERPLAY OF MULTIPLE EQUILIBRIA Bobone, S; Roversi, D; Savini, F; Vaezi, Z; Farrotti, A; Bocedi, A; Bocchinfuso, G; Palleschi, A; De Zotti, M; Formaggio, F; Park, Y; Luca, V; Mangoni, M; Stella, L Intervento a convegno
1-gen-2014 Aggregation propensity of Aib homo-peptides of different length: an insight from molecular dynamics simulations Bocchinfuso, G; Conflitti, P; Raniolo, S; Caruso, M; Mazzuca, C; Gatto, E; Placidi, E; Formaggio, F; Toniolo, C; Venanzi, M; Palleschi, A Articolo su rivista
1-gen-2020 Aggregation propensity of therapeutic fibrin-homing pentapeptides: insights from experiments and molecular dynamics simulations Zanuy, D; Puiggali-Jou, A; Conflitti, P; Bocchinfuso, G; Palleschi, A; Aleman, C Articolo su rivista
1-gen-2022 Aggregation properties of a therapeutic peptide for rheumatoid arthritis: a spectroscopic and molecular dynamics study Cimino, R; Savioli, M; Carrante, Nf; Placidi, E; Garay-Perez, H; López-Abad, M; Lasa, Am; Domínguez-Horta, Mdc; Gatto, E; Cavalieri, F; Bocchinfuso, G; Venanzi, M Articolo su rivista
1-gen-2009 Antimicrobial Peptides chelating Lanthanide ions: the Case of Trichogin GAIV analogues and Terbium(III) Venanzi, M; Gatto, E; Stella, L; Bocchinfuso, G; Palleschi, A; Formaggio, F; Toniolo, C Contributo in libro
1-gen-2014 Behaviour of antimicrobial peptides in phospholipid membranes: insights by combined spectroscopic and simulative studies Stella, L; Bocchinfuso, G; Bobone, S; Farrotti, A; Roversi, D; Vaezi, Z; Palleschi, A; Park, Y; De Zotti, M; Formaggio, F; Toniolo, C Articolo su rivista
1-gen-2007 Biochemical and Structural characterization of Noonan syndrome-causing mutations affecting SHP-2’s phoshotyrosyl-binding pockets. Martinelli, S; Torreri, P; Bocchinfuso, G; Stella, L; Flex, E; Grottesi, A; Chillemi, G; Ceccarini, M; Palleschi, A; Gelb, B; Petrucci, T; Tartaglia, M Intervento a convegno
1-gen-2022 Caenorhabditis elegans provides an efficient drug screening platform for GNAO1-related disorders and highlights the potential role of caffeine in controlling dyskinesia Di Rocco, M; Galosi, S; Lanza, E; Tosato, F; Caprini, D; Folli, V; Friedman, J; Bocchinfuso, G; Martire, A; Di Schiavi, E; Leuzzi, V; Martinelli, S Articolo su rivista
1-gen-2016 Carnitine palmitoyl transferase-1A (CPT1A): A new tumor specific target in human breast cancer Pucci, S; Zonetti, M; Fisco, T; Polidoro, C; Bocchinfuso, G; Palleschi, A; Novelli, G; Spagnoli, Lg; Mazzarelli, P Articolo su rivista
1-gen-2018 Clinical and functional characterization of two novel ZBTB20 mutations causing Primrose syndrome Stellacci, E; Steindl, K; Joset, P; Mercurio, L; Anselmi, M; Cecchetti, S; Gogoll, L; Zweier, M; Hackenberg, A; Bocchinfuso, G; Stella, L; Tartaglia, M; Rauch, A Articolo su rivista
1-gen-2020 Co-occurring WARS2 and CHRNA6 mutations in a child with a severe form of infantile parkinsonism Martinelli, S; Cordeddu, V; Galosi, S; Lanzo, A; Palma, E; Pannone, L; Ciolfi, A; Di Nottia, M; Rizza, T; Bocchinfuso, G; Traversa, A; Caputo, V; Farrotti, A; Carducci, C; Bernardini, L; Cogo, S; Paglione, M; Venditti, M; Bentivoglio, A; Ng, J; Kurian, Ma; Civiero, L; Greggio, E; Stella, L; Trettel, F; Sciaccaluga, M; Roseti, C; Carrozzo, R; Fucile, S; Limatola, C; Di Schiavi, E; Tartaglia, M; Leuzzi, V Articolo su rivista
1-gen-2021 Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2-related disorders Lorca, R; Pannone, L; Cuesta-Llavona, E; Bocchinfuso, G; Rodriguez-Reguero, J; Carpentieri, G; Hernando, I; Flex, E; Tartaglia, M; Coto, E; Gomez, J; Martinelli, S Articolo su rivista