PRANDINI, PAOLA

PRANDINI, PAOLA  

DIPARTIMENTO DI MEDICINA  

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A molecular signature associated with prolonged survival in glioblastoma patients treated with Regorafenib 1-gen-2021 Santangelo, Alessandra; Rossato, Marzia; Lombardi, Giuseppe; Benfatto, Salvatore; Lavezzari, Denise; Luca De Salvo, Gian; Indraccolo, Stefano; Cristina Dechecchi, Maria; Prandini, Paola; Gambari, Roberto; Scapoli, Chiara; DI GENNARO, Gianfranco; Caccese, Mario; Eoli, Marica; Rudà, Roberta; Ariela Brandes, Alba; Ibrahim, Toni; Rizzato, Simona; Lolli, Ivan; Lippi, Giuseppe; Delledonne, Massimo; Zagonel, Vittorina; Cabrini, Giulio
A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome 1-gen-2009 Pereira, P. L.; Magnol, L.; Sahún, I.; Brault, V.; Duchon, A.; Prandini, Paola; Gruart, A.; Bizot, J. C.; Chadefaux Vekemans, B.; Deutsch, S.; Trovero, F.; Delgado García, J. M.; Antonarakis, S. E.; Dierssen, M.; Herault, Y.
A novel out-of-frame mutation in the neurofilament light chain gene (NEFL) does not result in Charcot-Marie-Tooth disease type 2E. 1-gen-2005 Andrigo, C.; Boito, C.; Prandini, Paola; Mostacciuolo, M. L.; Siciliano, G.; Angelini, C.; Pegoraro, E.
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 1-gen-2011 Costantini, Silvia; Prandini, Paola; Corradi, Massimiliano; Pasquali, Alessandra; Contreas, Giovanna; Pignatti, Pierfranco; Pinelli, Leonardo; Trabetti, Elisabetta; Maffeis, Claudio
Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs. 1-gen-2014 Prandini, Paola; Zusi, Chiara; Malerba, Giovanni; Itan, ; Pignatti, Pierfranco; Trabetti, Elisabetta
Association between genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and cardiovascular events in type 2 diabetes mellitus patients 1-gen-2008 Zanoni, Martina; Prandini, Paola; Malerba, Giovanni; Angiolillo, D. J.; Bernardo, E.; Fernandez Ortiz, A.; Macaya, C.; Bass, T. A.; Trabetti, Elisabetta; Pignatti, Pierfranco
Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I. 1-gen-2005 Boito, C. A.; Melacini, P.; Vianello, A.; Prandini, Paola; Gavassini, B. F.; Bagattin, A.; Siciliano, G.; Angelini, C.; Pegoraro, E.
Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency. 1-gen-2003 Tezak, Z.; Prandini, Paola; Boscaro, M.; Marin, A.; Devaney, J.; Marino, M.; Fanin, M.; Trevisan, C. P.; Park, J.; Tyson, W.; Finkel, R.; Garcia, C.; Angelini, C.; Hoffman, E. P.; Pegoraro, E.
Detection of allele-specific gene expression on next generation sequencing data 1-gen-2013 Mijatovic, Vladan; Xumerle, Luciano; Trabetti, Elisabetta; Prandini, Paola; Zusi, Chiara; Buson, Genny; Ferrarini, Alberto; Zamo', Alberto; Delledonne, Massimo; Pignatti, Pierfranco; Malerba, Giovanni
Genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and profiles of clopidogrel-induced antiplatelet effects in type 2 diabetes mellitus patients with coronary artery disease 1-gen-2008 Zanoni, Martina; Prandini, Paola; Angiolillo, D. J.; Bernardo, E.; Fernandez Otiz, A.; Macaya, C.; Bass, T. A.; Trabetti, Elisabetta; Pignatti, Pierfranco
Genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and profiles of clopidogrel-induced antiplatelet effects in type 2 diabetes mellitus patients with coronary artery disease 1-gen-2008 Zanoni, Martina; Prandini, Paola; Angiolillo, D. J.; Bernardo, E.; Fernandez Ortiz, A.; Macaya, C.; Bass, T. A.; Trabetti, Elisabetta; Pignatti, Pierfranco
Impact of insulin receptor substrate-1 genotypes on platelet reactivity and cardiovascular outcomes in patients with type 2 diabetes mellitus and coronary artery disease 1-gen-2011 Angiolillo, D. J.; Bernardo, E.; Zanoni, Martina; Vivas, D.; Capranzano, P.; Malerba, Giovanni; Capodanno, D.; Prandini, Paola; Pasquali, Alessandra; Trabetti, Elisabetta; Sabaté, M.; Jimenez Quevedo, P.; Ferreiro, J. L.; Ueno, M.; Bass, T. A.; Pignatti, Pierfranco; Fernandez Ortiz, A.; Macaya, C.
Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology. 1-gen-2002 Pegoraro, E.; Cepollaro, F.; Prandini, Paola; Marin, A.; Fanin, M.; Trevisan, C. P.; El Messlemani, A. H.; Tarone, G.; Engvall, E.; Hoffman, E. P.; Angelini, C.
Islands of euchromatic-like sequence and expressed genes within the heterochromatic regions: lessons from the initial sequence analysis of 21p. 1-gen-2005 Prandini, Paola; Lyle, R.; Osoegawa, K.; ten Hallers, B.; Humphray, S.; Zhu, B.; Eyras, E.; Castelo, R.; Bird, C.; Cruts, M.; Dahoun, S.; She, X.; van Broeckhoven, C.; Eichler, E.; Guigo, R.; Rogers, J.; de Jong, P.; Reymond, A.; Antonarakis, S. E.
Islands of euchromatic-like sequence and expressed genes within the short arm of HSA21: sequence and copy number variability. 1-gen-2006 Prandini, Paola; Lyle, R.; Osoegawa, K.; ten Hallers, B.; Humphray, S.; Zhu, B.; Eyras, E.; Castelo, R.; Bird, C.; Cruts, M.; Dahoun, S.; She, X.; van Broeckhoven, C.; Eichler, E.; Guigo, R.; Rogers, J.; de Jong, P.; Reymond, A.; Antonarakis, S. E.
Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21. 1-gen-2007 Lyle, R.; Prandini, Paola; Osoegawa, K.; Ten Hallers, B.; Humphray, S.; Zhu, B.; Eyras, E.; Castelo, R.; Bird, C. P.; Gagos, S.; Scott, C.; Cox, A.; Deutsch, S.; Ucla, C.; Cruts, M.; Dahoun, S.; She, X.; Bena, F.; Wang, S. Y.; Van Broeckhoven, C.; Eichler, E. E.; Guigo, R.; Rogers, J.; de Jong, P. J.; Reymond, A.; Antonarakis, S. E.
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy. 1-gen-2004 Prandini, Paola; Berardinelli, A.; Fanin, M.; Morello, F.; Zardini, E.; Pichiecchio, A.; Uggetti, C.; Lanzi, G.; Angelini, C.; Pegoraro, E.
Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy. 1-gen-2005 Brockington, M.; Torelli, S.; Prandini, Paola; Boito, C.; Dolatshad, N. F.; Longman, C.; Brown, S. C.; Muntoni, F.
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan. 1-gen-2001 Brockington, M.; Blake, D. J.; Prandini, Paola; Brown, S. C.; Torelli, S.; Benson, M. A.; Ponting, C. P.; Estournet, B.; Romero, N. B.; Mercuri, E.; Voit, T.; Sewry, C. A.; Guicheney, P.; Muntoni, F.
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. 1-gen-2001 Brockington, M.; Yuva, Y.; Prandini, Paola; Brown, S. C.; Torelli, S.; Benson, M. A.; Herrmann, R.; Anderson, L. V.; Bashir, R.; Burgunder, J. M.; Fallet, S.; Romero, N.; Fardeau, M.; Straub, V.; Storey, G.; Pollitt, C.; Richard, I.; Sewry, C. A.; Bushby, K.; Voit, T.; Blake, D. J.; Muntoni, F.