VENTURIN, MARCO
VENTURIN, MARCO
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability
2016 S. Moncini, P. Castronovo, A. Murgia, S. Russo, M.F. Bedeschi, M. Lunghi, A. Selicorni, M.T. Bonati, P. Riva, M. Venturin
The miR-15/107 Family of microRNA Genes Regulates CDK5R1/p35 with Implications for Alzheimer’s Disease Pathogenesis
2017 S. Moncini, M. Lunghi, A. Valmadre, M. Grasso, V. Del Vescovo, P.V. Riva, M.A. Denti, M. Venturin
hnRNPA2/B1 and nELAV proteins bind to a specific U-rich element in CDK5R1 3'-UTR and oppositely regulate its expression
2014 P. Zuccotti, C. Colombrita, S. Moncini, A. Barbieri, M. Lunghi, C. Gelfi, S. De Palma, A. Nicolin, A. Ratti, M. Venturin, P. Riva
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome
2014 M. Venturin, S. Carra, G. Gaudenzi, S. Brunelli, G.R. Gallo, S. Moncini, F. Cotelli, P. Riva
ATRX mutation in two adult brothers with non-specific moderate intellectual disability identified by exome sequencing
2013 S. Moncini, M.F. Bedeschi, P. Castronovo, M. Crippa, M. Calvello, R.R. Garghentino, G. Scuvera, P. Finelli, M. Venturin
Centaurin-α2 Interacts with β-Tubulin and Stabilizes Microtubules
2012 P. Zuccotti, D. Cartelli, M. Stroppi, V. Pandini, M. Venturin, A. Aliverti, E. Battaglioli, G. Cappelletti, P.V. Riva
The Role of miR-103 and miR-107 in Regulation of CDK5R1 Expression and in Cellular Migration
2011 S. Moncini, A. Salvi, P. Zuccotti, G. Viero, A. Quattrone, S. Barlati, G. De Petro, M. Venturin, P.V. Riva
Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutations
2010 M. Longoni, S. Moncini, M. Cisternino, I.M. Morella, S. Ferraiuolo, S. Russo, S. Mannarino, V. Brazzelli, P. Coi, R. Zippel, M. Venturin, P.V. Riva
MicroRNA-23b mediates urokinase and c-met downmodulation and a decreased migration of human hepatocellular carcinoma cells
2009 A. Salvi, C. Sabelli, S. Moncini, M. Venturin, B. Arici, P. Riva, N. Portolani, S.M. Giulini, G. De Petro, S. Barlati
The 3' untranslated region of human cyclin-dependent kinase 5 regulatory subunit 1 contains regulatory elements affecting transcript stability
2007 S. Moncini, A. Bevilacqua, M. Venturin, C. Fallini, A. Ratti, A. Nicolin, P. Riva
Mental retardation and cardiovascular malformations are significantly present in NF1-microdeleted patients and point to candidate genes in 17q11.2
2004 M. Venturin, P. Guarnieri, F. Natacci, M. Stabile, R. Tenconi, M. Clementi, C. Hernandez, P. Thompson, M. Upadhyaya, L. Larizza, P. Riva
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions
2004 M. Venturin , C. Gervasini, F. Orzan, A. Bentivegna, L. Corrado, P. Colapietro , A. Friso, R. Tenconi, M. Upadhyaya, L. Larizza, P. Riva