Sfoglia per Autore
Search of candidate genes for cardiovascular malformation in NF1 microdeletion syndrome
2004 A. Bentivegna, M. Venturin, S. Moncini, L. Larizza, P. Riva
Functional study of transcription cis-regulatory elements predicted in the CDK5R1 3’UTR
2006 S. Moncini, M. Venturin, A. Bevilacqua, A. Nicolin, P. Riva
Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with nonsyndromic mental retardation
2006 M. Venturin, S. Moncini, V. Villa, S. Russo, M.T. Bonati, L. Larizza, P.V. Riva
The human CDK5R1 3'UTR contains distinct subregions affecting transcript stability
2007 S. Moncini, M. Venturin, A. Bevilacqua, A. Ratti, A. Nicolin, P. Riva
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
Functional study of regulatory elements in CDK5R1 3’-UTR: evidence on post-transcriptional gene expression regulation
2007 S. Moncini
Identification of a potential regulatory element forming a hairpin structure within the 3’UTR of CDK5R1
2008 M. Venturin, S. Moncini, P. Zuccotti, A. Nicolin, P. Riva
Evidence on microRNA-mediated regulation of CDK5R1 gene expression
2008 S. Moncini, M. Venturin, A. Salvi, V. Lanzi, C. Sabelli, G. De Petro, S. Barlati, P. Riva
The regulation of CDK5R1 gene expression by miRNAs may have a role in Alzheimer’s disease
2009 S. Moncini, M. Venturin, A. Salvi, P. Zuccotti, V. Lanzi, C. Sabelli, G. De Petro, S. Barlati, P. 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
miR-103 and miR-107 are involved in the regulation of CDK5R1/p35 expression
2010 S. Moncini, A. Salvi, M. Venturin, P. Zuccotti, A. Nicolin, G. De Petro, S. Barlati, P. Riva
Identification of a new Jnk-activating familial SOS1 and a de novo RAF1 mutations in a Noonan syndrome patient
2010 M. Longoni, S. Moncini, M. Cisternino, I. Morella, S. Ferraiuolo, S. Russo, P. Coi, R. Zippel, M. Venturin, P. 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
Identification of post-transcriptional regulatory elements in CDK5R1 3’UTR gene involved in CNS development and functioning
2011 P. Zuccotti, A. Barbieri, C. Colombrita, S. De Palma, S. Moncini, C. Gelfi, A. Ratti, M. Venturin, P. 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
Extensive mutational analysis of CDK5 and CDK5R1 in patients with non-syndromic mental retardation reveals novel variants in CDK5R1 3’-UTR
2012 S. Moncini, P. Castronovo, A. Murgia, S. Russo, M.F. Bedeschi, P. Riva, M. Venturin
Identification and functional characterization of trans-acting factors involved in the post-transcriptional regulation of CDK5R1
2012 P. Zuccotti, A. Barbieri, C. Colombrita, S. De Palma, S. Moncini, C. Gelfi, A. Ratti, M. Venturin, 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
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
Transcriptional dysregulation and impairment of PHOX2B auto-regulatory mechanism in the pathogenesis of Congenital Central Hypoventilation Syndrome
2014 S. Di Lascio, S. Moncini, T. Bachetti, I. Ceccherini, R. Benfante, D. Fornasari
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