VENTURIN, MARCO
VENTURIN, MARCO
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
The 3' untranslated region of human cyclin-dependent kinase 5 regulatory subunit 1 contains regulatory elements affecting transcript stability
2007-12-03 S. Moncini, A. Bevilacqua, M. Venturin, C. Fallini, A. Ratti, A. Nicolin, P. Riva
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome
2010-04-01 E. Martinoli, G.V. Zuccotti, L. Pogliani, M. Volontè, M. Venturin, P. Fortina, A. Ertel, S. Redaelli, P.V. Riva, L. Dalprà
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome
2014-01-01 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
2013-01-01 S. Moncini, M.F. Bedeschi, P. Castronovo, M. Crippa, M. Calvello, R.R. Garghentino, G. Scuvera, P. Finelli, M. Venturin
Breakpoint characterization of a novel NF1 multiexonic deletion : a case showing expression of the mutated allele
2008-05-01 F. Orzan, M. Stroppi, M. Venturin, M.C. Valero, C. Hernández, P. Riva
Candidate Genes and MiRNAs Linked to the Inverse Relationship Between Cancer and Alzheimer’s Disease: Insights From Data Mining and Enrichment Analysis
2019-09-24 C. Battaglia, M. Venturin, A. Sojic, N. Jesuthasan, A. Orro, R. Spinelli, M. Musicco, G. De Bellis, F. Adorni
Centaurin-α2 Interacts with β-Tubulin and Stabilizes Microtubules
2012-12-01 P. Zuccotti, D. Cartelli, M. Stroppi, V. Pandini, M. Venturin, A. Aliverti, E. Battaglioli, G. Cappelletti, P.V. Riva
Characterization of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements
2006-01-01 G. Portera, M. Venturin, A. Patrizi, E. Martinoli, P. Riva, L. Dalprà
Emerging Role of Genetic Alterations Affecting Exosome Biology in Neurodegenerative Diseases
2019-09-01 P. Riva, C. Battaglia, M. Venturin
Erratum: Fish with locus-specific probes on stretched chromosomes: A useful tool for genome organization studies (Chromosome reseach (2001) 9 (167-170))
2001-08-01 A. Bentivegna, M. Venturin, C. Gervasini, L. Corrado, L. Larizza, P. Riva
Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval
2005-01-01 M. Venturin, A. Bentivegna, R. Moroni, L. Larizza, P. Riva
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions
2004-01-01 M. Venturin , C. Gervasini, F. Orzan, A. Bentivegna, L. Corrado, P. Colapietro , A. Friso, R. Tenconi, M. Upadhyaya, L. Larizza, P. Riva
FISH with locus-specific probes on stretched chromosomes : a useful tool for genome organization studies
2001-02-01 A. Bentivegna, M. Venturin, C. Gervasini, L. Corrado, L. Larizza, P. Riva
Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability
2016-04-01 S. Moncini, P. Castronovo, A. Murgia, S. Russo, M.F. Bedeschi, M. Lunghi, A. Selicorni, M.T. Bonati, P. Riva, M. Venturin
hnRNPA2/B1 and nELAV proteins bind to a specific U-rich element in CDK5R1 3'-UTR and oppositely regulate its expression
2014-05-02 P. Zuccotti, C. Colombrita, S. Moncini, A. Barbieri, M. Lunghi, C. Gelfi, S. De Palma, A. Nicolin, A. Ratti, M. Venturin, P. Riva
Identification of duplicated genes in 17q11.2 by using FISH on stretched chromosomes and DNA fibers
2001-07-01 A. Bentivegna, M. Venturin, C. Gervasini, L. Corrado, L. Larizza, P. Riva
The long non-coding RNAs in neurodegenerative diseases : novel mechanisms of pathogenesis
2016-01-01 P. Riva, A. Ratti, M. Venturin
Mapping of genes and EST to 17q11.2 to a YAC contig centered on the NF1 gene
2000-01-01 L. Corrado, P. Riva, M. Venturin, A. Bentivegna, C. Gervasini, L. Larizza
Mental retardation and cardiovascular malformations are significantly present in NF1-microdeleted patients and point to candidate genes in 17q11.2
2004-01-01 M. Venturin, P. Guarnieri, F. Natacci, M. Stabile, R. Tenconi, M. Clementi, C. Hernandez, P. Thompson, M. Upadhyaya, L. Larizza, P. Riva
MicroRNA-23b mediates urokinase and c-met downmodulation and a decreased migration of human hepatocellular carcinoma cells
2009-06-01 A. Salvi, C. Sabelli, S. Moncini, M. Venturin, B. Arici, P. Riva, N. Portolani, S.M. Giulini, G. De Petro, S. Barlati