VENTURIN, MARCO
VENTURIN, MARCO
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome
2010 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 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
Breakpoint characterization of a novel NF1 multiexonic deletion : a case showing expression of the mutated allele
2008 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 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 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 G. Portera, M. Venturin, A. Patrizi, E. Martinoli, P. Riva, L. Dalprà
Emerging Role of Genetic Alterations Affecting Exosome Biology in Neurodegenerative Diseases
2019 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 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 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 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 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 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 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 A. Bentivegna, M. Venturin, C. Gervasini, L. Corrado, L. Larizza, P. Riva
Lost in HELLS: Disentangling the mystery of SALNR existence in senescence cellular models
2023 A. Consiglio, M. Venturin, S. Briguglio, C. Rossi, G. Grillo, S. Bellosta, M.G. Cattaneo, F. Licciulli, C. Battaglia
Mapping of genes and EST to 17q11.2 to a YAC contig centered on the NF1 gene
2000 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 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 A. Salvi, C. Sabelli, S. Moncini, M. Venturin, B. Arici, P. Riva, N. Portolani, S.M. Giulini, G. De Petro, S. Barlati
Multiple Layers of CDK5R1 Regulation in Alzheimer’s Disease Implicate Long Non-Coding RNAs
2018 M. Spreafico, B. Grillo, F. Rusconi, E. Battaglioli, M. Venturin