VENTURIN, MARCO
VENTURIN, MARCO
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
Unravelling the enigma of the complex relationship between aging, senescence, molecular biomarkers and sex/gender influences: a roadmap of open questions
2024 C. Battaglia, M.G. Cattaneo, C. Germiniani, M. Venturin
PURPL and NEAT1 Long Non-Coding RNAs Are Modulated in Vascular Smooth Muscle Cell Replicative Senescence
2023 C. Rossi, M. Venturin, J. Gubala, A. Frasca, A. Corsini, C. Battaglia, S. Bellosta
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
Unraveling the genetic causes of Moebius syndrome
2022 G. Moresco, O. Rondinone, J. Costanza, C. Santaniello, L. Fontana, A. Mauri, M. Venturin, O. Picciolini, R. Villa, M. Miozzo, M.F. Bedeschi
Psychiatric Disorders and lncRNAs: A Synaptic Match
2020 F. Rusconi, E. Battaglioli, M. Venturin
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
Emerging Role of Genetic Alterations Affecting Exosome Biology in Neurodegenerative Diseases
2019 P. Riva, C. Battaglia, M. Venturin
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
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
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 long non-coding RNAs in neurodegenerative diseases : novel mechanisms of pathogenesis
2016 P. Riva, A. Ratti, 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
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
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
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
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
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