VENTURIN, MARCO

VENTURIN, MARCO  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Risultati 1 - 12 di 12 (tempo di esecuzione: 0.015 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability 2016 MONCINI, SILVIACASTRONOVO, PAOLALUNGHI, MARTARIVA, PAOLA VANDAM. Venturin + Article (author) -
The miR-15/107 Family of microRNA Genes Regulates CDK5R1/p35 with Implications for Alzheimer’s Disease Pathogenesis 2017 S. MonciniM. LunghiA. ValmadreP.V. RivaM. Venturin + Article (author) -
hnRNPA2/B1 and nELAV proteins bind to a specific U-rich element in CDK5R1 3'-UTR and oppositely regulate its expression 2014 P. ZuccottiC. ColombritaS. MonciniA. BarbieriM. LunghiC. GelfiS. De PalmaA. NicolinA. RattiM. VenturinP. Riva Article (author) -
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome 2014 M. VenturinS. CarraG. GaudenziG.R. GalloS. MonciniF. CotelliP. Riva + Article (author) -
ATRX mutation in two adult brothers with non-specific moderate intellectual disability identified by exome sequencing 2013 S. MonciniP. CastronovoM. CrippaP. FinelliM. Venturin + Article (author) -
Centaurin-α2 Interacts with β-Tubulin and Stabilizes Microtubules 2012 P. ZuccottiD. CartelliV. PandiniM. VenturinA. AlivertiE. BattaglioliG. CappellettiP.V. Riva + Article (author) -
The Role of miR-103 and miR-107 in Regulation of CDK5R1 Expression and in Cellular Migration 2011 S. MonciniP. ZuccottiM. VenturinP.V. Riva + Article (author) -
Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutations 2010 M. LongoniS. MonciniI.M. MorellaR. ZippelM. VenturinP.V. Riva + Article (author) -
MicroRNA-23b mediates urokinase and c-met downmodulation and a decreased migration of human hepatocellular carcinoma cells 2009 S. MonciniM. VenturinP. Riva + Article (author) -
The 3' untranslated region of human cyclin-dependent kinase 5 regulatory subunit 1 contains regulatory elements affecting transcript stability 2007 S. MonciniA. BevilacquaM. VenturinA. RattiA. NicolinP. Riva + Article (author) -
Mental retardation and cardiovascular malformations are significantly present in NF1-microdeleted patients and point to candidate genes in 17q11.2 2004 M. VenturinL. LarizzaP. Riva + Article (author) -
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions 2004 M. VenturinC. GervasiniF. OrzanP. ColapietroL. LarizzaP. Riva + Article (author) -