VENTURIN, MARCO

VENTURIN, MARCO  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Titolo Data di pubblicazione Autori Tipo File Abstract
The 3' untranslated region of human cyclin-dependent kinase 5 regulatory subunit 1 contains regulatory elements affecting transcript stability 3-dic-2007 S. MonciniA. BevilacquaM. VenturinA. RattiA. NicolinP. Riva + Article (author) -
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome 1-apr-2010 E. MartinoliG.V. ZuccottiM. VolontèM. VenturinP.V. Riva + Article (author) -
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome 1-gen-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 1-gen-2013 S. MonciniP. CastronovoM. CrippaP. FinelliM. Venturin + Article (author) -
Breakpoint characterization of a novel NF1 multiexonic deletion : a case showing expression of the mutated allele 1-mag-2008 F. OrzanM. StroppiM. VenturinP. Riva + Article (author) -
Candidate Genes and MiRNAs Linked to the Inverse Relationship Between Cancer and Alzheimer’s Disease: Insights From Data Mining and Enrichment Analysis 24-set-2019 Battaglia, CristinaVenturin, Marco + Article (author) -
Centaurin-α2 Interacts with β-Tubulin and Stabilizes Microtubules 1-dic-2012 P. ZuccottiD. CartelliV. PandiniM. VenturinA. AlivertiE. BattaglioliG. CappellettiP.V. Riva + Article (author) -
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 1-gen-2006 M. VenturinA. PatriziMARTINOLI, EMANUELAP. Riva + Article (author) -
Emerging Role of Genetic Alterations Affecting Exosome Biology in Neurodegenerative Diseases 1-set-2019 Riva, PaolaBattaglia, CristinaVenturin, Marco Article (author) -
Erratum: Fish with locus-specific probes on stretched chromosomes: A useful tool for genome organization studies (Chromosome reseach (2001) 9 (167-170)) 1-ago-2001 Bentivegna A.Venturin M.Gervasini C.Corrado L.Larizza L.Riva P. Article (author) -
Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval 1-gen-2005 M. VenturinL. LarizzaP. Riva + Article (author) -
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions 1-gen-2004 M. VenturinC. GervasiniF. OrzanP. ColapietroL. LarizzaP. Riva + Article (author) -
FISH with locus-specific probes on stretched chromosomes : a useful tool for genome organization studies 1-feb-2001 M. VenturinC. GervasiniL. LarizzaP. Riva + Article (author) -
Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability 1-apr-2016 MONCINI, SILVIACASTRONOVO, PAOLALUNGHI, MARTARIVA, PAOLA VANDAM. Venturin + Article (author) -
hnRNPA2/B1 and nELAV proteins bind to a specific U-rich element in CDK5R1 3'-UTR and oppositely regulate its expression 2-mag-2014 P. ZuccottiC. ColombritaS. MonciniA. BarbieriM. LunghiC. GelfiS. De PalmaA. NicolinA. RattiM. VenturinP. Riva Article (author) -
Identification of duplicated genes in 17q11.2 by using FISH on stretched chromosomes and DNA fibers 1-lug-2001 M. VenturinC. GervasiniL. LarizzaP. Riva + Article (author) -
The long non-coding RNAs in neurodegenerative diseases : novel mechanisms of pathogenesis 1-gen-2016 P. RivaA. RattiM. Venturin Article (author) -
Mapping of genes and EST to 17q11.2 to a YAC contig centered on the NF1 gene 1-gen-2000 P. RivaM. VenturinC. GervasiniL. Larizza + Article (author) -
Mental retardation and cardiovascular malformations are significantly present in NF1-microdeleted patients and point to candidate genes in 17q11.2 1-gen-2004 M. VenturinL. LarizzaP. Riva + Article (author) -
MicroRNA-23b mediates urokinase and c-met downmodulation and a decreased migration of human hepatocellular carcinoma cells 1-giu-2009 S. MonciniM. VenturinP. Riva + Article (author) -