MONCINI, SILVIA

MONCINI, SILVIA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

Mostra records
Risultati 1 - 20 di 26 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
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) -
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) -
Differential allelic expression of SOS1 and hyperexpression of the activating SOS1 c.755C variant in a Noonan syndrome family 2015 S. MonciniI. MorellaL. FerrariP. Riva + Article (author) -
Differential allelic expression of the SOS1 c.755C activating variant in a Noonan syndrome family 2014 S. MonciniL. FerrariP. Riva + Article (author) -
Transcriptional dysregulation and impairment of PHOX2B auto-regulatory mechanism in the pathogenesis of Congenital Central Hypoventilation Syndrome 2014 S. Di LascioS. MonciniR. BenfanteD. Fornasari + Article (author) -
The role of p35/CDK5 regulation by miR-15/107 family in Alzheimer’s disease 2014 S. MonciniM. LunghiA. ValmadreP. 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) -
Extensive mutational analysis of CDK5 and CDK5R1 in patients with non-syndromic mental retardation reveals novel variants in CDK5R1 3’-UTR 2012 S. MonciniP. CastronovoP. RivaM. Venturin + Article (author) -
Identification and functional characterization of trans-acting factors involved in the post-transcriptional regulation of CDK5R1 2012 P. ZuccottiA. BarbieriC. ColombritaS. De PalmaS. MonciniC. GelfiA. RattiM. VenturinP. Riva Article (author) -
Identification of post-transcriptional regulatory elements in CDK5R1 3’UTR gene involved in CNS development and functioning 2011 P. ZuccottiA. BarbieriC. ColombritaS. De PalmaS. MonciniC. GelfiA. RattiM. VenturinP. 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) -
miR-103 and miR-107 are involved in the regulation of CDK5R1/p35 expression 2010 S. MonciniM. VenturinP. ZuccottiA. NicolinP. Riva + Article (author) -
Identification of a new Jnk-activating familial SOS1 and a de novo RAF1 mutations in a Noonan syndrome patient 2010 M. LongoniS. MonciniR. ZippelM. VenturinP. 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) -
The regulation of CDK5R1 gene expression by miRNAs may have a role in Alzheimer’s disease 2009 S. MonciniM. VenturinP. ZuccottiP. 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) -
Identification of a potential regulatory element forming a hairpin structure within the 3’UTR of CDK5R1 2008 M. VenturinS. MonciniA. NicolinP. Riva + Article (author) -
Evidence on microRNA-mediated regulation of CDK5R1 gene expression 2008 S. MonciniM. VenturinP. Riva + Article (author) -