MicroRNA‐23b mediates urokinase and c‐met downmodulation and a decreased migration of human hepatocellular carcinoma cells

Alessandro Salvi, Cristiano Sabelli, Silvia Moncini, +7

FEBS Journal

The Role of miR-103 and miR-107 in Regulation of CDK5R1 Expression and in Cellular Migration

Silvia Moncini, Alessandro Salvi, Paola Zuccotti, +6

PLoS ONE

The miR-15/107 Family of microRNA Genes Regulates CDK5R1/p35 with Implications for Alzheimer’s Disease Pathogenesis

Silvia Moncini, Marta Lunghi, Alice Valmadre, +5

Molecular Neurobiology

Neurodegenerative DiseasesAlzheimer's DiseaseMedicineDegenerative PathologyMir-15/107 Family +7

Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation

Marco Venturin, Silvia Moncini, Valentina Villa, +4

Neurogenetics

Omg GenesMendelian DisorderPsychiatrySyndromic AutismGenetic Disorder +9

<i>ADAP2</i> in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome

Marco Venturin, Silvia Carra, Germano Gaudenzi, +5

Journal of Medical Genetics

The 3' untranslated region of human Cyclin-Dependent Kinase 5 Regulatory subunit 1 contains regulatory elements affecting transcript stability

Silvia Moncini, Annamaria Bevilacqua, Marco Venturin, +4

BMC Molecular Biology

Noonan syndrome associated with both a new Jnk‐activating familial <i>SOS1</i> and a de novo <i>RAF1</i> mutations

Longoni Mauro, Silvia Moncini, Mariangela Cisternino, +9

American Journal of Medical Genetics Part A

Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability

Silvia Moncini, Paola Castronovo, Alessandra Murgia, +7

Journal of Human Genetics

Intellectual ImpairmentMendelian DisorderNon-syndromic Intellectual DisabilityCdk5r1 MutationsGenetic Disorder +6

Differential allelic expression of SOS1 and hyperexpression of the activating SOS1 c.755C variant in a Noonan syndrome family

Silvia Moncini, Maria Teresa Bonati, Ilaria Morella, +3

European Journal of Human Genetics

Allelic VariantGenetic DisorderGeneticsPathologyAutoimmunity +5

ATRX mutation in two adult brothers with non-specific moderate intellectual disability identified by exome sequencing

Silvia Moncini, Maria Francesca Bedeschi, Paola Castronovo, +6

Meta Gene

EngineeringExome SequencingGeneticsPathologyMinor Facial Anomalies +17