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

Moncini S, Lunghi M, Valmadre A, Grasso M, Del Vescovo V, Riva P, Denti MA, Venturin M. Moncini S, et al. Mol Neurobiol. 2017 Aug;54(6):4329-4342. doi: 10.1007/s12035-016-0002-4. Epub 2016 Jun 24. Mol Neurobiol. 2017. PMID: 27343180 Free article.

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

Moncini S, Castronovo P, Murgia A, Russo S, Bedeschi MF, Lunghi M, Selicorni A, Bonati MT, Riva P, Venturin M. Moncini S, et al. J Hum Genet. 2016 Apr;61(4):283-93. doi: 10.1038/jhg.2015.144. Epub 2015 Dec 10. J Hum Genet. 2016. PMID: 26657932

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The role of miR-103 and miR-107 in regulation of CDK5R1 expression and in cellular migration.

Moncini S, Salvi A, Zuccotti P, Viero G, Quattrone A, Barlati S, De Petro G, Venturin M, Riva P. Moncini S, et al. PLoS One. 2011;6(5):e20038. doi: 10.1371/journal.pone.0020038. Epub 2011 May 23. PLoS One. 2011. PMID: 21625387 Free PMC article.

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

Moncini S, Bedeschi MF, Castronovo P, Crippa M, Calvello M, Garghentino RR, Scuvera G, Finelli P, Venturin M. Moncini S, et al. Meta Gene. 2013 Oct 29;1:102-8. doi: 10.1016/j.mgene.2013.09.004. eCollection 2013 Dec. Meta Gene. 2013. PMID: 25606380 Free PMC article.

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ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome.

Venturin M, Carra S, Gaudenzi G, Brunelli S, Gallo GR, Moncini S, Cotelli F, Riva P. Venturin M, et al. Among authors: moncini s. J Med Genet. 2014 Jul;51(7):436-43. doi: 10.1136/jmedgenet-2013-102240. Epub 2014 Apr 7. J Med Genet. 2014. PMID: 24711647 Free article.

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

Moncini S, Bonati MT, Morella I, Ferrari L, Brambilla R, Riva P. Moncini S, et al. Eur J Hum Genet. 2015 Nov;23(11):1531-7. doi: 10.1038/ejhg.2015.20. Epub 2015 Feb 25. Eur J Hum Genet. 2015. PMID: 25712082 Free PMC article.

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Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutations.

Longoni M, Moncini S, Cisternino M, Morella IM, Ferraiuolo S, Russo S, Mannarino S, Brazzelli V, Coi P, Zippel R, Venturin M, Riva P. Longoni M, et al. Among authors: moncini s. Am J Med Genet A. 2010 Sep;152A(9):2176-84. doi: 10.1002/ajmg.a.33564. Am J Med Genet A. 2010. PMID: 20683980

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

Salvi A, Sabelli C, Moncini S, Venturin M, Arici B, Riva P, Portolani N, Giulini SM, De Petro G, Barlati S. Salvi A, et al. Among authors: moncini s. FEBS J. 2009 Jun;276(11):2966-82. doi: 10.1111/j.1742-4658.2009.07014.x. Epub 2009 Apr 16. FEBS J. 2009. PMID: 19490101 Free article.

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hnRNPA2/B1 and nELAV proteins bind to a specific U-rich element in CDK5R1 3'-UTR and oppositely regulate its expression.

Zuccotti P, Colombrita C, Moncini S, Barbieri A, Lunghi M, Gelfi C, De Palma S, Nicolin A, Ratti A, Venturin M, Riva P. Zuccotti P, et al. Among authors: moncini s. Biochim Biophys Acta. 2014 Jun;1839(6):506-16. doi: 10.1016/j.bbagrm.2014.04.018. Epub 2014 May 2. Biochim Biophys Acta. 2014. PMID: 24792867

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

Moncini S, Bevilacqua A, Venturin M, Fallini C, Ratti A, Nicolin A, Riva P. Moncini S, et al. BMC Mol Biol. 2007 Dec 3;8:111. doi: 10.1186/1471-2199-8-111. BMC Mol Biol. 2007. PMID: 18053171 Free PMC article.

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