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Page 1
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism.
Piccoli C, Ripoli M, Quarato G, Scrima R, D'Aprile A, Boffoli D, Margaglione M, Criscuolo C, De Michele G, Sardanelli A, Papa S, Capitanio N. Piccoli C, et al. Among authors: criscuolo c. J Med Genet. 2008 Sep;45(9):596-602. doi: 10.1136/jmg.2008.058628. Epub 2008 Jun 4. J Med Genet. 2008. PMID: 18524835
DNA damage induced by polyglutamine-expanded proteins.
Giuliano P, De Cristofaro T, Affaitati A, Pizzulo GM, Feliciello A, Criscuolo C, De Michele G, Filla A, Avvedimento EV, Varrone S. Giuliano P, et al. Among authors: criscuolo c. Hum Mol Genet. 2003 Sep 15;12(18):2301-9. doi: 10.1093/hmg/ddg242. Epub 2003 Jul 22. Hum Mol Genet. 2003. PMID: 12915485
A new model to study neurodegeneration in ataxia oculomotor apraxia type 2.
Becherel OJ, Sun J, Yeo AJ, Nayler S, Fogel BL, Gao F, Coppola G, Criscuolo C, De Michele G, Wolvetang E, Lavin MF. Becherel OJ, et al. Among authors: criscuolo c. Hum Mol Genet. 2015 Oct 15;24(20):5759-74. doi: 10.1093/hmg/ddv296. Epub 2015 Jul 30. Hum Mol Genet. 2015. PMID: 26231220 Free PMC article.
Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2.
Fogel BL, Cho E, Wahnich A, Gao F, Becherel OJ, Wang X, Fike F, Chen L, Criscuolo C, De Michele G, Filla A, Collins A, Hahn AF, Gatti RA, Konopka G, Perlman S, Lavin MF, Geschwind DH, Coppola G. Fogel BL, et al. Among authors: criscuolo c. Hum Mol Genet. 2014 Sep 15;23(18):4758-69. doi: 10.1093/hmg/ddu190. Epub 2014 Apr 23. Hum Mol Genet. 2014. PMID: 24760770 Free PMC article.
125 results