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Role of epigenetics in human aging and longevity: genome-wide DNA methylation profile in centenarians and centenarians' offspring.
Gentilini D, Mari D, Castaldi D, Remondini D, Ogliari G, Ostan R, Bucci L, Sirchia SM, Tabano S, Cavagnini F, Monti D, Franceschi C, Di Blasio AM, Vitale G. Gentilini D, et al. Among authors: sirchia sm. Age (Dordr). 2013 Oct;35(5):1961-73. doi: 10.1007/s11357-012-9463-1. Epub 2012 Aug 25. Age (Dordr). 2013. PMID: 22923132 Free PMC article.
Misbehaviour of XIST RNA in breast cancer cells.
Sirchia SM, Tabano S, Monti L, Recalcati MP, Gariboldi M, Grati FR, Porta G, Finelli P, Radice P, Miozzo M. Sirchia SM, et al. PLoS One. 2009;4(5):e5559. doi: 10.1371/journal.pone.0005559. Epub 2009 May 15. PLoS One. 2009. PMID: 19440381 Free PMC article.
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction.
Tabano S, Colapietro P, Cetin I, Grati FR, Zanutto S, Mandò C, Antonazzo P, Pileri P, Rossella F, Larizza L, Sirchia SM, Miozzo M. Tabano S, et al. Among authors: sirchia sm. Epigenetics. 2010 May 16;5(4):313-24. doi: 10.4161/epi.5.4.11637. Epub 2010 May 28. Epigenetics. 2010. PMID: 20418667 Free article.
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
Calvello M, Tabano S, Colapietro P, Maitz S, Pansa A, Augello C, Lalatta F, Gentilin B, Spreafico F, Calzari L, Perotti D, Larizza L, Russo S, Selicorni A, Sirchia SM, Miozzo M. Calvello M, et al. Among authors: sirchia sm. Epigenetics. 2013 Oct;8(10):1053-60. doi: 10.4161/epi.25812. Epub 2013 Aug 5. Epigenetics. 2013. PMID: 23917791 Free PMC article.
PDGFB hypomethylation is a favourable prognostic biomarker in primary myelofibrosis.
Augello C, Gianelli U, Falcone R, Tabano S, Savi F, Bonaparte E, Ciboddo M, Paganini L, Parafioriti A, Ricca D, Lonati S, Cattaneo D, Fracchiolla NS, Iurlo A, Cortelezzi A, Bosari S, Miozzo M, Sirchia SM. Augello C, et al. Among authors: sirchia sm. Leuk Res. 2015 Feb;39(2):236-41. doi: 10.1016/j.leukres.2014.11.012. Epub 2014 Dec 2. Leuk Res. 2015. PMID: 25498506 Clinical Trial.
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, Calcagno A, Maghnie M, Divizia MT, Melis D, Manfredini E, Ferrero GB, Pecile V, Larizza L. Russo S, et al. Clin Epigenetics. 2016 Mar 1;8:23. doi: 10.1186/s13148-016-0183-8. eCollection 2016. Clin Epigenetics. 2016. PMID: 26933465 Free PMC article.
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