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Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: The impact of full-length dystrophin deficiency.
Pioner JM, Santini L, Palandri C, Langione M, Grandinetti B, Querceto S, Martella D, Mazzantini C, Scellini B, Giammarino L, Lupi F, Mazzarotto F, Gowran A, Rovina D, Santoro R, Pompilio G, Tesi C, Parmeggiani C, Regnier M, Cerbai E, Mack DL, Poggesi C, Ferrantini C, Coppini R. Pioner JM, et al. Among authors: rovina d. Front Physiol. 2022 Nov 7;13:1030920. doi: 10.3389/fphys.2022.1030920. eCollection 2022. Front Physiol. 2022. PMID: 36419836 Free PMC article.
Differential signature of the centrosomal MARK4 isoforms in glioma.
Magnani I, Novielli C, Fontana L, Tabano S, Rovina D, Moroni RF, Bauer D, Mazzoleni S, Colombo EA, Tedeschi G, Monti L, Porta G, Bosari S, Frassoni C, Galli R, Bello L, Larizza L. Magnani I, et al. Among authors: rovina d. Anal Cell Pathol (Amst). 2011;34(6):319-38. doi: 10.3233/ACP-2011-0031. Anal Cell Pathol (Amst). 2011. PMID: 22156016 Free PMC article.
Epigenetic effects of chromatin remodeling agents on organotypic cultures.
Sirchia SM, Faversani A, Rovina D, Russo MV, Paganini L, Savi F, Augello C, Rosso L, Del Gobbo A, Tabano S, Bosari S, Miozzo M. Sirchia SM, et al. Among authors: rovina d. Epigenomics. 2016 Mar;8(3):341-58. doi: 10.2217/epi.15.111. Epub 2016 Mar 7. Epigenomics. 2016. PMID: 26949823 Free article.
Generation of the Rubinstein-Taybi syndrome type 2 patient-derived induced pluripotent stem cell line (IAIi001-A) carrying the EP300 exon 23 stop mutation c.3829A > T, p.(Lys1277*).
Alari V, Russo S, Rovina D, Gowran A, Garzo M, Crippa M, Mazzanti L, Scalera C, Prosperi E, Giardino D, Gervasini C, Finelli P, Pompilio G, Larizza L. Alari V, et al. Among authors: rovina d. Stem Cell Res. 2018 Jul;30:175-179. doi: 10.1016/j.scr.2018.06.009. Epub 2018 Jun 18. Stem Cell Res. 2018. PMID: 29944992 Free article.
Generation of three iPSC lines (IAIi002, IAIi004, IAIi003) from Rubinstein-Taybi syndrome 1 patients carrying CREBBP non sense c.4435G>T, p.(Gly1479*) and c.3474G>A, p.(Trp1158*) and missense c.4627G>T, p.(Asp1543Tyr) mutations.
Alari V, Russo S, Rovina D, Garzo M, Crippa M, Calzari L, Scalera C, Concolino D, Castiglioni E, Giardino D, Prosperi E, Finelli P, Gervasini C, Gowran A, Larizza L. Alari V, et al. Among authors: rovina d. Stem Cell Res. 2019 Oct;40:101553. doi: 10.1016/j.scr.2019.101553. Epub 2019 Aug 28. Stem Cell Res. 2019. PMID: 31491690 Free article.
31 results