Induced Pluripotent Stem Cells to Study Mechanisms of Laminopathies: Focus on Epigenetics

по Crasto, Silvia, Di Pasquale, Elisa
Опубликовано в: Front Cell Dev Biol (2018)

The Broad Spectrum of LMNA Cardiac Diseases: From Molecular Mechanisms to Clinical Phenotype

по Crasto, Silvia, My, Ilaria, Di Pasquale, Elisa
Опубликовано в: Front Physiol (2020)

Wnt signalling mediates miR-133a nuclear re-localization for the transcriptional control of Dnmt3b in cardiac cells

по Di Mauro, Vittoria, Crasto, Silvia, Colombo, Federico Simone, Di Pasquale, Elisa, Catalucci, Daniele
Опубликовано в: Sci Rep (2019)

Divergent Transcription of the Nkx2-5 Locus Generates Two Enhancer RNAs with Opposing Functions

по Salamon, Irene, Serio, Simone, Bianco, Simona, Pagiatakis, Christina, Crasto, Silvia, Chiariello, Andrea M., Conte, Mattia, Cattaneo, Paola, Fiorillo, Luca, Felicetta, Arianna, di Pasquale, Elisa, Kunderfranco, Paolo, Nicodemi, Mario, Papait, Roberto, Condorelli, Gianluigi
Опубликовано в: iScience (2020)

The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy

по Salvarani, Nicolò, Crasto, Silvia, Miragoli, Michele, Bertero, Alessandro, Paulis, Marianna, Kunderfranco, Paolo, Serio, Simone, Forni, Alberto, Lucarelli, Carla, Dal Ferro, Matteo, Larcher, Veronica, Sinagra, Gianfranco, Vezzoni, Paolo, Murry, Charles E., Faggian, Giuseppe, Condorelli, Gianluigi, Di Pasquale, Elisa
Опубликовано в: Nat Commun (2019)

Cofilin-1 phosphorylation catalyzed by ERK1/2 alters cardiac actin dynamics in dilated cardiomyopathy caused by lamin A/C gene mutation

по Chatzifrangkeskou, Maria, Yadin, David, Marais, Thibaut, Chardonnet, Solenne, Cohen-Tannoudji, Mathilde, Mougenot, Nathalie, Schmitt, Alain, Crasto, Silvia, Di Pasquale, Elisa, Macquart, Coline, Tanguy, Yannick, Jebeniani, Imen, Pucéat, Michel, Morales Rodriguez, Blanca, Goldmann, Wolfgang H, Dal Ferro, Matteo, Biferi, Maria-Grazia, Knaus, Petra, Bonne, Gisèle, Worman, Howard J, Muchir, Antoine
Опубликовано в: Hum Mol Genet (2018)