DNMT3B Functions: Novel Insights From Human Disease

著者: Gagliardi, Miriam, Strazzullo, Maria, Matarazzo, Maria R.
出版年 Front Cell Dev Biol (2018)

Chromosome territory reorganization in a human disease with altered DNA methylation

著者: Matarazzo, Maria R., Boyle, Shelagh, D'Esposito, Maurizio, Bickmore, Wendy A.
出版事項 2007

Non-coding RNAs in chromatin disease involving neurological defects

著者: Della Ragione, Floriana, Gagliardi, Miriam, D'Esposito, Maurizio, Matarazzo, Maria R.
出版事項 2014

Persistent epigenetic memory impedes rescue of the telomeric phenotype in human ICF iPSCs following DNMT3B correction

著者: Toubiana, Shir, Gagliardi, Miriam, Papa, Mariarosaria, Manco, Roberta, Tzukerman, Maty, Matarazzo, Maria R, Selig, Sara
出版年 eLife (2019)

DDX11L: a novel transcript family emerging from human subtelomeric regions

著者: Costa, Valerio, Casamassimi, Amelia, Roberto, Roberta, Gianfrancesco, Fernando, Matarazzo, Maria R, D'Urso, Michele, D'Esposito, Maurizio, Rocchi, Mariano, Ciccodicola, Alfredo
出版事項 2009

MeCP2 and Major Satellite Forward RNA Cooperate for Pericentric Heterochromatin Organization

著者: Fioriniello, Salvatore, Csukonyi, Eva, Marano, Domenico, Brancaccio, Arianna, Madonna, Michele, Zarrillo, Carmela, Romano, Alessia, Marracino, Federico, Matarazzo, Maria R., D'Esposito, Maurizio, Della Ragione, Floriana
出版年 Stem Cell Reports (2020)

Complex Events in the Evolution of the Human Pseudoautosomal Region 2 (PAR2)

著者: Charchar, Fadi J., Svartman, Marta, El-Mogharbel, Nisrine, Ventura, Mario, Kirby, Patrick, Matarazzo, Maria R., Ciccodicola, Alfredo, Rocchi, Mariano, D'Esposito, Maurizio, Graves, Jennifer A. Marshall
出版事項 2003

ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing

著者: Gatto, Sole, Gagliardi, Miriam, Franzese, Monica, Leppert, Sylwia, Papa, Mariarosaria, Cammisa, Marco, Grillo, Giacomo, Velasco, Guillame, Francastel, Claire, Toubiana, Shir, D’Esposito, Maurizio, Angelini, Claudia, Matarazzo, Maria R.
出版年 Nucleic Acids Res (2017)

L-Proline Induces a Mesenchymal-like Invasive Program in Embryonic Stem Cells by Remodeling H3K9 and H3K36 Methylation

著者: Comes, Stefania, Gagliardi, Miriam, Laprano, Nicola, Fico, Annalisa, Cimmino, Amelia, Palamidessi, Andrea, De Cesare, Dario, De Falco, Sandro, Angelini, Claudia, Scita, Giorgio, Patriarca, Eduardo J., Matarazzo, Maria R., Minchiotti, Gabriella
出版事項 2013

Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient

著者: Heyn, Holger, Vidal, Enrique, Sayols, Sergi, Sanchez-Mut, Jose V., Moran, Sebastian, Medina, Ignacio, Sandoval, Juan, Simó-Riudalbas, Laia, Szczesna, Karolina, Huertas, Dori, Gatto, Sole, Matarazzo, Maria R., Dopazo, Joaquin, Esteller, Manel
出版事項 2012