Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells

por Tabolacci, Elisabetta, Mancano, Giorgia, Lanni, Stella, Palumbo, Federica, Goracci, Martina, Ferrè, Fabrizio, Helmer-Citterich, Manuela, Neri, Giovanni
Publicado 2016

Role of CTCF Protein in Regulating FMR1 Locus Transcription

por Lanni, Stella, Goracci, Martina, Borrelli, Loredana, Mancano, Giorgia, Chiurazzi, Pietro, Moscato, Umberto, Ferrè, Fabrizio, Helmer-Citterich, Manuela, Tabolacci, Elisabetta, Neri, Giovanni
Publicado 2013

FAN1, a DNA Repair Nuclease, as a Modifier of Repeat Expansion Disorders

por Deshmukh, Amit L., Porro, Antonio, Mohiuddin, Mohiuddin, Lanni, Stella, Panigrahi, Gagan B., Caron, Marie-Christine, Masson, Jean-Yves, Sartori, Alessandro A., Pearson, Christopher E.
Publicado 2021

CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy

por Barbé, Lise, Lanni, Stella, López-Castel, Arturo, Franck, Silvie, Spits, Claudia, Keymolen, Kathelijn, Seneca, Sara, Tomé, Stephanie, Miron, Ioana, Letourneau, Julie, Liang, Minggao, Choufani, Sanaa, Weksberg, Rosanna, Wilson, Michael D., Sedlacek, Zdenek, Gagnon, Cynthia, Musova, Zuzana, Chitayat, David, Shannon, Patrick, Mathieu, Jean, Sermon, Karen, Pearson, Christopher E.
Publicado 2017

Slipped-CAG DNA binding small molecule induces trinucleotide repeat contractions in vivo

por Nakamori, Masayuki, Panigrahi, Gagan B., Lanni, Stella, Gall-Duncan, Terence, Hayakawa, Hideki, Tanaka, Hana, Luo, Jennifer, Otabe, Takahiro, Li, Jinxing, Sakata, Akihiro, Caron, Marie-Christine, Joshi, Niraj, Prasolava, Tanya, Chiang, Karen, Masson, Jean-Yves, Wold, Marc S., Wang, Xiaoxiao, Lee, Marietta Y. W. T., Huddleston, John, Munson, Katherine M., Davidson, Scott, Layeghifard, Mehdi, Edward, Lisa-Monique, Gallon, Richard, Santibanez-Koref, Mauro, Murata, Asako, Takahashi, Masanori P., Eichler, Evan E., Shlien, Adam, Nakatani, Kazuhiko, Mochizuki, Hideki, Pearson, Christopher E.
Publicado 2020