A repetitive elements perspective in Polycomb epigenetics

por Casa, Valentina, Gabellini, Davide
Publicado 2012

Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophy

por Casa, Valentina, Runfola, Valeria, Micheloni, Stefano, Aziz, Arif, Dilworth, F. Jeffrey, Gabellini, Davide
Publicado 2017

A Long ncRNA Links Copy Number Variation to a Polycomb/Trithorax Epigenetic Switch in FSHD Muscular Dystrophy

por Cabianca, Daphne S., Casa, Valentina, Bodega, Beatrice, Xynos, Alexandros, Ginelli, Enrico, Tanaka, Yujiro, Gabellini, Davide
Publicado 2012

Recognition of 5-Hydroxymethylcytosine by the Uhrf1 SRA Domain

por Frauer, Carina, Hoffmann, Thomas, Bultmann, Sebastian, Casa, Valentina, Cardoso, M. Cristina, Antes, Iris, Leonhardt, Heinrich
Publicado 2011

Direct Homo- and Hetero-Interactions of MeCP2 and MBD2

por Becker, Annette, Allmann, Lena, Hofstätter, Maria, Casà, Valentina, Weber, Patrick, Lehmkuhl, Anne, Herce, Henry D., Cardoso, M. Cristina
Publicado 2013

Redundant and specific roles of cohesin STAG subunits in chromatin looping and transcriptional control

por Casa, Valentina, Moronta Gines, Macarena, Gade Gusmao, Eduardo, Slotman, Johan A., Zirkel, Anne, Josipovic, Natasa, Oole, Edwin, van IJcken, Wilfred F.J., Houtsmuller, Adriaan B., Papantonis, Argyris, Wendt, Kerstin S.
Publicado 2020

Regulation of the cohesin-loading factor NIPBL: Role of the lncRNA NIPBL-AS1 and identification of a distal enhancer element

por Zuin, Jessica, Casa, Valentina, Pozojevic, Jelena, Kolovos, Petros, van den Hout, Mirjam C. G. N., van Ijcken, Wilfred F. J., Parenti, Ilaria, Braunholz, Diana, Baron, Yorann, Watrin, Erwan, Kaiser, Frank J., Wendt, Kerstin S.
Publicado 2017