FSHD: copy number variations on the theme of muscular dystrophy

بواسطة Cabianca, Daphne Selvaggia, Gabellini, Davide
منشور في 2010

Spatial segregation of heterochromatin: Uncovering functionality in a multicellular organism

بواسطة Cabianca, Daphne S., Gasser, Susan M.
الحاوية / القاعدة Nucleus (2016)

A novel molecular mechanism in human genetic disease: A DNA repeat-derived lncRNA

بواسطة Cabianca, Daphne S., Casa, Valentina, Gabellini, Davide
منشور في 2012

Chromatin states and nuclear organization in development — a view from the nuclear lamina

بواسطة Mattout, Anna, Cabianca, Daphne S., Gasser, Susan M.
الحاوية / القاعدة Genome Biol (2015)

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

بواسطة Cabianca, Daphne S., Casa, Valentina, Bodega, Beatrice, Xynos, Alexandros, Ginelli, Enrico, Tanaka, Yujiro, Gabellini, Davide
منشور في 2012

HnRNP A1 controls a splicing regulatory circuit promoting mesenchymal-to-epithelial transition

بواسطة Bonomi, Serena, di Matteo, Anna, Buratti, Emanuele, Cabianca, Daphne S., Baralle, Francisco E., Ghigna, Claudia, Biamonti, Giuseppe
منشور في 2013