SIGNAROLDI, ELENA
SIGNAROLDI, ELENA
Dipartimento di Oncologia ed Emato-Oncologia
MGUS and clonal hematopoiesis show unrelated clinical and biological trajectories in an older population cohort
2022 M.C. Da Vià, M. Lionetti, A. Marella, A. Matera, E. Travaglino, E. Signaroldi, A.A. Galbussera, U. Lucca, S. Mandelli, E. Riva, M. Tettamanti, L. Pettine, A. Pompa, L. Baldini, A. Neri, M.G. Della Porta, N. Bolli
Polycomb dysregulation in gliomagenesis targets a Zfp423-dependent differentiation network
2016 E. Signaroldi, P. Laise, S. Cristofanon, A. Brancaccio, E. Reisoli, S. Atashpaz, M.R. Terreni, C. Doglioni, G. Pruneri, P. Malatesta, G. Testa
FUNCTIONAL DISSECTION OF HISTONE H3 LYSINE 27 METHYLATION IN GLIOMAGENESIS
2013 E. Signaroldi
Cell reprogramming requires silencing of a core subset of polycomb targets
2013 G. Fragola, P. Germain, P. Laise, A. Cuomo, A. Blasimme, F. Gross, E. Signaroldi, G. Bucci, C. Sommer, G. Pruneri, G. Mazzarol, T. Bonaldi, G. Mostoslavsky, S. Casola, G. Testa
New molecular findings in congenital myopathies due to selenoprotein N gene mutations
2011 R. Cagliani, M.E. Fruguglietti, A. Berardinelli, M.G. D'Angelo, A. Prelle, S. Riva, L. Napoli, K. Gorni, S. Orcesi, C. Lamperti, A. Pichiecchio, E. Signaroldi, R. Tupler, F. Magri, A. Govoni, S. Corti, N. Bresolin, M. Moggio, G.P. Comi
Comment on 'Huntington's disease presenting as ALS'
2010 J. Mandrioli, C. Bernabei, E. Georgoulopoulou, P. Nichelli, P. Cortelli, R. Tupler, E. Signaroldi, P. Sola
New Molecular and Ultrastructural Findings in Congenital Myopathies Due to Selenoprotein N1 Gene Mutations
2008 R. Cagliani, A. Berardinelli, M.G. D'Angelo, A. Prelle, E. Fruguglietti, K. Gorni, S. Orcesi, C. Lamperti, E. Signaroldi, R. Tupler, N. Bresolin, M. Moggio, G.P. Comi
Peculiar ultrastructural findings in congenital myopathies due to selenoprotein N1 gene new mutations
2008 M.E. Fruguglietti, R. Cagliani, L. Napoli, A. Berardinelli, M.G. D'Angelo, K. Gorni, S. Orcesi, C. Lamperti, E. Signaroldi, R. Tupler, N. Bresolin, M. Moggio, G.P. Comi, A. Prelle
Genetic and ultrastructural findings in Selenoprotein N1-related congenital myopathies
2008 R. Cagliani, E. Fruguglietti, A. Berardinelli, M.G. D’Angelo, A. Prelle, K. Gorni, S. Orcesi, C. Lamperti, E. Signaroldi, R. Tupler, M. Moggio, G.P. Comi