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Titolo Data di pubblicazione Autori Tipo File Abstract
Genetic and ultrastructural findings in Selenoprotein N1-related congenital myopathies 2008 R. CaglianiC. LampertiE. SignaroldiG.P. Comi + Article (author) -
New Molecular and Ultrastructural Findings in Congenital Myopathies Due to Selenoprotein N1 Gene Mutations 2008 R. CaglianiSIGNAROLDI, ELENAN. BresolinG. P. Comi + Article (author) -
Peculiar ultrastructural findings in congenital myopathies due to selenoprotein N1 gene new mutations 2008 R. CaglianiC. LampertiE. SignaroldiN. BresolinG.P. Comi + Article (author) -
Comment on 'Huntington's disease presenting as ALS' 2010 E. Signaroldi + Article (author) -
New molecular findings in congenital myopathies due to selenoprotein N gene mutations 2011 E. SignaroldiS. CortiN. BresolinG.P. Comi + Article (author) -
Cell reprogramming requires silencing of a core subset of polycomb targets 2013 G. FragolaP. GermainA. BlasimmeF. GrossE. SignaroldiG. BucciG. PruneriT. BonaldiG. Testa + Article (author) -
FUNCTIONAL DISSECTION OF HISTONE H3 LYSINE 27 METHYLATION IN GLIOMAGENESIS 2013 E. Signaroldi Doctoral Thesis -
Polycomb dysregulation in gliomagenesis targets a Zfp423-dependent differentiation network 2016 E. SignaroldiG. PruneriG. Testa + Article (author) -
MGUS and clonal hematopoiesis show unrelated clinical and biological trajectories in an older population cohort 2022 Lionetti, MartaMarella, AlessioMatera, AntonioSignaroldi, ElenaPettine, LoredanaBaldini, LucaNeri, AntoninoBolli, Niccolo + Article (author) -
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