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Titolo Data di pubblicazione Autori Tipo File Abstract
Differential signature of the centrosomal MARK4 isoforms in glioma 2011 I. MagnaniC. NovielliL. FontanaS. TabanoD. RovinaD. BauerE.A. ColomboG. TedeschiL. MontiS. BosariL. BelloL. Larizza + Article (author) -
Microtubule-associated protein/microtubule affinity-regulating kinase 4 (MARK4) plays a role in cell cycle progression and cytoskeletal dynamics 2014 D. RovinaL. FontanaC. NovielliS.M. SirchiaI. MagnaniL. Larizza + Article (author) -
NEW INSIGHTS INTO THE ROLE OF THE CENTROSOMAL MARK4 KINASE IN REGULATING THE DYNAMICS AND REMODELLING OF CYTOSKELETON FROM OVEREXPRESSION STUDIES OF ITS TWO ISOFORMS IN NORMAL AND TUMOR CELLS 2014 D. Rovina Doctoral Thesis -
Overall and allele-specific expression of the SMC1A gene in female Cornelia de Lange syndrome patients and healthy controls 2014 I. ParentiD. RovinaM. MasciadriA. CeredaJ. AzzolliniP. FinelliC. GervasiniL. Larizza + Article (author) -
Functional characterisation of a novel mutation affecting the catalytic domain of MMP2 in siblings with multicentric osteolysis, nodulosis and arthropathy 2014 J. AzzolliniD. RovinaC. GervasiniI. ParentiA. FratoniA. CerriL. PietrograndeL. Larizza + Article (author) -
Suggestive evidence on the involvement of polypyrimidine-tract binding protein in regulating alternative splicing of MAP/microtubule affinity-regulating kinase 4 in glioma 2015 L. FontanaD. RovinaC. NovielliE. MaffioliG. TedeschiI. MagnaniL. Larizza Article (author) -
Epigenetic effects of chromatin remodeling agents on organotypic cultures 2016 S.M. SirchiaA. FaversaniD. RovinaM.V. RussoL. PaganiniF. SaviC. AugelloL. RossoA. Del GobboS. TabanoS. BosariM. Miozzo Article (author) -
Derivation of the Duchennemuscular dystrophy patient-derived induced pluripotent stem cell line lacking DMD exons 49 and 50 (CCMi001DMD-A-3, Δ49, Δ50) 2017 G. SpaltroE. CastiglioniD. RovinaC. GervasiniG. Pompilio + Article (author) -
Generation of induced pluripotent stem cells from a Becker muscular dystrophy patient carrying a deletion of exons 45-55 of the dystrophin gene (CCMi002BMD-A-9 ∆45-55) 2018 G. SpaltroSPINELLI, GIAN PAOLOD. RovinaPAGANINI, SILVIAC. GervasiniG. Pompilio + Article (author) -
Dystrophin Cardiomyopathies: Clinical Management, Molecular Pathogenesis and Evolution towards Precision Medicine 2018 Castiglioni, ElisaRovina, DavidePerrucci, Gianluca LorenzoPompilio, Giulio + Article (author) -
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins 2018 Paganini, LedaCHETTA, MASSIMILIANORovina, DavideFontana, LauraColapietro, PatriziaBonaparte, EleonoraPezzani, LidiaMarchisio, PaolaTabano, Silvia MSirchia, Silvia MRiboni, LauraMilani, DonatellaMiozzo, Monica + Article (author) -
Establishment of a Duchenne muscular dystrophy patient-derived induced pluripotent stem cell line carrying a deletion of exons 51–53 of the dystrophin gene (CCMi003-A) 2019 D. RovinaM. BelicchiC. GervasiniY. TorrenteG. Pompilio + Article (author) -
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients 2020 Rovina D.Fontana L.Tabano S.Bodega B.Miozzo M.Sirchia S. M. + Article (author) -
Multiomic approaches to uncover the complexities of dystrophin-associated cardiomyopathy 2021 Rovina D.Piacentini L.Pompilio G. + Article (author) -
The endocannabinoid system and cannabidiol: Past, present, and prospective for cardiovascular diseases 2021 Rovina D.Pompilio G. + Article (author) -
Spectrum of Rare and Common Genetic Variants in Arrhythmogenic Cardiomyopathy Patients 2022 Ascione C.Pedrazzini M.Rovina D.Riggio D.Pompilio G. + Article (author) -
Mostrati risultati da 1 a 16 di 16
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