ROVINA, DAVIDE

ROVINA, DAVIDE  

Dipartimento di Scienze della Salute  

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Risultati 1 - 15 di 15 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Derivation of the Duchennemuscular dystrophy patient-derived induced pluripotent stem cell line lacking DMD exons 49 and 50 (CCMi001DMD-A-3, Δ49, Δ50) 1-dic-2017 G. SpaltroE. CastiglioniD. RovinaC. GervasiniG. Pompilio + Article (author) -
Differential signature of the centrosomal MARK4 isoforms in glioma 1-gen-2011 I. MagnaniC. NovielliL. FontanaS. TabanoD. RovinaD. BauerE.A. ColomboG. TedeschiL. MontiS. BosariL. BelloL. Larizza + Article (author) -
Dystrophin Cardiomyopathies: Clinical Management, Molecular Pathogenesis and Evolution towards Precision Medicine 19-set-2018 Castiglioni, ElisaRovina, DavidePerrucci, Gianluca LorenzoPompilio, Giulio + Article (author) -
The endocannabinoid system and cannabidiol: Past, present, and prospective for cardiovascular diseases 17-set-2021 Rovina D.Pompilio G. + Article (author) -
Epigenetic effects of chromatin remodeling agents on organotypic cultures 1-mar-2016 S.M. SirchiaA. FaversaniD. RovinaM.V. RussoL. PaganiniF. SaviC. AugelloL. RossoA. Del GobboS. TabanoS. BosariM. Miozzo 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) 1-ott-2019 D. RovinaM. BelicchiC. GervasiniY. TorrenteG. Pompilio + Article (author) -
Functional characterisation of a novel mutation affecting the catalytic domain of MMP2 in siblings with multicentric osteolysis, nodulosis and arthropathy 1-nov-2014 J. AzzolliniD. RovinaC. GervasiniI. ParentiA. FratoniA. CerriL. PietrograndeL. Larizza + 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) 1-gen-2018 G. SpaltroSPINELLI, GIAN PAOLOD. RovinaPAGANINI, SILVIAC. GervasiniG. Pompilio + Article (author) -
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins 24-nov-2018 Paganini, LedaCHETTA, MASSIMILIANORovina, DavideFontana, LauraColapietro, PatriziaBonaparte, EleonoraPezzani, LidiaMarchisio, PaolaTabano, Silvia MSirchia, Silvia MRiboni, LauraMilani, DonatellaMiozzo, Monica + Article (author) -
Microtubule-associated protein/microtubule affinity-regulating kinase 4 (MARK4) plays a role in cell cycle progression and cytoskeletal dynamics 1-gen-2014 D. RovinaL. FontanaC. NovielliS.M. SirchiaI. MagnaniL. Larizza + Article (author) -
Multiomic approaches to uncover the complexities of dystrophin-associated cardiomyopathy 19-ago-2021 Rovina D.Piacentini L.Pompilio G. + 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 24-gen-2014 D. Rovina Doctoral Thesis -
Overall and allele-specific expression of the SMC1A gene in female Cornelia de Lange syndrome patients and healthy controls 1-lug-2014 I. ParentiD. RovinaM. MasciadriA. CeredaJ. AzzolliniP. FinelliC. GervasiniL. Larizza + Article (author) -
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients 19-mag-2020 Rovina D.Fontana L.Tabano S.Bodega B.Miozzo M.Sirchia S. M. + 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 1-gen-2015 L. FontanaD. RovinaC. NovielliE. MaffioliG. TedeschiI. MagnaniL. Larizza Article (author) -