| Microtubule-associated protein/microtubule affinity-regulating kinase 4 (MARK4) plays a role in cell cycle progression and cytoskeletal dynamics D Rovina, L Fontana, L Monti, C Novielli, N Panini, SM Sirchia, E Erba, ... European journal of cell biology 93 (8-9), 355-365, 2014 | 44 | 2014 |
| Dystrophin Cardiomyopathies: Clinical Management, Molecular Pathogenesis and Evolution towards Precision Medicine D D’Amario, A Gowran, F Canonico, E Castiglioni, D Rovina, R Santoro, ... Journal of Clinical Medicine 7 (9), 291, 2018 | 36 | 2018 |
| Fibrosis Rescue Improves Cardiac Function in Dystrophin-Deficient Mice and Duchenne Patient–Specific Cardiomyocytes by Immunoproteasome Modulation A Farini, A Gowran, P Bella, C Sitzia, A Scopece, E Castiglioni, D Rovina, ... The American journal of pathology 189 (2), 339-353, 2019 | 35 | 2019 |
| Differential signature of the centrosomal MARK4 isoforms in glioma I Magnani, C Novielli, L Fontana, S Tabano, D Rovina, RF Moroni, ... Analytical Cellular Pathology 34 (6), 319-338, 2011 | 27 | 2011 |
| The Endocannabinoid System and Cannabidiol: Past, Present, and Prospective for Cardiovascular Diseases M Rabino, S Mallia, E Castiglioni, D Rovina, G Pompilio, A Gowran Pharmaceuticals 14 (9), 936, 2021 | 22 | 2021 |
| A HS6ST2 gene variant associated with X‐linked intellectual disability and severe myopia in two male twins L Paganini, LA Hadi, M Chetta, D Rovina, L Fontana, P Colapietro, ... Clinical genetics 95 (3), 368-374, 2019 | 21 | 2019 |
| Functional characterisation of a novel mutation affecting the catalytic domain of MMP2 in siblings with multicentric osteolysis, nodulosis and arthropathy J Azzollini, D Rovina, C Gervasini, I Parenti, A Fratoni, MV Cubellis, ... Journal of human genetics 59 (11), 631-637, 2014 | 21 | 2014 |
| Profound alterations of the chromatin architecture at chromosome 11p15. 5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients D Rovina, M La Vecchia, A Cortesi, L Fontana, M Pesant, S Maitz, ... Scientific Reports 10 (1), 1-19, 2020 | 16 | 2020 |
| Suggestive evidence on the involvement of polypyrimidine-tract binding protein in regulating alternative splicing of MAP/microtubule affinity-regulating kinase 4 in glioma L Fontana, D Rovina, C Novielli, E Maffioli, G Tedeschi, I Magnani, ... Cancer letters 359 (1), 87-96, 2015 | 16 | 2015 |
| Overall and allele-specific expression of the SMC1A gene in female Cornelia de Lange syndrome patients and healthy controls I Parenti, D Rovina, M Masciadri, A Cereda, J Azzollini, C Picinelli, ... epigenetics 9 (7), 973-979, 2014 | 16 | 2014 |
| Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: the impact of full-length dystrophin deficiency JM Pioner, L Santini, C Palandri, M Langione, B Grandinetti, S Querceto, ... Frontiers in Physiology, 2297, 0 | 12 | |
| Derivation of the Duchenne muscular dystrophy patient-derived induced pluripotent stem cell line lacking DMD exons 49 and 50 (CCMi001DMD-A-3,∆ 49,∆ 50) G Spaltro, V Vigorelli, F Casalnuovo, P Spinelli, E Castiglioni, D Rovina, ... Stem cell research 25, 128-131, 2017 | 10 | 2017 |
| Generation of three iPSC lines (IAIi002, IAIi004, IAIi003) from Rubinstein-Taybi syndrome 1 patients carrying CREBBP non sense c. 4435G> T, p.(Gly1479*) and c. 3474G> A, p … V Alari, S Russo, D Rovina, M Garzo, M Crippa, L Calzari, C Scalera, ... Stem Cell Research, 101553, 2019 | 8 | 2019 |
| 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) A Gowran, G Spaltro, F Casalnuovo, V Vigorelli, P Spinelli, E Castiglioni, ... Stem cell research 28, 21-24, 2018 | 8 | 2018 |
| Epigenetic effects of chromatin remodeling agents on organotypic cultures SM Sirchia, A Faversani, D Rovina, MV Russo, L Paganini, F Savi, ... Epigenomics 8 (3), 341-358, 2016 | 8 | 2016 |
| Spectrum of Rare and Common Genetic Variants in Arrhythmogenic Cardiomyopathy Patients M Lippi, M Chiesa, C Ascione, M Pedrazzini, S Mushtaq, D Rovina, ... Biomolecules 12 (8), 1043, 2022 | 7 | 2022 |
| Generation of the Rubinstein-Taybi syndrome type 2 patient-derived induced pluripotent stem cell line (IAIi001-A) carrying the EP300 exon 23 stop mutation c … V Alari, S Russo, D Rovina, A Gowran, M Garzo, M Crippa, L Mazzanti, ... Stem Cell Research, 2018 | 7 | 2018 |
| 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) D Rovina, E Castiglioni, A Farini, M Bellichi, C Gervasini, S Paganini, ... Stem cell research 40, 101544, 2019 | 6 | 2019 |
| Cohesin Mutations Induce Chromatin Conformation Perturbation of the H19/IGF2 Imprinted Region and Gene Expression Dysregulation in Cornelia de Lange Syndrome Cell Lines S Pileggi, M La Vecchia, EA Colombo, L Fontana, P Colapietro, D Rovina, ... Biomolecules 11 (11), 1622, 2021 | 5 | 2021 |
| “Betwixt Mine Eye and Heart a League Is Took”: The Progress of Induced Pluripotent Stem-Cell-Based Models of Dystrophin-Associated Cardiomyopathy D Rovina, E Castiglioni, F Niro, S Mallia, G Pompilio, A Gowran International Journal of Molecular Sciences 21 (19), 6997, 2020 | 5 | 2020 |
