| The extra-virgin olive oil polyphenols oleocanthal and oleacein counteract inflammation-related gene and miRNA expression in adipocytes by attenuating NF-κB activation S Carpi, E Scoditti, M Massaro, B Polini, C Manera, M Digiacomo, ... Nutrients 11 (12), 2855, 2019 | 75 | 2019 |
| Cerium oxide nanoparticles: the regenerative redox machine in bioenergetic imbalance I Pezzini, A Marino, S Del Turco, C Nesti, S Doccini, V Cappello, M Gemmi, ... Nanomedicine 12 (4), 403-416, 2017 | 63 | 2017 |
| Powerhouse failure and oxidative damage in autosomal recessive spastic ataxia of Charlevoix-Saguenay C Criscuolo, C Procaccini, MC Meschini, A Cianflone, R Carbone, ... Journal of neurology 262 (12), 2755-2763, 2015 | 48 | 2015 |
| Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs disease R Di Fabio, F Moro, L Pestillo, MC Meschini, F Pezzini, S Doccini, ... Neurology 83 (19), 1769-1770, 2014 | 32 | 2014 |
| Functional transcriptome analysis in ARSACS KO cell model reveals a role of sacsin in autophagy F Morani, S Doccini, R Sirica, M Paterno, F Pezzini, I Ricca, A Simonati, ... Scientific reports 9 (1), 11878, 2019 | 29 | 2019 |
| Proteomic and functional analyses in disease models reveal CLN5 protein involvement in mitochondrial dysfunction S Doccini, F Morani, C Nesti, F Pezzini, G Calza, R Soliymani, G Signore, ... Cell death discovery 6 (1), 18, 2020 | 28 | 2020 |
| Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD S Doccini, S Sartori, S Maeser, F Pezzini, S Rossato, F Moro, I Toldo, ... Journal of neurology 263, 1029-1032, 2016 | 27 | 2016 |
| Integrative analysis of differentially expressed genes and miRNAs predicts complex T3-mediated protective circuits in a rat model of cardiac ischemia reperfusion F Forini, G Nicolini, C Kusmic, R D’Aurizio, M Rizzo, M Baumgart, M Groth, ... Scientific Reports 8 (1), 13870, 2018 | 25 | 2018 |
| Mitochondrial dysfunction in hereditary spastic paraparesis with mutations in DDHD1/SPG28 A Mignarri, A Rubegni, A Tessa, S Stefanucci, A Malandrini, E Cardaioli, ... Journal of the Neurological Sciences 362, 287-291, 2016 | 24 | 2016 |
| Tumor suppressor role of hsa-miR-193a-3p and-5p in cutaneous melanoma B Polini, S Carpi, S Doccini, V Citi, A Martelli, S Feola, FM Santorelli, ... International Journal of Molecular Sciences 21 (17), 6183, 2020 | 19 | 2020 |
| Dolichol-phosphate mannose synthase depletion in zebrafish leads to dystrophic muscle with hypoglycosylated α-dystroglycan M Marchese, A Pappalardo, J Baldacci, T Verri, S Doccini, D Cassandrini, ... Biochemical and biophysical research communications 477 (1), 137-143, 2016 | 18 | 2016 |
| SPG2 mimicking multiple sclerosis in a family identified using next generation sequencing A Rubegni, C Battisti, A Tessa, A Cerase, S Doccini, A Malandrini, ... Journal of the Neurological Sciences 375, 198-202, 2017 | 17 | 2017 |
| Bi‐allelic mutations in HARS1 severely impair histidyl‐tRNA synthetase expression and enzymatic activity causing a novel multisystem ataxic syndrome D Galatolo, ME Kuo, P Mullen, R Meyer‐Schuman, S Doccini, R Battini, ... Human mutation 41 (7), 1232-1237, 2020 | 16 | 2020 |
| Progressive myoclonus epilepsy and ceroidolipofuscinosis 14: The multifaceted phenotypic spectrum of KCTD7-related disorders M Mastrangelo, S Sartori, A Simonati, M Brinciotti, F Moro, M Nosadini, ... European Journal of Medical Genetics 62 (12), 103591, 2019 | 16 | 2019 |
| The networks of genes encoding palmitoylated proteins in axonal and synaptic compartments are affected in PPT1 overexpressing neuronal-like cells F Pezzini, M Bianchi, S Benfatto, F Griggio, S Doccini, R Carrozzo, ... Frontiers in molecular neuroscience 10, 266, 2017 | 16 | 2017 |
| Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy C Nesti, MC Meschini, B Meunier, M Sacchini, S Doccini, A Romano, ... Human Molecular Genetics 24 (11), 3248-3256, 2015 | 16 | 2015 |
| Development of nanostructured lipid carriers for the delivery of idebenone in autosomal recessive spastic ataxia of charlevoix-saguenay C Martinelli, M Battaglini, C Pucci, S Gioi, C Caracci, G Macaluso, ... ACS omega 5 (21), 12451-12466, 2020 | 15 | 2020 |
| Expanding the clinical and genetic heterogeneity of SPAX5 C Dosi, D Galatolo, A Rubegni, S Doccini, R Pasquariello, C Nesti, ... Annals of Clinical and Translational Neurology 7 (4), 595-601, 2020 | 15 | 2020 |
| Protein delivery by peptide-based stealth liposomes: A biomolecular insight into enzyme replacement therapy M Santi, F Finamore, A Cecchettini, FM Santorelli, S Doccini, ... Molecular Pharmaceutics 17 (12), 4510-4521, 2020 | 14 | 2020 |
| In vitro study of polydopamine nanoparticles as protective antioxidant agents in fibroblasts derived from ARSACS patients M Battaglini, A Carmignani, C Martinelli, J Colica, A Marino, S Doccini, ... Biomaterials Science 10 (14), 3770-3792, 2022 | 12 | 2022 |
