RIPOLONE, MICHELA

RIPOLONE, MICHELA  

DIPARTIMENTO DI BIOLOGIA (attivo dal 01/07/1979 al 26/04/2012)  

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Risultati 1 - 20 di 29 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls 2023 Magri, FrancescaRipolone, MichelaCorti, StefaniaComi, Giacomo Pietro + Article (author) -
Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant 2023 Magri, FrancescaRipolone, MichelaSalani, SabrinaFortunato, FrancescoCorti, StefaniaComi, Giacomo PietroRonchi, Dario + Article (author) -
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in Phospholamban Gene 2023 Ripolone, MichelaSalani, SabrinaCorti, StefaniaComi, Giacomo + Article (author) -
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization 2023 Ripolone, MichelaRonchi, DarioComi, Giacomo Pietro + Article (author) -
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy 2022 Ripolone M.Magri F.Fortunato F.Comi G. P. + Article (author) -
Expanding the phenotypic spectrum of non-alcoholic fatty liver disease and hypertriglyceridemia 2022 Marica MeroniMiriam LongoErika PaoliniMichela RipoloneLaura NapoliAnna Ludovica FracanzaniPaola Dongiovanni + Article (author) -
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy 2021 Mauri E.Pagliarani S.Magri F.Manini A.Ripolone M.Borellini L.Cinnante C.Corti S.Bresolin N.Comi G. P. + Article (author) -
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies 2021 Mauri, EleonoraGovoni, AlessandraBrusa, RobertaPagliarani, SerenaRipolone, MichelaCinnante, ClaudiaBresolin, NereoCorti, StefaniaComi, Giacomo PMagri, Francesca + Article (author) -
Drp1 overexpression induces desmin disassembling and drives kinesin-1 activation promoting mitochondrial trafficking in skeletal muscle 2020 Giovarelli M.Zecchini S.Ripolone M.Coazzoli M.Roux-Biejat P.Moscheni C.Perrotta C.Clementi E.De Palma C. + Article (author) -
Elucidating the role of Agl in bladder carcinogenesis by generation and characterization of genetically engineered mice 2019 Pagliarani, SerenaLucchiari, SabrinaRipolone, MichelaComi, Giacomo P + Article (author) -
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1 2018 M. RipoloneV. LucchiniD. RonchiY. TorrenteS. CortiG. P. Comi + Article (author) -
Reversal of Defective Mitochondrial Biogenesis in Limb-Girdle Muscular Dystrophy 2D by Independent Modulation of Histone and PGC-1α Acetylation 2016 S. PambiancoM. GiovarelliC. PerrottaS. ZecchiniI. Di RenzoC. MoscheniM. RipoloneE. ClementiC. De Palma + Article (author) -
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy 2015 M. RipoloneD. RonchiV. LucchiniI. ColomboL. VillaA. BordoniF. FortunatoS. CortiG.P. Comi + Article (author) -
Autophagy as a new therapeutic target in Duchenne muscular dystrophy 2012 C. De PalmaS. CheliS. PambiancoM. RipoloneM. FrancoliniE. Clementi + Article (author) -
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions 2012 D. RonchiA. BordoniM. RipoloneM. RanieriF. MagriS. CortiN. BresolinG.P. Comi + Article (author) -
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects 2011 D. RonchiA. CosiA. BordoniV. LucchiniF. FortunatoE. FassoneD. TondutiM. RanieriM. RipoloneS. CortiP. VeggiottiG.P. Comi + Conference Object -
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders 2011 M. RanieriD. RonchiA. BordoniV. LucchiniF. FortunatoE. FassoneD. TondutiM. RipoloneS. CortiP. VeggiottiG.P. Comi + Article (author) -
Low anaerobic threshold and increased skeletal muscle lactate production in subjects with Huntington's Disease 2011 N.E. MencacciM. RipoloneBIZZI, CATERINACOLCIAGO, CLARISSAV. SilaniG.G. Malfatto + Article (author) -
Oxidative defect in a large cohort of genetically-determined SMA cases 2011 V. LucchiniA. BordoniC. LampertiM. RipoloneS. CortiN. BresolinG. Comi + Article (author) -
USP8, a regulator of endosomal sorting, is involved in mouse acrosome biogenesis through interaction with the spermatid ESCRT-0 complex and microtubules 2010 G. BerrutiM. Ripolone + Article (author) -