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
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) -
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) -
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) -
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) -
Expanding the phenotypic spectrum of non-alcoholic fatty liver disease and hypertriglyceridemia 2022 Marica MeroniMiriam LongoErika PaoliniMichela RipoloneLaura NapoliAnna Ludovica FracanzaniPaola Dongiovanni + 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) -
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) -