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: 0.001 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Autophagy as a new therapeutic target in Duchenne muscular dystrophy 2012 C. De PalmaS. CheliS. PambiancoM. RipoloneM. FrancoliniE. Clementi + 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) -
cAMP-Epac2-mediated activation of Rap1 in developing male germ cells : RA-RhoGAP as a possible direct down-stream effector 2009 E. AivatiadouM. RipoloneBRUNETTI, FRANCESCO CARMELOG. Berruti 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) -
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) -
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 -
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) -
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) -
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) -
Expanding the phenotypic spectrum of non-alcoholic fatty liver disease and hypertriglyceridemia 2022 Marica MeroniMiriam LongoErika PaoliniMichela RipoloneLaura NapoliAnna Ludovica FracanzaniPaola Dongiovanni + 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) -
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) -
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) -
mUBPy and the Hrs-STAM complex in developing male germ cells 2006 M. RipoloneG. Berruti + Conference Object -
mUBPy in spermatogenic cells of Wobbler Mice 2007 M. RipoloneG. Berruti Conference Object -
mUBPY, endocytic vesicle traffic and microtubule mediated transport in acrosome biogenesis. Comparative study between wild-type and Wobbler (L967Q Vps54) mice 2009 M. Ripolone Doctoral Thesis -
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) -
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of Andersen Disease associated with a new mutation in GBE1 gene 2006 Costanza LampertiSabrina SalaniElisa FrugugliettiAndreina BordoniMichela RipoloneVeronica CrugnolaNereo BresolinGiacomo Pietro Comi + Article (author) -
Neuropathological study of skeletal muscle, heart, liver, and brainin a neonatal form of glycogen storage disease type IV associated with a newmutation in GBE1 gene 2009 7. C. LampertiS. SalaniS. LucchiariA. BordoniM. RipoloneME FrugugliettiV. CrugnolaN. BresolinG.P. Comi + 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) -