RIPOLONE, MICHELA

RIPOLONE, MICHELA  

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

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Risultati 1 - 20 di 25 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Autophagy as a new therapeutic target in Duchenne muscular dystrophy 1-gen-2012 C. De PalmaS. CheliS. PambiancoM. RipoloneM. FrancoliniE. Clementi + Article (author) -
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy 1-gen-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 1-gen-2009 E. AivatiadouM. RipoloneBRUNETTI, FRANCESCO CARMELOG. Berruti Article (author) -
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders 1-mag-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 1-gen-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 1-ago-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 28-giu-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 1-gen-2019 Pagliarani, SerenaLucchiari, SabrinaRipolone, MichelaComi, Giacomo P + Article (author) -
Expanding the phenotypic spectrum of non-alcoholic fatty liver disease and hypertriglyceridemia 1-set-2022 Marica MeroniMiriam LongoErika PaoliniMichela RipoloneLaura NapoliAnna Ludovica FracanzaniPaola Dongiovanni + Article (author) -
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy 1-gen-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 1-gen-2011 N.E. MencacciM. RipoloneBIZZI, CATERINACOLCIAGO, CLARISSAV. SilaniG.G. Malfatto + Article (author) -
mUBPy and the Hrs-STAM complex in developing male germ cells 1-gen-2006 M. RipoloneG. Berruti + Conference Object -
mUBPy in spermatogenic cells of Wobbler Mice 1-gen-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 1-gen-2009 M. Ripolone Doctoral Thesis -
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy 8-apr-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 1-lug-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 1-apr-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 1-nov-2012 D. RonchiA. BordoniM. RipoloneM. RanieriF. MagriS. CortiN. BresolinG.P. Comi + Article (author) -
Novel missense GARS gene mutation in an Italian family with hereditary distal motor neuropathy 1-gen-2005 R. Del BoF. LocatelliS. CortiM. RipoloneM. CarpoN. BresolinG.P. Comi + Article (author) -
Oxidative defect in a large cohort of genetically-determined SMA cases 1-gen-2011 V. LucchiniA. BordoniC. LampertiM. RipoloneS. CortiN. BresolinG. Comi + Article (author) -