Arnoldi, Michele

Arnoldi, Michele  

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Titolo Anno di pubblicazione Autori Unitn File
CHD mutations in autism spectrum disorders and epilepsy: alterations of epigenetic landscape and new approaches for therapeutic development. 28-apr-2022 Arnoldi, Michele
CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing 1-gen-2022 Kerschbamer, EmanuelaArnoldi, MicheleTripathi, TakshashilaPellegrini, MiguelDi Leva, FrancescaDassi, ErikBenelli, MatteoPiazza, SilvanoDemichelis, FrancescaBiagioli, Marta +
Design and Delivery of SINEUP: A New Modular Tool to Increase Protein Translation 1-gen-2022 Michele ArnoldiFrancesca Di LevaMarta Biagioli +
Natural SINEUP RNAs in Autism Spectrum Disorders: RAB11B-AS1 Dysregulation in a Neuronal CHD8 Suppression Model Leads to RAB11B Protein Increase 1-gen-2021 Arnoldi M.Filosi M.Tebaldi T.Domenici E.Di Leva F.Biagioli M. +
SINEUP RNA rescues molecular phenotypes associated with CHD8 suppression in autism spectrum disorder model systems 1-gen-2024 Di Leva, FrancescaArnoldi, MicheleSantarelli, StefaniaPellegrini, MiguelCastellini, Maria ElenaMessina, AndreaBozzi, YuriCasarosa, SimonaDassi, ErikMorandell, JasminBiagioli, Marta +