MORO, ENRICO

MORO, ENRICO  

Dipartimento di Medicina Molecolare - DMM  

Mostra records
Risultati 1 - 20 di 124 (tempo di esecuzione: 0.043 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
GBA1 inactivation in oligodendrocytes affects myelination and induces neurodegenerative hallmarks and lipid dyshomeostasis in mice 2024 Gregorio, IlariaRusso, LorisContarini, GabriellaPacinelli, GiadaBizzotto, DarioBraghetta, PaolaMoro, EnricoCescon, Matilde + MOLECULAR NEURODEGENERATION - -
Hampered differentiation and disrupted endo-lysosomal function in a human neuronal in vitro model of mucopolysaccharidosis type II 2024 Lorenzo BadenettiRosa ManzoliEnrico Moro MOLECULAR GENETICS AND METABOLISM - Hampered differentiation and disrupted endo-lysosomal function in human neuronal in vitro model of Mucopolysaccharidosis type II
Mucopolysaccharidosis type II zebrafish model exhibits early impaired proteasomal-mediated degradation of the axon guidance receptor Dcc 2024 Manzoli, RosaBadenetti, LorenzoBruzzone, MatteoMacario, Maria CarlaRubin, MichelaDal Maschio, MarcoRoveri, AntonellaMoro, Enrico CELL DEATH & DISEASE - -
The Antioxidant Drug Edaravone Binds to the Aryl Hydrocarbon Receptor (AHR) and Promotes the Downstream Signaling Pathway Activation 2024 Manzoli, RosaMacario, Maria CarlaMoro, Enrico + BIOMOLECULES - -
A novel CRISPR/Cas9-based iduronate-2-sulfatase (IDS) knockout human neuronal cell line reveals earliest pathological changes 2023 Badenetti L.Manzoli R.Trevisan M.Tomanin R.Moro E. + SCIENTIFIC REPORTS - -
Genome-wide screening in pluripotent cells identifies Mtf1 as a suppressor of mutant huntingtin toxicity 2023 Gambetta, Anna MariaAmato, SoniaAngiolillo, SilviaDiamante, LindaCarbognin, ElenaRomani, PatriziaLa Torre, FedericoZennaro, LucioMartello, GrazianoMoro, Enrico + NATURE COMMUNICATIONS - -
Monitoring Nrf2/ARE Pathway Activity with a New Zebrafish Reporter System 2023 Badenetti L.Manzoli R.Rubin M.Cozza G.Moro E. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES - -
Early axon guidance and synapse maturation defects in a zebrafish model of Mucopolysaccharidosis type II 2022 Rosa ManzoliLorenzo BadenettiRosella TomaninEnrico Moro - - Early axon guidance and synapse maturation defects in a zebrafish model of Mucopolysaccharidosis type II
Lysosomal function and axon guidance: Is there a meaningful liaison? 2021 Manzoli R.Badenetti L.Rubin M.Moro E. BIOMOLECULES - -
Lysosomal storage disorders: Molecular basis and therapeutic approaches 2021 Moro E. - - Lysosomal Storage Disorders: Molecular Basis and Therapeutic Approaches
A transcriptional and post-transcriptional dysregulation of Dishevelled 1 and 2 underlies the Wnt signaling impairment in type I Gaucher disease experimental models 2020 Costa RobertoBellesso StefaniaManzoli RosaMoro Enrico + HUMAN MOLECULAR GENETICS ONLINE - -
Temporal control of Wnt signaling is required for habenular neuron diversity and brain asymmetry 2020 Moro E.Argenton F. + DEVELOPMENT - -
“Janus” efficacy of CX-5011: CK2 inhibition and methuosis induction by independent mechanisms 2020 D'Amore C.Moro E.Borgo C.Salvi M. + BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH - -
A conditional mouse model and in vitro system to study Gba1 in myelinating glia: novel contribution for Gaucher Disease and Parkinson's Disease 2019 gregorio ilariachrisam martinabizzotto dariomoro enricocescon matilde GLIA - -
Impaired Mitochondrial ATP Production Downregulates Wnt Signaling via ER Stress Induction 2019 Costa R.Peruzzo R.Bachmann M.Vicario M.Santinon G.Mattarei A.Moro E.Scorrano L.Zeviani M.Vallese F.Zoratti M.Paradisi C.Argenton F.Brini M.Cali T.Dupont S.Szabo I.Leanza L. + CELL REPORTS - -
Corrigendum: FGF signaling deregulation is associated with early developmental skeletal defects in animal models for mucopolysaccharidosis type II (MPSII) [Human Molecular Genetics, 27, 13, (2018) (2262-2275)] DOI: 10.1093/hmg/ddy131 2018 Bellesso S.Salvalaio M.Costa R.Braghetta P.Giraudo C.Stramare R.Rigon L.Tomanin R.Moro E. + HUMAN MOLECULAR GENETICS - -
FGF signaling deregulation is associated with early developmental skeletal defects in animal models for mucopolysaccharidosis type II (MPSII). 2018 Bellesso StefaniaSalvalaio MarikaCosta RobertoBraghetta PaolaGiraudo ChiaraStramare RobertoRigon LauraTomanin RosellaMoro Enrico + HUMAN MOLECULAR GENETICS ONLINE - -
The Golgi ‘casein kinase’ Fam20C is a genuine ‘phosvitin kinase’ and phosphorylates polyserine stretches devoid of the canonical consensus 2018 Cozza, GiorgioMoro, EnricoMarin, OrianoSalvi, MauroVenerando, AndreaPinna, Lorenzo A. + THE FEBS JOURNAL - -
The pathogenesis of lysosomal storage disorders: beyond the engorgement of lysosomes to abnormal development and neuroinflammation. 2018 Enrico Moro + HUMAN MOLECULAR GENETICS ONLINE - -
Perturbations in cell signaling elicit early cardiac defects in mucopolysaccharidosis type II 2017 COSTA, ROBERTOURBANI, ANDREASALVALAIO, MARIKABELLESSO, STEFANIACIERI, DOMENICOZANCAN, ILARIABONALDO, PAOLOSZABO', ILDIKO'TOMANIN, ROSELLAMORO, ENRICO + HUMAN MOLECULAR GENETICS - -