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Mostrati risultati da 1 a 20 di 122
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
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 - -
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
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 - -
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 - -
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
Temporal control of Wnt signaling is required for habenular neuron diversity and brain asymmetry 2020 Moro E.Argenton F. + DEVELOPMENT - -
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 - -
“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 - -
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 - -
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 - -
The pathogenesis of lysosomal storage disorders: beyond the engorgement of lysosomes to abnormal development and neuroinflammation. 2018 Enrico Moro + 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 - -
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 - -
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 - -
Glucocerebrosidase deficiency in zebrafish affects primary bone ossification through increased oxidative stress and reduced Wnt/β-catenin signaling. 2015 COSTA, ROBERTOARGENTON, FRANCESCOMORO, ENRICO + HUMAN MOLECULAR GENETICS - -
Smad3 mediated TGFbeta signalling controls the progenitor/precursor switch during zebrafish CNS development 2014 M. SchiavoneVETTORI, ANDREATISO, NATASCIAARGENTON, FRANCESCOMORO, ENRICO + - - EZPM 2014 Abstract Book
Mostrati risultati da 1 a 20 di 122
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