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IANNIELLI, ANGELO

IANNIELLI, ANGELO  

Istituto di Neuroscienze - IN - Sede Secondaria Milano  

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Risultati 1 - 11 di 11 (tempo di esecuzione: 0.027 secondi).
Titolo Data di pubblicazione Autore(i) File
Generation of iPSCs from identical twin, one affected by LHON and one unaffected, both carrying a combination of two mitochondrial variants: m.14484 T>C and m.10680G>A 1-gen-2024 Peron, Camille; Cavaliere, Andrea; Fasano, Chiara; Iannielli, Angelo; Spagnolo, Manuela; Legati, Andrea; Nicol Colombo, Maria; Rizzo, Ambra; Sciacca, Francesca L.; Carelli, Valerio; Broccoli, Vania; Lamperti, Costanza; Tiranti, Valeria
New AAV9 engineered variants with enhanced neurotropism and reduced liver off-targeting in mice and marmosets 1-gen-2024 Giannelli, Serena Gea; Luoni, Mirko; Iannielli, Angelo; Middeldorp, Jinte; Philippens, Ingrid; Bido, Simone; Körbelin, Jakob; Broccoli, Vania
Enhanced production of mesencephalic dopaminergic neurons from lineage-restricted human undifferentiated stem cells 1-gen-2023 Maimaitili, M.; Chen, M.; Febbraro, F.; Ucuncu, E.; Kelly, R.; Niclis, J. C.; Christiansen, J. R.; Mermet-Joret, N.; Niculescu, D.; Lauritsen, J.; Iannielli, A.; Klaestrup, I. H.; Jensen, U. B.; Qvist, P.; Nabavi, S.; Broccoli, V.; Nykjaer, A.; Romero-Ramos, M.; Denham, M.
MCT1-dependent energetic failure and neuroinflammation underlie optic nerve degeneration in Wolfram syndrome mice 1-gen-2023 Rossi, Greta; Ordazzo, Gabriele; Vanni, Niccolò N; Castoldi, Valerio; Iannielli, Angelo; Di Silvestre, Dario; Bellini, Edoardo; Bernardo, Letizia; Giannelli, Serena G; Luoni, Mirko; Muggeo, Sharon; Leocani, Letizia; Mauri, Pierluigi; Broccoli, Vania
Synthesis and Preliminary Characterization of Putative Anle138b-Centered PROTACs against α-Synuclein Aggregation 1-gen-2023 Pedrini, Martina; Iannielli, Angelo; Meneghelli, Lorenzo; Passarella, Daniele; Broccoli, Vania; Seneci, Pierfausto
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives 1-gen-2021 Peron, C; Maresca, A; Cavaliere, A; Iannielli, A; Broccoli, V; Carelli, V; Di Meo, I; Tiranti, V
Generation of two human iPSC lines, FINCBi002-A and FINCBi003-A, carrying heteroplasmic macrodeletion of mitochondrial DNA causing Pearson's syndrome 1-gen-2021 Peron, C; Mauceri, R; Iannielli, A; Cavaliere, A; Legati, A; Rizzo, A; Sciacca, Fl; Broccoli, V; Tiranti, V
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs 1-gen-2021 Palombo, F; Peron, C; Caporali, L; Iannielli, A; Maresca, A; Di Meo, I; Fiorini, C; Segnali, A; Sciacca, Fl; Rizzo, A; Levi, S; Suomalainen, A; Prigione, A; Broccoli, V; Carelli, V; Tiranti, V
Frataxin gene editing rescues Friedreich's ataxia pathology in dorsal root ganglia organoid-derived sensory neurons 1-gen-2020 Mazzara, Pg; Muggeo, S; Luoni, M; Massimino, L; Zaghi, M; Valverde, Ptt; Brusco, S; Marzi, Mj; Palma, C; Colasante, G; Iannielli, A; Paulis, M; Cordiglieri, C; Giannelli, Sg; Podini, P; Gellera, C; Taroni, F; Nicassio, F; Rasponi, M; Broccoli, V
Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON) 1-gen-2020 Peron, C; Mauceri, R; Cabassi, T; Segnali, A; Maresca, A; Iannielli, A; Rizzo, A; Sciacca, Fl; Broccoli, V; Carelli, V; Tiranti, V
Whole brain delivery of an instability-prone Mecp2 transgene improves behavioral and molecular pathological defects in mouse models of Rett syndrome 1-gen-2020 Luoni, M; Giannelli, S; Indrigo, Mt; Niro, A; Massimino, L; Iannielli, A; Passeri, L; Russo, F; Morabito, G; Calamita, P; Gregori, S; Deverman, B; Broccoli, V