CARELLI, STEFANA
CARELLI, STEFANA
Dipartimento di Scienze Biomediche e Cliniche
Mitochondrial Acetoacetyl-CoA Thiolase Deficiency: Three New Cases Detected by Newborn Screening Confirming the Significance of C4OH Elevation
2025 A. Vasco, C. Berardo, S. Lucchi, L. Cappelletti, G. Tamburello, S. Fazzone, A. Mauri, F. Fiumani, D. Postorivo, L. Alberti, M. Perrone Donnorso, S. Gasperini, F. Furlan, L. Fiori, S. Carelli, L.A. Saielli, C. Montrasio, C. Cereda
Further insights into Allan-Herndon-Dudley syndrome: a novel SLC16A2 splice site variant
2024 L. Esposito, A. Mauri, F. Rey, E. Maghraby, B. Castellotti, G. Zuccotti, D. Tonduti, S. Carelli, C. Cereda
Insights on ZEB1-AS1: emerging roles from cancer to neurodegeneration
2024 S. Carelli, F. Rey, E. Maghraby, C. Cereda
Characterization of the molecular dysfunctions occurring in Aicardi-Goutières syndrome patients with mutations in ADAR1
2024 S. Al Wardat, L. Frassinelli, E. Orecchini, F. Rey, S.A. Ciafre, S. Galardi, J. Garau, S. Gagliardi, S. Orcesi, D. Tonduti, S. Carelli, C. Cereda, E. Picardi, A. Michienzi
Production of an induced pluripotent stem cell line CSSi018-A (14192) from a patient with hypomyelinating leukodystrophy 7 (HLD7) carrying biallelic variants of POLR3A (c.1802 T > A; c.4072G > A)
2024 A. Casamassa, G. Rotundo, C. Ceresoni, E.M. Turco, I. Torrente, O. Candido, F. Nicita, D. Tonduti, E. Bertini, M. Marano, D. Ferrari, C. Cereda, M. Pennuto, A.L. Vescovi, S. Carelli, J. Rosati
Further insights into Allan-Herndon-Dudley syndrome: characterization of two genetic variants in SLC16A2 gene
2023 L. Esposito, F. Rey, E. Maghraby, G. Zuccotti, D. Tonduti, S. Carelli, C. Cereda
TDP-43 PROTEINOPATHIES: THE ROLE OF EXTRACELLULAR VESICLES
2023 E. Casarotto, L. Messa, M. Chierichetti, L. Cornaggia, M. Cozzi, R. Cristofani, V. Ferrari, M. Galbiati, G. Patelli, M. Piccolella, P. Pramaggiore, P. Rusmini, B. Tedesco, S. Gagliardi, S. Carelli, C. Cereda, A. Poletti, V. Crippa
lncRNAs at the interplay between neurodegeneration and cancer: a role for MINCR
2023 C. Pandini, I. Cassotti, M. Garofalo, F. Rey, S. Carelli, C. Cereda, S. Gagliardi, P. Gandellini
3D photopolymerized microstructured scaffolds influence nuclear deformation, nucleo/cytoskeletal protein organization, and gene regulation in mesenchymal stem cells
2023 F. Donnaloja, M.T. Raimondi, L. Messa, B. Barzaghini, F. Carnevali, E. Colombo, D. Mazza, C. Martinelli, L. Boeri, F. Rey, C. Cereda, R. Osellame, G. Cerullo, S. Carelli, M. Soncini, E. Jacchetti
Identification of a novel pathway in sporadic Amyotrophic Lateral Sclerosis mediated by the long non-coding RNA ZEB1-AS1
2023 F. Rey, E. Maghraby, L. Messa, L. Esposito, B. Barzaghini, C. Pandini, M. Bordoni, S. Gagliardi, L. Diamanti, M.T. Raimondi, M. Mazza, G. Zuccotti, S. Carelli, C. Cereda
How PQC inhibition modulates miRNA loading in large and small extracellular vesicles
2022 E. Casarotto, M. Garofalo, L. Messa, D. Sproviero, S. Carelli, M. Cozzi, M. Chierichetti, R. Cristofani, V. Ferrari, M. Galbiati, F. Mina, M. Piccolella, P. Rusmini, B. Tedesco, P. Pramaggiore, C. Cereda, S. Gagliardi, A. Poletti, V. Crippa
COMPUTATIONAL AND BIOLOGICAL VALIDATION OF A NEW NICHOID SCAFFOLD OPTIMIZED FOR HUMAN MESENCHYMAL STEM CELLS
2022 B. Barzaghini, L. Messa, F. Rey, F. Fanizza, M. Antonella Sforazzini, G.V. Zuccotti, R. Osellame, G. Cerullo, E. Jacchetti, S. Carelli, M. Teresa Raimondi
Correspondence on “Expanded phenotype of AARS1-related white matter disease” by Helman et al
2022 A. Leidi, R. Previtali, C. Parazzini, F. Raviglione, S. Carelli, M.I. Mendes, G.S. Salomons, M. Iascone, D. Tonduti
Large and small extracellular vesicles may contribute to the propagation of ALS and FTD carrying toxic TDP species and potentially harmful miRNAs
2022 E. Casarotto, M. Garofalo, L. Messa, D. Sproviero, S. Carelli, M. Cozzi, M. Chierichetti, R. Cristofani, V. Ferrari, M. Galbiati, M. Piccolella, P. Rusmini, B. Tedesco, P. Pramaggiore, C. Cereda, S. Gagliardi, A. Poletti, V. Crippa
Mitochondrial dysfunctions in neurodegenerative diseases: role in disease pathogenesis, strategies for analysis and therapeutic prospects
2022 F. Rey, S. Ottolenghi, G. Zuccotti, M. Samaja, S. Carelli
RNA molecular signature profiling in PBMCs of sporadic ALS patients: HSP70 overexpression is associated with nuclear SOD1
2022 M. Garofalo, C. Pandini, M. Bordoni, E. Jacchetti, L. Diamanti, S. Carelli, M.T. Raimondi, D. Sproviero, V. Crippa, S. Carra, A. Poletti, O. Pansarasa, S. Gagliardi, C. Cereda
Oxygen sensing in neurodegenerative diseases: current mechanisms, implication of transcriptional response and pharmacological modulation
2022 F. Rey, L. Messa, E. Maghraby, G. Casili, S. Ottolenghi, B. Barzaghini, M.T. Raimondi, C. Cereda, S. Cuzzocrea, G.V. Zuccotti, E. Esposito, I. Paterniti, S. Carelli
SNCA-AS1 in aging and Parkinson's disease
2022 S. Carelli, F. Rey, C. Cereda
LncRNAs associated with neuronal development and oncogenesis are deregulated in SOD1-G93A murine model of Amyotrophic Lateral Sclerosis
2021 S. Carelli, F. Rey, S. Marcuzzo, S. Bonanno, C. Cereda, G.V. Zuccotti
LncRNAs associated with neuronal development and oncogenesis are deregulated in SOD1-G93A murine model of Amyotrophic Lateral Sclerosis
2021 S. Carelli, F. Rey, S. Marcuzzo, S. Bonanno, C. Cereda, G.V. Zuccotti