BERTOCCHI, MARTINA
BERTOCCHI, MARTINA
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
Leveraging Brain Organoids to Explore Neurodevelopmental Mechanisms in Congenital Central Hypoventilation Syndrome (CCHS)
2025 E. Piscitelli, S. Di Lascio, F. Chiesa, A. Chiodi, C. Cocola, P. Pelucchi, D. Gaglio, M. Bonanomi, R. Vanna, V. Alcolea Rodriguez, A. Lucia Cuadros Gamboa, M. Bertocchi, D. Fornasari, R. Benfante
Expression Deregulation of lncRNA PHOX2B-AS1 in the Pathogenesis of CCHS
2025 S. Di Lascio, E. Piscitelli, M. Bertocchi, F. Chiesa, A. Lucia Cuadros Gamboa, E. Mosca, P. Pelucchi, A. Chiodi, R. Benfante, D. Fornasari
The natural antisense lncRNA PHOX2B-AS1 in the pathogenesis and as potential drug target in Congenital Central Hypoventilation Syndrome (CCHS)
2025 R. Benfante, A.L. Cuadros Gamboa, M. Bertocchi, F. Chiesa, S. Di Lascio, D. Fornasari
Study of the function of the natural antisense lncRNA PHOX2B-AS1 in 2D and 3D iPSc derived neuronal models of Congenital Central Hypoventilation Syndrome
2025 S. Di Lascio, E. Piscitelli, A. Lucia Cuadros Gamboa, M. Bertocchi, F. Chiesa, A. Chiodi, E. Mosca, P. Pelucchi, R. Benfante, D. Fornasari
Generation of 2D and 3D iPSC-derived neuronal models for the study of Congenital Central Hypoventilation Syndrome (CCHS)
2024 A.L. Cuadros Gamboa, E. Piscitelli, M. Bertocchi, F. Chiesa, P. Pelucchi, S. Di Lascio, R. Benfante, D. Fornasari
2D and 3D iPSC-derived neuronal models for the study of the role of lncRNA PHOX2B-AS1 in the pathogenesis of Congenital Central Hypoventilation Syndrome
2024 M. Bertocchi, S. Di Lascio, A.L. Cuadros, F. Chiesa, E. Piscitelli, P. Pelucchi, D. Fornasari, R. Benfante
Study of the role of lncRNA PHOX2B-AS1 in the pathogenesis of Congenital Central Hypoventilation Syndrome
2024 M. Bertocchi, A.L. Cuadros Gamboa, F. Chiesa, R. Benfante, D. Fornasari, S. Di Lascio
iPSC-derived autonomic neurons for the study of the role of lncRNA PHOX2B-AS1 in the pathogenesis of Congenital Central Hypoventilation Syndrome
2024 M. Bertocchi, S. Di Lascio, A.L. Cuadros, F. Chiesa, E. Piscitelli, P. Pelucchi, R. Benfante, D. Fornasari
Characterization of iPSC-motoneurons from a HSP patient with a novel mutation in KIF5A N-terminal region Characterization of iPSCmotoneurons from a HSP patient with a novel mutation in KIF5A N-terminal region
2022 S. Santangelo, P. Bossolasco, C. Fallini, S. Magri, M. Bertocchi, S. Invernizzi, D. Di Bella, D. Bardelli, C. Colombrita, V. Silani, F. Taroni, A. Ratti
Modeling a novel N-terminal mutation of KIF5A gene in patient-derived iPSC-motoneurons
2022 S. Santangelo, P. Bossolasco, C. Fallini, S. Magri, M. Bertocchi, S. Invernizzi, D. Di Bella, D. Bardelli, C. Colombrita, V. Silani, F. Taroni, A. Ratti