NOORI, Leila
NOORI, Leila
Biomedicina, Neuroscienze e Diagnostica avanzata
Contribution of Extracellular Vesicles and Molecular Chaperones in Age-Related Neurodegenerative Disorders of the CNS
2023-01-04 Noori, L; Filip, K; Nazmara, Z; Mahakizadeh, S; Hassanzadeh, G; Caruso Bavisotto, C; Bucchieri, F; Marino Gammazza, A; Cappello, F; Wnuk, M; Scalia, F
Histopathological abnormalities of the skeletal muscle tissue from a patient aff ected by a rare genetic neuromyopathy
2022-01-01 Federica Scalia, Rosario Barone, Antonella Marino Gammazza, Francesca Rappa, Leila Noori, Filippo Macaluso, Fabrizio Lo Celso, Everly Conway de Macario, Alberto J. L. Macario, Francesco Cappello.
Investigation on the relationship between the Leu224Val mutation in the gene encoding the subunit 5 of the chaperonin CCT with a rare genetic neuromyopathy, and study of the potential oxidative stress alterations associated with the CCT5 subunit
2024-07-01
Putative Roles and Therapeutic Potential of the Chaperone System in Amyotrophic Lateral Sclerosis and Multiple Sclerosis
2024-01-24 Noori, Leila; Saqagandomabadi, Vahid; Di Felice, Valentina; David, Sabrina; Caruso Bavisotto, Celeste; Bucchieri, Fabio; Cappello, Francesco; Conway de Macario, Everly; Macario, Alberto J. L.; Scalia, Federica
Structural and Dynamic Disturbances Revealed by Molecular Dynamics Simulations Predict the Impact on Function of CCT5 Chaperonin Mutations Associated with Rare Severe Distal Neuropathies
2023-01-19 Scalia F.; Lo Bosco G.; Paladino L.; Vitale A.M.; Noori L.; Conway de Macario E.; Macario A.J.L.; Bucchieri F.; Cappello F.; Lo Celso F.