FADDA, MANUELA

FADDA, MANUELA  

100008 - Dipartimento di medicina sperimentale  

Mostra records
Risultati 1 - 10 di 10 (tempo di esecuzione: 0.021 secondi).
Titolo Data di pubblicazione Autore(i) File
Arf6 regulates the cycling and the readily releasable pool of synaptic vesicles at hippocampal synapse. 1-gen-2016 Tagliatti E1, 2; Fadda, Manuela; Falace, Antonio; Benfenati, Fabio; Fassio, Anna
Constitutive Inactivation of the PRRT2 Gene Alters Short-Term Synaptic Plasticity and Promotes Network Hyperexcitability in Hippocampal Neurons 1-gen-2019 Valente, Pierluigi; Romei, Alessandra; Fadda, Manuela; Sterlini, Bruno; Lonardoni, Davide; Forte, Nicola; Fruscione, Floriana; Castroflorio, Enrico; Michetti, Caterina; Giansante, Giorgia; Valtorta, Flavia; Tsai, Jin-Wu; Zara, Federico; Nieus, Thierry; Corradi, Anna; Fassio, Anna; Baldelli, Pietro; Benfenati, Fabio
Molecular Machines Determining the Fate of Endocytosed Synaptic Vesicles in Nerve Terminals 1-gen-2016 Fassio, Anna; Fadda, Manuela; Benfenati, Fabio
Neuronal hyperactivity causes Na+/H+ exchanger-induced extracellular acidification at active synapses 1-gen-2017 Chiacchiaretta, Martina; Latifi, Shahrzad; Bramini, Mattia; Fadda, Manuela; Fassio, Anna; Benfenati, Fabio; Cesca, Fabrizia
PRRT2 Is a Key Component of the Ca2+-Dependent Neurotransmitter Release Machinery 1-gen-2016 Valente, Pierluigi; Castroflorio, Enrico; Rossi, Pia; Fadda, Manuela; Sterlini, Bruno; Cervigni, Romina Ines; Prestigio, Cosimo; Giovedi', Silvia; Onofri, Franco; Mura, Elisa; Guarnieri, Fabrizia C.; Marte, Antonella; Orlando, Marta; Zara, Federico; Fassio, Anna; Valtorta, Flavia; Baldelli, Pietro; Corradi, ANNA MARGHERITA; Benfenati, Fabio
SYN1loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function 1-gen-2011 Fassio, Anna; Patry, L; Congia, S; Onofri, Franco; Piton, A; Gauthier, J; Pozzi, D; Messa, M; Defranchi, E; Fadda, Manuela; Corradi, ANNA MARGHERITA; Baldelli, Pietro; Lapointe, L; ST ONGE, J; Meloche, C; Mottron, L; Valtorta, F; KHOA NGUYEN, D; Rouleau, Ga; Benfenati, Fabio; Cossette, P.
SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicles cycling and axon outgrowth 1-gen-2014 Corradi, ANNA MARGHERITA; Fadda, Manuela; Amelie, Piton; Lysanne, Patry; Marte, Antonella; Rossi, Pia; Maxime Cadieux, Dion; Julie, Gauthier; Line, Lapointe; Laurent, Mottron; Flavia, Valtorta; Guy A., Rouleau; Fassio, Anna; Benfenati, Fabio; Patrick, Cossette
Synapsin I Senses Membrane Curvature by an Amphipathic Lipid Packing Sensor Motif. 1-gen-2011 Krabben, L; Fassio, Anna; Bhatia, Vk; Pechstein, A; Onofri, Franco; Fadda, Manuela; Messa, M; Rao, Y; Shupliakov, O; Stamou, D; Benfenati, Fabio; Haucke, V.
TBC1D24 regulates axonal outgrowth and membrane trafficking at the growth cone in rodent and human neurons 1-gen-2019 Aprile, D.; Fruscione, F.; Baldassari, S.; Fadda, M.; Ferrante, D.; Falace, A.; Buhler, E.; Sartorelli, J.; Represa, A.; Baldelli, P.; Benfenati, F.; Zara, F.; Fassio, A.
TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathway. 1-gen-2014 Falace, A; Buhler, E; Fadda, Manuela; Watrin, F; Lippiello, P; Pallesi Pocachard, E; Baldelli, Pietro; Benfenati, Fabio; Zara, F; Represa, A; Fassio, Anna; Cardoso, C. *.