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Titolo Data di pubblicazione Autore(i) File
Both Schwann cell and axonal defects cause motor peripheral neuropathy in Ebf2-/- mice. 1-gen-2011 Giacomini, C; La Padula, V; Schenone, Angelo; Leandri, Massimo; Contestabile, A; Moruzzo, Diego; Goutebroze, L; Consalez, Gg; Benfenati, Fabio; Corradi, ANNA MARGHERITA
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.
Ebf Genes In Peripheral Nerve Myelination 1-gen-2012 Moruzzo, Diego; Nobbio, Lucilla; Schenone, Angelo; Consalez, G. G.; Benfenati, Fabio; Corradi, ANNA MARGHERITA
Synapsin II mutations associated with autism or epilepsy: effects on neuronal development and synaptic vesicle cycling 1-gen-2012 Fadda, Manuela; Marte, Antonella; Fassio, Anna; Corradi, ANNA MARGHERITA; Patrick, Cossette; Benfenati, Fabio
Hyccin, the Molecule Mutated in the Leukodystrophy Hypomyelination and Congenital Cataract (HCC), Is a Neuronal Protein. 1-gen-2012 Gazzerro, E; Baldassari, Simona; Giacomini, C; Musante, V; Fruscione, Floriana; La Padula, V; Biancheri, R; Scarfi', Sonia; Prada, V; Sotgia, F; Duncan, Id; Zara, F; Werner, Hb; Lisanti, Mp; Nobbio, Lucilla; Corradi, ANNA MARGHERITA; Minetti, Carlo
Biochimica del Sistema Nervoso 1-gen-2013 Benfenati, Fabio; Corradi, ANNA MARGHERITA; Giovedi', Silvia; Onofri, Franco
Ebf genes' silencing impairs myelin formation 1-gen-2013 Moruzzo, Diego; Nobbio, Lucilla; Schenone, Angelo; Consalez, Gg; Benfenati, Fabio; Corradi, ANNA MARGHERITA
PHOSPHORYLATION OF SYNAPSIN I BY CYCLIN-DEPENDENT KINASE-5 REGULATES SYNAPTIC VESICLE SPATIAL DISTRIBUTION AND RECRUITMENT TO RECYCLING POOL AT HIPPOCAMPAL SYNAPSES. 1-gen-2014 Tagliatti, Erica; Verstegen, A.; Lignani, G.; Marte, Antonella; Corradi, ANNA MARGHERITA; Valtorta, F.; Gitler, D.; Onofri, Franco; Fassio, Anna; Benfenati, Fabio
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
Involvement of Synaptic Genes in the Pathogenesis of Autism Spectrum Disorders: The Case of Synapsins 1-gen-2014 Giovedi', Silvia; Corradi, ANNA MARGHERITA; Fassio, Anna; Benfenati, Fabio
Phosphorylation of Synapsin I by Cyclin-Dependent Kinase-5 Sets the Ratio between the Resting and Recycling Pools of Synaptic Vesicles at Hippocampal Synapses 1-gen-2014 A. M. J., Verstegen; Tagliatti, Erica; Lignani, Gabriele; Marte, Antonella; T., Stolero; M., Atias; Corradi, ANNA MARGHERITA; F., Valtorta; D., Gitler; Onofri, Franco; Fassio, Anna; Benfenati, Fabio
Synapsin knockdown is associated with decreased neurite outgrowth, functional synaptogenesis impairment, and fast high-frequency neurotransmitter release. 1-gen-2015 Brenes, O; Giachello, Cn; Corradi, ANNA MARGHERITA; Ghirardi, M; Montarolo, P. g.
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
A Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2): HINTS FOR AN INTRACELLULAR FUNCTION AT THE SYNAPSE 1-gen-2016 Rossi, Pia; Sterlini, Bruno; Castroflorio, Enrico; Marte, Antonella; Onofri, Franco; Valtorta, Flavia; Maragliano, Luca; Corradi, ANNA MARGHERITA; Benfenati, Fabio
The PRRT2 knockout mouse recapitulates the neurological diseases associated with PRRT2 mutations. 1-gen-2017 Michetti, C; Castroflorio, Enrico; Marchionni, I; Forte, N; Sterlini, Bruno; Binda, F; Fruscione, F; Baldelli, Pietro; Valtorta, F; Zara, F; Corradi, ANNA MARGHERITA; Benfenati, Fabio
PRRT2, a network stability gene 1-gen-2017 Michetti, C; Corradi, ANNA MARGHERITA; Benfenati, Fabio
The transcription factors EBF1 and EBF2 are positive regulators of myelination in Schwann cells 1-gen-2017 Moruzzo, Diego; Nobbio, Lucilla; Sterlini, Bruno; Giacomo Consalez, G.; Benfenati, Fabio; Schenone, Angelo; Corradi, ANNA MARGHERITA
PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity 1-gen-2018 Fruscione, F; Valente, P; Sterlini, B; Romei, A; Baldassari, S; Fadda, M; Prestigio, C; Giansante, G; Sartorelli, J; Rossi, P; Rubio, A; Gambardella, A; Nieus, T; Broccoli, V; Fassio, A; Baldelli, P; Corradi, A; Zara, F; Benfenati, F.
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
Red-hot chili receptors: a systematic review of TRPV1 antagonism in animal models of psychiatric disorders and addiction 1-gen-2020 Escelsior, Andrea; Sterlini, Bruno; Murri, Martino Belvederi; Serafini, Gianluca; Aguglia, Andrea; Silva, Beatriz Pereira da; Corradi, Anna; Valente, Pierluigi; Amore, Mario
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