Rezultati - Anna Corradi

  • Showing 1 - 12 results of 12
Refine Results
  1. 1
    Involvement of Synaptic Genes in the Pathogenesis of Autism Spectrum Disorders: The Case of Synapsins

    Involvement of Synaptic Genes in the Pathogenesis of Autism Spectrum Disorders: The Case of Synapsins od Silvia Giovedí, Anna Corradi, Anna Fassio, Fabio Benfenati

    Izdano 2014
    Polni tekst Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  2. 2
    Phosphorylation of Synapsin I by cAMP-Dependent Protein Kinase Controls Synaptic Vesicle Dynamics in Developing Neurons

    Phosphorylation of Synapsin I by cAMP-Dependent Protein Kinase Controls Synaptic Vesicle Dynamics in Developing Neurons od Dario Bonanomi, Andrea Menegon, Annarita Miccio, Giuliana Ferrari, Anna Corradi, Hung-Teh Kao, Fabio Benfenati, Flavia Valtorta

    Izdano 2005
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  3. 3
    A Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2)

    A Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2) od Pia Rossi, Bruno Sterlini, Enrico Castroflorio, Antonella Marte, Franco Onofri, Flavia Valtorta, Luca Maragliano, Anna Corradi, Fabio Benfenati

    Izdano 2016
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  4. 4
    MAPK/Erk-dependent phosphorylation of synapsin mediates formation of functional synapses and short-term homosynaptic plasticity

    MAPK/Erk-dependent phosphorylation of synapsin mediates formation of functional synapses and short-term homosynaptic plasticity od Carlo Natale Giuseppe Giachello, Ferdinando Fiumara, Caterina Giacomini, Anna Corradi, Chiara Milanese, Mirella Ghirardi, Fabio Benfenati, Pier Giorgio Montarolo

    Izdano 2010
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  5. 5
    A key role for the HLH transcription factor EBF2COE2,O/E-3 in Purkinje neuron migration and cerebellar cortical topography

    A key role for the HLH transcription factor EBF2COE2,O/E-3 in Purkinje neuron migration and cerebellar cortical topography od Laura Croci, Seung‐Hyuk Chung, Giacomo Masserdotti, Sara Gianola, Antonella Bizzoca, Gianfranco Gennarini, Anna Corradi, Ferdinando Rossi, Richard Hawkes, G. Giacomo Consalez

    Izdano 2006
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  6. 6
    The PRRT2 knockout mouse recapitulates the neurological diseases associated with PRRT2 mutations

    The PRRT2 knockout mouse recapitulates the neurological diseases associated with PRRT2 mutations od Caterina Michetti, Enrico Castroflorio, Ivan Marchionni, Nicola Forte, Bruno Sterlini, Francesca Binda, Floriana Fruscione, Pietro Baldelli, Flavia Valtorta, Federico Zara, Anna Corradi, Fabio Benfenati

    Izdano 2016
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  7. 7
    Phosphorylation of Synapsin I by Cyclin-Dependent Kinase-5 Sets the Ratio between the Resting and Recycling Pools of Synaptic Vesicles at Hippocampal Synapses

    Phosphorylation of Synapsin I by Cyclin-Dependent Kinase-5 Sets the Ratio between the Resting and Recycling Pools of Synaptic Vesicles at Hippocampal Synapses od Anne M.J. Verstegen, Erica Tagliatti, Gabriele Lignani, Antonella Marte, Tamar Stolero, Merav Atias, Anna Corradi, Flavia Valtorta, Daniel Gitler, Franco Onofri, Anna Fassio, Fabio Benfenati

    Izdano 2014
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  8. 8
    SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth

    SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth od Anna Corradi, Manuela Fadda, Amélie Piton, Lysanne Patry, Antonella Marte, Pia Rossi, Maxime Cadieux‐Dion, Julie Gauthier, Line Lapointe, Laurent Mottron, Flavia Valtorta, Guy A. Rouleau, Anna Fassio, Fabio Benfenati, Patrick Cossette

    Izdano 2013
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  9. 9
    Optimization of Transcription Factor-Driven Neuronal Differentiation from Human Induced Pluripotent Stem Cells for Disease Modelling and Drug Screening

    Optimization of Transcription Factor-Driven Neuronal Differentiation from Human Induced Pluripotent Stem Cells for Disease Modelling and Drug Screening od Martina Servetti, Martino Caramia, Giulia Parodi, Fabrizio Loiacono, Ennio Nano, Giorgia Biddau, Lorenzo Ferrando, Lisastella Morinelli, Pierluigi Valente, Sérgio Martinoia, Andrea Escelsior, Gianluca Serafini, Serena Tamburro, Sımona Baldassari, Anna Fassio, Fabio Benfenati, Anna Corradi, Bruno Sterlini

    Izdano 2025
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  10. 10
    PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity

    PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity od Floriana Fruscione, Pierluigi Valente, Bruno Sterlini, Alessandra Romei, Sımona Baldassari, Manuela Fadda, Cosimo Prestigio, Giorgia Giansante, Jacopo Sartorelli, Pia Rossi, Alicia Rubio, Antonio Gambardella, Thierry Nieus, Vania Broccoli, Anna Fassio, Pietro Baldelli, Anna Corradi, Federico Zara, Fabio Benfenati

    Izdano 2018
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  11. 11
    PRRT2 Is a Key Component of the Ca 2+ -Dependent Neurotransmitter Release Machinery

    PRRT2 Is a Key Component of the Ca 2+ -Dependent Neurotransmitter Release Machinery od Pierluigi Valente, Enrico Castroflorio, Pia Rossi, Manuela Fadda, Bruno Sterlini, Romina Inès Cervigni, Cosimo Prestigio, Silvia Giovedı̀, Franco Onofri, Elisa Mura, Fabrizia Claudia Guarnieri, Antonella Marte, Marta Orlando, Federico Zara, Anna Fassio, Flavia Valtorta, Pietro Baldelli, Anna Corradi, Fabio Benfenati

    Izdano 2016
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  12. 12
    SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function

    SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function od Anna Fassio, Lysanne Patry, Sonia Congia, Franco Onofri, Amélie Piton, Julie Gauthier, Davide Pozzi, Mirko Messa, Enrico Defranchi, Manuela Fadda, Anna Corradi, Pietro Baldelli, Line Lapointe, Judith St‐Onge, Caroline Meloche, Laurent Mottron, Flavia Valtorta, Dang Khoa Nguyen, Guy A. Rouleau, Fabio Benfenati, Patrick Cossette

    Izdano 2011
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:

Iskalna orodja: