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Anna Corradi

Showing results (31-40 of 40) with videos related to

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Cell Reports|June 16, 2021
PRRT2 modulates presynaptic Ca<sup>2+</sup> influx by interacting with P/Q-type channelsDaniele Ferrante, Bruno Sterlini, Cosimo Prestigio, et al.
Human Molecular Genetics|August 20, 2013
SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowthAnna Corradi, Manuela Fadda, Amélie Piton, et al.
Neurology. Genetics|February 3, 2026
Functional Characterization of a De Novo <i>SCN2A</i> Mixed Variant Linked to Early Infantile Developmental and Epileptic EncephalopathyAnna Corradi, Antonella Riva, Bruno Sterlini, et al.
Cell Death Discovery|June 5, 2026
An electrophysiological and proteomics roadmap for human induced glutamatergic neurons: fine-tuning of culture conditions for pathophysiological studiesMartina Servetti, Giulia Parodi, Martino Caramia, et al.
Stem Cell Reviews and Reports|January 31, 2025
Optimization of Transcription Factor-Driven Neuronal Differentiation from Human Induced Pluripotent Stem Cells for Disease Modelling and Drug ScreeningMartina Servetti, Martino Caramia, Giulia Parodi, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 19, 2018
Constitutive Inactivation of the PRRT2 Gene Alters Short-Term Synaptic Plasticity and Promotes Network Hyperexcitability in Hippocampal NeuronsPierluigi Valente, Alessandra Romei, Manuela Fadda, et al.
Brain : a Journal of Neurology|March 20, 2018
PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activityFloriana Fruscione, Pierluigi Valente, Bruno Sterlini, et al.
Plos One|March 31, 2012
Hyccin, the molecule mutated in the leukodystrophy hypomyelination and congenital cataract (HCC), is a neuronal proteinElisabetta Gazzerro, Simona Baldassari, Caterina Giacomini, et al.
Cell Reports|April 8, 2016
PRRT2 Is a Key Component of the Ca(2+)-Dependent Neurotransmitter Release MachineryPierluigi Valente, Enrico Castroflorio, Pia Rossi, et al.
Human Molecular Genetics|March 29, 2011
SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic functionAnna Fassio, Lysanne Patry, Sonia Congia, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Cell Reports|June 16, 2021
PRRT2 modulates presynaptic Ca<sup>2+</sup> influx by interacting with P/Q-type channelsDaniele Ferrante, Bruno Sterlini, Cosimo Prestigio, et al.
Human Molecular Genetics|August 20, 2013
SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowthAnna Corradi, Manuela Fadda, Amélie Piton, et al.
Neurology. Genetics|February 3, 2026
Functional Characterization of a De Novo <i>SCN2A</i> Mixed Variant Linked to Early Infantile Developmental and Epileptic EncephalopathyAnna Corradi, Antonella Riva, Bruno Sterlini, et al.
Cell Death Discovery|June 5, 2026
An electrophysiological and proteomics roadmap for human induced glutamatergic neurons: fine-tuning of culture conditions for pathophysiological studiesMartina Servetti, Giulia Parodi, Martino Caramia, et al.
Stem Cell Reviews and Reports|January 31, 2025
Optimization of Transcription Factor-Driven Neuronal Differentiation from Human Induced Pluripotent Stem Cells for Disease Modelling and Drug ScreeningMartina Servetti, Martino Caramia, Giulia Parodi, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 19, 2018
Constitutive Inactivation of the PRRT2 Gene Alters Short-Term Synaptic Plasticity and Promotes Network Hyperexcitability in Hippocampal NeuronsPierluigi Valente, Alessandra Romei, Manuela Fadda, et al.
Brain : a Journal of Neurology|March 20, 2018
PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activityFloriana Fruscione, Pierluigi Valente, Bruno Sterlini, et al.
Plos One|March 31, 2012
Hyccin, the molecule mutated in the leukodystrophy hypomyelination and congenital cataract (HCC), is a neuronal proteinElisabetta Gazzerro, Simona Baldassari, Caterina Giacomini, et al.
Cell Reports|April 8, 2016
PRRT2 Is a Key Component of the Ca(2+)-Dependent Neurotransmitter Release MachineryPierluigi Valente, Enrico Castroflorio, Pia Rossi, et al.
Human Molecular Genetics|March 29, 2011
SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic functionAnna Fassio, Lysanne Patry, Sonia Congia, et al.
Pageof 4