Search research articles
Contact Us
Filters
Showing results (81-90 of 94) with videos related to
Page
of 10
Sort By:
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 23, 2014
Phosphorylation of synapsin I by cyclin-dependent kinase-5 sets the ratio between the resting and recycling pools of synaptic vesicles at hippocampal synapses
Anne M J Verstegen, Erica Tagliatti, Gabriele Lignani, et al.
International Journal of Bipolar Disorders
|
December 10, 2019
Investigating the relationship between melatonin levels, melatonin system, microbiota composition and bipolar disorder psychopathology across the different phases of the disease
Mirko Manchia, Alessio Squassina, Claudia Pisanu, et al.
Brain, Behavior, and Immunity
|
October 26, 2017
Synapsin I deletion reduces neuronal damage and ameliorates clinical progression of experimental autoimmune encephalomyelitis
Fabrizia C Guarnieri, Serena Bellani, Latefa Yekhlef, et al.
Human Molecular Genetics
|
August 20, 2013
SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth
Anna Corradi, Manuela Fadda, Amélie Piton, 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 Neurons
Pierluigi Valente, Alessandra Romei, Manuela Fadda, et al.
Cell Reports
|
December 21, 2017
APache Is an AP2-Interacting Protein Involved in Synaptic Vesicle Trafficking and Neuronal Development
Alessandra Piccini, Enrico Castroflorio, Pierluigi Valente, et al.
Human Molecular Genetics
|
October 2, 2002
Deletion of the mental retardation gene Gdi1 impairs associative memory and alters social behavior in mice
Patrizia D'Adamo, Hans Welzl, Stavros Papadimitriou, et al.
Cell Reports
|
April 8, 2016
PRRT2 Is a Key Component of the Ca(2+)-Dependent Neurotransmitter Release Machinery
Pierluigi Valente, Enrico Castroflorio, Pia Rossi, et al.
Cell Death & Disease
|
November 11, 2020
Pharmacological antagonism of kainate receptor rescues dysfunction and loss of dopamine neurons in a mouse model of human parkin-induced toxicity
Maria Regoni, Stefano Cattaneo, Daniela Mercatelli, et al.
Human Molecular Genetics
|
March 29, 2011
SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function
Anna Fassio, Lysanne Patry, Sonia Congia, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 94) with videos related to
Sort By:
Page
of 10
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 23, 2014
Phosphorylation of synapsin I by cyclin-dependent kinase-5 sets the ratio between the resting and recycling pools of synaptic vesicles at hippocampal synapses
Anne M J Verstegen, Erica Tagliatti, Gabriele Lignani, et al.
International Journal of Bipolar Disorders
|
December 10, 2019
Investigating the relationship between melatonin levels, melatonin system, microbiota composition and bipolar disorder psychopathology across the different phases of the disease
Mirko Manchia, Alessio Squassina, Claudia Pisanu, et al.
Brain, Behavior, and Immunity
|
October 26, 2017
Synapsin I deletion reduces neuronal damage and ameliorates clinical progression of experimental autoimmune encephalomyelitis
Fabrizia C Guarnieri, Serena Bellani, Latefa Yekhlef, et al.
Human Molecular Genetics
|
August 20, 2013
SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth
Anna Corradi, Manuela Fadda, Amélie Piton, 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 Neurons
Pierluigi Valente, Alessandra Romei, Manuela Fadda, et al.
Cell Reports
|
December 21, 2017
APache Is an AP2-Interacting Protein Involved in Synaptic Vesicle Trafficking and Neuronal Development
Alessandra Piccini, Enrico Castroflorio, Pierluigi Valente, et al.
Human Molecular Genetics
|
October 2, 2002
Deletion of the mental retardation gene Gdi1 impairs associative memory and alters social behavior in mice
Patrizia D'Adamo, Hans Welzl, Stavros Papadimitriou, et al.
Cell Reports
|
April 8, 2016
PRRT2 Is a Key Component of the Ca(2+)-Dependent Neurotransmitter Release Machinery
Pierluigi Valente, Enrico Castroflorio, Pia Rossi, et al.
Cell Death & Disease
|
November 11, 2020
Pharmacological antagonism of kainate receptor rescues dysfunction and loss of dopamine neurons in a mouse model of human parkin-induced toxicity
Maria Regoni, Stefano Cattaneo, Daniela Mercatelli, et al.
Human Molecular Genetics
|
March 29, 2011
SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function
Anna Fassio, Lysanne Patry, Sonia Congia, et al.
Page
of 10