about
Kidins220/ARMS is transported by a kinesin-1-based mechanism likely to be involved in neuronal differentiationStepping Out of the Shade: Control of Neuronal Activity by the Scaffold Protein Kidins220/ARMSKidins220/ARMS is a novel modulator of short-term synaptic plasticity in hippocampal GABAergic neuronsKidins220/ARMS binds to the B cell antigen receptor and regulates B cell development and activation.Regulation of neural gene transcription by optogenetic inhibition of the RE1-silencing transcription factorEpileptogenic Q555X SYN1 mutant triggers imbalances in release dynamics and short-term plasticityBio-inspired hybrid microelectrodes: a hybrid solution to improve long-term performance of chronic intracortical implants.The synapsins: key actors of synapse function and plasticity.Synapsin I is an oligomannose-carrying glycoprotein, acts as an oligomannose-binding lectin, and promotes neurite outgrowth and neuronal survival when released via glia-derived exosomes.Neuronal hyperactivity causes Na+/H+ exchanger-induced extracellular acidification at active synapses.Intrathecal immunoglobulin A and G antibodies to synapsin in a patient with limbic encephalitis.Specificity protein 1 (Sp1)-dependent activation of the synapsin I gene (SYN1) is modulated by RE1-silencing transcription factor (REST) and 5'-cytosine-phosphoguanine (CpG) methylation.Optogenetic Modulation of Intracellular Signalling and Transcription: Focus on Neuronal Plasticity.Kidins220/ARMS is an essential modulator of cardiovascular and nervous system development.Kidins220/ARMS as a functional mediator of multiple receptor signalling pathways.Kidins220/ARMS mediates the integration of the neurotrophin and VEGF pathways in the vascular and nervous systems.Synapsin II desynchronizes neurotransmitter release at inhibitory synapses by interacting with presynaptic calcium channels.Functional Interaction between the Scaffold Protein Kidins220/ARMS and Neuronal Voltage-Gated Na+ Channels.ZDHHC3 Tyrosine Phosphorylation Regulates Neural Cell Adhesion Molecule Palmitoylation.Synaptic and extrasynaptic origin of the excitation/inhibition imbalance in the hippocampus of synapsin I/II/III knockout mice.Cortico-hippocampal hyperexcitability in synapsin I/II/III knockout mice: age-dependency and response to the antiepileptic drug levetiracetam.APache Is an AP2-Interacting Protein Involved in Synaptic Vesicle Trafficking and Neuronal Development.Imaging and structural studies of DNA-protein complexes and membrane ion channels.Graphene Oxide Nanosheets Disrupt Lipid Composition, Ca(2+) Homeostasis, and Synaptic Transmission in Primary Cortical Neurons.Delivery of Brain-Derived Neurotrophic Factor by 3D Biocompatible Polymeric Scaffolds for Neural Tissue Engineering and Neuronal Regeneration.Interfacing Graphene-Based Materials With Neural Cells.Fabrication of biocompatible free-standing nanopatterned films for primary neuronal culturesNanostructured Superhydrophobic Substrates Trigger the Development of 3D Neuronal NetworksSafety Assessment of Graphene-Based Materials: Focus on Human Health and the EnvironmentKidins220/ARMS transgenic lines could be instrumental in the understanding of the molecular mechanisms leading to spastic paraplegia and obesityKidins220/ARMS controls astrocyte calcium signaling and neuron-astrocyte communication
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description
researcher, ORCID id # 0000-0003-2190-6314
@en
wetenschapper
@nl
name
F Cesca
@nl
Fabrizia Cesca
@en
Fabrizia Cesca
@es
type
label
F Cesca
@nl
Fabrizia Cesca
@en
Fabrizia Cesca
@es
altLabel
F Cesca
@en
prefLabel
F Cesca
@nl
Fabrizia Cesca
@en
Fabrizia Cesca
@es
P106
P21
P31
P496
0000-0003-2190-6314