Search Results - "Becq, Hélène"
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The conversion of glutamate by glutamine synthase in neocortical astrocytes from juvenile rat is important to limit glutamate spillover and peri/extrasynaptic activation of NMDA receptors
Published in Glia (01-02-2017)“…Glutamate transporters (EAATs) are important to maintain spatial and temporal specificity of synaptic transmission. Their efficiency to uptake and transport…”
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A Kv7.2 mutation associated with early onset epileptic encephalopathy with suppression‐burst enhances Kv7/M channel activity
Published in Epilepsia (Copenhagen) (01-05-2016)“…Summary Mutations in the KCNQ2 gene encoding the voltage‐gated potassium channel subunit Kv7.2 cause early onset epileptic encephalopathy (EOEE). Most…”
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A recurrent KCNQ2 pore mutation causing early onset epileptic encephalopathy has a moderate effect on M current but alters subcellular localization of Kv7 channels
Published in Neurobiology of disease (01-08-2015)“…Abstract Mutations in the KCNQ2 gene encoding the voltage-dependent potassium M channel Kv7.2 subunit cause either benign epilepsy or early onset epileptic…”
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Knocking down of the KCC2 in rat hippocampal neurons increases intracellular chloride concentration and compromises neuronal survival
Published in The Journal of physiology (15-05-2011)“…Non‐technical summary ‘To be, or not to be’– thousands of neurons are facing this Shakespearean question in the brains of patients suffering from epilepsy or…”
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The Epilepsy of Infancy With Migrating Focal Seizures: Identification of de novo Mutations of the KCNT2 Gene That Exert Inhibitory Effects on the Corresponding Heteromeric KNa1.1/KNa1.2 Potassium Channel
Published in Frontiers in cellular neuroscience (24-01-2020)“…Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) (previously called Malignant migrating partial seizures of infancy) are early-onset epileptic…”
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A possible link between KCNQ2‐ and STXBP1‐related encephalopathies: STXBP1 reduces the inhibitory impact of syntaxin‐1A on M current
Published in Epilepsia (Copenhagen) (01-12-2017)“…Summary Objective Kv7 channels mediate the voltage‐gated M‐type potassium current. Reduction of M current due to KCNQ2 mutations causes early onset epileptic…”
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Inhibition of Glutamate Transporters Results in a “Suppression‐Burst” Pattern and Partial Seizures in the Newborn Rat
Published in Epilepsia (Copenhagen) (01-01-2007)“…Purpose: To determine the electrophysiological pattern and propose a clinical relevance of a deficient glutamate transport in the developing brain. Methods:…”
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Time‐limited alterations in cortical activity of a knock‐in mouse model of KCNQ2‐related developmental and epileptic encephalopathy
Published in The Journal of physiology (01-05-2022)“…De novo missense variants in the KCNQ2 gene encoding the Kv7.2 subunit of voltage‐gated potassium Kv7/M channels are the main cause of developmental and…”
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Inhibition of the Mitochondrial Glutamate Carrier SLC25A22 in Astrocytes Leads to Intracellular Glutamate Accumulation
Published in Frontiers in cellular neuroscience (31-05-2017)“…The solute carrier family 25 (SLC25) drives the import of a large diversity of metabolites into mitochondria, a key cellular structure involved in many…”
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An epilepsy-related ARX polyalanine expansion modifies glutamatergic neurons excitability and morphology without affecting GABAergic neurons development
Published in Cerebral cortex (New York, N.Y. 1991) (01-06-2013)“…Epileptic encephalopathies comprise a heterogeneous group of severe infantile disorders for which the pathophysiological basis of epilepsy is inaccurately…”
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Dynamic changes in interneuron morphophysiological properties mark the maturation of hippocampal network activity
Published in The Journal of neuroscience (09-05-2012)“…During early postnatal development, neuronal networks successively produce various forms of spontaneous patterned activity that provide key signals for circuit…”
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Abnormal Network Activity in a Targeted Genetic Model of Human Double Cortex
Published in The Journal of neuroscience (14-01-2009)“…In human patients, cortical dysplasia produced by Doublecortin (DCX) mutations lead to mental retardation and intractable infantile epilepsies, but the…”
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Spontaneous Epileptic Manifestations in a DCX Knockdown Model of Human Double Cortex
Published in Cerebral cortex (New York, N.Y. 1991) (01-11-2010)“…Previous reports indicate that in utero knockdown of doublecortin (DCX) results in the genesis of a subcortical heterotopia reminiscent of the doublecortex…”
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Paracrine intercellular communication by a Ca2+- and SNARE-independent release of GABA and glutamate prior to synapse formation
Published in Neuron (Cambridge, Mass.) (19-12-2002)“…GABA and glutamate receptors are expressed in immature "silent" CA1 pyramidal neurons prior to synapse formation, but their function is unknown. We now report…”
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Glutamate Transporters Prevent the Generation of Seizures in the Developing Rat Neocortex
Published in The Journal of neuroscience (31-03-2004)“…Glutamate transporters are operative at an early developmental stage well before synapse formation, but their functional significance has not been determined…”
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A possible link between KCNQ 2 ‐ and STXBP 1 ‐related encephalopathies: STXBP 1 reduces the inhibitory impact of syntaxin‐1A on M current
Published in Epilepsia (Copenhagen) (01-12-2017)Get full text
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18
The Epilepsy of Infancy With Migrating Focal Seizures: Identification of de novo Mutations of the KCNT2 Gene That Exert Inhibitory Effects on the Corresponding Heteromeric K Na 1.1/K Na 1.2 Potassium Channel
Published in Frontiers in cellular neuroscience (2020)“…The epilepsy of infancy with migrating focal seizures (EIMFS; previously called Malignant migrating partial seizures of infancy) are early-onset epileptic…”
Get full text
Journal Article -
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Paracrine Intercellular Communication by a Ca 2+- and SNARE-Independent Release of GABA and Glutamate Prior to Synapse Formation
Published in Neuron (Cambridge, Mass.) (19-12-2002)“…GABA and glutamate receptors are expressed in immature “silent” CA1 pyramidal neurons prior to synapse formation, but their function is unknown. We now report…”
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Quantal Release of Glutamate Generates Pure Kainate and Mixed AMPA/Kainate EPSCs in Hippocampal Neurons
Published in Neuron (Cambridge, Mass.) (03-07-2002)“…The relative contribution of kainate receptors to ongoing glutamatergic activity is at present unknown. We report the presence of spontaneous, miniature, and…”
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