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NMDA Receptors in the Central Nervous System

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1677, p.1

2017

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Genetics of infantile seizures with paroxysmal dyskinesia: the infantile convulsions and choreoathetosis (ICCA) and ICCA-related syndromes

Journal of medical genetics, 2008-12, Vol.45 (12), p.773-779

2008

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Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortex

Brain (London, England : 1878), 2006-03, Vol.129 (3), p.625-641

2006

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PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome

Neurology, 2003-06, Vol.60 (11), p.1811

2003

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NMDA Receptor Activity in Circulating Red Blood Cells: Methods of Detection

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.265

2017

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OP13 – 2799: Landau-Kleffner syndrome (LKS), continuous spike and waves during slow-wave sleep syndrome (CSWSS), and Rolandic epilepsy (RE) – A genetic and immunological study

European journal of paediatric neurology, 2015-05, Vol.19, p.S5-S5

2015

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Selective Cell-Surface Expression of Triheteromeric NMDA Receptors

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.145

2017

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Analysis of the dinucleotide repeat polymorphism in the epidermal growth factor receptor (EGFR) gene in head and neck cancer patients

Annals of oncology, 2005-06, Vol.16 (6), p.934-941

2005

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Analysis of Functional NMDA Receptors in Astrocytes

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1677, p.241

Kirchhoff, Frank

2017

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Detection of NMDARs Antibodies in Encephalitis

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.117

2017

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Magnetofection™ of NMDA Receptor Subunits GluN1 and GluN2A Expression Vectors in Non-Neuronal Host Cells

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.129

2017

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Transfection in Primary Cultured Neuronal Cells

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.137

2017

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Genetic and Functional Analysis of GRIN2A in Tumor Samples

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.93

2017

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Design of Light-Sensitive NMDARs by Genetically Encoded Photo-Cross-Linkers

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.185

2017

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Gene Targeted Mice with Conditional Knock-In (-Out) of NMDAR Mutations

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.201

2017

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Electrophysiological Investigation of NMDA Current Properties in Brain Slices

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.231

2017

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GluN2B Subunit Labeling with Fluorescent Probes and High-Resolution Live Imaging

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1677, p.171

2017

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Development of a Computational Approach/Model to Explore NMDA Receptors Functions

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.291

2017

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Quantification of NMDAR Subunit Genes Expression by qRT-PCR

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.83

Pallesi-Pocachard, Emilie

2017

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NMDA Receptors as Voltage Sensors

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.283

Khazipov, Roustem

2017

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Functional Analysis of Recombinant Channels in Host Cells Using a Fast Agonist Application System

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.163

2017

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GluNs Detection and Functions in Microglial Cells

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1677, p.253

2017

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Severe epilepsy, retardation, and dysmorphic features with a 2q deletion including SCN1A and SCN2A

Neurology, 2004-07, Vol.63 (1), p.191-192

2004

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PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine

Neurology, 2012-11, Vol.79 (21), p.2097-2103

2012

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SRPX2 mutations in disorders of language cortex and cognition

NMDA Receptors in the Central Nervous System

Genetics of infantile seizures with paroxysmal dyskinesia: the infantile convulsions and choreoathetosis (ICCA) and ICCA-related syndromes

Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortex

PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome

NMDA Receptor Activity in Circulating Red Blood Cells: Methods of Detection

OP13 – 2799: Landau-Kleffner syndrome (LKS), continuous spike and waves during slow-wave sleep syndrome (CSWSS), and Rolandic epilepsy (RE) – A genetic and immunological study

Selective Cell-Surface Expression of Triheteromeric NMDA Receptors

Analysis of the dinucleotide repeat polymorphism in the epidermal growth factor receptor (EGFR) gene in head and neck cancer patients

Analysis of Functional NMDA Receptors in Astrocytes

Detection of NMDARs Antibodies in Encephalitis

Magnetofection™ of NMDA Receptor Subunits GluN1 and GluN2A Expression Vectors in Non-Neuronal Host Cells

Transfection in Primary Cultured Neuronal Cells

Genetic and Functional Analysis of GRIN2A in Tumor Samples

Design of Light-Sensitive NMDARs by Genetically Encoded Photo-Cross-Linkers

Gene Targeted Mice with Conditional Knock-In (-Out) of NMDAR Mutations

Electrophysiological Investigation of NMDA Current Properties in Brain Slices

GluN2B Subunit Labeling with Fluorescent Probes and High-Resolution Live Imaging

Development of a Computational Approach/Model to Explore NMDA Receptors Functions

Quantification of NMDAR Subunit Genes Expression by qRT-PCR

NMDA Receptors as Voltage Sensors

Functional Analysis of Recombinant Channels in Host Cells Using a Fast Agonist Application System

GluNs Detection and Functions in Microglial Cells

Severe epilepsy, retardation, and dysmorphic features with a 2q deletion including SCN1A and SCN2A

PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine

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