UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

NMDA Receptors in the Central Nervous System

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

2017

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

2003

Volltextzugriff (PDF)

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

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

2017

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Selective Cell-Surface Expression of Triheteromeric NMDA Receptors

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

2017

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Analysis of Functional NMDA Receptors in Astrocytes

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

Kirchhoff, Frank

2017

Volltextzugriff (PDF)

Detection of NMDARs Antibodies in Encephalitis

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

2017

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Transfection in Primary Cultured Neuronal Cells

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

2017

Volltextzugriff (PDF)

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

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

2017

Volltextzugriff (PDF)

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

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

2017

Volltextzugriff (PDF)

Genetic and Functional Analysis of GRIN2A in Tumor Samples

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

2017

Volltextzugriff (PDF)

Electrophysiological Investigation of NMDA Current Properties in Brain Slices

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

2017

Volltextzugriff (PDF)

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

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

2017

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

NMDA Receptors as Voltage Sensors

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

Khazipov, Roustem

2017

Volltextzugriff (PDF)

GluNs Detection and Functions in Microglial Cells

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

2017

Volltextzugriff (PDF)

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

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

2004

Volltextzugriff (PDF)

Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse

American journal of human genetics, 2002-03, Vol.70 (3), p.726-736

2002

Volltextzugriff (PDF)

Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16

American journal of human genetics, 1997-10, Vol.61 (4), p.889-898

1997

Volltextzugriff (PDF)

Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis Syndrome

American journal of human genetics, 2001-03, Vol.68 (3), p.788-794

2001

Volltextzugriff (PDF)

1 – 25 von 76

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(53)
Mit Volltextzugriff
(46)

Publikationsform

Artikel
(76)

Sprache

Englisch
(71)
Französisch
(5)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(54)
Science & Technology
(54)
Humans
(51)
Neurosciences & Neurology
(30)
Animals
(25)
Biological And Medical Sciences
(24)
Genetics & Heredity
(23)
Biochemistry & Molecular Biology
(21)
Female
(21)
Medical Sciences
(18)
Neurosciences
(18)
Biochemical Research Methods
(17)
Male
(17)
Chromosome Mapping
(16)
Receptors, N-Methyl-D-Aspartate - Metabolism
(16)
Rezeptor
(15)
Chromosomes, Human, Pair 11
(13)
Clinical Neurology
(13)
Neurology
(13)
Pedigree
(13)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

NMDA Receptors in the Central Nervous System

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

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

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

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

Genetic and Functional Analysis of GRIN2A in Tumor Samples

Electrophysiological Investigation of NMDA Current Properties in Brain Slices

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

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

Quantification of NMDAR Subunit Genes Expression by qRT-PCR

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

NMDA Receptors as Voltage Sensors

GluNs Detection and Functions in Microglial Cells

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

Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse

Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16

Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis Syndrome

Suchergebnisse filtern