Biochemistry, Genetics and Molecular Biology
Agonist
20%
Allele
8%
Aspartic Acid
13%
Binding Domain
6%
Binding Site
20%
Bioinformatics
10%
C-Terminus
6%
Calcium Transport
6%
Case-Control Study
10%
Cholinergic
20%
CNTNAP2
20%
Comorbidity
15%
Confocal Microscopy
6%
Copy-Number Variation
20%
Gene Frequency
10%
Gene Linkage
38%
Gene Locus
20%
Genetic Risk
14%
Genetics
68%
Genotyping
17%
Glutamate Receptor
6%
Glutamic Acid
13%
GRIN2A
68%
HEK 293 Cells
6%
Inherited Mutation
6%
Language Ability
10%
Linkage Analysis
7%
Major Gene
6%
MicroRNA
20%
Minor Allele Frequency
10%
Missense Mutation
6%
NMDA Receptor
24%
Patch Clamp Technique
6%
Patient Coding
6%
PAX6
30%
Pedigree
9%
Prevalence
20%
Proband
22%
Rare Variant
10%
Receptor Gene
6%
Rolandic Epilepsy
100%
Sex Chromosome Aneuploidies
20%
Single Nucleotide Polymorphism
12%
Single-Nucleotide Polymorphism
23%
Slow-Wave Sleep
17%
Speech and Language
23%
Spike
54%
Synapse
20%
Western Blot
6%
Written Language
13%
Neuroscience
Agonist
13%
Allele Frequency
20%
Aphasia
6%
Aspartic Acid
10%
Attention Deficit Hyperactivity Disorder
20%
Autism
25%
Benign Epilepsy
10%
Brain Disease
25%
C-Terminus
6%
Calcium Transport
6%
Childhood Absence Epilepsy
13%
Cholinergic
20%
Comparative Genomics
5%
Copy Number Variation
41%
Dyslexia
20%
Epileptic Absence
20%
Exome Sequencing
10%
Focal Epilepsy
41%
Gene Locus
20%
Glutamic Acid
13%
GRIN2A
68%
HEK 293 Cells
6%
Hyperactivity
10%
KCNA2
10%
KCNB1
10%
Landau Kleffner Syndrome
25%
Language Disorder
10%
Language Disorders
20%
MECP2
10%
Migraine
20%
Missense Mutation
6%
N Methyl Dextro Aspartic Acid Receptor 2A
5%
NMDA Receptor
20%
Patch Clamp Technique
6%
PAX6
10%
Pediatric Epilepsy
8%
Pervasive Developmental Disorder
30%
Positive Allosteric Modulator
6%
Receptor
6%
Receptor Agonist
20%
Receptor Gene
6%
Receptor Trafficking
20%
Rolandic Epilepsy
75%
Seizure Types
10%
Single-Nucleotide Polymorphism
22%
Slow-Wave Sleep
13%
Speech Disorder
5%
Spike-and-Wave
13%
Synapse
22%
Western Blot
6%
Medicine and Dentistry
Allosteric Modulator
6%
Aphasia
6%
Benign Childhood Epilepsy
25%
Benign Epilepsy
10%
Brain Disease
27%
Calcium Transport
6%
Carboxy Terminal Sequence
6%
Cell Surface
6%
Cholinergic Synapse
20%
Comorbidity
6%
Confocal Microscopy
6%
Disease
17%
Epilepsy Syndromes
12%
Epileptic Seizure
12%
Exon
5%
Fisher Exact Test
10%
Flux Assay
6%
Genetic Analysis
20%
Genetic Risk Factor
5%
Glutamate Receptor Agonist
6%
Glutamic Acid
6%
Glycine Receptor Agonist
6%
GRIN2A
68%
HEK 293 Cells
6%
Landau-Kleffner Syndrome
27%
Language Disorder
10%
Missense Mutation
6%
Molecular Profiling
20%
Multimodal Imaging
10%
N Methyl Dextro Aspartic Acid Receptor 2A
5%
N Methyl-D-Aspartate Receptor
6%
NMDA Receptor
20%
Partial Epilepsy
5%
Partial Seizure
61%
Patch Clamp
6%
Patient-Data
6%
Pediatric Epilepsy
20%
Receptor
6%
Receptor Gene
6%
Rolandic Epilepsy
56%
Slow-Wave Sleep
15%
Specific Language Impairment
10%
Speech and Language
20%
Speech Disorder
8%
Speech Sound Disorder
10%
Western Blot
6%
