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Keyphrases
Loss Function
100%
Brain Development
100%
Neuronal Migration
100%
Protocadherin 19
100%
PCDH19
44%
Central Nervous System
11%
X-linked Genes
11%
Cassette
11%
Loss of Heterozygosity
11%
Cell Adhesion
11%
Gain-of-function mutation
11%
Adult Brain
11%
Motility
11%
Null Allele
11%
Postnatal Brain
11%
Embryonic Brain
11%
Migration Assay
11%
Null Cell
11%
Morphological Defects
11%
Epilepsy Syndrome
11%
Human Epilepsy
11%
Axon Guidance
11%
Childhood Epilepsy
11%
Axon-dendrite
11%
Protocadherin
11%
In Vitro Migration
11%
Self-avoidance
11%
Endogenous Promoter
11%
PCDH19 mutation
11%
Mammalian Model
11%
Girls Clustering Epilepsy
11%
Neuroscience
In Vitro
100%
Brain Development
100%
Neuronal Migration
100%
Epilepsy
66%
In Vivo
33%
Promoter Region
33%
Central Nervous System
33%
Dendrite
33%
Cell Adhesion
33%
Axon Guidance
33%
Loss of Function Mutation
33%
Pediatric Epilepsy
33%
Null Allele
33%
Biochemistry, Genetics and Molecular Biology
Brain Development
100%
Protocadherin
100%
Morphology
10%
Promoter Region
10%
X Chromosomal Inheritance
10%
Cell Adhesion
10%
Loss of Function Mutation
10%
Null Allele
10%
Axon Guidance
10%
Mammalian Model
10%
Dendrite
10%