Netrin-G2 dysfunction causes a Rett-like phenotype with areflexia

Keyphrases

• Areflexia 100%
• Rett-like 100%
• Netrin-G2 100%
• Rett Syndrome 80%
• Netrin 40%
• Knockdown 40%
• NTNG1 40%
• Neuronal Morphology 40%
• Early Brain Development 20%
• N-methyl-D-aspartate 20%
• Gene Knockout 20%
• Family Members 20%
• G Protein 20%
• Genetic Causes 20%
• Whole Exome Sequencing 20%
• Cortical Migration 20%
• Axonal Guidance 20%
• Primary Hippocampal Neurons 20%
• Methyl-CpG-binding Protein 2 (MeCP2) 20%
• Neurodevelopmental Phenotypes 20%
• G-family 20%
• Homozygous Frameshift mutation 20%
• Short Hairpin RNA (shRNA) 20%
• Synaptic Transmission 20%
• Sanger Sequencing 20%
• Neuronal Migration 20%
• Neurodevelopmental Defects 20%
• Functional Studies 20%
• In Utero Electroporation 20%
• Severe Impairment 20%
• Nonsense-mediated Decay 20%
• Targeted Gene 20%

Neuroscience

• Netrin 100%
• Rett Syndrome 57%
• Synaptic Transmission 14%
• In Vivo 14%
• Brain Development 14%
• Dextro Aspartic Acid 14%
• G Protein 14%
• Gene Knockdown 14%
• Small Hairpin RNA 14%
• Nonsense Mediated mRNA Decay 14%
• Electroporation 14%
• Exome Sequencing 14%
• Methyl CpG Binding Protein 2 14%
• Transfection 14%
• Frameshift Mutation 14%
• Dideoxynucleotide Sequencing 14%