A Human TSC1 Variant Screening Platform in Gabaergic Cortical Interneurons for Genotype to Phenotype Assessments-Reference-Cited by-同舟云学术

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A Human TSC1 Variant Screening Platform in Gabaergic Cortical Interneurons for Genotype to Phenotype Assessments

Published:2020-09-18 Issue: Volume:13 Page:
ISSN:1662-5099
Container-title:Frontiers in Molecular Neuroscience
language:
Short-container-title:Front. Mol. Neurosci.

Author:

Wundrach Dean,Martinetti Luis E.,Stafford April M.,Bilinovich Stephanie M.,Angara Kartik,Prokop Jeremy W.,Crandall Shane R.,Vogt Daniel

Publisher

Frontiers Media SA

Subject

Cellular and Molecular Neuroscience,Molecular Biology

Reference35 articles.

1. Nf1 deletion results in depletion of the Lhx6 transcription factor and a specific loss of parvalbumin+ cortical interneurons;Angara;Proc. Natl. Acad. Sci. U S A,2020

2. Dapper antagonist of catenin-1 cooperates with dishevelled-1 during postsynaptic development in mouse forebrain GABAergic interneurons;Arguello;PLoS One,2013

3. Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder;Bahl;Mol. Autism.,2013

4. Parvalbumin in most gamma-aminobutyric acid-containing neurons of the rat cerebral cortex;Celio;Science,1986

5. A corticothalamic switch: controlling the thalamus with dynamic synapses;Crandall;Neuron,2015

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