Pathogenic potential of human SLC12A5 variants causing KCC2 dysfunction
Authors:
Open Access
- 1 May 2019
- journal article
- review article
- Published by Elsevier in Brain Research
- Vol. 1710, 1-7
Abstract
No abstract availableKeywords
Funding Information
- Japan Society for the Promotion of Science
- Ministry of Education, Culture, Sports, Science and Technology (17H04025, 17K19682)
This publication has 52 references indexed in Scilit:
- Hyperpolarizing GABAergic Transmission Requires the KCC2 C-Terminal ISO DomainJournal of Neuroscience, 2012
- Taurine Inhibits K+-Cl− Cotransporter KCC2 to Regulate Embryonic Cl− Homeostasis via With-no-lysine (WNK) Protein Kinase Signaling PathwayJournal of Biological Chemistry, 2012
- Cortical parvalbumin interneurons and cognitive dysfunction in schizophreniaTrends in Neurosciences, 2012
- Tyrosine phosphorylation regulates the membrane trafficking of the potassium chloride co-transporter KCC2Molecular and Cellular Neuroscience, 2010
- Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental RetardationArchives of General Psychiatry, 2009
- Making sense of nonsense GABAA receptor mutations associated with genetic epilepsiesTrends in Molecular Medicine, 2009
- Sites of Regulated Phosphorylation that Control K-Cl Cotransporter ActivityCell, 2009
- Defining the role of GABA in cortical developmentThe Journal of Physiology, 2009
- Alterations in GABA-related transcriptome in the dorsolateral prefrontal cortex of subjects with schizophreniaMolecular Psychiatry, 2007
- Is there more to gaba than synaptic inhibition?Nature Reviews Neuroscience, 2002