IndraLab
Statements
Gamma-aminobutyric acid activates KCNQ3. 14 / 14
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2
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reach
"Electrophysiological recordings of cloned channels in Xenopus oocytes and CHO cells and endogenous M-current in PC12 cells and mouse dorsal root ganglia (DRG) neurons showed that KCNQ3 and 5, but not KCNQ2 or 4, are " activated " by sub-micromolar to micromolar levels of GABA, making these channels more sensitive than many canonical GABA receptors."
reach
"Here, phylogenetic analysis, electrostatic potential mapping, in silico docking, electrophysiology, and radioligand binding assays reveal that the anticonvulsant binding pocket evolved to accommodate endogenous neurotransmitters including gamma-aminobutyric acid (GABA), which directly activates KCNQ5 and KCNQ3 via W265."
reach
"Here, phylogenetic analysis, electrostatic potential mapping, in silico docking, electrophysiology, and radioligand binding assays reveal that the anticonvulsant binding pocket evolved to accommodate endogenous neurotransmitters including gamma-aminobutyric acid (GABA), which directly activates KCNQ5 and KCNQ3 via W265."
reach
"Here, phylogenetic analysis, electrostatic potential mapping, in silico docking, electrophysiology, and radioligand binding assays reveal that the anticonvulsant binding pocket evolved to accommodate endogenous neurotransmitters including gamma-aminobutyric acid (GABA), which directly activates KCNQ5 and KCNQ3 via W265."