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  • Search Condition : Filter (MeSH = Membrane Potentials / genetics)
Species Resource Title
C.elegans tm776 A V-to-F substitution in SK2 channels causes Ca2+ hypersensitivity and improves locomotion in a C. elegans ALS model.
Prokaryotes E. coli Obg and Membrane Depolarization Are Part of a Microbial Bet-Hedging Strategy that Leads to Antibiotic Tolerance.
C.elegans tm6834 Complex Locomotion Behavior Changes Are Induced in Caenorhabditis elegans by the Lack of the Regulatory Leak K+ Channel TWK-7.
C.elegans tm1392 , tm2913 Amphetamine potentiates the effects of β-phenylethylamine through activation of an amine-gated chloride channel.
C.elegans tm2034 Toxic role of K+ channel oxidation in mammalian brain.
C.elegans tm1552 The DEG/ENaC protein MEC-10 regulates the transduction channel complex in Caenorhabditis elegans touch receptor neurons.
C.elegans tm2484 A seven-transmembrane receptor that mediates avoidance response to dihydrocaffeic acid, a water-soluble repellent in Caenorhabditis elegans.
Rats F344-Adms/Kyo(strainID=724) Kcna1-mutant rats dominantly display myokymia, neuromyotonia and spontaneous epileptic seizures.
Rats SER/Kyo(strainID=28) Inhibitory effects of levetiracetam on the high-voltage-activated L-type Ca²⁺ channels in hippocampal CA3 neurons of spontaneously epileptic rat (SER).
Drosophila Kinesin heavy chain function in Drosophila glial cells controls neuronal activity.
C.elegans tm1896 Interactions between innexins UNC-7 and UNC-9 mediate electrical synapse specificity in the Caenorhabditis elegans locomotory nervous system.
C.elegans tm2913 A tyramine-gated chloride channel coordinates distinct motor programs of a Caenorhabditis elegans escape response.
Barley EST clones An aluminum-activated citrate transporter in barley.
Rats GRY/Idr(strainID=498) Increased Ca2+ channel currents in cerebellar Purkinje cells of the ataxic groggy rat.
C.elegans tm1402 Caenorhabditis elegans TRPA-1 functions in mechanosensation.
Rats GRY/Idr(strainID=498) , BN/SsNSlc(strainID=371) The ataxic groggy rat has a missense mutation in the P/Q-type voltage-gated Ca2+ channel alpha1A subunit gene and exhibits absence seizures.