1. ホーム
  2. 一覧
論文 特許

論文 - 一覧

  • 16 Hits
  • 検索条件 : 絞込み (MeSH = Membrane Potentials / genetics)
生物種 リソース名 タイトル
線虫 tm776 A V-to-F substitution in SK2 channels causes Ca2+ hypersensitivity and improves locomotion in a C. elegans ALS model.
原核生物(大腸菌) Obg and Membrane Depolarization Are Part of a Microbial Bet-Hedging Strategy that Leads to Antibiotic Tolerance.
線虫 tm6834 Complex Locomotion Behavior Changes Are Induced in Caenorhabditis elegans by the Lack of the Regulatory Leak K+ Channel TWK-7.
線虫 tm1392 , tm2913 Amphetamine potentiates the effects of β-phenylethylamine through activation of an amine-gated chloride channel.
線虫 tm2034 Toxic role of K+ channel oxidation in mammalian brain.
線虫 tm1552 The DEG/ENaC protein MEC-10 regulates the transduction channel complex in Caenorhabditis elegans touch receptor neurons.
線虫 tm2484 A seven-transmembrane receptor that mediates avoidance response to dihydrocaffeic acid, a water-soluble repellent in Caenorhabditis elegans.
ラット F344-Adms/Kyo(strainID=724) Kcna1-mutant rats dominantly display myokymia, neuromyotonia and spontaneous epileptic seizures.
ラット 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).
ショウジョウバエ Kinesin heavy chain function in Drosophila glial cells controls neuronal activity.
線虫 tm1896 Interactions between innexins UNC-7 and UNC-9 mediate electrical synapse specificity in the Caenorhabditis elegans locomotory nervous system.
線虫 tm2913 A tyramine-gated chloride channel coordinates distinct motor programs of a Caenorhabditis elegans escape response.
オオムギ EST clones An aluminum-activated citrate transporter in barley.
ラット GRY/Idr(strainID=498) Increased Ca2+ channel currents in cerebellar Purkinje cells of the ataxic groggy rat.
線虫 tm1402 Caenorhabditis elegans TRPA-1 functions in mechanosensation.
ラット 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.