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Journal Abstract Search

511 related items for PubMed ID: 26910900

  • 1. Retigabine, a Kv7.2/Kv7.3-Channel Opener, Attenuates Drug-Induced Seizures in Knock-In Mice Harboring Kcnq2 Mutations.
    Ihara Y, Tomonoh Y, Deshimaru M, Zhang B, Uchida T, Ishii A, Hirose S.
    PLoS One; 2016; 11(2):e0150095. PubMed ID: 26910900
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  • 2. Sequence determinants of subtype-specific actions of KCNQ channel openers.
    Wang AW, Yang R, Kurata HT.
    J Physiol; 2017 Feb 01; 595(3):663-676. PubMed ID: 27506413
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  • 5. Functional and behavioral signatures of Kv7 activator drug subtypes.
    Kanyo R, Wang CK, Locskai LF, Li J, Allison WT, Kurata HT.
    Epilepsia; 2020 Aug 01; 61(8):1678-1690. PubMed ID: 32652600
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  • 6. Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization.
    Singh NA, Otto JF, Dahle EJ, Pappas C, Leslie JD, Vilaythong A, Noebels JL, White HS, Wilcox KS, Leppert MF.
    J Physiol; 2008 Jul 15; 586(14):3405-23. PubMed ID: 18483067
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  • 8. Personalized treatment with retigabine for pharmacoresistant epilepsy arising from a pathogenic variant in the KCNQ2 selectivity filter.
    Nissenkorn A, Kornilov P, Peretz A, Blumkin L, Heimer G, Ben-Zeev B, Attali B.
    Epileptic Disord; 2021 Oct 01; 23(5):695-705. PubMed ID: 34519644
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  • 9. Molecular Mechanisms and Structural Basis of Retigabine Analogues in Regulating KCNQ2 Channel.
    Shi S, Li J, Sun F, Chen Y, Pang C, Geng Y, Qi J, Guo S, Wang X, Zhang H, Zhan Y, An H.
    J Membr Biol; 2020 Apr 01; 253(2):167-181. PubMed ID: 32170353
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  • 11. The mechanism of action of retigabine (ezogabine), a first-in-class K+ channel opener for the treatment of epilepsy.
    Gunthorpe MJ, Large CH, Sankar R.
    Epilepsia; 2012 Mar 01; 53(3):412-24. PubMed ID: 22220513
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  • 15. Kv7.3 Compound Heterozygous Variants in Early Onset Encephalopathy Reveal Additive Contribution of C-Terminal Residues to PIP2-Dependent K+ Channel Gating.
    Ambrosino P, Freri E, Castellotti B, Soldovieri MV, Mosca I, Manocchio L, Gellera C, Canafoglia L, Franceschetti S, Salis B, Iraci N, Miceli F, Ragona F, Granata T, DiFrancesco JC, Taglialatela M.
    Mol Neurobiol; 2018 Aug 01; 55(8):7009-7024. PubMed ID: 29383681
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  • 18. The KCNQ2/3 selective channel opener ICA-27243 binds to a novel voltage-sensor domain site.
    Padilla K, Wickenden AD, Gerlach AC, McCormack K.
    Neurosci Lett; 2009 Nov 13; 465(2):138-42. PubMed ID: 19733209
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  • 19. Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits.
    Miceli F, Soldovieri MV, Ambrosino P, Barrese V, Migliore M, Cilio MR, Taglialatela M.
    Proc Natl Acad Sci U S A; 2013 Mar 12; 110(11):4386-91. PubMed ID: 23440208
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