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Journal Abstract Search

445 related items for PubMed ID: 16735477

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  • 3. Calmodulin orchestrates the heteromeric assembly and the trafficking of KCNQ2/3 (Kv7.2/3) channels in neurons.
    Liu W, Devaux JJ.
    Mol Cell Neurosci; 2014 Jan; 58():40-52. PubMed ID: 24333508
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  • 4. An Ankyrin-G N-terminal Gate and Protein Kinase CK2 Dually Regulate Binding of Voltage-gated Sodium and KCNQ2/3 Potassium Channels.
    Xu M, Cooper EC.
    J Biol Chem; 2015 Jul 03; 290(27):16619-32. PubMed ID: 25998125
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  • 5. Heteromeric Assembly of Truncated Neuronal Kv7 Channels: Implications for Neurologic Disease and Pharmacotherapy.
    Li J, Maghera J, Lamothe SM, Marco EJ, Kurata HT.
    Mol Pharmacol; 2020 Sep 03; 98(3):192-202. PubMed ID: 32580997
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  • 6. Requirement of subunit co-assembly and ankyrin-G for M-channel localization at the axon initial segment.
    Rasmussen HB, Frøkjaer-Jensen C, Jensen CS, Jensen HS, Jørgensen NK, Misonou H, Trimmer JS, Olesen SP, Schmitt N.
    J Cell Sci; 2007 Mar 15; 120(Pt 6):953-63. PubMed ID: 17311847
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  • 8. Structural determinants of M-type KCNQ (Kv7) K+ channel assembly.
    Schwake M, Athanasiadu D, Beimgraben C, Blanz J, Beck C, Jentsch TJ, Saftig P, Friedrich T.
    J Neurosci; 2006 Apr 05; 26(14):3757-66. PubMed ID: 16597729
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  • 10. A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon.
    Pan Z, Kao T, Horvath Z, Lemos J, Sul JY, Cranstoun SD, Bennett V, Scherer SS, Cooper EC.
    J Neurosci; 2006 Mar 08; 26(10):2599-613. PubMed ID: 16525039
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  • 12. Identification by mass spectrometry and functional characterization of two phosphorylation sites of KCNQ2/KCNQ3 channels.
    Surti TS, Huang L, Jan YN, Jan LY, Cooper EC.
    Proc Natl Acad Sci U S A; 2005 Dec 06; 102(49):17828-33. PubMed ID: 16319223
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  • 15. Developmental changes in KCNQ2 and KCNQ3 expression in human brain: possible contribution to the age-dependent etiology of benign familial neonatal convulsions.
    Kanaumi T, Takashima S, Iwasaki H, Itoh M, Mitsudome A, Hirose S.
    Brain Dev; 2008 May 06; 30(5):362-9. PubMed ID: 18166285
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  • 20. Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC).
    Bassi MT, Balottin U, Panzeri C, Piccinelli P, Castaldo P, Barrese V, Soldovieri MV, Miceli F, Colombo M, Bresolin N, Borgatti R, Taglialatela M.
    Neurogenetics; 2005 Dec 06; 6(4):185-93. PubMed ID: 16235065
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