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Pubmed for Handhelds

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Journal Abstract Search

247 related items for PubMed ID: 33463481

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  • 5. KATP channel subunits in rat dorsal root ganglia: alterations by painful axotomy.
    Zoga V, Kawano T, Liang MY, Bienengraeber M, Weihrauch D, McCallum B, Gemes G, Hogan Q, Sarantopoulos C.
    Mol Pain; 2010 Jan 26; 6():6. PubMed ID: 20102598
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  • 6. Effects of ZD0947, a novel and potent ATP-sensitive K+ channel opener, on smooth muscle-type ATP-sensitive K+ channels.
    Mori K, Yamashita Y, Teramoto N.
    Eur J Pharmacol; 2016 Nov 15; 791():773-779. PubMed ID: 27693800
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  • 9. Sulfonylureas suppress the stimulatory action of Mg-nucleotides on Kir6.2/SUR1 but not Kir6.2/SUR2A KATP channels: a mechanistic study.
    Proks P, de Wet H, Ashcroft FM.
    J Gen Physiol; 2014 Nov 15; 144(5):469-86. PubMed ID: 25348414
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  • 12. Structure of an open KATP channel reveals tandem PIP2 binding sites mediating the Kir6.2 and SUR1 regulatory interface.
    Driggers CM, Kuo YY, Zhu P, ElSheikh A, Shyng SL.
    Nat Commun; 2024 Mar 20; 15(1):2502. PubMed ID: 38509107
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  • 13. The Pharmacology of ATP-Sensitive K+ Channels (KATP).
    Li Y, Aziz Q, Tinker A.
    Handb Exp Pharmacol; 2021 Mar 20; 267():357-378. PubMed ID: 34247283
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  • 15. ATP-sensitive potassium currents from channels formed by Kir6 and a modified cardiac mitochondrial SUR2 variant.
    Aggarwal NT, Shi NQ, Makielski JC.
    Channels (Austin); 2013 Mar 20; 7(6):493-502. PubMed ID: 24037327
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  • 16. Stoichiometry of sulfonylurea-induced ATP-sensitive potassium channel closure.
    Dörschner H, Brekardin E, Uhde I, Schwanstecher C, Schwanstecher M.
    Mol Pharmacol; 1999 Jun 20; 55(6):1060-6. PubMed ID: 10347249
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  • 17. ATP binding without hydrolysis switches sulfonylurea receptor 1 (SUR1) to outward-facing conformations that activate KATP channels.
    Sikimic J, McMillen TS, Bleile C, Dastvan F, Quast U, Krippeit-Drews P, Drews G, Bryan J.
    J Biol Chem; 2019 Mar 08; 294(10):3707-3719. PubMed ID: 30587573
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  • 20. Hybrid assemblies of ATP-sensitive K+ channels determine their muscle-type-dependent biophysical and pharmacological properties.
    Tricarico D, Mele A, Lundquist AL, Desai RR, George AL, Conte Camerino D.
    Proc Natl Acad Sci U S A; 2006 Jan 24; 103(4):1118-23. PubMed ID: 16418275
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