These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
8. Role of sulfonylurea receptor type 1 subunits of ATP-sensitive potassium channels in myocardial ischemia/reperfusion injury. Elrod JW, Harrell M, Flagg TP, Gundewar S, Magnuson MA, Nichols CG, Coetzee WA, Lefer DJ. Circulation; 2008 Mar 18; 117(11):1405-13. PubMed ID: 18316485 [Abstract] [Full Text] [Related]
9. Diazoxide maintenance of myocyte volume and contractility during stress: evidence for a non-sarcolemmal K(ATP) channel location. Sellitto AD, Maffit SK, Al-Dadah AS, Zhang H, Schuessler RB, Nichols CG, Lawton JS. J Thorac Cardiovasc Surg; 2010 Nov 18; 140(5):1153-9. PubMed ID: 20804990 [Abstract] [Full Text] [Related]
10. N-terminal transmembrane domain of SUR1 controls gating of Kir6.2 by modulating channel sensitivity to PIP2. Pratt EB, Tewson P, Bruederle CE, Skach WR, Shyng SL. J Gen Physiol; 2011 Mar 18; 137(3):299-314. PubMed ID: 21321069 [Abstract] [Full Text] [Related]
11. HMR 1098 is not an SUR isotype specific inhibitor of heterologous or sarcolemmal K ATP channels. Zhang HX, Akrouh A, Kurata HT, Remedi MS, Lawton JS, Nichols CG. J Mol Cell Cardiol; 2011 Mar 18; 50(3):552-60. PubMed ID: 21185839 [Abstract] [Full Text] [Related]
12. Disruption of sarcolemmal ATP-sensitive potassium channel activity impairs the cardiac response to systolic overload. Hu X, Xu X, Huang Y, Fassett J, Flagg TP, Zhang Y, Nichols CG, Bache RJ, Chen Y. Circ Res; 2008 Oct 24; 103(9):1009-17. PubMed ID: 18802029 [Abstract] [Full Text] [Related]
13. Transgenic overexpression of SUR1 in the heart suppresses sarcolemmal K(ATP). Flagg TP, Remedi MS, Masia R, Gomes J, McLerie M, Lopatin AN, Nichols CG. J Mol Cell Cardiol; 2005 Oct 24; 39(4):647-56. PubMed ID: 16099470 [Abstract] [Full Text] [Related]
14. Random assembly of SUR subunits in K(ATP) channel complexes. Cheng WW, Tong A, Flagg TP, Nichols CG. Channels (Austin); 2008 Oct 24; 2(1):34-8. PubMed ID: 18690055 [Abstract] [Full Text] [Related]
15. Antisense oligodeoxynucleotides of sulfonylurea receptors inhibit ATP-sensitive K+ channels in cultured neonatal rat ventricular cells. Yokoshiki H, Sunagawa M, Seki T, Sperelakis N. Pflugers Arch; 1999 Feb 24; 437(3):400-8. PubMed ID: 9914396 [Abstract] [Full Text] [Related]
17. Sulfonylurea receptors type 1 and 2A randomly assemble to form heteromeric KATP channels of mixed subunit composition. Chan KW, Wheeler A, Csanády L. J Gen Physiol; 2008 Jan 24; 131(1):43-58. PubMed ID: 18079561 [Abstract] [Full Text] [Related]
18. Syntaxin-1A inhibits KATP channels by interacting with specific conserved motifs within sulfonylurea receptor 2A. Chao C, Liang T, Kang Y, Lin X, Xie H, Feng ZP, Gaisano HY. J Mol Cell Cardiol; 2011 Nov 24; 51(5):790-802. PubMed ID: 21884702 [Abstract] [Full Text] [Related]
19. Characterization of K(ATP)-channels in rat basilar and middle cerebral arteries: studies of vasomotor responses and mRNA expression. Jansen-Olesen I, Mortensen CH, El-Bariaki N, Ploug KB. Eur J Pharmacol; 2005 Oct 31; 523(1-3):109-18. PubMed ID: 16226739 [Abstract] [Full Text] [Related]
20. The ATP-sensitive K(+) channel ABCC8 S1369A type 2 diabetes risk variant increases MgATPase activity. Fatehi M, Raja M, Carter C, Soliman D, Holt A, Light PE. Diabetes; 2012 Jan 31; 61(1):241-9. PubMed ID: 22187380 [Abstract] [Full Text] [Related] Page: [Next] [New Search]