Citations for
1ABCC9, NKAPL, TMEM132C
ABCC9, NKAPL, and TMEM132C are potential diagnostic and prognostic markers in triple-negative breast cancer
Zhang X, Kang X, Jin L, Bai J, Zhang H, Liu W, Wang Z.
Cell Biol Int. Oct;44(10):2002-2010. doi: 10.1002/cbin.11406. Epub 2020 Jul 1. 2020
2ABCC9, HCOD
Dominant missense mutations in ABCC9 cause Cantú syndrome.
Harakalova M, van Harssel JJ, Terhal PA, van Lieshout S, Duran K, Renkens I, Amor DJ, Wilson LC, Kirk EP, Turner CL, Shears D, Garcia-Minaur S, Lees MM, Ross A, Venselaar H, Vriend G, Takanari H, Rook MB, van der Heyden MA, Asselbergs FW, Breur HM, Swinkels ME, Scurr IJ, Smithson SF, Knoers NV, van der Smagt JJ, Nijman IJ, Kloosterman WP, van Haelst MM, van Haaften G, Cuppen E.
Nat Genet 44(7):793-6. doi: 10.1038/ng.2324. 2012
3ABCC9, HCOD
Cantú Syndrome Is Caused by Mutations in ABCC9.
van Bon BW, Gilissen C, Grange DK, Hennekam RC, Kayserili H, Engels H, Reutter H, Ostergaard JR, Morava E, Tsiakas K, Isidor B, Le Merrer M, Eser M, Wieskamp N, de Vries P, Steehouwer M, Veltman JA, Robertson SP, Brunner HG, de Vries BB, Hoischen A.
Am J Hum Genet 90(6):1094-101. Epub 2012 May 17. 2012
4ABCC9
The ATPase activities of sulfonylurea receptor 2A and sulfonylurea receptor 2B are influenced by the C-terminal 42 amino acids.
de Wet H, Fotinou C, Amad N, Dreger M, Ashcroft FM.
FEBS J 277(12):2654-62. 2010
5ABCC9
Interaction of asymmetric ABCC9-encoded nucleotide binding domains determines KATP channel SUR2A catalytic activity.
Park S, Lim BB, Perez-Terzic C, Mer G, Terzic A.
J Proteome Res 7(4):1721-8. Epub 2008 Mar 1. 2008
6ABCC8, ABCC9
ABCC8 and ABCC9: ABC transporters that regulate K+ channels.
Bryan J, Muñoz A, Zhang X, Düfer M, Drews G, Krippeit-Drews P, Aguilar-Bryan L.
Pflugers Arch 453(5):703-18. Epub 2006 Aug 8. Review. 2007
7ABCC9
A novel Val734Ile variant in the ABCC9 gene associated with myocardial infarction.
Minoretti P, Falcone C, Aldeghi A, Olivieri V, Mori F, Emanuele E, Calcagnino M, Geroldi D.
Clin Chim Acta 370(1-2):124-8. Epub 2006 Mar 6. 2006
8ABCC9, CMD10
ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating.
Bienengraeber M, Olson TM, Selivanov VA, Kathmann EC, O'Cochlain F, Gao F, Karger AB, Ballew JD, Hodgson DM, Zingman LV, Pang YP, Alekseev AE, Terzic A.
Nat Genet 36(4):382-7. Epub 2004 Mar 21. 2004
9ABCC8, ABCC9, KCNJ11, KCNJ8
The molecular basis of the specificity of action of K(ATP) channel openers.
Moreau C, Jacquet H, Prost AL, D'hahan N, Vivaudou M.
EMBO J 19(24):6644-6651. 2000
10ABCC8, ABCC9
The mitochondrial sulfonylurea receptor : identification and characterization.
Szewczyk A, et al.
Biochem Biophys Res Commun 230 : 611-615. 1997
11ABCC9
Cloning, tissue expression, and chromosomal localization of SUR2, the putative drug-binding subunit of cardiac, skeletal muscle, and vascular KATP channels.
Chutkow WA, et al.
Diabetes 45 : 1439-1445. 1996
12ABCC9
A novel sulfonylurea receptor forms with BIR (Kir6.2) a smooth muscle type ATP-sensitive K+ channel.
Isomoto S, Kondo C, Yamada M, Matsumoto S, Higashiguchi O, Horio Y, Matsuzawa Y, Kurachi Y.
J Biol Chem 271(40):24321-4. 1996