579 related articles for article (PubMed ID: 13679426)
1. Functional coupling between sulfonylurea receptor type 1 and a nonselective cation channel in reactive astrocytes from adult rat brain.
Chen M; Dong Y; Simard JM
J Neurosci; 2003 Sep; 23(24):8568-77. PubMed ID: 13679426
[TBL] [Abstract][Full Text] [Related]
2. Regulation by sulfanylurea receptor type 1 of a non-selective cation channel involved in cytotoxic edema of reactive astrocytes.
Simard JM; Chen M
J Neurosurg Anesthesiol; 2004 Jan; 16(1):98-9. PubMed ID: 14676579
[TBL] [Abstract][Full Text] [Related]
3. Involvement of the n-terminus of Kir6.2 in coupling to the sulphonylurea receptor.
Reimann F; Tucker SJ; Proks P; Ashcroft FM
J Physiol; 1999 Jul; 518 ( Pt 2)(Pt 2):325-36. PubMed ID: 10381582
[TBL] [Abstract][Full Text] [Related]
4. Sulfonylurea and K(+)-channel opener sensitivity of K(ATP) channels. Functional coupling of Kir6.2 and SUR1 subunits.
Koster JC; Sha Q; Nichols CG
J Gen Physiol; 1999 Aug; 114(2):203-13. PubMed ID: 10435998
[TBL] [Abstract][Full Text] [Related]
5. Cell-type specific expression of ATP-sensitive potassium channels in the rat hippocampus.
Zawar C; Plant TD; Schirra C; Konnerth A; Neumcke B
J Physiol; 1999 Jan; 514 ( Pt 2)(Pt 2):327-41. PubMed ID: 9852317
[TBL] [Abstract][Full Text] [Related]
6. Pharmacology of human sulphonylurea receptor SUR1 and inward rectifier K(+) channel Kir6.2 combination expressed in HEK-293 cells.
Gopalakrishnan M; Molinari EJ; Shieh CC; Monteggia LM; Roch JM; Whiteaker KL; Scott VE; Sullivan JP; Brioni JD
Br J Pharmacol; 2000 Apr; 129(7):1323-32. PubMed ID: 10742287
[TBL] [Abstract][Full Text] [Related]
7. Altered functional properties of KATP channel conferred by a novel splice variant of SUR1.
Sakura H; Trapp S; Liss B; Ashcroft FM
J Physiol; 1999 Dec; 521 Pt 2(Pt 2):337-50. PubMed ID: 10581306
[TBL] [Abstract][Full Text] [Related]
8. 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; 437(3):400-8. PubMed ID: 9914396
[TBL] [Abstract][Full Text] [Related]
9. Sensitivity of Kir6.2-SUR1 currents, in the absence and presence of sodium azide, to the K(ATP) channel inhibitors, ciclazindol and englitazone.
McKay NG; Kinsella JM; Campbell CM; Ashford ML
Br J Pharmacol; 2000 Jun; 130(4):857-66. PubMed ID: 10864893
[TBL] [Abstract][Full Text] [Related]
10. The effects of mitiglinide (KAD-1229), a new anti-diabetic drug, on ATP-sensitive K+ channels and insulin secretion: comparison with the sulfonylureas and nateglinide.
Sunaga Y; Gonoi T; Shibasaki T; Ichikawa K; Kusama H; Yano H; Seino S
Eur J Pharmacol; 2001 Nov; 431(1):119-25. PubMed ID: 11716850
[TBL] [Abstract][Full Text] [Related]
11. Regulation of cloned ATP-sensitive K channels by adenine nucleotides and sulfonylureas: interactions between SUR1 and positively charged domains on Kir6.2.
John SA; Weiss JN; Ribalet B
J Gen Physiol; 2001 Oct; 118(4):391-405. PubMed ID: 11585851
[TBL] [Abstract][Full Text] [Related]
12. Testing the bipartite model of the sulfonylurea receptor binding site: binding of A-, B-, and A + B-site ligands.
Winkler M; Stephan D; Bieger S; Kühner P; Wolff F; Quast U
J Pharmacol Exp Ther; 2007 Aug; 322(2):701-8. PubMed ID: 17495126
[TBL] [Abstract][Full Text] [Related]
13. Stoichiometry of sulfonylurea-induced ATP-sensitive potassium channel closure.
Dörschner H; Brekardin E; Uhde I; Schwanstecher C; Schwanstecher M
Mol Pharmacol; 1999 Jun; 55(6):1060-6. PubMed ID: 10347249
[TBL] [Abstract][Full Text] [Related]
14. 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; 103(4):1118-23. PubMed ID: 16418275
[TBL] [Abstract][Full Text] [Related]
15. 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; 131(1):43-58. PubMed ID: 18079561
[TBL] [Abstract][Full Text] [Related]
16. Functional involvement of sulphonylurea receptor (SUR) type 1 and 2B in the activity of pig urethral ATP-sensitive K+ channels.
Yunoki T; Teramoto N; Ito Y
Br J Pharmacol; 2003 Jun; 139(3):652-60. PubMed ID: 12788825
[TBL] [Abstract][Full Text] [Related]
17. The cytoplasmic C-terminus of the sulfonylurea receptor is important for KATP channel function but is not key for complex assembly or trafficking.
Giblin JP; Quinn K; Tinker A
Eur J Biochem; 2002 Nov; 269(21):5303-13. PubMed ID: 12392564
[TBL] [Abstract][Full Text] [Related]
18. Pharmacological comparison of native mitochondrial K(ATP) channels with molecularly defined surface K(ATP) channels.
Liu Y; Ren G; O'Rourke B; Marbán E; Seharaseyon J
Mol Pharmacol; 2001 Feb; 59(2):225-30. PubMed ID: 11160857
[TBL] [Abstract][Full Text] [Related]
19. The Kir6.2-F333I mutation differentially modulates KATP channels composed of SUR1 or SUR2 subunits.
Tammaro P; Ashcroft F
J Physiol; 2007 Jun; 581(Pt 3):1259-69. PubMed ID: 17395632
[TBL] [Abstract][Full Text] [Related]
20. Characterisation of sulphonylurea and ATP-regulated K+ channels in rat pancreatic A-cells.
Bokvist K; Olsen HL; Høy M; Gotfredsen CF; Holmes WF; Buschard K; Rorsman P; Gromada J
Pflugers Arch; 1999 Sep; 438(4):428-36. PubMed ID: 10519134
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
