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2. Evidence for a K+ channel in bovine chromaffin granule membranes: single-channel properties and possible bioenergetic significance. Ashley RH; Brown DM; Apps DK; Phillips JH Eur Biophys J; 1994; 23(4):263-75. PubMed ID: 7528657 [TBL] [Abstract][Full Text] [Related]
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4. Multiple types of voltage-dependent Ca2+-activated K+ channels of large conductance in rat brain synaptosomal membranes. Farley J; Rudy B Biophys J; 1988 Jun; 53(6):919-34. PubMed ID: 2456105 [TBL] [Abstract][Full Text] [Related]
5. Direct control of a large conductance K(+)-selective channel by G-proteins in adrenal chromaffin granule membranes. Arispe N; De Mazancourt P; Rojas E J Membr Biol; 1995 Sep; 147(2):109-19. PubMed ID: 8568848 [TBL] [Abstract][Full Text] [Related]
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7. In vitro reconstitution of chromaffin granule-cytoskeleton interactions: ionic factors influencing the association of F-actin with purified chromaffin granule membranes. Fowler VM; Pollard HB J Cell Biochem; 1982; 18(3):295-311. PubMed ID: 7068784 [TBL] [Abstract][Full Text] [Related]
8. Cation specificity and pharmacological properties of the Ca(2+)-dependent K+ channel of rat cortical collecting ducts. Schlatter E; Bleich M; Hirsch J; Markstahler U; Fröbe U; Greger R Pflugers Arch; 1993 Feb; 422(5):481-91. PubMed ID: 7682688 [TBL] [Abstract][Full Text] [Related]
9. Calcium-mediated agonists activate an inwardly rectified K+ channel in colonic secretory cells. Devor DC; Frizzell RA Am J Physiol; 1993 Nov; 265(5 Pt 1):C1271-80. PubMed ID: 7694492 [TBL] [Abstract][Full Text] [Related]
10. The heterogeneity of ion channels in chromaffin granule membranes. Hordejuk R; Szewczyk A; Dołowy K Cell Mol Biol Lett; 2006; 11(3):312-25. PubMed ID: 16847559 [TBL] [Abstract][Full Text] [Related]
11. NSF and SNAP are present on adrenal chromaffin granules. Burgoyne RD; Williams G FEBS Lett; 1997 Sep; 414(2):349-52. PubMed ID: 9315716 [TBL] [Abstract][Full Text] [Related]
12. Electron probe microanalysis of the subcellular compartments of bovine adrenal chromaffin cells. Comparison of chromaffin granules in situ and in vitro. Ornberg RL; Kuijpers GA; Leapman RD J Biol Chem; 1988 Jan; 263(3):1488-93. PubMed ID: 3335554 [TBL] [Abstract][Full Text] [Related]
13. Inactivation of the catecholamine transporter during the preparation of chromaffin granule membrane 'ghosts'. Gasnier B; Scherman D; Henry JP FEBS Lett; 1987 Sep; 222(1):215-9. PubMed ID: 3653399 [TBL] [Abstract][Full Text] [Related]
14. Phospholipids as adjuncts for calcium ion stimulated release of chromaffin granule contents: implications for mechanisms of exocytosis. Nayar R; Hope MJ; Cullis PR Biochemistry; 1982 Sep; 21(19):4583-9. PubMed ID: 7138818 [TBL] [Abstract][Full Text] [Related]
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16. A novel large-conductance Ca(2+)-activated potassium channel and current in nerve terminals of the rat neurohypophysis. Wang G; Thorn P; Lemos JR J Physiol; 1992 Nov; 457():47-74. PubMed ID: 1284313 [TBL] [Abstract][Full Text] [Related]
17. A molecular basis for synexin-driven, calcium-dependent membrane fusion. Pollard HB; Burns AL; Rojas E J Exp Biol; 1988 Sep; 139():267-86. PubMed ID: 2974861 [TBL] [Abstract][Full Text] [Related]
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19. Mode of action of iberiotoxin, a potent blocker of the large conductance Ca(2+)-activated K+ channel. Candia S; Garcia ML; Latorre R Biophys J; 1992 Aug; 63(2):583-90. PubMed ID: 1384740 [TBL] [Abstract][Full Text] [Related]