58 related articles for article (PubMed ID: 8826098)
1. FS2. a mamba venom toxin, is a specific blocker of the L-type calcium channels.
Yasuda O; Morimoto S; Jiang B; Kuroda H; Kimura T; Sakakibara S; Fukuo K; Chen S; Tamatani M; Ogihara T
Artery; 1994; 21(5):287-302. PubMed ID: 8826098
[TBL] [Abstract][Full Text] [Related]
2. Flanking proline residues identify the L-type Ca2+ channel binding site of calciseptine and FS2.
Kini RM; Caldwell RA; Wu QY; Baumgarten CM; Feher JJ; Evans HJ
Biochemistry; 1998 Jun; 37(25):9058-63. PubMed ID: 9636051
[TBL] [Abstract][Full Text] [Related]
3. Calciseptine binding to a 1,4-dihydropyridine recognition site of the L-type calcium channel of rat synaptosomal membranes.
Yasuda O; Morimoto S; Chen Y; Jiang B; Kimura T; Sakakibara S; Koh E; Fukuo K; Kitano S; Ogihara T
Biochem Biophys Res Commun; 1993 Jul; 194(2):587-94. PubMed ID: 8393668
[TBL] [Abstract][Full Text] [Related]
4. Effects of N- and L-type calcium channel antagonists and (+/-)-Bay K8644 on nerve-induced catecholamine secretion from bovine perfused adrenal glands.
O'Farrell M; Ziogas J; Marley PD
Br J Pharmacol; 1997 Jun; 121(3):381-8. PubMed ID: 9179377
[TBL] [Abstract][Full Text] [Related]
5. Voltage-dependent calcium channels in the rat retina: involvement in NMDA-stimulated influx of calcium.
Melena J; Osborne NN
Exp Eye Res; 2001 Apr; 72(4):393-401. PubMed ID: 11273667
[TBL] [Abstract][Full Text] [Related]
6. Comparison of binding affinities of omega-conotoxin and amlodipine to N-type Ca2+ channels in rat brain.
Qu YL; Sugiyama K; Ohnuki T; Hattori K; Watanabe K; Nagatomo T
Zhongguo Yao Li Xue Bao; 1998 Mar; 19(2):97-100. PubMed ID: 10374627
[TBL] [Abstract][Full Text] [Related]
7. Role of basic residues for the binding of omega-conotoxin GVIA to N-type calcium channels.
Sato K; Park NG; Kohno T; Maeda T; Kim JI; Kato R; Takahashi M
Biochem Biophys Res Commun; 1993 Aug; 194(3):1292-6. PubMed ID: 8394704
[TBL] [Abstract][Full Text] [Related]
8. Different contributions of voltage-sensitive Ca2+ channels to histamine-induced catecholamine release and tyrosine hydroxylase activation in bovine adrenal chromaffin cells.
O'Farrell M; Marley PD
Cell Calcium; 1999 Mar; 25(3):209-17. PubMed ID: 10378082
[TBL] [Abstract][Full Text] [Related]
9. Selective peptide antagonist of the class E calcium channel from the venom of the tarantula Hysterocrates gigas.
Newcomb R; Szoke B; Palma A; Wang G; Chen Xh; Hopkins W; Cong R; Miller J; Urge L; Tarczy-Hornoch K; Loo JA; Dooley DJ; Nadasdi L; Tsien RW; Lemos J; Miljanich G
Biochemistry; 1998 Nov; 37(44):15353-62. PubMed ID: 9799496
[TBL] [Abstract][Full Text] [Related]
10. Blockade of T-type voltage-dependent Ca2+ channels by benidipine, a dihydropyridine calcium channel blocker, inhibits aldosterone production in human adrenocortical cell line NCI-H295R.
Akizuki O; Inayoshi A; Kitayama T; Yao K; Shirakura S; Sasaki K; Kusaka H; Matsubara M
Eur J Pharmacol; 2008 Apr; 584(2-3):424-34. PubMed ID: 18331727
[TBL] [Abstract][Full Text] [Related]
11. Membrane-delimited G protein-mediated coupling between V1a vasopressin receptor and dihydropyridine binding sites in rat glomerulosa cells.
Grazzini E; Durroux T; Payet MD; Bilodeau L; Gallo-Payet N; Guillon G
Mol Pharmacol; 1996 Nov; 50(5):1273-83. PubMed ID: 8913359
[TBL] [Abstract][Full Text] [Related]
12. Characterization of the outer pore region of the apamin-sensitive Ca2+-activated K+ channel rSK2.
Jäger H; Grissmer S
Toxicon; 2004 Jun; 43(8):951-60. PubMed ID: 15208028
[TBL] [Abstract][Full Text] [Related]
13. Extracellular localization of the benzothiazepine binding domain of L-type Ca2+ channels.
Hering S; Savchenko A; Strübing C; Lakitsch M; Striessnig J
Mol Pharmacol; 1993 May; 43(5):820-6. PubMed ID: 8388993
[TBL] [Abstract][Full Text] [Related]
14. Identification of omega-conotoxin binding sites on adrenal medullary membranes: possibility of multiple calcium channels in chromaffin cells.
Jan CR; Titeler M; Schneider AS
J Neurochem; 1990 Jan; 54(1):355-8. PubMed ID: 2152797
[TBL] [Abstract][Full Text] [Related]
15. Effects of Ca2+ channel blocker neurotoxins on transmitter release and presynaptic currents at the mouse neuromuscular junction.
Katz E; Protti DA; Ferro PA; Rosato Siri MD; Uchitel OD
Br J Pharmacol; 1997 Aug; 121(8):1531-40. PubMed ID: 9283685
[TBL] [Abstract][Full Text] [Related]
16. Effect of cilnidipine, a novel dihydropyridine Ca++-channel antagonist, on N-type Ca++ channel in rat dorsal root ganglion neurons.
Fujii S; Kameyama K; Hosono M; Hayashi Y; Kitamura K
J Pharmacol Exp Ther; 1997 Mar; 280(3):1184-91. PubMed ID: 9067302
[TBL] [Abstract][Full Text] [Related]
17. Conserved Ca2+-antagonist-binding properties and putative folding structure of a recombinant high-affinity dihydropyridine-binding domain.
Huber I; Wappl E; Herzog A; Mitterdorfer J; Glossmann H; Langer T; Striessnig J
Biochem J; 2000 May; 347 Pt 3(Pt 3):829-36. PubMed ID: 10769189
[TBL] [Abstract][Full Text] [Related]
18. Competitive and cooperative effects of Bay K8644 on the L-type calcium channel current inhibition by calcium channel antagonists.
Zahradníková A; Minarovic I; Zahradník I
J Pharmacol Exp Ther; 2007 Aug; 322(2):638-45. PubMed ID: 17475903
[TBL] [Abstract][Full Text] [Related]
19. Smooth muscle relaxing and hypotensive activities of synthetic calciseptine and the homologous snake venom peptide FS2.
Watanabe TX; Itahara Y; Kuroda H; Chen YN; Kimura T; Sakakibara S
Jpn J Pharmacol; 1995 Jul; 68(3):305-13. PubMed ID: 7474554
[TBL] [Abstract][Full Text] [Related]
20. Subunit composition is a major determinant in high affinity binding of a Ca2+ channel blocker.
Suh-Kim H; Wei X; Birnbaumer L
Mol Pharmacol; 1996 Nov; 50(5):1330-7. PubMed ID: 8913365
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]