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165 related items for PubMed ID: 3178834

  • 1. The calcium channel antagonist omega-conotoxin inhibits secretion from peptidergic nerve terminals.
    Dayanithi G, Martin-Moutot N, Barlier S, Colin DA, Kretz-Zaepfel M, Couraud F, Nordmann JJ.
    Biochem Biophys Res Commun; 1988 Oct 14; 156(1):255-62. PubMed ID: 3178834
    [Abstract] [Full Text] [Related]

  • 2. Two types of high-threshold calcium currents inhibited by omega-conotoxin in nerve terminals of rat neurohypophysis.
    Wang X, Treistman SN, Lemos JR.
    J Physiol; 1992 Jan 14; 445():181-99. PubMed ID: 1323666
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  • 3. Ca2+ and vasopressin release in isolated rat neurohypophysis: differential effects of four classes of Ca2+ channel ligands.
    von Spreckelsen S, Lollike K, Treiman M.
    Brain Res; 1990 Apr 23; 514(1):68-76. PubMed ID: 2357532
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  • 4. Role of Q-type Ca2+ channels in vasopressin secretion from neurohypophysial terminals of the rat.
    Wang G, Dayanithi G, Kim S, Hom D, Nadasdi L, Kristipati R, Ramachandran J, Stuenkel EL, Nordmann JJ, Newcomb R, Lemos JR.
    J Physiol; 1997 Jul 15; 502 ( Pt 2)(Pt 2):351-63. PubMed ID: 9263915
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  • 5. Effects of membrane depolarization on intracellular calcium in single nerve terminals.
    Stuenkel EL.
    Brain Res; 1990 Oct 08; 529(1-2):96-101. PubMed ID: 2282508
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  • 6. Effects of toxins on Ca2+ currents and peptide release from nerve terminals.
    Lemos JR, Wang G, Wang X, Stuenkel EL, Nordmann JJ, Treistman SN.
    Ann N Y Acad Sci; 1994 Mar 09; 710():11-29. PubMed ID: 8154740
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  • 7. Intracellular calcium and vasopressin release of rat isolated neurohypophysial nerve endings.
    Stuenkel EL, Nordmann JJ.
    J Physiol; 1993 Aug 09; 468():335-55. PubMed ID: 8254513
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  • 12. An R-type Ca(2+) current in neurohypophysial terminals preferentially regulates oxytocin secretion.
    Wang G, Dayanithi G, Newcomb R, Lemos JR.
    J Neurosci; 1999 Nov 01; 19(21):9235-41. PubMed ID: 10531427
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  • 15. Intracellular calcium and hormone release from nerve endings of the neurohypophysis in the presence of opioid agonists and antagonists.
    Dayanithi G, Stuenkel EL, Nordmann JJ.
    Exp Brain Res; 1992 Nov 01; 90(3):539-45. PubMed ID: 1358668
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  • 16. Voltage-sensitive calcium flux into bovine chromaffin cells occurs through dihydropyridine-sensitive and dihydropyridine- and omega-conotoxin-insensitive pathways.
    Rosario LM, Soria B, Feuerstein G, Pollard HB.
    Neuroscience; 1989 Nov 01; 29(3):735-47. PubMed ID: 2739907
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  • 17. Adenosine inhibition via A(1) receptor of N-type Ca(2+) current and peptide release from isolated neurohypophysial terminals of the rat.
    Wang G, Dayanithi G, Custer EE, Lemos JR.
    J Physiol; 2002 May 01; 540(Pt 3):791-802. PubMed ID: 11986369
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  • 18. Calcium channels that are required for secretion from intact nerve terminals of vertebrates are sensitive to omega-conotoxin and relatively insensitive to dihydropyridines. Optical studies with and without voltage-sensitive dyes.
    Obaid AL, Flores R, Salzberg BM.
    J Gen Physiol; 1989 Apr 01; 93(4):715-29. PubMed ID: 2471780
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  • 19. Inhibition of histamine release from rat hypothalamic slices by omega-conotoxin GVIA, but not by nilvadipine, a dihydropyridine derivative.
    Takemura M, Kishino J, Yamatodani A, Wada H.
    Brain Res; 1989 Sep 04; 496(1-2):351-6. PubMed ID: 2553205
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