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Journal Abstract Search

165 related items for PubMed ID: 3178834

  • 41. Requirements for hormone release from permeabilized nerve endings isolated from the rat neurohypophysis.
    Cazalis M, Dayanithi G, Nordmann JJ.
    J Physiol; 1987 Sep; 390():71-91. PubMed ID: 2451000
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  • 42. Ethanol reduces vasopressin release by inhibiting calcium currents in nerve terminals.
    Wang XM, Lemos JR, Dayanithi G, Nordmann JJ, Treistman SN.
    Brain Res; 1991 Jun 14; 551(1-2):338-41. PubMed ID: 1913165
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  • 43. Effects of omega-conotoxin GVIA on the activation of capsaicin-sensitive afferent sensory nerves in guinea pig airway tissues.
    Morimoto H, Matsuda A, Ohori M, Fujii T.
    Jpn J Pharmacol; 1996 Jun 14; 71(2):161-6. PubMed ID: 8835642
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  • 44. Chloride and magnesium dependence of vasopressin release from rat permeabilized neurohypophysial nerve endings.
    Dayanithi G, Nordmann JJ.
    Neurosci Lett; 1989 Dec 04; 106(3):305-9. PubMed ID: 2601885
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  • 45. Effect of sodium and calcium on basal secretory activity of rat neurohypophysial peptidergic nerve terminals.
    Toescu EC, Nordmann JJ.
    J Physiol; 1991 Feb 04; 433():127-44. PubMed ID: 1841936
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  • 46. Multiple Ca2+ channel types coexist to regulate synaptosomal neurotransmitter release.
    Turner TJ, Adams ME, Dunlap K.
    Proc Natl Acad Sci U S A; 1993 Oct 15; 90(20):9518-22. PubMed ID: 8415733
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  • 47. K(+)-Evoked [(3)H]D-aspartate release in rat spinal cord synaptosomes: modulation by neuropeptide Y and calcium channel antagonists.
    Martire M, Altobelli D, Maurizi S, Preziosi P, Fuxe K.
    J Neurosci Res; 2000 Dec 01; 62(5):722-9. PubMed ID: 11104511
    [Abstract] [Full Text] [Related]

  • 48. Differential blockade of rat alpha3beta4 and alpha7 neuronal nicotinic receptors by omega-conotoxin MVIIC, omega-conotoxin GVIA and diltiazem.
    Herrero CJ, García-Palomero E, Pintado AJ, García AG, Montiel C.
    Br J Pharmacol; 1999 Jul 01; 127(6):1375-87. PubMed ID: 10455287
    [Abstract] [Full Text] [Related]

  • 49. Secretion from rat neurohypophysial nerve terminals (neurosecretosomes) rapidly inactivates despite continued elevation of intracellular Ca2+.
    Fatatis A, Holtzclaw L, Payza K, Russell JT.
    Brain Res; 1992 Mar 06; 574(1-2):33-41. PubMed ID: 1638405
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  • 52. omega-Conotoxin exerts functionally distinct low and high affinity effects in the neuronal cell line NG108-15.
    Werth JL, Hirning LD, Thayer SA.
    Mol Pharmacol; 1991 Nov 06; 40(5):742-9. PubMed ID: 1944242
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  • 56. Release of vasopressin from isolated permeabilized neurosecretory nerve terminals is blocked by the light chain of botulinum A toxin.
    Dayanithi G, Ahnert-Hilger G, Weller U, Nordmann JJ, Gratzl M.
    Neuroscience; 1990 Nov 06; 39(3):711-5. PubMed ID: 2097523
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  • 57. Differential sensitivity of synaptosomal calcium entry and endogenous dopamine release to omega-conotoxin.
    Woodward JJ, Rezazadeh SM, Leslie SW.
    Brain Res; 1988 Dec 13; 475(1):141-5. PubMed ID: 3214720
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  • 58. Omega-conotoxin inhibits the acute activation of tyrosine hydroxylase and the stimulation of norepinephrine release by potassium depolarization of sympathetic nerve endings.
    Rittenhouse AR, Zigmond RE.
    J Neurochem; 1991 Feb 13; 56(2):615-22. PubMed ID: 1671089
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  • 59. Calcium channels responsible for potassium-induced transmitter release at rat cerebellar synapses.
    Momiyama A, Takahashi T.
    J Physiol; 1994 Apr 15; 476(2):197-202. PubMed ID: 7913967
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