Ca2+ channel agonists enhance thyrotropin-releasing hormone-induced inositol phosphates and prolactin secretion.
暂无分享,去创建一个
[1] K. Catt,et al. Calcium mobilization and influx during the biphasic cytosolic calcium and secretory responses in agonist-stimulated pituitary gonadotrophs. , 1989, Archives of biochemistry and biophysics.
[2] I. Parnas,et al. Membrane depolarization evokes neurotransmitter release in the absence of calcium entry , 1989, Nature.
[3] S. Shibata,et al. Bay K 8644-induced potentiation of the contractile response of rabbit iliac artery to caffeine in a Ca2+-free medium. , 1989, General pharmacology.
[4] D. Eberhard,et al. Intracellular Ca2+ activates phospholipase C , 1988, Trends in Neurosciences.
[5] M. Lazdunski,et al. Targets for calcium channel blockers in mammalian skeletal muscle and their respective functions in excitation-contraction coupling. , 1988, Biochemical and biophysical research communications.
[6] A. Zavacki,et al. Calcium channel agonists and antagonists: effects of chronic treatment on pituitary prolactin synthesis and intracellular calcium. , 1988, Molecular endocrinology.
[7] P. Dannies,et al. TRH and BAY K 8644 synergistically stimulate prolactin release but not 45Ca2+ uptake. , 1988, The American journal of physiology.
[8] P. Dannies,et al. Dopamine has no effect on thyrotropin-releasing hormone mobilization of calcium from intracellular stores in rat anterior pituitary cells. , 1988, Molecular endocrinology.
[9] K. Catt,et al. Participation of voltage-sensitive calcium channels in pituitary hormone release. , 1988, The Journal of biological chemistry.
[10] P. Dannies,et al. Bombesin stimulates inositol polyphosphate production in GH4C1 pituitary tumor cells: comparison with TRH. , 1988, Biochemical and biophysical research communications.
[11] E. Woodcock,et al. Angiotensin II-stimulated phosphatidylinositol turnover in rat adrenal glomerulosa cells has a complex dependence on calcium. , 1988, Endocrinology.
[12] B. Fredholm,et al. Interaction of dihydropyridine calcium channel agonists and antagonists with adenosine receptors. , 1987, Pharmacology & toxicology.
[13] V. Flockerzi,et al. Primary structure of the receptor for calcium channel blockers from skeletal muscle , 1987, Nature.
[14] J. Cox,et al. Calcium-calmodulin stimulates inositol 1,4,5-trisphosphate kinase activity from insulin-secreting RINm5F cells. , 1987, The Journal of biological chemistry.
[15] J. Young,et al. Inhibition of radioligand binding to A1 adenosine receptors by Bay K8644 and nifedipine. , 1987, Biochemical pharmacology.
[16] W. S. Agnew. Dual roles for DHP receptors in excitation-contraction coupling? , 1987, Nature.
[17] J. G. Sarmiento,et al. [3H]BAY K 8644, a 1,4-dihydropyridine Ca++ channel activator: characteristics of binding to high and low affinity sites in cardiac membranes. , 1987, The Journal of pharmacology and experimental therapeutics.
[18] R. Inhorn,et al. Pathway for inositol 1,3,4-trisphosphate and 1,4-bisphosphate metabolism. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[19] F. Hofmann,et al. Purified dihydropyridine-binding site from skeletal muscle t-tubules is a functional calcium channel , 1986, Nature.
[20] T. Martin,et al. Thyrotropin-releasing hormone stimulation of polyphosphoinositide hydrolysis in GH3 cell membranes is GTP dependent but insensitive to cholera or pertussis toxin. , 1986, The Journal of biological chemistry.
[21] P. M. Hinkle,et al. Interaction of dihydropyridine Ca2+ agonist Bay K 8644 with normal and transformed pituitary cells. , 1986, The American journal of physiology.
[22] A. Schonbrunn,et al. Adenosine inhibits prolactin and growth hormone secretion in a clonal pituitary cell line. , 1985, Endocrinology.
[23] A. Rogol,et al. Calcium channel agonist BAY k8644 enhances anterior pituitary secretion in rat and monkey. , 1985, The American journal of physiology.
[24] P. M. Hinkle,et al. Dihydropyridine Ca2+ antagonists: potent inhibitors of secretion from normal and transformed pituitary cells. , 1985, The American journal of physiology.
[25] P. Albert,et al. Relationship of thyrotropin-releasing hormone-induced spike and plateau phases in cytosolic free Ca2+ concentrations to hormone secretion. Selective blockade using ionomycin and nifedipine. , 1984, The Journal of biological chemistry.
[26] Richard W. Taylor,et al. IONOPHORE A23187: CATION BINDING AND TRANSPORT PROPERTIES * , 1978 .
[27] W. Douglas,et al. Stimulus‐secretion coupling: the concept and clues from chromaffin and other cells , 1968, British journal of pharmacology.