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Journal Abstract Search

76 related items for PubMed ID: 8654566

  • 1. Basal phosphorylation of mu opioid receptor is agonist modulated and Ca2+-dependent.
    Wang Z, Arden J, Sadée W.
    FEBS Lett; 1996 May 27; 387(1):53-7. PubMed ID: 8654566
    [Abstract] [Full Text] [Related]

  • 2. Effects of naloxone and D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2 and the protein kinase inhibitors H7 and H8 on acute morphine dependence and antinociceptive tolerance in mice.
    Bilsky EJ, Bernstein RN, Wang Z, Sadée W, Porreca F.
    J Pharmacol Exp Ther; 1996 Apr 27; 277(1):484-90. PubMed ID: 8613958
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  • 3. Reversible phosphorylation as a controlling factor for sustaining calcium oscillations in HeLa cells: Involvement of calmodulin-dependent kinase II and a calyculin A-inhibitable phosphatase.
    Zhu DM, Tekle E, Chock PB, Huang CY.
    Biochemistry; 1996 Jun 04; 35(22):7214-23. PubMed ID: 8679550
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  • 4. Chronic opioids regulate KATP channel subunit Kir6.2 and carbonic anhydrase I and II expression in rat adrenal chromaffin cells via HIF-2α and protein kinase A.
    Salman S, Holloway AC, Nurse CA.
    Am J Physiol Cell Physiol; 2014 Aug 01; 307(3):C266-77. PubMed ID: 24898587
    [Abstract] [Full Text] [Related]

  • 5. Possible involvement of protein kinases in physical dependence on opioids: studies using protein kinase inhibitors, H-7 and H-8.
    Tokuyama S, Feng Y, Wakabayashi H, Ho IK.
    Eur J Pharmacol; 1995 Sep 15; 284(1-2):101-7. PubMed ID: 8549612
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  • 6. A protein kinase inhibitor, H-7, inhibits the development of tolerance to opioid antinociception.
    Narita M, Feng Y, Makimura M, Hoskins B, Ho IK.
    Eur J Pharmacol; 1994 Dec 27; 271(2-3):543-5. PubMed ID: 7705456
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  • 7. Inhibition of regulated catecholamine secretion from PC12 cells by the Ca2+/calmodulin kinase II inhibitor KN-62.
    Schweitzer ES, Sanderson MJ, Wasterlain CG.
    J Cell Sci; 1995 Jul 27; 108 ( Pt 7)():2619-28. PubMed ID: 7593303
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  • 8. delta- and mu-opioid receptor mobilization of intracellular calcium in SH-SY5Y human neuroblastoma cells.
    Connor M, Henderson G.
    Br J Pharmacol; 1996 Jan 27; 117(2):333-40. PubMed ID: 8789387
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  • 12. mu-Opioid receptor-induced Ca2+ mobilization and astroglial development: morphine inhibits DNA synthesis and stimulates cellular hypertrophy through a Ca(2+)-dependent mechanism.
    Hauser KF, Stiene-Martin A, Mattson MP, Elde RP, Ryan SE, Godleske CC.
    Brain Res; 1996 May 13; 720(1-2):191-203. PubMed ID: 8782912
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  • 14. Phosphorylation and agonist-specific intracellular trafficking of an epitope-tagged mu-opioid receptor expressed in HEK 293 cells.
    Arden JR, Segredo V, Wang Z, Lameh J, Sadée W.
    J Neurochem; 1995 Oct 13; 65(4):1636-45. PubMed ID: 7561859
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  • 17. mu-Opioid receptor internalization-dependent and -independent mechanisms of the development of tolerance to mu-opioid receptor agonists: Comparison between etorphine and morphine.
    Narita M, Suzuki M, Narita M, Niikura K, Nakamura A, Miyatake M, Yajima Y, Suzuki T.
    Neuroscience; 2006 Oct 13; 138(2):609-19. PubMed ID: 16417975
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  • 18. MAP kinase activation by mu opioid receptor involves phosphatidylinositol 3-kinase but not the cAMP/PKA pathway.
    Ai W, Gong J, Yu L.
    FEBS Lett; 1999 Jul 30; 456(1):196-200. PubMed ID: 10452557
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  • 19. Agonist-induced mu opioid receptor phosphorylation and functional desensitization in rat thalamus.
    Deng HB, Yu Y, Wang H, Guang W, Wang JB.
    Brain Res; 2001 Apr 20; 898(2):204-14. PubMed ID: 11306006
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  • 20. A selective Ca2+/calmodulin-dependent protein kinase II inhibitor, KN-62, inhibits the enhanced phosphorylation and the activation of tyrosine hydroxylase by 56 mM K+ in rat pheochromocytoma PC12h cells.
    Ishii A, Kiuchi K, Kobayashi R, Sumi M, Hidaka H, Nagatsu T.
    Biochem Biophys Res Commun; 1991 May 15; 176(3):1051-6. PubMed ID: 1674865
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