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Journal Abstract Search


703 related items for PubMed ID: 12606628

  • 1. Endogenous opioid peptides contribute to antinociceptive potency of intrathecal [Dmt1]DALDA.
    Szeto HH, Soong Y, Wu D, Qian X, Zhao GM.
    J Pharmacol Exp Ther; 2003 May; 305(2):696-702. PubMed ID: 12606628
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  • 2. Comparison of [Dmt1]DALDA and DAMGO in binding and G protein activation at mu, delta, and kappa opioid receptors.
    Zhao GM, Qian X, Schiller PW, Szeto HH.
    J Pharmacol Exp Ther; 2003 Dec; 307(3):947-54. PubMed ID: 14534366
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  • 4. Dynorphinergic mechanism mediating endomorphin-2-induced antianalgesia in the mouse spinal cord.
    Wu HE, Sun HS, Darpolar M, Leitermann RJ, Kampine JP, Tseng LF.
    J Pharmacol Exp Ther; 2003 Dec; 307(3):1135-41. PubMed ID: 14557378
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  • 6. Characterization of the binding of [3H][Dmt1]H-Dmt-D-Arg-Phe-Lys-NH2, a highly potent opioid peptide.
    Neilan CL, Janvey AJ, Bolan E, Berezowska I, Nguyen TM, Schiller PW, Pasternak GW.
    J Pharmacol Exp Ther; 2003 Aug; 306(2):430-6. PubMed ID: 12663687
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  • 10. Differential analgesic effects of a mu-opioid peptide, [Dmt(1)]DALDA, and morphine.
    Shimoyama M, Szeto HH, Schiller PW, Tagaito Y, Tokairin H, Eun Cm, Shimoyama N.
    Pharmacology; 2009 Aug; 83(1):33-7. PubMed ID: 18987489
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  • 11. Differential mechanisms mediating descending pain controls for antinociception induced by supraspinally administered endomorphin-1 and endomorphin-2 in the mouse.
    Ohsawa M, Mizoguchi H, Narita M, Chu M, Nagase H, Tseng LF.
    J Pharmacol Exp Ther; 2000 Sep; 294(3):1106-11. PubMed ID: 10945866
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  • 12. Structure-constrained endomorphin analogs display differential antinociceptive mechanisms in mice after spinal administration.
    Wang Y, Zhou J, Liu X, Zhao L, Wang Z, Zhang X, Wang K, Wang L, Wang R.
    Peptides; 2017 May; 91():40-48. PubMed ID: 28363796
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  • 13. Roles of endogenous opioid peptides in modulation of nocifensive response to formalin.
    Wu HE, Hung KC, Mizoguchi H, Nagase H, Tseng LF.
    J Pharmacol Exp Ther; 2002 Feb; 300(2):647-54. PubMed ID: 11805228
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  • 15. Selective antagonism by naloxonazine of antinociception by Tyr-D-Arg-Phe-beta-Ala, a novel dermorphin analogue with high affinity at mu-opioid receptors.
    Sakurada S, Takeda S, Sato T, Hayashi T, Yuki M, Kutsuwa M, Tan-No K, Sakurada C, Kisara K, Sakurada T.
    Eur J Pharmacol; 2000 Apr 28; 395(2):107-12. PubMed ID: 10794815
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  • 18. Nonopioidergic mechanism mediating morphine-induced antianalgesia in the mouse spinal cord.
    Wu HE, Thompson J, Sun HS, Leitermann RJ, Fujimoto JM, Tseng LF.
    J Pharmacol Exp Ther; 2004 Jul 28; 310(1):240-6. PubMed ID: 14999057
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