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zobag's Piomelli [12 articles]

Recent papers posted to zobag's library by the author Piomelli. You can also see everyone's Piomelli.
  • Structural determinants for recognition and translocation by the anandamide transporter
    PNAS, Vol. 96, No. 10. (11 May 1999), pp. 5802-5807.
    by D Piomelli, M Beltramo, S Glasnapp, SY Lin, A Goutopoulos, Xiang-Qun Xie, A Makriyannis
    posted to transport by zobag on 2007-05-08 09:14:38 as **
  • Formation and inactivation of endogenous cannabinoid anandamide in central neurons.
    Nature, Vol. 372, No. 6507. (15 December 1994), pp. 686-691.
    posted to anandamide synthesis by zobag on 2007-05-05 04:48:19 as **
  • Role of Endogenous Cannabinoids in Synaptic Signaling
    Physiol. Rev., Vol. 83, No. 3. (1 July 2003), pp. 1017-1066.
    by Tamas F Freund, Istvan Katona, Daniele Piomelli
  • Characterization of the fatty acid amide hydrolase inhibitor cyclohexyl carbamic acid 3'-carbamoyl-biphenyl-3-yl ester (URB597): effects on anandamide and oleoylethanolamide deactivation.
    J Pharmacol Exp Ther, Vol. 313, No. 1. (April 2005), pp. 352-358.
    posted to faahdetail inhibition urb597 by zobag on 2007-04-27 04:22:51 as **
  • Pharmacological profile of the selective FAAH inhibitor KDS-4103 (URB597).
    CNS Drug Rev, Vol. 12, No. 1. (2006), pp. 21-38.
    by D Piomelli, G Tarzia, A Duranti, A Tontini, M Mor, TR Compton, O Dasse, EP Monaghan, JA Parrott, D Putman
    posted to faahdetail inhibition urb597 by zobag on 2007-04-27 04:20:13 as **
  • The fatty-acid amide hydrolase inhibitor URB597 (cyclohexyl carbamic acid 3'-carbamoyl-biphenyl-3-yl ester) reduces neuropathic pain after oral administration in mice.
    J Pharmacol Exp Ther (5 April 2007)
    by Roberto Russo, Jesse Loverme, Giovanna La Rana, Timothy Compton, Jeff Parrot, Andrea Duranti, Andrea Tontini, Marco Mor, Giorgio Tarzia, Antonio Calignano, Daniele Piomelli
    posted to faahdetail inhibition urb597 by zobag on 2007-04-27 04:18:46 as **
  • Actions of the FAAH inhibitor URB597 in neuropathic and inflammatory chronic pain models.
    Br J Pharmacol, Vol. 147, No. 3. (February 2006), pp. 281-288.
    posted to faah inhibition pain by zobag on 2007-04-25 01:28:00 as **
  • The endogenous cannabinoid anandamide produces delta-9-tetrahydrocannabinol-like discriminative and neurochemical effects that are enhanced by inhibition of fatty acid amide hydrolase but not by inhibition of anandamide transport.
    J Pharmacol Exp Ther, Vol. 321, No. 1. (April 2007), pp. 370-380.
    posted to faah inhibition transport by zobag on 2007-04-25 00:28:28 as **
  • Modulation of neuropathic and inflammatory pain by the endocannabinoid transport inhibitor AM404 [N-(4-hydroxyphenyl)-eicosa-5,8,11,14-tetraenamide].
    J Pharmacol Exp Ther, Vol. 317, No. 3. (June 2006), pp. 1365-1371.
    posted to anandamide inhibition neuropathic pain transport by zobag on 2007-04-23 09:25:13 as **
  • Functional Role of High-Affinity Anandamide Transport, as Revealed by Selective Inhibition
    Science, Vol. 277, No. 5329. (22 August 1997), pp. 1094-1097.
    posted to anandamide transport by zobag on 2007-03-26 09:53:28 as ***
  • Brain monoglyceride lipase participating in endocannabinoid inactivation.
    Proc Natl Acad Sci U S A, Vol. 99, No. 16. (6 August 2002), pp. 10819-10824.
    by TP Dinh, D Carpenter, FM Leslie, TF Freund, I Katona, SL Sensi, S Kathuria, D Piomelli
    posted to anandamide inactivation by zobag on 2007-03-24 06:21:27 as ***
  • Anandamide transport is independent of fatty-acid amide hydrolase activity and is blocked by the hydrolysis-resistant inhibitor AM1172.
    Proc Natl Acad Sci U S A, Vol. 101, No. 23. (8 June 2004), pp. 8756-8761.
    posted to anandamide faah transport by zobag on 2007-03-24 06:16:24 as read
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