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Inhibiteur de la recapture (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Inhibiteur de la recapture" in French language version.

refsWebsite
Global rank French rank
26nih.gov
4th place
12th place
23doi.org
2nd place
3rd place
3zenodo.org
621st place
3,834th place
1europepmc.org
8,929th place
2,510th place
1wiley.com
222nd place
129th place

doi.org

dx.doi.org

  • (en) Iversen L., « Neurotransmitter transporters and their impact on the development of psychopharmacology. », Br J Pharmacol, vol. 147, no 1,‎ , S82–88 (PMID 16402124, PMCID 1760736, DOI 10.1038/sj.bjp.0706428, lire en ligne Accès libre [PDF])
  • « Inhibition of glutamate reuptake potentiates endogenous nitric oxide-facilitated dopamine efflux in the rat striatum: an in vivo microdialysis study », Neurosci. Lett., vol. 230, no 1,‎ , p. 21–4 (PMID 9259454, DOI 10.1016/S0304-3940(97)00465-5)
  • « The selective GABA reuptake inhibitor tiagabine for the treatment of generalized anxiety disorder: results of a placebo-controlled study », J Clin Psychiatry, vol. 66, no 11,‎ , p. 1401–8 (PMID 16420077, DOI 10.4088/JCP.v66n1109)
  • « Glycine reuptake inhibitor RG1678: a pharmacologic characterization of an investigational agent for the treatment of schizophrenia », Neuropharmacology, vol. 62, no 2,‎ , p. 1152–61 (PMID 22138164, DOI 10.1016/j.neuropharm.2011.11.008)
  • « The effects of the adenosine reuptake inhibitor soluflazine on synaptic potentials and population hypoxic depolarizations in area CA1 of rat hippocampus in vitro », Neuropharmacology, vol. 32, no 2,‎ , p. 149–55 (PMID 8383814, DOI 10.1016/0028-3908(93)90095-K)
  • « Evaluation of the inhibition of choline uptake in synaptosomes by capillary electrophoresis with electrochemical detection », Electrophoresis, vol. 23, no 21,‎ , p. 3699–704 (PMID 12432531, DOI 10.1002/1522-2683(200211)23:21<3699::AID-ELPS3699>3.0.CO;2-E)
  • « AM404, an inhibitor of anandamide uptake, prevents pain behaviour and modulates cytokine and apoptotic pathways in a rat model of neuropathic pain », Br J Pharmacol, vol. 148, no 7,‎ , p. 1022–32 (PMID 16770320, PMCID 1751928, DOI 10.1038/sj.bjp.0706798)
  • « Distinct effects of imipramine on 5-hydroxytryptamine uptake mediated by the recombinant rat serotonin transporter SERT1. », Journal of Neurochemistry, vol. 70, no 6,‎ , p. 2545–2553 (PMID 9603221, DOI 10.1046/j.1471-4159.1998.70062545.x, lire en ligne [PDF])
  • « Molecular mechanism of citalopram and cocaine interactions with neurotransmitter transporters. », J Pharmacol Exp Ther, vol. 307, no 1,‎ , p. 34–41 (PMID 12944499, DOI 10.1124/jpet.103.054593)
  • « Antidepressants targeting the serotonin reuptake transporter act via a competitive mechanism. », J Pharmacol Exp Ther, vol. 327, no 3,‎ , p. 982–990 (PMID 18801947, DOI 10.1124/jpet.108.142315)
  • « The role of antagonism of NMDA receptor-mediated neurotransmission and inhibition of the dopamine reuptake in the neuroendocrine effects of phencyclidine », Life Sci., vol. 78, no 17,‎ , p. 2006–11 (PMID 16288927, DOI 10.1016/j.lfs.2005.09.018)
  • « Ketamine inhibits monoamine transporters expressed in human embryonic kidney 293 cells », Anesthesiology, vol. 88, no 3,‎ , p. 768–74 (PMID 9523822, DOI 10.1097/00000542-199803000-00029)
  • « MK-801 blocks monoamine transporters expressed in HEK cells. », FEBS Lett., vol. 423, no 3,‎ , p. 376–380 (PMID 9515743, DOI 10.1016/S0014-5793(98)00126-4)
  • « [3H]1-[2-(2-thienyl)cyclohexyl]piperidine labels two high-affinity binding sites in human cortex: further evidence for phencyclidine binding sites associated with the biogenic amine reuptake complex. », Synapse, vol. 8, no 4,‎ , p. 289–300 (PMID 1833849, DOI 10.1002/syn.890080407, lire en ligne)
  • « RTI-4793-14, a new ligand with high affinity and selectivity for the (+)-MK801-insensitive [3H]1-]1-(2-thienyl)cyclohexyl]piperidine binding site (PCP site 2) of guinea pig brain. », Synapse, vol. 16, no 1,‎ , p. 59–65 (PMID 8134901, DOI 10.1002/syn.890160107, lire en ligne)
  • Rothman RB., « PCP site 2: a high affinity MK-801-insensitive phencyclidine binding site. », Neurotoxicol Teratol, vol. 16, no 4,‎ , p. 343–353 (PMID 7968938, DOI 10.1016/0892-0362(94)90022-1, lire en ligne)
  • « The S-enantiomer of R,S-citalopram, increases inhibitor binding to the human serotonin transporter by an allosteric mechanism. Comparison with other serotonin transporter inhibitors. », Eur. Neuropsychopharmacol., vol. 15, no 2,‎ , p. 193–198 (PMID 15695064, DOI 10.1016/j.euroneuro.2004.08.008)
  • « Allosteric modulation of the effect of escitalopram, paroxetine and fluoxetine: in-vitro and in-vivo studies. », Int J Neuropsychopharmacol, vol. 10, no 1,‎ , p. 31–40 (PMID 16448580, DOI 10.1017/S1461145705006462)
  • « Hyperforin – antidepressant activity by a novel mechanism of action », Pharmacopsychiatry, vol. 34 Suppl 1,‎ , S98–102 (PMID 11518085, DOI 10.1055/s-2001-15512)
  • « Hyperforin as a possible antidepressant component of hypericum extracts », Life Sci., vol. 63, no 6,‎ , p. 499–510 (PMID 9718074, DOI 10.1016/S0024-3205(98)00299-9)
  • « The involvement of sodium and calcium ions in the release of amino acid neurotransmitters from mouse cortical slices elicited by hyperforin », Life Sciences, vol. 71, no 22,‎ , p. 2645–55 (PMID 12354583, DOI 10.1016/S0024-3205(02)02104-5)
  • « Dual modulation of striatal acetylcholine release by hyperforin, a constituent of St. John's wort », The Journal of Pharmacology and Experimental Therapeutics, vol. 301, no 2,‎ , p. 714–9 (PMID 11961077, DOI 10.1124/jpet.301.2.714)
  • « Hyperforin – a key constituent of St. John's wort specifically activates TRPC6 channels », The FASEB Journal, vol. 21, no 14,‎ , p. 4101–11 (PMID 17666455, DOI 10.1096/fj.07-8110com)

europepmc.org

nih.gov

ncbi.nlm.nih.gov

  • (en) Iversen L., « Neurotransmitter transporters and their impact on the development of psychopharmacology. », Br J Pharmacol, vol. 147, no 1,‎ , S82–88 (PMID 16402124, PMCID 1760736, DOI 10.1038/sj.bjp.0706428, lire en ligne Accès libre [PDF])
  • « Inhibition of glutamate reuptake potentiates endogenous nitric oxide-facilitated dopamine efflux in the rat striatum: an in vivo microdialysis study », Neurosci. Lett., vol. 230, no 1,‎ , p. 21–4 (PMID 9259454, DOI 10.1016/S0304-3940(97)00465-5)
  • « The selective GABA reuptake inhibitor tiagabine for the treatment of generalized anxiety disorder: results of a placebo-controlled study », J Clin Psychiatry, vol. 66, no 11,‎ , p. 1401–8 (PMID 16420077, DOI 10.4088/JCP.v66n1109)
  • « Glycine reuptake inhibitor RG1678: a pharmacologic characterization of an investigational agent for the treatment of schizophrenia », Neuropharmacology, vol. 62, no 2,‎ , p. 1152–61 (PMID 22138164, DOI 10.1016/j.neuropharm.2011.11.008)
  • « The effects of the adenosine reuptake inhibitor soluflazine on synaptic potentials and population hypoxic depolarizations in area CA1 of rat hippocampus in vitro », Neuropharmacology, vol. 32, no 2,‎ , p. 149–55 (PMID 8383814, DOI 10.1016/0028-3908(93)90095-K)
  • « Evaluation of the inhibition of choline uptake in synaptosomes by capillary electrophoresis with electrochemical detection », Electrophoresis, vol. 23, no 21,‎ , p. 3699–704 (PMID 12432531, DOI 10.1002/1522-2683(200211)23:21<3699::AID-ELPS3699>3.0.CO;2-E)
  • « AM404, an inhibitor of anandamide uptake, prevents pain behaviour and modulates cytokine and apoptotic pathways in a rat model of neuropathic pain », Br J Pharmacol, vol. 148, no 7,‎ , p. 1022–32 (PMID 16770320, PMCID 1751928, DOI 10.1038/sj.bjp.0706798)
  • « Distinct effects of imipramine on 5-hydroxytryptamine uptake mediated by the recombinant rat serotonin transporter SERT1. », Journal of Neurochemistry, vol. 70, no 6,‎ , p. 2545–2553 (PMID 9603221, DOI 10.1046/j.1471-4159.1998.70062545.x, lire en ligne [PDF])
  • « Molecular mechanism of citalopram and cocaine interactions with neurotransmitter transporters. », J Pharmacol Exp Ther, vol. 307, no 1,‎ , p. 34–41 (PMID 12944499, DOI 10.1124/jpet.103.054593)
  • « Antidepressants targeting the serotonin reuptake transporter act via a competitive mechanism. », J Pharmacol Exp Ther, vol. 327, no 3,‎ , p. 982–990 (PMID 18801947, DOI 10.1124/jpet.108.142315)
  • « The role of antagonism of NMDA receptor-mediated neurotransmission and inhibition of the dopamine reuptake in the neuroendocrine effects of phencyclidine », Life Sci., vol. 78, no 17,‎ , p. 2006–11 (PMID 16288927, DOI 10.1016/j.lfs.2005.09.018)
  • « Ketamine inhibits monoamine transporters expressed in human embryonic kidney 293 cells », Anesthesiology, vol. 88, no 3,‎ , p. 768–74 (PMID 9523822, DOI 10.1097/00000542-199803000-00029)
  • « MK-801 blocks monoamine transporters expressed in HEK cells. », FEBS Lett., vol. 423, no 3,‎ , p. 376–380 (PMID 9515743, DOI 10.1016/S0014-5793(98)00126-4)
  • « [3H]1-[2-(2-thienyl)cyclohexyl]piperidine labels two high-affinity binding sites in human cortex: further evidence for phencyclidine binding sites associated with the biogenic amine reuptake complex. », Synapse, vol. 8, no 4,‎ , p. 289–300 (PMID 1833849, DOI 10.1002/syn.890080407, lire en ligne)
  • « The psychotomimetic drug phencyclidine labels two high affinity binding sites in guinea pig brain: evidence for N-methyl-D-aspartate-coupled and dopamine reuptake carrier-associated phencyclidine binding sites. », Mol. Pharmacol., vol. 36, no 6,‎ , p. 887–896 (PMID 2557536)
  • « RTI-4793-14, a new ligand with high affinity and selectivity for the (+)-MK801-insensitive [3H]1-]1-(2-thienyl)cyclohexyl]piperidine binding site (PCP site 2) of guinea pig brain. », Synapse, vol. 16, no 1,‎ , p. 59–65 (PMID 8134901, DOI 10.1002/syn.890160107, lire en ligne)
  • Rothman RB., « PCP site 2: a high affinity MK-801-insensitive phencyclidine binding site. », Neurotoxicol Teratol, vol. 16, no 4,‎ , p. 343–353 (PMID 7968938, DOI 10.1016/0892-0362(94)90022-1, lire en ligne)
  • « Studies of the biogenic amine transporters. VI. Characterization of a novel cocaine binding site, identified with [125I]RTI-55, in membranes prepared from whole rat brain minus caudate. », J Pharmacol Exp Ther, vol. 274, no 1,‎ , p. 385–395 (PMID 7616423)
  • « Studies of the biogenic amine transporters. IV. Demonstration of a multiplicity of binding sites in rat caudate membranes for the cocaine analog [125I]RTI-55. », J Pharmacol Exp Ther, vol. 270, no 1,‎ , p. 296–309 (PMID 8035327)
  • « The S-enantiomer of R,S-citalopram, increases inhibitor binding to the human serotonin transporter by an allosteric mechanism. Comparison with other serotonin transporter inhibitors. », Eur. Neuropsychopharmacol., vol. 15, no 2,‎ , p. 193–198 (PMID 15695064, DOI 10.1016/j.euroneuro.2004.08.008)
  • « Allosteric modulation of the effect of escitalopram, paroxetine and fluoxetine: in-vitro and in-vivo studies. », Int J Neuropsychopharmacol, vol. 10, no 1,‎ , p. 31–40 (PMID 16448580, DOI 10.1017/S1461145705006462)
  • « Hyperforin – antidepressant activity by a novel mechanism of action », Pharmacopsychiatry, vol. 34 Suppl 1,‎ , S98–102 (PMID 11518085, DOI 10.1055/s-2001-15512)
  • « Hyperforin as a possible antidepressant component of hypericum extracts », Life Sci., vol. 63, no 6,‎ , p. 499–510 (PMID 9718074, DOI 10.1016/S0024-3205(98)00299-9)
  • « The involvement of sodium and calcium ions in the release of amino acid neurotransmitters from mouse cortical slices elicited by hyperforin », Life Sciences, vol. 71, no 22,‎ , p. 2645–55 (PMID 12354583, DOI 10.1016/S0024-3205(02)02104-5)
  • « Dual modulation of striatal acetylcholine release by hyperforin, a constituent of St. John's wort », The Journal of Pharmacology and Experimental Therapeutics, vol. 301, no 2,‎ , p. 714–9 (PMID 11961077, DOI 10.1124/jpet.301.2.714)
  • « Hyperforin – a key constituent of St. John's wort specifically activates TRPC6 channels », The FASEB Journal, vol. 21, no 14,‎ , p. 4101–11 (PMID 17666455, DOI 10.1096/fj.07-8110com)

wiley.com

onlinelibrary.wiley.com

zenodo.org

  • « [3H]1-[2-(2-thienyl)cyclohexyl]piperidine labels two high-affinity binding sites in human cortex: further evidence for phencyclidine binding sites associated with the biogenic amine reuptake complex. », Synapse, vol. 8, no 4,‎ , p. 289–300 (PMID 1833849, DOI 10.1002/syn.890080407, lire en ligne)
  • « RTI-4793-14, a new ligand with high affinity and selectivity for the (+)-MK801-insensitive [3H]1-]1-(2-thienyl)cyclohexyl]piperidine binding site (PCP site 2) of guinea pig brain. », Synapse, vol. 16, no 1,‎ , p. 59–65 (PMID 8134901, DOI 10.1002/syn.890160107, lire en ligne)
  • Rothman RB., « PCP site 2: a high affinity MK-801-insensitive phencyclidine binding site. », Neurotoxicol Teratol, vol. 16, no 4,‎ , p. 343–353 (PMID 7968938, DOI 10.1016/0892-0362(94)90022-1, lire en ligne)