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Journal Abstract Search

109 related items for PubMed ID: 7498295

  • 1. First delineation of 5-HT1A receptors in human brain with PET and [11C]WAY-100635.
    Pike VW, McCarron JA, Lammerstma AA, Hume SP, Poole K, Grasby PM, Malizia A, Cliffe IA, Fletcher A, Bench CJ.
    Eur J Pharmacol; 1995 Sep 05; 283(1-3):R1-3. PubMed ID: 7498295
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  • 5. Characterisation of the appearance of radioactive metabolites in monkey and human plasma from the 5-HT1A receptor radioligand, [carbonyl-11C]WAY-100635--explanation of high signal contrast in PET and an aid to biomathematical modelling.
    Osman S, Lundkvist C, Pike VW, Halldin C, McCarron JA, Swahn CG, Farde L, Ginovart N, Luthra SK, Gunn RN, Bench CJ, Sargent PA, Grasby PM.
    Nucl Med Biol; 1998 Apr 05; 25(3):215-23. PubMed ID: 9620626
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  • 6. [11C]WAY 100635: a radioligand for imaging 5-HT1A receptors with positron emission tomography.
    Mathis CA, Simpson NR, Mahmood K, Kinahan PE, Mintun MA.
    Life Sci; 1994 Apr 05; 55(20):PL403-7. PubMed ID: 7968222
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  • 7. Two C-methyl derivatives of [11C]WAY-100635--effects of an amido alpha-methyl group on metabolism and brain 5-HT1A receptor radioligand behavior in monkey.
    McCarron JA, Marchais-Oberwinkler S, Pike VW, Tarkiainen J, Halldin C, Sóvagó J, Gulyas B, Wikström HV, Farde L.
    Mol Imaging Biol; 2005 Apr 05; 7(3):209-19. PubMed ID: 15912425
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  • 8. The selective 5-HT1A antagonist radioligand [3H]WAY 100635 labels both G-protein-coupled and free 5-HT1A receptors in rat brain membranes.
    Gozlan H, Thibault S, Laporte AM, Lima L, Hamon M.
    Eur J Pharmacol; 1995 Jan 16; 288(2):173-86. PubMed ID: 7720779
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  • 10. Evaluation of [O-methyl-3H]WAY-100635 as an in vivo radioligand for 5-HT1A receptors in rat brain.
    Hume SP, Ashworth S, Opacka-Juffry J, Ahier RG, Lammertsma AA, Pike VW, Cliffe IA, Fletcher A, White AC.
    Eur J Pharmacol; 1994 Dec 27; 271(2-3):515-23. PubMed ID: 7705452
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  • 15. 5-Hydroxytryptamine1A receptor occupancy by novel full antagonist 2-[4-[4-(7-chloro-2,3-dihydro-1,4-benzdioxyn-5-yl)-1-piperazinyl]butyl]-1,2-benzisothiazol-3-(2H)-one-1,1-dioxide: a[11C][O-methyl-3H]-N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-(2-pyridinyl)cyclohexanecarboxamide trihydrochloride (WAY-100635) positron emission tomography study in humans.
    Rabiner EA, Wilkins MR, Turkheimer F, Gunn RN, Udo de Haes J, de Vries M, Grasby PM.
    J Pharmacol Exp Ther; 2002 Jun 27; 301(3):1144-50. PubMed ID: 12023549
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  • 16. Antagonist properties of (-)-pindolol and WAY 100635 at somatodendritic and postsynaptic 5-HT1A receptors in the rat brain.
    Corradetti R, Laaris N, Hanoun N, Laporte AM, Le Poul E, Hamon M, Lanfumey L.
    Br J Pharmacol; 1998 Feb 27; 123(3):449-62. PubMed ID: 9504386
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  • 19. Selective in vivo labelling of brain 5-HT1A receptors by [3H]WAY 100635 in the mouse.
    Laporte AM, Lima L, Gozlan H, Hamon M.
    Eur J Pharmacol; 1994 Dec 27; 271(2-3):505-14. PubMed ID: 7705451
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