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Journal Abstract Search

143 related items for PubMed ID: 8773468

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  • 3. [carbonyl-11C]Desmethyl-WAY-100635 (DWAY) is a potent and selective radioligand for central 5-HT1A receptors in vitro and in vivo.
    Pike VW, Halldin C, McCarron JA, Lundkvist C, Hirani E, Olsson H, Hume SP, Karlsson P, Osman S, Swahn CG, Hall H, Wikström H, Mensonidas M, Poole KG, Farde L.
    Eur J Nucl Med; 1998 Apr; 25(4):338-46. PubMed ID: 9553162
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  • 6. Autoradiographic localization of 5-HT1A receptors in the post-mortem human brain using [3H]WAY-100635 and [11C]way-100635.
    Hall H, Lundkvist C, Halldin C, Farde L, Pike VW, McCarron JA, Fletcher A, Cliffe IA, Barf T, Wikström H, Sedvall G.
    Brain Res; 1997 Jan 16; 745(1-2):96-108. PubMed ID: 9037397
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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 Jan 16; 7(3):209-19. PubMed ID: 15912425
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  • 8. Quantitative analyses of carbonyl-carbon-11-WAY-100635 binding to central 5-hydroxytryptamine-1A receptors in man.
    Farde L, Ito H, Swahn CG, Pike VW, Halldin C.
    J Nucl Med; 1998 Nov 16; 39(11):1965-71. PubMed ID: 9829590
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  • 9. The PET radioligand [carbonyl-(11)C]desmethyl-WAY-100635 binds to 5-HT(1A) receptors and provides a higher radioactive signal than [carbonyl-(11)C]WAY-100635 in the human brain.
    Andrée B, Halldin C, Pike VW, Gunn RN, Olsson H, Farde L.
    J Nucl Med; 2002 Mar 16; 43(3):292-303. PubMed ID: 11884487
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  • 12. Synthesis and biologic evaluation of a novel serotonin 5-HT1A receptor radioligand, 18F-labeled mefway, in rodents and imaging by PET in a nonhuman primate.
    Saigal N, Pichika R, Easwaramoorthy B, Collins D, Christian BT, Shi B, Narayanan TK, Potkin SG, Mukherjee J.
    J Nucl Med; 2006 Oct 16; 47(10):1697-706. PubMed ID: 17015907
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  • 13. [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 Oct 16; 55(20):PL403-7. PubMed ID: 7968222
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  • 16. The pyridinyl-6 position of WAY-100635 as a site for radiofluorination--effect on 5-HT1A receptor radioligand behavior in vivo.
    McCarron JA, Pike VW, Halldin C, Sandell J, Sóvágó J, Gulyas B, Cselényi Z, Wikström HV, Marchais-Oberwinkler S, Nowicki B, Dollé F, Farde L.
    Mol Imaging Biol; 2004 Oct 16; 6(1):17-26. PubMed ID: 15018825
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  • 17. Imaging 5-HT1A receptors with positron emission tomography: initial human studies with [11C]CPC-222.
    Houle S, Wilson AA, Inaba T, Fisher N, DaSilva JN.
    Nucl Med Commun; 1997 Dec 16; 18(12):1130-4. PubMed ID: 9481759
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  • 19. Tracer kinetic modeling of the 5-HT1A receptor ligand [carbonyl-11C]WAY-100635 for PET.
    Gunn RN, Sargent PA, Bench CJ, Rabiner EA, Osman S, Pike VW, Hume SP, Grasby PM, Lammertsma AA.
    Neuroimage; 1998 Nov 16; 8(4):426-40. PubMed ID: 9811559
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  • 20. In vivo binding of [123I]4-(2'-methoxyphenyl)-1-[2'-(N-2"-pyridinyl)- p-iodobenzamido-]ethyl-piperazine, p-MPPI, to 5-HT1A receptors in rat brain.
    Kung MP, Zhuang ZP, Frederick D, Kung HF.
    Synapse; 1994 Dec 16; 18(4):359-66. PubMed ID: 7886629
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