Search Results - "Dasilva, J N"

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  1. 1

    Kinetic model-based factor analysis of dynamic sequences for 82-rubidium cardiac positron emission tomography by Klein, R., Beanlands, R. S., Wassenaar, R. W., Thorn, S. L., Lamoureux, M., DaSilva, J. N., Adler, A., deKemp, R. A.

    Published in Medical physics (Lancaster) (01-08-2010)
    “…Purpose: Factor analysis has been pursued as a means to decompose dynamic cardiac PET images into different tissue types based on their unique temporal…”
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    Journal Article
  2. 2

    In Vivo Imaging of the Brain Vesicular Monoamine Transporter by Frey, K.A, Vander Borght, T.M, Killbourn, M.R, DaSilva, J.N, Carey, J.E, Kuhl, D.E

    Published in The Journal of nuclear medicine (1978) (01-12-1995)
    “…In the search for an in vivo marker of monoamine nerve terminal integrity, we investigated methoxytetrabenazine (MTBZ) as a tracer of the brain synaptic…”
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    Journal Article
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    Naturally occurring R225W mutation of the gene encoding AMP-activated protein kinase (AMPK)gamma(3) results in increased oxidative capacity and glucose uptake in human primary myotubes by Crawford, S A, Costford, S R, Aguer, C, Thomas, S C, deKemp, R A, DaSilva, J N, Lafontaine, D, Kendall, M, Dent, R, Beanlands, R S B, McPherson, R, Harper, M-E

    Published in Diabetologia (01-09-2010)
    “…AMP-activated protein kinase (AMPK) has a broad role in the regulation of glucose and lipid metabolism making it a promising target in the treatment of type 2…”
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    Journal Article
  5. 5

    In vivo evaluation of [ 11C]-and [ 18F]-labelled cocaine analogues as potential dopamine transporter ligands for positron emission tomography by Wilson, Alan A., DaSilva, Jean N., Houle, Sylvain

    Published in Nuclear medicine and biology (01-02-1996)
    “…Four analogues of the potent dopamine transporter ligand, WIN 35,428, were radiolabelled with 11C and 18F at the 2-β-carboxy position for evaluation as…”
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    Journal Article
  6. 6

    Dysfunctional Attitudes and 5-HT2 Receptors During Depression and Self-Harm by Meyer, Jeffrey H., McMain, Shelley, Kennedy, Sidney H., Korman, Lorne, Brown, Gregory M., DaSilva, Jean N., Wilson, Alan A., Blak, Thomas, Eynan-Harvey, Rahel, Goulding, Verdell S., Houle, Sylvain, Links, Paul

    Published in The American journal of psychiatry (01-01-2003)
    “…OBJECTIVE: Dysfunctional attitudes are negatively biased assumptions and beliefs regarding oneself, the world, and the future. In healthy subjects, increasing…”
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    Journal Article
  7. 7

    Imaging 5-HT1A receptors with positron emission tomography: initial human studies with [11C]CPC-222 by Houle, S, Wilson, A A, Inaba, T, Fisher, N, DaSilva, J N

    Published in Nuclear medicine communications (01-12-1997)
    “…The novel radioligand [11C]CPC-222 (N-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]-N-(2-pyridinyl)-2-bicyclo [2,2,2]octane carboxamide) was evaluated as an in…”
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  8. 8

    Derivatives of WAY 100635 as potential imaging agents for 5-HT1A receptors : Syntheses, radiosyntheses, and in vitro and in vivo evaluation by WILSON, A. A, INABA, T, FISCHER, N, DIXON, L. M, NOBREGA, J, DASILVA, J. N, HOULE, S

    Published in Nuclear medicine and biology (01-11-1998)
    “…Analogues of the potent and selective 5-HT1A ligand, WAY 100635, were synthesized and examined as potential candidates for imaging 5-HT1A receptors by positron…”
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    Conference Proceeding Journal Article
  9. 9

    Neuromodulation of frontal and temporal cortex by intravenous d-fenfluramine : an [15O]H2O PET study in humans by MEYER, J. H, KAPUR, S, WILSON, A. A, DASILVA, J. N, HOULE, S, BROWN, G. M

    Published in Neuroscience letters (22-03-1996)
    “…This study assessed the modulatory effect of a serotonergic agonist, d-fenfluramine, on localized neuronal firing as indexed by changes in regional cerebral…”
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    Journal Article
  10. 10

    [18F]fluoroalkyl analogues of the potent 5-HT1A antagonist WAY 100635 : Radiosyntheses and In vivo evaluation by WILSON, A. A, DASILVA, J. N, HOULE, S

    Published in Nuclear medicine and biology (01-05-1996)
    “…Two analogues of the potent 5-HT1A antagonist WAY 100635 have been synthesized and radiolabelled with 18F, namely N-[2-[4-(2-2'-[18F]…”
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    Journal Article
  11. 11

    An admonition when measuring the lipophilicity of radiotracers using counting techniques by Wilson, Alan A, Jin, Li, Garcia, Armando, DaSilva, Jean N, Houle, Sylvain

    Published in Applied radiation and isotopes (01-02-2001)
    “…Log P measurements are a fundamental physico-chemical parameter and one of the cornerstones of structure–activity relationships in medicinal chemistry. Despite…”
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    Journal Article
  12. 12

    Characterization of [11C]tetrabenazine as an in vivo radioligand for the vesicular monoamine transporter by DaSilva, J N, Carey, J E, Sherman, P S, Pisani, T J, Kilbourn, M R

    Published in Nuclear medicine and biology (01-02-1994)
    “…[11C]Tetrabenazine ([11C]TBZ) is a new in vivo radioligand for positron emission tomographic (PET) imaging of vesicular monoamine transporters. The in vivo…”
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    Journal Article
  13. 13

    Application of cardiac molecular imaging using positron emission tomography in evaluation of drug and therapeutics for cardiovascular disorders by Yoshinaga, Keiichiro, Chow, Benjamin J W, dekemp, Robert A, Thorn, Stephanie, Ruddy, Terrence D, Davies, Ross A, DaSilva, Jean N, Beanlands, Rob

    Published in Current pharmaceutical design (01-03-2005)
    “…The incidence of cardiovascular disease is increasing with the aging population. This has stimulated a need for innovative means to evaluate and develop…”
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    Journal Article
  14. 14

    Synthesis of a [11C]methoxy derivative of alpha-dihydrotetrabenazine: a radioligand for studying the vesicular monoamine transporter by DaSilva, J N, Kilbourn, M R, Mangner, T J

    Published in Applied radiation and isotopes (01-12-1993)
    “…The synthesis of [11C]TBZOMe, a [11C]methoxy derivative at the 2-hydroxy position of alpha-dihydrotetrabenazine, was carried out by an O-[11C]methylation…”
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    Journal Article
  15. 15

    Synthesis and structure-affinity of a series of 7α-undecylestradiol derivatives: a potential vector for therapy and imaging of estrogen-receptor-positive cancers by DASILVA, J. N, VAN LIER, J. E

    Published in Journal of medicinal chemistry (1990)
    “…A series of 7 alpha-undecylestradiol derivatives, featuring various substituents at the end of the undecyl spacer chain, were synthesized and evaluated for…”
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    Journal Article
  16. 16

    In vivo imaging of vesicular monoamine transporters in human brain using [11C]tetrabenazine and positron emission tomography by Kilbourn, M R, DaSilva, J N, Frey, K A, Koeppe, R A, Kuhl, D E

    Published in Journal of neurochemistry (01-06-1993)
    “…The pharmacokinetics of [11C]tetrabenazine, a high-affinity radioligand for the monoamine vesicular transporter, were determined in living human brain using in…”
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  17. 17

    Dopamine D1 agonist R-[11C]SKF 82957 : Synthesis and in vivo characterization in rats by DASILVA, J. N, SCHWARTZ, R. A, GREENWALD, E. R, LOURENCO, C. M, WILSON, A. A, HOULE, S

    Published in Nuclear medicine and biology (01-07-1999)
    “…The active enantiomer R-SKF 82957 was labeled with 11C by N-[11C]methylation of the full dopamine (D1) agonist R-SKF 81297, using [11C]methyl iodide in the…”
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    Journal Article
  18. 18

    Solid-phase radiosynthesis of [11C]WAY 100635 by Wilson, Alan A., DaSilva, Jean N., Houle, Sylvain

    “…An efficient, fast and simple method is described for the radiosynthesis of the potent and selective 5‐HT1A antagonist…”
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    Journal Article
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    In vivo binding of [11C]tetrabenazine to vesicular monoamine transporters in mouse brain by DaSilva, J N, Kilbourn, M R

    Published in Life sciences (1973) (1992)
    “…The time course of regional mouse brain distribution of radioactivity after i.v. injection of a tracer dose of [11C]tetrabenazine ([11C]TBZ) has been…”
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  20. 20

    Analogues of WAY 100635 as radiotracers for in vivo imaging of 5-HT1A receptors by Wilson, Alan A., Garcia, Armando, Li, Jin, Dasilva, Jean N., Houle, Sylvain

    “…Two diastereoisomeric analogues of the potent 5‐HT1A antagonist W A Y 100635 have been synthesized and radiolabelled with 11C; namely trans‐ and…”
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    Journal Article