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1 ponse studies, insulin and/or TNF-alpha were coinfused.
3 (to measure 11beta-reductase activity) were coinfused and venous samples obtained from skeletal musc
4 erted upon the dopamine transporter (DAT) by coinfusing DA (1 microM) in the presence or absence of T
5 which lpr and normal bone marrow cells were coinfused into lpr hosts, have demonstrated that only T
7 tion, both of which were prevented either by coinfusing noggin or by treating the isolated aortas wit
9 TMX was specific for MA-evoked DA output by coinfusing TMX with a depolarizing concentration of pota
10 lecule; (14)C glycerol and (14)C oleate were coinfused to quantify the systemic and forearm release o
13 dac inhibited cholyltaurine uptake, and when coinfused with cholyltaurine, induced acute cholestasis.
14 at donor-derived T regulatory cells (Tregs), coinfused with conventional T cells (Tcons), protected r
17 or, L-N(G)-monomethylarginine [8 mumol/min], coinfused with nitric oxide donor, sodium nitroprusside
18 0, 120, and 240 pmol/min) were compared when coinfused with placebo and perindoprilat (5 nmol/mL).
19 stinotrophic response to a low dose of GLP-2 coinfused with PN in a rat model of SBS (60% jejunoileal
20 amino) tetralin (8-OH-DPAT; 200 ng), or were coinfused with the 5-HT1A receptor agonist and the 5-HT3
21 3 carbonylate (tropisetron; 500 ng), or were coinfused with the 5-HT3 receptor antagonist and the 5-H
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