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1 receptors and not through H2-histamine or I1-imidazoline receptors.
2 yperthermic effect of morphine by activating imidazoline receptors.
3 ), the H2 histamine receptor antagonist with imidazoline receptor activating properties, prevented th
5 ha2-AR) agonist guanabenz, but not by the Ih-imidazoline receptor agonists moxonidine or rilmenidine.
7 contrast, pretreatment with the specific I1 imidazoline receptor blocker, efaroxan (100-500 microg;
8 ion, i.c.v. or i.v. pretreatment with the I1-imidazoline receptor blocker, efaroxan, failed to inhibi
11 e cross-reactivity of alpha2AR agonists with imidazoline receptors has precluded an understanding of
13 te signal transduction pathways for the I(1)-imidazoline receptor in PC12 cells and their interaction
16 line compound with preferential affinity for imidazoline receptors (IR) over alpha(2)-adrenoceptors (
18 ine is known to bind to alpha-adrenergic and imidazoline receptors, it has been suggested that some o
21 ity and selectivity of some compounds for I1 imidazoline receptors over alpha2-adreergic receptors.
22 vous system with a polyclonal antibody to an imidazoline receptor protein (IRP) with binding characte
24 nd tested for their binding properties on I1 imidazoline receptors vs alpha2-adrenergic receptors and
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