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1 eraction of the same alphai subunit with the alpha2A-adrenergic receptor.
2 a well-defined allosteric site on the human alpha2A-adrenergic receptor.
3 0, a PC12 cell line overexpressing the human alpha2A-adrenergic receptor.
4 receptor could be replaced by activation of alpha2A-adrenergic receptors.
5 eurons, while POMC neurons are inhibited via alpha2A - adrenergic receptors.
7 is specifically stimulated by the selective alpha2A-adrenergic receptor agonist UK14304 and by lysop
8 nstrates that agonist-mediated activation of alpha2A adrenergic receptors (alpha(2A)AR) is voltage-de
10 intracellular (3i) loop of the heptahelical alpha2A-adrenergic receptor (alpha2A AR) is critical for
13 ne expressing a point mutation (D79N) in the alpha2a adrenergic receptor (alpha2aAR) to investigate t
14 was tethered to the carboxyl terminus of the alpha2A adrenergic receptor (alpha2AAR-Galphai2YFP).
15 inent feature of long-term regulation of the alpha2A-adrenergic receptor (alpha2AAR) is a loss of cel
16 novel direct interaction between APP and the alpha2A-adrenergic receptor (alpha2AAR) that occurs at t
19 etween delta opioid receptors (deltaORs) and alpha2A adrenergic receptors (alpha2AARs) require protei
20 competing at the one allosteric site on the alpha2A-adrenergic receptor and rules out the possibilit
21 alter subsequent radioligand binding to the alpha2a-adrenergic receptor and the dopaminergic D1 rece
22 293 cells, stimulation of either alpha1B- or alpha2A-adrenergic receptors (ARs) leads to rapid 5-10-f
24 ith fluorescent proteins and four GPCRs: the alpha2A-adrenergic receptor, GABAB, cannabinoid receptor
25 fluorescently labeled Galphai1 subunits and alpha2A-adrenergic receptor, GABAB, or dopamine receptor
26 receptor complexes between micro-opioid and alpha2A-adrenergic receptors has been demonstrated in tr
27 e RVL, 59% of c-Fos-positive cells contained alpha2A-adrenergic receptor-like immunoreactivity in clo
28 uggest that the effects of the overexpressed alpha2A-adrenergic receptor on PLD activity are mediated
29 tion of Gi-coupled lysophosphatidic acid and alpha2A adrenergic receptors or overexpression of Gbeta1
31 and 0.97) with the affinities for the human alpha2A adrenergic receptor subtype and poorly correlate
32 this inhibition is relieved by activation of alpha2A-adrenergic receptor, suggesting that the interac
33 f9 cell membranes expressing the recombinant alpha2A-adrenergic receptor were used to assess the cont
34 abeled agonist and antagonist binding to the alpha2a-adrenergic receptor with an IC50 value of 0.5 mi
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