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1 ously defined constitutive activation of the alpha 2-adrenergic receptor.
2 otein expression of NE transporter (NET) and alpha(2) adrenergic receptor.
3 that control song contain high densities of alpha(2)adrenergic receptors.
4 a(1)- and beta-adrenergic receptors, but not alpha(2)-adrenergic receptors.
5 ted secretion, in the cell surface export of alpha(2)-adrenergic receptors.
6 hat it is primarily mediated by postsynaptic alpha(2)-adrenergic receptors.
7 morphisms of the adenosine A2A receptors and alpha(2)-adrenergic receptors.
9 olin-stimulated cAMP accumulation induced by alpha(2)-adrenergic receptor activation is altered follo
13 ergic receptor antagonist, prazosin, and the alpha(2)-adrenergic receptor agonist, clonidine, reduced
14 ohimbine (1.0 microm), and attenuated by the alpha(2)-adrenergic receptor agonist, UK 14,304 (1.0 mic
17 Ang II-sensitive cells were inhibited by alpha 2-adrenergic receptor agonists (12 of 15 neurons).
18 e is reduced responsiveness to alpha(1)- and alpha(2)-adrenergic receptor agonists in skeletal muscle
19 tially localized apically, whereas the three alpha 2-adrenergic receptor (alpha 2 AR) subtypes are lo
20 mically the distribution of the A subtype of alpha 2-adrenergic receptor (alpha 2A-AR) in the rat cen
23 sly identified spinophilin as a regulator of alpha(2) adrenergic receptor (alpha(2)AR) trafficking an
24 receptor) and inhibitory (Galpha(i)-mediated alpha(2)-adrenergic receptor (alpha(2)-AR)) signals to a
26 d the role of the extracellular N termini of alpha(2)-adrenergic receptors (alpha(2)-ARs) in the ante
28 olateral localization and trafficking of the alpha(2)-adrenergic receptors (alpha(2)AR) are not; inst
30 everal studies have shown that activation of alpha(2)-adrenergic receptors (alpha(2)ARs) leads to mil
36 y stenosis before and during infusion of the alpha 2-adrenergic receptor antagonist idazoxan (1.0 mic
37 (iv) NA overflow for MA was enhanced by the alpha(2)-adrenergic receptor antagonist, yohimbine (1.0
38 t of human melanocyte cell cultures with the alpha-2 adrenergic receptor antagonist yohimbine results
39 mmonis 3 (CA3) epileptiform activity through alpha(2) adrenergic receptor (AR) activation on pyramida
40 regulating trafficking and signaling of the alpha(2)-adrenergic receptor (AR) both in vitro and in v
47 e activation of either supraspinal or spinal alpha(2) adrenergic receptors can induce antinociception
48 Chinese hamster ovary-K1 cells impaired the alpha(2)-adrenergic receptor G(s)-mediated stimulation o
49 ed: Galpha(oA) = Galpha(oB) > Galpha(i2) for alpha(2)-adrenergic receptor; Galpha(i2) > Galpha(oA) =
54 ast to that which occurs in the hippocampus, alpha(2)-adrenergic receptor inhibition of NE release is
56 gulates the Golgi to cell surface traffic of alpha(2)-adrenergic receptors, likely through a physical
57 on a natively expressed signalling pathway, alpha(2)-adrenergic receptor-mediated I(Ca) modulation,
59 r nerve injury, the cascade of activation of alpha(2) adrenergic receptors-muscarinic receptors-NO in
61 (3)R) was increased but not signaling of the alpha(2) adrenergic receptor or bradykinin BK(2) recepto
63 ts suggest that spinal (but not supraspinal) alpha(2) adrenergic receptors play a significant role in
65 aused an approximate 50% decrease in NET and alpha(2) adrenergic receptor protein expression in sever
67 l epithelial cells, all three epitope-tagged alpha 2-adrenergic receptor subtypes were found in neuro
68 -PCR was performed to detect the mRNA of the alpha(2)-adrenergic receptor subtypes alpha(2)A, alpha(2
69 ugh regulation of TNF expression, transforms alpha(2)-adrenergic receptors such that they function to
70 ation/down-regulation of the chromaffin cell alpha(2)-adrenergic receptors that normally inhibit CA s
72 BRET signals were observed for AGS4-RLuc and alpha(2)-adrenergic receptor-Venus, which were Galpha(i)
74 le in vivo interactions between dopamine and alpha(2)-adrenergic receptors was investigated in quail,
75 avian brain, indicating that the density of alpha(2) adrenergic receptors within the song system mig
76 volumes of song nuclei, and the densities of alpha(2) adrenergic receptors within the song system of
77 e largest, T was highest, and the density of alpha(2) adrenergic receptors (within HVc and RA) was lo
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