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1 es a reversible conformational change of the beta 2 receptor.
2 are supported by experimental studies of the beta 2 receptor.
3 olidine) as a PET agent for nicotine alpha(4)beta(2) receptors.
4 in double KO mice lacking both beta(1)- and beta(2)-receptors.
5 enol was reduced in mice lacking beta(1)- or beta(2)-receptors.
6 osition reduced activity at the beta(1)- and beta(2)-receptors.
7 , IL-23alpha subunit p19 (IL23A), adrenergic beta-2 receptor (ADRB2), oxidized LDL (lectin-like) rece
8 SD) but only weak relaxations to salbutamol (beta(2)-receptor agonist; 13 +/- 3%; P < 0.05) or BRL-37
10 of IL-6 by salmeterol was dependent upon the beta(2) receptor and could also be induced by cAMP or cA
11 intrinsic activity at either the beta(1) or beta(2) receptor, and significant thermogenesis effects
12 ut were unaffected by ICI-118,551 (selective beta(2)-receptor antagonist) or SR-59,230A (selective be
14 s are expressed in rat footpads; alpha 1 and beta 2 receptors are localized specifically to sweat gla
16 rent consensus on the relative importance of beta(2) receptor blockade in treating glaucoma may have
17 depression and activation slowing of alpha 1 beta 2 receptors, but had little effect on currents from
18 Zn2+ slowed macroscopic gating of alpha 1 beta 2 receptors by inducing a novel slow exponential co
20 fector of acute stress, and that beta(1) and beta(2) receptors can have quite distinct roles in CNS s
21 nuclear phospho-ERK1/2 than the chimeric V2 beta 2 receptor, consistent with the cytosolic retention
25 eptor cross-talk, which in turn could modify beta-2 receptor downregulation and associated tolerance
27 ABA (5 microM)-triggered currents of alpha 1 beta 2 receptors in a concentration-dependent manner (in
28 nses in K-177 cells expressing human alpha 4 beta 2 receptors, in IMR-32 and SH-SY5Y cells expressing
29 In stably transfected HEK-293 cells, the V2 beta 2 receptor increased ERK1/2-mediated, Elk-1-driven
32 polymerase chain reaction analyses show that beta(2)-receptor mRNA is the predominant beta-receptor m
33 lmeterol induced high-affinity states of the beta 2-receptor (pKh 9.6 +/- 0.4 and 10.4 +/- 0.7, respe
37 97), destroyed ligand binding of the alpha(M)beta(2) receptor, suggesting that these function-blockin
38 open and closed conformation of the alpha(M)beta(2) receptor, thereby indirectly affecting alpha(M)b
41 -fold selectivity over the human beta(1) and beta(2) receptors, which also displays good oral bioavai
42 eptors and enhanced activity at beta(1)- and beta(2)-receptors, while fluorination at the 6-position
43 also biexponential for preactivated alpha 1 beta 2 receptors with current depression more than fourf
44 substitution of the I domain of the alpha(L)beta(2) receptor with that of alpha(M) confers the alpha
45 or with that of alpha(M) confers the alpha(L)beta(2) receptor with the ability to interact with LRP1.
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