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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
9 pointing and less effective than long-acting beta(2)-receptor agonists.
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
13                      alpha 1B, alpha 2B, and beta 2 receptors are expressed in rat footpads; alpha 1
14 s are expressed in rat footpads; alpha 1 and beta 2 receptors are localized specifically to sweat gla
15       Because the gene coding the adrenergic beta(2) receptor (beta(2)AR) is embedded in the 5-HT(4)R
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
19           These results demonstrate that the beta(2) receptor can be a critical effector of acute str
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
22                                Surprisingly, beta(2)-receptors contribute to adrenergic vasodilation
23             alpha 1 and, to a lesser extent, beta 2 receptors decrease during development, whereas al
24                    The number of alpha 1 and beta 2 receptors decreases after P21, when the sympathet
25 eptor cross-talk, which in turn could modify beta-2 receptor downregulation and associated tolerance
26           Analysis of CD spectra of purified beta 2 receptor in the detergent micelle indicated that
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
30                              In summary, the beta-2 receptor mediates beta-adrenergic stimulation of
31 t, it is not known whether the beta-1 or the beta-2 receptor mediates this effect.
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
34      Binding of (18)F-nifrolidine to alpha(4)beta(2) receptor-rich regions in rats and monkeys indica
35                             Nicotine alpha(4)beta(2) receptor subtypes are implicated in the study of
36 ion pattern of nAChR containing alpha(4) and beta(2) receptor subunits (alpha(4)beta(2)*).
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
39        Similar contributions of beta(1)- and beta(2)-receptors to isoproterenol-induced vasorelaxatio
40                   Using these mutant alpha(M)beta(2) receptors, we have mapped the epitopes of nine 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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