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1  the beta2 receptor relative to that for the beta1 receptor.
2 These results establish alphavbeta1 as a LAP-beta1 receptor.
3 eval in mutant mice lacking either NE or the beta1 receptor.
4                            Inhibition of TGF-beta1 receptor 1 blocked Smad3 phosphorylation; reduced
5 1/2), and this was inhibited by blocking TGF-beta1 receptor 1, Smad3, or the Nox oxidases; ERK1/2 act
6                               Stimulation of beta1 receptors and activation of the cAMP pathway lead
7 ol (2 mug) or vehicle (Experiment 2), or the beta1-receptor antagonist, atenolol (Experiment 3).
8 activated within this pathway, alpha1 and/or beta1 receptors, are targets for clinically prescribed a
9 his signaling requires a functional integrin beta1 receptor as showed by RNA interference.
10  duration and with dogs with MR treated with beta1-receptor blockade (RB; extended-release metoprolol
11 se inhibitor), or practolol (10(-6) mol/L, a beta1-receptor blocker).
12  with attenuated thermal hyperalgesia in TGF-beta1 receptor conditional knock-out mice, where TGF-bet
13  soluble fibronectin to cells via the alpha5 beta1 receptor decreased only about 3-fold.
14 ction covering 15 years in an interleukin-12 beta1 receptor-deficient individual that developed into
15                                              beta1-receptor downregulation also occurred in human PAH
16 ion-blocking antibodies directed towards the beta1 receptors dramatically reduced the tensional force
17 RYD sequence bound to macrophages and alpha4/beta1 receptor-expressing cells as well as did wild-type
18 lls, we demonstrate that IL-4 suppresses TGF-beta1 receptor expression and signaling, and vice versa.
19  internalize complexes of E-cadherin and TGF-beta1 receptors, generate phospho-Smad2 (p-Smad2)-pY654-
20 s blocked by a specific inhibitor of the TGF-beta1 receptor I and antibodies directed against alpha5
21                            The levels of TGF-beta1 receptor II (TbetaRII) in adenovirus-infected cell
22 CDA1 deletion reduced gene expression of TGF-beta1 receptors in the kidney, resulting in a functional
23 wley rats to determine the expression of TGF-beta1 receptors including endoglin, and the role of Ang
24 n, whereas downstream signaling from the TGF-beta1 receptor increased in both injured epithelium and
25                             The specific TGF-beta1 receptor inhibitor SB431542 reduced ALI/ARDS BALF-
26                                        A TGF-beta1 receptor inhibitor, Rho-associated protein kinase
27 own receptors for OPN, and that the integrin beta1 receptor is involved in transmitting the prolifera
28 r if the latency-associated protein or a TGF-beta1 receptor kinase inhibitor was added to block the b
29 blocked by pre-incubation with a soluble TGF-beta1 receptor mimetic.
30  In intact failing hearts, downregulation of beta1-receptor mRNA and protein, upregulation of atrial
31 ifferent effects in patients with CYP2D6 and beta1-receptor polymorphisms.
32                                   Inhibiting beta1 receptors prevented the increase in glycinergic, b
33                        Additionally, the TGF-beta1 receptor-regulated Smad proteins, in particular Sm
34 selective antagonists to visualize beta2 and beta1 receptors, respectively).
35 ts with the transforming growth factor (TGF)-beta1 receptor/smad phosphorylation inhibitor SB431542 i
36 mesenchymal transition without immediate TGF-beta1 receptor (TbetaR) kinase inhibition.
37 eta1 (TGF-beta1), transforming growth factor-beta1 receptor (TGF-beta1R), let-7a, and downstream expr
38   We established that Tif1gamma controls TGF-beta1 receptor (Tgfbr1) turnover.
39  to preferentially recognize ligand-occupied beta1 receptors was used to stain keratinocytes.

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