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1  the current practice of adding bosentan, an endothelin receptor antagonist.
2 ral phosphodiesterase-5 inhibitor or an oral endothelin-receptor antagonist.
3 terase type 5 inhibitors, sodium nitrite and endothelin receptor antagonists.
4 bitors, niacin, inhaled carbon monoxide, and endothelin receptor antagonists.
5  mineralocorticoid receptor antagonists, and endothelin receptor antagonists.
6 se biological effects that are unaffected by endothelin receptor antagonists.
7 s of disease-targeted therapy (predominantly endothelin receptor antagonists [47.3%] or phosphodieste
8 gated for the treatment of nmCRPC, including endothelin receptor antagonists and bone-targeted therap
9 -3-methyl-glutaryl-CoA reductase inhibitors, endothelin receptor antagonists and phosphodiesterase ty
10                                  Conversely, endothelin receptor antagonists and/or KIT blocking anti
11 ple, with phosphodiesterase 5 inhibitors and endothelin receptor antagonists) and, if necessary, the
12 he treatment of PAH: prostacyclin analogues, endothelin receptor antagonists, and phosphodiesterase t
13                                              Endothelin receptor antagonists are first-line therapy f
14                                              Endothelin-receptor antagonists are in clinical use to t
15 ciated PH and 27 of 39 with PAH) received an endothelin receptor antagonist as initial therapy.
16 hese findings raise the possibility of using endothelin receptor antagonists as neuroprotective agent
17         These data do not support the use of endothelin receptor antagonists as therapy for ILD secon
18 a 12-month trial of bosentan, a nonselective endothelin receptor antagonist, as a therapy for SSc-rel
19 R trial assessed the association between the endothelin receptor antagonist atrasentan and pain and p
20                                BMS182874, an endothelin receptor antagonist, blocks the effects of ex
21                           Treatment with the endothelin receptor antagonist bosentan may be effective
22 liminary study, the orally administered dual endothelin-receptor antagonist bosentan improved exercis
23                                          The endothelin-receptor antagonist bosentan is beneficial in
24   We investigated whether treatment with the endothelin receptor antagonist, bosentan, decreased the
25                                          The endothelin receptor antagonist BQ-485 (ET(A) selective)
26                                              Endothelin receptor antagonist (ERA) and phosphodiestera
27 i) may offset fluid retaining effects of the endothelin receptor antagonist (ERA) atrasentan while ef
28                                              Endothelin receptor antagonists (ERA) and phosphodiester
29   Preclinical studies have demonstrated that endothelin receptor antagonists (ERAs) can reduce or pre
30                                         Oral endothelin receptor antagonists (ERAs) have been shown t
31                                              Endothelin receptor antagonists (ERAs) reduce albuminuri
32                                    Selective endothelin receptor antagonists (ERAs) that target the e
33                         Administration of an endothelin receptor antagonist (ETRA, SB 209670) to dogs
34 s sodium-glucose cotransporter 2 inhibitors, endothelin receptor antagonists, glucagon-like peptide 1
35                               Atrasentan, an endothelin receptor antagonist, has shown activity in pr
36                                              Endothelin receptor antagonists have emerged as a novel
37 rable hemodynamic and neurohormonal effects, endothelin receptor antagonists have not improved outcom
38                                              Endothelin receptor antagonists have revolutionized the
39 mineralocorticoid antagonist and a selective endothelin receptor antagonist, have now been demonstrat
40                        In cells treated with endothelin receptor antagonists, hydrogen peroxide scave
41   In many studies, such as the Study with an Endothelin Receptor Antagonist in Pulmonary Arterial Hyp
42  data support a potential role for selective endothelin receptor antagonists in protecting renal func
43 roenvironment and further support the use of endothelin receptor antagonists in the treatment of inva
44  changes of HPS and the effects of selective endothelin receptor antagonists in vivo were assessed af
45 he efficacy and safety of tezosentan, a dual endothelin receptor antagonist, in patients hospitalized
46 nd safety of tezosentan, an intravenous dual endothelin receptor antagonist, in patients with moderat
47 sess the hemodynamic effects of bosentan, an endothelin receptor antagonist, in patients with PHT, in
48                    Additionally, infusion of endothelin receptor antagonists into the bursa of wild-t
49                                          The endothelin receptor antagonist is among the most effecti
50                         Aprocitentan, a dual endothelin receptor antagonist, is the first agent from
51                                          The endothelin receptor antagonist macitentan has demonstrat
52 ar Disease]), we evaluated the effects of an endothelin receptor antagonist, macitentan, in patients
53                                    Moreover, endothelin receptor antagonists may have a therapeutic r
54                The vasodilator properties of endothelin receptor antagonists may prove valuable thera
55    Three patients required PH treatment with endothelin receptor antagonist (n=2) or calcium channel
56 us epoprostenol were weaned off post-LT, and endothelin receptor antagonist or phosphodiesterase type
57 y hypoxia but attenuated by either selective endothelin receptor antagonists or oligonucleotides targ
58 were receiving riociguat in combination with endothelin receptor antagonists or prostanoids, or both.
59 hypertension and patients who were receiving endothelin-receptor antagonists or (nonintravenous) pros
60  the disease and in those who were receiving endothelin-receptor antagonists or prostanoids.
61 ials continue to explore new applications of endothelin receptor antagonists, particularly in treatme
62          These effects were prevented by the endothelin receptor antagonist PD145065 (10 microM) and
63  144-363 d) after the initial combination of endothelin receptor antagonist + phosphodiesterase-5 inh
64 erent classes of drugs are now available-ie, endothelin receptor antagonists, phosphodiesterase-5 inh
65             Administration of a nonselective endothelin receptor antagonist provided essentially equi
66                      Novel agents, including endothelin receptor antagonists, pyruvate kinase activat
67                                     Although endothelin-receptor antagonists reduce albuminuria in di
68 udy examined the effects of the nonselective endothelin receptor antagonist SB-209,670, and the less
69   For instance, macitentan and bosentan from endothelin receptor antagonists show major concern while
70                                          The endothelin receptor antagonist tezosentan did not improv
71                         Tezosentan is a dual endothelin receptor antagonist that has been shown to im
72    Tezosentan is an intravenous short-acting endothelin receptor antagonist that has favorable hemody
73           Ambrisentan is an oral, once-daily endothelin receptor antagonist that is selective for the
74  the efficacy and safety of bosentan, a dual endothelin-receptor antagonist that can be taken orally,
75 mendation for either prostacyclin agonist or endothelin receptor antagonist therapy and a strong reco
76                           We used a specific endothelin receptor antagonist to determine whether ET-1
77 essed the efficacy of macitentan, a new dual endothelin-receptor antagonist, using a primary end poin
78 n of the endothelin system with bosentan, an endothelin receptor antagonist, was strongly protective
79  pulmonary arterial hypertension, other than endothelin-receptor antagonists, was allowed at study en
80 tment naive or on background therapy with an endothelin receptor antagonist, were eligible.
81 ts, which have been previously attributed to endothelin receptor antagonists, were more frequent in t
82  as aldosterone synthase inhibitors and dual endothelin receptor antagonists, whereas others may prov
83 g at the identification of novel potent dual endothelin receptor antagonists with high oral efficacy.
84                      Increasing doses of the endothelin receptor antagonist zibotentan and lower eGFR