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1 cal angiotensin II production and the type 2 angiotensin receptor.
2 asoconstriction via the activation of type 1 angiotensin receptors.
3 ing from elevated angiotensin II (AngII) and angiotensin receptor 2 (AT2R) producing increased plasma
4 1)-AA), stimulates sEng production via AT(1) angiotensin receptor activation in pregnant mice but not
5 covered that a circulating autoantibody, the angiotensin receptor agonistic autoantibody (AT(1)-AA),
6 onism of MAS1 receptors, beta-arrestin-based Angiotensin receptor agonists, and administration of sol
7 c administration of specific blockers of the angiotensin receptor and the Na-Ca exchanger.
8 embranes, which is distinctly different from angiotensin receptors and key proteases processing angio
9  colleagues present evidence that implicates angiotensin receptors and the relocation of beta-catenin
10 tural basis of the distinct functions of the angiotensin receptors, and may guide the design of new s
11 f angiotensin-converting enzyme inhibitor or angiotensin receptor antagonist (88.3% versus 86.6%), an
12                          Thus, this combined angiotensin receptor antagonist and neprilysin inhibitor
13 ll three isoforms of TGF-beta), losartan (an angiotensin receptor antagonist), or a combination of th
14  tumor's inner core, AD was combined with an angiotensin receptor antagonist, Telmisartan (TS), which
15 Heart Failure) trial demonstrated that a new angiotensin receptor antagonist-neprilysin inhibitor was
16 ay lead to the development of a new class of angiotensin receptor antagonists with activities biased
17 rs, calcium channel blockers, diuretics, and angiotensin receptor antagonists), smoking status, alcoh
18  of angiotensin-converting enzyme inhibitors/angiotensin receptor antagonists, use of beta-blocker, a
19                       Here, we show that the angiotensin-receptor-associated protein (ATRAP) localize
20                                     Recently angiotensin receptor AT(2)R has been associated negative
21 n and termination of signaling of the type I angiotensin receptor (AT(1)-R) can lead to dynamic chang
22 genic autoantibodies that activate the major angiotensin receptor, AT(1).
23                 Biased agonism on the type I angiotensin receptor (AT1-R) can achieve different outco
24  of beta-arrestins in cross-talk between the angiotensin receptor (AT1aR) and a member of the transie
25 beta-arrestin2 recruitment to unliganded AT1 angiotensin receptor (AT1R).
26                                     Using an angiotensin receptor bacterial artificial chromosome (BA
27                                              Angiotensin receptor blockade and inhibition of local An
28 odocytes, which was prevented by concomitant angiotensin receptor blockade application and TRPC6 knoc
29 hat inhibition of TGF-beta signaling through angiotensin receptor blockade can attenuate CS-induced l
30 ly, the addition of neprilysin inhibition to angiotensin receptor blockade has been shown to be even
31 erglycemia and the antiproteinuric effect of angiotensin receptor blockade or angiotensin-converting
32  injections (RR 0.45; 95% CI 0.24-0.83), and angiotensin receptor blockade vs placebo (RR 0.65; 95% C
33 egradation inhibition through neprilysin and angiotensin receptor blockade, has led to groundbreaking
34  to pharmacological reduction of fibrosis by angiotensin receptor blockade.
35              These effects did not depend on angiotensin receptor blockade.
36  mucociliary dysfunction, independent of its angiotensin receptor blockade.
37  combination therapy with NEP-inhibitors and angiotensin-receptor-blockade, which has been shown bein
38 otensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB) affected the results.
39 ]: 1.04 to 1.10) and discharge ACE inhibitor/angiotensin receptor blocker (ARB) in LV dysfunction (64
40 tensin-converting enzyme inhibitor (ACEI) or angiotensin receptor blocker (ARB) influences disease ou
41  comparable antihypertensive activity to the angiotensin receptor blocker (ARB) losartan.
42         The combination of a diuretic and an angiotensin receptor blocker (ARB) or angiotensin-conver
43 ology study uses claims data to characterize angiotensin receptor blocker (ARB) prescription trends t
44 ensin-converting enzyme inhibitor (ACEI) and angiotensin receptor blocker (ARB) should be used for se
45 ed in increased cancer risk, with a focus on angiotensin receptor blocker (ARB) therapy, as recent pu
46 giotensin-converting enzyme inhibitor (ACEI)/angiotensin receptor blocker (ARB) use and mortality in
47 otensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB) use, ESA use, dialysi
48 sing angiotensin-converting enzyme inhibitor/angiotensin receptor blocker (beta=0.36, P<0.001; CI: 0.
49                 LCZ696, which consists of an angiotensin receptor blocker (valsartan [VAL]) and a nep
50 : high dose, 0.55; low dose, 0.72; both ACEi/angiotensin receptor blocker and beta-blocker: high dose
51                         We hypothesized that angiotensin receptor blocker and neprilysin inhibitor, s
52 ate, angiotensin-converting enzyme inhibitor/angiotensin receptor blocker and oral anti-diabetic agen
53                              Telmisartan, an angiotensin receptor blocker and partial PPAR-gamma agon
54  angiotensin-converting enzyme inhibitor, or angiotensin receptor blocker as foundational therapy, wi
55 g angiotensin converting enzyme inhibitor or angiotensin receptor blocker background therapy.
56                                          The angiotensin receptor blocker component of LCZ696, valsar
57  angiotensin-converting enzyme inhibitor and angiotensin receptor blocker groups resulted in two simi
58 ted, whereas acute HF and patients receiving angiotensin receptor blocker had higher plasma Ang II wi
59 been demonstrated that Valsartan (Val) as an angiotensin receptor blocker has renoprotective effects,
60 (angiotensin-converting enzyme) inhibitor or angiotensin receptor blocker if left ventricular ejectio
61 r angiotensin-converting enzyme inhibitor or angiotensin receptor blocker in eligible patients.
62 n angiotensin-converting enzyme inhibitor or angiotensin receptor blocker in persons with CKD to impr
63               Treatment for 4 weeks with the angiotensin receptor blocker irbesartan, but not with th
64                  Providing the anti-fibrotic angiotensin receptor blocker losartan to mice in drinkin
65                                          The angiotensin receptor blocker losartan was given to half
66                                     Combined angiotensin receptor blocker neprilysin inhibitors (ARNI
67 giotensin receptor neprilysin inhibitor with angiotensin receptor blocker on Management Of heart fail
68 ting the renoprotective benefit of adding an angiotensin receptor blocker or a mineralocorticoid rece
69 eive angiotensin-converting enzyme inhibitor/angiotensin receptor blocker therapy (P<0.01).
70 d angiotensin-converting enzyme inhibitor or angiotensin receptor blocker therapy, 100% beta-blocker
71 d angiotensin-converting enzyme inhibitor or angiotensin receptor blocker therapy, 35% beta-blocker t
72 d angiotensin-converting enzyme inhibitor or angiotensin receptor blocker therapy, 51% beta-blocker t
73 n angiotensin-converting enzyme inhibitor or angiotensin receptor blocker throughout the study.
74                                              Angiotensin receptor blocker treatment may blunt the har
75 of associations and to explore the impact of angiotensin receptor blocker treatment.
76 nd to identify patients who can benefit from angiotensin receptor blocker treatment.
77 us, and has less advanced disease than prior angiotensin receptor blocker trials in HCM.
78      Angiotensin-converting enzyme inhibitor/angiotensin receptor blocker uptake increased from 46% t
79 r angiotensin-converting enzyme inhibitor or angiotensin receptor blocker usage during continuous flo
80 d angiotensin converting enzyme inhibitor or angiotensin receptor blocker usage were not significantl
81 .5%, angiotensin-converting enzyme inhibitor/angiotensin receptor blocker use in 24.9+/-1.9%, and asp
82  and angiotensin-converting enzyme inhibitor/angiotensin receptor blocker use in patients with an Ame
83 s in angiotensin-converting enzyme inhibitor/angiotensin receptor blocker use or anticoagulation for
84 , angiotensin-converting enzyme inhibitor or angiotensin receptor blocker use, and nonsmoking status-
85   Angiotensin-converting enzyme inhibitor or angiotensin receptor blocker use, beta-blocker use, anti
86 angiotensin-converting enzyme inhibitor use, angiotensin receptor blocker use, BMI z-score for age an
87  and angiotensin-converting enzyme inhibitor/angiotensin receptor blocker use-is well suited to provi
88 rketed by Novartis as Entresto) combines the angiotensin receptor blocker valsartan and the neprilysi
89 RNi with neprilysin inhibitor sacubitril and angiotensin receptor blocker valsartan on myocardial rem
90 loped by scientists at Novartis, combines an angiotensin receptor blocker with a neprilysin inhibitor
91 angiotensin converting enzyme inhibitor, and angiotensin receptor blocker), and N-terminal probrain n
92 nsin-converting enzyme) inhibitor or an ARB (angiotensin receptor blocker), at maximal or maximally t
93 tensin-converting enzyme inhibitor (ACEi, or angiotensin receptor blocker), beta-blocker, or both dru
94 f an angiotensin converting enzyme inhibitor/angiotensin receptor blocker, and hydrochlorothiazide 12
95  for angiotensin-converting enzyme inhibitor/angiotensin receptor blocker, beta-blocker, and mineralo
96 ent (angiotensin-converting enzyme inhibitor/angiotensin receptor blocker, beta-blocker, and mineralo
97 n patients receiving higher doses of ACEi or angiotensin receptor blocker, beta-blocker, or both (haz
98  an angiotensin-converting enzyme inhibitor, angiotensin receptor blocker, calcium channel blocker, o
99 DMT (angiotensin-converting enzyme inhibitor/angiotensin receptor blocker, or beta-blocker) at baseli
100 ngiotensin-converting enzyme inhibitor or an angiotensin receptor blocker, should generally be includ
101                                              Angiotensin receptor blocker-neprilysin inhibitor (ARNi)
102 n either stand-alone neprilysin inhibitor or angiotensin receptor blocker.
103  and angiotensin-converting enzyme inhibitor/angiotensin receptor blocker.
104 f angiotensin-converting enzyme inhibitor or angiotensin receptor blocker.
105 c agent that combines a NEP inhibitor and an angiotensin receptor blocker.
106 rd ratio for eplerenone versus placebo, ACEi/angiotensin receptor blocker: high dose, 0.67; low dose,
107 sin Receptor-Neprilysin Inhibitor] with ARB [Angiotensin Receptor Blocker] Global Outcomes in HFpEF),
108 tly less likely after dual treatment with an angiotensin-receptor blocker (ARB) and an angiotensin-co
109 erting-enzyme inhibitor (lisinopril) plus an angiotensin-receptor blocker (telmisartan) or lisinopril
110 st orally active direct renin inhibitor, the angiotensin-receptor blocker losartan, and their combina
111 scle fibrosis and improved pain Losartan, an angiotensin-receptor blocker with anti-fibrotic abilitie
112 in-converting enzyme inhibitor) or losartan (angiotensin-receptor blocker) in FSGS mice stimulated th
113 ngiotensin-converting-enzyme inhibitor or an angiotensin-receptor blocker.
114  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers (18.2% vs 16.9%, p = 1.000
115 for angiotensin-converting enzyme inhibitors/angiotensin receptor blockers (66% versus 68%; P=0.04) a
116 and angiotensin converting enzyme inhibitors/angiotensin receptor blockers (ACEI/ARB) in acute myocar
117 ic shock, and mortality than those receiving angiotensin receptor blockers (all p < 0.001).
118              Pre-hospital use vs. non-use of angiotensin receptor blockers (aOR 2.02, CI 1.03-3.96) a
119 ensin-converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB) are generally well t
120 nsin-converting enzyme inhibitors (ACEI) and angiotensin receptor blockers (ARB) doses on outcomes in
121 ensin-converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB) initiated after myoc
122 tensin-converting enzyme (ACE) inhibitors or angiotensin receptor blockers (ARB) were associated with
123 otensin-converting enzyme inhibitors (ACEI), angiotensin receptor blockers (ARB), beta-blockers (BB),
124 ensin-converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB).
125 tensin-converting enzyme (ACE) inhibitors or angiotensin receptor blockers (ARBs) and beta blockers.
126 nin angiotensin system pathways suggest that angiotensin receptor blockers (ARBs) are ideal drugs to
127 nsin-converting enzyme inhibitors (ACEIs) or angiotensin receptor blockers (ARBs) are widely prescrib
128 sin-converting-enzyme inhibitors (ACE-Is) or angiotensin receptor blockers (ARBs) both increased sign
129                                              Angiotensin receptor blockers (ARBs) convert myofibrobla
130                                   The use of angiotensin receptor blockers (ARBs) correlates with red
131 ertensive patients (n = 469), patients using angiotensin receptor blockers (ARBs) did not show a decl
132    PURPOSE OF REVIEW: As their introduction, angiotensin receptor blockers (ARBs) have been widely pr
133 tensin-converting enzyme (ACE) inhibitors or angiotensin receptor blockers (ARBs) in patients with ty
134  has revealed that ACE inhibitors (ACEIs) or angiotensin receptor blockers (ARBs) may be beneficial i
135 sin-converting enzyme inhibitors (ACEis) and angiotensin receptor blockers (ARBs) may increase the ri
136 otensin-converting enzyme inhibitors (ACEIs)/angiotensin receptor blockers (ARBs) may make patients m
137 in-converting enzyme inhibitors (ACE-Is) and angiotensin receptor blockers (ARBs) on the composite of
138 iotensin-converting enzyme (ACE) inhibitors, angiotensin receptor blockers (ARBs), and direct renin (
139 iotensin converting enzyme (ACE) inhibitors, angiotensin receptor blockers (ARBs), beta blockers, and
140 otensin-converting enzyme inhibitors (ACEI), angiotensin receptor blockers (ARBs), beta-blockers, and
141 target the renin angiotensin system, such as angiotensin receptor blockers (ARBs), have been associat
142 in-converting enzyme inhibitors (ACE-Is) and angiotensin receptor blockers (ARBs), may be associated
143 tensin-converting enzyme (ACE) inhibitors or angiotensin receptor blockers (ARBs).
144  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers (HR, 0.90; 95% CI, 0.79-1.
145  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers (ie, renin-angiotensin sys
146 for angiotensin-converting enzyme inhibitors/angiotensin receptor blockers (median, 85%; interquartil
147  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers (p = 0.029), higher biliru
148 ile lower ATP was associated with the use of angiotensin receptor blockers (P=0.015).
149 tensin-converting enzyme inhibitors [ACEIs], angiotensin receptor blockers [ARBs], and beta-blockers
150 nsin-converting enzyme inhibitors [ACEIs] or angiotensin receptor blockers [ARBs], and cilostazol) an
151 iotensin-converting enzyme inhibitors and/or angiotensin receptor blockers achieves only partial reno
152  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers and 82% were receiving bet
153 expression is ameliorated by antiproteinuric angiotensin receptor blockers and angiotensin-converting
154 ith angiotensin-converting enzyme inhibitors/angiotensin receptor blockers and beta-blockers and an o
155 use angiotensin-converting enzyme inhibitors/angiotensin receptor blockers and beta-blockers compared
156  Angiotensin-converting enzyme inhibitors or angiotensin receptor blockers and beta-blockers were pre
157                                              Angiotensin receptor blockers are renoprotective in hype
158  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers at admission), beta-blocke
159  of angiotensin-converting enzyme inhibitors/angiotensin receptor blockers at discharge decreased in
160 and angiotensin-converting enzyme inhibitors/angiotensin receptor blockers decreased from 89%, 84.9%,
161 f angiotensin-convering enzyme inhibitors or angiotensin receptor blockers during the study and a his
162  cardiovascular examples, such as the use of angiotensin receptor blockers for chronic heart failure,
163  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers for more than 90 days betw
164  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers for secondary prevention a
165  (3) angiotensin-converting enzyme inhibitor/angiotensin receptor blockers for systolic dysfunction,
166 he therapeutic benefits of beta-blockers and angiotensin receptor blockers given the emerging concept
167 angiotensin-converting enzyme inhibitors and angiotensin receptor blockers have demonstrated benefici
168        Thiazide diuretics, ACE-inhibitors or angiotensin receptor blockers if ACE-inhibitor-intoleran
169                       Six previous trials of angiotensin receptor blockers in HCM enrolled a median o
170  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers in patients with COVID-19.
171 ngiotensin-converting enzyme inhibitors, and angiotensin receptor blockers in patients with heart fai
172 ngiotensin-converting enzyme inhibitors, and angiotensin receptor blockers increased by 23%, 57%, 31%
173 ensin converting enzyme (ACE) inhibitors and angiotensin receptor blockers increases the likelihood o
174 and angiotensin-converting enzyme inhibitors/angiotensin receptor blockers on outcome in patients wit
175 angiotensin-converting enzyme inhibitors and angiotensin receptor blockers on the risk and outcomes o
176 he renin-angiotensin-aldosterone system with angiotensin receptor blockers or angiotensin-converting
177  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers requires further investiga
178 for angiotensin-converting enzyme inhibitors/angiotensin receptor blockers therapy, 1.08 (95% confide
179 angiotensin-converting enzyme inhibitors and angiotensin receptor blockers use, was similar between c
180                       Chronic treatment with angiotensin receptor blockers was associated with better
181  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers was indicated in 18.1% of
182                                              Angiotensin receptor blockers were associated with lower
183  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers with well controlled BP an
184 ensin-converting enzyme) inhibitors or ARBs (angiotensin receptor blockers) with beta-blockers (BBs)
185 ing angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, and 4.5 million not recei
186  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, and aldosterone antagonis
187 aneurysmal disease, including beta-blockers, angiotensin receptor blockers, and angiotensin-convertin
188 ns, angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, and beta-blockers, respec
189 s, ACE inhibitors, calcium channel blockers, angiotensin receptor blockers, and diuretics.
190  of angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, and more sunscreen use in
191  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, and P2Y12 antagonists) re
192 rs, angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, and statins after acute m
193 rs, angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, and statins reduces cardi
194  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, antiplatelet drugs, beta-
195  used in the clinic AT(1)R antagonist drugs (angiotensin receptor blockers, ARBs, or sartans) at prev
196  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, beta-blockers, aldosteron
197  of angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, beta-blockers, aldosteron
198    Angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, beta-blockers, and aldost
199 ns, angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, beta-blockers, and dual a
200 ns, angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, beta-blockers, and dual a
201 sed angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, beta-blockers, and statin
202 (angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, beta-blockers, spironolac
203 s, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, dihydropyridine calcium c
204 le angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, or both.
205 of angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, or sacubitril-valsartan.
206 rs, angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, P2Y12 inhibitors, and the
207 -blockers, angiotensin-converting inhibitors/angiotensin receptor blockers, statins, diabetic treatme
208 and -3.07 mm Hg (95% CI, -4.99 to -1.44) for angiotensin receptor blockers.
209  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers.
210  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers.
211  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers.
212 zyme, and synthesis of its inhibitors and of angiotensin receptor blockers.
213  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers.
214 angiotensin-converting enzyme inhibitors, or angiotensin receptor blockers.
215  of the next generation of beta-blockers and angiotensin receptor blockers.
216 angiotensin-converting enzyme inhibitors and angiotensin receptor blockers.
217 rt and compare to previous trials evaluating angiotensin receptor blockers.
218 .87 per 100 person-years for those receiving angiotensin receptor blockers.
219 .31; 95% CI, 1.22-1.40) than those receiving angiotensin receptor blockers.
220  angiotensin-converting enzyme inhibitors or angiotensin receptor blockers.
221 (+) intake and angiotensin converting enzyme/angiotensin receptors blockers Rx.
222 ing angiotensin-converting enzyme inhibitors/angiotensin receptors blockers, beta-blockers, and devic
223 (ACE) inhibitors (1.08, 1.02-1.15, p=0.008), angiotensin-receptor blockers (1.16, 1.07-1.25, p=0.0002
224   A potential association between the use of angiotensin-receptor blockers (ARBs) and angiotensin-con
225                                              Angiotensin-receptor blockers (ARBs) are a widely used d
226                                              Angiotensin-receptor blockers (ARBs) are effective treat
227 ensin-converting-enzyme (ACE) inhibitors and angiotensin-receptor blockers (ARBs) decreases proteinur
228 sin-converting enzyme inhibitors (ACEIs) and angiotensin-receptor blockers (ARBs) in coronavirus dise
229 ensin-converting-enzyme (ACE) inhibitors and angiotensin-receptor blockers (ARBs) in this clinical co
230 ensin-converting enzyme (ACE) inhibitors and angiotensin-receptor blockers (ARBs) reduce cardiovascul
231 tensin-converting enzyme (ACE) inhibitors or angiotensin-receptor blockers (ARBs) who filled brand-na
232 ensin-converting-enzyme (ACE) inhibitors and angiotensin-receptor blockers (ARBs), 3-hydroxy-3-methyl
233 tensin-converting-enzyme (ACE) inhibitors or angiotensin-receptor blockers (ARBs), and beta blockers
234 iotensin-converting enzyme (ACE) inhibitors, angiotensin-receptor blockers (ARBs), beta blockers, and
235 allergic myocardial infarction, anaphylaxis, angiotensin-receptor blockers (ARBs), beta-adrenergic bl
236  recent analysis showing increased risk with angiotensin-receptor blockers (ARBs).
237 ean BP reduction 12.9/7.7 mm Hg; p < 0.003), angiotensin-receptor blockers (mean BP reduction 13.3/7.
238  angiotensin-converting enzyme inhibitors or angiotensin-receptor blockers after SAVR for severe AS b
239  angiotensin-converting enzyme inhibitors or angiotensin-receptor blockers after surgical aortic valv
240 (angiotensin-converting enzyme inhibitors or angiotensin-receptor blockers and statins), and adverse
241 (angiotensin-converting enzyme inhibitors or angiotensin-receptor blockers and statins), and adverse
242 angiotensin-converting enzyme inhibitors and angiotensin-receptor blockers are not associated with gr
243                           ACE-inhibitors and angiotensin-receptor blockers remain excellent first lin
244 re angiotensin-converting enzyme inhibitors, angiotensin-receptor blockers, alpha-blockers, beta-bloc
245 irm the beneficial effect of ACE-inhibitors, angiotensin-receptor blockers, and diuretics and/or beta
246 of angiotensin-converting enzyme inhibitors, angiotensin-receptor blockers, beta blockers, calcium-ch
247 ng angiotensin-converting-enzyme inhibitors, angiotensin-receptor blockers, beta-blockers, and minera
248 ween previous treatment with ACE inhibitors, angiotensin-receptor blockers, beta-blockers, calcium-ch
249 ., angiotensin-converting enzyme inhibitors, angiotensin-receptor blockers, calcium channel blockers,
250  angiotensin-converting enzyme inhibitors or angiotensin-receptor blockers.
251 angiotensin-converting-enzyme inhibitors, or angiotensin-receptor blockers.
252 is of unproven value, even beta-blockers and angiotensin-receptor blockers.
253  angiotensin-converting enzyme inhibitors or angiotensin receptor blocking agents 85.3% versus 77.4%
254 ssociated with increased activation of brain angiotensin receptors, enhanced sympathetic nervous syst
255 sms for sexual dimorphism of regional aortic angiotensin receptor expression and AAA formation are un
256                           Mice lacking AT(1) angiotensin receptors have an impaired capacity to conce
257 s indicate widespread up-regulation of brain angiotensin receptors in SHR.
258 e findings suggest that activation of type 1 angiotensin receptors in the glomerulus is sufficient to
259 ies suggest that hyperactivation of brain AT angiotensin receptors is a major pathophysiological fact
260  In murine systems, there is a second type 1 angiotensin receptor isoform, AT1B, and its expression i
261 that are being probed include, among others, angiotensin receptors, matrix metalloproteinases, integr
262                                              Angiotensin receptor neprilysin inhibition (ARNI) therap
263 e based on type 2 diabetes status, age, sex, angiotensin receptor neprilysin inhibitor (ARNI) treatme
264 icacy and safety of LCZ696, a first-in-class angiotensin receptor neprilysin inhibitor (ARNI), in pat
265 eptide and left atrial size suggest that the angiotensin receptor neprilysin inhibitor LCZ696 may red
266 ioN fracTion (PARAMOUNT) trial, in which the angiotensin receptor neprilysin inhibitor LCZ696 reduced
267 ents with heart failure (HF) treated with an angiotensin receptor neprilysin inhibitor lived longer w
268                                          The angiotensin receptor neprilysin inhibitor sacubitril/val
269                                          The angiotensin receptor neprilysin inhibitor sacubitril/val
270 rtality and Morbidity in Heart Failure), the angiotensin receptor neprilysin inhibitor sacubitril/val
271 on enrolled in the Prospective comparison of angiotensin receptor neprilysin inhibitor with angiotens
272                                              Angiotensin receptor neprilysin inhibitors (ARNi), beyon
273 ACEI)/angiotensin II receptor blocker (ARB), angiotensin receptor-neprilysin inhibitor (ARNI), beta-b
274                              We compared the angiotensin receptor-neprilysin inhibitor LCZ696 with en
275  randomized in the Prospective Comparison of Angiotensin Receptor-Neprilysin Inhibitor With an Angiot
276  from PARADIGM-HF (Prospective Comparison of Angiotensin Receptor-Neprilysin Inhibitor With Angiotens
277 ence in the rate of mortality when comparing angiotensin receptor-neprilysin inhibitor+BB+mineralocor
278 c defibrillator+ACE inhibitor or ARB+BB, and angiotensin receptor-neprilysin inhibitor+BB+mineralocor
279 be treated with a beta-blocker and one of an angiotensin receptor-neprilysin inhibitor, angiotensin-c
280          Sacubitril/valsartan, a combination angiotensin receptor-neprilysin inhibitor, improves morb
281 GM-HF trial (Prospective Comparison of ARNI [Angiotensin Receptor-Neprilysin Inhibitor] With ACEI [An
282             (Prospective Comparison of ARNI [Angiotensin Receptor-Neprilysin Inhibitor] with ACEI [An
283 PARADIGM-HF (Prospective Comparison of ARNI [Angiotensin Receptor-Neprilysin Inhibitor] with ACEI [An
284  PARAGON-HF (Prospective Comparison of ARNI [Angiotensin Receptor-Neprilysin Inhibitor] with ARB [Ang
285 alocorticoid receptor antagonists (MRA), and angiotensin receptor-neprilysin inhibitors (ARNI), have
286 neralocorticoid receptor antagonists [MRAs], angiotensin receptor-neprilysin inhibitors [ARNIs], and
287 ive efficacy of pharmacological therapy with angiotensin receptor-neprilysin inhibitors and device th
288 or adverse outcomes in patients treated with angiotensin receptor-neprilysin inhibitors.
289 ening in the Prospective Comparison of ARNI (angiotensin-receptor-neprilysin inhibitor) with ACEI (an
290 duced ejection fraction treatment with ARNI (angiotensin receptor/neprilysin inhibitor) therapy or le
291 ystems diacylglycerol produced during type 1 angiotensin receptor signaling can be converted to 2-ara
292 al mechanism for biased ligand action at the angiotensin receptor that can be exploited to rationally
293 th an animal model of PTSD and the selective angiotensin receptor type 1 (AT1) antagonist losartan, w
294 played decreased fibrosis in response to the angiotensin receptor type 1 blocker losartan showed decr
295                          Use of losartan, an angiotensin receptor type 1 blocker used widely in the c
296 derlies increased placental HIF-1alpha in an angiotensin receptor type 1 receptor agonistic autoantib
297 sin I converting enzyme (ACE) inhibitors and angiotensin receptor type I (AT(1)R) antagonists.
298 eptors different from AT(1)R, in particular, angiotensin receptor type II (AT(2)R), resulting in biol
299                           ACE2 together with angiotensin receptor types 1 and 2 and ACE2 are componen
300 ance between angiotensin II, which activates angiotensin receptor types 1 and 2, and angiotensin 1-7

 
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