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1 in T) and dysfunction (N-terminal pro-B-type natriuretic peptide).
2 ate) on binding of ANP, BNP (atrial or brain natriuretic peptide).
3 tocrit, and NT-proBNP (N-terminal pro b-type natriuretic peptide).
4 of-life, and NT-proBNP (N-terminal pro-brain natriuretic peptide).
5  biomarkers (including N-terminal pro-B-type natriuretic peptide).
6 -dependent degradation of vasodilator atrial natriuretic peptide.
7 l strain, and N-terminal prohormone of brain natriuretic peptide.
8 grades vasoactive peptides, including atrial natriuretic peptide.
9 ic variables including N-terminal pro-B-type natriuretic peptide.
10 ype natriuretic peptide (BNP) and the C-type natriuretic peptide.
11  ejection fraction and N-terminal pro-B-type natriuretic peptide.
12 itional markers, such as N-terminal probrain natriuretic peptide.
13 nt, peripheral ischemic preconditioning, and natriuretic peptide.
14 x turnover), ST-2, and N-terminal pro-B-type natriuretic peptide.
15 ardiac troponin T, and N-terminal pro-B-type natriuretic peptide.
16 ith the cardiac marker N-terminal pro-B-type natriuretic peptide.
17 tion rate >=30 mL/min/1.73m(2), and elevated natriuretic peptides.
18 systolic function and remodeling and reduces natriuretic peptides.
19 riable changes in concentrations of multiple natriuretic peptides.
20  improvements in HF-related health status or natriuretic peptides.
21  (including NT-proBNP [N-terminal pro-B-type natriuretic peptide]).
22 , medical therapy escalation, and BNP [brain natriuretic peptide]).
23 -197) ng/L, NT-proBNP (N-terminal-pro-B-type natriuretic peptide) 624 (307-1312) ng/L, hs-cTnI (high
24 n (83.0 vs. 28.5 ng/L; P < 0.05), and B-type natriuretic peptide (7,424.5 vs. 3,209.5 pg/mL; P < 0.05
25 t AF-associated human variant p.Ile138Thr in natriuretic peptide A (NPPA) encoding the atrial natriur
26 he NT-proBNP (N-terminal prohormone of brain natriuretic peptide)-a biomarker that is used for screen
27 s pro-atrial natriuretic peptide into atrial natriuretic peptide, a cardiac hormone that regulates bl
28  Npr2 abolished protective effects of C-type natriuretic peptide, a ligand for Npr2, against death of
29  Vosoritide is a biologic analogue of C-type natriuretic peptide, a potent stimulator of endochondral
30       Also central to diagnosis are elevated natriuretic peptides above age- and context-specific thr
31                   Plasma aldosterone, B-type natriuretic peptide, active renin concentration, and cli
32 lar markers, including Nppb, encoding B-type natriuretic peptide, after infarction.
33 ocalin) and NT-proBNP (N-terminal pro-B-type natriuretic peptide; all P<0.001).
34             NT-proBNP (N-terminal pro-B-type natriuretic peptide) alone at a cutoff of >800 identifie
35           Preoperative N-terminal pro-B-type natriuretic peptide and cardiovascular events after nonc
36  signaling by extracellular peptides (C-type natriuretic peptide and EGF receptor ligands) maintain t
37 impairment, and higher N-terminal pro-B-type natriuretic peptide and high-sensitivity troponin T conc
38 obustly associated with N-terminal pro-brain natriuretic peptide and incident HF or death.
39  key zinc-dependent metallopeptidases in the natriuretic peptide and kinin systems and renin-angioten
40   To further investigate the local action of natriuretic peptide and p38 MAPK in podocytes, we genera
41  size) with concomitant N-terminal pro-brain natriuretic peptide and subsequent HF hospitalization or
42  biomarkers of post-MI HF: N-terminal B-type natriuretic peptide and troponin T, and newly emergent b
43 l capacity, biomarkers (N-terminal pro-brain natriuretic peptide and/or high-sensitivity troponin T),
44  the prognostic value of sST2 is additive to natriuretic peptides and (in the case of chronic HF) to
45    Changes in insulin signaling, circulating natriuretic peptides and adipokines, and varied expressi
46     Some ubiquitous biomarkers, for example, natriuretic peptides and cardiac troponin, may assist in
47 e regulation, indicated by the expression of natriuretic peptides and proteins related to the renin-a
48 oming the resistance to diuretics and atrial-natriuretic-peptide and inhibiting Na-H exchangers and s
49 re (1) mean NT-proBNP (N-terminal pro b-type natriuretic peptide) and (2) proportion of patients with
50                                  ANP (atrial natriuretic peptide) and BNP (B-type natriuretic peptide
51  of cardiac biomarkers (troponins and B-type natriuretic peptide) and cardiac dysfunction for 24-48 h
52 contrast to NT-proBNP (N-terminal pro-B-type natriuretic peptide) and hs-TnT (high-sensitivity tropon
53         NT-proBNP (N-terminal pro-brain-type natriuretic peptide) and myocardial perfusion reserve we
54                             Both BNP (B-type natriuretic peptide) and NT-proBNP (N-terminal pro B-typ
55  natriuretic peptides (N-terminal pro-B type natriuretic peptide) and rest/exercise echocardiography
56 atrial natriuretic peptide), BNP (brain-type natriuretic peptide), and cGMP, and decreased plasma end
57 ial volume, NT-proBNP (N-terminal pro-B-type natriuretic peptide), and fibrosis biomarkers; and lower
58 onin T (hsTnT), NT-proBNP (N-terminal B-type natriuretic peptide), and growth differentiation factor-
59 dinal strain, N-terminal prohormone of brain natriuretic peptide, and adverse cardiac outcomes compar
60 ve Risk Evaluation II, N-terminal pro-B-type natriuretic peptide, and cardiac troponin T concentratio
61 sma norepinephrine and N-terminal pro-B-type natriuretic peptide, and chemosensitivity to hypercapnia
62 , randomized treatment, N-terminal pro-brain natriuretic peptide, and clinical risk factors.
63 y greater reduction in N-terminal pro-B-type natriuretic peptide, and improved clinical outcomes comp
64 iltration rate, higher N-terminal pro-B-type natriuretic peptide, and lower peak Vo(2).
65 rular filtration rate, N-terminal pro-B-type natriuretic peptide, and peak oxygen consumption (Vo(2))
66 duced fat oxidation to affect cardiac atrial natriuretic peptide, and thus, induce adipose lipolysis,
67 otein, lipoprotein(a), N-terminal pro-B-type natriuretic peptide, and transferrin), and apolipoprotei
68 ndent prognostic value even beyond symptoms, natriuretic peptides, and Meta-Analysis Global Group in
69 ed to as atrial natriuretic factor or atrial natriuretic peptide (ANP) and brain or B-type natriureti
70 iuretic peptide A (NPPA) encoding the atrial natriuretic peptide (ANP) causes inflammation, fibroblas
71    Effects of sacubitril/valsartan on atrial natriuretic peptide (ANP) concentrations in patients are
72                                       Atrial natriuretic peptide (ANP) influences glucose homeostasis
73                                       Atrial natriuretic peptide (ANP) is a peptide hormone that in r
74                              Although atrial natriuretic peptide (ANP) is not amidated, Pam expressio
75 in the receptor-binding region of the A-type natriuretic peptide (ANP), demonstrating that they affec
76            Although neither atrial nor brain natriuretic peptide (ANP, BNP) is amidated, the major me
77 sin II (ANG II; vasoconstrictive) and atrial natriuretic peptide (ANP; vasodilatory) antagonize the b
78                                              Natriuretic peptides are substrates of neprilysin; hence
79 eptide) and NT-proBNP (N-terminal pro B-type natriuretic peptide) are widely used to aid diagnosis, a
80                                         NPs (natriuretic peptides) are cardiac-derived hormones that
81 ies study heart failure risk score excluding natriuretic peptides as the base model to which we added
82 igated the potential of uCNP (urinary C-type natriuretic peptide) as a biomarker for AKI.
83 cubitril/valsartan on results from different natriuretic peptide assays.
84  (28-scanning point method), and BNP (B-type natriuretic peptide) assessment during supine exercise e
85 de concentrations and compared the impact of natriuretic peptide-associated genetic variants on blood
86 ent effect on N-terminal prohormone of brain natriuretic peptide at 18 months was observed in the ove
87 siran lowered N-terminal prohormone of brain natriuretic peptide at 9 and 18 months (at 18 months, ra
88 ponin-T and NT-proBNP [N-terminal Pro-B-type natriuretic peptide]) at baseline (pre-ERT) and 12 month
89  associated with HF more closely than B-type natriuretic peptide (AUC = 0.97 versus 0.84, p = 0.011).
90  mRNA expression of myosin heavy chain 7 and natriuretic peptide B is up-regulated in both ventricles
91 ng, a 6-minute walk test, and measurement of natriuretic peptides before and 1 year after AVR.
92 e determined whether plasma levels of B-type natriuretic peptide (BNP) and cardiac troponin I are ass
93  (NP) family, which also includes the B-type natriuretic peptide (BNP) and the C-type natriuretic pep
94  With sacubitril/valsartan treatment, B-type natriuretic peptide (BNP) concentrations increase; it re
95  are substrates of neprilysin; hence, B-type natriuretic peptide (BNP) concentrations rise with nepri
96 at risk" for HFpEF given elevated brain-type natriuretic peptide (BNP) level; 160 had HFpEF by docume
97  class (HR 1.50; 95% CI 1.02-2.2), log brain natriuretic peptide (BNP) levels (HR 1.45; 95% CI 1.15-1
98 iac volume loading and increased serum brain natriuretic peptide (BNP) levels.
99 nnervated by pruritoceptors expressing brain natriuretic peptide (BNP) most of them contained mRNA fo
100 43 ms; P = 0.05), an elevated pre-TIPS brain natriuretic peptide (BNP) or N-terminal pro-brain natriu
101 t to derive a new staging system using brain natriuretic peptide (BNP) that would correlate with the
102                                        Brain natriuretic peptide (BNP) treatment increases heart func
103 ith an established biomarker for CVD, B-type Natriuretic Peptide (BNP), and echocardiographic paramet
104                Circulating RBP4, TTR, B-type natriuretic peptide (BNP), and troponin I (TnI) concentr
105                        The utility of B-type Natriuretic Peptide (BNP), N-terminal proBNP (NT-proBNP)
106 atriuretic peptide (ANP) and brain or B-type natriuretic peptide (BNP), thereby demonstrating an endo
107 divided into a labeled data set (with B-type natriuretic peptide [BNP] result as a marker of CHF) and
108 ckness, increased lung levels of ANP (atrial natriuretic peptide), BNP (brain-type natriuretic peptid
109 icular ejection fraction <=40%, and elevated natriuretic peptides: BNP >=150 pg/mL or NT-proBNP >=600
110 (P=0.0042) and reduced N-terminal pro-B-type natriuretic peptide by 28% (2%-47%), P=0.038.
111 e levels of NT-proBNP (N-terminal pro-B-type natriuretic peptide) by 36% (32 800 +/- 24 300 ng/L to 2
112 reatine kinase, myoglobin, N-terminal B-type natriuretic peptide, C-reactive protein, and leukocyte c
113  changes in NT-proBNP (N-terminal pro-B-type natriuretic peptide), cardiac reverse remodeling, and he
114              Biomarker measurements included natriuretic peptides, cardiac troponins, plasminogen act
115                                       C-type natriuretic peptide (CNP) is a fundamental endothelial s
116 ro-BNP (NT-proBNP), proBNP(1-108), or C-type natriuretic peptide (CNP) is not well understood.
117 sus 40), higher median N-terminal pro-B-type natriuretic peptide concentration (403 versus 320 pg/mL;
118 acellular fluid volume, and in plasma B-type natriuretic peptide concentration (ratio of intervention
119 e effects of genetic variants on circulating natriuretic peptide concentrations and compared the impa
120 in 6 min, and N-terminal prohormone of brain natriuretic peptide concentrations between the 2 groups.
121 ese findings are important for comparison of natriuretic peptide concentrations in heart failure and
122 of a nonhypotensive pGC-A activator/designer natriuretic peptide, CRRL269, in a short-term, large ani
123 ss and log-transformed N-terminal brain-type natriuretic peptide), cTSD was predictive of preclinical
124   Short-term mechanical circulatory support, natriuretic peptide decile, glomerular filtration rate,
125                     Plasma concentrations of natriuretic peptides decline with obesity in patients wi
126                        N-terminal pro-B-type natriuretic peptide declined significantly in all 4 subg
127                                              Natriuretic peptides decrease RV afterload by promoting
128 inical information (eg, N terminal pro-brain natriuretic peptide, distinctive chest x-ray findings, a
129  the relationship between cardiac troponins, natriuretic peptides, ECV and their associations with in
130 er adjustment for age, N-terminal pro-B-type natriuretic peptide, ejection fraction, E/E', and left v
131 baseline to week 12 in N-terminal pro-B-type natriuretic peptide, ejection fraction, global longitudi
132 (atrial natriuretic peptide) and BNP (B-type natriuretic peptide), encoded by the clustered genes Npp
133  with reduced ejection fraction and elevated natriuretic peptides enrolled in the COSMIC-HF trial (Ch
134  without hospitalization), and with elevated natriuretic peptides, enrolled at 167 sites in 21 countr
135 F proteins (NT-proBNP [N-terminal pro-B type natriuretic peptide], ESM [endothelial cell-specific mol
136 rotein kinase IIdelta phosphorylation, brain natriuretic peptide expression, and sustained capillariz
137 antly raised levels of N-terminal pro B-type natriuretic peptide, ferritin, D-dimers, and cardiac tro
138   Exercise testing, echocardiography, B-type natriuretic peptide, functional health assessment, and m
139 ensitivity troponin T, N-terminal pro-B-type natriuretic peptide, growth-differentiation factor-15, a
140               N-terminal prohormone of brain natriuretic peptide &gt;8500 ng/L could not be overcome for
141 ed cardiac biomarkers (N-terminal pro-B-type natriuretic peptide [&gt;40 pg/mL] or troponin T [>0.6 pg/m
142 core >2, or NT-proBNP (N-terminal pro-B-type natriuretic peptide) &gt;=40 pmol/L and among participants
143                               The concept of natriuretic peptide guidance has been extensively studie
144                    Assessment of BNP (B-type natriuretic peptide) has also been suggested by the Amer
145      Measures of serum cardiac troponins and natriuretic peptides have become established as prognost
146                               BACKGROUND AND Natriuretic peptides have led the way as a diagnostic an
147                                              Natriuretic peptides have many physiological actions and
148                             Plasma levels of natriuretic peptides have proven to be powerful diagnost
149 ional risk factors and N-terminal pro-B-type natriuretic peptide (hazard ratio per SD increment: 1.35
150  left atrium dimension, E/e', and pro B-type natriuretic peptide (hazard ratio, 1.05; 95% confidence
151 -1.39]) and NT-proBNP (N-terminal pro-B-type natriuretic peptide; hazard ratio, 1.73 [95% CI, 1.52-1.
152 e protein), NT-proBNP (N-terminal pro-B-type natriuretic peptide), HbA1C (glycated hemoglobin), and s
153 on, Galectin-3 (Gal-3), N-terminal proB-type natriuretic peptide, high sensitivity troponin T (hsTnT)
154 ronary artery calcium, N-terminal pro B-type natriuretic peptide, high-sensitivity cardiac troponin T
155 lso assayed NT-proBNP (N-terminal pro-B-type natriuretic peptide), hs-cTnT, CRP (C-reactive protein),
156 ion in inflammatory markers, D-dimer, B-type natriuretic peptide, IL-6, and IL-10 levels were common
157                        When including B-type natriuretic peptide in the model, only a decreasing myoc
158 linical model improved modestly after adding natriuretic peptides in men (DeltaC-statistic = 0.006; l
159  55 +/- 10%; p < 0.001; n = 259), and B-type natriuretic peptide increased (median [interquartile ran
160               Importantly, proBNP (pro-brain natriuretic peptide) increased at 12 months in 20 millio
161 cystatin C, NT-proBNP (N-terminal pro-B-type natriuretic peptide), interleukin (IL)-6, and E-selectin
162 rritin, procalcitonin, N-terminal pro B-type natriuretic peptide, interleukin-6 level, and D-dimers.
163 d in cardiomyocytes that converts pro-atrial natriuretic peptide into atrial natriuretic peptide, a c
164 yocardial infarction, indicating that B-type natriuretic peptide is required to preserve postinfarct
165  of pharmacological agents that are based on natriuretic peptides is an area of active research, with
166  Background NT-proBNP (N-terminal pro-B-type natriuretic peptide) is useful in diagnosis and prognost
167  EF was 56%; and median N-terminal pro-brain natriuretic peptide level was 1403 pg/mL; 761 (96.5%) co
168 ents were women, median N-terminal pro-brain natriuretic peptide level was 918 pg/ml (interquartile r
169 iastolic diameter; serum troponin level; and natriuretic peptide level) in each individual.
170                                  Age, B-type natriuretic peptide level, renal dysfunction, 24-h AHI,
171 have evaluated adjusting HF therapy based on natriuretic peptide levels ("guided therapy") with incon
172 ile concurrently reducing circulating atrial natriuretic peptide levels (p < 0.01).
173                        N-terminal pro-B-type natriuretic peptide levels decreased similarly in both g
174 roBNP levels of 1000 pg/mL or more or B-type natriuretic peptide levels of 250 pg/mL or more, regardl
175                        N-Terminal pro-B type natriuretic peptide levels were below the level consider
176 ociation class II or III HFpEF with elevated natriuretic peptide levels were enrolled between May 10,
177 aride binding protein, troponin T, and brain natriuretic peptide levels were measured.
178 h HFrEF (ejection fraction </=40%), elevated natriuretic peptide levels within the prior 30 days, and
179 uality of life, higher N-terminal pro-B-type natriuretic peptide levels, and a poorer prognosis.
180 s feasibility, on-study retention, trends in natriuretic peptide levels, quality of life, and safety
181 0.0001), despite lower N-terminal pro-B-type natriuretic peptide levels.
182              NT-proBNP (N-terminal pro brain natriuretic peptide) levels are included in the multipar
183 ukin-6) and NT-proBNP (N terminal pro B-type natriuretic peptide) levels were examined in multivariab
184 n fraction, NT-proBNP (N-terminal pro-B-type natriuretic peptide) levels, cardiac output/index, brach
185 <6 ng/L and NT-proBNP (N-terminal pro-B-type natriuretic peptide) &lt;100 pg/mL), and those with ECG-LVH
186 3, NAC+NaHCO3, ischemic preconditioning, and natriuretic peptide may have nephroprotective effects, t
187 ncluding 4-dimensional flow, BNP (brain-type natriuretic peptide) measurement, functional capacity as
188 he reduced fat oxidation and elevated atrial natriuretic peptide message of cardiac hypertrophy.
189 iography, increased plasma concentrations of natriuretic peptides, mild-to-moderate renal insufficien
190          Current guidelines recommend use of natriuretic peptides (N-terminal pro-B type natriuretic
191  cardiomyocytes and CFs via the atrial/brain natriuretic peptide-natriuretic peptide receptor-1 pathw
192                       ANP is a member of the natriuretic peptide (NP) family, which also includes the
193                                  Circulating natriuretic peptide (NP) levels are markedly lower in he
194           Phosphodiesterase-9 (PDE9) reduces natriuretic peptide (NP) signaling and may be involved i
195 thway, the evaluation of nitrates, synthetic natriuretic peptides (NP), and NP analogs has yielded mi
196                                              Natriuretic peptides (NPs) are hormones involved in main
197                                      Cardiac natriuretic peptides (NPs) play a fundamental role in ma
198                                  The cardiac natriuretic peptides (NPs), atrial NP and B-type NP, reg
199 ing coronary angiography, independent of the natriuretic peptide NT-proBNP, kidney function and of ma
200 alised, and who had an N-terminal pro-B-type natriuretic peptide (NT-pro-BNP) concentration less than
201 tion (LVEF) >=55%, and N-terminal pro-B-type natriuretic peptide (NT-proBNP) >=300 pg/ml.
202 ent staging systems use N-terminal pro-brain natriuretic peptide (NT-proBNP) and cardiac troponins T
203 awn for the biomarkers N-terminal pro-B-type natriuretic peptide (NT-proBNP) and high-sensitivity car
204                         N-terminal pro-brain natriuretic peptide (NT-proBNP) and high-sensitivity car
205                  Serum N-terminal-pro-B-type natriuretic peptide (NT-proBNP) and total testosterone l
206 roponin T (hs-cTnT) or N-terminal pro-B-type natriuretic peptide (NT-proBNP) are at high risk of infe
207 ce (6MWD) and change in N-terminal pro-brain natriuretic peptide (NT-proBNP) by after therapy.
208 g microRNA panels with N-terminal pro-B-type natriuretic peptide (NT-proBNP) clearly improved specifi
209 ortional change in the N-terminal pro-B-type natriuretic peptide (NT-proBNP) concentration from basel
210              Increased N-terminal pro-B-type natriuretic peptide (NT-proBNP) concentration predicts p
211 wever, the role of amino-terminal pro-B-type natriuretic peptide (NT-proBNP) concentrations among PHI
212 tril-valsartan reduces N-terminal pro-b-type natriuretic peptide (NT-proBNP) concentrations.
213 s biosensors to measure N-terminal pro-brain natriuretic peptide (NT-proBNP) in human serum within it
214                  Serum N-terminal pro-B-type natriuretic peptide (NT-proBNP) is considered a marker t
215 uretic peptide (BNP) or N-terminal pro-brain natriuretic peptide (NT-proBNP) level, an elevated E/A r
216 tone and usual care on N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels compared with usu
217  walk distance, plasma N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels, and health statu
218 phy, leading to elevated N-terminal probrain natriuretic peptide (NT-proBNP) levels.
219 -life (QOL) score, and N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels.
220 (GDMT) by reducing amino-terminal pro-B-type natriuretic peptide (NT-proBNP) was not superior to GDMT
221 c troponin T (hs-cTnT) and N-terminal B-type natriuretic peptide (NT-proBNP) were measured using seru
222 kers (such as N-terminal prohormone of brain natriuretic peptide (NT-proBNP)) and a measure of functi
223  troponin I (hs-cTnI), N-terminal pro-B-type natriuretic peptide (NT-proBNP), and high-sensitivity C-
224 eactive protein (CRP), N-terminal pro b-type natriuretic peptide (NT-proBNP), cardiac troponin I (cTn
225 ied the association of N-terminal pro-B-type natriuretic peptide (NT-proBNP), high-sensitive troponin
226 ary biomarkers such as N-terminal pro B-type natriuretic peptide (NT-proBNP), urine output (UOP), and
227 e assessments included N-terminal pro-B-type natriuretic peptide (NT-proBNP).
228 y score (KCCQ-OSS) and N-terminal pro-B-type natriuretic peptide (NT-proBNP).
229 questioned, and use of N-terminal pro-B-type natriuretic peptides (NT-proBNP) has been preferred and
230  >=6 ng/L] and stress (N-terminal pro-B-type natriuretic peptide [NT-proBNP] >=100 pg/mL) can inform
231 tom classification, and N-terminal pro-brain natriuretic peptide [NT-proBNP] level) at 6 months, 20 e
232 nins I and T, N-terminal prohormone of brain natriuretic peptide [NT-proBNP]) to predict baseline sus
233                                     Elevated natriuretic peptides occurring mid-first cycle of treatm
234 ic HF, ejection fraction >=45%, and elevated natriuretic peptides or a prior HF hospitalization.
235 troponin I, NT-proBNP (N-terminal pro-B-type natriuretic peptide), or high-sensitivity C-reactive pro
236  augmentation index at 12 months, BP, B-type natriuretic peptide, or physical function.
237 l cyclase activity, increased sensitivity to natriuretic peptide, or reduced the Michaelis constant i
238 p = 0.003), and higher N-terminal pro-B-type natriuretic peptide (p = 0.02) than those with <=Mild TR
239 e (p < 0.0001) or clinical score plus B-type natriuretic peptide (p = 0.02).
240  exercise capacity, and N-terminal pro-brain natriuretic peptide (P>0.30 for all).
241 .03]), and markers of cardiac stretch (brain natriuretic peptide [P < .001] and N-terminal fragment o
242  N-terminal fragment of the prohormone brain natriuretic peptide [P = .001]) in HIV.
243 stance, and NT-proBNP (N-terminal pro-B-type natriuretic peptide; P<0.05 for all).
244 decrease in NT-proBNP (N-terminal pro-B-type natriuretic peptide; P=0.002), and lower levels of PRA (
245                   Studies have reported that natriuretic peptides provide prognostic information for
246 or soluble ST2 and amino-terminal pro-B-type natriuretic peptide provides early risk assessment beyon
247 ; Meng test p = 0.03), N-terminal pro-B-type natriuretic peptide (r = 0.56 vs. r = 0.17; Meng test p
248 -type, endothelium-specific CNP(-/-), global natriuretic peptide receptor (NPR)-B(-/-) and NPR-C(-/-)
249         Human genetic variation in the NPR1 (natriuretic peptide receptor 1 gene, encoding NPR-A, atr
250 tide receptor 1 gene, encoding NPR-A, atrial natriuretic peptide receptor 1) was recently shown to af
251                                 Mutations in natriuretic peptide receptor 2 (Npr2) gene cause a rare
252 ferentiation via the guanylate cyclase NPR2 (natriuretic peptide receptor 2) and not the G-protein-co
253 e G-protein-coupled clearance receptor NPR3 (natriuretic peptide receptor 3).
254 the interaction between ANP and its receptor natriuretic peptide receptor A and reduces intracellular
255 cking gastrin-releasing peptide receptor and natriuretic peptide receptor A by genetic approaches or
256 ecifically for the interaction of human anti-natriuretic peptide receptor A IgG4 with the neonatal Fc
257 ncluding gastrin-releasing peptide receptor, natriuretic peptide receptor A, neuromedin B receptor, a
258  for IgG4 (S228P), an antibody targeting the natriuretic peptide receptor A, show a previously unreco
259                           ANP acting through natriuretic peptide receptor-A (NPRA) lowers blood press
260 nction using Npr1 (encoding guanylyl cyclase/natriuretic peptide receptor-A, GC-A/NPRA) gene-knockout
261 e learned of the potential role of an NPR-C (natriuretic peptide receptor-C) in atrial fibrosis and t
262 ough specific NP receptors, including NPR-C (natriuretic peptide receptor-C), are cardioprotective ho
263  in myocytes, as it was distinct from atrial natriuretic peptide receptor-cGMP-PKG-RyR2 Ser-2808 sign
264 lated manner, two polypeptide hormones - the natriuretic peptides - referred to as atrial natriuretic
265                                              Natriuretic peptides regulate multiple physiologic syste
266  T (cTnT) and N-terminal prohormone of brain natriuretic peptide) related to hemodynamic activity.
267 as endothelin-1 caused itch-selective B-type natriuretic peptide release.
268 rdiomyocyte death, and N-terminal pro B-type natriuretic peptide release; all are classical hallmarks
269  Important clinical entities associated with natriuretic peptide research include heart failure, obes
270 n- beyond traditional risk factors including natriuretic peptides, risk scores, and symptoms-in heart
271 betes, renal function, N-terminal pro-b-type natriuretic peptide serum concentration, and right ventr
272 hy (MRN) with hsTNT and N-terminal pro-brain natriuretic peptide serum levels in patients with T2D.
273 G1 is a primary effector of nitric oxide and natriuretic peptide signalling, and protects against hea
274                                These include natriuretic peptides, soluble suppressor of tumorgenicit
275 scovery of atrial secretory granules and the natriuretic peptides stored in them identified the atriu
276 ips between NT-proBNP (N-terminal Pro-B-type natriuretic peptide), systolic blood pressure, and diast
277  dyspnea, increased plasma concentrations of natriuretic peptides, systolic blood pressure of at leas
278 dy), high-sensitivity troponin I, and B-type natriuretic peptide ( Table 1 ).
279 g levels of NT-proBNP (N-terminal pro-B-type natriuretic peptide) than HF patients without AF.
280 d change in NT-proBNP [N-terminal pro-B-type natriuretic peptide]), there was a significant increase
281 yclase receptors that mediate the effects of natriuretic peptides through the generation of intracell
282                 After adjusting for baseline natriuretic peptides, time-updated Meta-Analysis Global
283 circulating NT-proBNP (N-terminal pro-B-type natriuretic peptide), TNF-alpha, IL-6, IL-12, IL-17, mal
284 of soluble ST2 and amino-terminal pro-B-type natriuretic peptide to clinical parameters for risk stra
285                                       Atrial natriuretic peptide together with PDE9a inhibitor were a
286 ft ventricular ejection fraction, pro-B-type natriuretic peptide, troponin I, and C-reactive protein
287 higher risk: NT-proBNP [N-terminal proB-type natriuretic peptide], TSP2 [thrombospondin-2], MBL [mann
288       In primary human keratinocytes, B-type natriuretic peptide upregulated genes promoting dermatol
289 s were normal, whereas N-terminal pro B-type natriuretic peptide was 10 times the upper limit of norm
290 quartile range) concentration of BNP (B-type natriuretic peptide) was 124 (69-197) ng/L, NT-proBNP (N
291                             Mean BNP (B-type natriuretic peptide) was elevated (5743 pg/mL).
292             NT-proBNP (N-terminal pro-B-type natriuretic peptide) was not affected.
293                                              Natriuretic peptides were highly predictive of CVAEs; ho
294 tients who fulfilled entry criteria for both natriuretic peptides were included in the present analys
295 levation of NT-proBNP (N-terminal pro-B-type natriuretic peptide) were eligible.
296 RI, and log NT-proBNP (N-Terminal Pro-B-Type Natriuretic Peptide) were retained (chi(2), 62.2; P<0.00
297 onal area, and the expression of ANP (atrial natriuretic peptide) were significantly attenuated in th
298 levation of NT-proBNP (N-terminal pro-B-type natriuretic peptide), were eligible.
299                                         NPs (natriuretic peptides), which elicit their effects throug
300  assessed the association of levels of these natriuretic peptides with the subsequent risk of cardiov

 
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