コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 arker, whereas the secondary definition used cardiac troponin.
2 Nearly all patients will have an elevated cardiac troponin.
5 I(R146G), and cTnI(R21C) were complexed into cardiac troponin and exchanged into rat ventricular myof
7 re observed across ncRNA types compared with cardiac troponins and cMyBP-C (cardiac myosin-binding pr
9 ype natriuretic peptide and high-sensitivity cardiac troponin), and clinical history (prior stroke).
12 led trial, we implemented a high-sensitivity cardiac troponin assay and the recommendations of the Un
13 agnosed due to the increasing sensitivity of cardiac troponin assays and is associated with adverse s
18 rdial injury was defined as any elevation in cardiac troponin at the time of clinical presentation or
19 r specificity, determination of the level of cardiac troponins became a predominant indicator for MI.
20 genase (LDH) and creatine kinase (CK), which cardiac troponins being the main accepted biomarkers for
21 as used to determine incorporation of mutant cardiac troponin C ( approximately 21%) into the KI-TnC-
22 c cardiomyopathy-associated mutant D145E, in cardiac troponin C (cTnC) C-domain, causes generalised i
24 ique 31-residue N-terminal region that binds cardiac troponin C (cTnC) to increase the calcium sensit
27 ac thin-filament activation, the N-domain of cardiac troponin C (N-cTnC) binds to Ca(2+) and interact
29 ation, in general, and for phospholamban and cardiac troponin C S-nitrosylation, in particular, in be
31 nt distance from the calcium binding site in cardiac troponin C, and do not affect either the binding
32 ndling proteins, including phospholamban and cardiac troponin C, thereby playing an essential and pre
35 ation of PKCepsilon expressing platelets and cardiac troponin clearly discriminates patients with 100
37 Troponin-I (cTnI) is one of the subunits of cardiac troponin complexes and a pivotal biochemical mar
39 of this study was to assess associations of cardiac troponin concentration with cardiovascular disea
40 September 2016, reporting on associations of cardiac troponin concentration with first-ever CVD outco
44 patients with renal impairment and elevated cardiac troponin concentrations had a 2-fold greater ris
45 S pathway incorporating low high-sensitivity cardiac troponin concentrations rules out myocardial inf
46 thway with a pathway that incorporates lower cardiac troponin concentrations to risk stratify patient
47 tations on the structure and kinetics of the cardiac troponin core domain associated with the Ca(2+)-
48 n of muscle-enriched miRNAs with cMyBP-C and cardiac troponins could open a new path of integrating c
55 ropriate clinical decision values (CDVs) for cardiac troponin (cTn) owing to limitations in the curre
56 hain (MHC)-beta to MHC-alpha and upregulated cardiac troponin (cTn)-T and tropomyosin, as well as cTn
57 estricted protein that is more abundant than cardiac troponins (cTn) and is released more rapidly aft
63 rest in widening the use of high-sensitivity cardiac troponins for population cardiovascular disease
70 nal proBNP (NT-proBNP), and high-sensitivity cardiac troponin (hs-cTn) concentrations for diagnosis a
71 myocardial infarction using high-sensitivity cardiac troponin (hs-cTn) concentrations irrespective of
73 on the association between high-sensitivity cardiac troponin (hs-cTn) levels and outcomes in patient
74 Society of Cardiology (ESC) high-sensitivity cardiac troponin (hs-cTn) measurement at presentation an
75 wledge the emerging role of high-sensitivity cardiac troponin (hs-cTnl) for risk stratification and t
76 a modified HEART score </=3 (which includes cardiac troponin I <0.04 ng/mL at 0 and 3 hours) were ra
77 fabricated with an immobilized antibody for cardiac troponin I (anti-cTnI) on a photoresponsive comp
78 dots (afGQDs) conjugated with antibody anti-cardiac Troponin I (anti-cTnI) to detect cardiac marker
79 most specific markers for cardiac injury are cardiac troponin I (cTnI) and cardiac troponin T (cTnT)
84 ifically monophosphorylates Ser(23) of human cardiac troponin I (cTnI) in isolation and in the trimer
87 Two hypertrophic cardiomyopathy-associated cardiac troponin I (cTnI) mutations, R146G and R21C, are
88 t proteins revealed site-specific changes in cardiac Troponin I (cTnI) phosphorylation, as well as a
89 , which coincided with a similar increase in cardiac troponin I (cTnI) protein, the established marke
91 ition, a competitive binding assay to detect cardiac Troponin I (cTnI) was used as an example to demo
92 highly sensitive and label-free detection of cardiac troponin I (cTnI), a biomarker for diagnosis of
93 the enrichment and comprehensive analysis of cardiac troponin I (cTnI), a gold-standard cardiac bioma
94 pro b-type natriuretic peptide (NT-proBNP), cardiac troponin I (cTnI), and fibrinogen- were rapidly
95 PKA targets the N-terminus (Ser-23/24) of cardiac troponin I (cTnI), cardiac myosin-binding protei
100 c troponin T (hs-cTnT), and high-sensitivity cardiac troponin I (hs-cTnI) were determined in plasma s
102 ed at baseline and 8 weeks: high-sensitivity cardiac troponin I (hs-cTnI), N-terminal pro-B-type natr
103 tionship between changes in high-sensitivity cardiac troponin I (hsTnI) and cardiovascular outcomes.
105 e molecular mechanism(s) of the mutant human cardiac troponin I (K206I), we tested the Ca(2+) depende
108 e is a progressive increase in expression of cardiac troponin I (TnI), with a concurrent decrease in
109 KEY POINTS: Mutations in genes encoding cardiac troponin I (TNNI3) and cardiac troponin T (TNNT2
111 : the sarcomeric mutations in genes encoding cardiac troponin I (TNNI3p.98truncation ) and cardiac tr
112 ors showed extraordinary sensitivity towards cardiac troponin I [1.7microA/(ng/mL) in phosphate buffe
113 rary primary prevention population, baseline cardiac troponin I and BNP were associated with the risk
114 n of CMBK resulted in higher serum levels of cardiac troponin I and elevated amounts of reactive oxyg
115 he measurement of the heart attack indicator cardiac troponin I and is shown to successfully combine
116 ncreased expression of the maturation marker cardiac troponin I and significantly increased action po
117 vels of B-type natriuretic peptide (BNP) and cardiac troponin I are associated with adverse outcomes
118 he impact of implementing a high-sensitivity cardiac troponin I assay with sex-specific diagnostic th
121 roperties and still enabled the detection of cardiac troponin I at pg/mL concentrations in 10% serum
122 us biomolecular recognition of model analyte cardiac troponin I by two antibody fragments brought the
123 rdial injury was defined as high-sensitivity cardiac troponin I concentration >99th centile of 16 ng/
124 acute coronary syndrome, a high-sensitivity cardiac troponin I concentration of less than 5 ng/L ide
126 e myocardial injury (high-sensitivity plasma cardiac troponin I concentration, 4.3 ng/L [interquartil
128 consecutive patients (n=2122) with elevated cardiac troponin I concentrations (>/=0.05 microg/L) at
129 ocardial ischemia, and an increase in plasma cardiac troponin I concentrations (1.4 [0.8-2.5] versus
131 ospective studies measuring high-sensitivity cardiac troponin I concentrations in patients with suspe
133 rating age, sex, and paired high-sensitivity cardiac troponin I concentrations, was trained on 3,013
137 valuated the performance of high-sensitivity cardiac troponin I in those with and without renal impai
140 syndrome (n=1218) underwent high-sensitivity cardiac troponin I measurement at presentation and 3 and
142 el we previously identified that HCM causing cardiac troponin I mutation Gly203Ser (cTnI-G203S) is as
147 f peptides afforded higher sensitivities for cardiac troponin I than those prepared by the chemisorpt
149 high sensitivity assay for the detection of cardiac troponin I using electrical double layer gated h
150 4 (307-1312) ng/L, hs-cTnI (high sensitivity cardiac troponin I) 6.3 (3.4-13.0) ng/L, hs-CRP (high se
151 croarray analysis of serum biomarkers (e.g., cardiac troponin I) afforded up to 130-fold enhancement
152 199 (equivalent to Ser200 in mouse) of cTnI (cardiac troponin I) is significantly hyperphosphorylated
153 .59 (95% CI, 1.76-3.83) for high-sensitivity cardiac troponin I, 1.65 (95% CI, 1.12-2.44) for NT-proB
155 implified Pulmonary Embolism Severity Index, cardiac troponin I, brain natriuretic peptide, and lower
156 ompe disease, the relationship between cTnT, cardiac troponin I, creatine kinase (CK), CK-myocardial
157 s: Risk score and clinical outcomes based on cardiac troponin I, N-terminal pro-B-type natriuretic pe
159 oprotein cholesterol ratio, high-sensitivity cardiac troponin I, NT-proBNP (N-terminal pro-B-type nat
160 system has been applied to the detection of cardiac Troponin I, the gold standard biomarker for the
161 he cardiac troponins, cardiac troponin T and cardiac troponin I, using sensitive methods, defines a t
164 oped for rapid and simultaneous screening of cardiac Troponin-I (cTnI) and cardiac-Troponin-T (cTnT)
166 injury, and markedly reduced elaboration of cardiac troponin-I in coronary effluent during ESHP.
167 RNA signatures correlated with elevations in cardiac Troponin-I in severely injured hearts during EVH
168 gens, like cardiac myosin heavy chain-alpha, cardiac troponin-I, and adenine nucleotide translocator
170 ed acute coronary syndrome, high-sensitivity cardiac troponin identified fewer patients with renal im
171 natriuretic peptide, ferritin, D-dimers, and cardiac troponin in addition to high C-reactive protein
172 i-square = 146; p < 0.001), and after adding cardiac troponins in women (DeltaC-statistic = 0.003; li
173 of a large proportion of patients with minor cardiac troponin increases (14 to 49 ng/l), the majority
178 ed mice at 24 hours, Ppara mice had elevated cardiac troponin levels compared with wild-type mice.
179 ial infarction and elevated high-sensitivity cardiac troponin levels often routinely undergo invasive
181 t size), a Biomarker Core (to measure plasma cardiac troponin levels), and a Data Coordinating Center
182 ble physiological effects (without affecting cardiac troponin levels), but short-term treatment did n
183 morphometry, neutrophil accumulation, blood cardiac troponin levels, and echocardiography and observ
184 rkers, for example, natriuretic peptides and cardiac troponin, may assist in the diagnosis of left ve
185 e sought to examine the relationship between cardiac troponins, natriuretic peptides, ECV and their a
186 ng, and cardiac biomarkers (high-sensitivity cardiac troponins, NT-proBNP [N-terminal pro-B-type natr
187 nal function, and the blood concentration of cardiac troponin often increases with declining glomerul
188 measurements included natriuretic peptides, cardiac troponins, plasminogen activator inhibitor-1, D-
189 IMI risk scores, which incorporate the first cardiac troponin, provided more diagnostic information.
192 , who experienced an event associated with a cardiac troponin T >99th percentile of a normal referenc
193 A total of 5460 patients had at least one cardiac troponin T >=0.01 ng/mL; 1365 of these patients
194 chronic myocardial injury (high-sensitivity cardiac troponin T >=6 ng/L] and stress (N-terminal pro-
195 -specific acute cardiac stress (by measuring cardiac troponin T (cTnT) and N-terminal prohormone of b
197 erified assumption that chronically elevated cardiac troponin T (cTnT) levels fluctuate randomly arou
199 The hypertrophic cardiomyopathy-causing cardiac troponin T (cTnT) mutation Delta160Glu (Delta160
201 esent study was to evaluate whether elevated cardiac troponin T (cTnT) was independently associated w
202 iac injury are cardiac troponin I (cTnI) and cardiac troponin T (cTnT) which have been considered as
204 splicing of TNNT2, the gene that encodes for cardiac troponin T (cTnT), a biomarker of myocardial inj
211 tiation factor-15 (GDF-15), high-sensitivity cardiac troponin T (cTnT-hs) and haemoglobin, age, and p
212 anterior circulation and a high-sensitivity cardiac troponin T (hs-cTnT) acquired on the day of admi
214 Although small elevations of high-sensitive cardiac troponin T (hs-cTnT) are associated with inciden
216 tional level, with elevated high-sensitivity cardiac troponin T (hs-cTnT) concentrations (>/=14 ng/L)
217 tic peptide (NT-proBNP) and high-sensitivity cardiac troponin T (hs-cTnT) concentrations were measure
218 rognostic value of baseline high-sensitivity cardiac troponin T (hs-cTnT) elevation in SCAD patients
219 implications of introducing high-sensitivity cardiac troponin T (hs-cTnT) into clinical practice and
221 f an undetectable (<5 ng/l) high-sensitivity cardiac troponin T (hs-cTnT) level and an electrocardiog
222 hesized that any detectable high-sensitivity cardiac troponin T (hs-cTnT) level is associated with ad
223 s are preferable when using high-sensitivity cardiac troponin T (hs-cTnT) levels in the diagnosis of
225 econdary endpoints included high-sensitivity cardiac troponin T (hs-cTnT) on day 4, left ventricular
226 CVD) but elevated levels of high-sensitivity cardiac troponin T (hs-cTnT) or N-terminal pro-B-type na
227 oninferiority of a 0/1-hour high-sensitivity cardiac troponin T (hs-cTnT) protocol in comparison with
229 A 1-h algorithm based on high-sensitivity cardiac troponin T (hs-cTnT) testing at presentation and
230 Thus, we assessed whether high-sensitivity cardiac troponin T (hs-cTnT), a marker of subclinical my
231 B-type natriuretic peptide, high-sensitivity cardiac troponin T (hs-cTnT), and high-sensitivity cardi
232 uretic peptide (NT-proBNP), high-sensitivity cardiac troponin T (hs-cTnT), and low-density lipoprotei
234 enes encoding cardiac troponin I (TNNI3) and cardiac troponin T (TNNT2) caused altered troponin prote
235 RNAs including the Insulin Receptor (Insr), Cardiac Troponin T (Tnnt2), Lim Domain Binding 3 (Ldb3)
236 ardiac troponin I (TNNI3p.98truncation ) and cardiac troponin T (TNNT2p.K217deletion ; also known as
240 protein expression of cardiomyogenic markers cardiac troponin T and alpha-smooth muscle actin in CPCe
242 f muscle-enriched miRNAs with high-sensitive cardiac troponin T and cMyBP-C returned the highest area
245 ype natriuretic peptide and high-sensitivity cardiac troponin T are frequently elevated in severe sep
246 per reference limit for the high-sensitivity cardiac troponin T assay (hs-cTnT) in 3 large independen
249 terminal pro-B-type natriuretic peptide, and cardiac troponin T concentrations in multivariate analys
250 type natriuretic peptide or high-sensitivity cardiac troponin T concentrations were independently ass
251 e ESC 0/1-h algorithm using high-sensitivity cardiac troponin T embedded in routine clinical care and
252 n 97.4% of the patients and high-sensitivity cardiac troponin T in 84.5%, with higher concentrations
254 was defined as an absolute high-sensitivity cardiac troponin T increase of >/=14 ng/L from preoperat
255 acute chest pain, elevated high-sensitivity cardiac troponin T levels (>14 ng/l), and inconclusive e
259 ive and 24-hour postoperative high-sensitive cardiac troponin T measurements and the respective chang
260 ac investigations including high-sensitivity cardiac troponin T measurements at later time points or
262 sus without either elevated high-sensitivity cardiac troponin T or NT-proBNP had a 10-year CV inciden
265 s, we used 2 mouse models of sarcomeric HCM (cardiac troponin T R92L and R92W) with differential myoc
266 nhanced myocardial damage evidenced by serum cardiac troponin T release in the rat and mouse cardiac
267 ype natriuretic peptide and high-sensitivity cardiac troponin T were measured 1, 2, and 7 days after
269 hich most patients would have had a negative cardiac troponin T with older assays); and Group 4, thos
270 rmined pre- and postoperative high-sensitive cardiac troponin T with the occurrence of major adverse
271 144 patients with elevated high-sensitivity cardiac troponin T, 31 had signs of MI and 113 did not.
272 B-type natriuretic peptide, high-sensitivity cardiac troponin T, and high-sensitivity C-reactive prot
273 B-type natriuretic peptide, high-sensitivity cardiac troponin T, and high-sensitivity C-reactive prot
274 e protein, procalcitonin, ferritin, D-dimer, cardiac troponin T, and N-terminal pro-B-type natriureti
281 women; 21.5% with elevated high-sensitivity cardiac troponin T; 17.7% with elevated NT-proBNP) with
282 ro-brain natriuretic peptide (NT-proBNP) and cardiac troponins T and I (TnT and TnI) for prognosticat
283 nano-gap device provides the capability for cardiac-troponin T (cTnT) measurements with co-existed 1
285 AT), matrix metalloproteinase-9 (MMP-9), and cardiac Troponin-T (cTnT) were evaluated by appropriate
287 rdial Infarction) evaluated high-sensitivity cardiac troponin-T (hs-cTnT) in a 1-hour acute myocardia
288 th myocardial damage (using high-sensitivity cardiac troponin-T [hs-cTnT]) and with coronary heart di
289 ificantly more cardiomyocytes, determined by cardiac troponin-T staining, in the MI zone of the QHG21
290 Left ventricular structure and function and cardiac troponin-T were among the top predictors for inc
291 normal biomarkers (hs-cTnT (high sensitivity cardiac troponin-T) <6 ng/L and NT-proBNP (N-terminal pr
292 tions between or near residues 112 to 136 of cardiac troponin-T, the crucial TnT1 (N-terminal domain
293 s screening of cardiac Troponin-I (cTnI) and cardiac-Troponin-T (cTnT) in a point-of-care sensor form
295 rdial Infarction recommends high-sensitivity cardiac troponin testing and classification of patients
297 ectrochemical sensor platform for monitoring cardiac troponins through the detection and quantificati