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1 Nearly all patients will have an elevated cardiac troponin.
2 yocytes between days 7 and 14, and expressed cardiac troponin.
4 I(R146G), and cTnI(R21C) were complexed into cardiac troponin and exchanged into rat ventricular myof
6 ype natriuretic peptide and high-sensitivity cardiac troponin), and clinical history (prior stroke).
10 r of time before the use of high-sensitivity cardiac troponin assays (hs-cTn) becomes common througho
11 tected more frequently once high-sensitivity cardiac troponin assays are approved for clinical use in
13 ) and cardiomyocyte damage using 2 different cardiac troponin assays in 718 consecutive patients pres
17 r specificity, determination of the level of cardiac troponins became a predominant indicator for MI.
18 as used to determine incorporation of mutant cardiac troponin C ( approximately 21%) into the KI-TnC-
20 c cardiomyopathy-associated mutant D145E, in cardiac troponin C (cTnC) C-domain, causes generalised i
22 ique 31-residue N-terminal region that binds cardiac troponin C (cTnC) to increase the calcium sensit
24 ac thin-filament activation, the N-domain of cardiac troponin C (N-cTnC) binds to Ca(2+) and interact
26 ation, in general, and for phospholamban and cardiac troponin C S-nitrosylation, in particular, in be
28 nt distance from the calcium binding site in cardiac troponin C, and do not affect either the binding
29 ndling proteins, including phospholamban and cardiac troponin C, thereby playing an essential and pre
32 trated by increased myocardial injury, serum cardiac troponin, cellular infiltration, complement depo
35 of this study was to assess associations of cardiac troponin concentration with cardiovascular disea
36 September 2016, reporting on associations of cardiac troponin concentration with first-ever CVD outco
39 patients with renal impairment and elevated cardiac troponin concentrations had a 2-fold greater ris
40 S pathway incorporating low high-sensitivity cardiac troponin concentrations rules out myocardial inf
41 thway with a pathway that incorporates lower cardiac troponin concentrations to risk stratify patient
47 ropriate clinical decision values (CDVs) for cardiac troponin (cTn) owing to limitations in the curre
48 ues 1-40) has not been resolved in the whole cardiac troponin (cTn) structure, little is known about
51 estricted protein that is more abundant than cardiac troponins (cTn) and is released more rapidly aft
55 was abolished by mutagenesis, and effects on cardiac troponin dynamics were mapped by hydrogen-deuter
56 G changes for pericarditis, arrhythmias, and cardiac troponin elevation or new or worsening ventricul
60 myocardial infarction using high-sensitivity cardiac troponin (hs-cTn) concentrations irrespective of
61 on the association between high-sensitivity cardiac troponin (hs-cTn) levels and outcomes in patient
62 a modified HEART score </=3 (which includes cardiac troponin I <0.04 ng/mL at 0 and 3 hours) were ra
63 fabricated with an immobilized antibody for cardiac troponin I (anti-cTnI) on a photoresponsive comp
64 dots (afGQDs) conjugated with antibody anti-cardiac Troponin I (anti-cTnI) to detect cardiac marker
65 farction (AMI) when used in combination with cardiac troponin I (cTnI) <99 th percentile and a nondia
66 most specific markers for cardiac injury are cardiac troponin I (cTnI) and cardiac troponin T (cTnT)
70 )O(4) MNPs in the enhancement of LSPR assay, cardiac troponin I (cTnI) for myocardial infarction diag
74 Two hypertrophic cardiomyopathy-associated cardiac troponin I (cTnI) mutations, R146G and R21C, are
75 t proteins revealed site-specific changes in cardiac Troponin I (cTnI) phosphorylation, as well as a
76 , which coincided with a similar increase in cardiac troponin I (cTnI) protein, the established marke
80 ition, a competitive binding assay to detect cardiac Troponin I (cTnI) was used as an example to demo
81 highly sensitive and label-free detection of cardiac troponin I (cTnI), a biomarker for diagnosis of
82 PKA targets the N-terminus (Ser-23/24) of cardiac troponin I (cTnI), cardiac myosin-binding protei
83 ncluding titin, myosin-binding protein-C and cardiac troponin I (cTnI), we sought to define if phosph
87 c troponin T (hs-cTnT), and high-sensitivity cardiac troponin I (hs-cTnI) were determined in plasma s
90 tionship between changes in high-sensitivity cardiac troponin I (hsTnI) and cardiovascular outcomes.
92 e molecular mechanism(s) of the mutant human cardiac troponin I (K206I), we tested the Ca(2+) depende
96 sites located in the N-terminal extension of cardiac troponin I (S4, S5, Y25), an increase in phospho
98 e is a progressive increase in expression of cardiac troponin I (TnI), with a concurrent decrease in
100 : the sarcomeric mutations in genes encoding cardiac troponin I (TNNI3p.98truncation ) and cardiac tr
101 ors showed extraordinary sensitivity towards cardiac troponin I [1.7microA/(ng/mL) in phosphate buffe
102 ssociated with PAPP-A stratified by baseline cardiac troponin I [Accu-TnI >0.04 mug/l], p interaction
103 ning reduces the incidence of postprocedural cardiac troponin I after elective PCI and confers an MAC
104 Patients with an MACCE had a higher mean cardiac troponin I after PCI (+/-SD): 2.07+/-6.99 versus
105 rary primary prevention population, baseline cardiac troponin I and BNP were associated with the risk
106 n of CMBK resulted in higher serum levels of cardiac troponin I and elevated amounts of reactive oxyg
107 ncreased expression of the maturation marker cardiac troponin I and significantly increased action po
108 vels of B-type natriuretic peptide (BNP) and cardiac troponin I are associated with adverse outcomes
111 ntervention for such patients, the dosage of cardiac troponin I at admission could not help in the de
112 roperties and still enabled the detection of cardiac troponin I at pg/mL concentrations in 10% serum
113 us biomolecular recognition of model analyte cardiac troponin I by two antibody fragments brought the
114 rched to evaluate if an early measurement of cardiac troponin I can help to detect a recent coronary
115 acute coronary syndrome, a high-sensitivity cardiac troponin I concentration of less than 5 ng/L ide
117 e myocardial injury (high-sensitivity plasma cardiac troponin I concentration, 4.3 ng/L [interquartil
119 consecutive patients (n=2122) with elevated cardiac troponin I concentrations (>/=0.05 microg/L) at
120 ocardial ischemia, and an increase in plasma cardiac troponin I concentrations (1.4 [0.8-2.5] versus
121 ospective studies measuring high-sensitivity cardiac troponin I concentrations in patients with suspe
125 of the sarcomere and potential signaling to cardiac troponin I in a network involving the ends of th
127 terations occurred on individual residues of cardiac troponin I in heart failure, likely reflecting a
128 valuated the performance of high-sensitivity cardiac troponin I in those with and without renal impai
129 We review how phosphorylation signaling to cardiac troponin I is integrated, with parallel signals
131 study were to assess the prognostic value of cardiac troponin I levels, measured with a new high-sens
133 syndrome (n=1218) underwent high-sensitivity cardiac troponin I measurement at presentation and 3 and
136 the modulation of thin filament activity by cardiac troponin I phosphorylation as an integral and ad
137 ural symptoms, ECG ST-segment deviation, and cardiac troponin I release after elective PCI and reduce
141 f peptides afforded higher sensitivities for cardiac troponin I than those prepared by the chemisorpt
143 high sensitivity assay for the detection of cardiac troponin I using electrical double layer gated h
144 count and myocardial blush grade), and serum cardiac troponin I were assessed before and after PCI.
145 rs of a recent coronary occlusion (including cardiac troponin I) and their respective contribution.
146 ication of cardiac biomarkers (myoglobin and cardiac troponin I) in the clinically significant sensin
147 199 (equivalent to Ser200 in mouse) of cTnI (cardiac troponin I) is significantly hyperphosphorylated
150 implified Pulmonary Embolism Severity Index, cardiac troponin I, brain natriuretic peptide, and lower
151 ompe disease, the relationship between cTnT, cardiac troponin I, creatine kinase (CK), CK-myocardial
153 s: Risk score and clinical outcomes based on cardiac troponin I, N-terminal pro-B-type natriuretic pe
154 t amplitude but decreased phosphorylation of cardiac troponin I, suggesting direct effects on the con
155 system has been applied to the detection of cardiac Troponin I, the gold standard biomarker for the
156 he cardiac troponins, cardiac troponin T and cardiac troponin I, using sensitive methods, defines a t
161 oped for rapid and simultaneous screening of cardiac Troponin-I (cTnI) and cardiac-Troponin-T (cTnT)
162 RNA signatures correlated with elevations in cardiac Troponin-I in severely injured hearts during EVH
163 F) nanoelectrode arrays for the detection of cardiac troponin-I in the early diagnosis of myocardial
164 ther confirmed by a significant reduction of cardiac troponin-I release and less myocardial apoptosis
165 gens, like cardiac myosin heavy chain-alpha, cardiac troponin-I, and adenine nucleotide translocator
166 ed acute coronary syndrome, high-sensitivity cardiac troponin identified fewer patients with renal im
168 of a large proportion of patients with minor cardiac troponin increases (14 to 49 ng/l), the majority
173 ed mice at 24 hours, Ppara mice had elevated cardiac troponin levels compared with wild-type mice.
175 t size), a Biomarker Core (to measure plasma cardiac troponin levels), and a Data Coordinating Center
176 ble physiological effects (without affecting cardiac troponin levels), but short-term treatment did n
177 morphometry, neutrophil accumulation, blood cardiac troponin levels, and echocardiography and observ
178 ng, and cardiac biomarkers (high-sensitivity cardiac troponins, NT-proBNP [N-terminal pro-B-type natr
179 nal function, and the blood concentration of cardiac troponin often increases with declining glomerul
180 IMI risk scores, which incorporate the first cardiac troponin, provided more diagnostic information.
182 ative myocardial injury and death, measuring cardiac troponin routinely after noncardiac surgery has
186 ical and biological significance of elevated cardiac troponin T (cTnT) in patients with neuromuscular
189 erified assumption that chronically elevated cardiac troponin T (cTnT) levels fluctuate randomly arou
193 esent study was to evaluate whether elevated cardiac troponin T (cTnT) was independently associated w
195 iac injury are cardiac troponin I (cTnI) and cardiac troponin T (cTnT) which have been considered as
197 splicing of TNNT2, the gene that encodes for cardiac troponin T (cTnT), a biomarker of myocardial inj
198 interaction between LVH, low but detectable cardiac troponin T (cTnT), and elevated N-terminal pro-B
202 tiation factor-15 (GDF-15), high-sensitivity cardiac troponin T (cTnT-hs) and haemoglobin, age, and p
203 cardiograms and serial serum measurements of cardiac troponin T (cTnT; cardiac injury biomarker), N-t
204 anterior circulation and a high-sensitivity cardiac troponin T (hs-cTnT) acquired on the day of admi
205 Although small elevations of high-sensitive cardiac troponin T (hs-cTnT) are associated with inciden
207 tional level, with elevated high-sensitivity cardiac troponin T (hs-cTnT) concentrations (>/=14 ng/L)
208 tic peptide (NT-proBNP) and high-sensitivity cardiac troponin T (hs-cTnT) concentrations were measure
209 rognostic value of baseline high-sensitivity cardiac troponin T (hs-cTnT) elevation in SCAD patients
210 ated hemoglobin (HbA1c) and high-sensitivity cardiac troponin T (hs-cTnT) in 9,661 participants free
211 sponse to mental stress and high-sensitivity cardiac troponin T (hs-cTnT) in healthy older individual
212 implications of introducing high-sensitivity cardiac troponin T (hs-cTnT) into clinical practice and
214 f an undetectable (<5 ng/l) high-sensitivity cardiac troponin T (hs-cTnT) level and an electrocardiog
215 hesized that any detectable high-sensitivity cardiac troponin T (hs-cTnT) level is associated with ad
216 s are preferable when using high-sensitivity cardiac troponin T (hs-cTnT) levels in the diagnosis of
218 econdary endpoints included high-sensitivity cardiac troponin T (hs-cTnT) on day 4, left ventricular
219 A 1-h algorithm based on high-sensitivity cardiac troponin T (hs-cTnT) testing at presentation and
220 Thus, we assessed whether high-sensitivity cardiac troponin T (hs-cTnT), a marker of subclinical my
221 B-type natriuretic peptide, high-sensitivity cardiac troponin T (hs-cTnT), and high-sensitivity cardi
222 uretic peptide (NT-proBNP), high-sensitivity cardiac troponin T (hs-cTnT), and low-density lipoprotei
225 eri-procedural increases of high-sensitivity cardiac troponin T (mean: 9.9 ng/ml, range: 2.7 to 19.0
226 enes encoding cardiac troponin I (TNNI3) and cardiac troponin T (TNNT2) caused altered troponin prote
227 RNAs including the Insulin Receptor (Insr), Cardiac Troponin T (Tnnt2), Lim Domain Binding 3 (Ldb3)
228 ardiac troponin I (TNNI3p.98truncation ) and cardiac troponin T (TNNT2p.K217deletion ; also known as
232 protein expression of cardiomyogenic markers cardiac troponin T and alpha-smooth muscle actin in CPCe
235 he 2 well-known biomarkers (high-sensitivity cardiac troponin T and N-terminal pro-brain natriuretic
236 ment of beating sheets of cells that express cardiac troponin T and show a full range of action poten
237 ype natriuretic peptide and high-sensitivity cardiac troponin T are frequently elevated in severe sep
238 per reference limit for the high-sensitivity cardiac troponin T assay (hs-cTnT) in 3 large independen
239 With the widespread use of high-sensitive cardiac troponin T assays, positive tests become frequen
240 17.8 ng/L and a perioperative high-sensitive cardiac troponin T change greater than or equal to 6.3 n
241 The risk predictive power of high-sensitive cardiac troponin T change in addition to the Revised Car
244 type natriuretic peptide or high-sensitivity cardiac troponin T concentrations were independently ass
246 mano-Ward syndrome and long-QT syndrome, and cardiac troponin T gene, tnnt2, affected in human cardio
248 n 97.4% of the patients and high-sensitivity cardiac troponin T in 84.5%, with higher concentrations
250 was defined as an absolute high-sensitivity cardiac troponin T increase of >/=14 ng/L from preoperat
251 Deletion of the 14 C-terminal residues of cardiac troponin T leads to hypertrophic cardiomyopathy.
254 acrophages, almost complete normalization of cardiac troponin T levels in serum and of left ventricul
256 ive and 24-hour postoperative high-sensitive cardiac troponin T measurements and the respective chang
261 and methylprednisolone significantly reduced cardiac troponin T release and the number of allograft i
262 nhanced myocardial damage evidenced by serum cardiac troponin T release in the rat and mouse cardiac
263 pro-brain natriuretic peptide (pro-BNP), and cardiac troponin T showed significant linear trends for
264 h no cardiovascular disease in our study had cardiac troponin T values above the current myocardial i
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
272 nges in markers of cardiac (high-sensitivity cardiac troponin T), renal (creatinine and cystatin-C),
273 144 patients with elevated high-sensitivity cardiac troponin T, 31 had signs of MI and 113 did not.
275 B-type natriuretic peptide, high-sensitivity cardiac troponin T, and high-sensitivity C-reactive prot
276 B-type natriuretic peptide, high-sensitivity cardiac troponin T, and high-sensitivity C-reactive prot
277 pe natriuretic peptide, and high-sensitivity cardiac troponin T, higher levels of Cp were associated
285 nano-gap device provides the capability for cardiac-troponin T (cTnT) measurements with co-existed 1
287 the pathologic free light chains (p < 0.05), cardiac troponin-T (cTnT) (p < 0.01), and the Karnofsky
289 rdial Infarction) evaluated high-sensitivity cardiac troponin-T (hs-cTnT) in a 1-hour acute myocardia
290 th myocardial damage (using high-sensitivity cardiac troponin-T [hs-cTnT]) and with coronary heart di
291 rdiac-selective expression of EcSOD from the cardiac troponin-T promoter after systemic administratio
292 ellular superoxide dismutase (EcSOD) via the cardiac troponin-T promoter would protect the mouse hear
293 ificantly more cardiomyocytes, determined by cardiac troponin-T staining, in the MI zone of the QHG21
294 Left ventricular structure and function and cardiac troponin-T were among the top predictors for inc
295 tions between or near residues 112 to 136 of cardiac troponin-T, the crucial TnT1 (N-terminal domain
296 s screening of cardiac Troponin-I (cTnI) and cardiac-Troponin-T (cTnT) in a point-of-care sensor form
299 ectrochemical sensor platform for monitoring cardiac troponins through the detection and quantificati
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