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1 roponin (the NH(2) terminus (TnT-(1-153)) of cardiac troponin T).
2 (endo)plasmic reticulum Ca(2+) ATPase 1, and cardiac troponin T.
3 e populations as determined by expression of cardiac troponin T.
4 2a, and very little of the mature isoform of cardiac troponin T.
5 n heavy chain, myosin binding protein C, and cardiac troponin T.
6 coronary syndrome (NSTE-ACS) and an elevated cardiac troponin T.
7 1,200 patients with NSTE-ACS and an elevated cardiac troponin T.
8 gy in patients with NSTE-ACS and an elevated cardiac troponin T.
9 -day mortality, better than high-sensitivity cardiac troponin T.
10 exon 5 with the adjoining exon 6 from avian cardiac troponin-T.
11 atric dosing resulted in fewer elevations of cardiac troponin T (0 of 12 piglets vs. 6 of 11 piglets,
12 women; 21.5% with elevated high-sensitivity cardiac troponin T; 17.7% with elevated NT-proBNP) with
13 144 patients with elevated high-sensitivity cardiac troponin T, 31 had signs of MI and 113 did not.
16 segment results in conformational changes in cardiac troponin T, an altered binding affinity for trop
17 protein expression of cardiomyogenic markers cardiac troponin T and alpha-smooth muscle actin in CPCe
18 urs within the tropomyosin-binding domain of cardiac troponin T and alters the charge of the residue.
20 onal antibodies (mAbs) raised against bovine cardiac troponin T and chicken tropomyosin to visualize
21 assess the usefulness of baseline levels of cardiac troponin T and CK-MB and the electrocardiographi
22 f muscle-enriched miRNAs with high-sensitive cardiac troponin T and cMyBP-C returned the highest area
25 he 2 well-known biomarkers (high-sensitivity cardiac troponin T and N-terminal pro-brain natriuretic
26 ment of beating sheets of cells that express cardiac troponin T and show a full range of action poten
27 this study was to investigate the utility of cardiac troponin T and troponin I for predicting outcome
32 ro-brain natriuretic peptide (NT-proBNP) and cardiac troponins T and I (TnT and TnI) for prognosticat
33 defects in beta-cardiac myosin heavy chain, cardiac troponin T, and alpha-tropomyosin account for >
34 B-type natriuretic peptide, high-sensitivity cardiac troponin T, and high-sensitivity C-reactive prot
35 B-type natriuretic peptide, high-sensitivity cardiac troponin T, and high-sensitivity C-reactive prot
36 e protein, procalcitonin, ferritin, D-dimer, cardiac troponin T, and N-terminal pro-B-type natriureti
37 min, beta-myosin heavy chain, alpha-actinin, cardiac troponin T, and phospholamban at levels comparab
41 ype natriuretic peptide and high-sensitivity cardiac troponin T are frequently elevated in severe sep
42 coding the thin-filament contractile protein cardiac troponin T are responsible for 15% of all cases
43 per reference limit for the high-sensitivity cardiac troponin T assay (hs-cTnT) in 3 large independen
44 With the widespread use of high-sensitive cardiac troponin T assays, positive tests become frequen
45 ide, alpha- and beta-myosin heavy chain, and cardiac troponin T) by day 3 with subsequent progression
47 onal analysis of all protein coding exons of cardiac troponin T, cardiac troponin I, alpha-tropomyosi
48 17.8 ng/L and a perioperative high-sensitive cardiac troponin T change greater than or equal to 6.3 n
49 The risk predictive power of high-sensitive cardiac troponin T change in addition to the Revised Car
52 terminal pro-B-type natriuretic peptide, and cardiac troponin T concentrations in multivariate analys
53 type natriuretic peptide or high-sensitivity cardiac troponin T concentrations were independently ass
54 ans, and patients were masked to study serum cardiac troponin-T concentrations and echocardiographic
55 s, serial endomyocardial biopsies, and serum cardiac troponin-T concentrations were obtained from 68
57 intronic elements (called MSEs) flanking the cardiac troponin T (cTNT) alternative exon 5 and promote
62 f two pre-mRNAs that are misregulated in DM, cardiac troponin T (cTNT) and insulin receptor (IR).
64 -specific acute cardiac stress (by measuring cardiac troponin T (cTnT) and N-terminal prohormone of b
69 r group previously identified elevated serum cardiac troponin T (cTnT) as the most powerful predictor
72 eins including myosin heavy chain (MyHC) and cardiac troponin T (cTnT) cause a dominant genetic heart
76 (ETR-3/NAPOR/BRUNOL3) promotes inclusion of cardiac troponin T (cTNT) exon 5 via binding between pos
77 to determine whether there is immunoreactive cardiac troponin T (cTnT) expression in diseased skeleta
79 nother purine-rich enhancer from the chicken cardiac troponin T (cTNT) gene for the ability to regula
80 ative exon 5 of the striated muscle-specific cardiac troponin T (cTNT) gene is included in mRNA from
81 Striated muscle-specific expression of the cardiac troponin T (cTNT) gene is mediated through two M
84 ical and biological significance of elevated cardiac troponin T (cTnT) in patients with neuromuscular
92 e investigated the physiological role of the cardiac troponin T (cTnT) isoforms in the presence of hu
95 prospectively evaluated the relation between cardiac troponin T (cTnT) level, the presence and severi
97 erified assumption that chronically elevated cardiac troponin T (cTnT) levels fluctuate randomly arou
101 a splice donor site mutation (trunc) in the cardiac troponin T (cTnT) model familial hypertrophic ca
102 of established interstitial fibrosis in the cardiac troponin T (cTnT) mouse model of human hypertrop
103 The hypertrophic cardiomyopathy-causing cardiac troponin T (cTnT) mutation Delta160Glu (Delta160
104 eporting the functional effects of the first cardiac troponin T (CTnT) mutation linked to infantile R
106 ial necrosis was assessed by measurements of cardiac troponin T (cTnT) on admission and 12 h after ad
108 MBNL1 controls the splicing of exon 5 in the cardiac troponin T (cTNT) pre-mRNA by competing directly
109 Regulated alternative splicing of avian cardiac troponin T (cTNT) pre-mRNA requires multiple int
110 st-procedure CK-MB, an isolated elevation in cardiac troponin T (cTnT) predicts long-term survival.
112 s to determine whether different profiles of cardiac troponin T (cTnT) values assessed over time woul
114 esent study was to evaluate whether elevated cardiac troponin T (cTnT) was independently associated w
118 iac injury are cardiac troponin I (cTnI) and cardiac troponin T (cTnT) which have been considered as
119 NT photodetector for an on-chip detection of cardiac troponin T (cTnT) with a detection limit of 12 p
121 splicing of TNNT2, the gene that encodes for cardiac troponin T (cTnT), a biomarker of myocardial inj
122 f body mass, heart rate, blood pressures and cardiac troponin T (cTnT), a biomarker of myocyte damage
123 interaction between LVH, low but detectable cardiac troponin T (cTnT), and elevated N-terminal pro-B
125 s insensitive to reconstitution of cTnI with cardiac troponin T (cTnT), cTnC, or cTnC and cTnT in the
128 t of expression of a mutant (Arg92Gln) human cardiac troponin T (cTnT), known to cause HCM in humans,
131 50%, and improved diastolic function in the cardiac troponin T (cTnT)-Q92 transgenic mouse model of
140 tiation factor-15 (GDF-15), high-sensitivity cardiac troponin T (cTnT-hs) and haemoglobin, age, and p
142 cardiograms and serial serum measurements of cardiac troponin T (cTnT; cardiac injury biomarker), N-t
143 the pathologic free light chains (p < 0.05), cardiac troponin-T (cTnT) (p < 0.01), and the Karnofsky
144 AT), matrix metalloproteinase-9 (MMP-9), and cardiac Troponin-T (cTnT) were evaluated by appropriate
147 nano-gap device provides the capability for cardiac-troponin T (cTnT) measurements with co-existed 1
148 s screening of cardiac Troponin-I (cTnI) and cardiac-Troponin-T (cTnT) in a point-of-care sensor form
150 (Ser532Pro and Phe764Leu) and a deletion in cardiac troponin T (deltaLys210) caused early-onset vent
151 eletion of the N-terminal variable region of cardiac troponin T demonstrates a novel mechanism by whi
152 e ESC 0/1-h algorithm using high-sensitivity cardiac troponin T embedded in routine clinical care and
155 ic cardiomyopathy caused by mutations in the cardiac troponin T gene (TNNT2) has been associated with
157 f a 9-bp segment from intron 7 of the turkey cardiac troponin T gene may be responsible for the weake
159 mano-Ward syndrome and long-QT syndrome, and cardiac troponin T gene, tnnt2, affected in human cardio
163 deaths compared with 29.5% among those with cardiac troponin T > or = 0.01 microg/L (p < .001).
164 43.7%, 33.8%, and 25.7% among patients with cardiac troponin T > or = 0.01 microg/L and 75.3%, 67.6%
165 , who experienced an event associated with a cardiac troponin T >99th percentile of a normal referenc
166 A total of 5460 patients had at least one cardiac troponin T >=0.01 ng/mL; 1365 of these patients
167 chronic myocardial injury (high-sensitivity cardiac troponin T >=6 ng/L] and stress (N-terminal pro-
168 GST) affinity tag at the N-terminus of human cardiac troponin T (hcTnT) and an intervening tobacco et
169 pe natriuretic peptide, and high-sensitivity cardiac troponin T, higher levels of Cp were associated
170 anterior circulation and a high-sensitivity cardiac troponin T (hs-cTnT) acquired on the day of admi
171 ween serial measurements of high-sensitivity cardiac troponin T (hs-cTnT) and future events in HF.
173 Although small elevations of high-sensitive cardiac troponin T (hs-cTnT) are associated with inciden
175 tional level, with elevated high-sensitivity cardiac troponin T (hs-cTnT) concentrations (>/=14 ng/L)
176 tic peptide (NT-proBNP) and high-sensitivity cardiac troponin T (hs-cTnT) concentrations were measure
177 rognostic value of baseline high-sensitivity cardiac troponin T (hs-cTnT) elevation in SCAD patients
178 ated hemoglobin (HbA1c) and high-sensitivity cardiac troponin T (hs-cTnT) in 9,661 participants free
179 sponse to mental stress and high-sensitivity cardiac troponin T (hs-cTnT) in healthy older individual
180 implications of introducing high-sensitivity cardiac troponin T (hs-cTnT) into clinical practice and
182 f an undetectable (<5 ng/l) high-sensitivity cardiac troponin T (hs-cTnT) level and an electrocardiog
183 hesized that any detectable high-sensitivity cardiac troponin T (hs-cTnT) level is associated with ad
184 s are preferable when using high-sensitivity cardiac troponin T (hs-cTnT) levels in the diagnosis of
186 econdary endpoints included high-sensitivity cardiac troponin T (hs-cTnT) on day 4, left ventricular
187 CVD) but elevated levels of high-sensitivity cardiac troponin T (hs-cTnT) or N-terminal pro-B-type na
188 oninferiority of a 0/1-hour high-sensitivity cardiac troponin T (hs-cTnT) protocol in comparison with
190 A 1-h algorithm based on high-sensitivity cardiac troponin T (hs-cTnT) testing at presentation and
191 Thus, we assessed whether high-sensitivity cardiac troponin T (hs-cTnT), a marker of subclinical my
192 B-type natriuretic peptide, high-sensitivity cardiac troponin T (hs-cTnT), and high-sensitivity cardi
193 uretic peptide (NT-proBNP), high-sensitivity cardiac troponin T (hs-cTnT), and low-density lipoprotei
194 uretic peptide (NT-proBNP), high-sensitivity cardiac troponin T (hs-cTnT), Cystatin-C (Cys-C), high-s
195 oponin T, measured by a new highly sensitive cardiac troponin T (hs-cTnT), may reflect ischemia witho
198 rdial Infarction) evaluated high-sensitivity cardiac troponin-T (hs-cTnT) in a 1-hour acute myocardia
199 ning with a biomarker (e.g. high sensitivity cardiac troponin T [hs-cTnT] or B-type natriuretic pepti
200 th myocardial damage (using high-sensitivity cardiac troponin-T [hs-cTnT]) and with coronary heart di
201 chain, myosin light chain 1/2, tropomyosin, cardiac troponins (T, I, C), and the trimeric troponin c
202 of wild-type (WT) cTn and cTn containing WT cardiac troponin T/I + cardiac troponin C (cTnC) D65A (a
203 ponin I was measured in 61,379 patients, and cardiac troponin T in 7880 patients (both proteins were
204 n 97.4% of the patients and high-sensitivity cardiac troponin T in 84.5%, with higher concentrations
207 was defined as an absolute high-sensitivity cardiac troponin T increase of >/=14 ng/L from preoperat
208 l prospective measurements were performed of cardiac troponin T, indexes of NO production (NO(2)(-) a
212 n of force development, the four known human cardiac troponin T isoforms, TnT1 (all exons present), T
213 Deletion of the 14 C-terminal residues of cardiac troponin T leads to hypertrophic cardiomyopathy.
215 level of 1.0 microg per liter or higher or a cardiac troponin T level of 0.1 microg per liter or high
216 acute chest pain, elevated high-sensitivity cardiac troponin T levels (>14 ng/l), and inconclusive e
221 acrophages, almost complete normalization of cardiac troponin T levels in serum and of left ventricul
226 ng hospitalization, 12.5% of patients with a cardiac troponin T < 0.01 microg/L suffered deaths compa
227 /L and 75.3%, 67.6%, and 62.9% in those with cardiac troponin T < 0.01 microg/L, respectively (p < .0
228 normal biomarkers (hs-cTnT (high sensitivity cardiac troponin-T) <6 ng/L and NT-proBNP (N-terminal pr
229 We also found that Max was a part of the cardiac troponin T M-CAT-TEF-1 complex even when the DNA
232 eri-procedural increases of high-sensitivity cardiac troponin T (mean: 9.9 ng/ml, range: 2.7 to 19.0
234 ive and 24-hour postoperative high-sensitive cardiac troponin T measurements and the respective chang
235 ac investigations including high-sensitivity cardiac troponin T measurements at later time points or
240 eins specifically activate exon inclusion of cardiac troponin T minigenes in vivo via muscle-specific
241 lure express an unusual low molecular weight cardiac troponin T missing 11 amino acids due to the spl
242 tide enhancer that has similarities with the cardiac Troponin T MSE3 enhancer, and a potentially nove
248 sus without either elevated high-sensitivity cardiac troponin T or NT-proBNP had a 10-year CV inciden
250 native splicing patterns (for example, human cardiac troponin T) or affects other aspects of RNA biol
251 e have asked whether serum concentrations of cardiac troponin-T predict development of coronary arter
253 combinase expressed under the control of the cardiac troponin T promoter resulted in death by E12.5;
254 rdiac-selective expression of EcSOD from the cardiac troponin-T promoter after systemic administratio
255 ellular superoxide dismutase (EcSOD) via the cardiac troponin-T promoter would protect the mouse hear
258 expression, transgenic mice carrying the rat cardiac troponin T proximal promoter (-497 bp from the t
259 igenic mice, turned on and off expression of cardiac troponin T-Q92 (cTnT-Q92), responsible for human
261 s, we used 2 mouse models of sarcomeric HCM (cardiac troponin T R92L and R92W) with differential myoc
262 and methylprednisolone significantly reduced cardiac troponin T release and the number of allograft i
263 nhanced myocardial damage evidenced by serum cardiac troponin T release in the rat and mouse cardiac
264 nges in markers of cardiac (high-sensitivity cardiac troponin T), renal (creatinine and cystatin-C),
265 ific antigens cardiac myosin heavy chain and cardiac troponin T, respectively (immunocytochemistry),
267 pro-brain natriuretic peptide (pro-BNP), and cardiac troponin T showed significant linear trends for
269 ificantly more cardiomyocytes, determined by cardiac troponin-T staining, in the MI zone of the QHG21
270 tions between or near residues 112 to 136 of cardiac troponin-T, the crucial TnT1 (N-terminal domain
271 enes encoding cardiac troponin I (TNNI3) and cardiac troponin T (TNNT2) caused altered troponin prote
272 RNAs including the Insulin Receptor (Insr), Cardiac Troponin T (Tnnt2), Lim Domain Binding 3 (Ldb3)
273 ted splicing of three CELF target pre-mRNAs, cardiac troponin T (Tnnt2), myotubularin-related 1 gene
275 ardiac troponin I (TNNI3p.98truncation ) and cardiac troponin T (TNNT2p.K217deletion ; also known as
276 estigated the prognostic value of detectable cardiac troponin T (TnT) and elevated N-terminal pro-B-t
277 ausing mutations associated with a truncated cardiac troponin T (TnT) and missense mutations in the b
283 t to evaluate the prognostic significance of cardiac troponin T (TnT) serum levels after noncardiac s
287 h no cardiovascular disease in our study had cardiac troponin T values above the current myocardial i
288 emoglobin A(1c), detectable high-sensitivity cardiac troponin T was associated with subsequent CVD (m
293 ype natriuretic peptide and high-sensitivity cardiac troponin T were measured 1, 2, and 7 days after
295 o cause HCM, both wild-type and mutant human cardiac troponin T were overexpressed in Escherichia col
296 Left ventricular structure and function and cardiac troponin-T were among the top predictors for inc
297 defect in the interactions between CTnC and cardiac troponin T, which are known to be necessary for
299 hich most patients would have had a negative cardiac troponin T with older assays); and Group 4, thos
300 rmined pre- and postoperative high-sensitive cardiac troponin T with the occurrence of major adverse