戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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.
3                      Blood concentrations of cardiac troponin above the 99(th) percentile are a key c
4                                              Cardiac troponin and B-type natriuretic peptide (BNP) co
5 I(R146G), and cTnI(R21C) were complexed into cardiac troponin and exchanged into rat ventricular myof
6 sessment algorithm based on high-sensitivity cardiac troponin and sampling at 0 and 1 hour.
7 re observed across ncRNA types compared with cardiac troponins and cMyBP-C (cardiac myosin-binding pr
8                            Measures of serum cardiac troponins and natriuretic peptides have become e
9 ype natriuretic peptide and high-sensitivity cardiac troponin), and clinical history (prior stroke).
10                           Elevated levels of cardiac troponin, and especially their relative changes
11                           Elevated levels of cardiac troponins are associated with adverse clinical o
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
14           Implementation of high-sensitivity cardiac troponin assays and the recommendations of the U
15                             High-sensitivity cardiac troponin assays enable myocardial infarction to
16           The introduction of more sensitive cardiac troponin assays has led to increased recognition
17                           The improvement in cardiac troponin assays, especially in conjunction with
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
23                                              Cardiac troponin C (cTnC) is the regulatory protein that
24 ique 31-residue N-terminal region that binds cardiac troponin C (cTnC) to increase the calcium sensit
25          The Ca(2+) sensor of the sarcomere, cardiac troponin C (cTnC), plays an important role in re
26 .I4M substitution in the N-terminal helix of cardiac troponin C (cTnC).
27 ac thin-filament activation, the N-domain of cardiac troponin C (N-cTnC) binds to Ca(2+) and interact
28                Coincident S-nitrosylation of cardiac troponin C decreases myocardial sensitivity to C
29 ation, in general, and for phospholamban and cardiac troponin C S-nitrosylation, in particular, in be
30           The ability of calcium-bound human cardiac troponin C to neutralize the inhibition of K206I
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
33 tivity in the absence of calcium-bound human cardiac troponin C.
34                           Measurement of the cardiac troponins, cardiac troponin T and cardiac tropon
35 ation of PKCepsilon expressing platelets and cardiac troponin clearly discriminates patients with 100
36 main of the troponin I subunit (TnIC) of the cardiac troponin complex.
37  Troponin-I (cTnI) is one of the subunits of cardiac troponin complexes and a pivotal biochemical mar
38                                            A cardiac troponin concentration of less than 5 ng/L ident
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
41              In the general population, high cardiac troponin concentration within the normal range i
42                                              Cardiac troponin concentrations are used to identify pat
43                                Variations in cardiac troponin concentrations by age, sex and time bet
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
49         The introduction of high-sensitivity cardiac troponin (cTn) assays has improved sensitivity f
50         It is unknown whether more sensitive cardiac troponin (cTn) assays maintain their clinical ut
51 institutions transitioning from conventional cardiac troponin (cTn) assays.
52                                              Cardiac troponin (cTn) elevation is a common finding in
53                                              Cardiac troponin (cTn) is a key molecule in the regulati
54                                  Measures of cardiac troponin (cTn) may have lower specificity for my
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
58 schemic stroke (AIS) have elevated levels of cardiac troponins (cTn).
59                                              Cardiac troponins (cTns) are the cornerstone of diagnosi
60                                              Cardiac troponin detected by new-generation, highly sens
61    IV histone infusion caused time-dependent cardiac troponin elevation to indicate cardiac injury.
62                             High-sensitivity-cardiac troponin for accelerated diagnosis of acute myoc
63 rest in widening the use of high-sensitivity cardiac troponins for population cardiovascular disease
64                                  Circulating cardiac troponin has been associated with adverse progno
65                 The structured use of serial cardiac troponin has the potential to facilitate risk st
66               Low values of high-sensitivity cardiac troponin (hs-cTn) and coronary artery calcium (C
67                             High-sensitivity cardiac troponin (hs-cTn) assays have been used clinical
68                  Until now, high-sensitivity cardiac troponin (hs-cTn) assays were mainly developed f
69                       Using high-sensitivity cardiac troponin (hs-cTn) assays with sex-specific 99th
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
72                             High-sensitivity cardiac troponin (hs-cTn) I or T methods have been in us
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)
80 ing in PKA-site dependent phosphorylation of cardiac troponin I (cTnI) and phospholamban (PLN).
81          Practice guidelines regard cTnT and cardiac troponin I (cTnI) as equally sensitive and speci
82 formance metrics of a novel high-sensitivity cardiac troponin I (cTnI) assay for this purpose.
83                                              Cardiac troponin I (cTnI) geometric mean decreased by 34
84 ifically monophosphorylates Ser(23) of human cardiac troponin I (cTnI) in isolation and in the trimer
85          During beta-adrenergic stimulation, cardiac troponin I (cTnI) is phosphorylated by protein k
86         Both tobacco smoking and circulating cardiac troponin I (cTnI) levels are associated with the
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
90                                          The cardiac troponin I (cTnI) R145W mutation is associated w
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
96 osed for the ultrasensitive immunosensing of Cardiac Troponin I (cTnI).
97  quantities of monoclonal antibodies against cardiac troponin I (cTnI).
98 Drug Administration-cleared high-sensitivity cardiac troponin I (hs-cTnI) assays.
99 myocardial infarction using high-sensitivity cardiac troponin I (hs-cTnI) have been identified.
100 c troponin T (hs-cTnT), and high-sensitivity cardiac troponin I (hs-cTnI) were determined in plasma s
101        Quartiles of BNP and high-sensitivity cardiac troponin I (hs-cTnI) were included in adjusted m
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.
104                 We measured high-sensitivity cardiac troponin I (hsTnI) in 12 956 and BNP in 11 076 p
105 e molecular mechanism(s) of the mutant human cardiac troponin I (K206I), we tested the Ca(2+) depende
106  with mice expressing a pseudophosphorylated cardiac troponin I (S23D and S24D; TnI-PP).
107                       Autoimmune response to cardiac troponin I (TnI) induces inflammation and fibros
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
110                                              Cardiac troponin I (TNNI3) gene mutations account for 3%
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
119                  Use of the high-sensitivity cardiac troponin I assay with sex-specific thresholds in
120 ons at presentation using a high-sensitivity cardiac troponin I assay.
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
125                                       Plasma cardiac troponin I concentration was measured with a hig
126 e myocardial injury (high-sensitivity plasma cardiac troponin I concentration, 4.3 ng/L [interquartil
127 y, as assessed by serial measurements of the cardiac troponin I concentration.
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
130                                  We measured cardiac troponin I concentrations in 725 participants (6
131 ospective studies measuring high-sensitivity cardiac troponin I concentrations in patients with suspe
132                                              Cardiac troponin I concentrations were less than 5 ng/L
133 rating age, sex, and paired high-sensitivity cardiac troponin I concentrations, was trained on 3,013
134       Low concentrations of high-sensitivity cardiac troponin I determined on presentation to the eme
135 vely enrolled and serial echocardiograms and cardiac troponin I evaluations were performed.
136 terferences when electrochemically detecting cardiac troponin I in complex biological samples.
137 valuated the performance of high-sensitivity cardiac troponin I in those with and without renal impai
138                                              Cardiac troponin I levels were normal in all patients, w
139 lic groups used to immobilise antibodies for cardiac troponin I marker.
140 syndrome (n=1218) underwent high-sensitivity cardiac troponin I measurement at presentation and 3 and
141 rds measured in transgenic mice expressing a cardiac troponin I mutation (R145G).
142 el we previously identified that HCM causing cardiac troponin I mutation Gly203Ser (cTnI-G203S) is as
143               We additionally measured human cardiac troponin I protein in 9 human plasma samples, an
144                               Periprocedural cardiac troponin I significantly increased (F=3.64; P=0.
145 r the interaction between the Ca(2+) ion and cardiac troponin I subunit.
146                             High-sensitivity cardiac troponin I testing is widely used to evaluate pa
147 f peptides afforded higher sensitivities for cardiac troponin I than those prepared by the chemisorpt
148             To evaluate the performance of a cardiac troponin I threshold of 5 ng/L at presentation a
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
154                  The device can detect serum cardiac troponin I, a biomarker of cardiac disease to 10
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
158                                              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
162                                  A series of cardiac troponin I-interacting kinase (TNNI3K) inhibitor
163         High-sensitivity assays can quantify cardiac troponins I and T (hs-cTnI, hs-cTnT) in individu
164 oped for rapid and simultaneous screening of cardiac Troponin-I (cTnI) and cardiac-Troponin-T (cTnT)
165                                          The cardiac Troponin-I (cTnI) is one of the subunits of card
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
169 of the clinical biomarker of cardiac injury, cardiac troponin-I, by 52+/-17% (P=1.01x10(-2)).
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
174                                 Increases in cardiac troponin indicative of myocardial injury are com
175                 The basal phosphorylation of cardiac troponin inhibitor (cTnI) and the myosin-binding
176                                              Cardiac troponin is an independent predictor of cardiova
177                                              Cardiac troponin is the preferred biomarker for diagnosi
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
180                     Circulating histones and cardiac troponin levels were obtained from serial blood
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.
190                     Minimally elevated serum cardiac troponin reflects myocardial injury and is assoc
191  and altered stoichiometry between the three cardiac troponin subunits.
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
196             However, it is not clear whether cardiac troponin T (cTnT) and troponin I (cTnI) are equi
197 erified assumption that chronically elevated cardiac troponin T (cTnT) levels fluctuate randomly arou
198                              Elevated plasma cardiac troponin T (cTnT) levels in patients with neurom
199      The hypertrophic cardiomyopathy-causing cardiac troponin T (cTnT) mutation Delta160Glu (Delta160
200 embled on a screen-printed electrode for the cardiac troponin T (cTnT) was developed.
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
203 isopropylacrylamide (PNIPAAm) functionalised cardiac troponin T (cTnT) with anti-cTnT.
204 splicing of TNNT2, the gene that encodes for cardiac troponin T (cTnT), a biomarker of myocardial inj
205 tic peptide (NT-proBNP) and high-sensitivity cardiac troponin T (cTnT), and genetic analysis.
206                                              Cardiac troponin T (cTnT), even at low concentrations, i
207             For the first time, we show that cardiac troponin T (cTnT), in part through its intrinsic
208 globin (MYG), bovine serum albumin (BSA) and cardiac troponin T (cTnT), respectively.
209 er Nkx2.5, or that of the myocardial marker, cardiac troponin T (cTnT).
210 rdial infarction, especially with the use of cardiac troponin T (cTnT).
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
213                             High-sensitivity cardiac troponin T (hs-cTnT) and N-terminal B-type natri
214  Although small elevations of high-sensitive cardiac troponin T (hs-cTnT) are associated with inciden
215                  High-sensitivity assays for cardiac troponin T (hs-cTnT) are sometimes used to rapid
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
220                             High-sensitivity cardiac troponin T (hs-cTnT) is a biomarker of cardiovas
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
224                       Their high-sensitivity cardiac troponin T (hs-cTnT) levels were measured.
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
228 ge, as assessed by elevated high-sensitivity cardiac troponin T (hs-cTnT) test results.
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
233 ge, as assessed by elevated high-sensitivity cardiac Troponin T (hs-cTnT).
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
237                     The C-terminal region of cardiac troponin T (TnT), a tropomyosin-associated prote
238 are mutations in the TNNT2 gene that encodes cardiac troponin T (TnT).
239                        Adding high-sensitive cardiac troponin T absolute change to the Revised Cardia
240 protein expression of cardiomyogenic markers cardiac troponin T and alpha-smooth muscle actin in CPCe
241        Measurement of the cardiac troponins, cardiac troponin T and cardiac troponin I, using sensiti
242 f muscle-enriched miRNAs with high-sensitive cardiac troponin T and cMyBP-C returned the highest area
243                             High-sensitivity cardiac troponin T and creatine kinase-myocardial band w
244  of these transcripts paralleled the rise in cardiac troponin T and decayed at 30 days.
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
247                              We measured the cardiac troponin T concentration at baseline with a high
248                                          The cardiac troponin T concentration was an independent pred
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
253 sing serial measurements of high-sensitivity cardiac troponin T in clinical routine.
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
256                       Serum high-sensitivity cardiac troponin T levels and electrocardiograms were ob
257                          However, changes in cardiac troponin T levels during the infusion did not di
258       In patients with NSTE-ACS and elevated cardiac troponin T levels, an early invasive strategy ha
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
261        Pre- and postoperative high-sensitive cardiac troponin T measurements demonstrated a majority
262 sus without either elevated high-sensitivity cardiac troponin T or NT-proBNP had a 10-year CV inciden
263               Elevations in high-sensitivity cardiac troponin T or NT-proBNP identify individuals wit
264 ociation rates in fully reconstituted WT and cardiac troponin T R92L and R92W thin filaments.
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
268                                  We measured cardiac troponin T with a highly sensitive assay (hs-cTn
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
275                           For a third trait, cardiac troponin T, investigation of regulatory domains
276 coronary syndrome (NSTE-ACS) and an elevated cardiac troponin T.
277 1,200 patients with NSTE-ACS and an elevated cardiac troponin T.
278 e populations as determined by expression of cardiac troponin T.
279 gy in patients with NSTE-ACS and an elevated cardiac troponin T.
280 -day mortality, better than high-sensitivity cardiac troponin T.
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
284                                              Cardiac Troponins (T and I) are well established protein
285 AT), matrix metalloproteinase-9 (MMP-9), and cardiac Troponin-T (cTnT) were evaluated by appropriate
286  through the detection and quantification of cardiac Troponin-T (cTnT).
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
294  (RV) dysfunction on imaging, and a positive cardiac troponin test result.
295 rdial Infarction recommends high-sensitivity cardiac troponin testing and classification of patients
296                             High-sensitivity cardiac troponin testing may improve the risk stratifica
297 ectrochemical sensor platform for monitoring cardiac troponins through the detection and quantificati
298                                              Cardiac troponin was detectable in 80.0% (hs-cTnI: 82.6%
299                                              Cardiac troponins were normal, whereas N-terminal pro B-
300 , and a vast majority of children had raised cardiac troponin when checked.

 
Page Top