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1 assessed by cardiac enzymes, troponin I, and creatine kinase.
2 ere modeled in the C terminus of muscle-type creatine kinase.
3 pyruvate kinase muscle isozyme, isoforms of creatine kinase.
4 including fasciculations and elevated serum creatine kinase.
5 pomyosin, myosin or an isoform of the enzyme creatine kinase.
6 d pathology and reduction in levels of serum creatine kinase.
7 ors make neurotransmission less dependent on creatine kinase.
8 ith significant reduction in levels of serum creatine kinase.
9 ansferase [ALT]), alkaline phosphastase, and creatine kinase.
10 ins such as myosin heavy chain fast type and creatine kinase.
11 ficulties, and normal to moderately elevated creatine kinase.
12 aminotransferase, lactate dehydrogenase, and creatine kinase.
13 thesis from OXPHOS, anaerobic glycolysis and creatine kinase.
14 table for bulky ASB9 substrates, such as the creatine kinases.
15 ut preinfarction angina (n=166) by both peak creatine kinase (1094+/-75 IU/L versus 2270+/-102 IU/L;
16 d in 9 healthy men (mean age 27.9 y, SE 3.3; creatine kinase 115 to 859 IU/L, median 358), was associ
19 fat, cold exposure stimulates mitochondrial creatine kinase activity and induces coordinated express
20 further explore the effect of calmodulin on creatine kinase activity and show that it is increased b
22 imus lumborum and a 5-fold increase in serum creatine kinase activity compared with healthy male litt
23 on and reduced the vascular adenylate kinase/creatine kinase activity ratio essential for the respons
24 l muscle health in mdx mice, reducing plasma creatine kinase activity, an established measure of musc
25 on of inflammatory markers of muscle damage (creatine kinase activity, C-reactive protein, proinflamm
26 f differentiation, demonstrated by increased creatine kinase activity, fusion index and myotube diame
27 e, as evidenced by i) normal levels of serum creatine kinase activity, ii) a lack of Evans blue dye u
31 lar to enolase, pyruvate kinase, isoforms of creatine kinase, aldolase A and an isoform of glyceralde
32 ne blood chemistry was normal, as were serum creatine kinase and aldolase levels and thyroid, hepatic
33 ngs to the phosphagen kinase family of which creatine kinase and arginine kinase are the typical repr
36 boratory analysis showed alteration of serum creatine kinase and creatinine in the Leu389Ser ALS4 coh
38 ult onset muscular dystrophy with high serum creatine kinase and that mutation screening, particularl
39 rast-enhanced cardiac MRI (CMRI; day 3+/-1), creatine kinase and troponin I area-under-the-curve, and
42 Of the 1,800 patients enrolled, 1,652 with creatine kinase and/or creatine kinase-myocardial band (
43 ased lactate dehydrogenase, pyruvate kinase, creatine kinase, and cytochrome c oxidase activities, an
44 derived from lactate dehydrogenase, one from creatine kinase, and four from serum albumin protein.
46 ge, sex, and admission levels of troponin I, creatine kinase, and N-terminal pro-brain natriuretic pe
47 size distribution, centralized nuclei, serum creatine kinase, and quantitative histopathology scores.
48 f such therapy, the levels of troponin T and creatine kinase, and the rates of bleeding and stroke di
49 5 IU/L versus 2270+/-102 IU/L; P<0.0001) and creatine kinase area under curve (18 420+/-18 941 versus
50 terquartile range, 14-42; P<0.01) and median creatine kinase areas under the curve were 22 000 and 38
51 with serum muscle enzyme levels (P<0.05 for creatine kinase, aspartate aminotransferase, and aldolas
52 variability compared with the commonly used creatine kinase assay, and correlated better with the re
53 y plus rifaximin group showed an increase in creatine kinase at the end of treatment compared with pa
55 e levels of creatine kinase, MB isoenzyme of creatine kinase, blood urea nitrogen, creatinine, K(+) i
56 sed guanidinoacetate N-methyltransferase and creatine kinase, both at the protein and RNA levels, and
61 ce of isotopically enriched magnesium on the creatine kinase catalyzed phosphorylation of adenosine d
62 ription, and QI 3 = complete blood count and creatine kinase check every 6 months for gout patients r
63 s critical role in hair bundle function, the creatine kinase circuit is essential for high-sensitivit
64 hypothesized that ATP transfer rate through creatine kinase (CK) (k(f)(CKrest)) would be increased,
68 kinases of known structure (the homodimeric creatine kinase (CK) and the monomeric arginine kinase (
72 We investigate the hypothesis that reduced creatine kinase (CK) capacity and flux is associated wit
73 utilization networks in response to chronic creatine kinase (CK) deficiency, a hallmark of cardiovas
75 f the absolute level and rate of increase of creatine kinase (CK) elevation after primary percutaneou
79 n the anti-Jo-1 antibody level and the serum creatine kinase (CK) level, as well as muscle and joint
81 a 2-tiered approach to NBS with screening by creatine kinase (CK) levels in dried blood spots followe
85 ovascular death or nonfatal MI, defined as a creatine kinase (CK) MB fraction of at least 100 ng/mL o
86 iation of a recently reported variant in the creatine kinase (CK) muscle gene, CKM Glu83Gly (rs115590
87 ATP production rate constants (k(f)) through creatine kinase (CK) or ATP synthase (ATPase) with 2 spe
91 lationship between cTnT, cardiac troponin I, creatine kinase (CK), CK-myocardial band levels, and ske
92 tions, and measurements of serum cTnT, cTnI, creatine kinase (CK), creatine kinase myocardial band (C
94 a showing reduced metabolism through cardiac creatine kinase (CK), the major myocardial energy reserv
95 enosine triphosphate (ATP) synthesis through creatine kinase (CK), the primary myocardial energy rese
96 or decreased intracellular ATP generation by creatine kinase (CK), the prime energy reserve of the he
97 erase (AST), lactate dehydrogenase (LDH) and creatine kinase (CK), which cardiac troponins being the
99 Creatine treatment enhanced cell fusion in a creatine kinase (CK)-dependent manner suggesting that AT
102 ir of high-energy phosphate (HEP) bonds, and creatine kinases (CK) catalyze the transfer of HEP from
104 Gower score, time to run 30 feet, and serum creatine kinase [CK] level) and with nonquantitative MR
105 re we report cryo-EM data for the substrate, creatine kinase (CKB) bound to ASB9-ELOB/C, and for full
106 s, we identified that brain-type cytoplasmic creatine kinase (Ckb) was greatly induced in mature oste
107 identified the ATP-buffering, mitochondrial creatine kinase CKMT1 as necessary for survival of EVI1-
109 e dye uptake into muscle and increased serum creatine kinase compared to the 129T2/SvEmsJ background.
110 he most common adverse event was an elevated creatine kinase concentration to more than ten times the
111 ical and functional changes using the muscle creatine kinase conditional frataxin knockout (KO) mouse
112 Ablation of Vps34 in the heart of muscle creatine kinase-Cre;Vps34(f/f) mice led to cardiomegaly
114 mechanical overload, which decreased muscle creatine kinase-driven TEAD-1 transgene expression, and
116 on and the contribution of other isoforms of creatine kinase during RANKL-induced osteoclastogenesis
117 different than control in terms of myalgia, creatine kinase elevation, cancer, and discontinuations
119 tin at its highest doses was associated with creatine kinase elevations (odds ratio, 4.14; 95% credib
120 00 patients [RD], 2.7; 95% CI, -3.2 to 8.7), creatine kinase elevations (RD, 0.2; 95% CI, -0.6 to 0.9
123 (STOMP) study assessed symptoms and measured creatine kinase, exercise capacity, and muscle strength
124 3 and miR-551a expression, which derepresses creatine kinase expression and allows energy to be captu
126 common grade 3-4 adverse events were raised creatine kinase (five [6%] in the 200 mg group vs 19 [13
127 nally, these mice exhibited increased plasma creatine kinase following exhaustive exercise when unfed
128 ne kinase reaction, we have now measured the creatine kinase forward reaction rate constant in BD.
130 hy control participants at 4T and quantified creatine kinase forward reaction rate constant using (31
132 ants or isoforms of tropomyosin, arginine or creatine kinase, glyceraldehyde-3-phosphate dehydrogenas
133 R, 2.620; 95% CI, 1.073-6.399; P = .035) and creatine kinase (>800 U/L; OR, 2.328; 95% CI, 1.129-4.80
134 ice exhibited progressive MD, elevated serum creatine kinase, heart dilation, blood vessel irregulari
135 Consistent with this model, inhibition of creatine kinase in avascular retinas blocks synaptic tra
136 on by OXPHOS (vOX), anaerobic glycolysis and creatine kinase in moderate and severe intensity exercis
137 here was a significant increase in mean peak creatine kinase in the oxygen group compared with the no
139 value exceeded 10 times normal, but average creatine kinase increased 20.8+/-141.1 U/L (P<0.0001) wi
140 ant bundle protein; at approximately 0.5 mM, creatine kinase is capable of maintaining high ATP level
151 = 0.45; I2 = 0%), and increases in the serum creatine kinase level were reduced (OR, 0.72 [CI, 0.54 t
153 ntractures, severe scoliosis, elevated serum creatine kinase level, myopathic electrodiagnostic chang
155 ecificity had proximal weakness (100%), high creatine kinase levels (mean maximum 10,333 IU/liter), a
157 d by adult onset muscle weakness, high serum creatine kinase levels and a prominent inflammatory infi
162 Myopathy--muscle pain or weakness with blood creatine kinase levels more than ten times the upper lim
163 ociated with an increased incidence of serum creatine kinase levels that were more than 10 times the
165 ntral nucleation, tissue fibrosis, and serum creatine kinase levels were dramatically reduced in Sgcd
169 thy characterized by mildly increased plasma creatine kinase levels, a variation in myofibre size and
171 distribution and significantly reduced serum creatine kinase levels, but had limited effect on muscle
172 of Dmdmdx-5Cv mice results in reduced serum creatine kinase levels, improved sarcolemmal integrity,
173 ake, increased muscle fibre necrosis, plasma creatine kinase levels, muscle PDK4, muscle atrophy F-bo
174 is was associated with greatly reduced serum creatine kinase levels, near-normal histology, and funct
175 ut without an earlier onset, increased serum creatine kinase levels, or decreased muscle strength.
188 globin and somatic cytochrome-C) and others (creatine kinase M, malate dehydrogenase cytosolic, fibri
189 Fractional synthesis rate (FSR) of plasma creatine kinase M-type (CK-M) and carbonic anhydrase 3 (
191 protein expression of creatine kinase-mt and creatine kinase-m isoforms was significantly reduced in
193 ved hemodynamics and decreased the levels of creatine kinase, MB isoenzyme of creatine kinase, blood
194 similar or lower in HBOC than HEX pigs, but creatine kinase-MB (but not creatine kinase-MB/creatine
197 (TnI), B-type natriuretic peptide (BNP), and creatine kinase-MB (CK-MB), and TnI and BNP by CART.
198 MI (PMI(Prot)) required a large elevation of creatine kinase-MB (CK-MB), with identical threshold for
199 similar information as a value of 5x ULN for creatine kinase-MB (hazard ratio, 4.31; 99% confidence i
200 rocedural MI, the primary MI definition used creatine kinase-MB as the preferred biomarker, whereas t
201 re hemodynamic deterioration, preangiography creatine kinase-MB isoenzyme rise >2 x normal, and time
202 images provided equal performance, and peak creatine kinase-MB levels correlated with MRI infarct si
207 43; P=0.003 and hazard ratio per doubling of creatine kinase-MB, 1.30; 95% confidence interval, 1.05-
208 ity C-reactive protein (hs-CRP), Troponin-T, creatine kinase-MB, fibrinogen, and D-Dimer concentratio
212 an HEX pigs, but creatine kinase-MB (but not creatine kinase-MB/creatine kinase ratio) was higher wit
213 function, and perfusion), injury biomarkers (creatine-kinase-MB and troponin I), and histopathologic
215 inol-binding protein (hRBP) under the muscle creatine kinase (MCK) promoter (MCKhRBP) with the PKCdel
216 ified a conserved sequence within the Muscle creatine kinase (MCK) promoter that is critical for high
219 ke signaling in this process, we used muscle creatine kinase (MCK)-Cre to disrupt expression of insul
220 omatic gene transfer or transgenesis (muscle creatine kinase [MCK]-EcSOD) in mice significantly atten
221 -activated receptor alpha (PPARalpha; muscle creatine kinase [MCK]-PPARalpha) or PPARbeta/delta (MCK-
222 5:00 am onset of reperfusion, with the peak creatine kinase measured at the peak of the curve being
223 n of total reverse T3, high concentration of creatine kinase, mild anaemia), and radiological (thicke
224 st notably the regions harboring CKMT2 gene (creatine kinase, mitochondrial 2) and RASGRF2 gene (Ras
225 ltiplexed detection of 100 fg/ml troponin T, creatine kinase MM, and creatine kinase MB in serum.
228 NAME induced elevation of cardiac output and Creatine Kinase Muscle-Brain (CKMB), but had no signific
229 ts, there was a reduction in serum levels of creatine kinase muscle-brain isoenzyme, a myocardial-spe
230 Prespecified secondary outcome measures of creatine kinase, muscle strength and function, motor ner
231 s of serum cTnT, cTnI, creatine kinase (CK), creatine kinase myocardial band (CK-MB), and N-terminal
234 enrolled, 1,652 with creatine kinase and/or creatine kinase-myocardial band (CK-MB) post-procedure w
235 ention (PCI, procedural MI) using increasing creatine kinase-myocardial band (CK-MB) thresholds with
237 ethodology to assess the association between creatine kinase-myocardial band and 1-year mortality.
240 High-sensitivity cardiac troponin T and creatine kinase-myocardial band were measured before and
242 me parameter was the area under the curve of creatine kinase-myocardial brain fraction concentration.
244 arkers included high-sensitivity troponin T, creatine kinase, myoglobin, N-terminal B-type natriureti
245 o proceeded directly to phase B for elevated creatine kinase (N = 218, with 73 randomized to ezetimib
246 h large increases in blood concentrations of creatine kinase), new-onset diabetes mellitus, and, prob
248 ted by targeted replacement of mitochondrial creatine kinase or mitochondrial-targeted CaMKII inhibit
251 95% CI 1.34, 13.71; p = 0.014), and elevated creatine kinase (OR 3.79; 95% CI 1.06, 13.51; p = 0.04),
252 nfarction </=1 flow, there was reduced serum creatine kinase (P=0.030) and a 19% reduction in cardiac
253 rapid ATP generation via the phosphocreatine-creatine kinase (PCr/CK) system, as a unique gene family
254 7 g/m(2) vs. 21 +/- 14 g/m(2); p = 0.01) and creatine kinase peak serum level (median [interquartile
255 Structural analysis of modified muscle-type creatine kinase peptide variants by two-dimensional NMR
256 letal muscle under the control of the muscle creatine kinase promoter (MCKcre mice) with mice having
257 e overexpressing PGC-1alpha under the muscle creatine kinase promoter (MPGC-1alphaTG mice) displayed
260 conversion of phosphocreatine to creatine by creatine kinase provides an essential chemical energy so
261 eatine kinase-MB (but not creatine kinase-MB/creatine kinase ratio) was higher with HBOC in moderate
262 muscle anaerobic metabolism, the rate of the creatine kinase reaction, intracellular buffering of pro
263 is replenished from phosphocreatine via the creatine kinase reaction, we have now measured the creat
266 y (31)P nuclear MR spectroscopy, lactate and creatine kinase release spectrophotometrically, and hypo
267 e estimated by peak and area under the curve creatine kinase release was measured in all study popula
268 that the extent of infarct size measured by creatine kinase release was significantly associated wit
271 and increased aspartate aminotransferase and creatine kinase serum enzyme levels in cynomolgus macaqu
272 ed muscle degeneration and fibrosis, reduced creatine kinase serum levels, restored running capacity
274 Diagnosis using the classic blood marker creatine kinase sometimes yields unsatisfactory results
277 but not pravastatin, induced elevated serum creatine kinase; swollen, misaligned, size-variable, and
278 apacity of oxidative phosphorylation and the creatine kinase system to buffer the cellular ATP/ADP ra
279 to examine the bioenergetic reactions of the creatine-kinase system and the ATP synthesis/hydrolysis
280 es, including aspartate aminotransferase and creatine kinase, that are typically elevated as a result
281 We assessed whether the level of plasma creatine kinase, the enzyme that utilizes ADP and phosph
282 , the characteristic clearance properties of creatine kinase, the time course of muscle fiber regener
283 intra- and intermolecular cross-links within creatine kinase, then to map the interaction surfaces be
284 sterol, low-density lipoprotein cholesterol, creatine kinase, thyroid-stimulating hormones, and eryth
286 n, stabilized the sarcolemma, restored serum creatine kinase to wild-type levels, and protected muscl
287 olipoprotein A1 (apoA1), apoE, mitochondrial creatine kinase U-type, beta-synuclein, synaptogyrin-3,
289 lower limb weakness with highly raised serum creatine kinase values (average 4500 IU/l) and frequent
295 r beta-actin, the cytosolic brain isoform of creatine kinase was the next most abundant bundle protei
296 tions of serum transaminases, bilirubin, and creatine kinase were infrequent and similar between grou
297 ion of MyoD-target genes myogenin and muscle creatine kinase were suppressed by PAX3/FOXO1A or PAX7/F
298 erize the interaction between calmodulin and creatine kinase, which we identify as a novel calmodulin
299 tion of myocardial ATP, phosphocreatine, and creatine kinase with decreased efficiency of mechanical
300 catalytic site of bound hexokinase or bound creatine kinase without ATP dilution in the cytosol.