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1 ties (grade 3 diarrhoea and grade 3 elevated aspartate aminotransferase).
2 eased levels of alanine aminotransferase and aspartate aminotransferase.
3 serum levels of alanine aminotransferase and aspartate aminotransferase.
4 and eosin quantification, and serum alanine/aspartate aminotransferase.
5 ABDC active site is very similar to that of aspartate aminotransferase.
6 elevated serum alanine aminotransferase and aspartate aminotransferase.
7 n the various strata of intact PTH and serum aspartate aminotransferase.
8 ble the "open" and "closed" conformations of aspartate aminotransferase.
9 ably due to the high K(m) of the cytoplasmic aspartate aminotransferase.
10 us co factor for diverse enzymes, among them aspartate aminotransferase.
11 hydrogenase < 100 U/L, below analyzer range; aspartate aminotransferase 0 hour, 15.6 +/- 9.3 U/L vs 7
12 the role of endogenous sulfur dioxide (SO2)/ aspartate aminotransferase 1 (AAT1) pathway in stretch-i
13 573 patients vs six [1%] of 570), increased aspartate aminotransferase (103 [18%] vs 16 [3%]), hyper
15 dL), alanine aminotransferase (2288.82 U/L), aspartate aminotransferase (1251.76 U/L), gamma-glutamyl
17 enzymes (alanine aminotransferase, 657 U/L, aspartate aminotransferase, 1401 U/L), blood urea (53 mg
18 l thromboplastin time (8% and 18%); elevated aspartate aminotransferase (15% and 18%), alanine aminot
19 lanine aminotransferase compared to group B (aspartate aminotransferase, 168[166] vs. 57[67] IU/L; P=
20 vs six [0.9%]), and reversible increases in aspartate aminotransferase (22 [3.4%] vs three [0.5%]).
21 sterol, 42.80 mg/dL (39.84-45.76 mg/dL); for aspartate aminotransferase, 22.67 U/L (19.94-25.41 U/L);
22 s of hypertension (35% vs. 15%) and elevated aspartate aminotransferase (23% vs. 8%) were higher with
23 ted with significantly lower serum levels of aspartate aminotransferase (240+/-98 IU/L vs. 382+/-163
26 ed with -7.29 (-9.5, -5.1) IU/L; P < 0.001], aspartate aminotransferase [-31.33 (-32.1, -30.5) compar
27 group, SG induced significant improvement in aspartate aminotransferase (32.4 +/- 17.4 vs 21.5 +/- 6.
28 288 patients vs four [3%] of 140), elevated aspartate aminotransferase (51 [18%] vs four [3%]), hype
29 mia (86 [34%]), fatigue (83 [33%]), elevated aspartate aminotransferase (65 [26%]), and increased ala
31 Importantly, increasing peak perioperative aspartate aminotransferase, a surrogate marker of hepati
37 ed plasma glucose, alanine aminotransferase, aspartate aminotransferase, AGEs and insulin levels.
38 ur algorithm included data on age; levels of aspartate aminotransferase, alanine aminotransferase (AL
40 creatinine (indicator of renal dysfunction), aspartate aminotransferase, alanine aminotransferase (ma
41 of serum liver tests (alkaline phosphatase, aspartate aminotransferase, alanine aminotransferase) an
42 (international normalized ratio, bilirubin, aspartate aminotransferase, alanine aminotransferase) an
43 m injury by reducing the activities of serum aspartate aminotransferase, alanine aminotransferase, an
44 of hepatocyte injury and cholestasis (serum aspartate aminotransferase, alanine aminotransferase, bi
45 ic diagnoses and laboratory values (albumin, aspartate aminotransferase, alanine aminotransferase, cr
46 o routine markers of liver impairment (e.g., aspartate aminotransferase, alanine aminotransferase, la
48 is and a substantially higher AUROC than the aspartate aminotransferase-alanine aminotransferase rati
49 occur in previous studies showing increased aspartate aminotransferase-alanine aminotransferase rati
50 ly improved liver function assessed by serum aspartate aminotransferase/alanine aminotransferase leve
51 on age, viral genotype, initial viral load, aspartate aminotransferase/alanine aminotransferase rati
52 outcome in multivariate analyses were higher aspartate aminotransferase/alanine aminotransferase rati
53 s the elevation in alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, and ga
54 rtal areas in the biopsy, patient age, serum aspartate aminotransferase, alkaline phosphatase, and pl
55 trition and inflammation, minerals, PTH, and aspartate aminotransferase, AlkPhos > or =120 U/L was as
56 olesterol, whereas increasing plasma alanine/aspartate aminotransferases (ALT/AST) and hepatic trigly
57 ociated with liver-related complications; an aspartate aminotransferase/ALT ratio >1 and older age we
58 higher mean [+/-2 standard deviation] serum aspartate aminotransferase and alanine aminotransferase
59 ma and liver triglyceride content and plasma aspartate aminotransferase and alanine aminotransferase
60 ce exhibited earlier mortality, higher serum aspartate aminotransferase and alanine aminotransferase
61 ed NASH as reflected by reductions in plasma aspartate aminotransferase and alanine aminotransferase
62 ose-limiting toxicity (one grade 3 increased aspartate aminotransferase and alanine aminotransferase
63 ing induction (20 [54%] patients), increased aspartate aminotransferase and alanine aminotransferase
64 r, and skeletal muscle and had higher plasma aspartate aminotransferase and alanine aminotransferase,
65 score created from the platelet count, serum aspartate aminotransferase and alanine aminotransferase,
66 ed in hepatic steatosis and increased plasma aspartate aminotransferase and alanine aminotransferase.
67 pect to sex, age, duration of disease, serum aspartate aminotransferase and alkaline phosphatase leve
69 proportion of patients alanine transaminase, aspartate aminotransferase and AlkPhos >5x upper-limit-o
70 sis, decreased platelet count, and increased aspartate aminotransferase and alpha-fetoprotein levels
71 Similarities have been discovered between aspartate aminotransferase and citrate synthase that onl
72 cyte population, depleted KCs, and increased aspartate aminotransferase and creatine kinase serum enz
73 learance of several serum enzymes, including aspartate aminotransferase and creatine kinase, that are
74 ture, decreased apoptosis, and reduced serum aspartate aminotransferase and creatinine levels compare
75 tients; one patient had grade 3 increases in aspartate aminotransferase and gammaglutamyltransferase
77 cally by transamination to oxaloacetate with aspartate aminotransferase and then decarboxylation with
78 yde-3-phosphate dehydrogenase, aldolase, and aspartate aminotransferase and thus reactivates these pr
79 f serum transaminases (alanine transaminase, aspartate aminotransferase) and coagulation times (proth
80 e 3 increase of alanine aminotransferase and aspartate aminotransferase) and two (13%) patients given
81 (current hematocrit, albumin, total protein, aspartate aminotransferase), and baseline demographics a
82 r injury (serum alanine aminotransferase and aspartate aminotransferase), and circulatory failure (hy
83 by IP as measured by lactate dehydrogenase, aspartate aminotransferase, and alanine aminotransferase
84 e enzyme levels (P<0.05 for creatine kinase, aspartate aminotransferase, and aldolase) and inversely
85 chemistries, including alkaline phosphatase, aspartate aminotransferase, and bilirubin, were signific
87 as MCV and hemoglobin, alkaline phosphatase, aspartate aminotransferase, and direct bilirubin concent
88 speptidase, maximum alanine aminotransferase/aspartate aminotransferase, and fibrosis stage were asso
90 increases in alanine aminotransferase and in aspartate aminotransferase, and hyponatraemia, each occu
91 and liver enzymes (alanine aminotransferase, aspartate aminotransferase, and lactate dehydrogenase) w
92 rboxylase NAD-ME, a mitochondrial isoform of aspartate aminotransferase, and photorespiratory markers
93 els of lactate dehydrogenase, bilirubin, and aspartate aminotransferase; and higher reticulocyte, whi
94 vate carboxylase, alanine, and an isoform of aspartate aminotransferase are localized in the cytosol.
95 reticulocytes, bilirubin, plasma hemoglobin, aspartate aminotransferase, arginase, and soluble adhesi
96 d predictive clinical variables and revealed aspartate aminotransferase as an important, albeit previ
97 ctivity of PLP in both GabR and a homologous aspartate aminotransferase (Asp-AT) from Escherichia col
98 nternal aldimine in alanine racemase (AlaR), aspartate aminotransferase (AspAT), and poly-L-lysine.
99 ansferases (PPA-ATs) that belong to class-Ib aspartate aminotransferases (AspAT Ibs) and catalyze the
100 ctive pulmonary disease, history of syncope, aspartate aminotransferase (AST) >600 U/L, direct biliru
101 of NASH in elderly patients included higher aspartate aminotransferase (AST) (odds ratio [OR] = 1.12
102 with both alanine aminotransferase (ALT) and aspartate aminotransferase (AST) (P < 0.0001, analysis o
103 h K8/18/Ub foci (r(2) = 0.47, P < 0.001) and aspartate aminotransferase (AST) (r(2) = 0.15, P = 0.002
104 ysophosphatidylcholines were associated with aspartate aminotransferase (AST) 14-day post-transplanta
106 ity is elevated significantly by 30% whereas aspartate aminotransferase (AST) activity remains unchan
112 ed by pure fructose) increases liver fat and aspartate aminotransferase (AST) concentrations in healt
113 eiver operating characteristics curve showed aspartate aminotransferase (AST) had highest area under
114 Liver function tests showed higher levels of aspartate aminotransferase (AST) in blood samples from p
115 minases, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) increased in all mice i
116 nal logistic regression analysis, increasing aspartate aminotransferase (AST) level (odds ratio [OR],
117 of vomiting, lower platelet count, elevated aspartate aminotransferase (AST) level, positivity in th
118 Nine studies evaluated associations between aspartate aminotransferase (AST) levels and T2D risk, wi
119 ibrosis in these patients were defined using aspartate aminotransferase (AST) levels, fibrosis-4 (FIB
120 the lower alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels, less liver dama
121 fibrosis score determined by FibroSURE with aspartate aminotransferase (AST) measurements and HIV co
122 ith INH had asymptomatic, mild elevations of aspartate aminotransferase (AST) or alanine aminotransfe
123 ension with grade 3 rash and fevers, grade 4 aspartate aminotransferase (AST) or alanine aminotransfe
125 163-HCV-FS was significantly superior to the aspartate aminotransferase (AST) to platelet ratio index
127 nd plasma alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were increased in wildt
129 induced Liver Damage (MALD) uses a patient's aspartate aminotransferase (AST), alanine aminotransfera
130 injury was assessed by the levels of plasma aspartate aminotransferase (AST), alanine aminotransfera
131 ated measurements (mean, 17.5 days apart) of aspartate aminotransferase (AST), alanine aminotransfera
133 um levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (
134 ses in serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (
135 e (GGT), alanine aminotransferase (ALT), and aspartate aminotransferase (AST), among a discovery set
136 d nephropathy with alanine aminotransferase, aspartate aminotransferase (AST), and bilirubin levels <
137 sts, such as alanine aminotransferase (ALT), aspartate aminotransferase (AST), and gamma-glutamyltran
141 ate dehydrogenase, alanine aminotransferase, aspartate aminotransferase (AST), gamma-glutamyltransfer
142 s, increased alanine aminotransferase (ALT), aspartate aminotransferase (AST), nonsterified fatty aci
143 iabetes, hypertension, hypertriglyceridemia, aspartate aminotransferase (AST), platelets, and the hom
145 We evaluated the diagnostic accuracy of aspartate aminotransferase (AST)-to-platelet ratio index
146 less severe steatosis on biopsy, lower serum aspartate aminotransferase (AST)/alanine aminotransferas
147 gression identified mean corpuscular volume, aspartate aminotransferase (AST)/alanine aminotransferas
148 sex, high levels of TBL, and a high ratio of aspartate aminotransferase (AST):ALT were independent ri
149 aminotransferase (42 versus 27, P = 0.005), aspartate aminotransferase (AST; 26 versus 21, P = 0.01)
150 etween both eprotirome groups and placebo in aspartate aminotransferase (AST; p<0.0001), alanine amin
151 ng semiannual follow-up with LFTs, including aspartate-aminotransferase (AST), alanine aminotransfera
153 es (e.g., alanine aminotransferase [ALT] and aspartate aminotransferase [AST]) were compared between
154 ver enzymes (alanine aminotransferase [ALT], aspartate aminotransferase [AST], gamma-glutamyl transpe
157 antly superior to biochemical markers (e.g., aspartate aminotransferase [AST]/platelet ratio, FIB-4,
158 atelet ratio (APRI) was calculated as = 100*(aspartate aminotransferase [AST]/upper limit of AST)/pla
159 te aminotransferase-to-platelet ratio index (aspartate aminotransferase [AST]: platelet index), AST:a
160 ver function (alkaline phosphatase, ALP, and aspartate aminotransferase, AST) and total serum protein
161 FT abnormality was defined as an increase in aspartate aminotransferase, (AST), alanine aminotransfer
162 (SD) decreases for alanine transaminase and aspartate aminotransferase at week 12 compared to the ba
163 l, the G allele was associated directly with aspartate aminotransferase (beta = 2.60; 95% CI: 0.99, 4
165 ificantly higher in group 2, conversely mean aspartate aminotransferase, cholinesterases, and prothro
166 aminotransferase and a 3.5-fold reduction in aspartate aminotransferase) compared with WT littermates
167 progression (18 [6%] vs 11 [4%]), increased aspartate aminotransferase concentration (15 [5%] vs 23
168 ration (24 [21%] vs one [1%]), and increased aspartate aminotransferase concentration (16 [14%] vs on
169 [19%] vs one [1%]) and increased alanine or aspartate aminotransferase concentration (39 [10%] vs no
170 in serum triglycerides (eight patients) and aspartate aminotransferase concentrations (two patients)
172 weight, height, alanine aminotransferase or aspartate aminotransferase concentrations, or alcohol us
173 lel biochemical pathways, namely alanine and aspartate aminotransferases, could not compensate for th
175 ate that levels of alanine aminotransferase, aspartate aminotransferase, creatinine, lactate, tumor n
176 y decreased serum levels of both alanine and aspartate aminotransferases, decreased hepatic necrosis,
177 cificity of three aminotransferases (E. coli aspartate aminotransferase, E. coli branched-chain amino
178 the apo form of homodimeric Escherichia coli aspartate aminotransferase (eAATase) (molecular mass = 4
179 ed unfolding pathway of the Escherichia coli aspartate aminotransferase (eAATase) homodimer proceeds
180 ons in the stability of the Escherichia coli aspartate aminotransferase (eAATase) homodimer was inves
183 ded neutropenia, thrombocytopenia, increased aspartate aminotransferase, febrile neutropenia, and tum
184 re of NtdA shows that NtdA shares the common aspartate aminotransferase fold (Type 1) with residues f
187 aline phosphatase; alanine aminotransferase; aspartate aminotransferase; gamma-glutamyltransferase; a
188 can be confounded in the setting of abnormal aspartate aminotransferase, gammaglutamyl transpeptidase
191 t of a signal transduction pathway involving aspartate aminotransferase, Gln synthetase, and Asn synt
192 linked to the tricarboxylic acid cycle (eg, aspartate aminotransferase [Got2] and hydroxyacid-oxoaci
193 r Hy's criteria (alanine aminotransferase or aspartate aminotransferase greater than three times the
194 utive elevations of alanine aminotransferase/aspartate aminotransferase > or =3 times upper limit of
195 A vasopressor requirement (4 points), aspartate aminotransferase > or =80 IU/l (2 points), bil
196 nd/or levels of alanine aminotransferase and aspartate aminotransferase >30 mU/L, using magnetic reso
198 Seventy-two hrs after reperfusion, plasma aspartate aminotransferase, hepatic oxidative stress, me
199 ated levels of lactate dehydrogenase in 82%, aspartate aminotransferase in 70%, alanine aminotransfer
200 e in two patients at 20 mg/kg, and increased aspartate aminotransferase in one patient at 1 mg/kg, an
203 otransferase in two (8%) patients, increased aspartate aminotransferase in two (8%) patients, decreas
206 increase (five [14%]), pyrexia (four [11%]), aspartate aminotransferase increase (three [8%]), and ej
207 reated patients, with pneumonitis, increased aspartate aminotransferase, increased alanine aminotrans
208 dysfunction), alanine aminotransferase, and aspartate aminotransferase (indicators of liver injury)
210 ex, elevated serum alanine aminotransferase, aspartate aminotransferase, iron, transferrin-iron satur
211 roducible rise in liver enzymes (alanine and aspartate aminotransferases) is observed in 1 to 3% of p
213 TA) was cocrystallized with Escherichia coli aspartate aminotransferase (l-AspAT) at a series of pH v
215 liver enzymes (alanine aminotransferase and aspartate aminotransferase), lactate, albumin, and tumor
216 enzymes (i.e., alanine aminotransferase and aspartate aminotransferase), lactate, creatinine, proinf
218 ants, primarily those with a higher ratio of aspartate aminotransferase level to platelet count.
219 hrombocytopenia (70 [14%] of 490), increased aspartate aminotransferase levels (22 [5%]), and anaemia
220 inotransferase levels as it decreased plasma aspartate aminotransferase levels (by 40% vs. 21%, P=0.0
221 s also showed a significant correlation with aspartate aminotransferase levels (rs = 0.35; P = 0.02).
222 demonstrated by decreased serum alanine and aspartate aminotransferase levels and numbers of TUNEL-p
223 eight and serum alanine aminotransferase and aspartate aminotransferase levels at week 24 (P < 0.05).
227 mice with recombinant IL-22 decreased serum aspartate aminotransferase levels, ameliorated cardinal
228 y reduced serum alanine aminotransferase and aspartate aminotransferase levels, and by H&E staining.
229 A levels, serum alanine aminotransferase and aspartate aminotransferase levels, and hepatic inflammat
230 independently associated with HBV DNA load, aspartate aminotransferase levels, and platelet counts;
231 inotransferase levels, four (33%) had raised aspartate aminotransferase levels, and two (17%) had inc
232 se rates, serum alanine aminotransferase and aspartate aminotransferase levels, or longitudinal chang
238 increases (40% alanine aminotransferase, 17% aspartate aminotransferase), maculopapular rash (17%), a
239 rane fatty acid transporter as mitochondrial aspartate aminotransferase (mAsp-AT) indicated that the
241 creatine phosphokinase (n=2), and increased aspartate aminotransferase (n=2) each occurring in more
242 commonly reversible increases in alanine or aspartate aminotransferase) occurred in six (3%), two (1
243 nine aminotransferase of 63.9%, P<0.005; and aspartate aminotransferase of 45.0%, P<0.005) and increa
245 e round of DNA back-shuffling with wild-type aspartate aminotransferase on this variant generated mut
246 placebo 18.2%; p = 0.355) or adverse events (aspartate aminotransferase or alanine aminotransferase >
247 xclusion criteria were other liver diseases, aspartate aminotransferase or alanine aminotransferase c
248 grade 3-4 increases in levels of alanine or aspartate aminotransferases or bilirubin; there were no
249 ed concentrations of asymptomatic alanine or aspartate aminotransferase, or gamma-glutamyltransferase
250 h markers of hepatic inflammation (P=.02 for aspartate aminotransferase, P=.002 for ferritin) and fib
251 sis, the platelet count, age-platelet index, aspartate aminotransferase-platelet ratio index (APRI),
253 luronic acid measurement but superior to the aspartate aminotransferase/platelet ratio index, FIB-4 s
254 or 2 of the following: NAFLD fibrosis score, aspartate aminotransferase/platelet ratio index, FIB-4 s
255 3) and 20.9 (95% CI: 2.6-165.3) based on the aspartate aminotransferase/platelet ratio index; and 6.2
257 na that control the electronic modulation in aspartate aminotransferase.Pyridoxal 5'-phosphate (PLP)
258 imit the availability of oxaloacetate to the aspartate aminotransferase reaction, an important route
259 /- 77 U/L in the placebo group; P = .02) and aspartate aminotransferase (reduction, 31 +/- 52 vs 4 +/
260 Moreover, cellular injury demonstrated by aspartate aminotransferase release and cell death is les
262 nd AAT2 encoding mitochondrial and cytosolic aspartate aminotransferases, respectively; (iii) MDH1 an
263 erapy, based on alanine aminotransferase and aspartate aminotransferase response criteria, and more l
264 ic activity was associated with higher serum aspartate aminotransferase, rs12979860 IL28B genotype, a
265 (affecting >/=2% of patients) were elevated aspartate aminotransferase (six [2%] vs none), dyspnoea
268 old types of pyridoxal phosphate enzymes: an aspartate aminotransferase subgroup 1beta in tested alph
269 osphate (PLP) dependent enzymes known as the aspartate aminotransferase superfamily or alpha-family.
274 ethnicity, sex, alcohol, cirrhosis, ratio of aspartate aminotransferase to alanine aminotransferase,
275 h the inactive K258A mutant of PLP-dependent aspartate aminotransferase to give a stable external ald
276 of 3-year liver stiffness measurement (LSM), aspartate aminotransferase to platelet ratio index (APRI
277 mined by the NAFLD fibrosis score (NFS), the aspartate aminotransferase to platelet ratio index (APRI
278 f liver disease, fibrosis-4 (FIB-4), and the aspartate aminotransferase to platelet ratio index (APRI
279 luated the utility of two simple biomarkers, aspartate aminotransferase to platelet ratio index (APRI
280 level >/=3 times the upper limit of normal, aspartate aminotransferase to platelet ratio index score
281 kin 28B genotype, negatively associated with aspartate aminotransferase-to platelet ratio index, and
282 OMA-IR) and liver fibrosis defined using the aspartate aminotransferase-to-platelet ratio index (APRI
284 m (BA), which cross-check FibroTest with the aspartate aminotransferase-to-platelet ratio index (APRI
286 ld vs. nonmild), defining mild disease as an aspartate aminotransferase-to-platelet ratio index (APRI
287 tic resonance imaging and MRE, FIBROSpectII, aspartate aminotransferase-to-platelet ratio index (aspa
288 ore than or equal to stage 1 groups, whereas aspartate aminotransferase-to-platelet ratio index and A
289 , liver function test, complete blood count, aspartate aminotransferase-to-platelet ratio index and t
290 edictive values of blood markers [FibroSURE, aspartate aminotransferase-to-platelet-ratio index (APRI
296 lar injury markers lactate dehydrogenase and aspartate aminotransferase were persistently low (lactat
298 d both the elevation in plasma IFN-gamma and aspartate aminotransferase, whereas depletion of CD8(+)
299 igher levels of alanine aminotransferase and aspartate aminotransferase, whereas the diagnosis of SH
300 cture of a homodimeric PLP-dependent enzyme, aspartate aminotransferase, which was reacted in situ wi
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