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1 ties (grade 3 diarrhoea and grade 3 elevated aspartate aminotransferase).
2 us co factor for diverse enzymes, among them aspartate aminotransferase.
3 eased 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 serum levels of alanine aminotransferase and aspartate aminotransferase.
7 hydrogenase < 100 U/L, below analyzer range; aspartate aminotransferase 0 hour, 15.6 +/- 9.3 U/L vs 7
8 the role of endogenous sulfur dioxide (SO2)/ aspartate aminotransferase 1 (AAT1) pathway in stretch-i
9 573 patients vs six [1%] of 570), increased aspartate aminotransferase (103 [18%] vs 16 [3%]), hyper
10 %] among 68 who received placebo), increased aspartate aminotransferase (11 [8%] vs two [3%]), anaemi
12 dL), alanine aminotransferase (2288.82 U/L), aspartate aminotransferase (1251.76 U/L), gamma-glutamyl
14 quent grade 3-4 adverse events were elevated aspartate aminotransferase (14 of 44, 32%), elevated gam
15 enzymes (alanine aminotransferase, 657 U/L, aspartate aminotransferase, 1401 U/L), blood urea (53 mg
16 lanine aminotransferase compared to group B (aspartate aminotransferase, 168[166] vs. 57[67] IU/L; P=
17 vs six [0.9%]), and reversible increases in aspartate aminotransferase (22 [3.4%] vs three [0.5%]).
18 sterol, 42.80 mg/dL (39.84-45.76 mg/dL); for aspartate aminotransferase, 22.67 U/L (19.94-25.41 U/L);
19 s of hypertension (35% vs. 15%) and elevated aspartate aminotransferase (23% vs. 8%) were higher with
22 ed with -7.29 (-9.5, -5.1) IU/L; P < 0.001], aspartate aminotransferase [-31.33 (-32.1, -30.5) compar
23 group, SG induced significant improvement in aspartate aminotransferase (32.4 +/- 17.4 vs 21.5 +/- 6.
24 in alanine aminotransferase (7 [11.3%] SAD), aspartate aminotransferase (4 [6.5%] SAD), and creatinin
26 288 patients vs four [3%] of 140), elevated aspartate aminotransferase (51 [18%] vs four [3%]), hype
27 nine aminotransferase (ALT) (-67% and -60%), aspartate aminotransferase (-57% and -52%), and fibrogen
28 levels of alanine aminotransferase (64%) and aspartate aminotransferase (60%), hypoalbuminemia (55%),
30 mia (86 [34%]), fatigue (83 [33%]), elevated aspartate aminotransferase (65 [26%]), and increased ala
32 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 of serum liver tests (alkaline phosphatase, aspartate aminotransferase, alanine aminotransferase) an
41 (international normalized ratio, bilirubin, aspartate aminotransferase, alanine aminotransferase) an
42 of hepatocyte injury and cholestasis (serum aspartate aminotransferase, alanine aminotransferase, bi
43 ic diagnoses and laboratory values (albumin, aspartate aminotransferase, alanine aminotransferase, cr
44 easily available perfusate parameters (PP) (aspartate aminotransferase, alanine aminotransferase, la
45 o routine markers of liver impairment (e.g., aspartate aminotransferase, alanine aminotransferase, la
47 occur in previous studies showing increased aspartate aminotransferase-alanine aminotransferase rati
48 is and a substantially higher AUROC than the aspartate aminotransferase-alanine aminotransferase rati
49 ients with diabetes, and those with elevated aspartate aminotransferase/alanine aminotransferase (AST
50 on age, viral genotype, initial viral load, aspartate aminotransferase/alanine aminotransferase rati
51 outcome in multivariate analyses were higher aspartate aminotransferase/alanine aminotransferase rati
52 s the elevation in alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, and ga
53 ean difference for alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, and ga
54 olesterol, whereas increasing plasma alanine/aspartate aminotransferases (ALT/AST) and hepatic trigly
55 ociated with liver-related complications; an aspartate aminotransferase/ALT ratio >1 and older age we
56 ed NASH as reflected by reductions in plasma aspartate aminotransferase and alanine aminotransferase
57 ose-limiting toxicity (one grade 3 increased aspartate aminotransferase and alanine aminotransferase
58 ing induction (20 [54%] patients), increased aspartate aminotransferase and alanine aminotransferase
59 higher mean [+/-2 standard deviation] serum aspartate aminotransferase and alanine aminotransferase
60 ma and liver triglyceride content and plasma aspartate aminotransferase and alanine aminotransferase
61 iversity displayed significantly higher mean aspartate aminotransferase and alanine aminotransferase
62 r, and skeletal muscle and had higher plasma aspartate aminotransferase and alanine aminotransferase,
63 score created from the platelet count, serum aspartate aminotransferase and alanine aminotransferase,
64 pect to sex, age, duration of disease, serum aspartate aminotransferase and alkaline phosphatase leve
66 proportion of patients alanine transaminase, aspartate aminotransferase and AlkPhos >5x upper-limit-o
67 sis, decreased platelet count, and increased aspartate aminotransferase and alpha-fetoprotein levels
68 cyte population, depleted KCs, and increased aspartate aminotransferase and creatine kinase serum enz
69 learance of several serum enzymes, including aspartate aminotransferase and creatine kinase, that are
70 ture, decreased apoptosis, and reduced serum aspartate aminotransferase and creatinine levels compare
71 tients; one patient had grade 3 increases in aspartate aminotransferase and gammaglutamyltransferase
73 preserved kidneys showed significantly lower aspartate aminotransferase and lactate dehydrogenase lev
74 bilirubin and alanine aminotransferase; POD3 aspartate aminotransferase and prothrombin time-internat
75 yde-3-phosphate dehydrogenase, aldolase, and aspartate aminotransferase and thus reactivates these pr
76 e 3 increase of alanine aminotransferase and aspartate aminotransferase) and two (13%) patients given
77 (current hematocrit, albumin, total protein, aspartate aminotransferase), and baseline demographics a
78 chemistries, including alkaline phosphatase, aspartate aminotransferase, and bilirubin, were signific
81 speptidase, maximum alanine aminotransferase/aspartate aminotransferase, and fibrosis stage were asso
82 concentrations of alanine aminotransferase, aspartate aminotransferase, and gamma-glutamyltransferas
83 increases in alanine aminotransferase and in aspartate aminotransferase, and hyponatraemia, each occu
84 rboxylase NAD-ME, a mitochondrial isoform of aspartate aminotransferase, and photorespiratory markers
85 er of kidney injury (P = 0.01), lower plasma aspartate aminotransferase, and reduced rate of troponin
86 y-4-cholesten-3-one, bile acids, alanine and aspartate aminotransferases, and neoepitope-specific N-t
87 vate carboxylase, alanine, and an isoform of aspartate aminotransferase are localized in the cytosol.
88 d predictive clinical variables and revealed aspartate aminotransferase as an important, albeit previ
89 /tissue volume (BV/TV) by micro-CT analysis; aspartate aminotransferase (ASAT) and alanine aminotrans
90 ctivity of PLP in both GabR and a homologous aspartate aminotransferase (Asp-AT) from Escherichia col
91 nternal aldimine in alanine racemase (AlaR), aspartate aminotransferase (AspAT), and poly-L-lysine.
92 ansferases (PPA-ATs) that belong to class-Ib aspartate aminotransferases (AspAT Ibs) and catalyze the
93 of NASH in elderly patients included higher aspartate aminotransferase (AST) (odds ratio [OR] = 1.12
94 with both alanine aminotransferase (ALT) and aspartate aminotransferase (AST) (P < 0.0001, analysis o
95 h K8/18/Ub foci (r(2) = 0.47, P < 0.001) and aspartate aminotransferase (AST) (r(2) = 0.15, P = 0.002
96 ysophosphatidylcholines were associated with aspartate aminotransferase (AST) 14-day post-transplanta
98 mitted COVID-19 patients had elevated plasma aspartate aminotransferase (AST) and 35% had elevated al
103 ed by pure fructose) increases liver fat and aspartate aminotransferase (AST) concentrations in healt
104 eiver operating characteristics curve showed aspartate aminotransferase (AST) had highest area under
105 of vomiting, lower platelet count, elevated aspartate aminotransferase (AST) level, positivity in th
106 d lower serum alanine aminotransferase (ALT)/aspartate aminotransferase (AST) levels and less hepatic
107 Nine studies evaluated associations between aspartate aminotransferase (AST) levels and T2D risk, wi
108 g NMP grafts showed significantly lower peak aspartate aminotransferase (AST) levels than those recei
109 ibrosis in these patients were defined using aspartate aminotransferase (AST) levels, fibrosis-4 (FIB
110 the lower alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels, less liver dama
111 fibrosis score determined by FibroSURE with aspartate aminotransferase (AST) measurements and HIV co
112 ension with grade 3 rash and fevers, grade 4 aspartate aminotransferase (AST) or alanine aminotransfe
114 163-HCV-FS was significantly superior to the aspartate aminotransferase (AST) to platelet ratio index
115 cerides, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) using a general linear
116 analysis older patient's age, abnormal serum aspartate aminotransferase (AST) value, Hepatitis C viru
118 nd plasma alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were increased in wildt
119 According to reported data, patients with aspartate aminotransferase (AST)>100 IU/L and 50 IU/L sh
121 induced Liver Damage (MALD) uses a patient's aspartate aminotransferase (AST), alanine aminotransfera
122 injury was assessed by the levels of plasma aspartate aminotransferase (AST), alanine aminotransfera
124 hepatotoxicity with improved blood levels of aspartate aminotransferase (AST), alanine transaminase (
125 um levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (
126 ses in serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (
127 ood glucose, alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase,
128 e (GGT), alanine aminotransferase (ALT), and aspartate aminotransferase (AST), among a discovery set
129 d nephropathy with alanine aminotransferase, aspartate aminotransferase (AST), and bilirubin levels <
130 nd change in alanine aminotransferase (ALT), aspartate aminotransferase (AST), and gamma-glutamyl tra
133 ate dehydrogenase, alanine aminotransferase, aspartate aminotransferase (AST), gamma-glutamyltransfer
134 od levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), glucose, total cholest
135 the upper limit of normal (ULN), platelets, aspartate aminotransferase (AST), hemoglobin, sodium, pa
136 tal protein, alanine aminotransferase (ALT), aspartate aminotransferase (AST), lactate dehydrogenase
137 ved testing for the total enzyme activity of aspartate aminotransferase (AST), lactate dehydrogenase
138 iabetes, hypertension, hypertriglyceridemia, aspartate aminotransferase (AST), platelets, and the hom
139 lular carcinoma (HCC) and the performance of aspartate aminotransferase (AST)-platelet ratio index (A
141 We evaluated the diagnostic accuracy of aspartate aminotransferase (AST)-to-platelet ratio index
142 less severe steatosis on biopsy, lower serum aspartate aminotransferase (AST)/alanine aminotransferas
143 sex, high levels of TBL, and a high ratio of aspartate aminotransferase (AST):ALT were independent ri
144 aminotransferase (42 versus 27, P = 0.005), aspartate aminotransferase (AST; 26 versus 21, P = 0.01)
145 etween both eprotirome groups and placebo in aspartate aminotransferase (AST; p<0.0001), alanine amin
146 ng semiannual follow-up with LFTs, including aspartate-aminotransferase (AST), alanine aminotransfera
148 fined by changes in liver aminotransferases (aspartate aminotransferase [AST] and alanine aminotransf
149 es (e.g., alanine aminotransferase [ALT] and aspartate aminotransferase [AST]) were compared between
151 ver enzymes (alanine aminotransferase [ALT], aspartate aminotransferase [AST], gamma-glutamyl transpe
154 antly superior to biochemical markers (e.g., aspartate aminotransferase [AST]/platelet ratio, FIB-4,
155 atelet ratio (APRI) was calculated as = 100*(aspartate aminotransferase [AST]/upper limit of AST)/pla
156 te aminotransferase-to-platelet ratio index (aspartate aminotransferase [AST]: platelet index), AST:a
157 ver function (alkaline phosphatase, ALP, and aspartate aminotransferase, AST) and total serum protein
158 FT abnormality was defined as an increase in aspartate aminotransferase, (AST), alanine aminotransfer
159 (SD) decreases for alanine transaminase and aspartate aminotransferase at week 12 compared to the ba
160 l, the G allele was associated directly with aspartate aminotransferase (beta = 2.60; 95% CI: 0.99, 4
161 sfunction, supported by elevations in plasma aspartate aminotransferase, blood urea nitrogen, and cre
164 ificantly higher in group 2, conversely mean aspartate aminotransferase, cholinesterases, and prothro
165 progression (18 [6%] vs 11 [4%]), increased aspartate aminotransferase concentration (15 [5%] vs 23
166 ration (24 [21%] vs one [1%]), and increased aspartate aminotransferase concentration (16 [14%] vs on
167 [19%] vs one [1%]) and increased alanine or aspartate aminotransferase concentration (39 [10%] vs no
168 oncentrations (two [7%] patients), increased aspartate aminotransferase concentration (two [7%] patie
169 ase concentrations (74 [46%]), and increased aspartate aminotransferase concentrations (65 [41%]).
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
174 y decreased serum levels of both alanine and aspartate aminotransferases, decreased hepatic necrosis,
175 cificity of three aminotransferases (E. coli aspartate aminotransferase, E. coli branched-chain amino
177 ded neutropenia, thrombocytopenia, increased aspartate aminotransferase, febrile neutropenia, and tum
178 re of NtdA shows that NtdA shares the common aspartate aminotransferase fold (Type 1) with residues f
181 eductions in serum alanine aminotransferase, aspartate aminotransferase, gamma-glutamyl transferase,
182 aline phosphatase; alanine aminotransferase; aspartate aminotransferase; gamma-glutamyltransferase; a
183 can be confounded in the setting of abnormal aspartate aminotransferase, gammaglutamyl transpeptidase
186 linked to the tricarboxylic acid cycle (eg, aspartate aminotransferase [Got2] and hydroxyacid-oxoaci
188 r Hy's criteria (alanine aminotransferase or aspartate aminotransferase greater than three times the
189 nd/or levels of alanine aminotransferase and aspartate aminotransferase >30 mU/L, using magnetic reso
191 Seventy-two hrs after reperfusion, plasma aspartate aminotransferase, hepatic oxidative stress, me
192 ated levels of lactate dehydrogenase in 82%, aspartate aminotransferase in 70%, alanine aminotransfer
193 e in two patients at 20 mg/kg, and increased aspartate aminotransferase in one patient at 1 mg/kg, an
195 eased levels of alanine aminotransferase and aspartate aminotransferase in the plasma, indicating les
196 otransferase in two (8%) patients, increased aspartate aminotransferase in two (8%) patients, decreas
199 Hair colour changes (67%), fatigue (54%), aspartate aminotransferase increase (39%), nausea (38%),
200 increase (five [14%]), pyrexia (four [11%]), aspartate aminotransferase increase (three [8%]), and ej
201 Ewing sarcoma, three [7%] for osteosarcoma), aspartate aminotransferase increase (two [4%] for Ewing
202 reated patients, with pneumonitis, increased aspartate aminotransferase, increased alanine aminotrans
204 ex, elevated serum alanine aminotransferase, aspartate aminotransferase, iron, transferrin-iron satur
207 nternational normalized ratio <= 1, baseline aspartate aminotransferase level <= 49 U/L, and a decrea
208 e aminotransferase level (in 11%), increased aspartate aminotransferase level (in 9%), hyponatremia (
209 range, 39-99 U/L [0.65-1.65 ukat/L]), and an aspartate aminotransferase level of 88 U/L (1.47 ukat/L)
210 (normal range, 0-29 U/L [0-0.48 ukat/L]), an aspartate aminotransferase level of 98 U/L (1.6 ukat/L)
211 (normal range, 0-29 U/L [0-0.48 ukat/L]), an aspartate aminotransferase level of 98 U/L (1.6 ukat/L)
212 ants, primarily those with a higher ratio of aspartate aminotransferase level to platelet count.
213 hrombocytopenia (70 [14%] of 490), increased aspartate aminotransferase levels (22 [5%]), and anaemia
214 demonstrated by decreased serum alanine and aspartate aminotransferase levels and numbers of TUNEL-p
215 y reduced serum alanine aminotransferase and aspartate aminotransferase levels as well as proinflamma
216 eight and serum alanine aminotransferase and aspartate aminotransferase levels at week 24 (P < 0.05).
217 e also found that plasma creatine kinase and aspartate aminotransferase levels in Acsl1(M) (-/-) mice
220 nd creatinine, alanine aminotransferase, and aspartate aminotransferase levels were within normal lim
221 mice with recombinant IL-22 decreased serum aspartate aminotransferase levels, ameliorated cardinal
222 A levels, serum alanine aminotransferase and aspartate aminotransferase levels, and hepatic inflammat
223 independently associated with HBV DNA load, aspartate aminotransferase levels, and platelet counts;
224 inotransferase levels, four (33%) had raised aspartate aminotransferase levels, and two (17%) had inc
225 se rates, serum alanine aminotransferase and aspartate aminotransferase levels, or longitudinal chang
229 increases (40% alanine aminotransferase, 17% aspartate aminotransferase), maculopapular rash (17%), a
230 rane fatty acid transporter as mitochondrial aspartate aminotransferase (mAsp-AT) indicated that the
231 creatine phosphokinase (n=2), and increased aspartate aminotransferase (n=2) each occurring in more
232 commonly reversible increases in alanine or aspartate aminotransferase) occurred in six (3%), two (1
233 nine aminotransferase of 63.9%, P<0.005; and aspartate aminotransferase of 45.0%, P<0.005) and increa
234 proaches to show that Rv3722c is the primary aspartate aminotransferase of M. tuberculosis, and media
236 e round of DNA back-shuffling with wild-type aspartate aminotransferase on this variant generated mut
237 placebo 18.2%; p = 0.355) or adverse events (aspartate aminotransferase or alanine aminotransferase >
238 xclusion criteria were other liver diseases, aspartate aminotransferase or alanine aminotransferase c
239 grade 3-4 increases in levels of alanine or aspartate aminotransferases or bilirubin; there were no
240 ncreased levels of alanine aminotransferase, aspartate aminotransferase, or gamma-glutamyl transferas
241 ed concentrations of asymptomatic alanine or aspartate aminotransferase, or gamma-glutamyltransferase
242 lu457Lys) of ALDH2, and two traits including aspartate aminotransferase (P = 5.20 x 10(-13)) and alan
243 h markers of hepatic inflammation (P=.02 for aspartate aminotransferase, P=.002 for ferritin) and fib
244 vasive indices for ruling out cirrhosis: the aspartate aminotransferase-platelet ratio index (APRI) a
245 sis, the platelet count, age-platelet index, aspartate aminotransferase-platelet ratio index (APRI),
247 luronic acid measurement but superior to the aspartate aminotransferase/platelet ratio index, FIB-4 s
248 or 2 of the following: NAFLD fibrosis score, aspartate aminotransferase/platelet ratio index, FIB-4 s
249 3) and 20.9 (95% CI: 2.6-165.3) based on the aspartate aminotransferase/platelet ratio index; and 6.2
251 na that control the electronic modulation in aspartate aminotransferase.Pyridoxal 5'-phosphate (PLP)
252 alkaline phosphatase (R = 0.543, P = 0.003), aspartate aminotransferase (R = 0.420, P = 0.029), and l
253 /- 77 U/L in the placebo group; P = .02) and aspartate aminotransferase (reduction, 31 +/- 52 vs 4 +/
254 Moreover, cellular injury demonstrated by aspartate aminotransferase release and cell death is les
256 nd AAT2 encoding mitochondrial and cytosolic aspartate aminotransferases, respectively; (iii) MDH1 an
257 erapy, based on alanine aminotransferase and aspartate aminotransferase response criteria, and more l
258 ic activity was associated with higher serum aspartate aminotransferase, rs12979860 IL28B genotype, a
259 (affecting >/=2% of patients) were elevated aspartate aminotransferase (six [2%] vs none), dyspnoea
260 , hyponatraemia (11 [6%] vs 0) and increased aspartate aminotransferase (six [3%] vs five [5%]).
263 old types of pyridoxal phosphate enzymes: an aspartate aminotransferase subgroup 1beta in tested alph
267 ethnicity, sex, alcohol, cirrhosis, ratio of aspartate aminotransferase to alanine aminotransferase,
268 h the inactive K258A mutant of PLP-dependent aspartate aminotransferase to give a stable external ald
269 luated the utility of two simple biomarkers, aspartate aminotransferase to platelet ratio index (APRI
270 culated: NASH clinical scoring system (NCS), aspartate aminotransferase to platelet ratio index (APRI
271 of 3-year liver stiffness measurement (LSM), aspartate aminotransferase to platelet ratio index (APRI
272 mined by the NAFLD fibrosis score (NFS), the aspartate aminotransferase to platelet ratio index (APRI
273 f liver disease, fibrosis-4 (FIB-4), and the aspartate aminotransferase to platelet ratio index (APRI
274 ors and the decline or increase of FIB-4 and aspartate aminotransferase to platelet ratio index (APRI
275 assessed non-invasively via the serum tests Aspartate Aminotransferase to Platelet Ratio Index and H
276 level >/=3 times the upper limit of normal, aspartate aminotransferase to platelet ratio index score
277 kin 28B genotype, negatively associated with aspartate aminotransferase-to platelet ratio index, and
279 ld vs. nonmild), defining mild disease as an aspartate aminotransferase-to-platelet ratio index (APRI
281 m (BA), which cross-check FibroTest with the aspartate aminotransferase-to-platelet ratio index (APRI
282 cohort and outperformed the Mayo Clinic and aspartate aminotransferase-to-platelet ratio index (APRI
283 OMA-IR) and liver fibrosis defined using the aspartate aminotransferase-to-platelet ratio index (APRI
284 tic resonance imaging and MRE, FIBROSpectII, aspartate aminotransferase-to-platelet ratio index (aspa
285 ore than or equal to stage 1 groups, whereas aspartate aminotransferase-to-platelet ratio index and A
286 , liver function test, complete blood count, aspartate aminotransferase-to-platelet ratio index and t
287 al cutoffs for three noninvasive biomarkers (aspartate aminotransferase-to-platelet ratio index, Fibr
288 er waist circumference, levels of alanine or aspartate aminotransferase, total and low-density lipopr
289 elevation of serum alanine aminotransferase, aspartate aminotransferase, total bilirubin and direct b
291 erase (two [<1%] of 260 patients), increased aspartate aminotransferase (two [<1%]), and nausea (two
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