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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
11 e (15%), alanine aminotransferase (12%), and aspartate aminotransferase (11%).
12 dL), alanine aminotransferase (2288.82 U/L), aspartate aminotransferase (1251.76 U/L), gamma-glutamyl
13 %] of 573 vs one [<1%] of 570) and increased aspartate aminotransferase (14 [2%] vs one [<1%]).
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
20 ransferase (73 [30%] patients) and increased aspartate aminotransferase (25 [10%]).
21 nd elevations in alanine aminotransferase or aspartate aminotransferase (25 [12%]).
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
25 minotransferase (ALT) (-49%; P = 0.009), and aspartate aminotransferase (-42%; P = 0.019).
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%),
29              Mean postoperative day (POD) 7, aspartate aminotransferase (61.13 + 24.77 vs 73.17 + 53.
30 mia (86 [34%]), fatigue (83 [33%]), elevated aspartate aminotransferase (65 [26%]), and increased ala
31 0 IU/L alanine aminotransferase and 420 IU/L aspartate aminotransferase 9 hours after gavage.
32   Importantly, increasing peak perioperative aspartate aminotransferase, a surrogate marker of hepati
33                  Consistently, inhibition of aspartate-aminotransferase, a key enzyme of the shunt, i
34                                           In aspartate aminotransferase (AAT), an extended hydrogen b
35                                 SO2 synthase aspartate aminotransferase (AAT1 and AAT2) mRNA and prot
36 nalysis (fibrosis, alanine aminotransferase, aspartate aminotransferase, age, biopsy length).
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
39                                              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
46                                         Mean aspartate aminotransferase, alanine aminotransferase, to
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
65                              During therapy, 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
72                                              Aspartate aminotransferase and lactate dehydrogenase as
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
79  and elevated levels of blood urea nitrogen, aspartate aminotransferase, and creatinine.
80 pids, cholesterol, alanine aminotransferase, aspartate aminotransferase, and creatinine.
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
97                                              Aspartate aminotransferase (AST) activity at LT (hazard
98 mitted COVID-19 patients had elevated plasma aspartate aminotransferase (AST) and 35% had elevated al
99                                              Aspartate aminotransferase (AST) and alanine aminotransf
100              Alanine aminotransferase (ALT), aspartate aminotransferase (AST) and fetuin-A were deter
101               They found that an increase in aspartate aminotransferase (AST) and its dynamicity corr
102                              The increase of aspartate aminotransferase (AST) by >25% (hazard ratio [
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
113       The primary endpoint was postoperative aspartate aminotransferase (AST) peak value; early graft
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
117                                       Median aspartate aminotransferase (AST) was higher than alanine
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
120                          The serum levels of aspartate aminotransferase (AST), alanine aminotransfera
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
123                               Peak values of 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
131              Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and gamma-glutamyltran
132                    Transplant albumin, day-1 aspartate aminotransferase (AST), day-1 lactate, day-3 b
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
140                                              Aspartate aminotransferase (AST)-to-platelet ratio (APRI
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
147                    Plasma aminotransferases (aspartate aminotransferase [AST] and alanine aminotransf
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
150       Clinical characteristics, liver tests (aspartate aminotransferase [AST], alanine aminotransfera
151 ver enzymes (alanine aminotransferase [ALT], aspartate aminotransferase [AST], gamma-glutamyl transpe
152        Our analysis sought to validate APRI (aspartate aminotransferase [AST]-to-platelet ratio index
153              Four variables (platelet count, aspartate aminotransferase [AST]/alanine aminotransferas
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
162                    Alanine aminotransferase, aspartate aminotransferase, BMI, insulin, Quantitative I
163 f-function mutation of the cytosolic form of aspartate aminotransferase (Caa1).
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)
171                         Elevated alanine and aspartate aminotransferase concentrations and profound e
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
176 .5%) and reversible alanine aminotransferase/aspartate aminotransferase elevations (13.4%).
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
179  aminotransferase (five [6%]), and increased aspartate aminotransferase (four [5%]).
180            In Study 2, 16 g/d increased mean aspartate aminotransferase from baseline (19 U/L; 95% CI
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
184                                    Increased aspartate aminotransferase, gammaglutamyl transpeptidase
185                                          The aspartate aminotransferase gene AAT1 was found to be a c
186  linked to the tricarboxylic acid cycle (eg, aspartate aminotransferase [Got2] and hydroxyacid-oxoaci
187  findings, O2 saturation lower than 90%, and aspartate aminotransferase greater than 40 U/L.
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 &gt;30 mU/L, using magnetic reso
190                  Histologic features, plasma aspartate aminotransferase, hepatic cytokine profile, ox
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
194                                  Median peak aspartate aminotransferase in the first 7 days was signi
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
197 apoptosis, and activity of serum alanine and aspartate aminotransferases in wild-type mice.
198 (in 12%), alkaline phosphatase (in 21%), and aspartate aminotransferase (in 27%).
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
203                                Conversion of aspartate aminotransferase into tyrosine aminotransferas
204 ex, elevated serum alanine aminotransferase, aspartate aminotransferase, iron, transferrin-iron satur
205                                GTK/KAT I and aspartate aminotransferase/KAT IV possess cysteine S-con
206                              For instance, l-aspartate aminotransferase (l-AspAT) is inactivated by 4
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
218                            Serum alanine and aspartate aminotransferase levels were reduced with vita
219                                        Serum aspartate aminotransferase levels were the only clinical
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
226  elevated serum alanine aminotransferase and aspartate aminotransferase levels.
227 ld higher serum alanine aminotransferase and aspartate aminotransferase levels.
228       The screen yielded GOT1, the cytosolic aspartate aminotransferase, loss of which kills cells up
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
235                  Minimal parenchymal damage (aspartate aminotransferase) of the liver was seen after
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),
246                                     Based on aspartate aminotransferase/platelet ratio index and FIB-
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
250                                 For example, aspartate aminotransferase protonates the pyridine nitro
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
255 oadipate aminotransferase, and mitochondrial aspartate aminotransferase, respectively.
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%]).
261  seven [7%]), and increased concentration of aspartate aminotransferase (six [3%] vs two [2%]).
262 l homology with members of the PLP-dependent aspartate aminotransferase subfamily.
263 old types of pyridoxal phosphate enzymes: an aspartate aminotransferase subgroup 1beta in tested alph
264 l fold places it into the well-characterized aspartate aminotransferase superfamily.
265 tures place them into the well-characterized aspartate aminotransferase superfamily.
266                            Grade 3 increased aspartate aminotransferase, syncope, pericardial effusio
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
278       Liver fibrosis was predicted using the aspartate aminotransferase-to-platelet ratio index (APRI
279 ld vs. nonmild), defining mild disease as an aspartate aminotransferase-to-platelet ratio index (APRI
280                                  We used the 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
290                          This consists of an aspartate aminotransferase (TvAspAT1), which transaminat
291 erase (two [<1%] of 260 patients), increased aspartate aminotransferase (two [<1%]), and nausea (two
292  [5%]) and increased concentrations of serum aspartate aminotransferase (two [10%]) in cohort B.
293 10%]), and increased concentrations of serum aspartate aminotransferase (two [10%]).
294                                              Aspartate aminotransferase was significantly higher in D
295           Serum alanine aminotransferase and aspartate aminotransferase were increased by all three c
296 lar injury markers lactate dehydrogenase and aspartate aminotransferase were persistently low (lactat
297             Serum levels of both alanine and aspartate aminotransferases were also lower after intrap
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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