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1 Ser or Thr and at the carbohydrate sites of alpha 1-acid glycoprotein.
2 ich correlated with plasma concentrations of alpha-1 acid glycoprotein.
3 high binding affinity of UCN-01 to the human alpha-1-acid glycoprotein.
4 alin-like prostaglandin D synthase (L-PGDS), alpha(1) -acid glycoprotein (AAG), transferrin (TF), cer
5 omplexity in the carbohydrate composition of alpha(1)-acid glycoprotein (AAG) makes it an ideal model
8 ned by radioimmunoassays, and transthyretin, alpha(1)-acid glycoprotein (AGP), alpha(1)-antichymotryp
9 roteins (APPs), C-reactive protein (CRP) and alpha(1)-acid glycoprotein (AGP), individually and in co
10 We examined the associations between serum alpha(1)-acid glycoprotein (AGP), serum C-reactive prote
12 primarily responsible for drug binding, the alpha(1)-acid-glycoprotein (AGP) and human serum albumin
13 ed at a micro liquid-liquid interface, using alpha(1)-acid-glycoprotein (AGP) as a chiral acute phase
14 ere was a positive correlation between serum alpha-1 acid glycoprotein (AGP) concentration and plasma
15 tive protein (CRP) concentrations >5 mg/L or alpha-1-acid glycoprotein (AGP) concentrations >1 g/L, 2
16 tive protein (CRP) concentrations >5 mg/L or alpha-1-acid glycoprotein (AGP) concentrations >1 g/L, 2
17 tive protein (CRP) concentrations >5 mg/L or alpha-1-acid glycoprotein (AGP) concentrations >1 g/L; 3
19 biomarkers such as C-reactive protein (CRP), alpha-1-acid glycoprotein (AGP), ferritin, and retinol.
21 red the relation between C-reactive protein, alpha 1 acid glycoprotein and albumin, an acute phase pr
24 garded as being random, we have found, using alpha-1-acid glycoprotein and antitrypsin as model syste
25 ntly labeled proteins, ubiquitin, myoglobin, alpha-1-acid glycoprotein and lysozyme, were incubated w
27 hydratase, glutathione-s-transferase omega, alpha-1-acid-glycoprotein, and phosphatidylethanolamine-
28 t alpha 1-acid glycoprotein, fetuin or human alpha 1-acid glycoprotein as acceptors together with the
29 enzyme measurement, alpha1-microglobulin and alpha(1)-acid glycoprotein by immunonephelometry, and se
30 (C-reactive protein concentration >5 mg/L or alpha-1-acid glycoprotein concentration >1 g/L), 2) the
31 fused with protein A, was incubated with rat alpha 1-acid glycoprotein, fetuin or human alpha 1-acid
32 ctivity with N-acetylneuramin lactose, human alpha-1-acid glycoprotein, fetuin, colominic acid, and b
33 human IgG (for core fucosylation) and human alpha-1-acid-glycoprotein (for antenna fucosylation).
34 ns, full length heparins, and N-glycans from alpha-1-acid glycoproteins from four mammalian species.
36 easured by C-reactive protein (> 5 mg/L) and alpha(1)-acid glycoprotein (> 1 g/L) before applying cut
37 ter adjusting for conventional risk factors: alpha-1-acid glycoprotein (hazard ratio [HR] 1.67 per 1-
38 lls at 25.0-50.0 nM, even in the presence of alpha(1) acid glycoprotein, human serum albumin, normal
39 ycoproteins included ribonuclease B, fetuin, alpha(1)-acid glycoprotein, immunoglobulin, and thyroglo
40 ity failed to transfer sialic acid to asialo alpha(1)-acid glycoprotein, indicating that this enzyme
41 n increase in steady-state concentrations of alpha 1-acid glycoprotein messenger RNA that peaked at 1
44 ethylpyrocarbonate (DEPC) was used to modify alpha 1-acid glycoprotein (orosomucoid, OMD) under vario
46 more, they found that C-reactive protein and alpha-1-acid glycoprotein provide important and differen
48 in-1beta, interleukin-6, corticosterone, and alpha-1 acid glycoprotein were determined in serum, and
49 the levels of cytokines, corticosterone, and alpha-1 acid glycoprotein were significantly higher in t
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