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1 ion in a crystallized form of calcium-bovine prothrombin fragment 1.
2 to 0.30 ng/mL); -0.02 [corrected] nmol/L for prothrombin fragment 1 + 2 (95% CI, -0.03 to 0.01 nmol/L
3 f thrombin: thrombin-antithrombin III (TAT), prothrombin fragment 1 + 2 (F1 + 2), and fibrinopeptide
4 thrombin generation in vivo), tissue factor, prothrombin fragment 1 + 2 (F1+2), and normalized APC se
6 e plasminogen activator antigen, factor VII, prothrombin fragment 1 + 2, urinary fibrinopeptide A, C-
7 ian levels of thrombin-antithrombin complex, prothrombin fragments 1 + 2, and von Willebrand factor a
9 and future VTE have been found for d-dimer, prothrombin fragment 1+2, and soluble P-selectin and als
10 activity and antigen, activated factor XII, prothrombin fragment 1+2, fibrinopeptide A, and fibrinog
11 We analysed concentrations of prothrombin, prothrombin fragment 1+2, thrombin-antithrombin complex,
12 antly higher median plasma concentrations of prothrombin fragment 1+2, tissue plasminogen activator (
14 artial thromboplastin and prothrombin times, prothrombin fragments 1+2, fibrinogen, thrombomodulin, p
16 ecrosis factor-alpha, von Willebrand factor, prothrombin fragment 1-2, D-dimer, and plasmin antiplasm
17 extracorporeal membrane oxygenation therapy, prothrombin fragment 1.2 (F1.2) (1.36-2.4 microM), throm
18 ntithrombin III (TAT) complex formation, and prothrombin fragment 1.2 (F1.2) were measured via commer
20 reversed by prothrombin (1-3 microM) and by prothrombin fragment 1.2 (PF1.2), but not by prothrombin
24 n generation (thrombin antithrombin complex, prothrombin fragment 1.2), inflammation (C-reactive prot
25 ligand), coagulation activation/inhibition (prothrombin fragment 1.2, thrombin/antithrombin complex,
26 7.6 ng/ml to 33.2 +/- 17.4 ng/ml, p = 0.003; prothrombin fragment 1.2: 95.6 +/- 45.6 micromol/l to 24
28 significantly greater reduction in D-dimer, prothrombin fragments 1 and 2 (F1 + 2), endogenous throm
29 transient increases in levels of d-dimer and prothrombin fragments 1 and 2 were observed, which resol
30 positions in the crystal structure of bovine prothrombin fragment 1 bound with calcium ions (bf1/Ca).
32 we have evaluated three mechanisms by which prothrombin fragment 1 may inhibit factor X activation.
35 investigate the binding of the Gla domain of prothrombin fragment 1 (PT1) to anionic lipids in the pr
38 The three-dimensional structure of strontium-prothrombin fragment 1 shows that these positions are cl
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