ライフサイエンスコーパス: soybean trypsin inhibitor

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1 ty of BG-4 is 8.6 times higher than purified soybean trypsin inhibitor.

2 (2)-antiplasmin and was readily inhibited by soybean trypsin inhibitor.

3 of the epidermis of newborn rats, as well as soybean trypsin inhibitor.

4 ptase inhibitors (FUT-175 or MPI-0442352) or soybean trypsin inhibitor.

5 one (TLCK) (85.4%), benzamidine (80.2%), and soybean trypsin inhibitor (75.6%) and partially inhibite

6 Pretreating duodenase with soybean trypsin inhibitor abolished DNA synthesis, confi

7 Gabexate mesilate (acinar cell permeable) or soybean trypsin inhibitor (acinar cell nonpermeable) was

8 Feeding of soybean trypsin inhibitor and Aedes aegypti trypsin modu

9 does induce susceptibility to inhibition by soybean trypsin inhibitor and antithrombin III.

10 e soybean-derived serine protease inhibitors soybean trypsin inhibitor and Bowman-Birk inhibitor inhi

11 Soybean trypsin inhibitor and phenylmethylsulphonylflour

12 Soybean trypsin inhibitor and succinyl-L-Ala-Ala-Pro-Phe

13 This increase was abolished by soybean trypsin inhibitor and was susceptible to carboxy

14 ovine carbonic anhydrase, alpha-lactalbumin, soybean trypsin inhibitor, and ovalbumin was separated u

15 ction with proteinaceous inhibitors, such as soybean trypsin inhibitor, basic pancreatic trypsin inhi

16 Active monomers are inhibited by soybean trypsin inhibitor, bovine pancreatic trypsin inh

17 at a rate similar to the ADP-ribosylation of soybean trypsin inhibitor by ExoS.

18 larly effective at blocking the chymotrypsin-soybean trypsin inhibitor complex and that the mechanism

19 s study, we demonstrate that benzamidine and soybean trypsin inhibitor-conjugated Sepharose beads, wh

20 Soybean trypsin inhibitor exhibited a reciprocal pattern

21 similarity places the encoded protein in the soybean trypsin-inhibitor family (Kunitz).

22 tionary phases carrying long alkyl chains or soybean trypsin inhibitor have been prepared for use in

23 -linked, high-molecular-weight derivative of soybean trypsin inhibitor (hMW-SBTI) which was unable to

24 for six proteins (ovalbumin, ribonuclease A, soybean trypsin inhibitor, lysozyme, and beta-lactoglobu

25 The degrading protease is inhibited by soybean trypsin inhibitor or by low concentrations of bl

26 laminin, elastin, beta-casein, plasminogen, soybean trypsin inhibitor, or Bowman-Birk inhibitor.

27 ith Z-Pro-Prolinal or plasma kallikrein with soybean trypsin inhibitor, Pro-Phe-Arg-chloromethylketon

28 Soybean trypsin inhibitor reduced secretion to backgroun

29 efoil fold, similar to those found in Kunitz soybean trypsin inhibitors, ricin-like toxins, plant agg

30 g exoenzyme S)-dependent ADP-ribosylation of soybean trypsin inhibitor (SBTI) at 0.4% and of the Ras

31 stance to natural trypsin inhibitors such as soybean trypsin inhibitor (SBTI) or human pancreatic sec

32 Additionally, we found that when soybean trypsin inhibitor (SBTI), was added to rat heart

33 was a lower kcat in the ADP-ribosylation of soybean trypsin inhibitor (SBTI).

34 egrees C) in the presence and the absence of soybean trypsin inhibitor (SBTI; 100 units/g pretreated

35 Gabexate mesilate as well as soybean trypsin inhibitor significantly decreased TAP le

36 We also analyzed the soybean trypsin inhibitor (STI) gene family, important p

37 ide bonds affects the secondary structure of soybean trypsin inhibitor (STI).

38 Soybean trypsin inhibitor was added to serum before inje

39 Soybean trypsin inhibitor was functionalized with N-(4-p

40 Among several protease inhibitors, soybean trypsin inhibitor was one of two that inhibited

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