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1                                        Human pancreatic elastase 1 is a serine protease which maps to
2 ve been tested as inhibitors of both porcine pancreatic elastase and human leukocyte elastase.
3 le elastin following hydrolysis with porcine pancreatic elastase and human neutrophil elastase were p
4 la) and serpin-1F (P1 Val) inhibited porcine pancreatic elastase and human neutrophil elastase.
5 re perfused with saline (control) or porcine pancreatic elastase and studied on postperfusion days 1,
6 in ANS fluorescence on cleavage with porcine pancreatic elastase and thrombin, respectively.
7 ibroblast cultures were treated with porcine pancreatic elastase, and elastase-mediated changes in bF
8 inant TgPI-1 inhibits trypsin, chymotrypsin, pancreatic elastase, and neutrophil elastase.
9                 Strikingly, chymotrypsin and pancreatic elastase are negatively correlated (-0.10).
10  (uPA)-type plasminogen activators and human pancreatic elastase at pH 5.5-8.5.
11 d a broad range of proteases (neutrophil and pancreatic elastases, cathepsin G, subtilisin, and tryps
12 st other serine proteases, including porcine pancreatic elastase, chymotrypsin, and trypsin, was also
13 anin in combination with trypsin- or porcine pancreatic elastase-cleaved Fe-transferrin.
14 se-3, an elastase-like protease, and porcine pancreatic elastase demonstrated rapid inhibition rate c
15 -selected sequences as inhibitors of porcine pancreatic elastase demonstrates a significant differenc
16 es with human leukocyte elastase and porcine pancreatic elastase have been investigated.
17                                          The pancreatic elastase I gene (ELA1) is selectively transcr
18 ement of the transcriptional enhancer of the pancreatic elastase I gene (ELA1).
19                                    The human pancreatic elastase I gene is transcriptionally silent,
20 ancreatic trypsin, chymotrypsin, and porcine pancreatic elastase in varying measures.
21 he application of the MSCS method to porcine pancreatic elastase is discussed, and comparison of the
22 hymotrypsin A alpha (Tyr, Pro, Trp), porcine pancreatic elastase (Leu/Ala, Arg, Ala), subtilisin Carl
23 ibitor of the serine proteases chymotrypsin, pancreatic elastase, neutrophil elastase, and trypsin.
24 but pPG3 was relatively resistant to porcine pancreatic elastase or human neutrophil cathepsin G.
25  Sprague-Dawley rats to intra-aortic porcine pancreatic elastase (PPE) (12 U/mL), AAA rupture was ind
26 (rShPI-1/K13L) exhibits a novel anti-porcine pancreatic elastase (PPE) activity together with a signi
27 nalysis of the complex between 1 and porcine pancreatic elastase (PPE) and subsequently the complex b
28 form an inhibitory complex with both porcine pancreatic elastase (PPE) and trypsin.
29    We previously showed that inhaled porcine pancreatic elastase (PPE) causes bronchoconstriction in
30      Treatment of hamster lungs with porcine pancreatic elastase (PPE) causes emphysema and a decreas
31  human neutrophil elastase (HNE) and porcine pancreatic elastase (PPE) complexed to peptidic ligands,
32 rine models of experimental AAA: the porcine pancreatic elastase (PPE) infusion model in C57BL/6 mice
33 se inhibitor, to the serine protease porcine pancreatic elastase (PPE) using isothermal titration cal
34 owing cleavage at the P1-P1' bond by porcine pancreatic elastase (PPE), as shown by the spontaneous f
35                                      Porcine pancreatic elastase (PPE), which binds to and digests el
36 proteinase inhibitor (alpha1PI) with porcine pancreatic elastase (PPE), which differs from the only o
37 ated beta-casomorphin-7 peptides and porcine pancreatic elastase (PPE).
38     Moreover, commercially available porcine pancreatic elastase preparations also activated Stx2d cy
39 ncreatic acinar cells by using a full-length pancreatic elastase promoter-driven Cre.
40    Cleavage of the two proteins with porcine pancreatic elastase results in a 1.6- and 2.6-fold incre
41 trum inhibitor of trypsin, chymotrypsin, and pancreatic elastase that has previously been isolated fr
42 tion of elastin by human leukocyte elastase, pancreatic elastase, thermolysin, and Pseudomonas elasta
43                                              Pancreatic elastase was found to induce edema and enhanc
44                                      Porcine pancreatic elastase was used as a model enzyme with two
45                                      Porcine pancreatic elastase was used to recruit monocytes to the
46 solvent crystal structures (MSCS) of porcine pancreatic elastase were used to map the binding surface

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