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1 e cytokines IL-1beta and IL-13 or by porcine pancreatic elastase.
2                                        Human pancreatic elastase 1 is a serine protease which maps to
3 ficantly amplified after exposure to porcine pancreatic elastase, an emphysema model, and to oxidativ
4 ve been tested as inhibitors of both porcine pancreatic elastase and human leukocyte elastase.
5 le elastin following hydrolysis with porcine pancreatic elastase and human neutrophil elastase were p
6 la) and serpin-1F (P1 Val) inhibited porcine pancreatic elastase and human neutrophil elastase.
7 derwent surgical AAA formation using porcine pancreatic elastase and received daily beta-aminopropion
8 re perfused with saline (control) or porcine pancreatic elastase and studied on postperfusion days 1,
9 in ANS fluorescence on cleavage with porcine pancreatic elastase and thrombin, respectively.
10 ibroblast cultures were treated with porcine pancreatic elastase, and elastase-mediated changes in bF
11 inant TgPI-1 inhibits trypsin, chymotrypsin, pancreatic elastase, and neutrophil elastase.
12                 Strikingly, chymotrypsin and pancreatic elastase are negatively correlated (-0.10).
13  (uPA)-type plasminogen activators and human pancreatic elastase at pH 5.5-8.5.
14                       We also measured fecal pancreatic elastase by enzyme-linked immunosorbent assay
15 d a broad range of proteases (neutrophil and pancreatic elastases, cathepsin G, subtilisin, and tryps
16 -function mutations in the gene encoding the pancreatic elastase chymotrypsin-like elastase family me
17 st other serine proteases, including porcine pancreatic elastase, chymotrypsin, and trypsin, was also
18 anin in combination with trypsin- or porcine pancreatic elastase-cleaved Fe-transferrin.
19 se-3, an elastase-like protease, and porcine pancreatic elastase demonstrated rapid inhibition rate c
20 -selected sequences as inhibitors of porcine pancreatic elastase demonstrates a significant differenc
21                                      Porcine pancreatic elastase (ELANE homolog) resists tumor-derive
22 es with human leukocyte elastase and porcine pancreatic elastase have been investigated.
23                                          The pancreatic elastase I gene (ELA1) is selectively transcr
24 ement of the transcriptional enhancer of the pancreatic elastase I gene (ELA1).
25                                    The human pancreatic elastase I gene is transcriptionally silent,
26 eficient (Ldlr(-/-)) mice or topical porcine pancreatic elastase in C57BL/6J mice.
27 ancreatic trypsin, chymotrypsin, and porcine pancreatic elastase in varying measures.
28  the role of Olfr2 in AAA using PPE (porcine pancreatic elastase) infusion in Olfr2-deficient (Olfr2(
29 he application of the MSCS method to porcine pancreatic elastase is discussed, and comparison of the
30 hymotrypsin A alpha (Tyr, Pro, Trp), porcine pancreatic elastase (Leu/Ala, Arg, Ala), subtilisin Carl
31                               Differences in pancreatic elastase levels associated with significantly
32                         The tracheal porcine pancreatic elastase model (PPE) produces severe injury,
33 ibitor of the serine proteases chymotrypsin, pancreatic elastase, neutrophil elastase, and trypsin.
34 but pPG3 was relatively resistant to porcine pancreatic elastase or human neutrophil cathepsin G.
35  Sprague-Dawley rats to intra-aortic porcine pancreatic elastase (PPE) (12 U/mL), AAA rupture was ind
36 (rShPI-1/K13L) exhibits a novel anti-porcine pancreatic elastase (PPE) activity together with a signi
37 nalysis of the complex between 1 and porcine pancreatic elastase (PPE) and subsequently the complex b
38 form an inhibitory complex with both porcine pancreatic elastase (PPE) and trypsin.
39    We previously showed that inhaled porcine pancreatic elastase (PPE) causes bronchoconstriction in
40      Treatment of hamster lungs with porcine pancreatic elastase (PPE) causes emphysema and a decreas
41  human neutrophil elastase (HNE) and porcine pancreatic elastase (PPE) complexed to peptidic ligands,
42 rine models of experimental AAA: the porcine pancreatic elastase (PPE) infusion model in C57BL/6 mice
43 se inhibitor, to the serine protease porcine pancreatic elastase (PPE) using isothermal titration cal
44 owing cleavage at the P1-P1' bond by porcine pancreatic elastase (PPE), as shown by the spontaneous f
45                                      Porcine pancreatic elastase (PPE), which binds to and digests el
46 proteinase inhibitor (alpha1PI) with porcine pancreatic elastase (PPE), which differs from the only o
47 ated beta-casomorphin-7 peptides and porcine pancreatic elastase (PPE).
48     Moreover, commercially available porcine pancreatic elastase preparations also activated Stx2d cy
49 ncreatic acinar cells by using a full-length pancreatic elastase promoter-driven Cre.
50    Cleavage of the two proteins with porcine pancreatic elastase results in a 1.6- and 2.6-fold incre
51 trum inhibitor of trypsin, chymotrypsin, and pancreatic elastase that has previously been isolated fr
52 tion of elastin by human leukocyte elastase, pancreatic elastase, thermolysin, and Pseudomonas elasta
53 frarenal, intraluminal aorta to PPE (porcine pancreatic elastase) under pressure to induce aneurysmal
54                                              Pancreatic elastase was found to induce edema and enhanc
55                                      Porcine pancreatic elastase was used as a model enzyme with two
56                                      Porcine pancreatic elastase was used to recruit monocytes to the
57 solvent crystal structures (MSCS) of porcine pancreatic elastase were used to map the binding surface