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1 lar adhesion molecule-1 [sICAM-1], and human leukocyte elastase).
2 ch is to regulate the activity of neutrophil/leukocyte elastase.
3 f both porcine pancreatic elastase and human leukocyte elastase.
4 the primary physiological inhibitor of human leukocyte elastase.
5 nt serine proteases: beta-tryptase and human leukocyte elastase.
6                                    Increased leukocyte elastase activity in mice lacking secretory le
7  parotid saliva on exogenously applied human leukocyte elastase, allowing for the elastase-mediated d
8  two cytokine activities can be generated by leukocyte elastase, an extracellular protease.
9 for a member of the serpin superfamily and a leukocyte elastase and crosstalk between neurons and T c
10 physiologically important inhibitor of human leukocyte elastase and is able to inhibit elastase-media
11  glycoprotein, sensitivity against the human leukocyte elastase and microcolony formation.
12 ractions of three BPTI homologues with human leukocyte elastase and porcine pancreatic elastase have
13                  A leukocyte origin of human leukocyte elastase and proteinase-3 in diabetic ketoacid
14 -dimer, tissue plasminogen activator (t-PA), leukocyte elastase, and lipoprotein(a) (all P<0.01), as
15                               However, human leukocyte elastase, arriving in gingival exudates from i
16             For alpha-chymotrypsin and human leukocyte elastase, both interacting with turkey ovomuco
17     For instance, inflammatory cytokines and leukocyte elastase can downregulate natural anticoagulan
18 y efficient irreversible inhibitors of human leukocyte elastase, cathepsin G, and proteinase 3.
19 minus) and subfragments thereof, obtained by leukocyte elastase digestion.
20 rophil elastase (EC 3.4.21.37, also known as leukocyte elastase, elastase 2 and medullasin), a serine
21  which identified potent inhibitors of human leukocyte elastase from screening a combinatorial peptid
22                                        Human leukocyte elastase (HLE) and cathepsin G (CG) are expres
23 ocytic, killed bacteria, and expressed human leukocyte elastase (HLE) in a granule-like compartment (
24                                        Human leukocyte elastase (HLE) interacts with HIV-1 glycoprote
25 nalities that are potent inhibitors of human leukocyte elastase (HLE).
26 chymotrypsin and is comparable only to human leukocyte elastase, hornet chymotrypsin and fiddler crab
27 s, Pro, Leu) and B (Cys, Pro, Lys) and human leukocyte elastase (Ile, Asp, Ile).
28 rHME is approximately 30% as active as human leukocyte elastase in solubilizing elastin.
29 ologic concentrations of extracellular human leukocyte elastase inhibitors (32.8 microM), the radii o
30  proteins related to inflammation processes (leukocyte elastase inhibitors) in the cecum tissues of a
31 ike enzymes, including pancreatic proteases, leukocyte elastase, key enzymes of blood coagulation, th
32 trate the DRG after nerve injury and release leukocyte elastase (LE), which was inhibited by SerpinA3
33                                              Leukocyte elastase, likely via cleavage of E-cadherin, w
34 tion Scoring System; epithelial lining fluid leukocytes; elastase; myeloperoxidase; xanthine oxidase
35 in inhibited the proteolytic action of human leukocyte elastase on purified acidic proline-rich saliv
36 betic ketoacidosis patients, including human leukocyte elastase (p < 0.001), proteinase-3 (p < 0.01),
37  proteolytic degradation of elastin by human leukocyte elastase, pancreatic elastase, thermolysin, an
38 alloproteinase-8 [aMMP-8], polymorphonuclear leukocyte elastase [PMN elastase], and total protein, al
39                 Millimolar concentrations of leukocyte elastase, when released from single azurophil
40 l trifluoromethyl ketone inhibitors of human leukocyte elastase which are found to have excellent pha