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1 e acylation vs deacylation half-reactions of cathepsin C.
2 odial ortholog of the lysosomal exopeptidase cathepsin C.
3 et lysosomal thiol protease, consistent with cathepsin C.
4             OLFM4 was found to interact with cathepsin C, a cysteine protease that plays an important
5 trophil bactericidal activity by restricting cathepsin C activity and its downstream granule-associat
6 athepsin G, and proteinase 3), which require cathepsin C activity for processing and maturity, were a
7                                          The cathepsin C activity in neutrophils from OLFM4(-)/(-) mi
8 assay to demonstrate an almost total loss of cathepsin C activity in PLS patients and reduced activit
9         We demonstrated that OLFM4 inhibited cathepsin C activity in vitro and in vivo.
10 expression of cystatin F suppressed cellular cathepsin C activity.
11 ld-type and Lman1(-/-) mice in the levels of cathepsin C and cathepsin Z in liver lysates or alpha1-a
12                            The activities of cathepsin C and its downstream proteases (neutrophil ela
13 ld be necessary before cystatin F can engage cathepsin C and we show that the intracellular form of c
14                                              Cathepsin C, another cysteine proteinase with a rather d
15                                        Thus, cathepsin Cs are critical to T. gondii growth and differ
16  endopeptidases cathepsin B and L, T. gondii cathepsin Cs are exopeptidases and remove dipeptides fro
17                                    T. gondii cathepsin Cs are required for peptide degradation in the
18                                We identified cathepsin C as critical for Leu-Leu-OMe-induced cell dea
19                              We examined the cathepsin C-catalyzed hydrolysis of dipeptide substrates
20                        The cysteine protease cathepsin C (CatC) activates granule-associated proinfla
21         Despite previous reports identifying cathepsin C, cathepsin Z, and alpha1-antitrypsin as addi
22  mutations that inactivate cysteine protease cathepsin C (CTSC), which processes a variety of serine
23                                  Strikingly, cathepsin C deficiency not only blocked Leu-Leu-OMe-medi
24 ntified as the activator of NSP4 in vivo, as cathepsin C deficiency resulted in a complete absence of
25  activity of the lysosomal cysteine protease cathepsin C/dipeptidyl peptidase I (DPPI).
26 l loss of cathepsin C in mice with OLFM4 and cathepsin C double deficiency.
27                        ESCP is homologous to cathepsin C enzymes of higher eukaryotes, but is disting
28 re syndrome, and evaluated the gene encoding cathepsin C for mutations.
29          Mutations of the lysosomal protease cathepsin C gene (CTSC) have been shown to be the geneti
30                            Addition of these cathepsin C gene mutations into the expanding Papillon-L
31                      In contrast, removal of cathepsin C had no effect on either tumor formation or p
32     Recently, mutations in the gene encoding cathepsin C have been disclosed in a limited number of f
33 cantly compromised by the additional loss of cathepsin C in mice with OLFM4 and cathepsin C double de
34 recombinant cystatin F was unable to inhibit cathepsin C in vitro even though overexpression of cysta
35 60, which is currently in clinical trials as cathepsin C inhibitor for the treatment of cystic fibros
36                                 The specific cathepsin C inhibitor, Gly-Phe-dimethylketone, selective
37 precise N-terminal truncation that creates a cathepsin C inhibitor.
38  tachyzoites was completely inhibited by the cathepsin C inhibitor.
39                                              Cathepsin C inhibitors also limited the in vivo infectio
40                                 By targeting cathepsin C, it may regulate diverse immune cell effecto
41 /endosomal enzyme-related genes (cystatin C, cathepsin C, lysozyme, and prosaposin) did not require d
42 inetic parameters and sKIEs for the proposed cathepsin C mechanism, integration of both steady-state
43 sins from Toxoplasma gondii, including three cathepsin Cs, one cathepsin B, and one cathepsin L.
44  gene (CTSC) encoding the lysosomal protease cathepsin C (or dipeptidyl aminopeptidase I) lies within
45                                              Cathepsin C, or dipeptidyl peptidase I, is a lysosomal c
46 hly conserved amino acid residues within the cathepsin C polypeptide.
47 substrate of cathepsins B, L, and S, but not cathepsin C, potentially explaining their differential e
48 g retrovirus and analyzed the cystatin C and cathepsin C promoters.
49 he structural effects caused by mutations in cathepsin C protein (CTSC).
50 atumoral collagenase (to digest collagen) or cathepsin C (to digest decorin) each increased diffusion
51   Using the dipeptide substrate Ser-Tyr-AMC, cathepsin C was characterized in both steady-state and p
52                                    Moreover, cathepsin C was identified as the activator of NSP4 in v
53 rent immune cell types is the aminopeptidase cathepsin C, which regulates the activation of effector

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