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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 at glomerular tuft staining for cathepsin B, cathepsin C, and annexin A3 in cFSGS was significantly g
15                                              Cathepsin C, another cysteine proteinase with a rather d
16                                        Thus, cathepsin Cs are critical to T. gondii growth and differ
17  endopeptidases cathepsin B and L, T. gondii cathepsin Cs are exopeptidases and remove dipeptides fro
18                                    T. gondii cathepsin Cs are required for peptide degradation in the
19                                We identified cathepsin C as critical for Leu-Leu-OMe-induced cell dea
20                              We examined the cathepsin C-catalyzed hydrolysis of dipeptide substrates
21                        The cysteine protease cathepsin C (CatC) activates granule-associated proinfla
22                                              Cathepsin C (CatC) from zymogens activates the proteolyt
23                                              Cathepsin C (CatC) is a cysteine dipeptidyl aminopeptida
24         Despite previous reports identifying cathepsin C, cathepsin Z, and alpha1-antitrypsin as addi
25  mutations that inactivate cysteine protease cathepsin C (CTSC), which processes a variety of serine
26                                  Strikingly, cathepsin C deficiency not only blocked Leu-Leu-OMe-medi
27 ntified as the activator of NSP4 in vivo, as cathepsin C deficiency resulted in a complete absence of
28  activity of the lysosomal cysteine protease cathepsin C/dipeptidyl peptidase I (DPPI).
29 l loss of cathepsin C in mice with OLFM4 and cathepsin C double deficiency.
30                        ESCP is homologous to cathepsin C enzymes of higher eukaryotes, but is disting
31 re syndrome, and evaluated the gene encoding cathepsin C for mutations.
32          Mutations of the lysosomal protease cathepsin C gene (CTSC) have been shown to be the geneti
33                            Addition of these cathepsin C gene mutations into the expanding Papillon-L
34                      In contrast, removal of cathepsin C had no effect on either tumor formation or p
35     Recently, mutations in the gene encoding cathepsin C have been disclosed in a limited number of f
36 cantly compromised by the additional loss of cathepsin C in mice with OLFM4 and cathepsin C double de
37 recombinant cystatin F was unable to inhibit cathepsin C in vitro even though overexpression of cysta
38 60, which is currently in clinical trials as cathepsin C inhibitor for the treatment of cystic fibros
39                                 The specific cathepsin C inhibitor, Gly-Phe-dimethylketone, selective
40 precise N-terminal truncation that creates a cathepsin C inhibitor.
41  tachyzoites was completely inhibited by the cathepsin C inhibitor.
42                                              Cathepsin C inhibitors also limited the in vivo infectio
43                                 By targeting cathepsin C, it may regulate diverse immune cell effecto
44 /endosomal enzyme-related genes (cystatin C, cathepsin C, lysozyme, and prosaposin) did not require d
45 inetic parameters and sKIEs for the proposed cathepsin C mechanism, integration of both steady-state
46 sins from Toxoplasma gondii, including three cathepsin Cs, one cathepsin B, and one cathepsin L.
47  gene (CTSC) encoding the lysosomal protease cathepsin C (or dipeptidyl aminopeptidase I) lies within
48                                              Cathepsin C, or dipeptidyl peptidase I, is a lysosomal c
49 hly conserved amino acid residues within the cathepsin C polypeptide.
50 substrate of cathepsins B, L, and S, but not cathepsin C, potentially explaining their differential e
51 ipeptidyl peptidase-1 (DPP-1), also known as cathepsin C, processes and activates neutrophil serine p
52 g retrovirus and analyzed the cystatin C and cathepsin C promoters.
53 he structural effects caused by mutations in cathepsin C protein (CTSC).
54 atumoral collagenase (to digest collagen) or cathepsin C (to digest decorin) each increased diffusion
55   Using the dipeptide substrate Ser-Tyr-AMC, cathepsin C was characterized in both steady-state and p
56                                    Moreover, cathepsin C was identified as the activator of NSP4 in v
57 rent immune cell types is the aminopeptidase cathepsin C, which regulates the activation of effector