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1 nfected cells in a soluble truncated form by tumor necrosis factor alpha-converting enzyme.
2 drolyzed peptide substrates of matrixins and tumor necrosis factor-alpha converting enzyme.
3 of oxygen radicals, which in turn stimulate tumor necrosis factor alpha-converting enzyme (a disinte
4 on (knockout), we now demonstrate that TACE (tumor necrosis factor alpha converting enzyme), a member
5 ecretase activity and enhanced hydrolysis of tumor necrosis factor alpha-converting enzyme, a primary
6 from the surface of activated leukocytes by tumor necrosis factor-alpha converting enzyme, a cell su
8 odulin protein expressions, inhibited tissue tumor necrosis factor-alpha converting enzyme activity,
11 s had substantially elevated levels of basal tumor necrosis factor-alpha-converting enzyme activity t
12 GHR metalloproteolysis can be catalyzed by tumor necrosis factor-alpha-converting enzyme (ADAM-17)
13 DC lacking MT1-MMP, and instead requires the tumor necrosis factor alpha-converting enzyme ADAM17 (a
15 al H19-7/IGF-IR neuronal cells and inhibited tumor necrosis factor-alpha-converting enzyme alpha-secr
17 as ERBB4) undergoes sequential processing by tumor necrosis factor-alpha converting enzyme and presen
18 o be mediated by reduced cleavage of GPIb by tumor necrosis factor-alpha-converting enzyme and reduce
19 flammatory response syndrome, monocyte basal tumor necrosis factor-alpha-converting enzyme, and its i
20 y reduced, due to inhibition of the sheddase-tumor necrosis factor-alpha-converting enzyme by Abeta.
22 ptide, sol-tumor necrosis factor production, tumor necrosis factor-alpha-converting enzyme expression
24 idues 646-657 was incubated with recombinant tumor necrosis factor-alpha-converting enzyme, fragments
27 increased expression of ADAM 10 and ADAM 17 (tumor necrosis factor-alpha-converting enzyme) in antral
28 contrast, the matrix metalloproteinase/TACE (tumor necrosis factor-alpha-converting enzyme) inhibitor
29 and PMA and was specifically inhibited by a tumor necrosis factor alpha-converting enzyme metallopro
30 cies, increased expression of pro-HB-EGF and tumor necrosis factor alpha-converting enzyme (pro-HB-EG
31 ealth Evaluation II score and the attenuated tumor necrosis factor-alpha-converting enzyme response t
33 ch higher efficiency the hydrolysis of a pro-tumor necrosis factor-alpha converting enzyme synthetic
35 ning transmembrane protein but is cleaved by tumor necrosis factor alpha converting enzyme (TACE) to
36 etalloproteinase-3, TIMP-3, that can inhibit tumor necrosis factor alpha converting enzyme (TACE), bu
39 tion of the extracellular region of ADAM-17 (tumor necrosis factor alpha-converting enzyme (TACE)) by
41 In parallel, the proteolytic activity of tumor necrosis factor alpha-converting enzyme (TACE; ADA
44 d from chimeric mice, which express inactive tumor necrosis factor-alpha converting enzyme (TACE(Delt
48 secretion) of tumor necrosis factor (TNF) by tumor necrosis factor-alpha converting enzyme (TACE) may
50 ctivation gene 3 (LAG-3) and metalloprotease tumor necrosis factor-alpha converting enzyme (TACE) wor
52 Our study identifies ADAM17, also called tumor necrosis factor-alpha converting enzyme (TACE), as
54 PR), undergoes regulated cleavage by the MMP tumor necrosis factor-alpha converting enzyme (TACE).
55 as observed in newborn mice lacking EGFR and tumor necrosis factor-alpha converting enzyme (TACE).
56 racterization of a fluorogenic substrate for tumor necrosis factor-alpha converting enzyme (TACE).
57 disintegrin and metalloprotease) identified tumor necrosis factor-alpha converting enzyme (TACE)/ADA
58 ese hamster ovary cells that lack functional tumor necrosis factor-alpha converting enzyme (TACE, als
61 and genetic reconstitution studies identify tumor necrosis factor-alpha converting enzyme (TACE/ADAM
63 sed from cells, a process termed "shedding." Tumor necrosis factor-alpha converting enzyme (TACE/ADAM
64 -myristate 13-acetate (PMA), and we identify tumor necrosis factor-alpha converting enzyme (TACE; ADA
65 the cell surface death receptors mediated by tumor necrosis factor-alpha converting enzymes (TACE/ADA
67 from genetically deficient mice, we identify tumor necrosis factor-alpha-converting enzyme (TACE or A
68 owth factor)-like growth factor (HB-EGF) and tumor necrosis factor-alpha-converting enzyme (TACE) (AD
69 d is required for Notch processing by ADAM17/tumor necrosis factor-alpha-converting enzyme (TACE) and
70 cleaved in cells lacking the metalloprotease tumor necrosis factor-alpha-converting enzyme (TACE) and
72 , Src small interfering RNA (siRNA), and the tumor necrosis factor-alpha-converting enzyme (TACE) inh
73 FR phosphorylation inhibitor AG1478, and the tumor necrosis factor-alpha-converting enzyme (TACE) inh
74 The introduction of enzymatically active tumor necrosis factor-alpha-converting enzyme (TACE) int
79 diverse group of membrane ectoproteins, and tumor necrosis factor-alpha-converting enzyme (TACE), a
80 e form by proteolytic cleavage that involves tumor necrosis factor-alpha-converting enzyme (TACE), an
81 uction, leading to EPCR shedding mediated by tumor necrosis factor-alpha-converting enzyme (TACE), en
82 upport of this hypothesis, BDNF up-regulated tumor necrosis factor-alpha-converting enzyme (TACE)/ADA
84 a mechanism involving the phosphorylation of tumor necrosis factor-alpha-converting enzyme (TACE/ADAM
85 malian N-TIMP-3 in strongly inhibiting human tumor necrosis factor-alpha-converting enzyme (TACE/ADAM
86 s was impaired by inhibition or depletion of tumor necrosis factor alpha-converting enzyme, the enzym
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