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1 ion of kallikrein; factor XII alone does not autoactivate.
2 he propeptide domain controls its ability to autoactivate.
3 ata show that tethered PTH/PTH receptors can autoactivate.
4 ically inactive soluble hepsin was unable to autoactivate.
5 expressed in Escherichia coli, purified, and autoactivated.
6 alyses demonstrated that the cpxRA operon is autoactivated.
7 , except that constitutively active ARF6 was autoactivating.
9 lysosomal environment because the zymogen is autoactivated and remains optimally active in acidic con
11 cognition protein that binds to bacteria and autoactivates and triggers the prophenoloxidase activati
12 sor (pro-HP14) interacts with peptidoglycan, autoactivates, and initiates the proteinase cascade.
13 lytic cleavage of both the transducer, which autoactivates, and the repressor, which is inactivated,
16 ere identical; however, at pH 5.0, Ile-21-Tg autoactivated at an enhanced rate relative to Asn-21-Tg.
17 eatitis (N29I, N29T, V39A, R122C, and R122H) autoactivated at increased rates and reached markedly hi
19 e marRAB operon is autorepressed by MarR and autoactivated by MarA at a site that also can be activat
20 tron 1 that is activated by activin and Vg1, autoactivated by Xnrs, and suppressed by ventral inducer
29 tion of apoptosis and differentiation by the autoactivating enediyne, enediyne-5, and the non-enediyn
30 ry glands of transgenic mice that express an autoactivating form of MMP-3/stromelysin-1 under the con
32 An allele-specific interaction between an autoactivating form of Snake (Snk) and a gd allele alter
35 al control over the production of snc1-1 (an autoactivated immune receptor) in Arabidopsis thaliana a
37 ssistance of another protease and is able to autoactivate in acidic pH in vitro via a unimolecular me
40 sexta: hemolymph proteinase 14 (HP14), which autoactivates in the presence of microbial surface compo
42 nzymatically dephosphorylated purified Rad53 autoactivates in vitro through a phosphorylation-depende
43 omain propagates the death signal through an autoactivating interaction with the trigger site of inac
46 In primary T cells, c-Myb allows GATA-3 to autoactivate its own expression, an event that requires
51 that prostate carcinoma cells LNCaP and PC3 autoactivate latent full-length PDGF D into its active f
53 We previously showed that targeting of an autoactivating mutant of the matrix metalloproteinase st
56 other Gram-positive bacteria, agr encodes an autoactivating peptide (AIP) that is the inducing ligand
57 alleles under both constitutive (PrpsL) and autoactivated (Pmga4) promoters illustrated that an argi
58 cancer cells, where it displayed an enhanced autoactivating process and a distinct intracellular rout
62 1 transgenic animals with mice expressing an autoactivating stromelysin-1 transgene targeted to mamma
63 alveolar epithelial cells of mice expressing autoactivating stromelysin-1 underwent unscheduled apopt
66 ndicated that this receptor was sufficiently autoactivated to produce at least partial differentiatio
68 We show that, although MASP-2 is able to autoactivate under artificial conditions, MASP-1 dramati
70 activation by upstream kinases, p38alpha can autoactivate when interacting with transforming growth f
71 ses, MASP-1 and MASP-2, have been thought to autoactivate when MBL/ficolin.MASP complexes bind to pat
72 proDelta(260-508)MMP-19 has the tendency to autoactivate, whereby the Lys(97)-Tyr(98) peptide bond i
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