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1 with urease is not compatible with classical uncompetitive inhibition.
2 could be fit with the equation for complete uncompetitive inhibition and that the mechanism may be a
4 re also provided for competitive inhibition, uncompetitive inhibition, and mixed inhibition of ordere
7 pentameric complex, which suggests that the uncompetitive inhibition by BFA and the nucleotide allos
9 constant (K(ic)) of 0.12 +/- 0.02 mM and an uncompetitive inhibition constant (K(iu)) of 3.04 +/- 0.
10 how unimpaired inhibition by triclosan, with uncompetitive inhibition constants (K(i)') of 0.18+/-0.0
11 etitive inhibition (decreased V max), whilst uncompetitive inhibition (decreased V max and K m ) occu
12 Compound 4 shows a mix of competitive and uncompetitive inhibition for both the yeast and the huma
13 utant protease showed mixed-type competitive-uncompetitive inhibition for darunavir and the chemicall
17 inding of agonists to Epac1 and suggested an uncompetitive inhibition mechanism with respect to Epac1
18 ligand binding and kinetic data best fit an uncompetitive inhibition model in which the binding of t
19 lowed by naphthol substrate, as shown by the uncompetitive inhibition of 3HNR by tricyclazole with re
23 m and Vmax values, suggesting a mechanism of uncompetitive inhibition on GlyT1-mediated glycine uptak
27 -L-arginine was synthesized and demonstrated uncompetitive inhibition versus ATP and competitive patt
31 is unknown, the structural requirements for uncompetitive inhibition were investigated by applicatio
32 ding a series of parallel plots, typical for uncompetitive inhibition with a Ki for inhibition of app
34 calpains relative to other proteases, (iii) uncompetitive inhibition with respect to substrate, and
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