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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
3                                          The uncompetitive inhibition and the substrate-dependent bin
4 re also provided for competitive inhibition, uncompetitive inhibition, and mixed inhibition of ordere
5                               Theoretically, uncompetitive inhibition arises from preferential intera
6                                              Uncompetitive inhibition by arabinose 5-phosphate (Ara5P
7  pentameric complex, which suggests that the uncompetitive inhibition by BFA and the nucleotide allos
8           Finally, we note that the apparent uncompetitive inhibition by fluoride as reported for sev
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
14                            The appearance of uncompetitive inhibition, however, suggests that a more
15                                 RFA-P showed uncompetitive inhibition, K(i) = 0.210 mm, under varied
16                                 CO(2) showed uncompetitive inhibition, K(i) = 0.990 mm, under varied
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
20 o importantly, binding to this pocket causes uncompetitive inhibition of KSP ATPase activity.
21                       For this purpose, only uncompetitive inhibition of pyruvate export proves effec
22                                           An uncompetitive inhibition of the anaerobic reaction catal
23 m and Vmax values, suggesting a mechanism of uncompetitive inhibition on GlyT1-mediated glycine uptak
24       At the concentrations corresponding to uncompetitive inhibition, PDPA shows positive cooperativ
25  for Ca(2+) that mediated noncompetitive and uncompetitive inhibition, respectively.
26                                         This uncompetitive inhibition suggests that the probe can int
27 -L-arginine was synthesized and demonstrated uncompetitive inhibition versus ATP and competitive patt
28 d competitive inhibition vs saccharopine and uncompetitive inhibition vs NADP.
29                                              Uncompetitive inhibition was also observed with the synt
30 ns of agonist for "pure' non-competitive vs. uncompetitive inhibition was computer simulated.
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
33                                          The uncompetitive inhibition with respect to ATP is also con
34  calpains relative to other proteases, (iii) uncompetitive inhibition with respect to substrate, and

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