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1                                              Double reciprocal analysis of initial velocities of AcpS
2 -prone than the original Furchgott method of double-reciprocal fit and simpler than alternatives that
3 substrate concentration data were plotted in double-reciprocal form, all line patterns were intersect
4                                              Double-reciprocal patterns of velocity versus substrate
5 reated control eyes fit a straight line on a double reciprocal plot (r2 = 0.98) after the introductio
6                                              Double reciprocal plot analysis of glutamine synthesis v
7 d-end inhibitor for GGPP, gave a competitive double reciprocal plot for varied concentrations of GGPP
8 ndary to AMD Study), which were plotted on a double reciprocal plot of 1 / lesion size (disc area) vs
9                                       From a double-reciprocal plot of k(obs) versus [H(2)O(2)] at pH
10                                              Double reciprocal plots and preincubation studies reveal
11                                              Double reciprocal plots for coenzyme binding to DGD exhi
12                                              Double reciprocal plots for the peptide mimic Cys-AMBA-L
13                                              Double reciprocal plots of initial rates versus concentr
14                           In this mechanism, double reciprocal plots will appear nearly parallel (as
15                                              Double reciprocal plots with N-methyl-L-tryptophan as th
16 lar to MAO A, including biphasic kinetics in double reciprocal plots.
17                 Curvature is observed in the double-reciprocal plots for product inhibition by NADH a
18                                              Double-reciprocal plots for two-substrate kinetic data y
19                                              Double-reciprocal plots of initial velocities versus the
20                                              Double-reciprocal plots showed a competitive inhibition
21                                 Although the double-reciprocal plots with UTP produced parallel lines
22                     The linearity of primary double-reciprocal plots, in the presence and absence of
23 eine (AdoHcy) were obtained and evaluated as double-reciprocal plots.
24 se and phosphatase both yielded intersecting double-reciprocal plots.
25     Steady-state rate studies yield parallel double-reciprocal plots; however, we show that fluoride
26             These results were compared with double-reciprocal velocity plots and product analyses ob
27 sferase) and suggest a predictive ability of double-reciprocal velocity plots for single versus multi
28                                              Double-reciprocal velocity plots under catalytic conditi