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1 roscopy, the rapid freeze procedure, and the stopped-flow method.
2  duplex DNA was studied using a fluorescence stopped-flow method.
3 s observed in proton pumping analysis by the stopped-flow method.
4 10 has been examined, using the fluorescence stopped-flow method.
5 ratures (-80 to -40 degrees C) as studied by stopped flow methods.
6 dy the kinetic cycle of DsbB in detail using stopped flow methods.
7 tants, compound I itself is only detected by stopped flow methods.
8 itor has been studied using steady state and stopped-flow methods.
9 kinetics of FAD reduction by sarcosine using stopped-flow methods.
10 inetics as measured by both steady-state and stopped-flow methods.
11  further, we undertook kinetic studies using stopped-flow methods.
12 s are too fast to measure using conventional stopped-flow methods.
13                        We established by the stopped-flow method a two-step binding process: an initi
14  function of the permutein was assayed using stopped-flow methods and shown to be essentially identic
15 with nitrones were determined using a UV-vis stopped-flow method, and phenyl radical (Ph(*)) trapping
16 anges in the Hsc66 absorbance spectrum using stopped-flow methods at 23 degrees C.
17 conditions that favour folding, conventional stopped-flow methods at higher denaturant concentrations
18 ding and dissociation kinetics determined by stopped-flow methods demonstrated that although actin gl
19  an inexpensive and economical complement to stopped-flow methods for a broad range of time-resolved
20           Using single-turnover fluorescence stopped-flow methods, here we report that ClpA, when ass
21 e catalytic mechanism were studied using the stopped-flow method, including the insertion of CO into
22                                              Stopped-flow methods indicate a burst of cGDPR formation
23               We find that within error, our stopped-flow method reproduces both the rate and activat
24             Kinetic measurements made by the stopped-flow method show that the reaction between the m
25 t intermediate using combined continuous and stopped-flow methods showed the formation of a defined s
26  have developed single-turnover fluorescence stopped-flow methods that allow us to quantitatively exa
27                                        Using stopped flow methods, the rate at which the ferrocytochr
28 yrene) were mixed with ferric P450 1A2 using stopped-flow methods, the changes in the heme Soret spec
29                        In this work, we used stopped-flow methods to monitor the coupling of adenosin
30 hrome c have been investigated using pH jump stopped-flow methods to probe the nature of the ionizabl
31 ygenase domain of neuronal NOS (nNOSoxy) and stopped-flow methods to study formation and autooxidativ
32 t with steady state data confirming that the stopped-flow method used was appropriate for the reactio
33  The reactions have been monitored by UV-vis stopped-flow methods, using the different optical spectr
34                                        Using stopped-flow methods we have examined the kinetic mechan
35                                              Stopped-flow methods were then used to assess the rates
36                                 Fluorescence stopped-flow methods were used to record the kinetics of

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