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1 nd secondary RecBC translocases in a tightly coupled reaction.
2 to a sequential mechanism in the luciferase-coupled reaction.
3 both glyceraldehyde and glucose in an NADPH-coupled reaction.
4 rently about balancing the relative rates of coupled reactions.
5 vated hydrogen peroxide generation in poorly coupled reactions.
6 nto enzymes catalyzing multielectron, proton-coupled reactions.
7 d using Amplex red in horseradish peroxidase-coupled reactions.
8 termined for the FRG(F)-L(F) and FRP(H)-L(F) coupled reactions.
9 cid oxidase/horseradish peroxidase (DAO/HRP)-coupled reactions.
10 as partially limited by the flux through the coupled reactions.
11 e catalytic activity of FTO proceeds via two coupled reactions.
12 The activity of Alkbh5 comprises two coupled reactions.
13 of basis functions in such a manner that the coupled reaction and diffusion processes are propagated
14 ght chemical systems that integrate strongly coupled reaction and transport phenomena, identifying fr
15 O-producing reaction is considered to be the coupled reaction, and the uncoupled reactions are those
16 s at single-monomer resolution using CREATS (coupled reaction approach toward super-resolution imagin
17 lis RNase P protein as a model, we show that coupled reactions are best understood as a change in flu
19 enzyme reaction, functions in the luciferase-coupled reaction as a prebound substrate and is directly
23 d by the unexpectedly weak inhibition of the coupled reaction by the bisubstrate analog, N-(phosphona
24 anics (QM/MM) calculations of individual and coupled reaction center chromophores to describe reactio
25 acyl-CoA substrate, it is suggested that the coupled-reaction conditions must be carefully standardiz
26 somero-oxygenase that catalyze isomerization-coupled reactions crucial for production of vision-suppo
29 extending our previous in vivo mechanically-coupled reaction-diffusion modeling framework we develop
30 f periodic travelling waves predicted by two coupled reaction-diffusion models: a commonly used preda
32 oped a mathematical model that describes the coupled reaction-diffusion process in an established imm
33 computational model is used to show how two coupled reaction-diffusion systems reproduce both natura
34 achieved by standard (i.e., not mechanically coupled) reaction-diffusion predictive modeling (0.75),
36 ce of N-terminal domain of DNA ligase I in a coupled reaction governs the channeling of the pol beta
37 th slope Phi) for a bounded, linear chain of coupled reactions having arbitrary connecting rate const
38 ns over 2 microM significantly inhibited the coupled reaction in both light intensity and quantum yie
40 methionine quantification based on an enzyme-coupled reaction in which (S,S)-AdoMet reacts with 2-nit
43 The single observed product of the force-coupled reaction is a thermally inaccessible syn-tricycl
46 oduction of more complex oligosaccharides in coupled reaction mixtures, e.g., in the preparation of s
47 the O-O coupling in OER, yet they compose a coupled reaction network with competing kinetics depende
48 d over space and time by the kinetics of the coupled reaction network, they are autonomously self-hea
50 of surface silanols, in combination with the coupled reaction of "isolated" silanols and strained sil
51 MDa multiprotein complex, that catalyzes the coupled reaction of pre-mRNA cleavage and polyadenylatio
55 ic assay is no longer reliant on a secondary coupled reaction, on substrate labeling, or on detecting
56 the properties that emerge from a network of coupled reactions, particularly when the system contains
58 The surface confined template and covalently coupled reaction products are investigated and character
59 nover rate was 75 per minute, 63% of the ATP-coupled reaction rate for the nitrogenase complex under
60 ulatory indicates that the occurrence of the coupled reaction, rather than the accelerated uncoupled
62 onstrated that the rate-limiting step of the coupled reaction sequence resides in the second cyclizat
63 t junctions derived from wild-type U3 and U5 coupled reactions showed an approximately 70% fidelity f
65 e constituent strands lengthen through force-coupled reactions that are triggered as the strands reac
66 omalous effect of PALA suggests that, in the coupled reaction, the effective concentration of carbamo
68 etection of H2O2 in a horseradish peroxidase-coupled reaction using N-acetyl-3, 7-dihydroxyphenoxazin
70 on is typically performed through peroxidase-coupled reactions utilizing organic dyes that suffer, ho
71 erts UDP-GlcNAcA to UDP-GlcNAc(3NH(2))A in a coupled reaction via a unique NAD(+) recycling pathway.
72 llular PA, measured directly using an enzyme-coupled reaction, which resulted in a decreased rate of
73 the traditional endpoint assay based on the coupled reaction with formate dehydrogenase, and measuri
75 imeric recombinant AruH were determined by a coupled reaction with NAD(+) and L-alanine dehydrogenase
77 activity of this enzyme are based either on coupled reactions with other enzymes or on high-performa
78 at the mutant IDH1 is very efficient in this coupled reaction, with the ability to form alphaHG from