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1 opropylguanine (CPG) are used as kinetically fast electron and hole traps to probe the resulting elec
2 onic conductivity, structural stability, and fast electron and ion transport, are explored for boosti
3 w conformational changes mask the relatively fast electron and methyl transfer steps.
4                                              Fast electrons are preferentially emitted along the lase
5 l cyst, and renal parenchymal volumes, using fast electron-beam computerized tomography scanning, and
6 , captured at 2.5 ms time resolution using a fast electron camera.
7                 Here, recent developments in fast electron detectors and data processing capability i
8 ariable time interval, it was shown that the fast electron donating complex was reformed in about 60
9 ining cyt cy , however, was able to form the fast electron donating complex with the RC (half-time of
10 bance changes at 832 nm in the presence of a fast electron donor (phenazine methosulfate (PMS)).
11 cause the bound cytochrome is available as a fast electron donor in Chlorobium, it is not necessary t
12 rbance changes at 298 K in the presence of a fast electron donor indicate that two electron acceptors
13                          Using a kinetically fast electron hole trap, N(4)-cyclopropylcytosine ((CP)C
14 xamine the photooxidation of two kinetically fast electron hole traps, N4-cyclopropylcytosine (CPC) a
15 tocatalytic reactions remains low due to the fast electron-hole recombination and low light utilizati
16 e deltaG(ET) = 0.3-0.7 kcal mol(-1) for very fast electron hopping or peregrination around the hexago
17 ing electron beam damage, for example, using fast electron imaging and spectroscopy.
18 tials increases the driving force and favors fast electron injection.
19 shells and the polar Fe3 O4 cores facilitate fast electron/ion transport and promote continuous react
20              Such affinity together with the fast electron kinetics enables simultaneous and unambigu
21  solar cells, leading to the conclusion that fast electron motion is essential for efficient charge c
22 how to control signal transmission, i.e. how fast electrons or excitation energy could be transferred
23 lated uric acid and adenosine and engaged in fast electron/proton transfer in the oxidation of both a
24 tein, thereby eliminating the requirement of fast electron self-exchange, which is a condition that i
25 sorbing X-ray photons and converting them to fast electrons through the photoelectric effect.
26             Cu(H2 Tpy(NMes))Cl shows similar fast electron transfer ( approximately 10(5) m(-1) s(-1)
27 ol that enables quantitative measurements of fast electron transfer (ET) kinetics when coupled with m
28 organization free energies are necessary for fast electron transfer (ET) reactions.
29 lectrode surface in such a way that there is fast electron transfer and complete retention of the che
30 mV with enhanced peak currents, indicating a fast electron transfer at the modified electrode surface
31                                    Achieving fast electron transfer between a material and protein is
32     These structural features facilitate the fast electron transfer between the thin protein film and
33             The close packing contributes to fast electron transfer by increasing the rate of electro
34 the absence of cyt c2 because it can mediate fast electron transfer from the cyt bc1 complex to the R
35 eal the molecular driving force that ensures fast electron transfer in cryptochrome guaranteeing form
36                                              Fast electron transfer in less than 2 ps is observed for
37 duction by the imidazole bound complex under fast electron transfer is due to 1e(-)/1H(+) O2-reductio
38  guidance, a productive docking geometry for fast electron transfer is imposed by the guided trajecto
39 smitters because they are sensitive, exhibit fast electron transfer kinetics, and are more resistant
40 able devices show excellent conductivity and fast electron transfer kinetics.
41 iments and computation showing that the same fast electron transfer mechanism is operating in a diffe
42 ng photoexcitation of the electron acceptor, fast electron transfer occurs initially from the oligoqu
43 transfer on Pt, and catechol, which exhibits fast electron transfer on Au.
44 d two different species; l-dopa, which shows fast electron transfer on Pt, and catechol, which exhibi
45 pports the hypothesis that the exceptionally fast electron transfer rate between Tvfd and the drug me
46 in the co-crystals, which is the same as the fast electron transfer rate in vivo and in solution.
47 scopy shows that this catalyst features very fast electron transfer rates, facile oxygen binding and
48 onductive part of the composite, facilitated fast electron transfer rates.
49 thanol, no regeneration is observed due to a fast electron transfer reaction from the tocopheryl radi
50             NADP(H) binding is essential for fast electron transfer through the flavoprotein domain o
51 se with bound NADP(H) is essential to ensure fast electron transfer through the two flavin cofactors.
52 oketyl radical, CH(3)C(*)(SH)NHCH(3) (1), by fast electron transfer to protonated thioacetamide in th
53 orescence of Trp68 and Trp156 is quenched by fast electron transfer to the amide backbone.
54 does the dopamine modified electrode yield a fast electron transfer with lower DeltaE(p) (30 mV) than
55 rent responses, and capable of demonstrating fast electron transfer) for outer sphere redox couples,
56 ns all the data needed to estimate the (very fast) electron transfer rates (both rate constants >/= 4
57 ced kinetics for electrooxidation of NA, and fast electron-transfer between electrode-electrolyte int
58 y oriented nano-graphitic-edges that exhibit fast electron-transfer kinetics and high electroactive s
59                                          The fast electron-transfer rate in TiO(2) single crystals an
60                                              Fast electron-transfer rates found in the two ruthenium
61 cise kinetic data may be obtained for a very fast electron-transfer reaction using this technique.
62 ommon use of xenon flashlamps to photoexcite fast electron-transfer reactions are discussed with rela
63 ve material-current collector connection for fast electron transport.
64                              The emission of fast electrons with kinetic energies exceeding 3 keV is

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