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1 dration, resulting in a dramatic decrease in induction time.
4 of 10(6)-10(8)cm(-3)s(-1); (iv). nucleation induction times agree with an a priori prediction based
6 mented amyloplasts, gravitropic sensitivity (induction time and intermittent stimulation) and plastid
8 odels correlated with the prolongation of MT induction time and that knockdown of MT with RNA interfe
10 oved linseed oil stability, showing the same induction time at 110 degrees C (by Rancimat) of control
11 studies revealed a 29.53-46.44 % increase in induction time at 140 degrees C, demonstrating improved
13 etradecanoylphorbol-13-acetate (TPA) with an induction time course following the c-Jun induction in b
14 re stimulated at various times to provide an induction time course for c-fos mRNA which peaked at 30
15 ymerase chain reaction data from a low-CO(2) induction time-course experiment demonstrated that the u
16 ce on the nucleation, i.e. shorter or longer induction time, dependent on the concentrations of the l
17 equently used to explain the existence of an induction time during the reduction process can be impor
18 he formation of stable crystals within short induction times, followed by rapid spreading as corner f
19 is of tailor-made polymers that decrease the induction time for crystal appearance and may find appli
24 incorporated into an insoluble polymer, the induction time for the onset of crystal formation for bo
25 second-scale molecular dynamics simulations, induction times for nucleation of LiF solids from their
27 corporation of Anx-A5 markedly shortened the induction time, greatly increasing the rate and overall
30 r than those of EV oils and blends, in which induction time increased proportionally with the percent
31 as exciting classroom experiments, where an induction time is followed by rapidly changing colours t
33 ion theory, for both mechanisms, the typical induction time is shown to scale with the pore volume to
34 A-EDA (OLD), unsaturated/saturated ratio and induction time (IT) allowed the correct classification o
35 s NEgen1, establishes correlations among the induction time, nucleation rate, growth rate, bond-formi
40 hnique for direct determination of rates and induction times of primary nucleation of HbS fibers, bas
41 model revealed the stochastic nature of the induction timing of the key cell fate determinants and i
45 covery in 20 consecutive patients undergoing induction timed sequential chemotherapy for newly diagno
47 y was accompanied by an increase in reaction induction times, suggesting that increasing surface pres
48 over time exhibited two regimes: an initial induction time, t(s), with little decay was followed by
49 rations of trans-ferulic acid resulted in an induction time (tau) proportional to the antioxidant con
50 termining key kinetic parameters such as the induction time (tau), rates of inhibited (R(inh)) and un
52 Apo-TLs show a longer diffusion-dependent induction time than holo-TLs due to more extensive oligo
54 first-derivative analysis, which defines the induction time, the rate and the amount of initial miner
56 No effect on toluene degradation rate or induction time was observed when active cells of Rhodoco
59 nearly identical, the turnover time and the induction time were significantly shorter for the experi
62 rmation could be a determinant of beta-sheet induction time, with implications for the onset of amylo