ライフサイエンスコーパス: first-order reaction

1 ecially at 45 degrees C and did not follow a first order reaction.

2 tion of NAD+ from all four sites in a single first-order reaction.

3 n converted to the native dimer by a slower, first-order reaction.

4 he ferri-alpha-meso-hydroxyheme product in a first-order reaction.

5 and can be adequately described by a single first-order reaction.

6 d by a pair of sequentially-occurring pseudo-first order reactions.

7 ata are well described using a series of two first-order reactions.

8 ubulin subunits hydrolyze GTP according to a first-order reaction after they are incorporated into th

9 appearance of MGO were confirmed as overall, first order reactions, albeit probably composites of mul

10 Oxygen isotope exchange proceeds as a first-order reaction, and the exchange rate is strongly

11 ffecting calcium absorption in the gut, in a first-order reaction, as followed by a calcium electrode

12 Our study reveals a transition from a slow, first order reaction at low accumulated hole density to

13 ould be modeled as the competition between a first-order reaction (bacterial growth) and a second-ord

14 tical solutions indicate that ultrasensitive first-order reactions can yield switches that respond to

15 ponse data, previously modeled as the sum of first-order reactions, have been used to evaluate models

16 n pathway that can be well approximated by a first order reaction; if several pathways exist, the mod

17 ted by kinetic experiments which indicated a first order reaction in hydroxide and a full negative ch

18 concentration of Abeta fibrils and a pseudo-first-order reaction in the concentration of peptide moi

19 also decreases the time contaminants undergo first-order reaction in the sediment.

20 tween contaminant supply from the stream and first-order reaction in the sediment.

21 ions Gh or Sp is described by two sequential first-order reactions, in which the intermediate state i

22 Aerobically in Na(+)-Hepes, a first-order reaction (k = 0.032 hr(-)(1) at 37 degrees C

23 sociated with the release of pheromone, is a first-order reaction (k = 74.1 +/- 0.32 s(-1); t(1/2), 9

24 [(SBI)ZrMe(+).B(C(6)F(5))(4)(-)] in a pseudo-first-order reaction, k = 3 x 10(-4) s(-1), [(L(2)ZrMe)(

25 MYR inactivation rates were estimated by the first-order reaction kinetic model.

26 Dmc1 renatures linearized plasmid DNA with first order reaction kinetics and without requiring adde

27 HF and AA over a period of 12h both followed first order reaction kinetics.

28 tion of the antioxidant compounds followed a first-order reaction kinetics and the degradation rate c

29 Degradation followed first-order reaction kinetics and the temperature-depend

30 s a model reaction, we demonstrated that its first-order reaction kinetics could be accurately determ

31 The mechanism involves first-order reaction kinetics for the conversion of eith

32 by both UV and UV/H(2)O(2) exhibited pseudo-first-order reaction kinetics with half-lives ranging fr

33 Second, Rad59-promoted DNA annealing follows first-order reaction kinetics, whereas Rad52-promoted an

34 e described using Michaelis-Menten model and first order reaction model, respectively.

35 Anthocyanin degradation fitted a first-order reaction model and the rate constants ranged

36 conditions, anthocyanin degradation fitted a first-order reaction model.

37 Degradation kinetics were best fitted by first-order reaction models for both ascorbic acid and c

38 duration tau that is followed by the pseudo-first-order reaction of S.

39 The rates of the pseudo-first-order reactions of the complexes depend on the nuc

40 Dissociation conformed to a single first order reaction over a wide range of protein occupa

41 tration, suggesting that polymerization is a first-order reaction, perhaps occurring when two Hsc70 m

42 e emergence of ultrasensitivity from coupled first-order reactions provides a versatile mechanism for

43 Calculated pseudo-first order reaction rate constants were in the followin

44 The pseudo-first-order reaction rate between C60 and O3 ranges from

45 e presence of 100 mug/L graphene, the pseudo-first-order reaction rate constant was increased ~50 tim

46 The pseudo-first-order reaction rate constants of Co(III) and Co(IV

47 containing L-ascorbic acid proceeded with a first-order reaction rate during storage (40 degrees C f

48 ing l-ascorbic acid (0.050%) degraded with a first-order reaction rate during storage (40 degrees C/7

49 Kinetic studies revealed a first-order reaction rate.

50 o acids or peptides, anthocyanin degraded at first-order reaction rate.

51 A first-order reaction supports an intramolecular concerte

52 e successfully modeled as sequential, pseudo-first-order reactions that transition through a long-liv

53 The numerical solution of sequential first-order reactions was used to obtain kinetic paramet

54 f this coiled coil represents a single-stage first-order reaction, while the refolding represents a s

55 bance changes can be fit to five consecutive first order reactions with rate constants of 350 s-1, 13

56 lowly converts to the low-lability form in a first-order reaction with a characteristic lifetime (inv

57 ng kinetics of anastellin to III3-FRET fit a first-order reaction with a half-time of approximately 3

58 tion of native actin follows approximately a first-order reaction with a rate constant of about 0.03

59 omposition can be described as a second- and first-order reaction with respect to Fe(VI), respectivel