ライフサイエンスコーパス: all-or-nothing

1 In reality, however, cooperation is rarely all-or-nothing.

2 an signal the onset of a light step with 1-3 all-or-nothing action potentials that attain a peak ampl

3 o convert an initially graded signal into an all-or-nothing activation of JAK/STAT and thus to proper

4 = omega < or = 145.0 +/- 37.0) results in an all-or-nothing association pattern on short templates.

5 r= omega <or= 89.8 +/- 8.9), resulting in an all-or-nothing association pattern on short templates.

6 arabinose operon P(BAD) promoter exhibit the all-or-nothing (autocatalytic) induction of expression t

7 Multivariate analysis revealed that all-or-nothing behaviour was the key predictor for the o

8 perceptions, stress, anxiety, depression and all-or-nothing behaviour were associated with the risk o

9 Thus, while MAPK signaling is involved in all-or-nothing cell fate decisions for both Xenopus oocy

10 Zn(II) binding triggers a highly localized, all-or-nothing change of water accessibility to the tran

11 fullerene guests was observed to effect the all-or-nothing cooperative templation of an S6-symmetric

12 registered at FLC in individual cells in an all-or-nothing (digital) manner or is continuously varyi

13 escent, indicating that ComK synthesis is an all or nothing event.

14 sion following CRAC channel activation is an all-or-nothing event over a range of stimulus intensitie

15 approach, we demonstrate that MOMP is not an all-or-nothing event.

16 xpression of one isozyme or the other was an all-or-nothing event.

17 ds" of performance may make more sense than "all-or-nothing" expectations.

18 elays 1 bit of information to coordinate the all-or-nothing expression of early genes, but also over

19 d exposure, cells respond autonomously in an all-or-nothing fashion, with the fraction of cells that

20 ltidrug efflux pumps do not associate in an "all-or-nothing" fashion but accommodate a certain degree

21 was accepted for study if it gave a stable, all-or-nothing fluorescence response to an external shoc

22 om of the complex at the cost of its normal, all-or-nothing functionality.IMPORTANCECaudovirales enco

23 If vaccine action is all-or-nothing (ie, a proportion of vaccine recipients r

24 This strain avoids the problem of all-or-nothing induction of P(BAD) because it is deficie

25 We report an approach to avoid all-or-nothing induction of the pBAD promoter; the use o

26 ity may explain the experimentally observed 'all-or-nothing' LAX3 spatial expression pattern in corti

27 " to form a compact productive complex in an all or nothing like fashion with all the important molec

28 s and receptors are thought to operate in an all-or-nothing manner, existing in an immunologically ac

29 ed between pathogen types, rather than in an all-or-nothing manner.

30 ctive population, Ca(++) gating occurs in an all-or-nothing manner.

31 critical displacement threshold governing an all-or-nothing mechanically-induced calcium response.

32 verall dynamics of an enzyme and suggest an "all-or-nothing" mechanism for the opening and closing of

33 ment to RP promoters to provide more than an all-or-nothing mode of transcriptional regulation.

34 ion is vital in animals that reproduce in an all-or-nothing mode, such as bristle worms: females comm

35 ld discrimination that are characteristic of all-or-nothing Na(+) spikes.

36 donor sophistication and also displays the "all or nothing" nature of adverse events in donor and re

37 Here, we show that this all-or-nothing neuronal differentiation results from Hip

38 PA release during moist-heat treatment is an all-or-nothing phenomenon; these findings also suggest t

39 ratio 6:1 at the branches, we observed the "all-or-nothing" phenomenon with plasma only entering the

40 lly inactive and matures through a symmetric all-or-nothing process.

41 Although initially considered an all-or-nothing reflex [1], numerous studies on freely di

42 deletion of fliT or fliD did not lead to an all-or-nothing response in FlhD(4) C(2) activity.

43 e from asymmetric septation, can achieve the all-or-nothing response in sigmaF activity required by t

44 r and greater control of the emergence of an all-or-nothing response of a cell.

45 metabolizable lactose analogues generates an all-or-nothing response, where some cells express the la

46 en, e.g., nitazoxanide consistently shows an all-or-nothing response.

47 ng progesterone stimulus into a switch-like, all-or-nothing response.

48 it diverse responses, ranging from graded to all-or-nothing responses and combinations thereof.

49 r exhibits the important neural functions of all-or-nothing spiking with signal gain and diverse peri

50 replication, and cyclin E, which triggers an all-or-nothing transition from G1 to S phase.

51 ough the loading of a cofactor represents an all-or-nothing transition in regard to the enzymatic fun

52 ybridization are often assumed to involve an all-or-nothing two-state dissociation pathway, but devia

53 This all-or-nothing two-state solution is a hallmark of posit