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 in some, but not all veins, contrasting with all-or-nothing alternatives available with the single-or

5 tion to enable powerful capabilities such as all-or-nothing assembly of nanostructures larger than a

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

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

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

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

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

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

12 highly heterogeneous, but tightly regulated, all-or-nothing cellular decisions.

13 esponse, recorded extracellularly, showed an all-or-nothing change in both amplitude and duration, a

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

15 omologous recombination DNA repair is not an all-or-nothing concept, but a spectrum, and that where a

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

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

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

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

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

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

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

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

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

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

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

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

28 tterns by activating a subset of cells in an all-or-nothing (i.e. digital) manner.

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

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

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

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

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

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

35 tinspiration triggers swallow behavior in an all-or-nothing manner, while there is a higher probabili

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

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

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

39 terization of CasX specificity, revealing an all-or-nothing mechanism where mismatches can be bound,

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

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

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

43 models for DNA loop formation are one-step, all-or-nothing models with a looped state and an unloope

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

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

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

47 to lower participation costs and allowed for all-or-nothing orders to avoid fragmented share portfoli

48 n density and food availability to induce an all-or-nothing organismal-wide response, but the mechani

49 uous deliberation within the network into an all-or-nothing output, after which the male will no long

50 ally processed vegetarian diets represent an all-or-nothing phenomenon and whether consuming primaril

51 r by homologous recombination (HR) is not an all-or-nothing phenomenon, but that HR competency comes

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

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

54 However, some neurons exhibit all-or-nothing plateau potentials that, once elicited, c

55 actin filaments or microtubules can exhibit all-or-nothing polymerization in a kinetically controlle

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

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

58 This domain mediates all or nothing regulation of actin assembly through an i

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

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

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

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

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

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

65 Toxoplasma gondii motility is an all-or-nothing response.

66 424 nM trans) in vitro was translated to an "all or nothing" response with complete recovery in a mur

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

68 vital properties of a neuron, including the all or nothing spiking, the threshold driven spiking of

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

70 cellular organelle allowed for finely tuned "all-or-nothing" spine-to-dendrite calcium coupling; cont

71 es allow cooperative individuals to adopt an all or nothing strategy to tie strengthening based on th

72 tolerance pathway enabled transition from an all-or-nothing survival strategy to a hormone-modulated,

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

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

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

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

77 ence (ATGATATCAT) do we recover a canonical "all-or-nothing" two-state model of hybridization/dehybri