ライフサイエンスコーパス: futile cycle

1 back to cysteine sulfinic acid and AMP in a futile cycle.

2 sterol actively effluxed by ABC1, creating a futile cycle.

3 t bifunctional activities without creating a futile cycle.

4 coli, these functions are separated to avoid futile cycling.

5 d neutral invertase, associated with minimal futile cycling.

6 omote uncoupling of the Serca pump and cause futile cycling.

7 t they are coordinately regulated to prevent futile cycling.

8 gulate an activated FBPase in order to avoid futile cycling?

9 -AT target genes, as NF-ATs are subject to a futile cycling across the nuclear envelope owing to enga

10 This apparent futile cycle allows eggs to maintain elevated cytoplasmi

11 k(HR) estimates glucose/glucose-6-phosphate futile cycling, along with glucose recycling through the

12 embrane domains MalF and MalG that generated futile cycling; although interaction with MBP stimulated

13 yeast glycolysis and the coupled pathways of futile cycling and glycogen and trehalose synthesis (whi

14 birth-death process, an example of enzymatic futile cycle, and a stochastic switch model.

15 xperimental conditions and identified a high futile cycle between oxaloacetate and pyruvate, indicati

16 duction of beta-lapachone by NQO1 leads to a futile cycling between the quinone and hydroquinone form

17 tose-binding site of MalF likely generated a futile cycle by preventing maltose from binding to MalFG

18 Calcineurin suppresses this futile cycling by a non-catalytic mechanism involving th

19 Further experiments confirmed this futile cycle; cells without FepB transported FeEnt acros

20 To avoid infinite futile cycles, folded LRP6 molecules undergo palmitoylat

21 Our studies reveal that the zebrafish gene futile cycle (fue) is required in the zygote for male pr

22 This protein is related to zebrafish futile cycle (Fue), a nuclear envelope (NE) constituent

23 The zebrafish futile cycle gene is shown to encode a maternally expres

24 ed ultrasensitivity in a kinase/phosphatase "futile cycle" has been a paradigmatic example of collect

25 osphate-1-kinase coupled with the absence of futile cycling implies an undetermined mechanism of coor

26 on of alternative electron flow pathways and futile cycles in energy rebalancing.

27 urthermore, the ED pathway does not generate futile cycles in organisms that fix CO2 via the Calvin-B

28 and histochemical measurements, we show that futile cycling in roots of barley (Hordeum vulgare) seed

29 emingly opposed functions and explains how a futile cycle is avoided-cytoplasmic p300/CBP E4 activiti

30 evious reported noise-induced bistability in futile cycles is found to have originated from the kinas

31 ional functional modalities on the enzymatic futile cycle mechanism that include stochastic amplifica

32 ell maintenance costs, in agreement with the futile cycling model of ammonium toxicity.

33 Our study fundamentally revises the futile-cycling model by demonstrating that NH3 is the ma

34 this phenomenon is not exclusively due to a futile cycle of abortive TLS followed by exonucleolytic

35 involvement of the proofreading subunit in a futile cycle of base insertion/excision with the UmuC st

36 presence of free fatty acids and leads to a futile cycle of Ca(2+) accumulation and release when exo

37 ir target biosynthetic machinery involving a futile cycle of cell wall synthesis and degradation, the

38 persist to the next cell cycle, leading to a futile cycle of centriole formation and disintegration.

39 These findings link a futile cycle of creatine metabolism to adipose tissue en

40 e metabolic signature of WAT by activating a futile cycle of de novo fatty acid synthesis and beta-ox

41 iglycerides to the liver, which results in a futile cycle of enhanced VLDL production and increased k

42 AC3 regulates WAT metabolism by activating a futile cycle of fatty acid synthesis and oxidation, whic

43 rom the gluconeogenic process and prevents a futile cycle of glucose phosphorylation.

44 gulatory role of GltC may be prevention of a futile cycle of glutamate synthesis and degradation in t

45 s the mitochondrial inner membrane, create a futile cycle of nutrient oxidation without generating AT

46 sequence are not cleaved, thereby avoiding a futile cycle of removal and readdition of these essentia

47 erted to PC and TAG, and appeared to be in a futile cycle of synthesis and degradation.

48 f enduring lipid droplets that prevented the futile cycle of TAG biosynthesis/lipolysis and instead c

49 Collectively, the data reveal a futile cycle of unregulated transcription, siRNA product

50 flux systems, protects cells from continuous futile cycles of Ca(2+) across the inner mitochondrial m

51 Subsequent futile cycles of DNA mismatch repair can lead to a p53-a

52 Viomycin inhibition also promotes futile cycles of GTP hydrolysis by EF-G.

53 We suggest that these result from futile cycles of recombinational elongation and truncati

54 d therefore to drug resistance by preventing futile cycles of translesion synthesis and mismatch corr

55 It is hypothesized that futile cycles of translesion synthesis past cisplatin-DN

56 e that adipocytes lack GyK and thereby avoid futile cycles of triglyceride breakdown and resynthesis

57 iggering transcription-coupled repair (TCR), futile cycles of which may lead to repeat expansion or c

58 e turnover and suggesting that CD36 promotes futile cycling of fatty acids into triglyceride.

59 In conclusion, high futile cycling of fatty acids is important for maintaini

60 Elevated futile cycling of hepatic lipids was also observed.

61 By this mechanism, SLN promotes the futile cycling of SERCA, contributing to muscle heat pro

62 2014) report that memory T cells activate a "futile cycle" of de novo fatty-acid synthesis and concur

63 MMR-mediated damage tolerance and futile cycle repair processes are discussed, as well as

64 3R calcium channel leads to an ATP-depleting futile cycle, resulting in activation of the energy sens

65 te in the protocol but was timed to minimize futile cycling, since phosphorylase a became inhibited b

66 rate, can decompose to produce H(2)O(2) in a futile cycle that consumes NADPH.

67 which inhibit modularity, through enzymatic futile cycles that consume energy, typically in the form

68 This led to futile cycling the LLO pathway, exacerbated by GDP-manno

69 (bio)chemical-reaction mechanisms, enzymatic futile cycles, the external noise may induce a bistable

70 w that a single-player system may escape the futile cycle trap by limiting transfer of reducing equiv

71 malate into oil is low and that flux through futile cycles (wasting ATP) is low, which contrasts with

72 c regulatory properties for the formation of futile cycles were further considered in the model, resu

73 rylation of X-5-P by Pho13p might generate a futile cycle with xylulokinase overexpression.

74 which has implications for the coherence of futile cycles within an integrated tissue.