ライフサイエンスコーパス: autoinduction

1 naling events that are required for TGFbeta1 autoinduction.

2 ii) reveal the origin of stereochemistry and autoinduction.

3 in a wild-type strain due to the absence of autoinduction.

4 as to examine the mechanism of PTC TGF-beta1 autoinduction.

5 significant induction period consistent with autoinduction.

6 oduce the optimum level of OmpR-P needed for autoinduction.

7 eta release, an amplification process termed autoinduction.

8 vels, possibly caused by enzyme induction or autoinduction.

9 o that present in 6TG1.1 cells after 18 h of autoinduction.

10 ng lacZ fused to a gene that is regulated by autoinduction.

11 ncreased only threefold in vivo during phoPR autoinduction, a role for unphosphorylated PhoP in Pho r

12 These findings demonstrate that both autoinduction and autorepression play critical and oppos

13 to the receptor is potentially amplified by autoinduction and cross-signaling through epidermal grow

14 arthritis by using IL-1R antagonist to block autoinduction and IL-1alpha stimulation to simulate auto

15 from LPS-stimulated cells is attributable to autoinduction and that GLA reduces autoinduction of IL-1

16 e examined group-specific differences in agr autoinduction and virulence gene regulation by utilizing

17 up-regulation of T(3) receptor beta (TRbeta; autoinduction) and BTEB1 (basic transcription element-bi

18 uxIR QS system produces an 'outward wave' of autoinduction, and the Lsr QS system yields dispersed au

19 in adenosine receptors, and adenosine-IL-13 autoinduction are critical events in IL-13-induced patho

20 providing insight into the dynamics of this autoinduction behaviour.

21 th the TrbetaA promoter in vivo and enhances autoinduction, but this action does not depend on its DN

22 anscription of nisABTCIP and nisFEG requires autoinduction by external nisin via signal transducing b

23 Ms, a process that is partially dependent on autoinduction by IL-1.

24 Opines control autoinduction by regulating the expression of traR.

25 ological noise present in the quorum-sensing autoinduction circuit and ensures that ICEMlSym(R7A) tra

26 factor (VEGF) interact in a newly described autoinduction circuit, in which each of these cytokines

27 tion, and the Lsr QS system yields dispersed autoinduction from spatially-localized secretion and upt

28 Enantioselective autoinduction has also been reported for the process.

29 ucidation of cAMP-CRP involvement in E. coli autoinduction impacts many areas, including the growth o

30 dspI was shown to abolish biofilm dispersion autoinduction in continuous cultures of P. aeruginosa an

31 isopropyl beta-D-thiogalactopyranoside-free autoinduction in Escherichia coli.

32 e we examined the role of km23-1 in TGFbeta1 autoinduction in TGFbeta-sensitive epithelial cells.

33 In many gram-negative bacteria, autoinduction involves the production of and response to

34 Thus, the role of OmpR-P in autoinduction is to help to counteract repression by H-N

35 The autoinduction leads to a maximum 4-fold signal enhanceme

36 GPC1 may trigger the Skp2 autoinduction loop at least partially by suppressing p21

37 degradation of p27 is in the formation of an autoinduction loop that selectively controls the transit

38 kely that GPC1 stimulates the so-called Skp2 autoinduction loop, independent of cyclin D-CDK4/6.

39 y by activating the mitogen-independent Skp2 autoinduction loop.

40 Thus, reduction of IL-1beta autoinduction may be protective in some patients with en

41 ubunits (CylL(S)'') through a quorum-sensing autoinduction mechanism.

42 We report an autoinduction methodology that provides soluble cruzain

43 Growth factor autoinduction of cleavage could be stimulated by several

44 Previous suggestions of autoinduction of drug metabolism were not confirmed by t

45 receptor blockade reduces the IL-1-mediated autoinduction of IL-1, reduces the expression of ICAM-1

46 utable to autoinduction and that GLA reduces autoinduction of IL-1beta while leaving the initial IL-1

47 No autoinduction of metabolism was observed with dosing ove

48 Autoinduction of MIP-2 and KC mRNA was also noted.

49 ed cell growth, indicating that there was no autoinduction of production of ComX pheromone.

50 After 4 h, autoinduction of RANTES transcripts was observed.

51 er treatment with exogenous bFGF, suggesting autoinduction of the cytokine.

52 servations form the basis of a model for the autoinduction of the cytolysin by a quorum-sensing mecha

53 hat MisR phosphorylation is critical for the autoinduction of the misRS operon.

54 ion to investigate how estrogens repress the autoinduction of the TNFalpha gene.

55 XTC-2 cells caused accelerated and enhanced autoinduction of the TrbetaA gene.

56 dulates the acyl-homoserine lactone-mediated autoinduction of Ti plasmid conjugative transfer by inte

57 or the clinically important oxazaphosphorine autoinduction pharmacokinetics seen with these drugs in

58 iA, exhibiting features characteristic of an autoinduction (quorum sensing) mechanism.

59 eas induction of c-fos, Smad7, and TGF-beta1 autoinduction relied on expression of Smad3.

60 In summary, in PTCs, TGF-beta1 autoinduction requires the coordinated action of indepen

61 d in the extracellular matrix and acts as an autoinduction signal to stimulate neighboring cells to p

62 ctones (acyl-HSLs) that act as intercellular autoinduction signals.

63 alter the activity of the protein on TrbetaA autoinduction, suggesting that BTEB1 can function in thi

64 uction system is controlled both by a second autoinduction system and by the RpoS(Rso) sigma factor.

65 The acyl-HSL-dependent autoinduction system in R. solanacearum is part of a mor

66 e, in R. solanacearum the acyl-HSL-dependent autoinduction system is controlled both by a second auto

67 This acyl-HSL-dependent autoinduction system is noteworthy because (i) it is reg

68 AW1 has a functional autoinduction system, because (i) expression of solI req

69 Bacteria employ autoinduction systems to sense the onset of appropriate

70 uction and IL-1alpha stimulation to simulate autoinduction that approximately 40% of IL-1beta release

71 To assess reversible CYP3A4 autoinduction, the expanded part of the study tested thr

72 Thus, while quorum sensing is dependent upon autoinduction, the two phenomena are not synonymous.

73 ndicate that km23-1 is required for TGFbeta1 autoinduction through Smad2-independent Ras/ERK/JNK path

74 ulated IL-33 receptors and facilitated IL-33 autoinduction, thus establishing a feed-forward circuit.

75 egulated in Lactococcus lactis ATCC 11454 by autoinduction via a two-component NisRK-mediated system.

76 m Agrobacterium tumefaciens is controlled by autoinduction via the transcriptional activator TraR and