ライフサイエンスコーパス: flagellar motility

1 ant for C1 central microtubule stability and flagellar motility.

2 y, but no centrin has been found to regulate flagellar motility.

3 optimal alignment of doublets for productive flagellar motility.

4 entral role in the regulation of ciliary and flagellar motility.

5 kely serve different functions in regulating flagellar motility.

6 emal dynein activity and thus of ciliary and flagellar motility.

7 m that plays a key role in the regulation of flagellar motility.

8 iding and attaching to prey and then ceasing flagellar motility.

9 rocesses ranging from mitosis and meiosis to flagellar motility.

10 ing molecules that are predicted to regulate flagellar motility.

11 ine the role of DegU for GmaR production and flagellar motility.

12 n axonemal CK1 regulates dynein activity and flagellar motility.

13 lia and is required for axonemal sliding and flagellar motility.

14 ADP) is known to have interesting effects on flagellar motility.

15 chment was somewhat slower in the absence of flagellar motility.

16 nd suggest that it may act in the control of flagellar motility.

17 lagellar compartment is essential for normal flagellar motility.

18 a motor protein and is essential for normal flagellar motility.

19 plex in the 9 + 2 axoneme for the control of flagellar motility.

20 t intermediate in the pathway that regulates flagellar motility.

21 uired for DRC assembly and the regulation of flagellar motility.

22 oneme central apparatus that is required for flagellar motility.

23 egulating such processes as capacitation and flagellar motility.

24 DRC mutants, the drc3 mutant has a defect in flagellar motility.

25 ition to modify dynein activity and regulate flagellar motility.

26 modify the activity of the I1 dynein during flagellar motility.

27 he synthesis of exopolysaccharide; and (iii) flagellar motility.

28 is an important target for the regulation of flagellar motility.

29 ctures play a significant role in regulating flagellar motility.

30 al microtubule assembly and/or stability and flagellar motility.

31 ctures play a significant role in regulating flagellar motility.

32 Although axDHCs are integral participants in flagellar motility, a role in flagellar morphogenesis ha

33 gellates suggest the protein plays a role in flagellar motility across phyla.

34 ced by a reduction in secretory activity and flagellar motility and an increase in adenosine triphosp

35 Bacterial flagellar motility and chemotaxis help cells to reach th

36 ilm formation in the presence of bile, while flagellar motility and expression of type 1 fimbriae wer

37 role in other organisms, CsrA also regulated flagellar motility and glycogen levels.

38 rther revealed the role of the 1alpha Dhc in flagellar motility and phototactic behavior.

39 ccurs in swarmer cells and is facilitated by flagellar motility and pili.

40 inhardtii hydin is a CP protein required for flagellar motility and probably involved in the CP-radia

41 indicated that GM-CSF induced the genes for flagellar motility and pyocin production in the persiste

42 adillo repeats predicted to be important for flagellar motility and stability of the axoneme central

43 e conclude that Spag6 is essential for sperm flagellar motility and that it is important for the main

44 cess previously suggested to firstly require flagellar motility and then flagellar shedding upon prey

45 in C. difficile was recently shown to reduce flagellar motility and to increase cell aggregation.

46 gen Clostridium difficile, c-di-GMP inhibits flagellar motility and toxin production and promotes pil

47 yclic di-GMP (c-di-GMP) negatively regulates flagellar motility and, in some cases, virulence.

48 ng retrograde vesicular trafficking, ciliary/flagellar motility, and cell division.

49 The DeltaprfA mutant exhibited wild-type flagellar motility, and its biofilm defect occurred afte

50 hydin is a central pair protein required for flagellar motility, and mice with Hydin defects develop

51 d and coordinated to produce ordered ciliary/flagellar motility, but how this is achieved is not unde

52 axoneme, plays a central role in ciliary and flagellar motility; but, its contribution to adaptive im

53 Furthermore, phase variation of flagellar motility by targeting flgR may be a phenomenon

54 ncodes a GTP-binding protein, is part of the flagellar-motility-chemotaxis operon.

55 RC), which is a major hub for the control of flagellar motility, contains at least 11 different subun

56 Our study of dimeric NDK5 in a flagellar motility control complex, the radial spoke (RS

57 pacitation, the transition to hyperactivated flagellar motility, develops with a similar time course

58 Deletion of podJ1 interferes with flagellar motility, exopolysaccharide production, cell e

59 In this study, we tested the contribution of flagellar motility, flagellin structure, and its glycosy

60 These studies indicate that regulation of flagellar motility gene expression and/or other genes co

61 lar pathogen that represses transcription of flagellar motility genes at physiological temperatures (

62 Temperature-dependent expression of flagellar motility genes is mediated by the opposing act

63 udies have shown that Listeria monocytogenes flagellar motility genes, including flaA, encoding flage

64 Flagellar motility has long been regarded as an importan

65 us and functions in a complex that regulates flagellar motility in a calcium-dependent manner.

66 ere obtained in visN and visR, activators of flagellar motility in A. tumefaciens, now found to inhib

67 nfection assays in which the requirement for flagellar motility in adherence and invasion was bypasse

68 Flagellar motility in Campylobacter jejuni mediates opti

69 We propose that Ca(2+) regulation of flagellar motility in Chlamydomonas may be achieved in p

70 Flagellar motility in Listeria monocytogenes (Lm) is res

71 Our findings reveal that flagellar motility in Lm is governed by both temperature

72 the receiver domain of DegU has no effect on flagellar motility in Lm.

73 Flagellar motility in Rhodobacter sphaeroides is notably

74 A qseC mutant was impaired in flagellar motility, in invasion of epithelial cells, and

75 a crucial role in regulation of ciliary and flagellar motility, including control of waveform.

76 We conclude that calcium regulation of flagellar motility involves regulation of dynein-driven

77 We previously demonstrated that bacterial flagellar motility is a fundamental mechanism by which h

78 Bacterial flagellar motility is among the most extensively studied

79 Flagellar motility is an essential mechanism by which ba

80 Flagellar motility is an important determinant of Campyl

81 Flagellar motility is an important virulence factor for

82 the challenges in understanding ciliary and flagellar motility is determining the mechanisms that lo

83 Flagellar motility is generated by the activity of multi

84 Results of mutant studies indicate that flagellar motility is involved in the observed preferenc

85 of YFP-labelled prey bacteria, showing that flagellar motility is not essential for prey entry but i

86 Ciliary and flagellar motility is regulated by changes in intraflage

87 were selected in a screen for Chlamydomonas flagellar motility mutations.

88 Flagellar motility of Campylobacter jejuni and Helicobac

89 library identified 28 mutants defective for flagellar motility, one of the few known virulence deter

90 simple means to prevent steric hindrance of flagellar motility or to ensure that phage-mediated gene

91 ed rice genes, type II secretion competence, flagellar motility, or resistance to two phytoalexins or

92 ass of motor protein involved in ciliary and flagellar motility, organelle transport, and chromosome

93 Regulation of ciliary and flagellar motility requires spatial control of dynein-dr

94 After septation, Bdellovibrio flagellar motility resumes inside the prey bdelloplast p

95 face, or epiphytic, sites specifically favor flagellar motility, swarming motility based on 3-(3-hydr

96 complex (N-DRC), a key regulator of ciliary/flagellar motility that is conserved from algae to human

97 Unlike ciliary or flagellar motility, the biophysics of this mode is not w

98 ylori, and Bartonella bacilliformis, require flagellar motility to efficiently infect mammalian hosts

99 ry bacterium Bdellovibrio bacteriovorus uses flagellar motility to locate regions rich in Gram-negati

100 Interestingly, flagellar motility was abolished in the ssaI and ssaR mu

101 had defects in both phototactic behavior and flagellar motility were identified and characterized.

102 Sp-AK activity and flagellar motility were studied using demembranated sper