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1 is an important target for the regulation of flagellar motility.
2 ctures play a significant role in regulating flagellar motility.
3 al microtubule assembly and/or stability and flagellar motility.
4 ctures play a significant role in regulating flagellar motility.
5 entral role in the regulation of ciliary and flagellar motility.
6 ant for C1 central microtubule stability and flagellar motility.
7  dissect individual protein contributions to flagellar motility.
8 ellar transport (IFT), and power ciliary and flagellar motility.
9 DRC mutants, the drc3 mutant has a defect in flagellar motility.
10 in Caenorhabditis elegans, but up-regulating flagellar motility.
11 y, but no centrin has been found to regulate flagellar motility.
12 optimal alignment of doublets for productive flagellar motility.
13 kely serve different functions in regulating flagellar motility.
14 emal dynein activity and thus of ciliary and flagellar motility.
15 m that plays a key role in the regulation of flagellar motility.
16 rodigiosin antibiotic, and downregulation of flagellar motility.
17 iding and attaching to prey and then ceasing flagellar motility.
18 rocesses ranging from mitosis and meiosis to flagellar motility.
19 ing molecules that are predicted to regulate flagellar motility.
20 ine the role of DegU for GmaR production and flagellar motility.
21 n axonemal CK1 regulates dynein activity and flagellar motility.
22 lia and is required for axonemal sliding and flagellar motility.
23 ADP) is known to have interesting effects on flagellar motility.
24 chment was somewhat slower in the absence of flagellar motility.
25 nd suggest that it may act in the control of flagellar motility.
26 lagellar compartment is essential for normal flagellar motility.
27  a motor protein and is essential for normal flagellar motility.
28 plex in the 9 + 2 axoneme for the control of flagellar motility.
29 CWDEs), type III secretion system (T3SS) and flagellar motility.
30 t intermediate in the pathway that regulates flagellar motility.
31 uired for DRC assembly and the regulation of flagellar motility.
32 oneme central apparatus that is required for flagellar motility.
33 egulating such processes as capacitation and flagellar motility.
34 ition to modify dynein activity and regulate flagellar motility.
35  modify the activity of the I1 dynein during flagellar motility.
36 he synthesis of exopolysaccharide; and (iii) flagellar motility.
37 Although axDHCs are integral participants in flagellar motility, a role in flagellar morphogenesis ha
38 gellates suggest the protein plays a role in flagellar motility across phyla.
39 ein, FleQ acts as a master regulator of both flagellar motility and adherence factor secretion and us
40 ced by a reduction in secretory activity and flagellar motility and an increase in adenosine triphosp
41                                    Bacterial flagellar motility and chemotaxis help cells to reach th
42                This response is dependent on flagellar motility and correlated with higher swimming s
43 athogenic mode, Sulfitobacter D7 upregulated flagellar motility and diverse transport systems, presum
44 ilm formation in the presence of bile, while flagellar motility and expression of type 1 fimbriae wer
45 role in other organisms, CsrA also regulated flagellar motility and glycogen levels.
46 y illuminates structural dynamics underlying flagellar motility and identifies pathogen-specific prot
47 rther revealed the role of the 1alpha Dhc in flagellar motility and phototactic behavior.
48 ccurs in swarmer cells and is facilitated by flagellar motility and pili.
49 inhardtii hydin is a CP protein required for flagellar motility and probably involved in the CP-radia
50  indicated that GM-CSF induced the genes for flagellar motility and pyocin production in the persiste
51 adillo repeats predicted to be important for flagellar motility and stability of the axoneme central
52 e conclude that Spag6 is essential for sperm flagellar motility and that it is important for the main
53 cess previously suggested to firstly require flagellar motility and then flagellar shedding upon prey
54 in C. difficile was recently shown to reduce flagellar motility and to increase cell aggregation.
55 gen Clostridium difficile, c-di-GMP inhibits flagellar motility and toxin production and promotes pil
56 yclic di-GMP (c-di-GMP) negatively regulates flagellar motility and, in some cases, virulence.
57 ng retrograde vesicular trafficking, ciliary/flagellar motility, and cell division.
58     The DeltaprfA mutant exhibited wild-type flagellar motility, and its biofilm defect occurred afte
59 hydin is a central pair protein required for flagellar motility, and mice with Hydin defects develop
60  which bacterial cells build their intricate flagellar motility apparatuses has long fascinated scien
61          The role of ArcZ as an activator of flagellar motility appears to be unique to E. amylovora
62 d and coordinated to produce ordered ciliary/flagellar motility, but how this is achieved is not unde
63 axoneme, plays a central role in ciliary and flagellar motility; but, its contribution to adaptive im
64  RmaA play an integral role in regulation of flagellar motility by acting primarily on the master reg
65              Furthermore, phase variation of flagellar motility by targeting flgR may be a phenomenon
66 ncodes a GTP-binding protein, is part of the flagellar-motility-chemotaxis operon.
67 RC), which is a major hub for the control of flagellar motility, contains at least 11 different subun
68               Our study of dimeric NDK5 in a flagellar motility control complex, the radial spoke (RS
69 pacitation, the transition to hyperactivated flagellar motility, develops with a similar time course
70 rther show that the underlying cause is that flagellar motility drives bacterial dispersal along the
71 that proper B-tubule closure is critical for flagellar motility, exemplifying how integrating structu
72            Deletion of podJ1 interferes with flagellar motility, exopolysaccharide production, cell e
73 In this study, we tested the contribution of flagellar motility, flagellin structure, and its glycosy
74    These studies indicate that regulation of flagellar motility gene expression and/or other genes co
75 lar pathogen that represses transcription of flagellar motility genes at physiological temperatures (
76          Temperature-dependent expression of flagellar motility genes is mediated by the opposing act
77 udies have shown that Listeria monocytogenes flagellar motility genes, including flaA, encoding flage
78                                              Flagellar motility has independently arisen three times
79                                              Flagellar motility has long been regarded as an importan
80 us and functions in a complex that regulates flagellar motility in a calcium-dependent manner.
81 ere obtained in visN and visR, activators of flagellar motility in A. tumefaciens, now found to inhib
82 nfection assays in which the requirement for flagellar motility in adherence and invasion was bypasse
83                            While the role of flagellar motility in bacterial survival has been widely
84                                              Flagellar motility in Campylobacter jejuni mediates opti
85         We propose that Ca(2+) regulation of flagellar motility in Chlamydomonas may be achieved in p
86  of the chemosensory machinery that controls flagellar motility in Escherichia coli.
87 tants have reduced swimming speed when using flagellar motility in liquid.
88                                              Flagellar motility in Listeria monocytogenes (Lm) is res
89                     Our findings reveal that flagellar motility in Lm is governed by both temperature
90 the receiver domain of DegU has no effect on flagellar motility in Lm.
91                                              Flagellar motility in Rhodobacter sphaeroides is notably
92                A qseC mutant was impaired in flagellar motility, in invasion of epithelial cells, and
93  a crucial role in regulation of ciliary and flagellar motility, including control of waveform.
94       We conclude that calcium regulation of flagellar motility involves regulation of dynein-driven
95    We previously demonstrated that bacterial flagellar motility is a fundamental mechanism by which h
96                                    Bacterial flagellar motility is among the most extensively studied
97                                              Flagellar motility is an energy-demanding process, where
98                                              Flagellar motility is an essential mechanism by which ba
99                                              Flagellar motility is an important determinant of Campyl
100                                              Flagellar motility is an important virulence factor for
101                                    Bacterial flagellar motility is controlled by the binding of CheY
102  the challenges in understanding ciliary and flagellar motility is determining the mechanisms that lo
103                                              Flagellar motility is generated by the activity of multi
104      Results of mutant studies indicate that flagellar motility is involved in the observed preferenc
105  of YFP-labelled prey bacteria, showing that flagellar motility is not essential for prey entry but i
106                                  Ciliary and flagellar motility is regulated by changes in intraflage
107                                              Flagellar motility is seen in various parasitic protozoa
108  were selected in a screen for Chlamydomonas flagellar motility mutations.
109                                              Flagellar motility of Campylobacter jejuni and Helicobac
110  library identified 28 mutants defective for flagellar motility, one of the few known virulence deter
111  simple means to prevent steric hindrance of flagellar motility or to ensure that phage-mediated gene
112 ed rice genes, type II secretion competence, flagellar motility, or resistance to two phytoalexins or
113 ass of motor protein involved in ciliary and flagellar motility, organelle transport, and chromosome
114                    Regulation of ciliary and flagellar motility requires spatial control of dynein-dr
115                After septation, Bdellovibrio flagellar motility resumes inside the prey bdelloplast p
116 face, or epiphytic, sites specifically favor flagellar motility, swarming motility based on 3-(3-hydr
117  complex (N-DRC), a key regulator of ciliary/flagellar motility that is conserved from algae to human
118                            Unlike ciliary or flagellar motility, the biophysics of this mode is not w
119 expansion such as B-vitamin biosynthesis and flagellar motility to be mapped to the phylogeny.
120     Helicobacter pylori has evolved distinct flagellar motility to colonize the human stomach.
121 ylori, and Bartonella bacilliformis, require flagellar motility to efficiently infect mammalian hosts
122 ry bacterium Bdellovibrio bacteriovorus uses flagellar motility to locate regions rich in Gram-negati
123    To reach these openings, the bacteria use flagellar motility to swim from stigma tips to the hypan
124                               Interestingly, flagellar motility was abolished in the ssaI and ssaR mu
125 had defects in both phototactic behavior and flagellar motility were identified and characterized.
126                           Sp-AK activity and flagellar motility were studied using demembranated sper

 
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