ライフサイエンスコーパス: nonmotile

1 hment to surfaces and were almost completely nonmotile.

2 few or no flagella and are poorly motile or nonmotile.

3 lonies, and individual cells were completely nonmotile.

4 Moreover, the flagella in mutant sperm are nonmotile.

5 te into a cargo binding primed state that is nonmotile.

6 ated cells and aglZ sglK double mutants were nonmotile.

7 motY and motCD mutations rendered the cells nonmotile.

8 lonies, and individual cells were completely nonmotile.

9 ain PAO1 was constructed and was shown to be nonmotile.

10 haracterized invasion-deficient mutants were nonmotile.

11 w), while bacteria grown at 37 degrees C are nonmotile.

12 km, which produced neither flagellin and was nonmotile.

13 tectable in the uninflamed dermis, most were nonmotile.

14 These mutants are nonmotile.

15 ction as anion exchangers but are apparently nonmotile.

16 s reports have concluded that H. volcanii is nonmotile.

17 In contrast, single nonmotile 9 + 0 primary cilia are found on epithelial ce

18 Although myosin-XXI dimers might act as nonmotile actin cross-linkers, the calmodulin-binding mo

19 We isolated an asporogenous, nonmotile, aerobic gram-positive rod from a transplant r

20 o surfaces and to improve nutrient uptake by nonmotile and attached cells.

21 Despite their utility, these cell lines are nonmotile and cannot build polarized structures or cell-

22 to wild-type ES4326, ES4326 rpoN::Km(r) was nonmotile and could not utilize nitrate, urea, C(4)-dica

23 Mutants in the Tax3 locus are nonmotile and do not make type IV pili.

24 7; however, clinical isolates are frequently nonmotile and do not produce detectable H antigen.

25 FliL- mutants are nonmotile and fail to synthesize flagellin, while comple

26 The hp0958:aphA3 mutant was nonmotile and failed to produce flagella.

27 The mutants were nonmotile and had deletions of various lengths beginning

28 t II-3 is unable to attach to host cells and nonmotile and has a branched cellular morphology compare

29 However, a strain null for taxAY1 was nonmotile and hyperpiliated.

30 rain containing a single mutation in flaA is nonmotile and lacks a flagellum, while strains containin

31 , we found that uninjured podocytes remained nonmotile and maintained a canopy-shaped structure over

32 In eukaryotes, both nonmotile and motile cilia possess sensory functions.

33 This mutant was also nonmotile and nonadhesive.

34 Consequently, nonmotile and nonchemotactic mutants are susceptible to

35 the paradigm which held that S. pullorum is nonmotile and nonflagellated, motility can be induced in

36 pathogen of poultry previously thought to be nonmotile and nonflagellated.

37 Overall, the nonmotile and nonmotile/quorum-sensing-deficient mutants

38 All strains were nonmotile and nonpigmented.

39 ormation of highly clonogenic cells that are nonmotile and prone to undergo apoptosis.

40 We find that stimulation of nonmotile and quiescent cells with growth factors or ECM

41 ve a flat-wave morphology, mutant cells were nonmotile and rod shaped.

42 55 selected by the intestine are shown to be nonmotile and to have deletions in the flhDC operon, whi

43 STEC serotype found was O91:NM (NM indicates nonmotile), and others included O128:NM, O88:NM, O6:H49,

44 nts display membrane-associated defects, are nonmotile, and are unable to form an optimal symbiosis w

45 eletion of rpoN rendered V. parahaemolyticus nonmotile, and it caused reduced biofilm formation and a

46 h an incomplete O-antigen, mutants that were nonmotile, and mutants deficient in quorum sensing were

47 obacillary to rod-shaped, catalase positive, nonmotile, and nonlipophilic.

48 ty, is gram-negative, aerobic, coccobacilli, nonmotile, and nonspore forming bacteria.

49 m, which expressed FlaB but not FlaA and was nonmotile; and N6flaA::cat/flaB::km, which produced neit

50 lity than the wild type; the motAB mutant is nonmotile; and the cheW and cheY mutants are motile but

51 Primary cilia are single, nonmotile, antenna-like structures extending from the ap

52 for polycystin-2 proteins in both motile and nonmotile axonemal-containing structures.

53 ta C and wild-type beta 2-tubulin results in nonmotile axonemes because of a disruption of the period

54 on loss by 18 hours after infection, whereas nonmotile B. thuringiensis infections required 30 hours

55 s were performed with flagellated motile and nonmotile bacteria and nonflagellated bacteria.

56 We observed that flagellated but nonmotile bacteria do not adhere to or invade human epit

57 ch mice were infected orally with motile and nonmotile bacteria in a 1:1 ratio.

58 demonstrated that motile bacteria outcompete nonmotile bacteria in the colonization of the intestines

59 easurements are performed on both motile and nonmotile bacteria.

60 report direct experimental evidence that the nonmotile bacterium Staphylococcus aureus possesses a ta

61 tile (Cytophaga hutchinsonii) and apparently nonmotile (Bacteroides thetaiotaomicron, Bacteroides fra

62 The nonmotile BRUME also carries many flagellar genes but th

63 chanism can impart motility to aggregates of nonmotile but active bacteria; we show that SSB in this

64 o strongly express arginine kinase; they are nonmotile but are undergoing repeated rounds of (ATP-dep

65 flaA (flaB+) filament mutant was found to be nonmotile but Cia protein secretion competent (Mot-, S+)

66 cted and characterized a motB mutant that is nonmotile but retains its periplasmic flagella.

67 esponses, we compared in two animal models a nonmotile, but flagellin-expressing and -secreting serot

68 M. pneumoniae HA mutant II-3 lacking P30 was nonmotile, but HA mutant II-7 producing a truncated P30

69 k such complex adhesion systems and are also nonmotile, but they are shown here to dynamically evolve

70 The resulting flaB mutants not only were nonmotile, but were rod-shaped.

71 ice and between 80 and 90% of the cells were nonmotile by day 15 after feeding.

72 strain MG1655, 45 to 50% of the cells became nonmotile by day 3 after feeding of the strain to mice a

73 Analysis of the invasive ability of a nonmotile C. jejuni 11168H rpoN mutant in the VDC model

74 In the nonmotile case, we obtain the power spectrum of the magn

75 hat this depends on primary cilia, which are nonmotile, cell-surface structures that serve as platfor

76 ing in an increase in the ratio of motile to nonmotile cells and in the succession of populations.

77 traction force patterns of small clusters of nonmotile cells and larger sheets of motile Madin-Darby

78 rugated surfaces, in stark contrast to where nonmotile cells attach.

79 These results indicate that in nonmotile cells dynamic actin filaments can function to

80 Nonmotile cells extend and retract pseudopodia-like stru

81 How nonmotile cells might filter out noise is unknown.

82 te that assembly of some actin structures in nonmotile cells of multicellular organisms utilizes the

83 noise filtering by time averaging, allowing nonmotile cells to track shallow gradients.

84 tal observations in trypsinized cells and in nonmotile cells transfected with Prestin.

85 tingly, we also found that a small number of nonmotile cells were sufficient to block the swarming be

86 ore than 1000-fold faster than in most other nonmotile cells where this property has been measured.

87 talked-cell transition and form flagellated, nonmotile cells, also fail to localize DivJ.

88 d on the observation that Myxococcus xanthus nonmotile cells, by a Tra-dependent mechanism, block swa

89 Mark broadening is also observed in nonmotile cells, indicating that this aspect of transpor

90 ence show that, compared with MTs in control nonmotile cells, MT turnover is increased twofold in the

91 to a 4-fold nutrient exposure compared with nonmotile cells.

92 ls became highly aligned, and can even align nonmotile cells.

93 fastest 20% of the population compared with nonmotile cells.

94 tact inhibition in which a nonproliferative, nonmotile cellular state is achieved once stable interce

95 d that ectopic expression of FleQ in mucoid, nonmotile CF isolates restored flagellum biosynthesis an

96 protofilament ribbon-associated proteins in nonmotile cilia and cellular signaling have not been inv

97 d to be required for transport in motile and nonmotile cilia and flagella where it is essential for p

98 ow that PACRG localizes to a small subset of nonmotile cilia in Caenorhabditis elegans, suggesting an

99 Nonmotile cilia on olfactory sensory neurons (OSNs) comp

100 ut has not been extensively investigated for nonmotile cilia or for sensory cilia such as vertebrate

101 For years these nonmotile cilia were considered evolutionary remnants of

102 Here we investigate the nonmotile ciliary signaling roles of parkin coregulated

103 drome (BBS), a monogenic autosomal recessive nonmotile ciliopathy, as an archetypal condition.

104 imental evidence indicates that the primary, nonmotile cilium is a mechanosensory organelle in severa

105 Most neurons possess a single, nonmotile cilium that projects out from the cell surface

106 A nonmotile clone of sorbitol-fermenting O157 has rapidly

107 ng indicated that the wild-type flaB gene in nonmotile clones was present in the introduced extrachro

108 is and thereby gain a fitness advantage over nonmotile competitors.

109 Primary cilia were the largely neglected nonmotile counterparts of their better-known cousin, the

110 ents of plus-end-directed motor proteins and nonmotile cross-linker proteins are needed to explain th

111 nstrate, with the use of motile and isogenic nonmotile deletion mutants of two independent strains of

112 Throughout IBC formation, nonmotile DeltafliC mutants achieved the same number of

113 tudies determined that the presence of these nonmotile DeltamotB cells has no effect on the clearance

114 t SAHH, which is diffuse in the cytoplasm of nonmotile Dictyostelium amoebae and human neutrophils, c

115 In the absence of calmodulin, nonmotile dimers that cross-linked actin filaments were

116 ocal adhesions in normally non-ECM-adherent, nonmotile Drosophila S2 cells.

117 European Escherichia coli O157:H- isolate is nonmotile due to a 12-bp deletion in the flagellar regul

118 nt carbon sources than the wild type and was nonmotile due to deletion of the flhD gene.

119 In experiments on nonmotile E. coli exposed to polymyxin B, cell-generated

120 55 mutants with improved colonizing ability: nonmotile E. coli MG1655 flhDC deletion mutants that gre

121 PCR analysis of several nonmotile E. coli O157 strains from various geographical

122 to confirm the species identification of two nonmotile E. gallinarum isolates which had been previous

123 two EPEC O55:H7 (SOR(+) GUD(+)) strains, two nonmotile EHEC O157:H(-) strains (SOR(+) GUD(+)) contain

124 hemorrhagic Escherichia coli O157:H7 or O157:nonmotile (EHEC O157) in feces and on hides within group

125 de fruiting bodies differentiate into round, nonmotile, environmentally resistant spores.

126 odel system consisting of two populations of nonmotile Escherichia coli bacteria competing within ope

127 phimurium flagellar motor, overproduced in a nonmotile Escherichia coli host, has revealed a variatio

128 treptomycin-treated mouse intestine selected nonmotile Escherichia coli MG1655 flhDC deletion mutants

129 he entire cell periphery in serum-starved or nonmotile fibroblasts.

130 with Edwardsiella piscicida, while atypical nonmotile fish-pathogenic E. tarda isolates are equivale

131 We recently reported that a nonmotile flaB mutant that lacks periplasmic flagella is

132 id not lead to functional restoration of the nonmotile flaB null mutant.

133 ht-organ morphogenesis even when placed in a nonmotile flaJ mutant that cannot infect the light-organ

134 Myo1p localizes to nonmotile foci that cluster in sterol-rich plasma membra

135 NP-A with little or no phosphorylated H3 and nonmotile fragments that contain exclusively phosphoryla

136 sinking speed, and this may explain why some nonmotile genera are rod-like.

137 mean length of 0.8 micron, whereas 18 of 94 nonmotile genera are smaller.

138 spherical and have larger axial ratios than nonmotile genera.

139 These filaments are absent in cells of a nonmotile gldF mutant but are restored upon expression o

140 Pasteurella multocida is a small nonmotile gram-negative coccobacillus that is found in t

141 a pertussis and Bordetella parapertussis are nonmotile human pathogens, while Bordetella bronchisepti

142 V. cholerae flhF and flhG mutants appeared nonmotile in a soft agar assay.

143 ococcus faecium isolates were observed to be nonmotile in all media and by the direct microscopic met

144 we found that R. solanacearum is essentially nonmotile in planta, although it can be highly motile in

145 bacteria which were hyperfimbriated but were nonmotile in soft agar.

146 detect motility in 40 isolates that appeared nonmotile in the motility media investigated.

147 irmed that organisms previously described as nonmotile, including Croceibacter atlanticus, "Gramella

148 of the gldNO deletion mutant were completely nonmotile, indicating that cells require GldN, or the Gl

149 r, like its wild-type parent, it was largely nonmotile inside plants.

150 Capsid was also found in larger nonmotile internal structures that colocalized with cell

151 To further characterize nonmotile isolates (designated NM), we developed a PCR-r

152 namics in live cells suggests that KinG is a nonmotile kinesin that promotes the pausing of SHR-assoc

153 iosis requires the proper function of NOD, a nonmotile kinesin-10.

154 Nod, a nonmotile kinesin-like protein, plays a critical role in

155 or not the microbes produced flagellin, all nonmotile L. pneumophila mutants bound BMM less efficien

156 A fliX null mutant is nonmotile, lacks a flagellum, and exhibits a marked cell

157 was confirmed by showing that the mutant is nonmotile, lacks flagella, is attenuated in mice, and do

158 competent in causing aggressive motility in nonmotile MCF-10A human breast cells (with endogenous AT

159 pha (PKCalpha) was previously shown to endow nonmotile MCF-10A human breast cells with aggressive mot

160 Primary cilia are nonmotile microtubule structures that assemble from basa

161 ese mutants retain flagella (Fla(+)) but are nonmotile (Mot(-)).

162 affected filament assembly were found to be nonmotile (Mot-) and did not secrete Cia proteins (S-),

163 distinct cell types: motile individuals and nonmotile multicellular chains.

164 Controls with limited nutrient flux and a nonmotile mutant (Delta flag) show that cells cannot col

165 e plasmid vector control, or an fliC mutant (nonmotile mutant control).

166 blood mononuclear cells, while its isogenic nonmotile mutant lacking PF resulted in significantly di

167 describe isolation and characterization of a nonmotile mutant of B. cepacia with reduced invasiveness

168 In a previous study, we identified a nonmotile mutant of C. jejuni 81-176 with a transposon i

169 We complemented a nonmotile mutant of F. johnsoniae (UW102-09) with a libr

170 aerobe that is chemotactic to oxygen, and a nonmotile mutant of the alga Chlamydomonas reinhardtii,

171 Complementation of the nonmotile mutant UW102-48 identified another gene, gldJ,

172 vitro assays, the genetically characterized nonmotile mutant was found to be internalized by culture

173 Internalization of the nonmotile mutant was increased significantly (14- to 21-

174 ain between confined birds was modest, but a nonmotile mutant was less able to spread between birds.

175 ate the tissue layers effectively, whereas a nonmotile mutant was unable to overcome the tissue barri

176 Deletion of fliG resulted in a nonmotile mutant with a markedly decreased number of fla

177 In contrast, a nonmotile mutant with unpowered flagella was clearly deb

178 R1 was isolated as a spontaneously occurring nonmotile mutant, and HL51 was isolated as a site-direct

179 d virulence indistinguishable from that of a nonmotile mutant, demonstrating that directed motility,

180 ion of terminal organelles was impaired in a nonmotile mutant, indicating a requirement for gliding i

181 In general, nonmotile mutants displayed few or no defects in intesti

182 All nonmotile mutants examined, including those with inserti

183 In contrast, nonmotile mutants exhibited autoagglutination under grow

184 Demonstrating the utility of the system, six nonmotile mutants from a total of nine exhibited inserti

185 Ten nonmotile mutants isolated from mice were sequenced, and

186 have tested this system in the isolation of nonmotile mutants of C. jejuni.

187 rates) and spontaneous or transposon-induced nonmotile mutants of strain 0395 were obtained.

188 A large number of nonmotile mutants of the gliding bacterium Flavobacteriu

189 y into 50 spontaneous and chemically induced nonmotile mutants restored motility to each of them, sug

190 -negative mutants were avirulent whereas the nonmotile mutants showed no loss of virulence.

191 Complementation of the nonmotile mutants UW102-41, UW102-85, and UW102-92 ident

192 Both nonmotile mutants were defective in biofilm development,

193 We observed that nonmotile mutants were defective in biofilm formation.

194 marEm2 each transposed in F. johnsoniae, and nonmotile mutants were identified and analyzed.

195 Nonmotile mutants were significantly deficient in biofil

196 soil-soak inoculation virulence assay, both nonmotile mutants were significantly reduced in the abil

197 Like previously described nonmotile mutants, gldJ mutants were deficient in chitin

198 these pathogens, we constructed flagellated nonmotile mutants.

199 d motility to 4 of 61 independently isolated nonmotile mutants.

200 m and stabilizes the calmodulin-dissociated, nonmotile myosin.

201 Finally, the nonmotile nature of the cells allows for the retrograde

202 s induce AVM-like migrations in the normally nonmotile neuron PVM; this indicates that serotonin was

203 0 times as much [3H]leucine into IL-8 as did nonmotile neutrophils exposed to chemoattractants.

204 rotype Typhimurium strain (flgK mutant) to a nonmotile, non-flagellin-expressing strain (flgK fliC fl

205 A subset of nonmotile, nonpolarized cells also exhibited focal adhes

206 erated with rotations of podosome rings in a nonmotile, nonrotating cell, suggesting a unique feature

207 aused by Proteus mirabilis, we constructed a nonmotile, nonswarming flagellum mutant of strain WPM111

208 are detected in the redox responses given by nonmotile, nontransformed human breast epithelial cells,

209 ile Inaba(+) vaccine candidate, Peru-2, to a nonmotile Ogawa(+) phenotype using a mariner-based trans

210 otactic, copiotrophic populations outcompete nonmotile, oligotrophic populations during diatom blooms

211 The resulting mutants were nonmotile on motility agar plates, but under a light mic

212 Both mutants were completely nonmotile on soft agar plates, in minimal broth, and in

213 Subspecies IIIa is nonmotile on swarming agar and thus may also have reduce

214 bnormal cells are relatively nonadhesive and nonmotile on the protein ligands of these receptors.

215 PAF-stimulated neutrophils were nonmotile on the surface of the fibroblast, but subseque

216 ith aberrant phototaxis; mutants were either nonmotile or exhibited an "inverted motility response" (

217 rains containing these mutations were either nonmotile or had severely impaired motility.

218 Cilia may be nonmotile or motile, the latter having additional specif

219 ulted in either aflagellate, flagellated but nonmotile, or flagellated but nonchemotactic A. tumefaci

220 lly with approximately 100 cfu of wild type, nonmotile, or nonmotile/quorum-sensing-deficient Bacillu

221 bacterium Flavobacterium johnsoniae and the nonmotile oral pathogen Porphyromonas gingivalis.

222 Primary cilia are nonmotile organelles implicated in signaling and sensory

223 Haemophilus influenzae is considered a nonmotile organism that expresses neither flagella nor t

224 at the onset of feeding, formed networks of nonmotile organisms that advanced toward the basolateral

225 Fungi are nonmotile organisms that obtain carbon from compounds in

226 itical role in cell physiology in motile and nonmotile organisms.

227 Importantly, nonmotile P. aeruginosa also elicits reduced IL-1beta le

228 T inhibits flagellum biosynthesis in mucoid, nonmotile P. aeruginosa cystic fibrosis isolates by prom

229 Nonmotile P. aeruginosa elicits reduced IL-1beta product

230 on facilitates the uptake of both motile and nonmotile P. aeruginosa However, unexpectedly, mechanist

231 ssor of fleQ, we mutated amrZ in the mucoid, nonmotile P. aeruginosa strain FRD1.

232 mmasome activation is reduced in response to nonmotile P. aeruginosa.

233 apable of inducing 1D diffusion of otherwise nonmotile PARP1, while excess APE1 also facilitated the

234 Analysis of 22 nonmotile Peru-2 mutants showed that two were Ogawa(+),

235 the cell to form the irregular shape, as two nonmotile, PF-deficient mutants (JR1 and HL51) were no l

236 n Escherichia coli, this plasmid conferred a nonmotile phenotype and a reduction in flagellar number.

237 generally motile but frequently convert to a nonmotile phenotype as the disease progresses.

238 of the sokA301 allele of ctrA to bypass the nonmotile phenotype of the pleC null mutation provides e

239 with TICs adopting the expected rounded and nonmotile phenotype on soft ECMs.

240 Deletion of flgN (yvyG) results in a nonmotile phenotype that is attributable to a decrease i

241 Deletion of flgP results in a nonmotile phenotype, demonstrating the requirement of th

242 tX, or motY in Vibrio cholerae resulted in a nonmotile phenotype, whereas deletion of fliG gave a non

243 of the mutant with amrZ restored the mucoid, nonmotile phenotype.

244 c fibrosis lung frequently display a mucoid, nonmotile phenotype.

245 olera toxin and hemolysin, and resulted in a nonmotile phenotype.

246 rved that in CF isolates, the mucoid and the nonmotile phenotypes occur predominantly together.

247 ontaining monocilia generate nodal flow, and nonmotile polycystin-2 containing cilia sense nodal flow

248 ecialization, we initially hypothesized that nonmotile prestin orthologs, while functioning as anion

249 Nonmotile primary cilia are sensory organelles composed

250 The majority of mammalian cells have nonmotile primary cilia on their surface that act as ant

251 line mammalian kidney nephrons have solitary nonmotile primary cilium projecting from their surface i

252 Motile cilia generate fluid flow, whereas nonmotile (primary) cilia are required for sensory physi

253 In the new century, interest in nonmotile (primary) cilia, never lost from the cradle, w

254 Many cells possess a single, nonmotile, primary cilium highly enriched in receptors a

255 derived signal could be amplified from a few nonmotile producers to act on many responder cells.

256 cosylated asparagines of FlgA1 renders cells nonmotile, providing direct evidence for the first time

257 f infection resulted from infection with the nonmotile/quorum-sensing-deficient B. thuringiensis stra

258 ximately 100 cfu of wild type, nonmotile, or nonmotile/quorum-sensing-deficient Bacillus thuringiensi

259 Overall, the nonmotile and nonmotile/quorum-sensing-deficient mutants were signific

260 92 in uidA was found only in O157:H7 and its nonmotile relatives, including a SOR+ O157:H clone impli

261 g approach to study the self-organization of nonmotile rod-shaped bacterial cells growing on a solid

262 In the first phase, bacteria in the IBC were nonmotile, rod shaped, and grew rapidly in loosely organ

263 A previously described nonmotile, rod-shaped, kanamycin-resistant B. burgdorfer

264 sembly of all eukaryotic motile flagella and nonmotile sensory cilia.

265 onellosis and one outbreak of infection with nonmotile Shiga toxin-producing Escherichia coli O157 oc

266 Here, we show that the nonmotile, single-celled marine dinoflagellate Pyrocysti

267 its gonidia (asexual reproductive cells) are nonmotile, specialized for growth and reproduction, and

268 The device isolates motile sperm from nonmotile sperm and other cellular debris, based on the

269 on because it is the mechanism through which nonmotile sperm cells are delivered to ovules, thus allo

270 etophyte or pollen tube (PT) [5] carries two nonmotile sperm cells to the female gametophyte (FG) or

271 llen tubes undergo tip growth to deliver two nonmotile sperm to the ovule where they fuse with an egg

272 During sperm differentiation, nonmotile spermatids are remodeled into motile spermatoz

273 In the second phase of dissemination, the nonmotile spirochetes transitioned into motile organisms

274 tensile stress and forces the tissue into a nonmotile state characterized by a broad distribution of

275 control of the transition between motile and nonmotile states in E. coli.

276 l regulator of cell motility that promotes a nonmotile stationary cell state by preventing p21 from i

277 A nonmotile strain of E. coli (E. coli O39), which was neg

278 When BMM contact by each nonmotile strain was promoted by centrifugation, all the

279 indistinguishable from that of a completely nonmotile strain.

280 motaxis genes are lost in many, but not all, nonmotile strains but are well preserved in all motile s

281 Nonmotile strains of Y. enterocolitica were less invasiv

282 Thirteen of 15 nonmotile strains that did not produce the A pattern had

283 the assay, and 13 (2.6%) were monophasic or nonmotile strains that possessed flagellar antigen genes

284 mensalism could have delayed the recovery of nonmotile, suspension-feeding epifauna in the Early Tria

285 Nonmotile tatC mutant cells lacked detectable flagella,

286 Despite being nonmotile, the brucellae contain flagellum gene clusters

287 Compared to the lpp DKO mutant, which was nonmotile, the motility of the lpp SKO mutants was signi

288 2-5 min, suggesting that although yeast are nonmotile, their actin filaments undergo rapid cycles of

289 Switches from a nonmotile to a motile phenotype and from a fim on to off

290 This strain has been shown to be nonmotile, to be a poor invader in vitro, and to be a po

291 in discrete steps before forming long-lived, nonmotile UV-DDB dimers (DDB1-DDB2)2 at sites of damage.

292 s used to detect the presence of flagella in nonmotile variants of several pathogenic Escherichia col

293 exhibited enhanced virulence compared to the nonmotile variants.

294 tent of 24 isolates of serotype O121:H19 and nonmotile variants.

295 , a regulator of JMY's nuclear functions, on nonmotile vesicles with no associated actin networks.

296 By constructing a flaB mutant that is nonmotile, we investigated for the first time the absolu

297 Previously thought to be nonmotile, we show here that Mycobacterium smegmatis can

298 ed to be deficient in invasin production and nonmotile when grown at 23 degrees C.

299 utants lacked PFs, were rod shaped, and were nonmotile, which substantiates previous evidence that PF

300 tal strain Sphingomonas wittichii RW1, and a nonmotile (with paralyzed flagella) Escherichia coli K12