ライフサイエンスコーパス: expulsion

1 eas enhancement of Dh44 signals delays sperm expulsion.

2 es are essential: atopic asthma and helminth expulsion.

3 iently inducing Nippostrongylus brasiliensis expulsion.

4 ld-type mice, but without increased parasite expulsion.

5 ite complex and induce TolC opening for drug expulsion.

6 IL-13 in basophils resulted in impaired worm expulsion.

7 immune signaling pathways that control their expulsion.

8 s and the BNSLs can occur faster than the NP expulsion.

9 e parasites, leading to their destruction or expulsion.

10 ng high-dose infections that result in fetal expulsion.

11 actomyosin ring is not essential for nuclear expulsion.

12 dered the view that mast cells mediate rapid expulsion.

13 be unique to rats and has been called rapid expulsion.

14 on occurs when challenged rats exhibit rapid expulsion.

15 ociate mast cell degranulation from parasite expulsion.

16 RMCPII), was detected in sera at the time of expulsion.

17 activity in neonatal rats that display rapid expulsion.

18 release of RMCPII is not sufficient to cause expulsion.

19 d smooth muscle thickness, and impaired worm expulsion.

20 eby allowing ring fragmentation and nitrogen expulsion.

21 n intestinal smooth muscle function and worm expulsion.

22 reatly increased mortality, and delayed worm expulsion.

23 f conformational changes that result in drug expulsion.

24 arget pathogens for containment, killing, or expulsion.

25 talsis; and attaching to the midgut to avoid expulsion.

26 improve the likelihood of spontaneous stone expulsion.

27 , IL-4 and IL-13, and may contribute to worm expulsion.

28 rt Stat6-dependent effects that promote worm expulsion.

29 nd a competition between laser shadowing and expulsion.

30 tion of interleukin 13 (IL-13), which drives expulsion.

31 n and increased susceptibility to intestinal expulsion.

32 ircuitry are simultaneously involved in UPEC expulsion.

33 P and motor Myosin VIIa to mediate bacterial expulsion.

34 in intestinal function that facilitate worm expulsion.

35 e hypertrophy/hyperplasia, and impaired worm expulsion.

36 l responses to Hb2 infection that facilitate expulsion.

37 tic movement and facilitated Trichuris muris expulsion.

38 tionship between cell cycle exit and nuclear expulsion.

39 cus production, ultimately resulting in worm expulsion.

40 immunity, RELMbeta (Retnlb) can promote its expulsion.

41 .4 ppm) had very little or no impact on worm expulsion.

42 clear volume following cytoplasm/nucleoplasm expulsion.

43 plore mechanisms associated with the delayed expulsion, 3-week-old female BALB/c mice were placed on

44 20%), hyphema (41%), iris trauma (62%), lens expulsion (54%), subretinal hemorrhage (51%), and choroi

45 The primary outcome was the rate of IUD expulsion 6 months after IUD insertion; an expulsion rat

46 C-IUD users experienced significantly higher expulsion (8% versus 1%, p = 0.02) and elective disconti

47 similar elevations in Th2 cytokines and worm expulsion after N. brasiliensis inoculation.

48 ls elaborate diverse mechanisms for pathogen expulsion, amebae have also developed complex strategies

49 ial cells resulted in a marked delay in worm expulsion and abolished the expansion of the Lin(-)c-Kit

50 ropulsive motor pattern, associated with gas expulsion and anal sphincter relaxation, inferred to be

51 ng the genetic determinants that control the expulsion and death of epithelial cells.

52 the child's history of school suspension or expulsion and difficulty in getting along with others.

53 tactic mutants are susceptible to intestinal expulsion and experience large fluctuations in absolute

54 infection, deficient mice had impaired worm expulsion and higher worm fecundity despite normal produ

55 ies in which no dewetting is observed, water expulsion and hydrophobic collapse occur simultaneously,

56 ELM-beta is essential for normal spontaneous expulsion and IL-4-induced expulsion of Nippostrongylus

57 - and WASp in the process of secretory cargo expulsion and integration of vesicular membranes with th

58 uc5ac, which is detected shortly before worm expulsion and is associated with the production of inter

59 ing sites while Msn2 can promote reposition, expulsion and recruitment of nucleosomes to alter gene e

60 s provided by the final step of hinge-region expulsion and subsequent closure of the main beta-sheet

61 erol is associated with school suspension or expulsion and that low total cholesterol may be a risk f

62 he inflammatory response following both worm expulsion and the peak in Mphi accumulation.

63 tinal nematode parasites contributes to worm expulsion and tolerance to associated tissue damage.

64 motility by assessing stool frequency, bead expulsion, and isometric muscle recordings of colonic lo

65 llet output, total gut transit, colonic bead expulsion, and muscle tension recordings.

66 Pups born to infected dams displayed rapid expulsion, and RMCPII was detected in their sera.

67 region may have been a steady site for flux expulsion, and triggering of geomagnetic reversals, for

68 s, shortening the time to stone and fragment expulsion as well as minimizing pain.

69 lammation develops) and then, following worm expulsion (as the inflammation resolves), both the resid

70 This suggests a corollary: following ion expulsion at neutral pH, a spontaneous global conformati

71 llular gate is spontaneously followed by ion expulsion at the extracellular selectivity filter.

72 he only remaining steric barrier to complete expulsion being the "breathable" residue, P81.

73 nly in pathology (allergic disease, parasite expulsion) but also during normal postnatal development.

74 -type immune responses that can mediate worm expulsion, but the role of this response in controlling

75 tive response ultimately leading to parasite expulsion, but they also play a role in the regulation o

76 receive misoprostol, 71 percent had complete expulsion by day 3 and 84 percent by day 8 (95 percent c

77 While RELMalpha (Retnla) impairs helminth expulsion by inhibiting protective Th2 immunity, RELMbet

78 f mammalian red blood cells requires nuclear expulsion by orthochromatic erythoblasts late in termina

79 Water expulsion by the contractile vacuole (CV) in Dictyosteli

80 These results indicate that rapid expulsion can occur in the absence of either intestinal

81 the absence of Bcl11b leads to impaired worm expulsion, caused by a deficit in ILC2s, whereas Citroba

82 Organoazides and their nitrogen expulsion chemistry have attracted the attention of many

83 clohexane), and their gold-mediated nitrogen expulsion chemistry, and the isolation of formal nitrene

84 lminated in electrostatically driven protein expulsion, consistent with the chain ejection model (CEM

85 r motility in niche formation and collective expulsion-containment strategies beyond individual searc

86 e cell anal depressor muscle, used for waste expulsion, contains bilateral dorsal-ventral sarcomeres.

87 ed anterior body wall muscle contraction and expulsion defective (aex) mutants, exhibits similar defe

88 effector cell recruitment and impaired worm expulsion, demonstrating that T(ML) cells are not suffic

89 nts with IEC organoids demonstrated that IEC expulsion did not require other cell types.

90 cytokine production, leading to delayed worm expulsion during infection with the gastrointestinal hel

91 dings on Co(I) chemistry suggest that halide expulsion during reductive dehalogenation is initiated t

92 d effector function associated with helminth expulsion during type 2 inflammation.

93 on, caused by complex coacervation and water expulsion, enables us to reduce linear dimensions of pri

94 After diphosphate expulsion, farnesyl cation reacts with the distal 10,11-

95 parameters including the frequency of pellet expulsion, fecal weight and fecal water content.

96 he global DNA conformation to achieve lesion expulsion from DNA.

97 After expulsion from HE ipDNA-capsids, ipDNA forms sharp bands

98 The rhythm is driven by the host's expulsion from its light-emitting organ of most of the s

99 esulted in sanctions ranging from censure to expulsion from membership.

100 tages of a kinetic mechanism of lateral drug expulsion from the active site of HIV-1 protease, by con

101 ation of Robos in post-crossing axons allows expulsion from the floor plate and prevents recrossing.

102 as generally highest around the time of worm expulsion from the gut, at which point the inflammation

103 photosynthetic capability, resulting in its expulsion from the host.

104 ht absorbance, centrifugal instability, iron expulsion from the internal aqueous phase, color differe

105 pping (oxidation of the iodide site) and its expulsion from the lattice in the form of iodine provide

106 Water expulsion from the protein core is a key step in protein

107 lation induces phosphorylation of CPEB, PARN expulsion from the ribonucleoprotein complex, and polyad

108 ted commissural axons and facilitating their expulsion from the VM within the chick spinal cord.

109 ated repellents, Slit1-3, facilitating their expulsion from, and prohibiting their reentry into, the

110 reported over 24 ns, and subsequent complete expulsion, implemented using steered molecular dynamics

111 ufficient to restore IgE production and worm expulsion in inulin-fed mice.

112 Despite this, inulin prevented worm expulsion in normally resistant mice, instead resulting

113 lar vesicles was recognized and selected for expulsion in response to innate immune signaling.

114 y with indomethacin resulted in delayed worm expulsion in selenium-adequate mice.

115 Lack of expulsion in the mice fed inulin was accompanied by a si

116 (HPWP) to replicate petroleum generation and expulsion in uplifted onshore basins.

117 y effector cytokine responsible for T. muris expulsion, inhibits IL-13 function both in vitro and in

118 Our mathematical model reveals that expulsion is a combined effect of motility and alignment

119 oblet cell hyperplasia is abrogated and worm expulsion is compromised.

120 Compared to anhydrous pyrolysis where oil expulsion is limited, gas yields are much lower, and the

121 The water expulsion is reversible, and is attributed to the interf

122 tween photosynthetic competency and symbiont expulsion, little is known about the effect of thermal s

123 e nanocrystals undergo facile thermal ligand expulsion (</=200 degrees C), which was studied by TGA-m

124 cells, but not Th2 cells, caused rapid worm expulsion, marked basophilia, and increased mast cell nu

125 es work as bellows organs in a unique pollen expulsion mechanism activated by the passerines.

126 ing against a contractile ring-based nuclear expulsion mechanism.

127 sserine'), characterized by different pollen expulsion mechanisms and reward types, but not by tradit

128 g in vitro, uncoupling parasite killing from expulsion mechanisms.

129 Alongside increased parasite expulsion, MyD88-deficient mice showed heightened IL-4 a

130 ion of the metal-bound N2 and reforming with expulsion of [N2(SiMe3)3](-).

131 ed to the edges in a manner analogous to the expulsion of a magnetic field from superconductors.

132 Mucosal mast cells contribute to expulsion of a number of gastrointestinal nematode paras

133 activation intracellularly with concomitant expulsion of a phosphoramidate anion.

134 The resulting air flow causes the expulsion of a pollen jet and the deposition of pollen o

135 Here, we present evidence for a sudden expulsion of a reservoir-size quantity of methane from a

136 employed in order to achieve the controlled expulsion of a synergistic enzybiotic cocktail consistin

137 ubstitution of Ser residue by Thr caused the expulsion of a water molecule from the cavity, creating

138 The resultant expulsion of acetate into the extracellular environment

139 ional isolated actomyosin rings we show that expulsion of actin bundles does not require continuous p

140 the rate of ATP hydrolysis by retarding the expulsion of ADP.

141 previously demonstrated that host protective expulsion of adult H. bakeri worms from a challenge infe

142 mastocytosis in vivo, leading to accelerated expulsion of adult worms from the intestine.

143 losteric transition is stabilized further by expulsion of an aromatic residue from the cAMP-binding p

144 The 6-month rate of expulsion of an IUD after immediate insertion was higher

145 mer terminus base pair into the active site; expulsion of an unpaired pyrimidine, but not purine, bas

146 pumps with diverse functions, including the expulsion of antibiotics.

147 Inhibiting SFK signaling blocks both the expulsion of apoptotic cells and the rosette formation a

148 the streptavidin binding site (specifically expulsion of bound water molecules).

149 l compression of actomyosin rings results in expulsion of bundles predominantly at regions of high cu

150 opriately placed nucleophile facilitates the expulsion of carbon dioxide from the active site in many

151 zes the POT underlayer, which results in the expulsion of cations from the membrane at an appropriate

152 ypentachlorocyclohexadienones results in the expulsion of chloride and provides a direct route to the

153 are positioned at the oocyte cortex to allow expulsion of chromosomes into polar bodies.

154 h permeability of the vaginal epithelium and expulsion of conventional soluble drug dosage forms.

155 lts under ambient conditions resulted in the expulsion of crystalline, non-passivated HgTe quantum do

156 zil, which undergoes two parallel reactions: expulsion of cyanide to give the corresponding benzil an

157 5-methyl-6-Cys-81-S-5,6-dihydrocytosine and expulsion of Cys-81-S- provides the product DNA 5-methyl

158 These contractions drive the expulsion of damaged cells into the brain ventricle with

159 Slow expulsion of dinitrogen (N(2)) was observed at room temp

160 etonitrile at 254 and 300 nm, which involves expulsion of dinitrogen and sulfur to form the respectiv

161 t in the oligomerization process must be the expulsion of discrete water molecules that facilitates t

162 ular events culminating in the PAD4-mediated expulsion of DNA.

163 Expulsion of excess surfactant to the surfaces of superc

164 initiates lysosome exocytosis, resulting in expulsion of exosome-encased bacteria.

165 involving ejection of unfolded monomers, (2) expulsion of folded monomers from the intact tetramer, a

166 Expulsion of fracture fluids from basement systems with

167 s their dorsal tracheal trunks (DTTs) by the expulsion of gas bubbles into the body.

168 NA silencing of the host gene contributed to expulsion of group II introns from nuclear genomes and d

169 on technique because it usually involves the expulsion of impurities.

170 This capacity of TLR4 to mediate the expulsion of intracellular bacteria from infected cells

171 Here, we report that expulsion of intracellular E. coli by infected BECs is i

172 tion (driven by the solidifying inner core's expulsion of light elements), thermal convection (from s

173 Expulsion of lipid-oligonucleotide conjugates from the p

174 superconductivity: zero resistivity and the expulsion of magnetic flux (the Meissner effect).

175 xperimental and theoretical studies of rapid expulsion of microswimmers, such as motile bacteria, by

176 ing mechanisms underlying the production and expulsion of milk by mammary epithelial cells during lac

177 molysis of 1b at ~100 degrees C leads to the expulsion of N(2) and isolation of Ru(2)(D(3,5-Cl(2))PhF

178 azide nitrogen leads to cyclization with the expulsion of N2.

179 Expulsion of neutral alkenes via syn-elimination to give

180 ormal spontaneous expulsion and IL-4-induced expulsion of Nippostrongylus brasiliensis and Heligmosom

181 in vitro and in vivo and contributed to the expulsion of Nippostrongylus brasiliensis.

182 eorganization allowing for the thermoneutral expulsion of one CO ligand, which in turn generates an e

183 ng occurs, with the bud(s) formed by partial expulsion of one of the two polymer-rich aqueous phases.

184 llapse to new benzimidazole derivatives with expulsion of p-substituted anilines.

185 Expulsion of parasites from the intestine was significan

186 evelopment of nuocytes and their role in the expulsion of parasitic worms.

187 c infections by a combination of resistance (expulsion of pathogens) and tolerance (active mitigation

188 ded ((Ar)L)FeCl((*)NAd) (6) with concomitant expulsion of Ph3C(C6H5)CPh2.

189 us distribution of high heat flow areas, the expulsion of reactive DOM is spotty at any given time.

190 The expulsion of relatively nutrient-rich sea ice brine into

191 ed on short life span but is also driven via expulsion of resident thymocytes by fresh progenitors en

192 ofusely and may represent particles in which expulsion of scaffold and DNA packaging are incomplete.

193 el describing micelle formation by insertion/expulsion of single molecules under nonisothermal condit

194 tion model (CEM), which involves the gradual expulsion of stretched-out chains from the droplet.

195 yl, and acyl/alkoxy gold carbenes by in situ expulsion of sulfur dioxide.

196 crophages, angiogenesis, and PD-L1-dependent expulsion of T and B cells.

197 he events at C-20 leading to contraction and expulsion of the "C(2)" unit as acetic acid from a metal

198 ent with the experimental KIEs indicate that expulsion of the 5'O remains an integral feature of the

199 This is a complex morphogenetic event where expulsion of the apoptotic cell is accompanied by rearra

200 rnalized and fuse with autophagosomes before expulsion of the autophagosomal contents by exocytosis.

201 s involved in packing interactions, denoting expulsion of the bound antigen upon crystal formation.

202 independent, suggesting that CSNK-1 prevents expulsion of the entire meiotic spindle into a polar bod

203 rdination of the enzyme's catalytic zinc and expulsion of the enzyme's catalytic water were a consist

204 leukemia virus type 1 (HTLV-1) Env in which expulsion of the final bulky hydrophobic residue is impo

205 After expulsion of the formyl unit, both proton-independent an

206 uitment that was associated with accelerated expulsion of the gastrointestinal nematode Nippostrongyl

207 evidence that the transport process involves expulsion of the globular domain from the beta-barrel.

208 f the peptide tunnel appear to assist in the expulsion of the growing peptide chain, and clamps at th

209 1-136 with coincident, and possibly coupled, expulsion of the hinge of the reactive center loop.

210 ures show several differences, including the expulsion of the hinge region of the reactive centre loo

211 cles assemble in crystallographic alignment, expulsion of the intervening solvent and particle coales

212 d that interleukin-3 and c-Kit contribute to expulsion of the intestinal nematode Strongyloides venez

213 row-derived dendritic cells (BMDCs) enhanced expulsion of the intestinal nematode, Trichinella spiral

214 ther reaction of the intermediate results in expulsion of the leaving group to give an alpha-methylen

215 the protonation of the radical anion or the expulsion of the leaving group.

216 capsule rupture at the posterior pole, with expulsion of the lens nucleus and degenerating fiber cel

217 A related process, the expulsion of the lethal endosomal pathogen Cryptococcus

218 liferation, and lack of amphiregulin delayed expulsion of the nematode Trichuris muris.

219 cleolus occurs, and NE modifications promote expulsion of the nucleolus to the cytoplasm.

220 ll protease 1 (Mcpt-1), which contributes to expulsion of the parasite.

221 readily reorganize and pave the way for the expulsion of the product of the reaction from the active

222 ve to hydroxide ion, probably related to the expulsion of the relatively poor leaving group amide ani

223 5' nucleophile on the cyclic phosphate, with expulsion of the ribose O2' and generation of a 3',5'-ph

224 involving activation of the viral protease, expulsion of the scaffold proteins, and the uptake of vi

225 ll as DNA, suggesting that DNA packaging and expulsion of the scaffolding protein are coupled process

226 Decompression after reaction causes expulsion of the solution from the pores and spontaneous

227 ucleosome-remodeling activity and results in expulsion of the SWI/SNF complex from the Xi.

228 the peptide tunnel lining that assist in the expulsion of the synthesized peptide.

229 robial peptides, and the recently discovered expulsion of their nuclear contents to form neutrophil e

230 IL-31Ralpha(-/-) mice exhibited accelerated expulsion of Trichuris with significantly decreased worm

231 of Muc5ac caused a significant delay in the expulsion of two other gut-dwelling nematodes (Trichinel

232 A new study shows that phospho-dependent expulsion of type-1-phosphatase (PP1) from the spindle p

233 scription activation mechanism requiring the expulsion of Tyr-152 from the multidrug binding pocket.

234 of external urethral sphincter (EUS) EMG and expulsion of urine from the urethral meatus.

235 (Weibel-Palade bodies [WPBs]) and subsequent expulsion of von Willebrand factor (VWF) content.

236 the absorption of water and electrolytes and expulsion of waste contents, largely via regulation of e

237 tude and indicate that gel extensibility and expulsion of water are both manifestations of protein un

238 ty changes based on area models supports the expulsion of water from the interface of the Hoechst-DNA

239 tion-induced contraction of the hydrogel and expulsion of water generates a transient waveguide, whic

240 In particular, the expulsion of water molecules at the interface might be a

241 ce approach each other, fibril formation and expulsion of water molecules occur rapidly and nearly si

242 Expulsion of water, resulting in the formation of a dry

243 local effector mechanism culminating in the expulsion of worms from the large intestine is not known

244 tering remains a valid mechanism for droplet expulsion on the nanoscale, while irradiation induced st

245 ing-up the capsule seam, resulting in either expulsion or trapping of cesium ions depending on the an

246 release of bound phenolics arriving to their expulsion outside the cell.

247 o objectively assess arousal, orgasm and the expulsion phase of ejaculation such as functional MRI, d

248 dues, whereas the reactive center loop hinge expulsion plays only a minor additional role.

249 A dewetting transition, in which water expulsion precedes hydrophobic collapse, is observed for

250 Successful cell expulsion prevents the death of nearby cells and an exac

251 neering the enzyme to accelerate the product expulsion process and improve the efficiency of biomass

252 rption spectroscopy revealed that the iodide expulsion process leaves a defect-rich perovskite lattic

253 he changes in free energy during the product expulsion process.

254 ce of low field strengths reflects core flux expulsion promoted by the unusual core-mantle boundary (

255 Th2 cytokine responses and resulted in worm expulsion, providing the first demonstration of TSLPR-in

256 D expulsion 6 months after IUD insertion; an expulsion rate 8 percentage points higher in the immedia

257 Anal pressures, rectal balloon expulsion, rectal sensation, and pelvic floor structure

258 t the mechanism of helminth killing prior to expulsion remains unclear.

259 multifunctional stamens that provide pollen expulsion, reward and attraction.

260 The 6-month expulsion risk was 5.0% (13 of 258 women) after immediat

261 .46, compatible with significant amide anion expulsion/S-N fission in the transition state.

262 eed microscopy we uncover different particle expulsion scenarios depending on the mode of bubble defo

263 ion profile predicts the water-addition and -expulsion steps as the highest barriers along the pathwa

264 the cycloaddition as well as a formaldehyde expulsion steps were computed, and a multistep mechanism

265 LR2/4-deficient mice showed accelerated worm expulsion, suggesting that MyD88 was active in signaling

266 TLR5, or TLR9 did not show enhanced parasite expulsion, suggesting that these TLRs signal redundantly

267 known, our recent work on parasitic helminth expulsion suggests the possibility that, rather than T c

268 evaluate DD-a clinical DD score, the balloon expulsion test (BET) and a digital rectal examination (D

269 ation pattern on manometry, abnormal balloon expulsion test or impaired rectal evacuation by imaging.

270 >90 mm Hg, and have a normal rectal balloon expulsion test result.

271 sphincter, 41 had an abnormal rectal balloon expulsion test, and 20 had abnormal rectal sensation.

272 expand, resulting in a severe defect in worm expulsion that is rescued by the adoptive transfer of in

273 asion and involved a previously reported IEC expulsion that was coordinated with lipid mediator and c

274 After the dawn expulsion, the epithelium reestablished its polarity, an

275 Cell expulsion through neuroepithelial contraction represents

276 tion anorectal manometry, and rectal balloon expulsion time in 62 healthy women and 295 women with ch

277 people from patients with prolonged balloon expulsion time with 75% sensitivity and a specificity of

278 tients had prolonged (>180 s) rectal balloon expulsion time.

279 ng patients with normal and abnormal balloon expulsion time.

280 m those with constipation but normal balloon expulsion time.

281 dicting which patients had prolonged balloon expulsion times.

282 y people from patients with abnormal balloon expulsion times; 2 phenotypes discriminated healthy peop

283 -13 from Th2 cells was not required for worm expulsion, tissue inflammation, or airway hyperreactivit

284 de, which subsequently undergoes isobutylene expulsion to form [CF(3)-ONO]W horizontal lineCH(Et)(OSi

285 OTf, and B(C(6)F(5))(3) catalyze isobutylene expulsion to yield the tungsten-oxo complex [CF(3)-ONO]W

286 ae within Aiptasia larvae and observed algal expulsion under an environmental stressor.

287 st zooxanthellar phylotypes are dying during expulsion upon release from the host.

288 IEC expulsion was accompanied by a major actin rearrangement

289 Expulsion was associated with an increased local express

290 Furthermore, rapid worm expulsion was impaired in IgE-deficient but not in IgG1-

291 reatment on day 1, a second dose on day 3 if expulsion was incomplete, and vacuum aspiration on day 8

292 Worm expulsion was inhibited in H. polygyrus-inoculated B cel

293 Notably, the process of worm expulsion was restored within 2 to 4 days after feeding

294 ttenuated in IL-13Ralpha2(-/-) mice and worm expulsion was similar to that of wild-type mice.

295 ncomplete, and vacuum aspiration on day 8 if expulsion was still incomplete.

296 hout CGRP signaling, ILC2 responses and worm expulsion were enhanced.

297 ansit, small-bowel transit, and colonic-bead expulsion were normal in Met(fl/fl); Wnt1Cre+ mice.

298 mastocytosis, yet such rats exhibited rapid expulsion when challenged orally.

299 nisms of chemical transport, including water expulsion, will dictate the rate of transformation and h

300 jection of oxytocin could increase placental expulsion without the need for a surgeon or anaesthetic.