ライフサイエンスコーパス: noninfected

1 es were similar (96.9% infected versus 97.6% noninfected).

2 milar levels of wild type CLASP2 or that are noninfected.

3 ifference in mean microbial recovery between noninfected (1.2 isolates) and infected (2.7 isolates) d

4 EU/ml versus 51.4 +/- 12.5 EU/ml, p = 0.16; noninfected: 5.9 +/- 4.8 EU/ml versus 11.1 +/- 4.3 EU/ml

5 AB and NAB sutures were harvested from noninfected (70.9%) and infected (29.1%) sites in 158 pa

6 us (HIV)-infected adolescents and high-risk, noninfected adolescents (n = 182) were recruited at 16 l

7 tion of peripheral CD4+ cells from syngeneic noninfected adult mice prevents the autoimmune developme

8 as well as clinical studies of infected and noninfected adults indicate that systemic infections tha

9 l communication network between infected and noninfected AECs and alveolar macrophages that leads to

10 Ten wild-type C57BL/6 infected mice and 11 noninfected age-matched apoE(-/-) mice served as control

11 ents (n = 20) for RSV infection, and healthy noninfected age-matched controls (n = 18).

12 m samples of BAL fluid and lung tissues from noninfected and A. fumigatus-infected rabbits.

13 ersely, stretch produced opposite changes in noninfected and AdLacZ-infected myocytes: Aogen increase

14 elevated CO2 (eCO2 ; 650 mumol mol(-1) ) on noninfected and BYDV-infected wheat.

15 and 17, the %CD14 also was different between noninfected and infected survivors.

16 Compared to noninfected and simian immunodeficiency virus-infected,

17 om 85 (53.8%) explanted sites; 39 sites were noninfected, and 46 were infected.

18 PBMC isolated from noninfected animals and treated with morphine sulfate in

19 B cells from noninfected animals did not proliferate upon M. avium su

20 ination may be utilized to spare vaccinated, noninfected animals from slaughter and subsequent dispos

21 Johne's disease-infected animals relative to noninfected animals included those encoding tumor necros

22 brane-associated hsp60 seen in the livers in noninfected animals subsequently increased during infect

23 hsp60 was restricted to the mitochondria in noninfected animals, it was associated with the plasma m

24 els to an extent similar to that observed in noninfected animals.

25 is and Helicobacter pylori and compared with noninfected animals.

26 higher activation level than platelets from noninfected animals.

27 reased intimal cellularity compared with the noninfected apoE(-/-) mice.

28 total knee arthroplasty and 28 patients with noninfected arthroplasty were reviewed by two musculoske

29 agulase-negative staphylococci isolated from noninfected arthroplasty-associated specimens were scree

30 Similarly, noninfected ATAF2 knockout or ATAF2 repressor lines disp

31 nsactivation of the pol promoter by R in EBV-noninfected B cells.

32 timulation fall sharply in both infected and noninfected birds.

33 Minimal cell death occurred when noninfected BL-41 cells were incubated with valproate, w

34 r infection by a black fly bite, but because noninfected black flies acquired the virus while co-feed

35 eed on the same host in nature, infected and noninfected black flies were allowed to feed on the same

36 ntigens, monospecies malaria infections, and noninfected blood samples.

37 phages and is expressed in low levels in the noninfected brain.

38 one was found to react with a 3-kb mRNA from noninfected but not from P. carinii-infected rat lung, s

39 in infected cells but activates apoptosis in noninfected bystander cells.IMPORTANCE B cell lymphoma 2

40 d cell, but also allows it to trans-activate noninfected bystander leukemia B cells.

41 induced apoptosis of both infected cells and noninfected "bystander" cells.

42 owth inhibition and apoptosis in surrounding noninfected cancer cells but not in normal cells, thus e

43 The remaining 44 were from noninfected cases, of which 2 were culture positive.

44 ectomy is warranted in previously untreated, noninfected cases.

45 omen had rates that were similar to those of noninfected cases.

46 oped for discriminating between infected and noninfected cases.

47 f CD44 compared to lymphocytes from lungs of noninfected cattle.

48 CHF rabbits (Ad.nNOS CB versus contralateral noninfected CB respectively, P<0.05).

49 ency virus (HIV) has been reported to target noninfected CD4 and CD8 cells for destruction.

50 cted T cells form a virological synapse with noninfected CD4(+) T cells in order to efficiently trans

51 top signal and supramolecular segregation in noninfected CD4(+) T cells.

52 CD4+ cells and blocks fusion of infected and noninfected CD4+ cells.

53 was observed in both parasite-containing and noninfected cell populations represented in T. cruzi-inf

54 d at cell contact areas between infected and noninfected cells and at the edges of plaques.

55 uppressed, but the activation of surrounding noninfected cells and subsequent tissue damage are limit

56 When infected and noninfected cells are purified by cell sorting, the form

57 cyte cell cultures showed no difference from noninfected cells in mRNA expression of the caspase fami

58 s were trained to differentiate infected and noninfected cells with high accuracy (90%).

59 lase and arachidonic acid epoxygenase in the noninfected cells, (b) the CYP 4A3-dependent oxidation o

60 lysis in a host cell to analyze infected and noninfected cells, and compared this to microarray and p

61 Indeed, CstK co-localized with TBC1D5 in noninfected cells, and TBC1D5 was recruited to CCVs in i

62 When expressed in noninfected cells, E4orf3 overcame the mitotic arrest ca

63 In noninfected cells, N-cadherin and beta-catenin were colo

64 e same animals (28.1+/-5.2% reduction versus noninfected cells, P<0.01).

65 seradish peroxidase (HRP) uptake compared to noninfected cells, while coculture with a P. aeruginosa

66 xosomes to inhibit the NLRP3 inflammasome in noninfected cells.

67 ease from the infected cells and taken up by noninfected cells.

68 helial (Caco-2) cells as well as surrounding noninfected cells.

69 in comparison with that in nonexpressing and noninfected cells.

70 nectin-1 of infected cells at junctions with noninfected cells.

71 e pathogenic intracellular bacteria) than in noninfected cells.

72 were challenged with F. alocis, compared to noninfected cells.

73 n of the cytokine was strictly a property of noninfected cells.

74 arker, and could transfer virus particles to noninfected cells.

75 increased conduction velocity compared with noninfected cells.

76 of such compounds to act in infected versus noninfected cells.

77 regulated retrograde trafficking of MPRs in noninfected cells.

78 cient alveolar macrophages into the lungs of noninfected CF mice is sufficient to induce pneumonia.

79 fidence interval (CI) 0.38-1.53) relative to noninfected children of similar age.

80 r lung function measures, when compared with noninfected children.

81 h differences between C. parvum-infected and noninfected children.

82 mparison of growth in C. parvum-infected and noninfected children.

83 f weight gain between C. parvum-infected and noninfected children.

84 Immunocytochemistry of transfected noninfected CHO cells demonstrated that the distribution

85 r[Ca2+]i flux than did similarly stimulated, noninfected CLL cells or CLL cells infected with a contr

86 Compared to noninfected contemporary or historical controls, patient

87 among SARS-CoV-2 stroke patients compared to noninfected contemporary or historical stroke patients (

88 int Louis encephalitis virus (SLEV) and from noninfected control birds.

89 es was at least ninefold higher than that in noninfected control cells and significantly decreased in

90 al and clinical infection groups, along with noninfected control cows of similar parity, to study hos

91 herapy-suppressed HIV-infected subjects, and noninfected control donors.

92 ction were compared with those of a matched, noninfected control group (n = 98).

93 nfected population were less than those in a noninfected control group, but the difference was much l

94 ed DCs shows no significant differences over noninfected control lung DCs.

95 nkeys, compared with those in 8 primigravid, noninfected control monkeys.

96 Participants infected with HIV vs noninfected control participants with similar cardiac ri

97 erleukin-8 were different between sepsis and noninfected control patients at time 1.

98 d with saline-treated infected rats and with noninfected control rats.

99 ents, 7 RV-infected control subjects, and 14 noninfected control subjects.

100 the livers of Listeria-infected, relative to noninfected control, mice at 0.5-2 h after i.v. infectio

101 e DeltaEF mutant was similar to that for the noninfected control.

102 ions in the infected roots compared with the noninfected control.

103 rican, 8 other race) with candidemia and 351 noninfected controls (263 white, 88 African American).

104 us-infected subjects (n = 19) and comparable noninfected controls (n = 20) were studied before and 6

105 = 66), gram-negative bacteremia (n = 74), or noninfected controls (n = 35) were enrolled.

106 anked as follows: nonsurvivors > survivors > noninfected controls (p < .01).

107 fected subjects produced interleukin-10, but noninfected controls did not (P < .001).

108 A cohort of 338 candidemia patients and 351 noninfected controls were genotyped for single-nucleotid

109 -positive patients with persistent warts, 42 noninfected controls, and 46 HIV-positive controls.

110 Compared to noninfected controls, cumulative risks and burdens of re

111 ed in the mesenteric lymph nodes compared to noninfected controls, following oral infection.

112 ts of IL-5 into the airways as compared with noninfected controls, no IL-5 was detectable in both bro

113 t, and rate of protein synthesis relative to noninfected controls.

114 ORF2 or the parent Ab4 virus or were kept as noninfected controls.

115 s versus 0 of 11 liver tissue specimens from noninfected controls.

116 ocerca volvulus infection with 85 comparable noninfected controls.

117 h that in neutrophil-enriched fractions from noninfected controls.

118 This response was not seen in noninfected controls.

119 limited to select populations and often lack noninfected controls.

120 rally infected with Plasmodium falciparum or noninfected controls.

121 P = .002), compared with wart specimens from noninfected controls.

122 on, and IFN-gamma production were similar to noninfected controls.

123 in the cytoplasm of infected COS-7 cells and noninfected COS-7 cells transfected with plasmids contai

124 produces about four times more eggs than the noninfected counterpart.

125 Infected patients were sicker than their noninfected counterparts (Acute Physiology and Chronic H

126 ch experiment, raw milk samples from a known noninfected cow were inoculated with 10(2) to 10(8) CFU/

127 SS), 12 patients with severe sepsis (S), six noninfected critically ill patients (CINS), and nine nor

128 multiple organ dysfunction syndrome, and ten noninfected critically ill patients were studied.

129 s more pronounced in septic patients than in noninfected critically ill patients.

130 with this observation identical treatment of noninfected cultures decreased the contribution of endog

131 ing apoptosis on JCV infection compared with noninfected cultures; small interfering RNA inhibition o

132 No pathological changes were detected in noninfected d3Tx mice.

133 of the T cell responses; in contrast, these noninfected DC showed downregulation of major histocompa

134 infected cells, which can be internalized by noninfected DCs driving DC maturation in the presence of

135 ic MLR, in contrast to potent stimulation by noninfected DCs from the same cultures.

136 h CD86 and MHC class II, in contrast to many noninfected DCs.

137 lial cells and the other at the level of the noninfected DCs.

138 as present in 100% and 66.6% of infected and noninfected devices, respectively (P < 0.042).

139 hile commensal skin flora was recovered from noninfected devices.

140 on of increasing amounts of human serum from noninfected donors to the cell culture directly correlat

141 f IFN-gamma-producing NK cells compared with noninfected donors, independent of CD4(+) T cell counts.

142 as similar between adenovirally infected and noninfected EC over 4 hr.

143 ing of the cell to blood elements (including noninfected erythrocytes, leukocytes) and walls of micro

144 e or absence of a biofilm in infected versus noninfected explanted devices was noted.

145 established by housing infected ferrets with noninfected ferrets with no influenza antibody titer aga

146 L-28B pretreatment induced ISG expression in noninfected fibroblasts, but a relative decrease of ISG

147 nd patterns of (18)F-FDG uptake over time in noninfected grafts, in relationship to prosthetic materi

148 5) and IgG3 (P < 0.001) were observed in the noninfected group.

149 ity diameter or mobility between infected vs noninfected groups.

150 was transmitted from infected guinea pigs to noninfected guinea pigs housed in the same cage, an adja

151 f 10, and 67% of infected compared to 44% of noninfected had detectable IC50 titers (P < 0.001).

152 Exhaustion/burnout is common, even in noninfected HCWs.

153 levels of tyrosine phosphatase activity than noninfected hemocytes.

154 , as well as controls made from infected and noninfected HEp-2 cells, suspended in a formalin-fixed,

155 among SARS-CoV-2 stroke patients compared to noninfected historical controls (OR = 1.39, 95% CI = 1.0

156 Previously noninfected horses (control/Ab4) displayed clinical sign

157 nscytosis across the mucosal epithelium of a noninfected host.

158 r protection than picaridin provided against noninfected, host-seeking females of the southern house

159 ition, while infective vector preference for noninfected hosts will promote transmission.

160 Y. enterocolitica serotype O:8 compared with noninfected hosts.

161 ly lower incorporation of EdC than of EdU in noninfected human fibroblast cells or in cells infected

162 We have previously shown that noninfected human T-cell lines express the canonical 5.7

163 recognized by single-chain Fv fragments from noninfected humans with lupus that neutralized genetical

164 f serum CD4BD(core)-specific serum IgAs from noninfected humans without autoimmune disease isolated b

165 Comparison with noninfected ICU patients delineated a substantial common

166 tential pitfalls related to tracer uptake in noninfected implants have been described.

167 med ImmunoCAP tests in filarial-infected and noninfected individuals for IgE measurements to allergen

168 higher concentrations of BDNF than sera from noninfected individuals.

169 Sterile (noninfected) inflammation underlies the pathogenesis of

170 ies using microsomal fractions isolated from noninfected insect cells and from cells infected with CY

171 Because infected and noninfected insects potentially feed on the same host in

172 ut intraarticular bodies were more common in noninfected joints (53% vs 12%, P < .001).

173 but thin rim enhancement was more common in noninfected joints (62% vs 21%, P < .001) and diffuse jo

174 ondral cysts were seen almost exclusively in noninfected joints (76% vs 2%, P < .001).

175 We compared the proteomes of infected and noninfected L1s to identify proteins that display differ

176 cPLA(2) is present in Golgi fractions from noninfected LLC-PK(1) cells and rat kidney cortex.

177 These CTL lysed noninfected LNCap cells in a CD8-dependent manner.

178 expressed in JSRV-infected lung compared to noninfected lung, including many genes with roles in car

179 epitope density) than their counterparts in noninfected lungs, satisfying a need for memory effector

180 Sera from noninfected, M. bovis-infected, or M. avium subsp. parat

181 tissue (SCAT and VAT, respectively) from 14 noninfected macaques and 19 PHIV treated or not treated

182 xpression in SCAT and VAT from INSTI-treated noninfected macaques.

183 These cells, as well as noninfected macrophages, are stimulated to high levels o

184 exerted a low level of nonspecific lysis of noninfected macrophages.

185 ssessed vitamin D levels in HIV cases versus noninfected matched controls to determine if deficiency

186 Although MCs from the jejunum and spleen of noninfected mice failed to express mouse MC protease (mM

187 ived IgM only with IgM-containing serum from noninfected mice improved both survival rates and serum

188 ransferred transgenic T cells was reduced in noninfected mice that had been fed OVA.

189 Moreover, transfer of Fas-negative DCs from noninfected mice to preinfected animals results in eithe

190 e able to detect NP(+) GCs in the spleens of noninfected mice, but there were no detectible NP(+) GCs

191 In noninfected mice, most jejunal MCs reside in the submuco

192 In noninfected mice, no detectable chemokine gene expressio

193 Cs) from RRV-infected, but not with DCs from noninfected mice, which was correlated with an increased

194 nfected splenocytes (HSV-Spls) obtained from noninfected mice.

195 ed with nontransgenic mosquitoes when fed on noninfected mice.

196 feration compared with transplanted cells in noninfected mice.

197 DC and containing Ag85A were phagocytosed by noninfected migrating ALDC expressing SIRPalpha via acti

198 ial protection against ZIKV-infected and old noninfected mosquitoes was achieved with 5% DEET, which

199 Noninfected myocytes and myocytes infected with AdLacZ s

200 infection and end-stage liver disease and 20 noninfected negative controls.

201 timulating additional cytokine production by noninfected neighboring cells.

202 ing HMC-1 cells and in a paracrine manner in noninfected neighboring HMC-1 cells, IFN-I promoted a ce

203 athogens and communicating danger signals to noninfected neighbors; however, little is known about th

204 potentiated in infected compared with nearby noninfected neurons.

205 fected joint, were larger than those next to noninfected neuropathic joints (2.6 cm(2) [range, 0.3-8.

206 A subgroup of patients with noninfected neutrophilic RA was associated with systemic

207 were similar between mothers of infected and noninfected newborns.

208 Compared with noninfected normal BM cells or to cells infected with an

209 t H. pylori infection, than in the mucosa of noninfected normal subjects.

210 ter in the CHV1-infected strains than in the noninfected ones.

211 , cell numbers were reduced as compared with noninfected or AdLacZ-infected cells (157 780+/-8413 [Ad

212 , nitrogen-fixing nodules but not in that of noninfected or inactive nodule organs.

213 Noninfected or infected control Sf9 cells do not express

214 mal when treated with BAL fluid samples from noninfected or Toxoplasma gondii-infected rats.

215 nfected with P. gingivalis, nonimmunized and noninfected, or orally infected with P. gingivalis only.

216 -8413 [AdCat], P<0.05 versus 233 700+/-3032 [noninfected] or 222 410+/-5332 [AdLacZ]).

217 uded households comprised 71 infected and 41 noninfected participants.

218 d with both healthy volunteers (p < .01) and noninfected patients (p < .05), and was highest in the s

219 carriers as compared with 50% (11/21) of the noninfected patients (P=0.01).

220 obacteriaceae in previously noncolonized and noninfected patients and used the double disk synergy te

221 All 91830 nonpsychiatric, noninfected patients discharged from the participating m

222 ory activity between gonococcus-infected and noninfected patients in either cervical mucus or serum.

223 with a SIRS, the proportions of infected and noninfected patients manifesting worsening encephalopath

224 At present, noninfected patients on biologicals for the treatment of

225 in plasma samples of patients with sepsis or noninfected patients who were elderly (eg, age >65 years

226 re common in both Campylobacter-infected and noninfected patients.

227 endogenous components present in the PDE of noninfected patients.

228 fected patients compared with 31.7 months in noninfected patients.

229 ein cholesterol concentrations compared with noninfected patients.

230 transplantation (LDKT; P=0.02) than matched noninfected patients.

231 ) have lower rates of contraceptive use than noninfected peers, yet concerns regarding contraceptive

232 The immunoglobulins enable macrophages from noninfected persons to destroy healthy T cells in tissue

233 V)-infected persons are less likely than are noninfected persons to respond to vaccination with pneum

234 rsons with HCV infection, and 6.9 months for noninfected persons.

235 ted person are significantly higher than for noninfected persons.

236 Noninfected PHVs frequently display homogeneous FDG upta

237 otentially lower future aphid populations on noninfected plants but no change or increased aphid popu

238 ulation size and increased feeding damage on noninfected plants under eCO2 but no changes to populati

239 fitness of infected plants was smaller than noninfected plants, we found no correlation between the

240 igher drought stress tolerance compared with noninfected plants, whereas this effect is attenuated by

241 function of the infected cells vs coresident noninfected population, nor about the mechanisms that co

242 res of FDG uptake on PET/CT in patients with noninfected prosthetic heart valve (PHV).

243 statistically different between infected and noninfected rabbits.

244 dization on RNA from P. carinii-infected and noninfected rat lungs.

245 was observed for PuM from both infected and noninfected rats and depended on the interaction of C. n

246 Initial experiments conducted with noninfected rats showed that acute administration of 8-O

247 on between Pneumocystis carinii-infected and noninfected rats were examined.

248 or necrosis factor-alpha) in infected versus noninfected rats.

249 serum samples from infected individuals and noninfected recipients of a recombinant gp120 vaccine.

250 01-positive patients is not recapitulated in noninfected recipients of Gag-containing canarypox-based

251 Similar to endogenous PKA activity of noninfected red blood cells, the parasite enzyme can be

252 P9i roots showed, in part, extremely swollen noninfected root hairs and reduced numbers of deformed n

253 was significantly different compared to the noninfected roots.

254 und to be amplifiable from both infected and noninfected samples and were inferred to be human DNA no

255 gulation of both Mcl1 and Noxa compared with noninfected samples.

256 e within the range of properties observed in noninfected SCN neurons.

257 onabsorbable (NAB) sutures from infected and noninfected sites.

258 Piglets from PRRSV-infected and noninfected sows were randomly assigned to Streptococcus

259 staining demonstrates that infected, but not noninfected, splenic CD11c(+)Gr-1(+) dendritic cells are

260 r1 and Vir2, produce abundant transcripts in noninfected strains of the fungus, but the transcripts a

261 V1 containing strains was much lower than in noninfected strains, and the dwell time of cryparin with

262 tration in the CHV1-infected strains than in noninfected strains.

263 to follow secretion in virally infected and noninfected strains.

264 it of 1.05 cm (95% CI 0.46-1.66) relative to noninfected, stunted children of similar age.

265 ically ill with sepsis (CIS), critically ill noninfected subjects (CINS), and healthy controls (C).

266 terferon-gamma were significantly greater in noninfected subjects (P < .05, .001, and .05, respective

267 subjects infected despite vaccination and in noninfected subjects were not significantly different.

268 Among noninfected subjects, those circulating RV-A16-specific

269 itical illness between infected (septic) and noninfected subjects.

270 me, reaching significance (p < 0.05) between noninfected survivors (n = 74) and nonsurvivors (n = 21)

271 ence in microbial recovery from infected and noninfected sutures was noted, (ii) infected sutures har

272 ll polarizes and releases virions toward the noninfected target cell in a gp120- and intercellular ad

273 ression may enhance trafficking of potential noninfected target cells to the site of active infection

274 patients with THA PJI (infection group) and noninfected THA (control group) were retrospectively eva

275 sted in latently infected tissue, but not in noninfected tissue of the same mice.

276 e of proliferation in latently infected than noninfected tissue, which was associated with a reduced

277 We enriched nuclei from infected and noninfected tissues and quantitatively assessed changes

278 lso minimizing collateral damage to adjacent noninfected tissues.

279 infected cells and impart resistance to the noninfected tissues.

280 other examples of immune-mediated damage to noninfected tissues: Rejecting renal allografts, melanom

281 WAP-TGFalpha transgenic animals compared to noninfected transgenic controls, and > 30% of the corres

282 ndeed, in vitro p24 expression by cells from noninfected transgenic mice was up-regulated by polyclon

283 egs were significantly less suppressive than noninfected Tregs and demonstrated down-regulation of ge

284 In vitro HIV-GFP infected and noninfected Tregs were isolated by flow-based cell-sorti

285 om the peritoneal dialysis effluent (PDE) of noninfected uremic patients.

286 he second dose were measured in infected and noninfected vaccine recipients.

287 but its specificity is limited by uptake on noninfected valves.

288 erns, and persistence of (18)F-FDG uptake in noninfected vascular prostheses, misinterpretation of PE

289 Diffuse (18)F-FDG uptake was found in 92% of noninfected vascular prostheses, more in Dacron grafts t

290 Serum interleukin-6 in noninfected VDR(+/+) mice was undetectable, but was easi

291 this classifier, inflammatix-bacterial-viral-noninfected-version 1 (IMX-BVN-1), without retraining, t

292 The close proximity in the CNS of noninfected visceral circuits to infected somatic neuron

293 nd P4[10]; and NSP4 type [A] in the group of noninfected volunteers (n = 11) were significantly highe

294 IV-1 vectors as vaccine immunogens in HIV-1,-noninfected volunteers has produced CTL responses in a s

295 MMTV-infected WAP-TGFalpha tumors, and some noninfected WAP-TGFalpha tumors also showed evidence of

296 irus (BYDV) during in vitro feeding, prefers noninfected wheat plants, while noninfective aphids also

297 NF-kappaB p65 formed a complex with VDR in noninfected wild-type mouse intestine.

298 Compared with noninfected women, those with symptomatic COVID-19 had i

299 liver samples from 20 (17 WHV-infected and 3 noninfected) woodchucks, 10 with WHV-associated hepatic

300 ococcus sp. amplicons were detected in 11/13 noninfected wounds; S. aureus was not detected in these