ライフサイエンスコーパス: uninfected

1 : 101 had congenital infection, and 116 were uninfected.

2 attach to the surfaces of cells, infected or uninfected.

3 equently among CMV-infected (39.1%) than CMV-uninfected (2.1%) infants.

4 The prevalence of HS was highest in the uninfected (33%) and HIV-monoinfected (28%), followed by

5 cal membrane Ag-1 (AMA1) in HIV-infected and uninfected adults living in Kenya.

6 h records from 9310 HIV-infected and 510 313 uninfected adults over the period April 1, 1996, to Dec

7 Healthy, HIV-uninfected adults were randomized to receive 4 mg of PEN

8 specific CD4 T cells in HIV-infected and HIV-uninfected adults with LTBI.

9 TPP criteria for clinical utility among HIV-uninfected adults with presumed tuberculosis in high-vol

10 We tested blood samples from 755 HIV-uninfected adults with presumptive pulmonary tuberculosi

11 adults had significantly less liver fat than uninfected adults, even after adjusting for demographics

12 o are retained in care can approach those of uninfected adults.

13 F, alone or with emtricitabine (FTC), in HIV-uninfected African men and women.

14 <0.8 mmol/L) in 596 HIV-infected and 544 HIV-uninfected AGEhIV Cohort Study participants.

15 In contrast, uninfected aging Siglec-H KO mice developed a mild form

16 tococcus (GBS) surface proteins among 81 HIV-uninfected and 83 HIV-infected mother-newborn pairs usin

17 CI 38 to 97) in children exposed to HIV but uninfected and 90% (53 to 98) in malnourished children n

18 , nodule primordia formed, but most remained uninfected and bacterial entry via ITs into the root epi

19 rtaken in human immunodeficiency virus (HIV)-uninfected and HIV-infected child-mother dyads from 2007

20 y itself, cause increased chemotaxis of both uninfected and HIV-infected human monocytes, suggesting

21 acy among human immunodeficiency virus (HIV)-uninfected and HIV-infected pregnant women.

22 ess samples from longitudinal cohorts of HIV-uninfected and HIV-infected women and their infants to e

23 RNA from undifferentiated and differentiated uninfected and HPV16-positive keratinocytes showed that

24 gets, impacts the proteome and physiology of uninfected and infected cells.

25 When we compared uninfected and infected Fulani individuals, in contrast

26 infected Fulani individuals, in contrast to uninfected and infected individuals from the sympatric e

27 in KwaZulu-Natal, South Africa, who were HIV uninfected and sexually active consented to HIV-1 RNA te

28 a TB-endemic setting, either HIV-infected or uninfected and with latent or active TB (aTB), were scre

29 iplicate differentiated populations of NIKS (uninfected) and NIKS16 (infected).

30 ferent at 18 days post-infection compared to uninfected animals indicating that the immune response i

31 his resulted in three sublines per genotype: uninfected, +APSE8 and +APSE3.

32 t baseline versus four (<1%) of 518 contacts uninfected at baseline, respectively (p=1.00).

33 due to smoking into the HIV-infected and HIV-uninfected, at high risk for HIV populations.

34 of 3 populations: US general population; HIV-uninfected, at high risk for HIV; and PLWH.

35 n of apoptosis and defined a transition from uninfected B cells (BCL-2) to early-infected (MCL-1/BCL-

36 in was degraded less in EBV-infected than in uninfected B cells, induction of cathepsin G activity by

37 ty) and greater beta diversity compared with uninfected BAL.

38 ECs from subjects with asthma, compared with uninfected BECs from subjects with asthma, led to a sign

39 We found that compared to the uninfected BN rat, the uninfected LEW rat has inherently

40 to the US general population and persons HIV-uninfected, but at high risk for HIV.

41 terflies, they also reduced the life span of uninfected butterflies, resulting in a hump-shaped curve

42 roduced by HIV-infected cells, as well as by uninfected bystander cells, and that the dominant stimul

43 Apoptosis was observed in both infected and uninfected bystander cortical neurons, suggesting a role

44 lected for RNA-sequencing, with samples from uninfected C57BL/6 WT and C57BL/6 IL-17RA KO animals ser

45 of latently infected calves than in those of uninfected calves.

46 urons in latently infected calves but not in uninfected calves.

47 gonist venetoclax induced minimal killing of uninfected CD4 T cells but markedly increased the death

48 ition of HIV-1 transmission from infected to uninfected CD4(+) T cells through virological synapses (

49 ver, it demonstrates that ISG15 modifies the uninfected cell proteome in response to dsDNA, potential

50 packaged into CSC-exposed HIV-1-infected and uninfected cell-derived exosomes, on HIV-1 replication o

51 vely, these results imply that exosomes from uninfected cells activate latent HIV-1 in infected cells

52 in wild-type SA11-infected cells or (ii) in uninfected cells along with viroplasm-forming proteins N

53 natures successfully classified infected and uninfected cells and further identified signals that wer

54 e show that IRAV associates with P bodies in uninfected cells and with the dengue virus replication c

55 that levels of background expression due to uninfected cells are kept at a minimum.

56 xpression in VZV-infected cells and adjacent uninfected cells compared to mock-infected cells.

57 n this study, we asked whether exosomes from uninfected cells could activate latent HIV-1 in infected

58 fragmentation, and apoptosis of infected or uninfected cells could be found in ZIKV-infected brain t

59 nase (RACK1), that are not phosphorylated in uninfected cells or cells infected by other viruses.

60 The exosomes from CSC-treated uninfected cells showed a protective effect against cyto

61 e to limiting the spread of DENV to adjacent uninfected cells through contact dependent gap junctions

62 he bacteroids, ammonia is finally reduced in uninfected cells to allantoin and allantoic acid [1].

63 ve structures that form between infected and uninfected cells to enhance the spread of HIV-1.

64 that is distinct from its normal function in uninfected cells to fine-tune lipid raft cholesterol tha

65 Accumulation of ISGylated proteins in uninfected cells treated with dsDNA was prevented by exp

66 The infected radial units are surrounded by uninfected cells undergoing apoptosis, suggesting that p

67 ranscripts of the P-acquisition genes in the uninfected cells were enriched after P limitation, inclu

68 , dsDNA triggered ISG15 accumulation even in uninfected cells, and this was reduced by HCMV IE1 expre

69 n human cells ERI3 localizes to the Golgi in uninfected cells, but relocalizes near sites of DENV-2 r

70 caused by fusion of infected cells with many uninfected cells, increased cytoskeleton reorganization,

71 s and potentially be exported to neighboring uninfected cells, leading to increased cellular activati

72 In uninfected cells, spliced mRNAs emerge into the cytoplas

73 In uninfected cells, the impaired RNA-binding capacity of Y

74 cytoplasmic processing bodies (P bodies) in uninfected cells, where it interacts with the MOV10 RISC

75 ed upregulation of catalase in exosomes from uninfected cells, with a decrease in the levels of catal

76 t ISGylation in response to dsDNA sensing in uninfected cells.

77 nnot discriminate between HIV-1-infected and uninfected cells.

78 eriments when KSHV miRNAs were introduced to uninfected cells.

79 onomer and conjugate protein accumulation in uninfected cells.

80 cted cells exposed to purified exosomes from uninfected cells.

81 es the opportunity of the virus to spread to uninfected cells.

82 ed neuropathology may be defined by death of uninfected cells.

83 s and RNA from infected cells to neighboring uninfected cells.

84 e processes occur in both virus-infected and uninfected cells.

85 rategy of the virus to efficiently spread to uninfected cells.IMPORTANCE The Cbl E3 ligase suppresses

86 led in pretreatment HIV care, and had an HIV-uninfected child (aged 6-10 years) were randomly allocat

87 ted retrospectively by PCR (n = 55), and (3) uninfected children (RDT/PCR negative) (n = 434).

88 and fetal growth restriction are reported in uninfected children born to human immunodeficiency virus

89 therapy (ART) regimens were compared to HIV-uninfected children not on ART, all of whom required tre

90 er levels of TNF-alpha and IL-1beta than HIV-uninfected children with measles, and lower levels of in

91 Of 2322 HIV-uninfected children with respiratory syncytial virus (RS

92 al HIV-disclosure to primary school-aged HIV-uninfected children.

93 nt relapse and the resulting transmission to uninfected children.

94 th HIV was significantly greater than in the uninfected cohort and declined after treatment.

95 (MESA), a Human Immunodeficiency Virus (HIV)-uninfected cohort, which used a similar photographic met

96 stage AMD compared with that found in an HIV-uninfected cohort.

97 of 169 infected contacts and six (5%) of 111 uninfected contacts developed incident tuberculosis (p=0

98 with severe pneumococcal pneumonia and three uninfected control animals.

99 4.4 +/- 1.3 compared to 7.8 +/- 0.5 for the uninfected control mice (P < 0.05).

100 d samples from 150 subjects, of whom 30 were uninfected control patients and 120 had Chagas disease (

101 Uninfected controls had the lowest LN activity (mean [SD

102 dults and a demographically-matched group of uninfected controls performed a verbal working memory ta

103 Data were compared with uninfected controls similar in age, sex, and cardiovascu

104 e HSV-2 seropositive or seronegative and HIV-uninfected controls were analyzed by flow cytometry.

105 tion, and HCV-HIV coinfection, as well as in uninfected controls, before and after HIV antiretroviral

106 y lower in all three infected groups than in uninfected controls, but with the highest loss of bone d

107 Compared with uninfected controls, women with early Plasmodium falcipa

108 es of seminal HHV shedding compared with HIV-uninfected controls.

109 y expanded during ZIKV infection compared to uninfected controls.

110 with minimal changes in sections from the 16 uninfected controls.

111 rvum oocysts for 6-13 days and compared with uninfected controls.

112 d graft survival rates compared to their HIV-uninfected counterparts, despite a nearly threefold incr

113 survival rates similar to those of their HIV-uninfected counterparts.

114 idence of cardiovascular diseases than their uninfected counterparts; however, the underlying mechani

115 ceptors IP, EP2, and EP4 in infected but not uninfected cPLA2alpha(-/-)or COX-1(-/-)macrophages.

116 not with pandemic IAV, enhance maturation of uninfected DC and T cell proliferation.

117 m infected DCs and taken up and presented by uninfected DCs, possibly overcoming this blockade of ant

118 Women who remained uninfected displayed a greater frequency of positive CD4

119 fely receive an organ transplant from an HIV uninfected donor.

120 semen and blood using samples obtained from uninfected donors and spiked with inactivated EBOV.

121 se endogenous ligands that are released from uninfected dying cells, thereby activating immune respon

122 greater loss is caused by the elimination of uninfected erythrocytes, sometimes long after infection

123 males of Drosophila melanogaster crossed to uninfected females causes embryonic lethality.

124 c incompatibility (CI)(3-5), where eggs from uninfected females fail to develop when fertilized by sp

125 hality in crosses between infected males and uninfected females.

126 hality in crosses between infected males and uninfected females.

127 ines was performed in H. pylori-infected and uninfected gastric biopsy specimens.

128 ve reverse transcriptase PCR in infected and uninfected gastric mucosa obtained from Bhutan and from

129 cells eventually accumulated in infected and uninfected glands.

130 ibody concentrations were higher for the HIV-uninfected group than the HIV-infected groups.

131 1 (HIV-1)-infected (and 116 HIV-exposed but uninfected (HEU) African infants receiving pentavalent r

132 1 human immunodeficiency virus (HIV)-exposed uninfected (HEU) and 100 HIV-unexposed Zimbabwean infant

133 survived (controls), and in 194 HIV-exposed uninfected (HEU) and 197 HIV-unexposed infants.

134 ed children, but efficacy in HIV-exposed but uninfected (HEU) children in a non-malarial, low-breastf

135 to 21 years of age compared with HIV-exposed uninfected (HEU) youth.

136 mated at 20.5% in PLWH in care, 14.6% in HIV-uninfected high-risk persons, and 12.8% in the US genera

137 study comparing the fecal microbiomes of HIV-uninfected (HIV SN) to HIV-infected individuals on long-

138 ciency virus (HIV)-infected children and HIV-uninfected, HIV-exposed children as opportunistic infect

139 l were maintained when co-presented with the uninfected host odors, overriding attraction to uninfect

140 nfected host odors, overriding attraction to uninfected hosts.

141 t differences in the metabolic profile among uninfected I. scapularis nymphal ticks, B. burgdorferi-i

142 lower risk of parasitemia, compared with HIV-uninfected individuals (adjusted relative risk, 0.16; 95

143 9 patients with chronic HCV infection and 19 uninfected individuals (controls) and measured levels of

144 Among 479 HIV-infected and 377 HIV-uninfected individuals (median follow-up = 3.9/4.1 years

145 ining significantly higher compared with HIV-uninfected individuals (p = 0.0001).

146 ined greater than the rate of decline in HIV-uninfected individuals at the lumbar spine but not at th

147 e was no induction of any T cell response in uninfected individuals following parasite antigen stimul

148 5 S. stercoralis-infected individuals and 10 uninfected individuals stimulated with parasite antigen

149 ssues obtained from HIV-infected and control uninfected individuals to examine connexin 43 (Cx43) exp

150 12 mo) and compared with 19 age-matched HIV-uninfected individuals using flow cytometry.

151 polyfunctionality compared with healthy HIV-uninfected individuals with latent TB infection.

152 ntly decreased (p = 0.002) compared with HIV-uninfected individuals, a change that correlated inverse

153 Occasional false-reactive Aptima results in uninfected individuals, or nonreactive results in HIV-1-

154 Compared with uninfected individuals, those with HIV infection with a

155 tly higher levels of Ki67, compared with HIV-uninfected individuals, thus indicating recent activatio

156 1417806 was significantly overrepresented in uninfected individuals.

157 F, borderline HFpEF, and HFrEF compared with uninfected individuals.

158 g in HIV-infected individuals as compared to uninfected individuals.

159 HIV-infected individuals, compared with HIV-uninfected individuals.

160 and worsening albuminuria compared with HIV-uninfected individuals.

161 unctive corticosteroid responsiveness in HIV-uninfected individuals.

162 Here we report that uninfected infant rhesus macaques exhibited a higher phy

163 We observed that uninfected infant rhesus macaques exhibited higher physi

164 All HIV-exposed, uninfected infants (HEIs) at 8 weeks of age (n = 1984) w

165 paediatric HIV infection, but the number of uninfected infants exposed to HIV through their HIV-infe

166 We also excluded clinical harms to HIV-uninfected infants incorrectly treated with ART after fa

167 [SGA], and BW z scores [BWZ]) in HIV-exposed uninfected infants of PHIV vs nonperinatally HIV-infecte

168 of HIV infection is <100%, leading some HIV-uninfected infants to be incorrectly identified as HIV-i

169 averted costly HIV care and ART in truly HIV-uninfected infants, it was cost-saving: total cost US$1,

170 herent challenges in studies of HIV-exposed, uninfected infants, which need large populations with ap

171 lity for invasive GBS disease in HIV-exposed uninfected infants.

172 were similarly detected in CMV-infected and uninfected infants.

173 ective birth cohort of 30 highly exposed CMV-uninfected infants.

174 in medical intervention for large numbers of uninfected infants.

175 In the studies reported here, we found that uninfected Irgm1-deficient mice displayed high levels of

176 xposure accelerated rate of metamorphosis in uninfected larvae.

177 that compared to the uninfected BN rat, the uninfected LEW rat has inherently higher transcript leve

178 -infected livers in comparison with control, uninfected livers and HCC, allowing us to identify pre-n

179 Eighty-eight healthy, HIV-uninfected, low-risk participants were enrolled in 6 Uni

180 In uninfected lungs, 53 genes were already differentially e

181 cinated infected, unvaccinated infected, and uninfected macaques identified two main IRF4(hi) subsets

182 reverse transcriptase (RT-SHIV), compared to uninfected macaques, and interestingly, there was extens

183 ith those observed in SIV-noncontrolling and uninfected macaques, we aimed to identify markers and ac

184 bacteria transferred from infected cells to uninfected macrophages along with other cytosolic materi

185 Infected and uninfected macrophages interdigitate, assuming an altere

186 in exosomes derived from HIV-1-infected and uninfected macrophages.

187 rs [interquartile range, 49-59 years] and 29 uninfected male controls with a median age of 52 years [

188 Dual expression in transgenic, uninfected males of Drosophila melanogaster crossed to u

189 Eligible participants were HIV-uninfected men and transgender women reporting condomles

190 ting after 12 months ranged from 42.4% among uninfected men to 56.7% among infected men on the index

191 usly infected mice was sufficient to protect uninfected mice from lethal pathogen challenge.

192 induced overexpression of PTEN in B cells in uninfected mice led to suppression of antibody responses

193 essed in the salivary glands of infected and uninfected mice, and many of these could promote the mig

194 to heart sections from T. cruzi-infected and uninfected mice.

195 ell transfer did not trigger inflammation in uninfected mice.

196 t infected microglia produced type I IFN and uninfected microglia induced an innate immune response f

197 Uninfected monocytes treated with LDL or left untreated

198 -exposed uninfected newborns compared to HIV-uninfected mother-newborn dyads.

199 0.1 times (95% CI, 6.1-16.6) the risk of HIV-uninfected MSM.

200 to nonfrail, HIV-infected (n = 141) and HIV-uninfected (n = 150) men by age, calendar year, and anti

201 tuberculosis-specific CD4(+) T cells in HIV-uninfected (n = 20) and HIV-infected individuals (n = 20

202 plication (noncontrollers [NCs]), and 48 HIV-uninfected (NEG) subjects.

203 HIV-exposed uninfected neonates were more than twice as likely to ha

204 Ex vivo analysis of infected versus uninfected neutrophils revealed a deficiency in infectio

205 cted in HIV-infected mothers and HIV-exposed uninfected newborns compared to HIV-uninfected mother-ne

206 ted in mid or late biosynthetic steps induce uninfected nodule primordia.

207 modifies the proteomes of virus-infected and uninfected normal cells in response to cell-intrinsic ds

208 Here, we characterized exosomes derived from uninfected or HIV-1 infected T-cells and DCs.

209 a cohort of Ugandan patients, including HIV-uninfected or HIV-infected subjects and those either tre

210 patterns among primary human gastric cells, uninfected or infected with H pylori P12 wt or P12Deltac

211 s, Ulex europaeus and Acacia paradoxa either uninfected or infected with the hemiparasite Cassytha pu

212 ncluding AHR and eosinophil infiltration, in uninfected OVA-sensitized/challenged mice.

213 ed participants (13 [3%] women) and 1952 HIV-uninfected participants (154 [8%] women).

214 acute or chronic HIV infection and from HIV-uninfected participants from Bangkok, Thailand.

215 HIV-uninfected participants had higher odds of SDCS with par

216 ping of cagA from feces of both infected and uninfected participants revealed that the AB genotype ac

217 Compared with uninfected participants-and after adjusting for demograp

218 ART but remained elevated compared with HIV-uninfected participants.

219 ion was higher in O. viverrini-infected than uninfected participants.

220 t were similar to or lower than those in HIV-uninfected participants.

221 echanism for enhanced HIV transmission to an uninfected partner.

222 patients with AIDS were more likely than HIV-uninfected patients to be discharged to nonhospital inpa

223 of AIDS were significantly more likely than uninfected patients to die during hospitalization after

224 study analyzed 455 HIV-infected and 1945 HIV-uninfected patients, all of them members of the Kaiser P

225 Among HIV-uninfected patients, mortality was associated with highe

226 In HIV-uninfected patients, the corresponding sensitivities wer

227 rvival of human immunodeficiency virus (HIV)-uninfected patients, with TT-genotype patients significa

228 infected with influenza A(H3N2) viruses and uninfected patients.

229 ected patients without a history of AIDS and uninfected patients.

230 We recruited 64 HIV-infected and 107 HIV-uninfected patients.

231 d with P. aeruginosa but not in samples from uninfected patients.

232 e detection of HIV RNA decayed as background uninfected PBMC counts increased; proteinase K treatment

233 stive heart failure (CHF) risk compared with uninfected people.

234 lower in HIV-infected persons as compared to uninfected persons (P = .048), whereas blood responses w

235 ition was not reduced in HIV-infected, HSV-2-uninfected persons during TDF-containing ART.

236 oinfected, 17739 HIV-monoinfected, and 36604 uninfected persons in the Veterans Aging Cohort Study (2

237 s (HIV) have a 2.8-fold higher risk than HIV-uninfected persons of nonmelanoma skin cancer (NMSC), de

238 HIV-infected persons compared with HIV-uninfected persons were are at higher risk for subsequen

239 However, although HIV-uninfected persons with latent TB infection exhibited ex

240 3.8% in PLWH in care, 9.7% for high-risk HIV-uninfected persons, and 9.4% in the US general populatio

241 Compared with HIV-uninfected persons, HIV-infected individuals were slight

242 HIV-infected persons when compared with HIV-uninfected persons.

243 Results were similar among uninfected persons.

244 e restoration of weight gain to the level of uninfected pigs.

245 veral immune traits: Fish from the naturally uninfected population initiated a stronger granulocyte r

246 ad consistency of findings with those in HIV-uninfected population would suggest that the risk strati

247 earlier than would be expected in a typical uninfected population.

248 e as great (range = 0.23-0.29) as those from uninfected populations (range = 0.04-0.17).

249 mes among human immunodeficiency virus (HIV)-uninfected pregnant women protected by indoor residual s

250 errupt rapid transmission within networks of uninfected PWID.

251 golian gerbils (either H. pylori infected or uninfected) received a normal diet or one of three diets

252 estered parasitized erythrocytes and reduced uninfected red blood cell deformability (RCD) compromise

253 ial reservoirs of infection and to safeguard uninfected regions through enhanced biosecurity.

254 an Immunodeficiency Virus (SIV)-infected and uninfected rhesus macaques.

255 mmunodeficiency virus (SHIV)-infected and 16 uninfected rhesus macaques.

256 Compounds specific to the uninfected root and bacteria were also detected.

257 r the rapid analysis of intact root nodules, uninfected root segments, and free-living rhizobia.

258 ntegrin alpha4 mediate T cell recruitment to uninfected salivary glands but that redundant mechanisms

259 T cell recruitment to uninfected salivary glands depended on chemokines and th

260 zoite vaccinations, mice were immunized with uninfected salivary glands from a single mosquito.

261 XCR3 was critical for T cell accumulation in uninfected salivary glands.

262 The bites of uninfected sand flies favor the transmissibility of L. d

263 demonstrate that prior exposure to bites of uninfected sand flies potentiates their ability to trans

264 grees C, whilst growth was maintained at the uninfected skin temperature of 32 degrees C.

265 unless NAAT cost exceeded US$400 or the HIV-uninfected status of infants incorrectly identified as i

266 cts infected with HIV was similar to that in uninfected subjects.

267 turnover in HIV type 1 (HIV-1)-infected and -uninfected TB patients and controls, and a prospective c

268 ctivity differed between HIV-1-infected and -uninfected TB patients and corresponded with specific TB

269 t increased plasma PIIINP, compared to HIV-1-uninfected TB patients.

270 urified brain mitochondria from infected and uninfected Tg7 mice showed significant differences in th

271 omposition of exosomes from Mtb-infected and uninfected THP-1-derived macrophages was evaluated by ta

272 ulomas had higher [(64)Cu]-LLP2A uptake than uninfected tissues, and immunohistochemical analysis of

273 iral signals from infection sites to distant uninfected tissues.

274 Conversion from HIV-1-uninfected to -infected status was rapid, with no eviden

275 classification of apparently infected versus uninfected to a probability-based interpretation which i

276 dividuals were identified as converting from uninfected to infected status.

277 at a hospital in South Africa in healthy HIV-uninfected toddlers (aged 2 to <3 years) and term infant

278 ated higher amounts of catechin and PAs than uninfected trees.

279 HIV-uninfected, TT-genotype patients had high CSF proinflamm

280 ndividuals with (infected [INF]) or without (uninfected [UN]) S. stercoralis infections.

281 in most individuals classified as H. pylori uninfected using conventional methods.

282 vational cohort of HIV-infected veterans and uninfected veterans matched by age, sex, race/ethnicity,

283 Compared with uninfected veterans, HIV-infected veterans had an increa

284 articipants (37 PPI+ and 40 PPI-) and 20 HIV-uninfected volunteers.

285 and microbial translocation biomarkers than uninfected volunteers.

286 ulations of children who are HIV-exposed but uninfected will face the challenge of disclosure of pare

287 V-infected women compared with 32 in the HIV-uninfected women (6.8 vs 3.9 episodes per 1000 person-mo

288 antenatal enrollment compared to 7.7% among uninfected women (adjusted risk ratio [aRR] 1.14 [95% co

289 infection at delivery compared to 7.9% among uninfected women (aRR 1.32 [95% CI: 1.08, 1.62]; N = 11,

290 e burden of HPV in both HIV-infected and HIV-uninfected women (independent of pH).

291 of PCR-CI and SDI was 5.6% and 35.0% in HIV-uninfected women and 20.5% and 43.6% among HIV-infected

292 d >/=50, as well as between HIV-infected and uninfected women and between Hispanic and non-Hispanic w

293 nd cognition in a cohort of HIV-infected and uninfected women from the Women's Interagency HIV Study

294 HIV-uninfected women reporting condomless vaginal or anal in

295 Vaccine efficacy in HIV-uninfected women was similar for PCR-CI (66.9%; 95% conf

296 ow MUAC at enrollment compared to 8.4% among uninfected women with MUAC >/= 23 cm (joint aRR 2.13 [95

297 , during the second trimester: compared with uninfected women, women with positive RDT findings deliv

298 HSIL) and anal cancer (AC) compared with HIV-uninfected women.

299 QFT negative, HIV uninfected young children aged 18-24 weeks were enrolled

300 (PrEP) in human immunodeficiency virus (HIV)-uninfected young men who have sex with men, we measured