ライフサイエンスコーパス: -infected

1 ntrol, randomized, open-label study in HIV-1-infected antiretroviral therapy-naive adults (CD4+ >=50

2 nation eliminated reactivated latently HIV-1-infected cells in an ex vivo quantitative viral outgrowt

3 smaller reduction in the proportion of HIV-1-infected cells within LNs per year on therapy that was s

4 entions that do not rely on daily ART, HIV-1-infected children face lifelong medications to control i

5 to inform cure-directed approaches for HIV-1-infected children.

6 In three independent experiments in HIV-1-infected humanized mice and one pivotal experiment in si

7 bneutralizing plasma concentrations in HIV-1-infected humanized mice but elicited CD4-binding site mu

8 1-18 alone fully suppressed viremia in HIV-1-infected humanized mice without selecting for resistant

9 proteome arrays from chronic untreated HIV-1-infected individuals using the classificatory random for

10 dependent t-tests were used to compare HIV-1-infected individuals within or outside an identified clu

11 ured polarized endocervical cells with HIV-1-infected lymphocyte-derived cells, we discovered endocer

12 taneously enhance viral suppression in HIV-1-infected macrophages.

13 ECH clears HIV-1 in blood samples from HIV-1-infected patients.

14 llers (EC) represent a small subset of HIV-1-infected people that spontaneously control viral replica

15 ced pathogenic levels of VEGF-A within HSV-1-infected corneas, and CD4(+) cell depletion promoted rei

16 expression was transiently elevated in HSV-1-infected neurons, as well as in the presence of antivira

17 These data show that HTLV-1-infected T-cell clones carrying key oncogenic driver mut

18 d increases colorectal tumorigenesis in 11G5-infected Apc(Min/+) mice.

19 were observed in the colonic mucosa of 11G5-infected Apc(Min/+)/Atg16l1(DeltaIEC) mice vs 11G5-infec

20 ed Apc(Min/+)/Atg16l1(DeltaIEC) mice vs 11G5-infected Apc(Min/+) mice.

21 ubstantially restored in the HVT-DeltavNr-13-infected cells.

22 onfirmed coronavirus disease 2019 (COVID-19)-infected patients and specificity using 1,204 samples su

23 n of different leukocyte subsets in COVID-19-infected patients in relation to disease severity.

24 ity for all patients with HF and in COVID-19-infected patients with HF.

25 vels were significantly elevated in COVID-19-infected patients.

26 outcomes of 17 previously healthy SARS-CoV-2-infected children and adolescents with an inflammatory p

27 Treatment of SARS-CoV-2-infected hamsters with a low dose of favipiravir or hydr

28 Recent research suggests that SARS-CoV-2-infected individuals can be highly infectious while asym

29 SARS-CoV-2-infected lung tissues show a massively upregulated innat

30 ng between vaccinated and control SARS-CoV-2-infected macaques.

31 rigger immunopathogenic events in SARS-CoV-2-infected patients or enhance infection.

32 ence of antibody sequences across SARS-CoV-2-infected patients, highlighting stereotyped naive respon

33 ent an opportunity to improve care for HIV-2-infected individuals.

34 did not receive treatment, and 67% of HIV-2-infected mothers and 77% of their infants received ineff

35 ex vivo study of circulating Tfh from HIV-2-infected patients.

36 l six passages, comparable with that for 22L-infected cells.

37 ll functions in vivo Importantly, H5N1 (2:6)-infected mice displayed decreased numbers of tissue-resi

38 st T cell responses in the lungs, H5N1 (2:6)-infected mice showed inefficient and delayed viral clear

39 xpression by cytotoxic T cells in H5N1 (2:6)-infected mice, suggesting that delayed viral clearance o

40 lture, and increased survival of influenza A-infected mice.

41 Depletion of TREM-1 in EV-A71-infected PBMCs with peptide LP17 resulted in decreased l

42 nst fatal malaria in Plasmodium berghei ANKA-infected C57BL/6J mice, an experimental CM model.

43 ood meal is not known; however, an arbovirus-infected mosquito can inoculate extravascular host tissu

44 Aspergillus-infected monocyte-derived DCs and neutrophils recruit pD

45 Aspergillus-infected murine Mo-DCs and neutrophils recruited pDCs to

46 CD4(+) T-cells among influenza A/H3N2 and B-infected patients (p = 0.006 and 0.004 respectively).

47 Blastocystis-infected animals had non-inflammatory CHS with increased

48 Treatment of SINV-Broccoli-infected cells with antibody to the SINV E2 glycoprotein

49 yces dermatitidis and Histoplasma capsulatum-infected canine and feline lungs and airway epithelial c

50 his study, humoral immune responses in CHIKV-infected patients and vaccinees were analyzed.

51 We hypothesized that Chlamydia-infected DCs and epithelial cells present overlapping se

52 CDRH2 that was isolated from the chronically-infected individual from whom the bent CDRH3 bNAbs were

53 ) and that natural killer (NK) cells in CL13-infected mice are reduced in numbers and have an immatur

54 ding survival of cardiac allografts from CMV-infected donors.

55 n but lower capacity to respond to human CMV-infected cells; 2) term pregnancy dNK are not skewed tow

56 against HDV in 12 treatment-naive HBV/HDV co-infected patients.

57 PHHs, either HBV mono-infected or HBV/HDV co-infected.

58 is compared with APRI or FIB-4 in HBV/HIV co-infected adults on combined antiretroviral therapy.

59 In addition, HBV/HIV co-infected females presented at a younger mean age (36.8 y

60 of morbidity and mortality in the HBV/HIV co-infected patient population.

61 In co-infected non-human primates, Siglec-1 is highly expresse

62 The reduced survival times in mice co-infected with a low dose of T. muris on d 105 after CNS

63 Patients co-infected with hepatitis B virus (HBV) and the human immu

64 ticipants; 69.9% were male and 70.4% were co-infected with human immunodeficiency virus (HIV).

65 ased acquisition of Th cells in Coccidioides-infected lungs compared with vaccinated wild-type mice,

66 raze toxic endophyte (Epichloe coenophialum)-infected tall fescue (E+) and are hallmark signs of fesc

67 tive donor samples, but in 299 HIV confirmed-infected donor samples, 46 (15.4%; 95% confidence interv

68 ORF8b was abundantly expressed in MERS-CoV-infected Huh-7 cells.

69 oid assay in colonic crypts isolated from CR-infected mice revealed elevated levels of LRP5/6 and FZD

70 By 2019, CWD-infected cervids had been detected in 26 states, three C

71 ly with brain homogenate from individual CWD-infected elk of various genotypes (LL132, LM132, or MM13

72 In order to ascertain whether such CWD-infected elk carry distinct prion strains, groups of Tg1

73 All ASFV-G-DeltaI177L-infected animals had low viremia titers, showed no virus

74 nocytes isolated in an acute phase from DENV-infected pediatric patients correlates with severe disea

75 However, DENV-infected MEG-01 cells, when induced for differentiation

76 he wild-type virus and found that the DUBmut-infected mice had a statistically significant reduction

77 een groups following stimulation with an EBV-infected cell lysate.

78 a is subjected to ubiquitination in both EBV-infected and EBV-negative cells.

79 ather rewires intracellular signaling in EBV-infected B cells that optimizes cell survival and prolif

80 Proportions of EBV-infected cells correlated with blood EBV loads.

81 We showed that EBV-infected T cells had an effector memory activated phenot

82 ctor memory activated phenotype, whereas EBV-infected B cells expressed plasma cell differentiation m

83 aining lymph node of ectromelia virus (ECTV)-infected mice or at becoming effectors but proliferated

84 ment downregulated CCR7 on Y. enterocolitica-infected bone marrow-derived DCs and purified MLN DCs, w

85 ) were found in the RLN of Y. enterocolitica-infected TNFRp55(-/-) mice.

86 t of Tir clustering on the viability of EPEC-infected intestinal epithelial cells (IECs) is unknown.

87 uations analogous to the Susceptible-Exposed-Infected-Recovered (SEIR) model.

88 ophylaxis and bites from 12-15 P. falciparum-infected mosquitoes (CVac-chloroquine arm) at 3 monthly

89 participants underwent Plasmodium falciparum-infected mosquito challenge (controlled human malaria in

90 survival was also 12% lower on C. fioriniae-infected fruit.

91 T cell control of B cell lymphoma in gammaHV-infected mice overlap with those necessary for control o

92 xpression of Wnt3a and Dvl3 in P. gingivalis-infected gingival tissues, and increases disease severit

93 d delayed viral clearance compared with H1N1-infected mice.

94 e-resident memory T cells compared with H1N1-infected mice; however, despite the decreased number of

95 Indonesian patients and 20% of reported H5N1-infected patients globally.

96 uld be an effective strategy to identify HBV-infected pregnant women at risk of perinatal transmissio

97 countries hinders the identification of HBV-infected pregnant women at risk of perinatal transmissio

98 ntly, the transfer of EVs purified from HCMV-infected cells enhanced virus spread.

99 Indeed, survival of autophagy-inhibited HCMV-infected monocytes was rescued when MLKL and RIPK3 were

100 1035 HCV-infected patients were included, 667 (64%) coinfected wi

101 in 29 HCV-infected LTx-recipients and 17 HCV-infected patients during DAA-treatment.

102 virin) that enrolled chronic genotype 1a HCV-infected persons coinfected with suppressed HIV: 5 of 6

103 STAT-1 and STAT-4 phosphorylation in 29 HCV-infected LTx-recipients and 17 HCV-infected patients dur

104 in HCV-infected hepatocytes and chronic HCV-infected liver biopsy specimens.

105 strated that ATM expression is higher in HCV-infected hepatocytes and chronic HCV-infected liver biop

106 loping hepatocellular carcinoma (HCC) in HCV-infected patients who achieve sustained virological resp

107 2 (Day 7 in 4 of 5 participants), mean %HCV-infected cells = 1.0% (95% CI, 0.2%-1.7%) (P < .05 for c

108 At liver biopsy 1, mean %HCV-infected cells = 25.2% (95% confidence interval [CI], 7.

109 ession of miR-181c promoted apoptosis of HCV-infected hepatocytes and can be inhibited by overexpress

110 ntaining CDRH3 is specific to particular HCV-infected individuals, we solved a crystal structure of t

111 amplifying partial viral genomes from 6 HeV-infected tissue samples from Syrian hamsters and 4 tissu

112 Finally, RNA sequencing studies of HEV-infected primary human hepatocytes demonstrated a tempor

113 rinatally human immunodeficiency virus (HIV)-infected adolescents (PHIV+) compared to age-, sex-, eth

114 tudies in human immunodeficiency virus (HIV)-infected individuals suggest excess weight gain with int

115 luding 57 human immunodeficiency virus (HIV)-infected men with KS, multicentric Castleman disease, or

116 HIV-infected immunological non-responders (INR) fail to reco

117 ll incidence rate of 0.74 cases per 1000 HIV-infected person-years (95% confidence interval, 0.43-1.0

118 We conducted a study of 22 HIV-infected participants receiving modern ART to determine

119 replication, we studied blood pDCs in 29 HIV-infected participants who initiated antiretroviral thera

120 were performed on stool samples from 405 HIV-infected and 111 uninfected participants of the Copenhag

121 Aging HIV-infected (HIV+) men who have sex with men (MSM) and HIV-

122 nowledge regarding mechanisms that allow HIV-infected cells to persist in individuals during combinat

123 anti-CD3 stimulation (P = .19) although HIV-infected participants had significantly higher CD8+ T-ce

124 Graft and patient survival among HIV-infected LT recipients have shown improvement over time.

125 to infinity) but declined rapidly among HIV-infected participants (half-life; 39 years; 24-108 years

126 Among HIV-infected, model of end-stage liver disease (aHR, 1.04; P

127 ears old (age-ineligible for PCV13), and HIV-infected adults (18 to 40 years old) on antiretroviral t

128 lness among pregnant girls and women and HIV-infected persons.

129 the JCI, Chaillon and coworkers assessed HIV-infected cells from various anatomic compartments obtain

130 There was no difference between HIV-infected and HIV-uninfected study participants in terms

131 gen receptor (CAR) T cell to target both HIV-infected CD4(+) T cells and the FDC reservoir in vitro A

132 Among 1454 treatment-eligible HIV-infected MSM and 1939 PWID, older age (adjusted prevalen

133 natomic CMV compartmentalization in five HIV-infected mothers and identify the possibility of congeni

134 Kidney transplant (KT) outcomes for HIV-infected (HIV+) persons are excellent, yet acute rejecti

135 at fractionated SP enriched for EVs from HIV-infected men induces potent transcriptional responses in

136 Cryopreserved serum samples from HIV-infected Ugandans obtained as part of a prospective CrAg

137 fibrosis/cirrhosis in a cohort of Greek HIV-infected patients.

138 ession profiles, and immune responses in HIV-infected adult solid organ transplant (SOT) recipients o

139 ospinal fluid (CSF) by flow cytometry in HIV-infected adults with cryptococcal (n = 31) and noncrypto

140 T-treated HIV subjects occur in vitro in HIV-infected CD4 T cells remains unknown.

141 and regulates cell cycle progression in HIV-infected cells.

142 cal, cOgnitive and VIsual performance in hiv-infected Children cohort showed significant cognitive im

143 Our results suggest that timing of TI in HIV-infected children has a long-term and measurable impact

144 ct of long-term ART on gut microbiome in HIV-infected children.

145 STA on both CD4(+) and CD8(+) T cells in HIV-infected human patients.

146 (TAF) improves renal tubular markers in HIV-infected individuals but the impact on estimated glomeru

147 telomere erosion, and cell apoptosis in HIV-infected individuals on antiretroviral therapy (ART).

148 for bacterial respiratory infections in HIV-infected inpatients, but its value is limited as quantit

149 romotes the decline in CD4(+) T cells in HIV-infected mice.

150 lymorphisms that were overrepresented in HIV-infected patients in Japan sharing the same HLA genotype

151 The diagnosis of tuberculosis (TB) in HIV-infected patients is challenging.

152 In HIV-infected patients, higher plasma sodium was uniformly as

153 flammation and neurological disorders in HIV-infected patients.

154 levated production of HERV-K proteins in HIV-infected patients.

155 V-1 Rev-mediated expression of HERV-K in HIV-infected patients.

156 on is the main barrier to cure, and most HIV-infected cells reside in the gut, where distinct but unk

157 Most HIV-infected cells reside in tissues such as the gut, but it

158 WHIV (vs non-HIV-infected women) exhibited increased myocardial fibrosis

159 the potential locations of reservoirs of HIV-infected cells that persist during therapy.

160 oliferation counterbalanced the decay of HIV-infected cells throughout therapy.

161 to enhance immune-mediated clearance of HIV-infected cells.

162 he abundance of ABCA1 in brain tissue of HIV-infected human subjects diagnosed with HAND was lower, a

163 Treatment of HIV-infected macrophages and T cells with trehalose inhibite

164 leading to profound immunodeficiency of HIV-infected patients is still only partially understood.

165 igen-specific CD4 T cells in a cohort of HIV-infected persons starting antiretroviral treatment (ART)

166 In vivo clonal expansion of HIV-infected T cells is an important mechanism of viral pers

167 humoral response to KSHV in a cohort of HIV-infected Zambian mothers without KS and identify potenti

168 Thus, we studied 4 simian/HIV-infected, ART-suppressed rhesus macaques infused with vi

169 we analyze the TCR repertoire of single HIV-infected cells harboring translation-competent proviruse

170 on with CD4 count or HAND status for the HIV-infected cohort.

171 Median survival was 82 days among the HIV-infected HCC patients compared to 181 days among those w

172 antiretroviral therapy, children born to HIV-infected (HI) mothers are at a higher risk of early-life

173 herapies and insufficiencies in treating HIV-infected individuals.

174 who were HIV-uninfected (n = 314) versus HIV-infected (n = 42).

175 tiretroviral therapy (ART) in vertically HIV-infected children limits the size of the virus reservoir

176 Using an in vitro HIV-infected, ART-treated MDM model, we show that ZL0580 als

177 one quarter of the adult population was HIV-infected in 2012.

178 mprovements over time for both, but with HIV-infected patients having greater improvements (P-trends

179 In RSV- or HMPV-infected cells, cytosolic inclusion bodies containing th

180 s and promotes accelerated cell death in HSV-infected cells.

181 recipitation experiments with lysates of HSV-infected neurons showed that UL16 and three other tegume

182 nd explain, at least in part, why every HSV1-infected person is not equally likely to develop HSV1-as

183 In the wild-type HVT-infected cells, vNr-13 expression appeared to be directl

184 Pneumococcal ability to grow in the IAV-infected LRT depends on the nutrient-rich milieu with in

185 bodies (mAbs) that target IBV NA from an IBV-infected patient.

186 luenza B, and improved survival of influenza-infected mice.

187 ies, uterus, cervix, or vagina in FP isolate-infected dams.

188 lation of dsRNA and the IFN response in JUNV-infected cells.

189 In sharp contrast, KSHV-infected LECs predominantly entered lytic replication, u

190 The NE gene expression observed in KSHV-infected cells was recapitulated in uninfected endotheli

191 and underlying mechanisms of HIV Tat in KSHV-infected endothelial cells undergoing viral lytic reacti

192 bly counteract each other in regulating KSHV-infected endothelial cell proliferation.

193 BEC and LEC, respectively) to show that KSHV-infected BECs progressively lose viral genome as they pr

194 hedgehog (hh) signaling in LXA4-treated KSHV-infected cells.

195 ed infection rates in surviving S411A Kunjin-infected Culex quinquefasciatus mosquitoes were observed

196 LCMV-infected Il18-transgenic (Il18tg) mice developed cachexi

197 Nevertheless, Legionella-infected macrophages induce an interleukin-1 (IL-1)-depe

198 FN-gamma binds to its receptor on Leishmania-infected macrophages, resulting in their activation, pro

199 ized the interactions of lymphocytes and LVS-infected macrophages using confocal microscopy and chara

200 In contrast, co-culture of LVS-infected macrophages with LVS-immune lymphocytes halted

201 Here, we identified 7 SIV(mac239)-infected rhesus macaques (RMs), defined as PTCs, who sta

202 hanges in tissues collected from EBOV-Makona-infected cynomolgus macaques.

203 ms, including circulating rings from malaria-infected patients and artemisinin-induced quiescent para

204 he development of liver cancer in S. mansoni-infected patients.

205 e individuals and one from a previously MARV-infected individual were selected for testing as HCDR3 l

206 While MDV-infected chickens have normal serum concentrations of ch

207 RSV-infected cultures (>40%) than from mock-infected cultures (<5%) after 4 h.

208 VZV-infected qHA-sps, but not mock-infected qHA-sps, contained intracellular amylin, APP, a

209 h severe clinical disease compared with mock-infected controls.

210 days 8 and 28 on SACC-PHHs, either HBV mono-infected or HBV/HDV co-infected.

211 younger mean age (36.8 years) than HBV mono-infected women (50.5 years) (p = 0.09).

212 elevated in Mycobacterium tuberculosis (Mtb)-infected macrophages.

213 that acetylcholine is the top-scoring in Mtb-infected AMs.

214 azole are two top-scoring metabolites in Mtb-infected KCs and that acetylcholine is the top-scoring i

215 dings and show that in vivo treatment of Mtb-infected C57BL/6 mice with doramapimod, a p38 MAP-kinase

216 ysosomal system is a defining feature of Mtb-infected macrophages and suggest that this altered lysos

217 A metabolomics comparison of Mtb-infected macrophages indicates that ornithine and imidaz

218 We showed that Mtb-infected CSE(-/-) mice survive longer than WT mice, and

219 ian hamsters and 4 tissue samples from a NiV-infected African green monkey with viral loads as low as

220 roinflammatory cytokines (IL-6, IL-8) in NiV-infected PBEpC was not decreased.

221 nvestigate changes in blood chemistry in NiV-infected Syrian hamsters that survived or succumbed to d

222 tive control material, the evaluation of non-infected cells expressing coronavirus (SARS, MERS) spike

223 ells of the human body to eliminate pathogen-infected or tumorigenic cells (i.e., target cells).

224 In pathogen-infected cells, HLA class I expression is perturbed.

225 ellular antibiotic visualisation in pathogen-infected tissue is lacking.

226 ia is significantly decreased in Pbyop1Delta-infected mice.

227 In B. pertussis-infected mice, lung type I/III IFN responses correlated

228 Y. pestis-infected Mefv(M680I/M680I) FMF knock-in mice exhibited I

229 ection method to generate A. phagocytophilum-infected ticks in laboratory conditions.

230 thod for separating all stages of Plasmodium-infected erythrocytes through lysis and removal of uninf

231 in contrast to no mortality in S. pneumoniae-infected sham (Sham + Sp) animals.

232 At 3 days post-injury, S. pneumoniae-infected traumatic brain injury mice (TBI + Sp) had a 25

233 harvested from 1-, 2-, 3-, and 6-month post-infected hamsters compared to uninfected liver tissues.

234 ile brain homogenates from symptomatic prion-infected mice are highly toxic to cultured neurons, exce

235 ions in gastric epithelial cells of H pylori-infected INS-GAS mice was assessed by whole-exome sequen

236 Notably, H. pylori-infected AGS cells exhibited the loss of mitochondrial i

237 nfection rates, only a fraction of H. pylori-infected individuals develop gastric cancer.

238 e quaking-induced conversion assays with RML-infected cell lysates, we observed a strong signal over

239 e (n = 4446), and full-term (n = 33 417) RSV-infected infants were matched to 424, 791, 8875, and 66

240 on 3-wk- (juvenile) and 8-wk-old (adult) RSV-infected C57BL/6 mice to investigate age-related differe

241 glycol-conjugated catalase (PG-CAT) for RSV-infected mice.

242 ecovered more apoptotic neutrophils from RSV-infected cultures (>40%) than from mock-infected culture

243 Human tracheal aspirates from RSV-infected infants showed elevated pro-IL-1beta mRNA and p

244 5 in the bronchoalveolar lavage fluid of RSV-infected mice, without increasing viral replication in t

245 Airway sensitization of naive mice with RSV-infected BMDCs exacerbate a live challenge with RSV infe

246 ed inflammation, was also prevented in EW RV-infected mice.

247 Salmonella-infected, CD4-depleted 129X1/SvJ mice remained chronical

248 epletion was performed in five SHIV(SF162P3)-infected RMs treated with ART for 12 months and with pla

249 future therapeutic approaches to treat SFTSV-infected patients.

250 When infused into viremic simian HIV (SHIV)-infected rhesus macaques, there was a 21% difference in

251 n simian-human immunodeficiency virus (SHIV)-infected rhesus macaques, an earlier and sharper decline

252 ivation following antibody treatment of SINV-infected differentiated AP-7 neuronal cells.

253 SIV-infected animals showed decreased diversity of gut micro

254 al coordinates analysis (PCoA) clustered SIV-infected untreated animals away from healthy and treated

255 ith sustained viral control after ATI in SIV-infected RMs.IMPORTANCE While effective, antiretroviral

256 Using SIV-infected rhesus macaques, we analyzed multiple brain reg

257 ication, both in vitro and in vivo in SIVmac-infected macaques, by upregulating antioxidant pathways

258 ectly associated with exposure to sporozoite-infected mosquitoes (RR, 1.24; 95% CI, 1.11-1.38).

259 Of 927 STEC-infected children, 41 (4.4%) had HUS at presentation; of

260 nt therapy (RRT) (secondary outcome) in STEC-infected children without HUS at initial presentation.

261 ocalization in the spleens and livers of STm-infected IFN-gamma(-/-) and T-bet(-/-) mice.

262 The proximal colon of T. suis-infected pigs exhibited general inflammation around day

263 ulation by fitting compartmental susceptible-infected-susceptible (SIS) transmission models simultane

264 dynamics take place, e.g., as in susceptible-infected-recovered (SIR) models.

265 tions, similar to the well-known susceptible-infected-recovered (SIR) model.

266 lity data to estimate a modified susceptible-infected-recovered (SIR) model in the United States.

267 sing a computer-generated list, T. trichiura-infected adolescents were randomly assigned to 7 treatme

268 By killing trophozoite-infected erythrocytes, PfGARP could synergize with other

269 N RNA in the cytoplasm compared to wild-type-infected cells.

270 tes to mount responses to cancer and virally-infected cells, dendritic cells must capture antigens pr

271 +) T cells in the lungs of influenza A virus-infected mice.

272 tance capable of destroying tumors and virus-infected cells through cytotoxicity and rapid cytokine p

273 e has been a rapid rise in hepatitis C virus-infected (HCV+) heart transplantation.

274 natural killer cells to help eliminate virus-infected and transformed target cells.

275 Human immunodeficiency virus-infected children had significantly lower alpha-diversit

276 ity rates among human immunodeficiency virus-infected persons in Africa.

277 (ART)-treated simian immunodeficiency virus-infected rhesus macaques (RMs) undergoing CD8alpha deple

278 a methodology for analyzing influenza virus-infected lung in vivo by two-photon imaging microscopy.

279 decreased in modified avian influenza virus-infected mice.

280 interface, the immune synapse, to kill virus-infected and tumorigenic target cells.

281 a three-dimensional culture AD model, virus-infected APP/PS1 mice and the brains of patients with AD

282 nal capacity to accelerate the loss of virus-infected cells through Fc gamma receptor (FcgammaR)-medi

283 ecially true for scheduled necropsy of virus-infected ferrets, a standard component in evaluation of

284 Therefore, EBV BGLF2 might protect virus-infected cells from the type I interferon response in ce

285 n lipopolysaccharide-treated or Sendai virus-infected U937 or THP-1 cells, the mNLS variant reduced T

286 (ifnar1(-/-)ifngr1(-/-)) bitten by the virus-infected AaVA-1-deficient mosquitoes present a lower vir

287 culate extravascular host tissues with virus-infected saliva during probing.

288 udy 2, n = 24) were inoculated with P. vivax-infected red blood cells to initiate infection, and were

289 VZV-infected qHA-sps, but not mock-infected qHA-sps, contain

290 were detected, yet only supernatant from VZV-infected cells induced amylin aggregation and, to a less

291 induce a sustained antiviral response in WHV-infected woodchucks; the identification of a baseline in

292 lions of competitive, sterile male Wolbachia-infected mosquitoes, and use of these males in a large-s

293 verall state of ISGylation in wild-type (WT)-infected cells.

294 loped a consumptive coagulopathy whereas YFV-infected hFRG mice did not.

295 ZIKV-infected NSCs show global dampening of miRNA production,

296 Viremia was achieved in 3/3 FP ZIKV-infected dams and 2/3 PR ZIKV-infected dams.

297 as well as Guillain-Barre syndrome, in ZIKV-infected adults.

298 hypothesized that vaginal deposition of ZIKV-infected baboon semen would lead to maternal infection a

299 in 3/3 FP ZIKV-infected dams and 2/3 PR ZIKV-infected dams.

300 ructural and functional MRI showed that ZIKV-infected infant rhesus macaques had persistent enlargeme