ライフサイエンスコーパス: naive

1 ere disease, and were methotrexate treatment-naive.

2 ty-two of 69 study eyes (32%) were treatment naive.

3 Scale=30+/-6) and about half were treatment naive.

4 tment required significantly less C removal (naive=0.42 Tg C, optimized=0.25 Tg C) to achieve the sam

5 o B cells were dispensable for activation of naive 1-DER T cells but necessary for full expansion of

6 older (>/=65 years) patients with treatment-naive acute myeloid leukaemia who were not candidates fo

7 l, multicenter phase II trial, 152 treatment-naive adult solid organ transplant recipients, with CD20

8 tudy evaluated rWN/DEN4Delta30 in flavivirus-naive adults aged 50-65 years and found it to be safe an

9 es (95% confidence interval [CI]) in 815 ARV-naive adults, 136 ARV-experienced adults, and 36 predomi

10 three times at 8-wk intervals to 15 malaria-naive adults.

11 As recirculating naive Ag-specific B cells arrive in Ag-draining secondar

12 For treatment-naive and -experienced patients, ledipasvir-sofosbuvir f

13 I 82-100]) of 29 of those who were treatment-naive and 29 (100% [88-100]) of 29 who were treatment-ex

14 ug classes for both antiretroviral treatment-naive and antiretroviral treatment-experienced patients,

15 ity of the fusion proteins was assessed with naive and Bet v 1-specific T cells.

16 WIN55212 inhibited GABAergic mIPSCs in both naive and CFA-treated rats.

17 ncreased senescent CD4+ T cells, and reduced naive and effector and central memory CD8+ T cells.

18 Thus, memory cells embody features of both naive and effector cells, fuelling a long-standing debat

19 NA sequencing of unstimulated and stimulated naive and effector memory CD4(+) T cells from young and

20 Ag-dependent conjugate formation in primary naive and effector T cells.

21 ks by the ACK1 inhibitor (R)-9bMS-sensitized naive and enzalutamide-resistant prostate cancer cells a

22 food/water intake and body weight in ethanol-naive and ethanol-trained wild-type (WT), but not Tlr4 K

23 .1 years of age; 55% female) who were statin naive and free of cancer at baseline from the offspring

24 e cell reactivity and synaptic plasticity in naive and in MDA-kindled anaesthetised rats.

25 nctions toward allergic responses induced by naive and in vivo-primed human T helper 2 cells.

26 We found that EPNs can differentiate between naive and infected hosts, and that host attractiveness c

27 els of lipids that can differentiate between naive and irradiated samples, as well as providing poten

28 r relatively early (1 d) after activation of naive and memory cells and that demethylation is the pre

29 iases in both VH and VL sequences within the naive and memory compartments.

30 s, revealing distinct expression patterns in naive and memory subsets.

31 aling dampened activation of SMX-NO-specific naive and memory T cells, whereas blockade of TIM-3 prod

32 was expressed in osteocytes from bones from naive and myeloma-bearing mice.

33 hase was followed by 2 expansion cohorts (PI-naive and PI-exposed patients) at the maximum tolerated

34 Two phases of pluripotency, called naive and primed, have previously been described.

35 is C virus genotype (GT)1-infected treatment-naive and prior-relapse patients.

36 ed capacity to uptake allergen and stimulate naive and TH2 effector responses on allergen stimulation

37 To assess PD-L1 expression in treatment-naive and treated BCCs.

38 -episode psychosis (14 of them antipsychotic naive) and 20 healthy volunteers underwent a high-resolu

39 fied by treatment experience (experienced vs naive) and included block randomisation at nurse level w

40 ere black, 69% were male, 82% were treatment naive, and 20% had cirrhosis.

41 A majority (80%) were HCV treatment-naive, and 84% were infected through perinatal transmiss

42 ation strategies consider movements of young naive animals in addition to those of adults to account

43 suppress exploratory behaviours in recipient naive animals.

44 assive protection against virus challenge in naive animals.

45 Naive ants that arrived at an experimentally provided fe

46 vo methylation programs and re-expression of naive-associated genes.

47 Even in subjects with mild steroid-naive asthma, differences in the bronchial microbiome ar

48 te the subpassage of prions from infected to naive astrocyte cultures, indicating the generation of p

49 kers for discriminating bacterial infection (naive AUC = 0.94; nested CV-AUC = 0.86).

50 We show that naive B and T cells interact via the signaling lymphocyt

51 Additionally, CD40L-induced naive B cell genes were also significantly enriched in s

52 VH4-34-expressing clones are common in the naive B cell repertoire but are rarely found in IgG memo

53 In contrast, TET2 is expressed in normal naive B cells and ABC type lymphomas.

54 lie differences in function between MBCs and naive B cells and among MBC subsets and how this leads t

55 al step in this process is the activation of naive B cells expressing germline (gl) antibody precurso

56 This impairment was more profound in naive B cells from CVID 21low patients than CVID 21norm

57 ion transcription factors in memory, DN, and naive B cells in SLE show elevated levels of Aiolos, whe

58 ine designs because of the in vivo rarity of naive B cells that recognize broadly neutralizing epitop

59 ived from human immature dendritic cells and naive B cells to assess the expression of CD40-downstrea

60 nts, whereas frequencies of transitional and naive B cells were decreased.

61 onsive genes in immature dendritic cells and naive B cells were significantly enriched in synovial ti

62 ic SIV infection is characterized by loss of naive B cells, loss of resting memory B cells due to the

63 ire-sequencing method can use as few as 1000 naive B cells.

64 ere fully protected against disease, whereas naive baboons developed illness (with 1 death) and leuko

65 g cells that were isolated from the lungs of naive BALB/c mice and those treated with IL-33.

66 truct knowledge graphs: logistic regression, naive Bayes classifier and a Bayesian network using nois

67 We built 1,000 naive Bayes models on the training sets.

68 Here, the authors take an in silico naive Bayesian classifier approach to integrate multiple

69 L algorithms, specifically, a tree-augmented naive Bayesian network, a random forest algorithm, and a

70 erapy, or topical chemotherapy) vs treatment-naive BCCs.

71 n of the first MPH dose to 40 stimulant drug-naive boys newly diagnosed with ADHD while they performe

72 estigated the role of EGFR signaling in drug-naive cancer cells harboring these oncogene fusions.

73 We showed that naive CAST mice make low IFN-gamma and TNF-alpha respons

74 Naive CD4 T cell responses, especially their ability to

75 inhibition of the H3K27 demethylase JMJD3 in naive CD4 T cells demonstrates how critically important

76 ypes of pathogens through differentiation of naive CD4 T cells into functionally distinct subsets of

77 odels an abnormal distribution of memory and naive CD4 T cells occurred, and peripheral CD4 and CD8 T

78 urin inhibition leads the most self-reactive naive CD4 T cells to adopt the phenotype of their less s

79 miR-34c-5p in response to TCR stimulation in naive CD4 T cells.

80 confirming its role as a novel regulator of naive CD4 T-cell activation.

81 aphylococcal enterotoxin A (SEA)-nonreactive naive CD4 Tcon cells were cocultured with SEA-reactive a

82 eration of inducible Treg (iTreg) cells from naive CD4(+) human T cells.

83 n analysis identifies changes in neutrophil, naive CD4(+) T cell, and macrophage populations during p

84 mice, Stat3 is constitutively acetylated and naive CD4(+) T cells are potentiated in Th17/Treg cell d

85 In vitro polarization of DOCK8-deficient naive CD4(+) T cells revealed the TH2 bias and TH17 defe

86 his article, we report that murine and human naive CD4(+) T cells that sequester Pam3Cys4 (CD4(+) T(P

87 duced extensive proliferation of transferred naive CD4(+) T cells, and significant uveoretinitis.

88 ecombinant IL-2 induced expression of LAP on naive CD4(+) T cells, independent of Foxp3 or exogenous

89 ived mouse dendritic cells (BMDCs), and moDC/naive CD4(+) T-cell cocultures were analyzed by using EL

90 analysis of polarization, DCs and autologous naive CD4+ T cells were cocultured.

91 In naive CD4bs, unmutated common ancestor knock-in mice Env

92 The differentiation of naive CD8 T cells into effector cytotoxic T lymphocytes

93 trate that an intracellular pool of LFA-1 in naive CD8(+) T cells plays a key role in T cell activati

94 ly, knockdown of TMEM20 in miR-150-deficient naive CD8(+) T cells reduced intracellular Ca(2+) levels

95 stimulated CTLs directly activated bystander naive CD8(+) T cells to produce interferon-gamma (IFNgam

96 -presentation of Ags and priming the pool of naive CD8(+) T cells within the liver microenvironment.

97 nation, they failed to support activation of naive CD8(+) T cells.

98 in increased intracellular Ca(2+) levels in naive CD8(+) T cells.

99 associated with the early and late stages of naive cell formation.

100 nsights into the molecular events leading to naive cell resetting.

101 isplay higher ST6Gal-I levels than treatment-naive cells along with a reduced gemcitabine sensitivity

102 cally, the treatment of hormone therapy (HT)-naive cells or HT-treated metabolically dormant populati

103 ngs are consistent with the proposition that naive cells transition to a distinct formative phase of

104 but also have many properties in common with naive cells, including pluripotency and the ability to m

105 of viral or prion proteins from infected to naive cells, it is not clear whether the viral genome is

106 lls using ChIP-Seq and found that unlike the naive cells, the regulatory elements of the cytokine gen

107 celecoxib reduced the proliferation of LLC1 naive cells, while the opposite occurred with placebo-tr

108 ption of "memory-primed" genes compared with naive cells.

109 ne homolog 1 and 2 (GLI1/GLI2) compared with naive cells.

110 develop from effector cells or directly from naive cells.

111 2 eyes SND+ and 50 eyes SND-) with treatment-naive, center-involving DME were evaluated.

112 formed epigenetic profiling of human resting naive, central and effector memory T cells using ChIP-Se

113 ing >2 x 10(8) TCRB sequences of circulating naive, central memory, regulatory and stem cell-like mem

114 we randomly assigned (1:1) HIV-infected, ART-naive children aged 0-12 years who were eligible for tre

115 experienced adults, and 36 predominantly ARV-naive children were 9.4% (7.5%-11.7%), 12.5% (7.5%-19.3%

116 One hundred twenty-seven steroid-naive children with the first severe wheezing episode (9

117 studied, which included eyes with treatment-naive CNV due to AMD, non-neovascular AMD, and normal co

118 ome diversity of children from an antibiotic-naive community in Niger.

119 gut microbiome of children in an antibiotic-naive community.

120 we co-house MARV-inoculated donor ERBs with naive contact ERBs.

121 xposure comparisons) and 57 age-matched GBCA-naive control subjects.

122 some (Xi) of primed hESCs was reactivated in naive culture conditions.

123 -kappaB signaling was impaired in all mature naive CVID-derived B cells.

124 Naive-derived T cells showed the greatest rate of prolif

125 Although eyes with naive DME gained more vision than refractory eyes (P < 0

126 C virus-infected patients who are treatment-naive, do not have cirrhosis, and have a pretreatment vi

127 AN1 upregulation, overexpression of RCAN1 in naive DRG neurons recapitulated the effects of pharmacol

128 in histone), and gene-expression profiles in naive, effector memory (EM), and terminally differentiat

129 veness of different T cell subsets, that is, naive, effector, and memory T cells.

130 te complex host-microbe interactions in this naive epithelium.

131 g both CRVO and HRVO eyes and both treatment-naive eyes and eyes treated previously with anti-VEGF, w

132 vitreomacular adhesion (VMA) in consecutive naive eyes diagnosed with exudative age-related macular

133 Forty-two consecutive treatment-naive eyes with CRVO imaged with ultra-widefield angiogr

134 Treatment-naive eyes with neovascular age-related macular degenera

135 isual stimuli that are presented to visually naive ferrets can influence the parameters of speed tuni

136 Overall, priming naive ferrets with COBRA HA based viruses or using COBRA

137 ter influenza A infection of immunologically naive ferrets with various H1N1 or H3N2 strains, the acu

138 Compared to naive ferrets, all vaccinated ferrets showed improved ce

139 ficity of functional dysconnectivity in drug-naive first-episode psychosis (FEP).

140 Here, we examined 16 drug-naive, first-episode psychosis patients and 16 healthy c

141 Notably, naive Foxp3(Cre)xT-bet(fl/fl) mice, lacking Treg1 cells,

142 in the LAIV H5N2 experienced group than the naive group (p<0.0001).

143 d users (compared with those who were opioid-naive) had 9.2% higher costs [95% confidence interval (C

144 ally of the mTORC2 subunit, in the different naive hESCs.

145 that, in both sexes, fremanezumab inhibited naive high-threshold (HT) neurons, but not wide-dynamic

146 ART-naive HIV-1-infected patients from Cameroon were subject

147 We processed 66 ART-naive HIV-1-positive patients with highly diverse subtyp

148 In a cohort of 53 antiretroviral-naive HIV-infected subjects, the measure of thymic volum

149 ial was a randomised controlled trial in ART-naive HIV-positive patients with CD4 cell count of more

150 h hormone-based therapy for the treatment of naive hormone receptor-positive advanced breast cancer o

151 irus replication during acute infection of a naive host is subclinical in most individuals.

152 ost-generalist pathogens sporadically infect naive hosts, potentially triggering epizootics.

153 We find that naive hPSCs robustly engraft in both pig and cattle pre-

154 Naive human CD4(+) T cells were short-term activated in

155 Naive human embryonic stem cells (hESCs) can be derived

156 rythrocyte antibodies in ex vivo cultures of naive human peripheral blood mononuclear cells (PBMC) ex

157 ontrolled human malaria infection in malaria-naive individuals.

158 L tumor samples from 105 primarily treatment-naive individuals.

159 curs during early-use critical periods, when naive juveniles experience sensory input.

160 as reduced in epileptic mice but restored to naive levels in epileptic mice receiving MGE transplants

161 (YFV), we show that the recently described 'naive-like' memory population have significantly longer

162 after sound making compared with the initial naive listening.

163 Naive lymphocyte counts peaked around 1 year, whereas mo

164 y the mechanism of action of Rh-alpha4beta7, naive macaques were infused with Rh-alpha4beta7 and samp

165 METHOD: Adults aged 18-65 with treatment-naive major depression were randomly assigned with equal

166 tLTD), the predominant form of plasticity in naive male mice, to spike-timing-dependent long-term pot

167 Here we show that adult drug-naive male offspring of cocaine-exposed sires have memor

168 noglobulin heavy chain VDJ rearrangements of naive, mature CD5(+), IgM(+) memory, and class-switched

169 ber 31, 2014, to identify cases of treatment-naive mCNV, which was defined as the presence of myopic

170 ncy fluctuation (ALFF) in first-episode drug-naive MDD patients, using the Seed-based d Mapping metho

171 e approaches have drawbacks: 1) They rely on naive measures of network topology.

172 cision-analysis model was created for biopsy-naive men who had been recommended for prostate biopsy o

173 mally symptomatic patients with chemotherapy-naive metastatic castration-resistant prostate cancer wi

174 sistance to taxanes in men with chemotherapy-naive, metastatic, castration-resistant prostate cancer.

175 nd transfusion of these red blood cells into naive mice affords protection for up to 28 days.

176 H and germinal center (GC) B cell numbers in naive mice and hastened islet allograft rejection.

177 utaneous injection of recombinant TWEAK into naive mice induces cutaneous inflammation with histologi

178 +) mice after a fatal LPS dose compared with naive mice or Nb-infected hRETNTg(-) mice.

179 of the same subsets of cells harvested from naive mice resulted in inefficient invasion by the bacte

180 Naive mice were exposed to cytokines or natural allergen

181 rom UV-irradiated mice and transplanted into naive mice, the recipient mice (UV-chimeric) had reduced

182 nt to increase movement in the TST in stress-naive mice, while stimulating above the carrier frequenc

183 of cystitis, but had no effect in uninjured, naive mice.

184 king (HAD) mice does not differ from alcohol naive mice.

185 ed or even increased their activity in awake naive mice.

186 permeability, and induced histologic ALI in naive mice.

187 959-972) report that, in naive mouse embryonic stem cells (ESCs), p53 controls DN

188 We report that, in naive mouse ESCs (mESCs), p53 restricts the expression o

189 patterns and outcomes in eyes with treatment-naive myopic choroidal neovascularization (mCNV) in the

190 4 patients treated with DEX implant for DME (naive, n = 209; refractory, n = 90).

191 Sixty patients with treatment-naive neovascular AMD in 1 eye randomized 1:2 to monthly

192 can infect virtually all cell types, neither naive nor inflammatory Ly6C(hi) monocytes served as a pr

193 total of 119 patients with advanced EGFR-TKI-naive NSCLC and 15 EGFR-TKI-resistant patients to identi

194 current stage IIIb or stage IV, chemotherapy-naive NSCLC.

195 Forty eyes of 40 patients with treatment-naive NVAMD were managed with a TAE regimen of intravitr

196 Treatment-naive or -experienced kidney transplant recipients with

197 atients and Methods Patients with ipilimumab-naive or -treated advanced/metastatic melanoma received

198 Eligible patients were drug-naive or discontinued their antihypertensive medications

199 karyotype, early embryos must remain gender-naive; our findings show that the mir-35 family microRNA

200 in structure from a condensed maternal and a naive paternal genome to generate a totipotent embryo.

201 We identified a treatment-naive patient who has metastatic uterine leiomyosarcoma

202 ured in peripheral blood (PB) from treatment-naive patients in the CLL8, CLL10, and CLL11 clinical tr

203 ] and at risk of viral rebound) or treatment-naive patients initiating their first combination ART re

204 f liver and plasma compartments in treatment naive patients provides insight into viral quasispecies

205 d by 98% (39/40; 95% CI, 87-99) of treatment-naive patients treated for 12 weeks and 96% (45/47; 95%

206 fusion-weighted imaging data of 12 treatment-naive patients with 34 metastases acquired before and at

207 s as predictors of prognosis in chemotherapy-naive patients with advanced NSCLC, we recruited all tho

208 Patients and Methods BRAF inhibitor-naive patients with BRAF V600-mutant MM were randomly as

209 cation (CAC) is highly prevalent in dialysis-naive patients with chronic kidney disease (CKD).

210 t clinical study, investigating 52 nilotinib-naive patients with chronic-phase CML.

211 sease and all-cause mortality among dialysis-naive patients with CKD.

212 prospective longitudinal cohort of treatment-naive patients with IPF.

213 s were analyzed from 38 eyes of 38 treatment-naive patients with macular edema due to RVO, enrolled i

214 Chemotherapy-naive patients with metastatic colorectal cancer (WHO pe

215 Eligible participants were insulin-naive patients with type 2 diabetes, aged 18 years and o

216 Patients and Methods Chemotherapy-naive patients with unresectable, nonsarcomatoid MPM (Ea

217 CHB-treatment naive patients, patients treated with PEGylated IFN-alph

218 nd VEGF at the enhancing edge in bevacizumab-naive patients.

219 eonal boundaries than that of bisphosphonate-naive patients.

220 Naive PD-L2-deficient (PD-L2(-/-)) mice produced signifi

221 estinal mucosa are up-regulated in treatment-naive pediatric patients with UC compared with patients

222 ls in the maintenance/survival of the mature naive peripheral B cell population.

223 We collected naive peritoneal macrophages and plasma, at multiple tim

224 resent heterogeneous populations composed of naive phenotype (NP, CD44(low)) and memory phenotype (MP

225 ur hypothesis, we define 12 key hallmarks of naive pluripotency, five of which are specific to primat

226 r delineating developmental progression from naive pluripotency.

227 n), that modulates the dynamics of exit from naive pluripotency.

228 s of WNT and MAPK-ERK signaling to safeguard naive pluripotency.

229 eviously shown that E-cadherin regulates the naive pluripotent state of mouse embryonic stem cells (m

230 showed significantly better results in this naive population.

231 accination leading to a higher proportion of naive populations.

232 iruses can spread rapidly in immunologically naive populations.

233 and induced (i)Treg cells that develop from naive precursors, suppressive IL-17A(+)Foxp3(+) and ex-T

234 y other method significantly better than the naive prediction.

235 in CTCF occupancy during the transition from naive/primed pluripotency to multipotent primary neural

236 In total, 101 patients with treatment-naive progressive metastatic clear cell renal cell carci

237 lections that deviated from their respective naive QRS template.

238 Naive quantity-based models using treatment/control comp

239 ells, further corroborating the value of the naive rabbit antibody library as a rich and virtually un

240 by the CB1 receptor antagonist rimonabant in naive rats but not in CFA-treated rats.

241 Drug-naive rats did not self-administer CTDP-32476.

242 Nontreated, sham and naive rats were also included.

243 eta, to activate a systemic APR in recipient naive rats, as well as the behavioural consequences of E

244 in the RVM of CFA-treated rats compared with naive rats.

245 ation (LTP) at perforant path-DG synapses in naive rats.

246 rents were smaller, when compared to ethanol naive rats.

247 athecal injection of recombinant TNFalpha in naive rats.

248 ts (cytotoxicity and anti-migration) on drug-naive recipient cells (Recipient cells).

249 ar dysfunction, fibrosis, and hypertrophy in naive recipient mice.

250 zed T cells were able to transfer disease to naive recipients.

251 ubation in the four chemical inhibitors (4i)-naive reprogramming medium and showed transcriptional co

252 including 55% (six of 11) of transplantation-naive responders.

253 between 2 experts and between 1 expert and 1 naive sleep investigators gave similar results.

254 trial, we recruited patients with treatment-naive, stage IV NSCLC in 102 sites in 16 countries.

255 Both establishment of and exit from the naive state (differentiation) happened via an XIST-negat

256 e mouse embryonic stem cells (ESCs) in their naive state has been extensively characterized.

257 acts independently of PRDM14 to regulate the naive state of mouse ESCs.

258 tional regulation according to which, in the naive state, polycomb recessive complex 2 repressed the

259 Treatment-naive subjects harboring NRTI-DRMs had significantly low

260 rin spectroscopy studies in healthy epilepsy-naive subjects.

261 sleep greater than 8 hours), epigenetic age, naive T cell (CD8+CD45RA+CCR7+), and late differentiated

262 In contrast, permanence of naive T cell clones would be determined by their affinit

263 ly distinct from their more mature but still naive T cell counterparts, because they exhibit dampened

264 can be understood as mechanisms to maximize naive T cell diversity.

265 nt novel evidence that Treg-DC skewed CD4(+) naive T cell polarization toward a regulatory phenotype

266 To determine the contribution of naive T cell, memory stem T cell, central memory T cell,

267 n-educated" DCs stimulated the activation of naive T cells and polarized a subset of these cells into

268 +) T cells and includes only memory T cells; naive T cells are excluded to limit the potential for al

269 ogether with Egr2 and 3, T-bet is induced in naive T cells by Ag stimulation, but Egr2 and 3 expressi

270 nse to IL-7 signalling in order to reprogram naive T cells for proliferation and differentiation.

271 ted loci and show the advantage of utilizing naive T cells for understanding autoimmune diseases.

272 Piperacillin-primed naive T cells from healthy volunteers also secreted IFN-

273 ning protein coronin 1 in the maintenance of naive T cells in peripheral lymphoid organs.

274 central memory T cells were reduced, whereas naive T cells increased in treated patients.

275 the production of T cells declines with age, naive T cells must be long-lived.

276 However, it remains unclear how naive T cells survive for years while constantly travell

277 ergo an additional maturation step to mature naive T cells that circulate through secondary lymphoid

278 mune responses require a large repertoire of naive T cells that migrate throughout the body, rapidly

279 PD-1H in mice blocks the differentiation of naive T cells to Foxp3(+) inducible Treg cells (iTreg) w

280 About half of the patients had less than 10% naive T cells, reduced/absent T-cell proliferation, and

281 ssion of CD45RA is generally associated with naive T cells.

282 ls of protein expression in Mettl3-deficient naive T cells.

283 tion of antigens by dendritic cells (DCs) to naive T lymphocytes.

284 (EF4.1) expressing a limited, yet polyclonal naive T-cell repertoire was used.

285 phylaxis showed increased T-cell activation, naive T-cell skewing, and elevated serum CXCL9 and CXCL1

286 an adoptive-transfer approach, we show that naive Tg CD4 T cells become activated, proliferate, migr

287 Clonal expansions have differentiated from a naive to effector phenotype associated with CD27 downreg

288 s before screening who were either treatment naive to or relapsed after interferon-alpha based therap

289 dual cells undergo abrupt transitions from a naive to primed pluripotent state.

290 n this study, we hypothesized that MP cells, naive to TCR stimulation, constitute a transient populat

291 FGF4-FGFR1-ETS2 pathway in TECs and converts naive tumor cells to chemoresistant TSCs, thereby facili

292 rs heighten efficacy of our nanobiologics on naive tumors by augmenting HER3 expression.

293 to visualize the paravascular space (PVS) in naive uninjected mice, we show that a single wave of cor

294 were obtained with DCs obtained from malaria-naive US donors and malaria-experienced donors from Mali

295 parallel with hepcidin in serum from malaria-naive volunteers infected in controlled human malaria in

296 d in vitro, however, IFN-gamma production by naive wild type and tristetraprolin-deficient CD8(+) T-c

297 When inoculated into naive wild-type (WT) mice, this persistently circulating

298 given in combination with low-dose IL-33 to naive wild-type mice, led to synergistic increases in ai

299 olutegravir for HIV-1 infection in treatment-naive women.

300 is study assessed neural function among drug-naive youth with a behavioral addiction-Internet gaming