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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

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