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1 PPS and heparin also decreased MMP-9 (P < 0.001) after t
2 PPS by itself, or CCh and NE in the absence of synaptic
3 PPS encodes MAX2/ORE9 (for MORE AXILLARY BRANCHES2/ORESA
4 PPS is a promising new therapy for alphavirus-induced ar
5 PPS is an excellent permeation enhancer which provides n
6 PPS was found to improve sensitivity in MALDI analyses o
7 PPS was injected intramuscularly weekly for 3 weeks.
8 PPS was tested for dose- and time-dependent cytotoxicity
12 d with a 23-valent pneumococcal vaccine or a PPS 3-bovine serum albumin conjugate revealed that they
13 ulin loci (XenoMouse mice) vaccinated with a PPS-3-tetanus toxoid conjugate and their molecular genet
15 ospice programs develop clear policies about PPS and PSU, including mechanisms for training and ensur
17 generated B-1b cells and protective adaptive PPS-specific antibody responses, whereas hCD19Tg mice la
25 uctions in joint destruction with PB-145 and PPS treatments (P < 0.01) compared with buffer control.
27 At the population level, both PPS-6B and PPS-14 Abs expressed kappa and lambda chains, although 6
30 duced calcium responses, PD-1 induction, and PPS-3-specific IgG3 responses and restored protection du
34 s sequence to analyse the effect of VWS- and PPS-associated mutations in the DNA-binding domain of IR
35 ference between young and older adults, anti-PPS IgA or IgM antibodies were removed from immune sera
41 in IL-7Ralpha are severely impaired in anti-PPS responses and do not survive Streptococcus pneumonia
42 In order to determine the effects of anti-PPS IgA or IgM antibodies on the functional difference b
43 IgM antibody levels, the low levels of anti-PPS IgM antibody alone can explain the functional differ
44 enhanced both the primary and secondary anti-PPS responses in mice, especially the type 1 IgG isotype
48 antibody levels are high compared with anti-PPS IgM antibody levels, the low levels of anti-PPS IgM
49 rmal unfolding and the stabilization by APS, PPS-1 behaved like the unstable human PAPSS2 protein sug
59 Twelve hours after the induction of SE by PPS or 3 hr after pilocarpine administration, Gal-IR neu
61 Once the proteins are free from the cell, PPS also assists in protein solubilization by shielding
62 al variability (ITV) in brain regions coding PPS predicts individual differences of its boundary at t
67 throughout IRF6 may cause VWS; in contrast, PPS-causing mutations are highly associated with the DNA
68 acrylamide)-block-(N-isopropylacrylami de)] (PPS-b-PDMA-b-PNIPAAM) that forms physically cross-linked
71 g identified binding sites on PrP 23-106 for PPS, which include the octarepeat histidine and an N-ter
72 bs were found to have similar affinities for PPS-3 but different epitope specificities and CDR3 regio
73 V(H) was associated with lower affinity for PPS 14, a result suggesting that somatic mutation could
75 psular polysaccharide (PPS) are required for PPS-based vaccine-mediated protection against Streptococ
79 ic geranyl(geranyl)diphosphate synthase [G(G)PPS] is involved in myrcene biosynthesis in hop trichome
80 , we also assessed peripersonal space, e.g., PPS, the area around the body used to act on nearby obje
82 o catalyzes depupylation, it was unclear how PPS function could be maintained without Dop and PafA ca
83 ears to be a general characteristic of human PPS-specific Ab repertoires, and we suggest that this pr
85 s to identify some of the recent advances in PPS and to describe progress towards greater standardiza
88 This was explained by >10-fold increases in PPS-specific immunoglobulin G (IgG) levels in Pneumovax-
90 molecular basis for the defects observed in PPS and potential targets that contribute to the patholo
91 observation that B3GLCT mutant phenotypes in PPS patients are less severe than embryonic lethal pheno
93 ng of trunk-centered multisensory signals in PPS is of particular relevance for theoretical models an
97 rioception, body-related visual information, PPS, and embodiment) and argue that the fronto-parietal
99 We describe a severe syndrome of isolated PPS in the adult that mimics chronic pulmonary thromboem
100 n, and management of 12 adults with isolated PPS, 17 to 51 years of age (mean, 36.2 +/- 9.7 years), w
101 erience with 12 adult patients with isolated PPS, half of whom had been previously diagnosed with chr
104 e oxidants were found to oxidize the micelle PPS core, making it more hydrophilic and triggering mice
107 zing animals, 10 min after the end of 30 min PPS, was significantly less effective than pretreatment
109 Administration of diazepam after 60 min PPS was characterized by a further decrease of its effic
111 timulation of the perforant path for 30 min (PPS) or by injection of lithium and pilocarpine, Gal-IR
115 Polyphenylsilsesquioxane [PhSiO(1.5)](n) (PPS) and polyvinylsilsesquioxane [vinylSiO(1.5)](n) (PVS
124 e native PPS were able to inhibit binding of PPS-specific B cells in a flow cytometric assay demonstr
127 A major characteristic of the boundary of PPS in humans is the extremely high variability of its l
129 d-type C57BL/6 (Wt) mice with a conjugate of PPS of serotype 3 and tetanus toxoid (PPS3-TT) and deter
133 ns show high variability in the extension of PPS across individuals, but there is a lack of evidence
137 , we directly characterized the phenotype of PPS-specific B cells before and after vaccination with P
138 w cytometry to characterize the phenotype of PPS-specific B cells obtained from 18 young adults pre-
145 he TLR2/4 antagonist, OxPAPC, at the time of PPS immunization completely blocked the production of an
146 ective data demonstrate the potential use of PPS-b-PDMA-b-PNIPAAM as an injectable, cyto-protective h
148 cted diversity was a feature common to other PPS specificities, we examined the light (L)-chain expre
150 t anti-pneumococcal capsular polysaccharide (PPS) antibody avidity can influence protective efficacy.
151 ies to pneumococcal capsular polysaccharide (PPS) are a critical component of vaccine-mediated immuni
152 ies to pneumococcal capsular polysaccharide (PPS) are required for PPS-based vaccine-mediated protect
154 ies to pneumococcal capsular polysaccharide (PPS), we studied the response of transgenic mice reconst
156 . pneumoniae type 3 capsular polysaccharide (PPS-3) and other strong TI-2 Ags were significantly impa
157 type 3 pneumococcal capsular polysaccharide (PPS-3) were generated from transgenic mice reconstituted
159 By contrast, pneumococcal polysaccharide (PPS) immunization protected CD19(-/-) mice during lethal
160 ate that Abs to pneumococcal polysaccharide (PPS) serotypes 1 and 6B have limited clonal diversity.
161 Remarkably, pneumococcal polysaccharide (PPS) vaccination alone induced C4(-/-) mice to produce i
162 The current pneumococcal polysaccharide (PPS) vaccine is highly effective in young adults; howeve
163 o the 23-valent pneumococcal polysaccharide (PPS) vaccine, Pneumovax, such as children <2 y, the aspl
164 ibodies against pneumococcal polysaccharide (PPS), older adults had lower IgA and IgM antibody levels
165 ning to isolate pneumococcal polysaccharide (PPS)-specific Fab fragments from two vaccinated adults.
167 zed with native pneumococcal polysaccharide (PPS; Pneumovax23) or protein-PPS conjugate (Prevnar-13)
170 d to determine whether pentosan polysulfate (PPS) inhibited proliferation and altered extracellular m
175 Dimethyl palmitoyl ammonio propanesulfonate (PPS), with excellent enhancement potential and minimal t
176 e key population found to produce protective PPS-specific antibody in both wild-type and CD19(-/-) mi
179 ed a rapid primary pneumococcal capsular PS (PPS) response in mice that was dependent on CD4(+) T cel
181 costs of HAIs and AMU in Singapore, repeated PPSs over the next decade will be useful to gauge progre
184 atically, and pediatric procedural sedation (PPS) is increasingly performed by practitioners who are
187 sorimotor interface, the peripersonal space (PPS), mediates every physical interaction between our bo
189 r for N-(4-hydroxyphenylpropanoyl)-spermine (PPS), and virtually absent for philanthotoxin 343 (PhTX
190 olated peripheral pulmonary artery stenosis (PPS) in the adult is rare and frequently unsuspected.
194 ng SE induced by perforant path stimulation (PPS) at the ages of postnatal day 21 (P21) and P35 were
195 of intermittent perforant path stimulation (PPS) needed to induce self-sustaining status epilepticus
196 ief intermittent perforant path stimulation (PPS) was examined with regard to the effects of two conv
197 we discovered that paired-pulse stimulation (PPS) elicits a form of homosynaptic long-term depression
198 Here we demonstrate that random-structured PPS and PVS rearrange in the presence of catalytic amoun
201 onducted a national point prevalence survey (PPS) to determine the prevalence of healthcare-associate
202 ed to characterize postprogression survival (PPS) and assess with time-dependent covariates analysis
203 and severity ofpostpericardiotomy syndrome (PPS) in children after cardiac surgery with cardiopulmon
205 ns in B3GLCT result in Peters plus syndrome (PPS), an autosomal recessive disorder characterized by e
207 rome (VWS) and popliteal pterygium syndrome (PPS) are autosomal dominant disorders characterized by c
209 assessing paradoxical puborectalis syndrome (PPS) in patients with obstructive defecation syndrome (O
211 he Medicare ESRD prospective payment system (PPS) and changes to dosing guidelines for erythropoiesis
212 quitin-like protein (Pup)-proteasome system (PPS), the bacterial equivalent of the eukaryotic ubiquit
218 ammation and joint swelling, suggesting that PPS is a promising candidate for drug repurposing for th
220 4 vs 0.27 +/- 0.17, P = 0.009) analysis, the PPS(+) patients displayed a lower absolute ADC differenc
224 this prediction, we cloned and expressed the PPS-1 protein from the roundworm Caenorhabditis elegans
227 y of PPS rules, a stand-alone version of the PPS and guidance for PPS users are being developed.
228 dividual differences in the extension of the PPS are predicted by variability of BOLD responses in th
230 ART may influence qualitative aspects of the PPS response by restoring expression of certain V(H)3 ge
233 died PS-specific responses, we find that the PPS 6B repertoire makes use of a diverse collection of h
236 tween July 2015 and February 2016, using the PPS methodology developed by the European Centre for Dis
237 bservations in healthy young volunteers, the PPS-responding B-cell population consisted primarily of
238 ) emissions were 28% and 17% higher with the PPS-M compared to the SMPS for LSHFO and MGO, respective
240 n vitro opsonophagocytic activities of three PPS-specific mouse immunoglobulin G1 monoclonal antibodi
242 ctive, serotype-specific human antibodies to PPS 3, and they lend support to the proposal that these
243 ation immunoglobulin G2 (IgG2) antibodies to PPS serotypes 6B and 23F and examined the relationship b
245 ced fluorescence of PrP 23-106 when bound to PPS, consistent with the alignment of tryptophan side ch
246 pecificity, and efficacy for defined MAbs to PPS may identify antibody features that might be useful
247 sis of three monoclonal antibodies (MAbs) to PPS 3 generated from lymphoid cells from mice vaccinated
252 hin individual adults, serum Ab responses to PPS serotypes 6B, 14, and 23F derive from a small number
253 not adult mice are impaired in responses to PPS vaccination and to 4-hydroxy-3-nitrophenyl-acetyl-Fi
254 by the monoclonal antibody D12) responses to PPS were determined for first-time recipients of a 23-va
255 A single 526-kb haplotype mapped strongly to PPS levels, dramatically refining the mapped interval.
258 the hippocampus in P21 animals subjected to PPS, although extensive activation of hippocampal and ex
259 pal structures was seen in pups subjected to PPS-induced self-sustaining SE at P35 or LiPC SE at P21.
261 mirror website of the UM-BBD, UM-BPT and UM-PPS is being developed at ETH Zurich to improve speed an
264 y of Minnesota pathway prediction system (UM-PPS) recognizes functional groups in organic compounds t
265 d a rule-based Pathway Prediction System (UM-PPS) that predicts plausible pathways for microbial degr
269 ajority of PrP 23-106 remain disordered upon PPS binding, the octarepeat region adopts a repeating lo
271 ned for first-time recipients of a 23-valent PPS vaccine, both receiving and not receiving HAART, and
282 These data suggest that vaccination with PPS may not be effective for patients during and after l
283 ic B cells before and after vaccination with PPS vaccine (PPV) in elderly adults, using fluorescently
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