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1 PEM acquisition geometry limits sampling statistics at t
2 PEM and bacteria deposition, and heavy metal influence,
3 PEM and MR imaging had comparable breast-level sensitivi
4 PEM decreased maternal and fetal urea concentration, whi
5 PEM had greater specificity at the breast and lesion lev
6 PEM had little measureable effect on maternal and fetal
7 PEM microchambers "cap" and "wall" thickness depend on t
8 PEM was used to map SVs in an African and in a putativel
9 PEM, the percentage of 2.5-second intervals containing p
10 PEMs from MARCO-deficient mice exhibited 2.7 times lower
13 used a 5-point confidence scale to score 232 PEM images for the presence of up to 3 malignant lesions
16 ombe epistasis mapper' strategies, PEM-1 and PEM-2, which allow for high-throughput double mutant gen
18 ces in optimizing both cathode materials and PEMs as well as the future and peculiar challenges assoc
21 calculated for PET/CT patients, and PUV/BGV (PEM uptake value/background value) was calculated for PE
24 of the 82 breasts were identified with both PEM and MR imaging; 21 (26%) breasts, with MR imaging on
27 itive predictive value of biopsy prompted by PEM findings (47 [66%] of 71 cases) was higher than that
29 f operating conditions of these conventional PEM materials, mesoporous functionalised SiO(2) additive
31 ic methods of patterning and controlling 3-D PEM architectures and selective particle depositions.
33 This quantitative understanding will drive PEM design efforts towards optimal membrane transport, t
35 00 samples were analyzed for 34 gases during PEM-Tropics A, over 4,500 samples were analyzed for 58 g
37 boys and 3 girls aged 6-15 mo with edematous PEM and infection approximately 3 d after admission (stu
38 We assessed whether children with edematous PEM can mount a general APP response and compared the ki
41 were measured in 14 children with edematous PEM, aged 11.4 +/- 2 mo, and 9 children with nonedematou
43 ated GO can be built into a highly efficient PEM with a proton transfer rate of seven orders of magni
45 ore, the addition of exogenous IL-2 enhanced PEM Treg phosphorylated STAT5 signaling compared with PE
46 ork is to clarify the origin of the enhanced PEM-FC performance of catalysts prepared by the procedur
49 ransfer in polyelectrolyte multilayer films (PEM), as well as between biomolecules and redox centres,
51 R imaging and fluorine 18 fluorodeoxyglucose PEM in randomized order; resultant images were interpret
57 s layering approaches currently employed for PEMs, reducing the production time from ~2 days down to
64 e useful as a marker for isolating the human PEM gene, which has been impervious to cloning by conven
66 ndicate that immobilizing silver-impregnated PEMs on the wound-contact surface of Biobrane significan
68 BCG-mediated protection was abrogated in PEM derived from A1-a(-/-) mice, indicating a requiremen
69 PAR mRNA or protein or both were apparent in PEM from transgenic and control mice, even at a ratio of
74 el cells, oxygen evolution reaction (OER) in PEM based water electrolysis and metal air batteries rem
78 BRAF wild-type advanced melanoma, first-line PEM every 3 weeks followed by second-line IPI or first-l
81 n with LPS, peritoneal-elicited macrophages (PEM) from mammary tumor-bearing mice display a diminishe
82 ride (LPS), peritoneal-elicited macrophages (PEM) from mice bearing mammary tumors display alteration
86 oglycollate-elicited peritoneal macrophages (PEMs) with immobilized mAb costimulated IL-12 production
88 loss induced by protein-energy malnutrition (PEM) has been well documented, it is unclear whether the
91 nd the edema of protein-energy malnutrition (PEM) were investigated by measuring the plasma concentra
94 rpretation of positron emission mammography (PEM) images and compared image interpretation between 2
99 h-throughput and massive paired-end mapping (PEM), a large-scale genome-sequencing method to identify
100 primarily based on paired-end read mapping (PEM) as reported previously by Tuzun et al. and Korbel e
102 aliana, yellow poplar proembryogenic masses (PEMs) were transformed with three modified merA construc
104 construct a position-specific energy matrix (PEM) that allowed a reliable prediction of ArcA-P bindin
106 the ability of pediatric emergency medicine (PEM) physicians to perform a wide array of diagnostic an
109 e conventional polymer electrolyte membrane (PEM) materials for fuel cell applications strongly rely
111 such as in acidic proton exchange membrane (PEM) electrolyzers and photoelectrochemical cells (PEC).
112 energies, such as proton exchange membrane (PEM) electrolyzers and solar photoelectrochemical (PEC)
113 reaction (ORR) in proton exchange membrane (PEM) fuel cells, oxygen evolution reaction (OER) in PEM
114 fuel cells a novel proton exchange membrane (PEM) using inorganic phosphotungstic acid (HPW) as proto
115 e catalyst and the proton exchange membrane (PEM), have proven to be particularly demanding to overco
119 dely used polymer for electrolyte membranes (PEMs) in fuel cells, consists of a fluorocarbon backbone
121 M), ionomers, polymer electrolyte membranes (PEMs), and electrode structures designed for use in next
122 , using the phasic electromyographic metric (PEM), in relation to clinical features of idiopathic Par
128 modified using a polyelectrolyte multilayer (PEM) coating procedure in open-tubular capillary electro
130 ayer assembly of polyelectrolyte multilayer (PEM) films represents a bottom-up approach for re-engine
132 e compared with polyelectrolyte multilayers (PEM) thin films having array of hollow microchambers pro
133 itosan-alginate polyelectrolyte multilayers (PEM) with and without adsorbed Br(2)Y were analyzed by l
134 nanometer-thick polyelectrolyte multilayers (PEMs) impregnated with silver nanoparticles have been sh
135 Photoreactive polyelectrolyte multilayers (PEMs) that dissolve upon UV irradiation are described.
136 port the use of polyelectrolyte multilayers (PEMs) to alter the surface charge and control the direct
137 e, we have used polyelectrolyte multilayers (PEMs) to alter the surface of microchannels fabricated i
139 le, nanoscale 'polyelectrolyte multilayers' (PEMs) on the luminal surfaces of flexible catheters, and
140 Children with edematous and nonedematous PEM had higher plasma concentrations of 4 of 5 APPs in p
142 4 +/- 2 mo, and 9 children with nonedematous PEM, aged 10.1 +/- 1.4 mo, at 3 times: approximately 2 d
147 s work presents a 3D culture model and novel PEM coating procedure that enhances viability, maintains
149 the first successful in vivo application of PEM-engineered cells, which maintained viability and fun
154 s have addressed the potential influences of PEM on the immunogenicity and protective efficacy of avi
156 and "wall" thickness depend on the number of PEM bilayers, while the "cap" and "wall" of the PEC micr
160 t the rational engineering of a new class of PEMs with modular biological functionality and tunable p
162 disruption and facilitates the deposition of PEMs on cell surfaces that are tailorable in composition
163 he created m-dPEG acid monolayer patterns on PEMs act as resistive templates, and thus further deposi
167 d by only MR findings in five women, by only PEM findings in one, and by PEM and MR findings in five.
168 ntact printing of m-dPEG acid molecules onto PEM films to determine the optimal conditions for these
172 rmation of three-dimensional (3-D) patterned PEM films or selective particle depositions atop the ori
173 he formation of three-dimensional, patterned PEMs with high fidelity, micron-scale features by using
174 immune checkpoint inhibitors-pembrolizumab (PEM), nivolumab (NIVO), and ipilumumab (IPI)-demonstrate
176 yses indicate that both elicited peritoneal (PEMs) and bone marrow-derived macrophages (BMDMs) from t
177 ipotent erythrocyte-megakaryocyte precursor (PEM) population, and a CID-independent macrophage popula
179 When subjects are in the fed state, severe PEM induces a marked reduction in whole-body protein syn
180 A corollary is that children with severe PEM do not mount a protein catabolic response to infecti
181 proton migration within the HPW-meso-silica PEM and to determine the mechanism of proton hopping, we
185 ent two 'pombe epistasis mapper' strategies, PEM-1 and PEM-2, which allow for high-throughput double
186 rom mice bearing D1-DMBA-3 mammary tumors (T-PEM) are deficient in inflammatory functions and that th
200 whether the presence of infection alters the PEM-induced reduction in whole-body protein metabolism.
202 antification of whole air samples during the PEM-Tropics missions, along with an analysis of the anal
205 artitioned into heterogeneous regions of the PEM and Overhauser dynamic nuclear polarization relaxome
207 luate the chromatographic performance of the PEM coating as a chiral stationary phase, the separation
208 ia mesoporosity, favouring rigid link of the PEM on the sensor and improving the device sensitivity.
211 produce NO and lyse targets and, unlike the PEM, was not able to upregulate these functions even whe
212 capture of ROS generated in situ within the PEM for a period of about 7 h and the incorporation of C
215 brane electrode assemblies (MEAs) from these PEMs resulted in fuel cells that outperformed those base
220 -endothelium (postendothelial migrated Treg [PEM Treg ]) and the effect of subsequent interactions wi
221 2.4 and 1.8 times more IL-12 than wild-type PEMs in response to LPS or LPS and IFN-gamma, respective
222 r-operating-characteristic (ROC) study using PEM images reconstructed with different count levels exp
223 adjuvanted vaccination in populations where PEM is endemic may be one strategy to boost vaccination-
224 er, 279 (91.2%) were correctly assessed with PEM compared with 264 (86.3%) that were correctly assess
225 with MR imaging only; 14 (17%) breasts, with PEM only; and seven (8.5%) breasts, with mammography and
226 ematous and seven nonedematous children with PEM by using constant intragastric infusions of [2H3]leu
227 pletion of the albumin pool of children with PEM is not mediated by changes in the FSR, and the edema
233 epared in both PS and PETG are modified with PEMs, they demonstrate very similar electroosmotic mobil
234 ion could only detect Br(2)Y adsorbed within PEMs when using either higher photon energies or matrix
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