戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 the subjective experience of one's self (ego dissolution).
2 fidic conditions and subsequent Fe reductive dissolution.
3 nated by calcium carbonate precipitation and dissolution.
4 variables involved in the performance of the dissolution.
5 hest extraction of CuO NPs, while minimizing dissolution.
6 g the pH dependence of O(2)(*-)-mediated AFO dissolution.
7 perties, such as morphology, composition and dissolution.
8 Au core-shell nanocubes undergoing oxidative dissolution.
9 nto this microenvironment to promote CaCO(3) dissolution.
10 ntimicrobial lipids, and facilitate membrane dissolution.
11 n cell binding and extracellular virion (EV) dissolution.
12 NPs translocates from the lungs mainly after dissolution.
13 e Carbon ecosystems are sites of net CaCO(3) dissolution.
14 e deformation, and mineral precipitation and dissolution.
15 condensates, and oppose condensate reentrant dissolution.
16  including lipid interdigitation and bilayer dissolution.
17 hence the occurrence or not of LLPS upon ASD dissolution.
18 duced during elongation stimulate condensate dissolution.
19 e associated with positively experienced ego dissolution.
20 where the lowered polarity of water enhances dissolution.
21 t mechanisms of amyloid formation and fibril dissolution.
22  had significantly higher extractability and dissolution.
23 ed into soluble forms by sulfate-driven acid dissolution.
24 d for implant biofilm removal may lead to Ti dissolution.
25 generate a thin biofilm that induced mineral dissolution accompanied by water extraction.
26  flow-through and one flow-by) indicated 50% dissolution after 5 to 6 days at non-saturating conditio
27                  The overall rate of calcite dissolution along the fracture decreased over time, conf
28 fibrils, a potential method of cell-mediated dissolution, amyloid-like fibrils were labeled with the
29 rly vulnerable to ocean acidification due to dissolution and a reduction in shell-building carbonate
30 OF composites exhibit significantly enhanced dissolution and achieves high supersaturation in simulat
31                     We discovered a parallel dissolution and adsorption of Fe(2+) onto the metal, yie
32                               The sequential dissolution and autonomous release of the chemoattractan
33 n strategies are widely used for alleviating dissolution and diffusion of polysulfides, but they expe
34 e product of the solubility and ratio of the dissolution and diffusion rate-constants.
35 e(III)-reducing bacteria which favor mineral dissolution and drive mobilization of both iron and carb
36 mor localization, often exhibit little to no dissolution and excretion.
37 s might affect ligand-controlled (hydr)oxide dissolution and Fe acquisition.
38 ous sources such as atmospheric inputs, rock dissolution and fertilizer residues, and their concentra
39 ing slag was recycled via an integrated acid dissolution and hematite precipitation method.
40 imated groundwater recharge, suggesting that dissolution and leaching may be responsible for SIC loss
41                                          The dissolution and mass transport controls on divalent sili
42 ion is achieved by a combination of chemical dissolution and mechanical chip removal and ocean acidif
43 ere specifically favorable for retarding bio-dissolution and mechanical decay of scaffolds in vitro.
44  silicate addition, for reducing both pyrite dissolution and metalliferous drainage, may be applicabl
45  the subsurface and 2) the coupled carbonate dissolution and pyrite oxidation at depth in the rock.
46 rticles that was mediated by non-equilibrium dissolution and recrystallization.
47 er tendency of unwanted transition-metal-ion dissolution and side-reactions in Jahn-Teller-active oxi
48                       Application to improve dissolution and solubility for the hydrophobic small dru
49 tion protocol likely contributed to atrazine dissolution and subsequent underestimation of sorbed che
50 on processes associated with electrochemical dissolution and sulfur crossover through the membrane in
51 ion dictates phosphorylation-mediated fibril dissolution and that the hydrophobic effect drives fibri
52 ses drastically, suggesting the preferential dissolution and the formation of more stable Fe oxides.
53 fficient polarizing agents, providing, after dissolution and transfer (10 s), a (13) C liquid-state p
54                  The present methodology for dissolution and transformation fills a high priority gap
55  surface alterations and related Ti particle dissolution, and (3) cytocompatibility.
56 c interruption of the reaction for sampling, dissolution, and (bio)chemical analysis to monitor their
57 cantly reduced evaporative loss and material dissolution, and importantly, greatly suppressed competi
58           The combination of biodegradation, dissolution, and photo-oxidation depleted most PACs at s
59 ions between oil-gas phase transfer; aqueous dissolution; and densities and volumes of liquid oil dro
60             Because relationship discord and dissolution are common and costly, interventions are nee
61 ion of drug compounds in the solution during dissolution (as is commonly done), we monitor the decrea
62 ue to a greater leaf surface affinity and Cu dissolution, as determined computationally and experimen
63                The method is based on sample dissolution assisted by ultrasound energy in tetramethyl
64  position at 1 week post implantation, graft dissolution at 3 weeks, epithelialization of the ocular
65 data suggest that reef flat corals reach net dissolution at an aragonite saturation state (Omega(AR))
66 infrared spectroscopy showed that forsterite dissolution begins and electrical impedance spectroscopy
67 oil pH and organic matter content affect the dissolution behavior of CuO NP in soil in a predictable
68               Very little is known about the dissolution behavior of MC in the marine environment.
69  during the salt selection process, the salt dissolution behavior should be well understood.
70 t yet elaborate characterization of the salt dissolution behavior.
71                    Oil compound depletion by dissolution, biodegradation, and photo-oxidation was unt
72 nking were sensitive to the proximity to the dissolution ("boiling") temperature of the dense liquid:
73 on in target cell binding and an increase in dissolution, both of which correlated with a small-plaqu
74 (<6 h) via inhibiting arsenopyrite oxidative dissolution, but increased arsenic mobility over a longe
75 dification to regulate droplet formation and dissolution, but the physical basis of the regulatory me
76 id water required for the aqueous phase acid dissolution, but variability in WS-Fe was mainly driven
77             Here we show that static abiotic dissolution cannot rationalize this result, whereas two
78 ncomplete drug release under a wide range of dissolution conditions.
79 tored during rest periods, and lithium metal dissolution (corrosion) was observed in all electrolytes
80 t of galvanic interaction on reducing pyrite dissolution decreased with increasing pH and was greater
81 ), in terms of three components: enthalpy of dissolution (DeltaH(diss)), enthalpy of formation of aqu
82 t the anode carbon active material initiates dissolution, diffusion, and deposition of reaction side
83 lity, however, the phase solubility test and dissolution/disintegration tests (water and artificial s
84 ructural transformation and transition metal dissolution dominates the cathode capacity fading.
85 eted NMR-based metabolomic workflow based on dissolution dynamic nuclear polarization (d-DNP) for the
86         Hyperpolarization of ligand spins by dissolution dynamic nuclear polarization (D-DNP) is show
87 ar magnetic resonance (NMR) monitoring using dissolution dynamic nuclear polarization (D-DNP) to ampl
88        Here, folic acid is hyperpolarized by dissolution dynamic nuclear polarization (D-DNP).
89 e mostly to single voxel measurements unless dissolution dynamic nuclear polarization (dDNP) is used
90                   Herein we demonstrate that dissolution dynamic nuclear polarization (dDNP) provides
91 lomics combined with signal enhanced NMR via dissolution dynamic nuclear polarization (dDNP).
92                                    Advent of dissolution dynamic nuclear polarization (DNP) and its t
93                                           In dissolution-dynamic nuclear polarization, nuclear spins
94                          After assessment of dissolution effects, the resulting relationship between
95                                    Temporary dissolution enhancement during confinement is expected t
96 alytic effect of Fe(II) on ligand-controlled dissolution even at submicromolar Fe(II) concentrations
97 ipment, and provide only "snapshots" of drug dissolution every few minutes.
98 of the experimental design on the results of dissolution experiments of metal and metal oxide NPs is
99             We examined this effect in batch dissolution experiments using two structurally distinct
100 Additional simulations indicate that aqueous dissolution, fluid density changes, and gas-oil phase tr
101                                      In situ dissolution fluxes estimated in the current study were l
102 osed solid explosives to quantify in situ MC dissolution fluxes using dissolved MC gradients near the
103                       Plants could mobilize (dissolution followed by vertical transport) uranium (U)
104                             Transition-metal dissolution from cathode materials, manganese in particu
105 window of 3.3 V, suppresses transition metal dissolution from the cathode, and ensures singular inter
106  caused by reaction-driven precipitation and dissolution in a micromodel.
107                                    Oxidative dissolution in acidic solutions leads to increases in th
108 properties of bioelectronic implants such as dissolution in body fluids, biocompatibility, mechanical
109 through antisolvent precipitation, involving dissolution in ethanol or glacial acetic acid followed b
110 viding potentially higher resistance against dissolution in more corrosive waters.
111 hout sacrificing their dynamic formation and dissolution in response to physicochemical stimuli.
112 d gold nanoparticles (AuNPs), stable against dissolution in the absence of specific ligands, were add
113  interfaces from crystal formation in Bti to dissolution in the larval mosquito midgut.
114  exposure, respectively, with more extensive dissolution in the polar species.
115 play an important role in AFO photoreductive dissolution in the presence of the chosen surrogate of n
116                               Less extensive dissolution in the temperate brachiopod did not affect s
117 onation, phase transformation, and metal-ion dissolution in transition-metal oxides upon exposure to
118                    Mineral precipitation and dissolution induce complex dynamic pore structures, ther
119                                              Dissolution induces these natural convective flows that,
120 hat reactive iron minerals undergo reductive dissolution inside anoxic microsites of primarily unsatu
121  has been variously ascribed to drilling mud dissolution, interaction with pore fluids or shale excha
122 -called karst morphologies formed by mineral dissolution into water.
123                    Results show that methane dissolution is affected by heterogeneity, active versus
124 pendence of LMCT-mediated AFO photoreductive dissolution is mainly controlled by the influence of pH
125  be dominated by solid coating, whereas post dissolution it is dominated by receptor-bound drug (3.7
126 to develop an empirical model to predict the dissolution kinetics of CuO NPs in soil.
127 capability depends on the complex growth and dissolution kinetics of lithium sulfide (Li(2)S) and sul
128 NOM) and light on silver nanoparticle (AgNP) dissolution kinetics with particular emphasis on determi
129 oS(2) by NOM was mainly attributed to slower dissolution kinetics with rapid initial oxidation (i.e.,
130 tractions were applied to measure the CuO NP dissolution kinetics.
131 were traced to geogenic sources (weathering, dissolution, leaching) and anthropogenic emissions from
132 eached and unexpected mechanisms like quartz dissolution linked to shale degradation.
133 e associated with negatively experienced ego dissolution, lower levels in hippocampal glutamate were
134 on microscopy (TEM) imaging reveals that the dissolution mechanism changes from predominantly edge-se
135 ot and released over time to provide a depot dissolution mechanism.
136 lso provide new insights into the V(2) O(5) -dissolution mechanisms for different Zn-salt aqueous ele
137  study, the degree of supersaturation in the dissolution medium generated by the crosslinked systems
138  same nuclei undergoing growth, fluctuation, dissolution, merging and/or division, which are regulate
139                                The developed dissolution method allowed Ca, Fe, Zn, and Mg determinat
140 bed in the US Food and Drug Administration's Dissolution Methods Database.
141 fested by cytoskeletal remodelling, junction dissolution, migration and extracellular matrix turnover
142  after (57)Fe(II), suggesting that catalyzed dissolution occurred at or near the site of (57)Fe incor
143 ith the dietary exposures suggests that some dissolution occurred within fish organs.
144                  This allows for homogeneous dissolution of 1.3 ng of fluorescently labeled dAbs in 4
145                                            A dissolution of [Fe(CN)(6)](4-)/[Fe(CN)(6)](3-) as a redo
146                           The disaggregation/dissolution of Abeta fibrils occurred nearly instantly w
147  the contribution of O(2)(*)(-) to reductive dissolution of AFO is dependent on conditions such as th
148 on of AFO by O(2)(*)(-) occurs following the dissolution of AFO, and hence, the contribution of O(2)(
149 tial AFO concentration affecting the rate of dissolution of AFO.
150 to regulate the formation, modification, and dissolution of aggregates.
151 echanism via which NOM affects the oxidative dissolution of AgNPs, (ii) the role of photogenerated or
152 d reactive oxygen species (ROS) in oxidative dissolution of AgNPs, and (iii) the mechanism of formati
153 the kinetics and mechanism of photoreductive dissolution of amorphous iron oxyhydroxide (AFO) in view
154 Dealloying typically occurs via the chemical dissolution of an alloy component through a corrosion pr
155            Iron EC involves the electrolytic dissolution of an Fe(0) electrode to Fe(II).
156                                          The dissolution of anhydrous iron bromide in a mixture of py
157 ron donor for microbially-mediated reductive dissolution of As-bearing Fe(III) (oxyhydr)oxides.
158 n, As release is attributed to the oxidative dissolution of As-bearing pyrite.
159 f their many components is the formation and dissolution of biomolecular condensates through liquid-l
160 red that permethylation affords the complete dissolution of both soluble and insoluble polysaccharide
161  disintegration, have emerged to explain the dissolution of Cahokia, the largest prehistoric populati
162 emonstrate, using a mathematical model, that dissolution of calcium that has aggregated within the mi
163 km/s correspond with growth of porosity from dissolution of chlorite, the most reactive of the abunda
164  with longer crosslink lifetimes, there is a dissolution of clusters.
165 Mn from the alloy appeared to discourage the dissolution of Cr in the molten fluoride salts which is
166 cs of acute hypoxia; (ii) the initiation and dissolution of distinct hemodynamic niches; (iii) tumor
167 cantly accelerate rates of ligand-controlled dissolution of Fe(III) (hydr)oxides at circumneutral pH.
168                                              Dissolution of Fe(III) phases is a key process in making
169 clude that the catalytic effect of Fe(II) on dissolution of Fe(III)(hydr)oxides is likely important u
170               This electrolyte minimizes the dissolution of ferrocene; it raises the cation-insertion
171 d to quantitatively monitor phagocytosis and dissolution of fibrils concurrently.
172        Current drugs used for inhibiting the dissolution of fibrin, the main structural component of
173 ystem thus reveals the dynamic formation and dissolution of fusion pores.
174                                 However, the dissolution of high-order polysulfide in electrolytes an
175 ociated with the formation, development, and dissolution of intimate relationships.
176 (>12 kyr-old) aquifer promotes the reductive dissolution of iron oxides and the release of arsenic.
177 w of the recognition that the light-mediated dissolution of iron oxides controls Fe availability in m
178             The increased rate and extent of dissolution of iron oxyhydroxides on the acidification o
179                                              Dissolution of iron(III)phases is a key process in soils
180 d where reducing alkaline conditions favored dissolution of iron-manganese- (Fe-Mn-) oxyhydroxides (w
181                                              Dissolution of irradiated bismuth targets is accomplishe
182 e water irrigated areas, suggesting repeated dissolution of land applied fertilizer during recirculat
183 en no current is flowing, demonstrating that dissolution of lithium remains a critical issue for lith
184 to isotope exchange at the surface, with the dissolution of Lp by ligands accelerated by up to 60-fol
185                                       During dissolution of Lp with DFOB, ratios of released (56)Fe a
186 tics, reflecting the differential and faster dissolution of lumenal versus tissue-embedded coating ow
187     These results demonstrate that oxidative dissolution of magnetite can induce a rich array of stra
188                            The formation and dissolution of many RNP condensates are finely dependent
189 ew aims to elucidate nanospecific effects on dissolution of metallic NPs in freshwater and similar me
190 e catalyst enables the reversible growth and dissolution of micrometre-sized lithium oxide crystals t
191 e reference 316 H stainless steel due to the dissolution of Mn into the molten salt.
192 enetically deleted, leads to a near-complete dissolution of NS.
193                   Remarkably, layer-by-layer dissolution of Pd into Ag is always preceded by an encap
194 rphology of dendritic cells and mediates the dissolution of podosomes, which dendritic cells use to a
195 phosphate and exchangeable Ca(2+) and/or (2) dissolution of poorly crystalline Fe and Al oxides by 1
196 nic interaction and silicate addition on the dissolution of pyrite, the major contributor to acid and
197 e, overexpression of laccase showed enhanced dissolution of quartz phases by etching and pitting.
198      Washout experiments confirmed the rapid dissolution of SGs, accompanied by normalization of TDP-
199 sport resulting from cultivation may enhance dissolution of SIC, altering their local stock at decada
200 rrays of pinnacles, emerge robustly from the dissolution of solids with smooth initial shapes.
201 cate addition also significantly reduced the dissolution of sphalerite or galena (by 10-44%, except a
202 n is unknown, and quantification of flow and dissolution of stray gas is required.
203                                              Dissolution of the Au shell slows down when both metals
204  The synthetic compound ink derived from the dissolution of the bulk binary precursors in the right s
205  iodide ions, thus preventing the consequent dissolution of the cathode-plated iodine as triiodides.
206 al gradients, in agreement with preferential dissolution of the crystallite core in acidic media.
207 d two release processes intracellularly: the dissolution of the dye aggregates into dye molecules and
208 ingle capsule or tablet, measurements of the dissolution of the entire multi-particle capsule or tabl
209 XX interactions saturate, which leads to the dissolution of the gel and the appearance of a liquid ph
210                                              Dissolution of the iron trans-bimetallacycle in benzene-
211 ght chain fibrils by macrophages, leading to dissolution of the mass.
212 nsition happened, which resulted in the full dissolution of the network.
213 th conventional voltammetric analyzer, after dissolution of the samples in microwave oven, and with a
214 tions whereas relatively high levels promote dissolution of these condensates.
215                                  The aqueous dissolution of these materials creates high pH solutions
216  mechanisms that can allow the formation and dissolution of this membraneless body.
217 he more disordered nanoparticles showing the dissolution of tin and platinum species during electroca
218                                              Dissolution of U(70) in organic media reveals (by small-
219                                 However, the dissolution of U-As-Ca and U-Ca-bearing solids at pH 7 w
220 , and pore water chemical data, suggest that dissolution of V(III)-bearing magnetite, V(III)- and V(I
221 ntify a possible impact of calcium phosphate dissolution on the maintenance of F0F1-ATP synthase acti
222 treatment groups (n = 15) using gums of oral dissolution (one gum every 12 hours) for 10 days.
223                 Techniques for measuring the dissolution or degradation of a drug product in vitro pl
224 le sample preparation step that consisted of dissolution or dilution of the samples in water, followe
225 ver geological timescales until extracted by dissolution or fracturing of the olivine host.
226   Increased temperature did not impact shell dissolution or thickness.
227 educed corrosion resistance and increased Ti dissolution over 30 days of material aging as compared t
228 ripts are stabilized and stored until P-body dissolution permits transcript reentry into the cytosol.
229                              Subsequently, a dissolution phase was conducted by injecting clean water
230 ile other genomic regions promote condensate dissolution, potentially preventing aggregation of the l
231 d shear zones deforming via diffusion creep, dissolution-precipitation creep and grain boundary slidi
232 ine h-BNNS was achieved through a successive dissolution-precipitation/crystallization process in the
233 igation was attributed to film thinning by a dissolution/precipitation mechanism.
234   We accomplished this by inverting the drug dissolution problem: instead of measuring the increase i
235 reening of small sample amounts and detailed dissolution process analysis.
236  LiMn(2) O(4) -like sub-nanodomain formation/dissolution process during each charge/discharge, which
237                   Rational interpretation of dissolution process into a numerical problem led to a sm
238 solubility data, which demonstrated that the dissolution process is endothermic and non-spontaneous a
239 ry out time-resolved imaging of this "active dissolution" process.
240 performance properties, and studies of their dissolution processes define the underlying aspects.
241               The potential role of titanium dissolution products in peri-implantitis necessitate the
242  for pharmaceutical companies to obtain full dissolution profiles for drug products in a variety of d
243 sensor data revealed significantly different dissolution profiles for the different drugs, and in som
244  and fully-automated technique for obtaining dissolution profiles from single controlled-release pell
245  this technique to measure the single-pellet dissolution profiles of several commercial controlled-re
246                                 The improved dissolution properties of these phosphate prodrugs provi
247 freeze-drying of the extracts allowed better dissolution properties than spray-drying.
248 content, soil pH and moisture content on the dissolution rate and solubility of copper oxide nanopart
249                             In contrast, the dissolution rate constant correlated with pH for pH < 6.
250 om 5.9 to 6.8 in LUFA 2.2 soil decreased the dissolution rate constant from 0.56 mol(1/3).kg(1/3).s(-
251  (<15 nm) was observed, leading to increased dissolution rate constants and solubility in some cases.
252 es C) is demonstrated here, showing that the dissolution rate of pyrite significantly changes with th
253                                      Calcite dissolution rate quantified from the attenuation data wa
254 crystal, which has much lower solubility and dissolution rate than commercial powder reb B product.
255                                   The pyrite dissolution rate was reduced by 98% upon silicate additi
256 suffers from poor aqueous solubility and low dissolution rate, which greatly limits its application,
257 centrations with up to a 13-fold increase in dissolution rate.
258 pplied a simple empirical model to determine dissolution rates and a more complex kinetic model that
259 quantification of silver nanoparticle (AgNP) dissolution rates in simulated sweat.
260 conditions to investigate the mechanisms and dissolution rates of biogenic, noncrystalline UO(2)(s) b
261                      Surface area normalized dissolution rates of both the drug and the polymer from
262                                              Dissolution rates of UO(2)(s) with dissolved nitrite wer
263 ed in the current study were lower than most dissolution rates reported for laboratory experiments, b
264 -type T. denitrificans and nitrate, UO(2)(s) dissolution rates were similar to those of abiotic exper
265 ural convective flows that, in turn, enhance dissolution rates, and simulations show that this feedba
266 siological needs of different biota, mineral dissolution rates, and substrate nutrient availability r
267 mplementation of grouping and read-across by dissolution rates.
268 and single-cell analysis, we found that foci dissolution rather than formation promoted HSF1 activity
269                                       As the dissolution reaction progressed, the ESA is observed to
270 roscopy, revealing nonclassical pathways via dissolution-recrystallization of highly hydrated amorpho
271 as a simple anion exchange mechanism without dissolution-recrystallization or interstratification pro
272                                         This dissolution reduces the skeletal density and hardness an
273 nt, the Kirkendall effect, Ostwald ripening, dissolution-regrowth, and the surface-protected hollowin
274                   TAMOC reveals that aqueous dissolution removed >95% of the methane from ~3.5 mm liv
275 r steady flow conditions, this formation and dissolution repeats cyclically.
276                                       During dissolution, retention in porcine iliofemoral arteries i
277                                           Ti dissolution should become an important consideration in
278                                 Also, during dissolution study, the degree of supersaturation in the
279 y of protons, 2) better cycling stability by dissolution suppression, and 3) higher Coulombic efficie
280 ize this result, whereas two dynamic abiotic dissolution systems (one flow-through and one flow-by) i
281                                              Dissolution testing and content drug recovery was carrie
282  can augment and potentially replace current dissolution tests and support product development and qu
283                 During the Cu(2)O growth and dissolution, the cubic shape evolved with specific plane
284 inating from inhomogeneous Li deposition and dissolution, the formation of dendritic and/or dead Li l
285            Kinetic analyses revealed that Mg dissolution to Mg(2+) followed mostly a zero-order kinet
286 bolic activity accelerates calcium carbonate dissolution to rates exceeding accretion by healthy cora
287 on relations between particle properties and dissolution/transformation characteristics of metal and
288  results signify an increased plant-mediated dissolution, uptake, and leaching of radioactive contami
289 M) and atomic force microscopy (AFM), and Ti dissolution via light microscopy and Inductively-coupled
290 2) S composites and inhibits the polysulfide dissolution via the TM S bond, effectively addressing th
291                                        The U dissolution was further increased when chernikovite co-o
292 s enthalpy, entropy and Gibbs free energy of dissolution were obtained using experimental solubility
293                      There was no observable dissolution when Au NPs were incubated in abiotic soil.
294 s following amorphous solid dispersion (ASD) dissolution when the drug concentration exceeds the "amo
295 1k) and mPEG(2k)-LA(2).(7k) micelles favored dissolution whereas mPEG(5.4k)-LA(28.5k) micelles favore
296 e of thrombus, thus achieving efficient clot dissolution whilst minimising undesirable side effects.
297                            Substantial shell dissolution with decreasing pH posed a threat to both a
298 d this work by studying isotope exchange and dissolution with lepidocrocite (Lp) and goethite (Gt) in
299  faces several challenges including complete dissolution with maximum therapeutic efficiency over a s
300 le cycles of 53BP1 repair foci formation and dissolution, with the first cycle taking longer than sub

 
Page Top