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1 a up to 759 m(2) g(-1) mainly contributed by micropores).
2 -membrane mimics, with a well-defined single micropore.
3 er in between bran particles and probably in micropores.
4 layer and continuous water provision through micropores.
5 iquor is subsequently soaked off through the micropores.
6 erived carbon, with a narrow distribution of micropores.
7 ient) with the fraction of porosity in small micropores.
8 is attributed to the microenvironment of the micropores.
9 d survival in migration through constraining micropores.
10 sorbed, both to exterior surfaces and within micropores.
11 thick and contain a network of 0.5-nanometer micropores.
12 y due to desorption of chemicals from narrow micropores.
13 intergranular pores and the H(2) residing in micropores.
14  area and pore volume, respectively) is from micropores.
15  migrating through the size-restricted 3-mum micropores.
16 the chlorine groups, lining the walls of the micropores.
17 ed Cr cations stabilized by silanol nests in micropores.
18 edominantly occurs via diffusion through the micropores.
19  cations (Ni, Pd, Pt, Cr, Cu) in the zeolite micropores.
20 polymers thread into the particles' sub-2 nm micropores.
21 on of alcohol-hydronium ion complexes in the micropores.
22  spectrum of pores ranging from mesopores to micropores.
23  benefit from traditional confinement within micropores.
24 g through the pores or wireless ECL-emitting micropores.
25 electric double layers (EDLs) within charged micropores.
26 hey result from denser counterion packing in micropores.
27 upon MN length, number, and occlusion of the micropores.
28 e the penetration of liquid through putative micropores.
29 nes (MPMs) that present dense and continuous micropore (~0.8 nm) networks, we show significant uptake
30 onsisting of noncrystallographic extra-large micropores (13 angstrom) that connect with the character
31 cally porous COF foams consisting of ordered micropores (2-2.2 nm) and disordered meso and macropores
32                                          The micropore, a mysterious structure found in apicomplexan
33 bits a large surface area, a high content of micropores, a high content of graphitic N, and N-sites w
34                                              Micropores accelerate fragmentation by facilitating the
35 hibition of mesopore collapse, and therefore micropore accessibility, as the basis for the extraordin
36 s, nanopores in the range of 2 nm and below (micropores, according to IUPAC classification) are usual
37 s from limitations to molecular transport in micropores, across external crystal surfaces, but also a
38 tructural features-such as grain spacing and micropores-affect fracture behavior.
39 e framework structures with discrete uniform micropores allowing selective processing and sorption ba
40                     Containment within small micropores also protects clusters against thermal sinter
41 the interface between a single ion-selective micropore and aqueous solutions is quantitatively invest
42 nt with predicted values using surface area, micropore and mesopore volumes as the input values simul
43               This paper describes synthetic micropore and nanotube membranes that mimic the function
44 gates to the exterior through the membrane's micropore and pumps target objects into the cell, acting
45 ECL) is emitted in half of the electroactive micropore and reveals the asymmetric polarization in thi
46 ities that allow CO2 gas molecules to access micropores and adsorb effectively.
47 zed the literature on different apicomplexan micropores and found that T. gondii probably harbors a m
48 l, the absorption is most improved for IL in micropores and in nitrogen-doped carbon.
49 Here, in cancer cell migration through rigid micropores and in passive pulling into micropipettes, lo
50 arbons was characterized for the presence of micropores and macropores, when obtained from highly cro
51               The presence of interconnected micropores and mesopores is responsible for the enhanced
52       The unique nanoarchitectures with rich micropores and mesopores, as well as the high surface ar
53 of water molecules from the surfaces of coal micropores and mesopores.
54 only in CD34(+) cells, but migration through micropores and nuclear flexibility in micropipette aspir
55                         However, their dense micropores and poor pore connectivity hinder mass transp
56 pends on the solvating environments of their micropores and the proximity of their Bronsted acid site
57 ned polygonal lattices and built-in discrete micropores and/or mesopores.
58 tential drop at the level of the solid-state micropore, and thus to a locally enhanced polarization o
59 n essential intermediate for adsorption into micropores, and demonstrates how surrounding environment
60 erlayer macropores, narrowly distributed 7 A micropores, and ever most polar pore walls.
61 meable drugs by creating transient epidermal micropores, and micropore lifetime directly affects drug
62 for solution sampling from biological cells, micropores, and other microscopic objects.
63 h as disconnected micropores, interconnected micropores, and surface macropores, reveal that the hydr
64 ers with persistence lengths that exceed the micropore aperture size of zeolitic imidazolate framewor
65                                          NaA micropore apertures restrict access to encapsulated clus
66 deoxidized silicon electrodes located in the micropore are polarized at a very low potential (7 V), w
67   Ion-selective membranes with sub-nanometer micropores are essential in various separation processes
68 he clays by gas physisorption indicates that micropores are only partly accessible to N(2) (77 K) and
69  %), surface area up to 367 m(2) g(-1) , and micropores around 1.1 nm.
70 ti-channel device which utilized solid-state micropores array assembly for simultaneous measurement o
71                         Here we validate the micropore as an essential organelle for endocytosis of n
72 T-1 crystals and contained partially ordered micropores as well as disordered mesopores.
73 e Pd nanoparticles controlled by the zeolite micropores, as elucidated by competitive adsorption and
74 ts bi-microporous features with well-defined micropores at 0.86 nm and 1.51 nm.
75 trolite) irreversibly inserts xenon into its micropores at 1.7 GPa and 250 degrees C, while Ag(+) is
76  are observed: (1) minor sorption effects in micropores at low pressures; (2) capillary condensation
77 ns are increasingly desorbed from the carbon micropores at the negative electrode, while at the posit
78 ved the metal and acid functions by limiting micropore blockage by metal clusters and enhancing acces
79  deformability is reduced in sepsis but that micropore bulk-filtration methods may not be appropriate
80 ulatory disturbances in sepsis have prompted micropore bulk-filtration studies of red blood cell (RBC
81 species generated on the Pt sites within the micropores can be readily transported by these oxygenate
82                                  Solid-state micropores can characterize each cell in a sample provid
83                The ionic current across each micropore channel was continuously monitored and recorde
84 eaks and TEM images that reveal well-ordered micropore channels.
85 cancy-network polymorphs with very different micropore characteristics.
86 at includes both finite ion size effects and micropore chemical charge, which predicts such enhanceme
87 lored, and we report for the first time that micropore closure is delayed in elderly subjects in a ma
88 s (61.1 +/- 16.1 h) had significantly longer micropore closure time versus Asians (44.1 +/- 14.0 h).
89                                              Micropore closure was measured with impedance spectrosco
90  flow is synergistically fulfilled by robust micropore confinement and multi-interaction between ion
91            It is generally known that narrow micropores contribute to higher CO(2) adsorption capacit
92                       In addition to a large micropore contribution to the surface area, mesopores ar
93 distinctive advection domain, macropores and micropores created in silicon substrate.
94 s combining mesopores (d >/= 20 A) and large micropores (d = 10-20 A), due to the overlap of pore-fil
95                  We find that the density of micropores decreases monotonically along the Pr length w
96                             This interfacial micropore defect formation becomes more prominent with i
97    The present result shows the formation of micropore defects in the interface region of the PEDOT:P
98 d carbon samples with well-aligned, straight micropores demonstrate high specific capacitance of up t
99 axima proportional to the Pr length and that micropore diameters produce a Knudsen number at the boun
100                                 The measured micropore diffusion coefficient for CO2 in Cu-BTC is 1.7
101 tal size aids in the accurate measurement of micropore diffusion coefficients.
102 h the high external surface area and reduced micropore diffusion length, account for higher reaction
103                                        These micropore dimensions are relevant for many valuable chem
104 pirobifluorene, endowing these polymers with micropore dimensions attractive for gas separations.
105                                 We develop a micropore EDL theory that includes both finite ion size
106                                      Surface micropores enable permanent porosity by steric exclusion
107 nt membrane-like Matrigel on a polycarbonate micropore filter was evoked by vasoactive intestinal pep
108 d with a cell transit analyzer (containing a micropore filter with 30 identical, 8-microm diameter po
109 ctic mobility, assessed by migration through micropore filters without Matrigel, and in situ MMP acti
110 did not respond to VIP by chemotaxis through micropore filters without or with a top layer of basemen
111         The migration of RNK-16 cells across micropore filters, without or with a layer of Matrigel,
112 en CLL cells were separated from the MSCs by micropore filters.
113  were osmotically fragile, and ektacytometry/micropore filtration measurements demonstrated reduced d
114 cal behavior was tested using a computerized micropore filtration system (CTA) and a laser-diffractio
115 MN deformation behavior was investigated via micropore filtration, using the cell transit analyzer.
116 roton hopping across the channels, while the micropores follow sluggish vehicle conduction.
117 pplied suggests the ion rearrangement in the micropores following different mechanisms depending on t
118 anelle and functions as a protein hub at the micropore for endocytic uptake.
119 ificant in all groups (p < 0.05), confirming micropore formation regardless of skin type.
120 e T. gondii micropore, we propose a model of micropore formation, thus enriching our wider understand
121  measured at baseline and post-MN to confirm micropore formation.
122                     Stomata are controllable micropores formed between two adjacent guard cells (GCs)
123                                          The micropores formed by the AB stacking are highly accessib
124 porosity while borrowing the robustness of a micropore framework.
125 hell membranes (CSEMs) consisting of natural micropores function well as a polysulfide reservoir in L
126                           By integrating two micropore-generating units such as a water-soluble Troge
127 rug delivery), as well as calculation of the micropore half-life.
128 e involvement of subclinical inflammation in micropore healing.
129 ites vs. placebo, suggesting slower rates of micropore healing.
130 However, despite being extremely beneficial, micropores impose restrictions on the mass transport of
131                         Square arrays of 100 micropores in 130 mum thick borosilicate glass coverslip
132 ct the rate of ionic diffusion in the carbon micropores in an effort to understand supercapacitor cha
133 pens an avenue to exploit the sub-5 angstrom micropores in carbon and their desirable size-exclusion
134  suggesting that despite the vast numbers of micropores in shale, the micropores will be unavailable
135 ow-noise properties of bilayer recordings on micropores in Teflon AF films were exploited to record t
136 t ionic liquids spontaneously wet the carbon micropores in the absence of any applied potential and t
137 icroscopy showed that NaOH steeping produced micropores in the cell walls and light microscopy reveal
138 ng powdered allergen and adjuvants into many micropores in the epidermis.
139      It is most likely caused by the lack of micropores in the polymer structures.
140 ticles with protruding microneedles, to form micropores in the skin to increase skin permeability to
141 actional infrared laser ablation to generate micropores in the skin, and the effects of LamOVA on blo
142 nation via vaccine delivery into an array of micropores in the skin, instead of bolus injection at a
143 orresponding swollen material; the amount of micropores increased with increasing rigidity and size o
144  the synergetic actions of BPE and of planar micropores integrated in a microfluidic device lead to t
145 varied pore structures, such as disconnected micropores, interconnected micropores, and surface macro
146 DB2 at the subnuclear DNA damage foci within micropore irradiated cells.
147                                        Using micropore irradiation, we demonstrate that large amounts
148                           Filtration through micropores is frequently used to assess red blood cell d
149 ca or carbon nanospheres with size-selective micropores is presented.
150              LamOVA EPIT via laser-generated micropores is safe and equally effective compared to SCI
151 sults indicate that the surface chemistry in micropores is tunable thereby influencing the selectivit
152 action that cannot take place in the zeolite micropores, is observed.
153 sfer limitation due to the small size of the micropores (less than 1 nm).
154 ent, or replacement of framework atoms), the micropore level (e.g. template removal and functionalisa
155 ent the first human study demonstrating that micropore lifetime can be extended following MN treatmen
156 man proof-of-concept study demonstrates that micropore lifetime can be prolonged with simple topical
157            We report for the first time that micropore lifetime differences are present in human subj
158 creating transient epidermal micropores, and micropore lifetime directly affects drug diffusion timef
159 erent ethnic/racial backgrounds, with longer micropore lifetime in skin of color.
160 measured skin color is a better predictor of micropore lifetime than self-identified race/ethnicity.
161                                              Micropore lifetime was significantly longer in Blacks (6
162      When categorizing data according to L*, micropore lifetime was significantly longer in darker sk
163 pedance was repeated for 4 days to determine micropore lifetime.
164 ), and contained a significant population of micropores (&lt; or =20 A).
165 ion of well-separated mesopores (3-7 nm) and micropores (&lt;2 nm) were found to be most promising.
166 t monolith had relatively large fractions of micropores (&lt;2 nm, 11.9%) and mesopores in the range fro
167 y (cell-on-cell) or indirectly (separated by micropore membrane)] designed to interrogate the interpl
168 F)-positive cells separated by 0.4-mum-thick micropore membranes from stromal cells), indicating a pa
169 TPA, initially shows a broad distribution of micropores, mesopores, and macropores.
170 eport a simple strategy for partitioning the micropores/mesopores of multivariate COFs.
171  T(g)), sorption of TCE is well-described by micropore models, with enthalpies of sorption characteri
172 bution increases, making a portion of closed micropore network accessible.
173 rrangements are crucial because they control micropore-network characteristics, and hence the diffusi
174       Herein, a hierarchical nanoparticle-in-micropore (NP-MP) architecture in porous mechanochromic
175 le-sites anchored on the internal surface of micropores of a microporous silicate exhibit high select
176 urface interactions of water confined in the micropores of an MFI-type, hydrophilic zeolite with a Si
177  via redox between mainly Cl(2)/Cl(-) in the micropores of carbon and Na/Na(+) or Li/Li(+) redox on t
178 te LSBs, where sulfur is encapsulated in the micropores of carbon matrix and sealed by solid electrol
179 nd various forms of phase transitions in the micropores of electrodes interfacing with an organic ele
180        Ultrasmall Pd(4) clusters form in the micropores of FER zeolite during low-temperature treatme
181                    Ion migration through the micropores of the flow electrodes was facilitated in par
182 enotype of the endothelial cells through the micropores of the membrane and their spread morphology o
183                                          The micropores of the MOF crystals embedded within a semiper
184 showed that slow diffusion occurs within the micropores of the sol-gel films which could be modeled a
185  grafted at the Bronsted acid sites (BAS) in micropores of the zeolite, whereas silanoate- and alumin
186 tead of Pt(0) cluster-proton adducts, in the micropores of the ZSM-5 zeolite.
187         However, the differences between the micropores of these two parasites questions the nature o
188  within the smaller 12-membered ring (12-MR) micropores of Ti-Beta.
189 e of water, hydronium ions formed within the micropores of zeolite H-BEA significantly influence the
190  while acidity is retained solely within the micropores of ZSM-5.
191 gmented HDM extract via laser-generated skin micropores offers a safe and effective treatment option
192 environments, such as dental plaques or soil micropores, often characterized by noneven surfaces.
193 change are overcome by previously unreported micropores on the Pr surface and by superhydrophobic Tr
194 e invagination with a dense neck, termed the micropore, on the surface of intracellular parasites.
195 ated metal centers and two distinct types of micropores, one of which is lined by CrO4 (2-) (CROFOUR)
196 ur, compared with its counterparts with only micropores or bimodal micro/mesopores.
197 eronyssinus extract via laser-generated skin micropores or by subcutaneous injection with or without
198 ondensation reactions also occur within tiny micropores or defects in the topmost layer.
199 ctions, especially for catalysts with narrow micropores or large zeolite crystals.
200                           The sub-5 angstrom micropore orifices centered at 4.1-4.3 angstrom in PDA-C
201  temperature) with tailorable sub-5 angstrom micropore orifices together with larger microvoids by on
202 ined and arrange themselves according to the micropore pattern.
203 timated pore size that can contribute to the micropore peak is estimated to be around 2.4 nm.
204                    The chemical shift of the micropore peak is observed to evolve with changing press
205    Organic open frameworks with well-defined micropore (pore dimensions below 2 nm) structure are att
206                However, rapid healing of the micropores prevents further drug delivery, blunting the
207 structure, with no detectable interspaces or micropores; probiotic inclusion did not significantly ch
208 n, thus enriching our wider understanding of micropore protein function.
209              Here we show that the mordenite micropores provide a perfect confined environment for th
210 ures are an ideal solution, e.g., with small micropores providing large surface areas and larger macr
211 ]((1-n)+) complexes inside uniquely confined micropore reaction environments.
212 hile preserving micro- and mesoporosity, and micropore reaction rates.
213        Intriguingly, maximal activity of the micropore requires the ceramide de novo synthesis pathwa
214  to be partitioned into two or three smaller micropores, respectively.
215 pic energy barrier(8,9) brought about by the micropore's geometry retains the cargo even when the cat
216 terial with a periodic arrangement of narrow micropores, shows an increase in isosteric enthalpy with
217                   Modulation of the hydrated micropore size (less than two nanometres) enables direct
218                             This ease of the micropore size adjustment and the attained degree of str
219 r values (by ~20x) with further decreases in micropore size as Ti sites are confined within 10-MR por
220 se after bioconversion, while the accessible micropore size distribution increases, making a portion
221                      Both inaccessible meso-/micropore size distributions decrease after bioconversio
222 ganic polyhedra displaying a precise uniform micropore size of 1.0 nm.
223                               With a typical micropore size range of around 1 nm and a typical surfac
224    Through moderate activation, we achieve a micropore-size distribution consisting almost exclusivel
225 estions the nature of a general apicomplexan micropore structure and whether the formation process mo
226 n silanol (Si-OH) defects located within the micropore structure and/or on the external surface of ze
227 th large porosity and permanent well-defined micropore structures, which can overcome the ubiquitous
228 e average pore diameter increases, while the micropore surface area increases with pore volume decrea
229 tment, which is confirmed by the increase of micropore surface area.
230                                              Micropore Teflon diffusion chambers were implanted subcu
231  with a resistive pulse sensor (RPS) using a micropore that counts the released NPs, this method can
232 s in water while maintaining dry networks of micropores that are accessible to gas molecules.
233 like actuators from smart gels with embedded micropores that autonomically dilate and contract in res
234 skin-impermeable drugs by creating transient micropores that bypass the barrier function of the skin.
235 vitro inhibited macrophage migration through micropores that mimic features of dense 3D tissue.
236 lly owing to the formation of ultraselective micropores that selectively exclude the bulkier CH4 mole
237 hese endocytic structures correspond to the 'micropore' that has been observed throughout the Apicomp
238  both small (<0.7 nm) and large (0.7-1.0 nm) micropores, the former enhancing selectivity and the lat
239  to the mechanism whereby Y(2)O(3)NPs occupy micropores, thereby reducing active corrosion sites with
240                  By creating laser-generated micropores through the epidermis, we targeted a model pr
241 t pore sizes, which are gradually tuned from micropores to mesopores.
242 e synthetic protocols and the ability of NaA micropores to sieve reactants based on molecular size.
243 scutaneous immunotherapy via laser-generated micropores to subcutaneous injection.
244 agnitude-without changing the particle size, micropore topology, or polymer chain length-by rationall
245 s of magnitude is possible by minimizing the micropore tortuosity.
246  could enhance the exposure of the intrinsic micropores toward the pollutant environment, thereby, im
247 t of measurement and as the cells passed the micropores, tumor cells showed distinctive current block
248 ondii probably harbors a more representative micropore type than the more widely studied ones in Plas
249 d through the addition of chemical charge to micropores via surface functionalization.
250 rface area (SA(BET)) of 454 m(2) g(-1) and a micropore volume (V(mp)) of 0.22 mL g(-1).
251 e titration confirm the expected decrease of micropore volume and increase in external surface area f
252 This means that a particular surface area or micropore volume can be precisely tuned.
253                             Increasing their micropore volume could further improve their already exc
254 ith a continuously tuneable surface area and micropore volume over a wide range can be prepared.
255                               This increased micropore volume results from the opening of some of the
256 yte applications, the importance of matching micropore volume to sulfide loading and cycling rate is
257  and sorbent; this results in ca. 10% higher micropore volume with limited impact on its thermal stab
258 trend regularly with N2 or CO2 surface area, micropore volume, mesopore volume, H/C ratio, O/C ratio,
259  graphite due to the higher surface area and micropore volume.
260 r intensity, while a higher surface area and micropores volume were important for removing phenolic a
261 ciency was related to their surface area and micropores volume.
262 th high surface areas (up to 940 m(2)/g) and micropore volumes (0.36 cm(3)/g) were synthesized via K(
263 t properties such as large surface areas and micropore volumes, that favor a high adsorption capacity
264       The defects in the silica layer of the micropore wall enable the creation of an electric pathwa
265                       The MO adsorbed in the micropores was strongly adsorbed and difficult to remove
266 e weathering products dissolved in meso- and micropore water, which lysimeters cannot extract.
267                                       In the micropores, water adsorbs to Bronsted acid sites and def
268 d gene depletion phenotypes in the T. gondii micropore, we propose a model of micropore formation, th
269 nanoparticles exclusively deposited into the micropores, we demonstrate that activated hydrogen speci
270 ion, provided that distances between any two micropores were sufficient.
271 ere well tolerated and effective at creating micropores when applied to the skin of human participant
272 associated with the unique properties of the micropores, where the sharp potential drop is focused.
273  that the heel was mainly built up in narrow micropores which can be occupied or blocked by some of t
274 n of the total permeable area created by the micropores (which would approximate the area available f
275  holder from single crystalline silicon with micropores, which carries up to thousands of crystals an
276 f adsorbed and non-adsorbed molecules within micropores, which experience significantly different che
277 y and structure of these thermally regulated micropores, which is crucial to systematic engineering o
278 mn vacancies is proposed for the extra-large micropores, which is revealed unambiguously by high-reso
279 the vast numbers of micropores in shale, the micropores will be unavailable for storage for geologic
280 was fabricated in silicon in series with two micropores with 2 and 100 microm diameters.
281 nificantly dependent on the volume of narrow micropores with a pore size of less than 0.8 nm rather t
282 rd, accessible method for the fabrication of micropores with diameters from 2 to 800 micro m in films
283 simulate red cell motion through cylindrical micropores with diameters of 3.6, 5, and 6.3 microns, an
284       PIMs contain interconnected regions of micropores with high gas permeability but with a level o
285 d nitrogen-doped active carbons exhibit rich micropores with high surface area and high nitrogen cont
286 d polymeric backbones, resulting in membrane micropores with multimodal pore size distributions.
287 e majority of conventional MOFs possess only micropores with very limited accessibility to substances
288 (-1)) that arise almost entirely (>90%) from micropores, with an oxygen-rich nature.
289      Two binding energies are present in the micropores, with the lower, more dominant one being on t
290 oporosity maps show the spatial variation of micropores within a sample and offers insights into the
291 he lack of site intimacy and the presence of micropores within conventional catalysts create challeng
292 he thin inorganic barriers of interconnected micropores within deep-sea vents.
293                     The induction of ordered micropores within the disordered 3D architecture synergi
294 aker ionic interactions are allowed to enter micropores without sacrificing the power density.

 
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