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1 alcohol oxidation reactions performed in the liquid phase.
2 preimposed ion-concentration gradient in the liquid phase.
3 log reduction after 72 h), especially in the liquid phase.
4 or to the ice phase, without an intermediate liquid phase.
5 ly in the aerosol phase, further than in the liquid phase.
6 and remains disordered in the densely packed liquid phase.
7 ogenation of 1-hexene at 25 degrees C in the liquid phase.
8 rgies for solute or solvent molecules in the liquid phase.
9 echanism which proceeds through a metastable liquid phase.
10 w-cost and accurate detection of analytes in liquid phase.
11 re of 2.5 to 3.5 kilobar in the high-density liquid phase.
12  range of analyte types, in both the gas and liquid phases.
13 s between dilute liquid phases and condensed liquid phases.
14 itions where they exhibit coexistence of two liquid phases.
15 ults in the formation of a particle with two liquid phases.
16  facilitating CO(2) transfer in both gas and liquid phases.
17 transition between the molecular and network liquid phases.
18 nal energy transfer between molecules in the liquid phase, a difficult process hampered by weak inter
19 escriptions of toxin-MOF interactions, while liquid-phase adsorption isotherms readily allow for the
20 RNPA1, can assemble into both a polydisperse liquid phase and an ordered solid phase of amyloid fibri
21 -gfp) within an E. coli host (EcoFJ1) in the liquid phase and biofilms in bioreactors.
22  thermal energy in their metastable Z isomer liquid phase and release the energy by optically trigger
23 y driven separation techniques, the first in liquid phase and the second in gas phase, with a label-f
24 ind that oxygen vacancies stabilise the spin liquid phase and the stuffing of Ti sites by Yb suppress
25 ess that partitions molecules between dilute liquid phases and condensed liquid phases.
26  a variety of structures that are soluble in liquid phases and therefore amenable to homogeneous cata
27 A damage was previously shown to alter FUS's liquid-phase and solid-phase transitions in cell models
28 rate constants, and VTST in the solid phase, liquid phase, and enzymes.
29 ed on these rigid features, for both gas and liquid phase applications.
30 Q-rich sequence of FUS LC that stabilize the liquid phase are not known in detail.
31                In particular, two immiscible liquid phases are identified in bioadhesive fluid extrac
32 -dependence of the viscosity of the evolving liquid phase, as well as the distribution and longevity
33           These species remain stable in the liquid phase at room temperature but convert to gels upo
34                The precise mechanism for the liquid-phase autoxidation of anthrahydroquinone (AnH(2)Q
35 er and Pt foil as the working electrode in a liquid-phase auxiliary cell.
36 rmodynamic capillary condensation of a vapor-liquid phase between parallel plates, suggesting they co
37 een drawn to understand the role of water in liquid phase biomass conversions as well as the hydrothe
38 P) using virus neutralization test (VNT) and liquid-phase blocking ELISA (LPBE) is the standard proce
39  on the rates for crystal growth relative to liquid phase Ca diffusivity (R/D).
40  requires a structural reorganization of the liquid phase, called stress-driven ageing.
41 llenge in developing efficient and selective liquid phase catalytic processes, as predictive understa
42 les and catalytic reactions occurring in the liquid phase, catalyzed by either colloidal or supported
43 nstruction, taking advantage of the solid-to-liquid phase change of the metal at body temperature and
44 al-organic compounds as a new class of solid-liquid phase-change materials (PCMs) for thermal energy
45 k average decrease in the amount of water in liquid-phase clouds compared with unpolluted clouds.
46    An increase in the amount of water inside liquid-phase clouds induced by aerosols, through the sup
47    We further elucidate that DAXX drives p62 liquid phase condensation by inducing p62 oligomerisatio
48  and conformational fluctuations can promote liquid phase condensation of a pH-responsive, intrinsica
49  this basic site-C cGAS interface disrupting liquid-phase condensation, as monitored by cGAMP formati
50 nzymatic activity as a result of DNA-induced liquid-phase condensation.
51 -phase aggregation, while minimally altering liquid-phase condensation.
52                Co-assembly of gel phases and liquid phases confers local stability and long-range dyn
53                      We propose that a dense liquid phase (containing 4-7 H2O per CaCO3 unit) forms i
54 queous or solvent fraction of the bioreactor liquid phase (depending on the derivative and medium use
55 useful technological tool for the control of liquid phase deposition of 2D materials.
56 ed heterochromatin protein 1alpha (HP1alpha) liquid-phase disruptions, decreases in HP1alpha expressi
57   In this work, we present the first one-pot liquid-phase DNA synthesis technique which allows the ad
58 ssolution of the gel and the appearance of a liquid phase driven by weaker DAXX-DAXX interactions.
59 with hnRNPA2 yet partition specifically into liquid phase droplets with the low complexity domain (LC
60                                        Here, Liquid Phase Electron Microscopy (LPEM) captures the int
61                               Innovations in liquid-phase electron microscopy (LP-EM) have made it po
62 us feedstock solutions using electrochemical liquid phase epitaxy (ec-LPE) at low temperatures (T </=
63 OF crystallites onto substrates via stepwise liquid-phase epitaxy.
64                                              Liquid phase exfoliation and size selection were success
65 g the high yield sonication-assisted aqueous liquid phase exfoliation of size-selected nanomaterials.
66 g atomic sheets of borophene through a novel liquid-phase exfoliation and the reduction of borophene
67 synthesis of these nanomaterials, such as in liquid-phase exfoliation.
68 amorphous nanoclusters within the metal-rich liquid phase, followed by crystallization of these amorp
69 ave been reported to condensate into a dense liquid phase, forming a reversible droplet state.
70        Phase separation creates two distinct liquid phases from a single mixed liquid phase, like oil
71 with key advantages over strategies based on liquid phase (fusion) sintering that requires both oxide
72                   Transit through the carbon liquid phase has significant consequences for the subseq
73 0 nm gold particles supported on silica with liquid-phase hydrogen and deuterium peroxides at multipl
74 ve nanoreactors, void-confinement effects in liquid-phase hydrogenation are investigated in a two-cha
75  high activity and excellent selectivity for liquid-phase hydrogenation of substituted nitroaromatics
76 ce, locking in non-equilibrium shapes of one liquid phase in another.
77  have shown that nucleation occurs through a liquid phase in porous particles with narrow cracks or s
78             Our results indicate a non-Fermi liquid phase in the global phase diagram of heavy fermio
79                 The mechanisms that localize liquid phases in cells, however, are not fully understoo
80                                A vapor/vapor-liquid phase is observed at hydrophobic and hydrophilic
81 served and chemical exchange between gas and liquid phases is shown to play an important role on the
82 econd paragraph, which starts "Consequently, liquid-phase iterative synthetic methods...", and in the
83 emperature range, the binary mixture forms a liquid phase (Lalpha) and a coexistence of Lalpha and ei
84 o distinct liquid phases from a single mixed liquid phase, like oil droplets separating from water.
85 oach to produce ultrapure H(2) and O(2) from liquid-phase Martian regolithic brine at ~-36 degrees C.
86 rates embody a new class of high-temperature liquid-phase materials for carbon dioxide capture and we
87 ttachment kinetics of atomic clusters in the liquid phase, melting is instead barrier-less and limite
88 with the ease of downstream manipulation via liquid-phase methods-should enable the search for predic
89 rectly synthesized via bottom-up vapour- and liquid-phase methods.
90 carried out with deep eutectic solvent based liquid phase microextraction (DES-LPME) for trace determ
91 ncentration with deep eutectic solvent-based liquid phase microextraction (DES-LPME).
92                                              Liquid phase microextraction (LPME) was performed with a
93 form that accommodates electric-field-driven liquid phase microextraction (mu-EME) in a fully automat
94                   A switchable solvent based liquid phase microextraction (SS-LPME) has been proposed
95              QuEChERS and switchable solvent liquid phase microextraction (SS-LPME) were respectively
96 vortex-assisted supramolecular solvent-based liquid phase microextraction (VA-SUPRAS-LPME) prior to s
97 thiocarbamate) with a supramolecular solvent liquid phase microextraction method.
98 concept for at-line coupling of hollow fiber liquid-phase microextraction (HF-LPME) to commercial cap
99 ample preparation step involved membrane bag liquid-phase microextraction in which a synergistic mixt
100 d and successfully applied in the dispersive liquid-phase microextraction of seven representative pol
101 rokinetic concentration, we report one-step, liquid-phase NA purification that is simpler and faster
102                              An intermediate liquid phase-Na(2)Mo(2)O(7) is formed through a eutectic
103                                         Most liquid-phase nucleation processes are heterogeneous, occ
104 composition into solute-rich and solute-poor liquid phases, nucleation of amorphous nanoclusters with
105                        Here we demonstrate a liquid phase of actin filaments in the presence of the p
106 ormation about methanol concentration in the liquid phase of microbial cultures through headspace gas
107       These data reveal that a developmental liquid phase of scaffold molecules is essential for the
108 mals at the bottom of well plates, casting a liquid-phase of Pluronic on top that solidifies via a mo
109 tained material was tested for gas phase and liquid phase olefin metathesis and exhibited higher cata
110                                              Liquid-phase oligonucleotide synthesis (LPOS) uses solub
111  lipid mixtures we find that MBP forms dense liquid phases on top of the lipid membranes mediating at
112                  The formation of immiscible liquid phases or coacervates is a phenomenon widely obse
113 production process that requires homogeneous liquid-phase organometallic catalysts with corrosive hal
114 nia in the gas-phase are observed, as is the liquid-phase photoelectron angular anisotropy.
115 hase synthesis; it does not, and is a purely liquid-phase process.
116  gradients of E(h), pH, and temperature, and liquid-phase products would be able to diffuse to other
117 ectrolyte, solid catalyst, and gas-phase and liquid-phase reactants and products.
118  nanoparticles using different gas phase and liquid phase reactions.
119 inetics of multiple parallel and consecutive liquid-phase reactions.
120  vitro, we reconstitute the SYD-2 and ELKS-1 liquid-phase scaffold, and find that it is competent to
121             Correlative light microscopy and liquid-phase scanning transmission electron microscopy (
122 tes between the three isomers of xylene with liquid-phase selectivity in the order p-xylene >> m-xyle
123 echanical shear once present in their liquid-liquid phase separated form.
124 hich serve as models of charge-driven liquid-liquid phase separated systems.
125 he Escherichia coli SSB protein forms liquid-liquid phase-separated condensates in cellular-like cond
126 granules are biomolecular condensates-liquid-liquid phase-separated droplets that organize and manage
127 roceed through a dynamically arrested liquid-liquid phase-separated intermediate.
128 n protein 1alpha (HP1alpha) undergoes liquid-liquid phase separation (LLPS) and forms liquid droplets
129  Here, we asked whether PrP undergoes liquid-liquid phase separation (LLPS) and if this process is mo
130  activities, the CPC also can undergo liquid-liquid phase separation (LLPS) and proposed that the inn
131 that PcG condensates assemble through liquid-liquid phase separation (LLPS) and suggest that phase-se
132 2 (SARS-CoV-2) condenses with RNA via liquid-liquid phase separation (LLPS) and that N protein can be
133 re, we show that SGs assemble through liquid-liquid phase separation (LLPS) arising from interactions
134 tein kinase (PKA), RIalpha, undergoes liquid-liquid phase separation (LLPS) as a function of cAMP sig
135                     Here, we identify liquid-liquid phase separation (LLPS) as a mechanism for organi
136   Marine organisms, for instance, use liquid-liquid phase separation (LLPS) as the precursor phase to
137             Here, we uncover a common liquid-liquid phase separation (LLPS) behavior shared by these
138 cently, tau has been shown to undergo liquid liquid phase separation (LLPS) both in vivo and in vitro
139 rging) wetting layer when approaching liquid-liquid phase separation (LLPS) by changing protein conce
140                                       Liquid-liquid phase separation (LLPS) compartmentalizes transcr
141 e PEG400/Na(2)SO(4)/Water system near Liquid-Liquid Phase Separation (LLPS) conditions by both sittin
142 ecular condensate, whose formation by liquid-liquid phase separation (LLPS) facilitates the initial s
143                                       Liquid-liquid phase separation (LLPS) has been recognized as on
144 orm membraneless compartments through liquid-liquid phase separation (LLPS) has challenged long-stand
145   Prion-like domains (PLDs) can drive liquid-liquid phase separation (LLPS) in cells.
146 romatin undergoes histone tail-driven liquid-liquid phase separation (LLPS) in physiologic salt and w
147 red region (IDR) that facilitates its liquid-liquid phase separation (LLPS) in the nucleolus.
148 er, increase of NEAT1 promotes TDP-43 liquid-liquid phase separation (LLPS) in vitro.
149 and Axin interacting sites, undergoes liquid-liquid phase separation (LLPS) in vitro.
150                                       Liquid-liquid phase separation (LLPS) is involved in the format
151                                       Liquid-liquid phase separation (LLPS) is one proposed mechanism
152                         The idea that liquid-liquid phase separation (LLPS) may be a general mechanis
153                                       Liquid-liquid phase separation (LLPS) mediates formation of mem
154                                       Liquid-liquid phase separation (LLPS) occurs following amorphou
155                         Proteinaceous liquid-liquid phase separation (LLPS) occurs when a polypeptide
156 ere has been a jarring awakening that liquid-liquid phase separation (LLPS) of key protein and nuclei
157 rresponding to the droplet phase upon liquid-liquid phase separation (LLPS) of protein or protein-RNA
158 inning of biomolecular condensates is liquid-liquid phase separation (LLPS) of proteins and nucleic a
159                                       Liquid-liquid phase separation (LLPS) of proteins and nucleic a
160                                       Liquid-liquid phase separation (LLPS) of proteins into concentr
161                                       Liquid-liquid phase separation (LLPS) of proteins that leads to
162                                       Liquid-liquid phase separation (LLPS) of proteins underlies the
163 biomolecular condensates underlain by liquid-liquid phase separation (LLPS) of proteins, we conducted
164                                       Liquid-liquid phase separation (LLPS) of RNA-binding proteins p
165                                       Liquid-liquid phase separation (LLPS) of RNA-protein complexes
166           The mechanism that leads to liquid-liquid phase separation (LLPS) of the tau protein, whose
167                              Cellular liquid-liquid phase separation (LLPS) plays a key role in the d
168  recent study, Yasuda et al. show how liquid-liquid phase separation (LLPS) under hyperosmotic stress
169          It's widely appreciated that liquid-liquid phase separation (LLPS) underlies the formation o
170         Evidence is now mounting that liquid-liquid phase separation (LLPS) underlies the formation o
171 . melanogaster unexpectedly undergoes liquid-liquid phase separation (LLPS) upon binding DNA in vitro
172 ocapsid protein (N-protein) undergoes liquid-liquid phase separation (LLPS) with viral RNA.
173 -43 at its endogenous level undergoes liquid-liquid phase separation (LLPS) within nuclei in multiple
174 nelles, or condensates, that form via liquid-liquid phase separation (LLPS)(1,2).
175 tion is the macroscopic completion of liquid-liquid phase separation (LLPS), a process by which aqueo
176 triggers inclusion body formation via liquid-liquid phase separation (LLPS), a process underlying the
177 artments that are proposed to form by liquid-liquid phase separation (LLPS), a thermodynamic process
178 binding protein FUS (FUS LC) mediates liquid-liquid phase separation (LLPS), but the interactions bet
179              Biomolecules can undergo liquid-liquid phase separation (LLPS), forming dense droplets t
180 e of crowding agents, tau can undergo liquid-liquid phase separation (LLPS), forming highly dynamic l
181 nt reports that tau readily undergoes liquid-liquid phase separation (LLPS), here we explored the rel
182 membraneless organelles assembled via liquid-liquid phase separation (LLPS), known as condensates, al
183 at although they are likely formed by liquid-liquid phase separation (LLPS), they have a differential
184             RNA granules form through liquid-liquid phase separation (LLPS), whereby weak promiscuous
185 at human IAPP undergoes AWI-catalyzed liquid-liquid phase separation (LLPS), which initiates hydrogel
186 ganic/inorganic system that undergoes liquid-liquid phase separation (LLPS).
187 cellular material in a process termed liquid-liquid phase separation (LLPS).
188 h multivalent interactions that drive liquid-liquid phase separation (LLPS).
189 also has a high propensity to undergo liquid-liquid phase separation (LLPS).
190 isorders, has a propensity to undergo liquid-liquid phase separation (LLPS).
191 n of biomolecular condensates through liquid-liquid phase separation (LLPS).
192 inding proteins (RBPs), which undergo liquid-liquid phase separation (LLPS).
193 A-binding proteins and are formed via liquid-liquid phase separation (LLPS).
194      Tau protein in vitro can undergo liquid-liquid phase separation (LLPS); however, observations of
195                      The link between liquid-liquid phase separation and actin nucleation in the form
196 asmic mRNP granules that assemble via liquid-liquid phase separation and are implicated in the decay
197 re properties of systems that undergo liquid-liquid phase separation and could be investigated in thi
198          Moreover, we analyzed TDP-43 liquid-liquid phase separation and detected similar detergent-r
199                             Reentrant liquid-liquid phase separation can occur when the condensation
200 ia a two-step process involving first liquid-liquid phase separation followed by polymer microphase s
201                            Biological liquid-liquid phase separation has gained considerable attentio
202 tive disease, are also implicated in driving liquid phase separation has galvanized significant inter
203 proteins and nucleic acids to undergo liquid-liquid phase separation has recently emerged as an impor
204 ultivalent interactions necessary for liquid-liquid phase separation have been extensively studied in
205  Coacervate microdroplets produced by liquid-liquid phase separation have been used as synthetic prot
206 n, theory has been developed to model liquid-liquid phase separation in bulk systems.
207          Appreciation for the role of liquid-liquid phase separation in the functional organization o
208                      TIAR-2 undergoes liquid-liquid phase separation in vitro and forms granules with
209 ins-YTHDF1, YTHDF2 and YTHDF3-undergo liquid-liquid phase separation in vitro and in cells.
210 odulate TDP-43 CTD aggregation and/or liquid-liquid phase separation in vitro GRN-3 promoted insolubl
211                    Here, we show that liquid-liquid phase separation into solute-rich and solute-poor
212                                              Liquid phase separation into two or more coexisting phas
213                                       Liquid-liquid phase separation is emerging as the universal mec
214 ation of membrane-less organelles via liquid-liquid phase separation is one way cells meet the biolog
215 her tauopathies, was found to undergo liquid-liquid phase separation making it one of several protein
216          Specifically, we analyze the liquid-liquid phase separation of an in vitro model of cellular
217 mbrane-less organelles resulting from liquid-liquid phase separation of biopolymers into intracellula
218 and provides a scaffold that supports liquid-liquid phase separation of chromatin binding proteins.
219 microfluidic device that triggered liquid-to-liquid phase separation of FG-Nups, which yielded drople
220 nt phase, a process implicated in the liquid-liquid phase separation of intrinsically disordered prot
221                                       Liquid-liquid phase separation of intrinsically disordered prot
222  minimal model to study the effects of pH on liquid phase separation of macromolecules.
223                                       Liquid-liquid phase separation of multivalent intrinsically dis
224    Biomolecular condensates formed by liquid-liquid phase separation of proteins and nucleic acids ha
225 centration-dependent condensation and liquid-liquid phase separation of soluble proteins.
226                                       Liquid-liquid phase separation of tau protein has been implicat
227 zation might result from a process of liquid-liquid phase separation orchestrated by the epigenetic m
228                                       Liquid-liquid phase separation plays an important role in a var
229                                       Liquid-liquid phase separation plays an important role in cellu
230  m(6)A-modified mRNAs are governed by liquid-liquid phase separation principles.
231 in motor affect the efficiency of the liquid-liquid phase separation process.
232 n undergo a phase transition in which liquid-liquid phase separation results in the formation of a pa
233  (RNPs) form mesoscale condensates by liquid-liquid phase separation that play essential roles in sub
234 e we identify an in vivo regulator of liquid-liquid phase separation through a genetic screen targeti
235 TAZ forms nuclear condensates through liquid-liquid phase separation to compartmentalize its DNA-bind
236 tment domains, and that can engage in liquid-liquid phase separation to form subnuclear bodies, as we
237   This review summarizes recent work linking liquid phase separation to neurodegeneration, highlighti
238 tic theory of protein aggregation and liquid-liquid phase separation to study the spatial control of
239  zone proteins RIM and RIM-BP undergo liquid-liquid phase separation to tether Ca(2+) channels.
240 oprofen (KTP)-rich phase generated by liquid-liquid phase separation was evaluated.
241        SynGAP-alpha1, which undergoes liquid-liquid phase separation with PSD-95, is highly enriched
242 rganelles or condensates form through liquid-liquid phase separation(1-4), which is thought to underl
243                     Here we implicate liquid-liquid phase separation(3) as the underlying mechanism.
244  membraneless organelles form through liquid-liquid phase separation, but how their size is controlle
245      We suggest that consideration of liquid-liquid phase separation, leading to complete or partial
246 Formed from proteins and RNAs through liquid-liquid phase separation, membraneless organelles (MLOs)
247 ion of hnRNPA1 that synchronizes with liquid-liquid phase separation, regulates the fluidity and mobi
248 elow the saturation concentration for liquid-liquid phase separation, so they can compete subunits aw
249 indicate that the physical process of liquid-liquid phase separation, together with surface effects,
250 olecular condensates can be driven by liquid-liquid phase separation, which arises from weak, multiva
251 that coiled-coil proteins can promote liquid-liquid phase separation, which expands our understanding
252  that filaggrin assembles KGs through liquid-liquid phase separation.
253 to drive heterochromatin formation by liquid-liquid phase separation.
254 tion of how many proteins can undergo liquid-liquid phase separation.
255 nelles that assemble by intracellular liquid-liquid phase separation.
256 aterial properties of proteins assembled via liquid phase separation.
257 re formed from processes that include liquid-liquid phase separation.
258 ring YAP reprogramming is mediated by liquid-liquid phase separation.
259  membraneless domains, reminiscent of liquid-liquid phase separation.
260  structures form through a process of liquid-liquid phase separation.
261 Clustering is also a prerequisite for liquid-liquid phase separation.
262 rmation of biological condensates via liquid-liquid phase separation.
263 omponent condensates that assemble by liquid-liquid phase separation.
264 n-protein interactions analogous to a liquid-liquid phase separation.
265 f the TDP-43 CTD while GRN-5 mediated liquid-liquid phase separation.
266 enucleation species (PNS) that precede solid-liquid phase separation.
267 ies, which in some cases form through liquid-liquid phase separation.
268 osome remodeler Brg1 and FUS-assisted liquid-liquid phase separation.
269 wcomers covering proteins involved in liquid-liquid phase separation.
270 an RNA-binding protein in the case of liquid-liquid phase separation.
271 such as 53BP1, into foci that exhibit liquid-liquid phase-separation condensate properties.
272         Polysulfide intermediates (PSs), the liquid-phase species of active materials in lithium-sulf
273 bility of Z isomers at high temperatures and liquid-phase stability at temperatures below 0 degrees C
274  viscous, semisolid phase state at night and liquid phase state with phase separation during the day.
275  differentiation of the solid, semisolid and liquid phase states of individual particles without prio
276                 We observed that cytoplasmic liquid-phase structures contain FUS phosphorylated at no
277 e chromatographic purification and solid- or liquid-phase supports enabled synthesis of sequence-defi
278 w-electron dense entities from their similar liquid-phase surroundings presents signal-to-noise ratio
279  synthetic polymers through a combination of liquid-phase synthesis and selective molecular sieving.
280 rison between growth pathways in vapour- and liquid-phase synthesis techniques.
281   Nucleation underlies the formation of many liquid-phase synthetic and natural materials with applic
282 que insights into reaction mechanisms in the liquid phase that involve changes of the oxidation state
283 erivatives exhibiting coherent melting and a liquid phase that is stable over a large temperature win
284 ates with a behavior that is consistent with liquid phases that are modulated by a predicted disorder
285 IRs selectively extract cargo from condensed liquid phases thereby regulating functional phase separa
286 described that drives chemical cargo between liquid phases to generate a concentration gradient.
287  different means for triggering the solid-to-liquid phase transition are discussed.
288                            We found a liquid-liquid phase transition in the phase-change materials Ag
289 lt suggests that pressure causes a liquid-to-liquid phase transition in this metallic alloy supercool
290 y upon melting the PCM to trigger a solid-to-liquid phase transition.
291              Analogous to RNA-induced liquid-liquid phase transitions observed for other proteins imp
292 ling complexes, lead to intracellular liquid-liquid phase transitions, and seed crystallization or pa
293                                    Utilizing liquid-phase transmission electron microscopy, we map th
294 ly active Bi-Sn nano-alloys produced using a liquid-phase ultrasonication technique and investigate t
295 induced the selective crystallization of the liquid phase via Z-to-E isomerization, and the latent he
296 r Ni(2)(m-dobdc) in both the gaseous and the liquid phases via breakthrough and batch adsorption expe
297  narrow hydrophobic gate region may disfavor liquid-phase water, leading to local dewetting, which wi
298 edox reaction of the Cu(2)O nanocubes in the liquid phase were systematically studied.
299 minants and oxygen from the gas phase to the liquid phase, where pollutant biodegradation occurs.
300  over cyclohexane (20:1 for vapors, 92:1 for liquid phase), while 4 demonstrates unprecedented adsorp

 
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