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1 fall between traditional small molecules and large molecules).
2 formational, discontinuous epitope on a very large molecule.
3 nic transitions from a specific nucleus in a large molecule.
4 ltered, and the nucleus becomes permeable to large molecules.
5 that require fast mass transfer or deal with large molecules.
6 accessible to small apatite crystals but not large molecules.
7 s for the separation of small molecules from large molecules.
8 escribed for calculating the total energy of large molecules.
9 gulates the inward permeability of P2X7Rs to large molecules.
10 litate rather than hinder diffusion even for large molecules.
11 arily regulates the outward P2X7R current of large molecules.
12 he transdermal delivery of several small and large molecules.
13 raction speed and in their inability to load large molecules.
14 ydrophobicity of protein molecules and other large molecules.
15 used to enhance the ionization efficiency of large molecules.
16 sistance and increased flux of small but not large molecules.
17 nsitivity and signal stability for small and large molecules.
18 rophoresis and has comparable resolution for large molecules.
19 pulmonary microvascular barrier function to large molecules.
20 catalysis and adsorption processes involving large molecules.
21 molar mass determinations for both small and large molecules.
22 ates and are inherently multidimensional for large molecules.
23 viate these issues but are too expensive for large molecules.
24 e of following proton transfer (PT) in these large molecules.
25 rties in between that enable the building of large molecules.
26 hat hinder desorption/ionization by trapping large molecules.
27 e to a membrane pore allowing the passage of large molecules.
28 pletion increased epithelial permeability to large molecules.
29 e selective uptake or exclusion of small and large molecules.
30 fers from limited selectivity when analyzing large molecules.
31 is explanation seems to be true for cationic large molecules.
32 tent of cytoplasmic membrane permeability to large molecules.
33 the permeabilization of the cell membrane to large molecules.
34 terms of speed and memory, particularly for large molecules.
35 al ergodicity breaking in an unprecedentedly large molecule, (12)C(60), determined from its icosahedr
36 ne accessibility mutagenesis, the relatively large molecule [2-(trimethylammonium)] methanethiosulfon
37 us multicomponent analysis of both small and large molecules across a wide polarity range in single e
38 Vesicular transport enables the export of large molecules across the cell wall, and vesicles conta
39 t of fluid, solutes, hormones, and small and large molecules across the microvascular endothelium.
40 ifferences control the movement of fluid and large molecules across the microvascular wall of normal
43 rstanding of the dissociation mechanisms for large molecules adsorbed on surfaces is still a challeng
45 the brain parenchyma, and of both small and large molecule agents into the perivascular space from t
46 reated kidney value) clearance of small- and large-molecule agents and the urine flow rates that resu
47 o a constantly changing mixture of small and large molecules, along with an abundance of bacteria, vi
48 nanowires, nanotubes, nanoribbons, or other large molecules; among these complex materials, networks
50 urpose-built for targeted delivery of modern large molecule and temperature-sensitive therapeutics to
51 ine various biophysical characteristics of a large molecule and the biomechanical properties of human
52 ave a 6-fold higher sensitivity in detecting large molecules and a 33% improvement in detecting small
53 ons as a selectivity filter for transport of large molecules and a sieve-like filter for diffusion of
55 neurofilaments was detected by exclusion of large molecules and by direct force measurements with at
59 lenging target given its innate exclusion of large molecules and its defenses against bacterial invas
61 escriptions of mobility within structures of large molecules and membranes as well as in free space.
63 solution-phase approach to the formation of large molecules and nanostructures by coupling reactions
65 in the domain of inception that lies between large molecules and soot particles, we provide a new mec
66 water, the controlled covalent synthesis of large molecules and structures in vivo has remained chal
68 ol levels, capability of analyzing small and large molecules, and good spatial resolution (250 mum).
70 ll-cell channels are permeable to relatively large molecules, and it was thought that opening of hemi
71 t, permeable TJs become first restrictive to large molecules, and only later to small molecules, with
72 These NPs themselves can be considered as large molecules, and thus, applying a wet-chemical depro
73 key role in terminating the burst release of large molecules, and to provide a means for novel aqueou
74 ruggability (ligandability), suitability for large-molecule approaches (e.g. antibodies) or new modal
75 has revolutionized the manner by which many large molecules are characterized, the highly variable a
76 cromolecules, spurring investigations of how large molecules are distributed within the crystals with
80 ethod is especially superior for cases where large molecules are sedimented at faster rotor speeds, d
83 erred between coupled heteronuclear spins in large molecules at high magnetic fields in the presence
84 s describe vibrational dephasing dynamics in large molecules at intermediate times because of the loc
85 ation and dissociation of bonds between very large molecules at rates that change considerably under
88 is directly linked to permeation of ions and large molecules (ATP and fluorescent dyes) and occurs du
89 demonstrate a novel separation mechanism for large molecules based on their radial migration in capil
91 te is to selectively restrict the passage of large molecules between cells while allowing electrical
94 demand to allow adsorption and processing of large molecules but challenge our synthetic ability.
95 digests tissue HA and facilitates spread of large molecules but is not sufficient to cause subcutane
96 of P2X7R outward and inward permeability to large molecules by Cl-(o) and Na+(o), respectively, may
98 a of the slowly diffusing species (generally large molecules) by diffusion editing, the slowly relaxi
103 ules to traverse by passive diffusion, while large molecules can only translocate with the help of nu
104 on protein and shown that, in resting cells, large molecules can rapidly diffuse across the cell with
105 mers) because the degradation mechanisms for large molecules can result in hundreds of thousands to e
107 method for transporting colloidal particles, large molecules, cells, and other materials across surfa
108 ant polymer is beta-(1,6)-glucans, which are large molecules composed of a linear beta-(1,6)-glucan c
112 esolution mass spectrometry revealed several large-molecule DBPs, including chloroanilines, (chloro)h
114 duction potential of a factor of up to 5 for large molecules (dextran) under unretained conditions.
116 he first-time, buccal delivery of dry coated large molecule drug, vancomycin, through controlled depo
117 ped as new drugs for the brain because these large molecule drugs do not cross the brain capillary wa
119 filters are advantageous for the analysis of large molecules due to the ability to perform ion isolat
120 e made it possible to quantify expression of large molecules during embryogenesis, little information
121 preventing waste of expensive biologics and large molecules during proof-of-concept and pre-clinical
122 fter radiosynoviorthesis or extravasation of large molecules (e.g., [(90)Y]Y-ibritumomab tiuxetan).
123 rt decreases with increasing molecular size, large molecules (e.g., albumin) are nevertheless removed
124 between the separated channels but prevents large molecules, e.g., DNA, from traversing the membrane
125 ergence of new data, it became apparent that large molecules enter the cell directly through the pore
126 without template replication or assembly of large molecules; exhibits selection both without and wit
127 type G protein-coupled receptors (aGPCRs), a large molecule family with over 30 members in humans, op
129 2 diabetes mellitus, exclusively focusing on large-molecule formats (notably enteroendocrine peptides
130 me the highly charged, barrier-like layer of large molecules forming a target cell's glycocalyx.
133 ding of fluorescein-labeled Ficoll and other large molecules from the SE/CC complex showed an irregul
135 ' cage, making their replacement by a single large molecule (here adamantane or ferrocene) entropical
137 opportunities for probing atomic motion in a large molecule in a typical pump-probe measurement.
139 ble biochemical monitoring of both small and large molecules in a variety of body fluids, such as swe
142 we can detect interactions between small and large molecules in human blood serum and quantify the si
144 zation of adhered brain endothelial cells to large molecules in response to applied pulsed electric f
145 s a new approach for ionizing both small and large molecules in solids or liquid solvents with high s
148 eening method for examining the diffusion of large molecules in tissues, and for studying the effects
151 picomolar range were obtained for small- and large-molecule interactions in both synthetic and cell-d
155 Mechanistically, we found that the uptake of large molecules is a receptor-independent, fluid-phase p
156 ctrometry (CDMS) for measuring the masses of large molecules, macromolecular complexes, and synthetic
157 s found in nonribosomal peptide synthetases, large molecule mass spectrometry is shown to be a new, u
158 e studies indicate that intranasally applied large molecules may enter the brain and cerebrospinal fl
159 d current and an increase in permeability to large molecules, mediated by the opening of pannexin-1 h
161 ike studies of the structure and dynamics of large molecules, multispecies trace gas detection and is
162 cell-to-cell communication, via transfer of large molecules, occurs between the cell bodies of injur
163 compact form that allows comparatively very large molecules of DNA to fit inside the cell's nucleus.
164 nt investigations in animal models show that large molecules of neurotherapeutic potential can be con
165 assignments to individual nuclei, which for large molecules often can only be obtained by tedious po
169 ever, it has long been deemed infeasible for large molecules-particularly polymers, proteins and pept
170 but controversy persists as to whether such large molecules pass directly through the open ion chann
172 uced barrier loss by limiting both small and large molecule permeability but did not affect myosin li
175 e, there has been no direct demonstration of large molecule permeation via the Panx1 channel itself,
176 fields where the targets of the analyses are large molecules present in a matrix that would otherwise
177 trometry (HRMS) based approach for analyzing large-molecule proteins at the intact level in biologica
179 drug development of either small molecule or large molecule (recombinant proteins, gene medicines) ne
180 e intermediate states), and that crowding by large molecules reduces noise more efficiently than crow
181 However, they are highly hydrophobic and large molecules, regarded as difficult targets for in vi
184 strate enhanced paracellular permeability to large molecules, revealing a potential role of JAM-A in
187 These simulation results suggest that even large molecule solutes would be more easily cleared from
188 e signals generated by shape fluctuations of large molecules studied by feedback tracking microscopy.
190 hannels can be a release site for relatively large molecules such as ATP and glutamate, which can ser
191 model predicts the topological seclusion of large molecules such as CD43 from the site of closest co
192 sible dehydrogenation and rehydrogenation of large molecules such as cyclohexane and methylcyclohexan
193 first report of a method for introduction of large molecules such as DNA into amphioxus embryos, open
195 ely 12 angstroms) raises questions as to how large molecules such as LF and EF can move through the p
197 P2X7 receptor (P2X7R) expands to accommodate large molecules such as N-methyl-D-glucamine (NMDG+).
199 often intractable on classical computers for large molecules such as proteins and for protocols such
201 ges and slow sensor responses when detecting large molecules such as proteins and nucleic acids.
202 However, it is also common to observe that large molecules such as proteins and polymers often prod
203 ution, the determination of the structure of large molecules such as proteins, which is one of the mo
205 rgets, from rare atoms and molecules to very large molecules, such as a proteins, protein complexes,
210 ssential technique to characterize small and large molecules, such as organic compounds, metabolites,
211 l units, such as small molecular ligands, or large molecules, such as proteins, can be positioned wit
212 of cancer immunotherapeutic approaches using large molecules, such as T cell bispecific Abs (TCBs).
214 previously been used to select aptamers for large-molecule targets such as proteins, lipopolysacchar
216 edly enhanced tight junction permeability to large molecules that could be modeled by size-selective
218 een the initiator-coated pore structures and large molecules that hinder desorption/ionization by tra
219 Glycoproteins are biologically significant large molecules that participate in numerous cellular ac
220 mage(2), but it is unclear whether there are large molecules that regulate the integrity of the plasm
223 d BBB-targeted procedure for the delivery of large-molecule therapeutic agents to treat neurological
227 al for positive interplay between small- and large-molecule therapeutics against HIV entry, which may
228 osis is an attractive pathway for delivering large-molecule therapeutics to the central nervous syste
229 are a possible way out: they scale well for large molecules, they can be parallelized and their accu
232 hat pressure changes impact the retention of large molecules to a much greater degree than small mole
235 B) presents a major challenge for delivering large molecules to study and treat the central nervous s
237 uires modification for protein secretion and large-molecule transport as well as for bacterial growth
238 s requires conjugation of the PNA to another large molecule, typically a cell-penetrating peptide or
239 re complexes (NPCs), which act a barriers to large molecules unless they are escorted by specific LCD
242 Similar conductances that are permeable to large molecules were activated by extreme hyperpolarizat
244 spectra remains challenging, especially for large molecules, where the monoisotopic peak is often un
245 face speeding up the gas-phase conversion of large molecules while lessening possible memory effects.
247 of the human PKD1 gene, polycystin, shows a large molecule with a unique arrangement of extracellula
248 flagellate-derived polyketides are typically large molecules with complex structures, potent bioactiv
250 all molecules from salivary mucins and other large molecules with only a 29% reduction of signal comp
251 enables rapid vapor pressure measurements on large molecules with state-of-the-art measurement uncert
252 bling adsorption, activation and reaction of large molecules with sufficient versatility to drive abs
253 rules for renal filtration, given that these large molecules (with aspect ratios ranging from 100:1 t