ライフサイエンスコーパス: interface

1 r of syn- and anti-CH3 CHOO at the air-water interface.

2 f the lipid antigens trapped at the TCR-CD1d interface.

3 ace and the charge transfer at the SNNO/LSMO interface.

4 the research process, and the science-policy interface.

5 e captured on the substrate using a portable interface.

6 formational dynamics of the kinase-substrate interface.

7 quences can also be analyzed through the web interface.

8 ctin retrograde flow at the T-cell-substrate interface.

9 xide, an amorphous layer is generated at the interface.

10 on of the cis isomer of glyoxal at the water interface.

11 cterisation of antioxidant efficiency at the interface.

12 ssess the designability of a protein-protein interface.

13 iquid-vapor interface meets the solid-liquid interface.

14 NA scoring functions in one simple graphical interface.

15 unable stiffness gradient at the cell-matrix interface.

16 mb, available through a user-friendly online interface.

17 and by supplying nutrients at the NAPL/water interface.

18 from the droplet bulk to the droplet-vapour interface.

19 rces the user to become acquainted with each interface.

20 helial cells (EREC), grown at the air-liquid interface.

21 lt of only two mutations outside the binding interface.

22 ity are conformational epitopes at the dimer interface.

23 ons and improving its flexible visualization interface.

24 ow-affinity binding events at the QD/solvent interface.

25 cations being observed at the film-substrate interface.

26 lled through a custom-written graphical user interface.

27 sm for iron mineral formation at the protein interface.

28 bit enhanced concentrations at the air/water interface.

29 formation compromises the DNA-nuclear matrix interface.

30 e of the composition of the homodimerization interface.

31 hat are located distal to the Galpha-binding interface.

32 and analysing the properties of the protein interface.

33 ructions through an intuitive graphical user interface.

34 g delays in recruitment to the host-pathogen interface.

35 g striking conservation of their interaction interface.

36 nd formation and the nature of the resulting interface.

37 ylamide) (PNiPAm) microgels at the air/water interface.

38 ectrostatic effect at the electrode/solution interface.

39 d when the CNC-surfactants are jammed at the interface.

40 a3.1 and M72 on CaM at the KCa3.1-CaM-BD/CaM interface.

41 t most of these materials bear both types of interfaces.

42 wildlife-public health or wildlife-livestock interfaces.

43 istinct capacities to control brain-computer interfaces.

44 econfiguration of the NTD-CTD and CTD trimer interfaces.

45 cally and abiotically at natural oxic/anoxic interfaces.

46 aller micellar (curved) and planar oil-water interfaces.

47 nallyuniform chemical composition across the interfaces.

48 mparisons between different peripheral nerve interfaces.

49 ith the local strain existing at solid-solid interfaces.

50 (GO)-coated Surface Plasmon Resonance (SPR) interfaces.

51 thesis, gives enhanced electrode-electrolyte interfaces.

52 onic and catalytic properties of ceria-metal interfaces.

53 Therefore, we study two interfaces- {112}beta1/{100}Mg and {111}beta1/{110}Mg- t

54 ons greater than 15 A are at homo-oligomeric interfaces, 19% arise from family structural variation,

55 ress this, we apply the Onsager model to the interface accounting for the asymmetry.

56 hase boundary sliding at metal/intermetallic interfaces accounts for the extensive ductility observed

57 , in vitro, and in vivo analysis argues that interface add-ons are a practical and widespread evoluti

58 , growth experiments showed that the lack of interface add-ons can lead to physiologically harmful cr

59 ageous for surface functionalization, strong interface adhesion as well as boosting the interfacial c

60 epithelial cells were grown at an air-liquid interface (ALI) and subjected to light mechanical stimul

61 unction of TJs were determined in air-liquid interface (ALI) cultures of control and asthmatic primar

62 The interface allows data contributors to create a customize

63 reviously shown to bind the Nef dimerization interface also reduced Nef interactions with AP-2 and CD

64 binding by marked reorganization of subunit interface, altering the packing of beta-sheets to induce

65 the ST region, ions are blocked at the TT-ST interface and accumulated in the TT region and then can

66 t the predicted central core of the trimeric interface and are important for GP-alphaDG interaction.

67 quorum sensing, influence the water-membrane interface and are important for the bacterial attachment

68 t is derived, namely friction at the ice-bed interface and form drag, and the resistance to ice flow

69 pha2delta1 subunit at the predicted membrane interface and further suggest that preventing GPI anchor

70 complete profiling of the bio/nanomaterials interface and interaction should have profound impact on

71 with a higher adsorption capacity at the A/W interface and penetration into egg phosphatidylcholine m

72 s into an antiparallel beta-sheet at the A/W interface and presents strong intermolecular interaction

73 It has a user-friendly interface and produces graphical representations of the

74 srupts the BC-loop regions at the P450 dimer interface and results in a CYP126A1 monomeric crystal fo

75 Mutations in the hetero-tetramer interface and the active sites can abolish Pseudomonas a

76 between the charge screening at the PZT/SNNO interface and the charge transfer at the SNNO/LSMO inter

77 ses, i.e., the catalytic effect at the water interface and the differentially selective solvation, ac

78 astic concentration being the water-sediment interface and top 0.5 cm of sediments (66%).

79 ls mainly takes place at Li2 O2 /electrolyte interfaces and has obvious correspondence with the oxidi

80 the polar group next to the protein-solvent interface are difficult to compensate by interactions wi

81 The CTD dimer and CTD trimer interfaces are also intrinsically variable.

82 Convenient and intuitive data interfaces are critical for researchers to easily upload

83 Owing to the increased reaction interface area, the Janus catalyst exhibits a more than

84 Mutation of a charged residue at the interface (Arg-103) weakens the interface significantly,

85 nzee and gorilla A3C form dimers at the same interface as human A3C S188I, but through different amin

86 of 2D polymers synthesized at the air/water interface as it, in principle, allows estimation of the

87 ion by OH in the gas-phase, at the air-water interface as well as in the solid phase (dry film).

88 nts, are formed rapidly at the liquid/liquid interface, assemble into a monolayer, and, when jammed,

89 Brain-computer interface-assisted motor imagery (MI-BCI) or transcrania

90 entify in detail Gag residues and structural interfaces associated with the development of HIV-1 resi

91 ap plays a key role in stabilizing air-water interfaces at the pits between water- and gas-filled con

92 ovides insight into the platelet-endothelial interface, based on in vitro flow chamber studies and cr

93 performed with Bidirectional Brain-Computer-Interfaces (BBCI) can artificially strengthen connection

94 Brain-computer interface (BCI) controlled prosthetic arms are being dev

95 rable residence time and, using a 3D-printed interface, be directly interfaceable with LC-MS.

96 ipolaron sheet density >10(10) cm(-2) at the interface between an indium tin oxide anode and the comm

97 ing provided a valuable forum to explore the interface between developmental biology and metabolism.

98 A separate lipid bilayer formed at the interface between each droplet and the hydrogel; each bi

99 The third interface between Hda monomers occludes the active site

100 region, but in a distinct sub-pocket at the interface between helices V and VI, which may facilitate

101 are recognised to play a pivotal role at the interface between innate and acquired immunities followi

102 microstructural defects, and without obvious interface between printed layers, which overall result i

103 , structural differences are observed at the interface between protomers in the crystal structure of

104 We demonstrate a highly efficient optical interface between Si3N4 waveguides and single-quantum do

105 A lasso extension forms an interface between SUR1 and Kir6.2 adjacent to the ATP si

106 e structures reveal an unexpected tripartite interface between synaptotagmin-1 and both the SNARE com

107 ablish that small molecules that bind to the interface between TAM Ig1 domain and Gas6 Lg1 domain can

108 ne nucleus (PPN) has long been considered an interface between the basal ganglia and motor systems, a

109 astrointestinal tract represents the largest interface between the human body and the external enviro

110 a rotary injection valve, used as an online interface between the microextraction system and the det

111 The interface between the neural retina and the retinal pigm

112 nce of carbon or carbide-like species at the interface between the Ni cluster and its metal-oxide sup

113 represents a disruption of the biocompatible interface between the titanium dioxide layer of the impl

114 ified missense mutations, are located in the interface between the transmembrane domain and the C-ter

115 ic contacts and a strong charge clamp at the interface between these partners.

116 jor conformational changes to form a TM6/TM6 interface between TMDs of TAS1R2 and TAS1R3, which is co

117 e immunosuppression in tumors and act at the interface between tumor cells and host cells.

118 to investigate small numbers of bonds at the interface between two membranes.

119 rophobic cavity in the HA trimer stem at the interface between two protomers.

120 lectrostatic fields tune the ground state of interfaces between complex oxide materials.

121 e heterostructures possess a high density of interfaces between platinum-nickel and nickel sulfide co

122 he formation of homogeneous and barrier-free interfaces between the superconductor and semiconductor.

123 lled from water/hydrophobe (e.g., air/water) interfaces, both computer simulations and experiments ha

124 le of engineering an adaptive Li/electrolyte interface brings about a new and promising way to addres

125 cifically recruited to the macrophage-hyphal interface but not the macrophage-spore interface due to

126 Our aim is to bridge the science-policy interface by developing a natural capital accounting str

127 tion of Cr7C3 nanostructures at the MWCNT/Cu interface by reaction of diffused Cr atoms and amorphous

128 mon excitations at a single metal-dielectric interface can perform spatial differentiation.

129 However, we lack an understanding of how an interface can select some ligands, but not others.

130 density, grain boundary, triple junction and interface coherency affect the nucleus growth, shape and

131 influence of optical phonon coupling across interfaces comprised of different materials with varying

132 he mechanisms and allosteric sites [alpha(-)-interface containing] by which prototoxins can modulate

133 ith binding of one molecule of 11m per dimer interface, contrary to most benzothiadiazine dioxides de

134 ngiotensin I is demonstrated using the DRILL interface coupled to ESI-MS along with an improved limit

135 obal compaction of the extracellular subunit interface, coupled to an outward motion of the M2-M3 loo

136 Air-liquid interface cultures of primary nasal epithelial cells wer

137 Emergent self-induced interface currents promote active diffusion that could b

138 ent Schottky barrier height originating from interface defects between the electrodes and NbOx layer.

139 vin-Helmholtz instabilities occurring at the interface demonstrated that the biofilm flows like a vis

140 e either away from or towards the gas-liquid interface depending on their surface charge.

141 ogenous retinal detachment and vitreoretinal interface disorders, as well as potential future prophyl

142 umulation of oxygen vacancies at the Cu2O/Cu interface drives the collapse of the Cu2O lattice near t

143 yphal interface but not the macrophage-spore interface due to differences in carbohydrate antigen exp

144 of the parasitic channel formation at AlN/Si interfaces due to increased surface acceptor densities a

145 esce along the intermetallic compound/solder interface during EM testing.

146 el for control of the microtubule-actomyosin interfaces during neuronal differentiation.

147 represents a general approach to compatibly interface E-AB sensors with complex biological samples.

148 re understood on the basis of a quantitative interface energy level alignment model, which indicates

149 acid bovine whey were preserved at air water interface even after a heat treatment at 90 degrees C.

150 A comprehensive interface exchange between the TCR alpha/beta constant d

151 Reactive mineral-water interfaces exert control on the bioavailability of conta

152 helial cells (BEAS-2B) through an air-liquid interface exposure.

153 slip along the southern Hikurangi subduction interface; extensive uplift along much of the coastline;

154 he hinge center, whereas locking the SD3-SD4 interface flexibility in favor of an extended conformer

155 To correlate intraoperative interface fluid dynamics during Descemet stripping autom

156 complex, highlighting the importance of this interface for direct regulation of CLOCK:BMAL1 activity

157 acterial detection and provided a switchable interface for easy removal of bacterial cell.

158 encing and develop an open access, web-based interface for further interrogation of the data.

159 search engines and a convenient command line interface for high-performance data processing tasks.

160 A user-friendly NMR interface for the visual and accurate determination of e

161 physicochemical properties of heterogeneous interfaces for solar water splitting applications using

162 s binding fills a gap in the protein-protein interface, "freezes" one of the conformational states of

163 airment of each participant, we modified the interface gains to restore a higher level of upper body

164 Biosurfactants at the air-water interface generated by microorganisms as a result of quo

165 rmore, the erratic motion of spinners at the interface generates chaotic fluid flow reminiscent of 2D

166 The top SRO/BTO interface, grown at high PO2 (around 150 mTorr), usually

167 developed in MATLAB and has a graphical user interface (GUI) for visualization and user interaction.

168 To date, little information on the Vif-A3H interface has been available.

169 xcitons dissociate at organic donor-acceptor interfaces has been a long-standing question in the orga

170 induced Cr redistribution at the metal/oxide interfaces has drawn recent attention.

171 We present a user-friendly, graphically interfaced implementation and a quantitative analysis of

172 bserved to occur initially along the Cu2O/Cu interface in a layer-by-layer manner.

173 II heterojunction at the semiconductor-water interface in a photoelectrochemical cell (PEC) and theor

174 echanism, particularly at the sediment-water interface in many natural systems.

175 g to the alpha4:alpha4 subunit extracellular interface in nAChR potentiation.

176 ough the SH2 domain is a less common binding interface in Shc proteins, we demonstrate that it associ

177 increased surface acceptor densities at the interface in silicon.

178 and also reveals a potential oligomerization interface in the C-terminal domain as well as a conserve

179 perturbations at a specific protein-protein interface in the capsid lattice.

180 omain as well as a conserved oligomerization interface in the mVP40 N-terminal domain.

181 re and combination of metal and oxide at the interface in tuning selectivity, and identify the key de

182 e for determining intermolecular interaction interfaces in large biomolecular complexes in the solid

183 we use sPREs to characterize protein-protein interfaces in the GB1 complex with immunoglobulin G (IgG

184 Mutagenesis of the Fn2-Fn2 interface increased the basal phosphorylation of Tie2, s

185 d the latter contains important 'historical' interface information but often is overlooked.

186 rms, matching predictions from known protein interface information.

187 ults may help in understanding the origin of interface instabilities and the resulting non-uniform ph

188 -MS of selected zones, eluted via the TLC-MS Interface into MS, confirmed the identity of coumarin.

189 formation of a carboxylate ionic bond at the interface is characterized both with APXPS and in situ a

190 Importantly, we find that the HIV-1 Vif-A3H interface is distinct from the Vif-A3G and Vif-A3F inter

191 remained elusive because this abiotic-biotic interface is inaccessible to traditional structural meth

192 increase in the amount of ionic bonds at the interface is observed.

193 cular events that take place at the YAP:TEAD interface is therefore important not only to devise drug

194 Ion exchange at charged solid-liquid interfaces is central to a broad range of chemical and t

195 e of its infrastructure, such as the network interface, is the same as in the previously published R

196 , due to the transient behavior of the metal interface layer.

197 rom that observed in the bulk at defects and interfaces lead to significant compositional segregation

198 unctionalization of the monolayer/dielectric interfaces, leading to localized electronic states that

199 Here we selectively probe the interface magnetization of SrTiO3/La0.5Ca0.5MnO3/La0.7Sr

200 new spin-polarized current injection induced interface magnetoelectric (ME) effect.

201 hms, but NucliTrack's interactive, graphical interface makes it significantly more user friendly.

202 We attribute the current-induced interface ME effect to modulations of the strong double-

203 The placental interface mediates the interaction between two semiallog

204 by the contact angle where the liquid-vapor interface meets the solid-liquid interface.

205 ity of a region that combines hydrophobic-at-interface membrane-proximal external region aromatics wi

206 At the oxic/anoxic interface (OAI) of hyporheic zones subjected to redox os

207 t time to reconstruct the air-liquid crystal interface of a nematic material, namely, 4-pentyl-4'-cya

208 tropic surface tension and elasticity at the interface of beads with the liquid crystal.

209 that the dopant migration toward the alloyed interface of core/shell QDs is a thermodynamically drive

210 ility, we clearly demonstrate that CT at the interface of NCs can be tuned and promoted by metal ion

211 INO80 translocates along DNA at the H2A-H2B interface of nucleosomes and persistently displaces DNA

212 slocating along nucleosomal DNA at the H3-H4 interface of nucleosomes.

213 The web interface of pgRNAFinder contains both gRNA search and s

214 rectly weaken inhibitor binding at the dimer interface of the catalytic core domain but at the same t

215 res spanning the lipid bilayer formed at the interface of the encapsulated aqueous droplets and the e

216 ing with basal lamina (BL) attachment at the interface of the implant and the adjacent epithelium all

217 phipathic structure matches the polar/apolar interface of the lipid bilayer very well.

218 nlinearity polarization at the core-cladding interface of the PCF.

219 translocation pathway may lie at or near the interface of the protomers of a BR trimer.

220 de in solution) for the mica-nickel confined interface of total area approximately 0.03 mm(2) The ini

221 the microstructure and phases at the bonding interface of ultrasonically welded aluminum to copper jo

222 bles is proposed, and PFOS partitions to the interfaces of air bubbles with the hydro-oleophobic perf

223 ecific ion coactivation (SICA) effect at the interfaces of transient polymer solids and liquid soluti

224 Hybrid quantum networks rely on efficient interfacing of dissimilar quantum nodes, as elements bas

225 ACK region to guide an analysis of the Cdc42 interface on ACK, creating a panel of mutant proteins wi

226 Single point mutations at the interface on either CRY1 or CLOCK disrupt formation of t

227 croscopy analysis revealed the effect of the interface on the electrical transport behavior of a smal

228 Across this interface, one monomer supplied a catalytic arginine to

229 KB mutations in barttin-binding sites, dimer interface or selectivity filter often have severe functi

230 t were not solely dominated by the number of interfaces, or the number of discrete beads, in the conn

231 Interfaces play a crucial role in semiconductor devices,

232 his polarity are regulated hierarchically by interfacing protein modules that sort polarized motility

233 The dislocations and the Al/B4C interfaces provide more heterogeneous nucleation sites f

234 The graphical user interface provides visualization of multiple lines of sp

235 d at the surface and/or within the NS5 dimer interface, providing a functional significance to the cr

236 The imprinted surface interfaces readily with computers to display images as w

237 n antiferromagnetic LaMnO3-type phase at the interface region and explain the experimentally observed

238 The interface region is highlighted by interactions that dis

239 measured the (75)As signals arising from the interface region of single-crystal semi-insulating GaAs

240 es the collapse of the Cu2O lattice near the interface region, which results in a tilted Cu2O/Cu inte

241 ented as a heat map reflecting the potential interface regions in both query proteins.

242 nfluenza A(H5N1) viruses at the animal-human interface remain a major concern for emergence of viruse

243 -actin and the details of the intermolecular interface remain poorly understood at atomic resolution.

244 O2 reduces hydroxyl ion density at catalyst interface, resulting in poor kinetics and negative catal

245 Using the Rosetta interface score as a classifier, the cognate pair was th

246 e the charge transfer occurs mainly from the interface Si atoms to the neighboring B atoms.

247 sidue at the interface (Arg-103) weakens the interface significantly, whereas effects are negligible

248 d photoelectron probes often fail to provide interface-specific information in such systems.

249 to the ACh binding site, whereas the lack of interface specificity indicates that interaction with a

250 ons in and outside the highly interdigitated interface stabilize a specific integrin/pro-TGF-beta ori

251 or exfoliation, of graphite at an oil/water interface stabilizes water-in-oil emulsions, without the

252 Our results reveal that tuning the interface structure, distribution, and phase stability t

253 n, training on closed-loop (CL) sensorimotor interfaces, such as action video games and musical instr

254 Alanine substitutions of key residues in the interface support the functional significance of the str

255 The new user interface supports diverse search options and graphic re

256 ry strong electric field across the c-Si/a-B interface systems where the charge transfer occurs mainl

257 maging offers the opportunity to study these interfacing systems' distinct processes, to quantify the

258 a challenge for traditional measurement and interfacing techniques that typically couple to macrosco

259 gnetic transition depending on the Fe- or Rh-interface termination.

260 a flexible loop proximal to the dimer-dimer interface that is essential for catalysis (i.e. the "act

261 enyl]methanol induce an enlarged interaction interface that results in the open "face-back" tunnel th

262 nt is unable to form the conserved catalytic interface that was thought to be essential for ATP synth

263 n N-TIMP2 mutant, with five mutations in its interface, that has an MMP-14 inhibition constant (Ki )

264 n conjunction with a hand-held "cradle" that interfaces the phone with a silicon-based microfluidic c

265 h a predominantly hydrophobic intermolecular interface; this heterodimer formed a higher order comple

266 cloud-based technologies with a simple user interface to allow users to access large public datasets

267 Here, we present T2N, a powerful interface to control NEURON with Matlab and TREES toolbo

268 k linking a cryptic site at the dimerization interface to enzyme function.

269 a QTOF mass spectrometer using an ion funnel interface to evaluate the m/z range transmitted as compa

270 y which NO operates at the blood-endothelium interface to exert anti-inflammatory properties is large

271 pen-source web server providing an intuitive interface to genetic and phenotypic databases.

272 idues may act in concert along a replicative interface to promote prion conversion.

273 lator in R) is an R package that provides an interface to simulate gene expression data from a given

274 nal dynamics spanning from the trimerization interface to the regions mediating receptor binding.

275 BSI was interfaced to a capillary electrophoresis-UV instrument

276 es and direct targeting of their interaction interfaces to modulate GPCR functions selectively have n

277 However, interfacing to nanomaterials in complex biological envir

278 ization of the molecules at the solid/liquid interface was investigated by means of scanning tunnelin

279 esh electronics probe showed that the tissue interface was uniform and neurons and neurofilaments pen

280 using initially on a single pentacene-C60 DA interface, we confirm that the charge transfer transitio

281 on the V2 and V3 regions and the gp120-gp41 interface, we developed the CZA97 SOSIP.v4.2-M6.IT const

282 is internal model estimate for brain-machine interfaces, we performed an offline analysis showing tha

283 red MoS2 nanosheet as an ideal semiconductor interface, which is able to form a homogenous layer on t

284 induces nonuniform Marangoni stresses on the interface, which results in three-dimensional motion ins

285 ork, we report on a novel combined MALDI/ESI interface, which was coupled to different Orbitrap mass

286 Li(+) adsorbs to the aqueous solution-vapor interface, while K(+) does not.

287 an addition magnetic layer is formed at the interface whose properties are crucially important in sa

288 ce region, which results in a tilted Cu2O/Cu interface with concomitant Cu2O island rotation.

289 ine and we reveal its functional interaction interface with high-affinity ligands.

290 toluene, and anisole) react at the air-water interface with increasing O3(g) during tauc approximatel

291 s the first insight into a coronavirus PLP's interface with ISG15 via SARS-CoV PLpro in complex with

292 Metazoan eIF4Gs share this extended binding interface with m4E-BPs, with significant implications on

293 alled inclusion, which serves as a signaling interface with the host cell.

294 , circuits and radios designed to intimately interface with the soft tissues of the human body are of

295 opt the fractal geometry of the neurons they interface with.

296 rceived by the fetus, dependent on how light interfaces with maternal tissue.

297 Evanescent waves are ubiquitous at interfaces with optical, seismic or acoustic waves, and

298 ace is distinct from the Vif-A3G and Vif-A3F interfaces, with a small Vif region being important for

299 remain regarding freezing near vapor-liquid interfaces, with earlier experimental studies being most

300 Specific macular clinic user interfaces within the institutional hospital information