ライフサイエンスコーパス: concave

1 ted synergistically - the isobole curve was "concave".

2 he hydrophilic face of the lipid leaflets is concave.

3 increased virulence and as this trade-off is concave.

4 surface's silhouette was convex rather than concave.

5 of inverse sigmoidal shape that is initially concave.

6 ophilic face of the phospholipid leaflets is concave.

7 toacoustic scanner for human use, based on a concave 8-MHz transducer array, attaining 135 degrees an

8 Here, 3D-concave agarose micro-wells were used to culture robust

9 Interestingly, concave and convex complexes also include more arginine

10 "smooth" pores and channels (expressing both concave and convex curvatures).

11 -induced shifting of the patch shape between concave and convex features.

12 terface dynamics, leading to co-existence of concave and convex interfaces.

13 nct appearances in STM which are assigned to concave and convex intramolecular conformations.

14 adaptors use two helices to bind to both the concave and convex surfaces of the Fis1 TPR domain.

15 Five concave and six convex thrombi were initially identified

16 inus floor configuration was classified into concave, angle, and flat according to the sinus floor pr

17 of the cylindrical leaves that have a convex/concave architecture of size comparable to the drop.

18 hment of the cell membrane is facilitated in concave areas of the cell, where membrane tension produc

19 luential in suppressing mortality in low and concave areas, explaining an additional 10% of the varia

20 convex to the left atrium at midsystole and concave at maximal valve opening.

21 systole but convex near both commissures and concave at the belly at maximal valve opening.

22 n the acidic convex surface of cytb5 and the concave basic proximal surface of cytP4502B4.

23 tris(2-pyridylmethyl)amine (TPA) ligand, and concave baskets 2 and 3, having glycine and (S)-alanine

24 nges from rough to facet, and from convex to concave because of a surface instability, and thereby th

25 ed by an empirical power-law function with a concave behavior at higher densities than with a linear

26 Moreover, for concave bending, a significant improvement in detection

27 ing of the ClO4(-) anion to the hydrophobic, concave binding site of a deep-cavity cavitand is presen

28 ashion, classifying the contour and shape as concave (bowl-shaped) or inflective (S-shaped contour wi

29 uctures, often in the form of interconnected concave cavities, are typically assembled from convex mo

30 inding site for the single PDZ domain is the concave cavity of the BAR dimer.

31 Bridges developed large tensions where concave cell edges were anchored to FN by adhesion sites

32 higher prey diversity when the trade-off is concave (cheap).

33 /- 25 years (range 3-95) in the group with a concave contour (P = .001).

34 om the fovea was thicker in the group with a concave contour.

35 sensors is due to binding of biomolecules in concave corners where screening is reduced.

36 d via the controlled overgrowth of preformed concave cube seeds.

37 tion direction: the bath accentuates natural concave curvature caused by transmurally rotating fibers

38 mismatches between predictions (power-law or concave curvature) and observed empirical data (convex c

39 d progressively toward more acute convex and concave curvature, matching the neural recording results

40 d toward contours containing acute convex or concave curvature.

41 phasizing representation of acute convex and concave curvature.

42 velop thick peripheral stress fibers, with a concave curvature.

43 After adapting to a concave curve, subjects more frequently perceived faces

44 tatic screening is weaker in the vicinity of concave curved surfaces, and stronger in the vicinity of

45 verlapping, linear, convex, and occasionally concave curves with typically negative, but also sometim

46 We found that the concave (CV) fibril edge has significantly higher bindin

47 Our results indicate a strictly concave damage function and compounding benefits of prog

48 at is, either positive (convex) or negative (concave), depends on the curvatures of the interfaces.

49 f liposomes, FtsZ-YFP-mts bound and produced concave depressions, bending the membrane in the same di

50 be small Z rings, which still maintained the concave depressions.

51 he membrane in the direction opposite to the concave depressions.

52 s were then extruded at the intersections of concave depressions.

53 ellar liposomes formed patches that produced concave distortions when viewed at the equator of the li

54 two symmetrically located phosphates on the concave DNA face contributes -2.3 kcal mol(-1) to -0.9 k

55 ve (seven structures) correlation containing concave (DNA curved toward protein) and convex (DNA curv

56 mance relationships that were overwhelmingly concave down.

57 es, we reveal a globally consistent positive concave-down BPR, showing that continued biodiversity lo

58 at the model can explain both concave-up and concave-down force-velocity relations for growing actin

59 capita relationship has both concave-up and concave-down sections.

60 n-donating substituents is nonlinear, with a concave downward curvature.

61 sional environments by a system of conjugate concave downward faults instead of multiple normal fault

62 A concave downward Hammett plot is presumably the result o

63 ltrasonic communication in an amphibian, the concave-eared torrent frog (Amolops tormotus) from Huang

64 Here we show that the Chinese concave-eared torrent frog, Odorrana tormota, can tune i

65 The peptides bound to the concave edge have significantly lower free energy compar

66 n range of ceilings, and extended convex and concave edges in the orientation range of wall/floor/cei

67 ions at different bridge regions: (1) at the concave edges of bridges, MIIA force stimulates actin fi

68 , it is reported that the presence of highly concave edges, which are free or physically constrained

69 unctions, i.e., small triangular sheets with concave edges.

70 The unprecedented double concave encapsulation of a metal ion by two bowl-shaped

71 ons involving methyl iodide proceed from the concave (endo) face of the bicyclo[4.3.0]nonene ring sys

72 isomers but are destabilized within smaller concave environments (TON) because framework distortions

73 classified as flat (eta(1) coordination) and concave (eta(2) coordination) sites.

74 e waveguide geometries (such as with a flat, concave exterior and a round interior) is not as detrime

75 mbrane, is a cup-like structure with a clear concave face and a highly curved rim.

76 e surface to those that favor binding to the concave face and subsequent membrane bending.

77 ead dimer in the form of a C clamp, with its concave face containing a number of basic residues that

78 The structure resembles a boomerang with its concave face filled in and contains a triple tetratricop

79 n and projects its carbonyl group out of the concave face in the vicinity of the opposite allyl termi

80 he metalloproteinase-like domain held in the concave face of a rigid module formed by the disintegrin

81 Mutations on the concave face of decorin abolished collagen binding regar

82 We conclude that the concave face of decorin mediates collagen binding and th

83 amics simulations of membrane binding to the concave face of N-BAR domains are used along with discre

84 s that directly show membrane binding to the concave face of N-BAR domains, resulting in the generati

85 59), which reveals that PopB lies within the concave face of PcrH, employing mostly backbone residues

86 rgetic preference for methane binding to the concave face of sumanene.

87 Ssu72 is bound to the concave face of symplekin, and engineered mutations in t

88 Thus, the concave face of the BAR dimer accommodates the PDZ domai

89 ween the membrane and the positively charged concave face of the BAR, even when it is tightly bound t

90 to determine that electrophiles react at the concave face of the enolate derived from 1d.

91 The cystine knot of Spz binds the concave face of the Toll leucine-rich repeat solenoid in

92 d, right-handed, alpha-helical solenoid, the concave face of which completely covers the metal-bindin

93 ve a large radius of curvature, glycosylated concave face, and a novel C-terminal capping motif.

94 n the PDZ domain slides to the center of the concave face, where more favorable hydrophobic interacti

95 ctenone occur on the more sterically crowded concave face.

96 onto bilayers via surfaces other than their concave face.

97 he curvature of a putative membrane-engaging concave face.

98 nexpectedly on the apparently more hindered (concave) face; this result has been explained through co

99 Finally, the factors leading to concave-face alkylation of the enolate derived from 1d a

100 ne and amide resonance are proposed to favor concave-face alkylation.

101 by the association of two monomers via their concave faces.

102 Our model predicts that these concave faults accumulate large amounts of extension and

103 fect on the melting points of the convex and concave features.

104 stem and a multimode fiber-loop cavity using concave fiber lenses with matching numerical apertures a

105 edure was more predictable in sinuses with a concave floor and small implant-intruding angles.

106 dian is preferentially represented in sulci (concave folds), throughout visual cortex in both primate

107 The interacting binding surfaces, concave for IIA(Chb) and convex for HPr, complement each

108 r acted synergistically - isoboles adopted a concave form, while after digestion in vitro an additive

109 ed force of infection; iii) low-dose linear, concave functions allow the basic reproduction number to

110 relations satisfied by any nonnegative Schur-concave functions.

111 The convergent lens has a plano-concave geometry, in contrast to conventional dielectric

112 on by degenerate four-wave mixing in a plano-concave glass slide, obtaining magnified images.

113 in tetratricopeptide-like motifs that form a concave groove, but their relative orientation differs b

114 ed in the flat sinus group compared with the concave group (P <0.001).

115 time underlying saccades was found to have a concave growth, thereby confirming previous results on h

116 mus depth was classified as straight (3 mm), concave (>3 to </=5 mm), or pouchlike (>5 mm).

117 guests and illustrate the potential of these concave hosts to act as catalysts for controlling chemic

118 ith or without water-filled pores and uses a concave hull algorithm for surface-residue classificatio

119 This tiling has 694 distinct concave (i.e., nonconvex) repeat units, 24 of which poss

120 tral isthmus was straight in 8% of patients, concave in 47% of patients, and pouchlike (>5 mm) in 45%

121 ty and carboxylesterase activity predicted a concave increase in tumor SN-38 duration, which was conf

122 f the PIN-FORMED auxin efflux carrier at the concave (inner) versus convex (outer) side of the hook s

123 ces of the normal gyroid, as compared to the concave interfaces of a reverse spherical micelle.

124 r data suggest that the substrate enters the concave interior of the enzyme structure, is held in pla

125 (CNTs) and elastomeric polymer is formed on concave lenses, and used as an efficient optoacoustic so

126 The association of a concave macrocyclic compound to one or multiple fluoroph

127 ys, in the course of which it interacts with concave membrane necks and bud rims.

128 while the smaller defects found on flat and concave membrane surfaces inhibit folding by kinetically

129 reased, septin localization is diminished at concave membranes in these mutants.

130 out that this protein binds specifically to concave membranes.

131 able optical properties as a result of their concave menisci, the shape of which can be easily manipu

132 proposed method in tuning the profile of the concave microarray structures by changing the laser puls

133 efficient fabrication method of high-quality concave microarrays on fused silica substrates based on

134 nadherent cells within a gelatin plug on the concave microraft surface was developed, enabling releas

135 and that activity was best described using a concave model of effort-discounting.

136 t plays an essential role in controlling the concave morphology of the final product.

137 dex planes, we then fabricated monodispersed concave nanocages via a material-independent electroleac

138 Hollow and concave nanocrystals find applications in many fields, a

139 palladium nanocubes, the shape is evolved to concave nanocubes and finally hollow nanocages in the si

140 With the high-index facets exposed, these concave nanocubes and nanocages are 10- and 100-fold mor

141 The concave nanocubes exhibit higher chemical activities com

142 We prepared bimetallic FeNi concave nanocubes with high Miller index planes through

143 A new class of gold nanostructures, concave nanocubes, enclosed by 24 high-index {720} facet

144 Concave nanostructures are rare because of their thermod

145 In contrast, the M(CC) was concave near both commissures and convex at the belly at

146 At midsystole, the M(SL) was concave near the mitral annulus, turned from concave to

147 water density fluctuations are enhanced near concave nonpolar surfaces compared with those near flat

148 two thick "grips" separated by a large, deep concave opening.

149 ed to an endo- or an exoligand, possessing a concave or convex arrangement of ligating atoms, which i

150 ible sheets and further folded either into a concave or convex hemisphere.

151 PLEDs were repeatedly bent to 1.5 mm radius concave or convex with calculated strain in the emissive

152 e patches were tuned reversibly to be either concave or convex.

153 facilitated by escort ion (M) binding to the concave orientated amide carbonyl.

154 The concave orientated amide N-H is able to activate the lea

155 be facilitated by hydrogen-bonding with the concave orientated amide N-H; and (iii) pro-R delivery o

156 se of the shell, yielding Cu(2-x)S(y)Se(1-y) concave particles.

157 ed the lethal phenotype of a mutation in the concave patch, P540A.

158 The initial concave patchy particles were synthesized in a water sus

159 ects the best predictors of a phenotype by a concave penalized regression model, while estimating the

160 We implement both the L1 penalty and minimax concave penalty for variable selection and Laplacian pen

161 ed on sure independent screening and minimax concave penalty techniques, we use a joint significance

162 ted in a more hydrophilic environment, while concave plots originate from AOs in a more hydrophobic l

163 The concave pocket in the unbound state exhibits wet/dry hyd

164 natorial optimization is relaxed as a convex-concave problem, which is then transformed into a sequen

165 To optimize, we implement a Convex-Concave procedure-based algorithm.

166 -abundance, or rare, classes, accompanied by concave rank-abundance curves.

167 blocked by inhibition of EGFR signaling, the concave regions continued to move, suggesting that both

168 Dictyostelium cells preferentially bleb from concave regions, where membrane tension facilitates memb

169 s showed a preference for curvature that was concave relative to fixation.

170 he pitch plane, convex responses in dMNs and concave responses in vMNs to bending in mid-body segment

171 Stochasticity in time series explains concave responses of per capita growth rate to populatio

172 In the yaw plane, concave responses to bending of rostral segments and con

173 rface of the NusA-NTD, situated opposite its concave RNA polymerase (RNAP) binding surface.

174 nterface morphology appeared with convex and concave sections that cycled between growth and retreat.

175 peptide inserts or loops that pack to form a concave, semicircular surface around the substrate leavi

176 Observers viewed ambiguous convex/concave shaded surfaces, with or without highlights.

177 reveals contrasting behaviors: 1a exhibits a concave shape as B increases to a saturation field, B(c)

178 a C(1)-symmetric conformation, leading to a concave shape in the 13-membered chelate in which one am

179 e three domains of urokinase receptor form a concave shape with a central cone-shaped cavity where th

180 arger devaluations for higher effort-levels (concave shape).

181 Mutant discs also lost their characteristic concave shape, exhibited ectopic chondrocyte differentia

182 pressure, the thin planar membrane assumed a concave shape, representing a segment of the blood vesse

183 Furthermore, when the solute has a concave shape, we can also capture the water number insi

184 bining sites of antibodies interact with the concave shaped substrate-binding clefts of proteases, we

185 gands, as revealed in these structures, form concave shapes, or 'pockets', on the protein's surface.

186 e "platform" and three imide residues on its concave side carrying flexible alkane chains.

187 ere we show that an extensive surface on the concave side of both arrestin-2 domains is involved in r

188 ght to take place via tip-like growth on the concave side of lobes driven by localized concentrations

189 onfirms that conserved basic residues on the concave side of RecX are important for repression of Rec

190 root primordia, the vascular system, and the concave side of the apical hook.

191 ish an auxin maximum in the epidermis at the concave side of the apical hook.

192 nd PDZ domains adjacent to each other on the concave side of the banana-shaped PICK1 dimer.

193 calmodulin binding site is localized on the concave side of the C-domain and a loop in the center of

194 ple intramolecular hydrogen bonds within the concave side of the molecule.

195 t asymmetric ROS distribution, higher at the concave side of the root.

196 ccessible patches on the leucine-rich repeat concave side of the solenoid structure of NgR.

197 and were less concentrated or absent at the concave side where growth was promoted.

198 to be larger than steps across surfaces with concave silhouettes.

199 s it is delocalized on both C and O atoms on concave sites, increasing the back-bonding on these site

200 The concave stereoselectivities arise from alkene predistort

201 d bridging three polar chains underneath the concave steroid rings of cholate and capping with anothe

202 to construct an all-in-one evaporator with a concave structure for high-efficiency solar steam genera

203 al folding, characterized by convex gyri and concave sulci, has an intrinsic relationship to the brai

204 Pyrogallol[4]arene is a macrocycle with a concave surface and 12 peripheral hydroxyl groups that m

205 t examine in greater detail the roles of the concave surface and amphipathic helices in driving local

206 induce curvature in membranes via a charged concave surface and N-terminal amphipathic helices.

207 o undergo dynamic excursions that reveal the concave surface and therefore may be important for bindi

208 The concave surface assembled from the most highly variable

209 rase: the template channel and one face of a concave surface behind the template channel.

210 id cavity, in which light propagates along a concave surface by continuous total internal reflection,

211 VP55's concave surface docks the globular VP39.

212 bending, and that imposition of the module's concave surface forces fluid-phase bilayers to bend loca

213 Mdv1 recruitment: an N-terminal "arm" and a concave surface formed by evolutionarily conserved resid

214 UZ domain is mapped to the highly conserved, concave surface formed by the alpha 3 helix and the cent

215 The extensive beta-sheet on the molecule's concave surface forms a platform for several modificatio

216 positioned along a continuous groove on the concave surface generated by the aligned CasC1-6 subunit

217 ral scaffold projects its NH unit out of the concave surface in close vicinity to one allyl terminus.

218 athic helices that bind across the conserved concave surface of ALIX(Bro1).

219 Mutations directed toward the concave surface of C3d result in substantially compromis

220 ons in which CR2 SCR1-2 is docked within the concave surface of C3d.

221 tion in the initial beta sheets of the inner concave surface of CD14 are crucial for structure and fu

222 as the elbow joint, and occupies most of the concave surface of ELL2.

223 SART3 dimerizes through the concave surface of HAT-C, whereas the HAT-C convex surfa

224 domain of Skp1 associates with Sgt1 via the concave surface of its TPR domain using residues that ar

225 charge of +4 and are positioned on the inner concave surface of the 50 degree DNA bend that is induce

226 structural evidence showing that in WRAD, a concave surface of the Ash2L SPIa and ryanodine receptor

227 Spin-labeled side chains on the concave surface of the BAR domain do not penetrate into

228 ges that induce membrane curvature along the concave surface of the BAR domain.

229 rged cell membrane to the positively charged concave surface of the BAR domain.

230 The concave surface of the cavities is smooth, and the cavit

231 The concave surface of the crescent-shaped Bin-amphiphysin-R

232 harged patch and sulfate-binding site on the concave surface of the domain.

233 Our data indicate that the concave surface of the Fis1 tetratricopeptide repeat-lik

234 RBC36 binds the H-trisaccharide on the concave surface of the LRR modules of the solenoid struc

235 Spatzle binds to the concave surface of the membrane-distal LRR domain, in co

236 target, the Abl SH2 domain, revealed that a concave surface of the monobody, as intended in our desi

237 ding domain is centered in the middle of the concave surface of the NgR1 leucine-rich repeat domain a

238 site comprises the beta-sheet that forms the concave surface of the proteins.

239 he Cdc48-binding site could be mapped to the concave surface of the PUL domain by biochemical studies

240 ocation of the quinone site implies that the concave surface of the PutA dimer approaches the membran

241 s sandwiched between a variable loop and the concave surface of the VLR formed by the beta-strands of

242 F3b-containing domain and protrudes over the concave surface of tri-snRNP, where the U1 snRNP may res

243 A concave surface on the cytosolic domain of Fis1 from Sac

244 n-helix motifs scaffold a positively charged concave surface perfectly shaped for duplex DNA.

245 An engineered cysteine, I85C, located on the concave surface that lies underneath the Fis1 arm, was r

246 ankyrin repeat units, which provide a large concave surface to grip the two contiguous zinc fingers

247 the F-BAR dimer, but instead shift from its concave surface to positions on either side of the dimer

248 uires the stable presentation of the charged concave surface to the membrane and is not driven by the

249 tertiary fold containing a highly conserved concave surface where we predict its active site is loca

250 With its phosphate-binding concave surface, beta-arrestin-1 'reads' the message in

251 R-based receptors bind antigens though their concave surface, in addition to a unique hypervariable l

252 binds alpha/beta-tubulin via its conserved, concave surface, including part of the atypical blade.

253 e is positioned within a shallow hydrophobic concave surface, whereas the cytosine on the target stra

254 interactions of the membrane with the F-BAR concave surface.

255 ally to the catalytic domain through a large concave surface.

256 sheet and surface loops that together form a concave surface.

257 at is known for ligand interaction through a concave surface.

258 residues in the beta-sheets lining the VLR-B concave surface.

259 ly shaped to accommodate a DNA duplex on the concave surface.

260 inding is abolished by mutations to the Fis1 concave surface.

261 oworkers have implicated an electronegative "concave" surface on C3d in the binding process.

262 se near flat or convex ones, suggesting that concave surfaces are more hydrophobic.

263 surface contours of 6 with the corresponding concave surfaces of CB[7], desolvation of the CO portals

264 formed among the asparagine residues on the concave surfaces of neighboring leucine-rich repeat modu

265 Residues distributed over the concave surfaces of the two arrestin domains are involve

266 nts, highlights will occur on convex but not concave surfaces, due to occlusion of the illuminant.

267 , when the cell body switches from convex to concave, tension in the apical cortex is transmitted to

268 They are synthesized from a concave tetratopic pi-extended tetrathiafulvalene ligand

269 Two patients had stable concave thrombi, one with an initial concave thrombus de

270 stable concave thrombi, one with an initial concave thrombus developed convex thrombus, and one with

271 ne with an initial convex thrombus developed concave thrombus.

272 ese tilings generally possess 2,068 distinct concave tiling units, 62 of which are centrally symmetri

273 flat near the annulus, turned from slightly concave to convex across the belly, and flattened toward

274 concave near the mitral annulus, turned from concave to convex across the belly, and was convex along

275 ional switching of individual molecules from concave to convex and vice versa is observed.

276 terial growth-defense trade-off changes from concave to convex, i.e., defense is effective and cheap

277 ints on a curve where its shape changes from concave to convex, or vice versa.

278 d surface forms an RNA binding path from the concave to the convex side of MTERF4 and further along N

279 ism of predatory Venus flytraps that rely on concave-to-convex reconfigurations.

280 om other regions of the protein due to their concave topology combined with a pattern of hydrophobic

281 olded (C- or V-shaped) granule neuron layer, concave toward the hilus and delimited by a hippocampal

282 respectively, with positive curvature being concave toward the left atrium.

283 120-gp41 interactions, whereas a "flat open" concave trimer apex is observed consequent to gp120 tilt

284 removing higher trophic level individuals, a concave trophic distribution emerges.

285 The concave trophic distribution implies a more direct link

286 On coral reefs, managing for 'concave' trophic pyramids might be a win-win for people

287 reaches a step near 10.8 T and then becomes concave until saturation is reached at 15.8 T.

288 of the binding of EGF to its receptor yields concave up plots that indicate the presence of two class

289 a function of its extension has a nonconvex (concave up) region, the stretched polymer chain separate

290 demonstrate that the model can explain both concave-up and concave-down force-velocity relations for

291 s case, the per capita relationship has both concave-up and concave-down sections.

292 e curves of all corneal-scleral buttons were concave-up asymptotes, demonstrating elasticity.

293 Our results provide theoretical support for concave-up biodiversity-ecosystem functioning relationsh

294 d temperature dependence shows a significant concave upward curvature indicative of the influence of

295 A concave upward proton inventory suggests that more than

296 s and consumers with endowments and strictly concave utilities) the price-adjustment mechanism will a

297 function) for low reward and risk avoiding (concave utility function) with higher amounts.

298 illslopes and advective processes that carve concave valleys.

299 Here we show that an atomically sharp, concave wedge can further promote ice nucleation with sp

300 In particular, the concave (when viewed from the extracellular side) region

301 nd thermally interconvertible planar E-1 and concaved Z-1 were found to exhibit different affinities,

302 ke trend, and rank frequency plots exhibit a concave Zipf's curve.