ライフサイエンスコーパス: blade

1 g a craft-cutting tool equipped with a knife blade.

2 cave surface, including part of the atypical blade.

3 ing zones to one another and the mature leaf blade.

4 e harvest season, although lower than in the blade.

5 which extends from the N-terminal propeller blade.

6 the developing epithelium and the adult wing blade.

7 drop in the number of cell files across the blade.

8 critical to their ability to generate a leaf blade.

9 thelial cell adhesion in the Drosophila wing blade.

10 for disruption of adhesion in the adult wing blade.

11 fly unfold and expand to present a flat wing blade.

12 isotropic tissue flows that reshape the wing blade.

13 e lands to be removed without using a doctor blade.

14 03-0.43; P = .001) compared with nonelectric blades.

15 lated to a WD40 motif in place of one of its blades.

16 derstanding durability of jet engine turbine blades.

17 alized bone tools, body ornaments, and small blades.

18 developed for potential use in wind turbine blades.

19 speed particle impact for jet engine turbine blades.

20 drical structure composed of nine MT triplet blades.

21 ions such as aircraft cabins or wind turbine blades.

22 properly positioning the triplet microtubule blades.

23 ted to disrupt the molecule's beta-propeller blades.

24 d sometimes glutamine compared to older leaf blades.

25 genes was higher in younger than older leaf blades.

26 e amino acid levels in center and outer leaf blades.

27 idgeheads gave triptycenes with triphenylene blades.

28 microelectronics or superalloys for turbine blades.

29 increased up to 32.5-fold in 8-week-old leaf blades.

30 mooth, 5.3-mum-thick PbSe QD film via doctor-blading.

31 Cysteine 308 in Blade 1 of the beta-TrCP beta-propeller region was found

32 of arrestin2 interacts with a groove between blades 1 and 2 in the clathrin beta-propeller domain, wh

33 a conserved 7-amino acid motif that connects blades 1 and 6 of the beta-pinwheel and is a hallmark fe

34 ate serine protease active site to recognize blades 2, 3, and 4 of the beta-propeller fold of RON Sem

35 Selected antibodies directed against SEMA blades 2-3 and the PSI-IPT 1 region inhibited brain inva

36 ith the known HGF beta chain binding site on blades 2-3 of the SEMA domain beta-propeller.

37 emaphorin's 4c-4d loop into a deep groove in blade 3 of the PlexinC1 propeller.

38 lose to a hydrophobic groove located between blades 4 and 5 (beta4-beta5 groove) of the H protein bet

39 L) interacts with a binding pocket formed by blades 4 and 5 in clathrin.

40 4 binds a hydrophobic groove located between blades 4 and 5 of the hemagglutinin beta-propeller head.

41 ed to gauge impacts of scaling production to blades 40 m and longer.

42 nding, this quartet of residues on propeller blade 5 conducts conformational changes that are recepto

43 that a second and a third hotspot lie within blade 5 of the SEMA domain and IPT domains 2-3, both of

44 alizes Ile-194 at the interface of propeller blades 5 and 6, and our data indicate that a small aliph

45 wo pseudo-equivalent PI(3)P binding sites on blades 5 and 6.

46 pleckstrin homology domain of kindlin-3 and blades 5-7 of RACK1.

47 th membrane binding by a hydrophobic loop in blade 6, explaining the specificity of the PROPPINs for

48 In growing maize (Zea mays) leaf blades, a defined developmental gradient facilitates ana

49 ment caused cell death in B. distachyon leaf blades, an effect that was reversed by the addition of t

50 henotype with polarity defects in sheath and blade and a failure to differentiate vascular and photos

51 ipid content ranged from 17 to 45mg/g in the blade and between 21 and 63mg/g in the sporophyll.

52 and can substitute for STF function in leaf blade and flower development if expressed under the STF

53 b1-R) produces ectopic auricle tissue in the blade and increases the domain of LG1 accumulation.

54 Clovis, with its distinctive biface, blade and osseous technologies, is the oldest widespread

55 We identify both blade and petiole positioning as important components of

56 nt of the ligule, which separates the distal blade and proximal sheath of the leaf.

57 At the junction between blade and sheath are the ligule and auricles, both of wh

58 te cell proliferation in the developing leaf blade and specific floral tissues; a role that was not a

59 Third, "fused" wings became both the wing blade and surrounding regions of the dorsal thorax cutic

60 of the distinct tissues found in the distal blade and the proximal sheath.

61 ime-varying system, consisting of a rotating blade and the surrounding air.

62 ur specific clean delivery practices (boiled blade and thread, hand washing, and plastic sheet).

63 addressed in the contents of the kit (boiled blade and thread, plastic sheet, gloves, hand washing, a

64 onse is mediated by auxin synthesized in the blade and transported to the petiole.

65 adhesion to moving surfaces such as turbine blades and aircraft not only causes surface contaminatio

66 dissimilar to native SAPs, having wider leaf blades and greater leaf area, dense and evenly distribut

67 d devices as diverse as transistors, turbine blades and interfacial superconductors.

68 lopmental trajectories in Kranz (foliar leaf blade) and non-Kranz (husk leaf sheath) leaves of the C4

69 verrepresented among 25 E- > E+ DEGs in leaf blade, and a number of other DEGs were associated with d

70 tions of TGF-beta1 were wounded with a razor blade, and the wound area and time to closure were deter

71 llosum involvement with sparing of the outer blades, and involvement of corticospinal tracts, thalami

72 The flight muscles, dorsal air sacs, wing blades, and thoracic cuticle of the Drosophila adult fun

73 horetic deposition, hydrogel casting, doctor blading, and many others.

74 l-blade device; (2) microvitreoretinal (MVR) blade; and (3) Trabectome.

75 ved in sepal and petal development, but leaf blades are apparently normal.

76 hereas the dorsal flaps and associated setal blades are homologous with the flaps of gilled lobopodia

77 The reliability of BLADE arises from its reliance on recombinases under the

78 entral pair of flaps, with a series of setal blades attached at the base of the dorsal flaps.

79 m the presence of a dorsal array of flexible blades attached to a transverse rachis on the trunk segm

80 d forms corresponding to specific structural blades (B1-B4) of PEX9.

81 ated forms of GST-PEX9 containing structural blades B1B2 or B3B4, we have identified B3B4 as the prim

82 repared GST-PEX9 forms containing structural blades B1B2 or B3B4.

83 We recently described a sequence in blade B4 (P3 sequence) that bound alpha4beta1 integrin a

84 stablish new functions of PEX9 attributed to blades B4 and B1 and should help in designing specific i

85 ion, such that the hydrophobic sides of each blade bearing Trp-302 are facing inward and the polar si

86 Above the line, the cells become blade, below the line the cells become sheath and at the

87 h are connected to a carboxyl-terminal three-blade beta-propeller tip domain by flexible loops.

88 Each monomer forms a six-blade beta-propeller with a wide "top" and a narrower "b

89 The Balpha subunit comprises a seven-bladed beta propeller, with an acidic, substrate-binding

90 Gib2 contains a seven-bladed beta transducin structure and is emerging as a sc

91 nserved contacts of the amino-terminal seven-bladed beta-propeller (sema) domains of both semaphorin

92 The structure consists of a seven-bladed beta-propeller and, unexpectedly, contains two ps

93 Here, we show that Vps18 indeed has a seven-bladed beta-propeller as its N-terminal domain by reveal

94 The catalytic domain was a five-bladed beta-propeller consisting of five radially orient

95 HiAXHd3 displays an N-terminal five-bladed beta-propeller domain and a C-terminal beta-sandw

96 residue N-terminal domain and a C-terminal 8-bladed beta-propeller domain that are both required for

97 6 are proteins predicted to contain four six-bladed beta-propeller domains and both bind the bone-spe

98 Here we find that MojV-G displays a six-bladed beta-propeller fold bearing limited similarity to

99 native and recombinant PLL revealed a seven-bladed beta-propeller fold creating seven putative fucos

100 ture of UmAbf62A and PaAbf62A reveals a five-bladed beta-propeller fold that confirms their predicted

101 It adopts a seven-bladed beta-propeller fold with a rare nonvelcro propell

102 crystal structure of LJM11, revealing a six-bladed beta-propeller fold with a single ligand binding

103 structure of the OLF domain presents a five-bladed beta-propeller fold with unusual geometric proper

104 The protein has a 6-bladed beta-propeller fold, and it contains a single met

105 CyRPA has a six-bladed beta-propeller fold, and we identify the region t

106 he Dos1 WD repeat domain, revealing an eight-bladed beta-propeller fold.

107 wed that the enzyme displayed a type A seven-bladed beta-propeller fold.

108 Nup157 (residues 70-893), folds into a seven-bladed beta-propeller followed by an alpha-helical domai

109 The overall fold is a six-bladed beta-propeller formed by oligomerization as in th

110 eals the close interaction between the seven-bladed beta-propeller MEP50 and the N-terminal domain of

111 w that allosteric signalling through the six-bladed beta-propeller protein TolB is central to Tol fun

112 significant structural variation in the six-bladed beta-propeller scaffold of the GhV-G receptor-bin

113 PfCyRPA adopts a 6-bladed beta-propeller structure with similarity to the c

114 , folds into an extensively decorated, seven-bladed beta-propeller that forms the centerpiece of this

115 BamB forms an eight-bladed beta-propeller with a central pore and is shaped

116 Structurally, PON1 is a six-bladed beta-propeller with a flexible loop (residues 70-

117 The enzyme is a seven-bladed beta-propeller with an iron cofactor coordinated

118 Rae1 forms a seven-bladed beta-propeller with several extensive surface loo

119 In this study, we report that Bub3, a 7-bladed beta-propeller, is the MELT(P) reader.

120 se proximity by the formation of a novel six-bladed beta-propeller, where the first blade is not form

121 we determined that Nup37 folds into a seven-bladed beta-propeller.

122 N-terminal domain (TD), which forms a seven-bladed beta-propeller.

123 lutamines do cluster at the top of the seven-bladed beta-propeller.

124 the 46-kDa N-terminal domain reveals a seven-bladed beta-propeller.

125 l a new addition to the small family of five-bladed beta-propellers.

126 onsisting of a proximal petiole and a distal blade, but the molecular mechanisms that control proxima

127 by the synchronous activation of GCs in both blades by either somatic inhibition or dendritic excitat

128 The flexible propeller blades can adopt distinct conformations, and consist of

129 sion of Unpaired within the presumptive wing blade causes small, stunted adult wings.

130 The blade-coated polyethylenimine cathode interlayer and act

131 al in reducing the amount of ink used during blade coating and improving the reproducibility of print

132 A combination of surface energy-guided blade coating and inkjet printing is used to fabricate a

133 Here we present a new method based on blade coating of a blend of conjugated small molecules a

134 known attempt to print multiple materials by blade coating.

135 e sequenced four cDNA libraries created from blades collected at the sea surface and at 18 m depth du

136 erwood had higher fucoxanthin content in the blade compared to Pelorus Sound.

137 retardation in broadband, while the turbine blades consist of multiple polar sections, each of which

138 cy of polyploid cells in basal zones of leaf blades, consistent with the disruption of cytokinesis an

139 to a propeller-like homotrimer in which each blade contains a GT-B-type glycosyltransferase domain wi

140 e prevented from turning, yet decreased when blades could turn.

141 nd that air turbulence caused by fast-moving blades creates conditions that are less attractive to ba

142 mining the dependence of ribbon curvature on blade curvature, the longitudinal load imposed on the ri

143 beta-diketones in the peduncle and flag leaf blade cuticles.

144 ed to the cave and processed with the aid of blade cutting tools and fire.

145 bladekiller1-R (blk1-R) is defective in leaf blade development and meristem maintenance and exhibits

146 The genetic pathways underlying shoulder blade development are largely unknown, as gene networks

147 artially redundant, contributions to ectopic blade development in bop1 bop2 leaves.

148 To help understand regulation of maize leaf blade development, including sink-source transitions and

149 of JAK/STAT signaling is deleterious to wing blade development.

150 , WOX3 homologs are major regulators of leaf blade development.

151 rol points in gene expression along the leaf blade developmental gradient.

152 The dual-blade device achieved a more complete removal of TM with

153 The novel dual-blade device demonstrated a more complete removal of TM

154 Dual-blade device treatment across 157.5 +/- 26.3 degrees res

155 incised using 3 instruments: (1) novel dual-blade device; (2) microvitreoretinal (MVR) blade; and (3

156 ersity is achieved by the modulation of leaf blade dissection to form lobes or leaflets.

157 bdivided into a proximal sheath and a distal blade, each with distinct developmental patterning.

158 superposition of the pitch and the number of blade element.

159 BLADE enables execution of sophisticated cellular comput

160 In the Drosophila wing-blade epithelium, two cell types predominate: vein and i

161 The MVR blade exhibited minimal removal of TM and obvious injury

162 Post-germination cotyledon blade expansion in abcb19 was 65% slower than in wild-ty

163 trotransposon insertion leads to abortion of blade expansion in the mediolateral axis and disruption

164 , including shoestring leaves that lack leaf blade expansion.

165 pidermal, mesophyll and petiole cells during blade expansion.

166 synthesis and auxin biosynthesis in the leaf blade followed by auxin long-distance transport to the p

167 ystal, which acts as an all-optical, virtual blade for terahertz near-field imaging via a knife-edge

168 ion event and reveals a novel player in wing blade formation during Drosophila development.

169 ty, ranging from minute unicells to massive, bladed forms.

170 esults showed that the amino acid content in blades from the exposed farm was significantly higher (P

171 fficiently high to quantify the evolution of blade-generated coherent motions, such as the tip and tr

172 ic stages along the developmental maize leaf blade gradient.

173 ants and their submarine counterparts, algal blades, have a typical, saddle-like midsurface and rippl

174 The DP gives rise to the wing blade, hinge and dorsal mesothorax, whereas the PE makes

175 Blade I and IV mutants showed diminished enhancement of

176 cessary for MMP-14 homodimerization and that blade I is required for CD44 MMP-14 heterodimerization.

177 to be critical for homodimerization, whereas blade I was required for heterodimerization with CD44.

178 f collagen-like triple-helices occurs within blades I and II of this domain.

179 Blades I and IV were found to be involved in cell migrat

180 tricity generated with 5% CNF by mass in the blades if no increase in electrical output is realized.

181 elles and cells through distinct residues in blades III and IV of its hemopexin-like domain, while bi

182 defense response, being induced in seedling blades in response to herbivory by beet army worm.

183 age of using the 96-blade system, if all the blades in the brush are used, the sample preparation tim

184 ed leaves, sepals and petals with diminished blades, indicating a requirement for sly-miR160 for thes

185 ns in diagenetic carbonate rosettes, apatite blades intergrown among carbonate rosettes and magnetite

186 shows a novel phenotype: the infrapyramidal blade is absent, while the suprapyramidal blade is prese

187 curling a ribbon by running it over a sharp blade is commonly used when wrapping presents.

188 eaf blade is entire, or dissected, where the blade is divided into distinct leaflets.

189 s can be described as simple, where the leaf blade is entire, or dissected, where the blade is divide

190 l six-bladed beta-propeller, where the first blade is not formed by a Kelch repeat.

191 segmentation of the somitic component of the blade is partially lost; and third, there are striking d

192 al blade is absent, while the suprapyramidal blade is present and laminated.

193 and the somitic contribution to the scapular blade is significantly smaller than in previous models.

194 The flattening of leaves to form broad blades is an important adaptation that maximizes photosy

195 We found that blade IV is necessary for MMP-14 homodimerization and th

196 ution mutations within the MMP-9 PEX domain, blade IV was shown to be critical for homodimerization,

197 hed along the developmental axis of the leaf blade, leading from an undifferentiated leaf base just a

198 d 47-residue ancestral motifs that form five-bladed lectin propellers via oligomeric assembly.

199 n 8 different meat products (cutlets, bacon, blade loin, tenderloin, dry fermented sausage, cooked ha

200 am, minced meat, tenderloin, bacon, cutlets, blade loin, uncooked ham) or a melting step (salami saus

201 f the DG known as the lateral suprapyramidal blade (LSB).

202 nt the development of a new diminutive stone blade (microlithic) technology beginning at 35-30 ka, th

203 defined size and thickness using a vibrating blade microtome.

204 criptionally repress its targets during leaf blade morphogenesis.

205 d for trimers that yielded the expected "fan blade" motifs when visualized by cryoelectron microscopy

206 ine geometric repetition, such as the moving blade of a fan or the spinning of a car wheel.

207 ZCD is an N-truncated CCD4 form, lacking one blade of the beta-propeller structure conserved in all C

208 s innervate homogenously the lower and upper blade of the dentate gyrus, including the SGZ.

209 cells at the base and expanded cells in the blade of the maize (Zea mays) leaf.

210 n abrupt change in their kinematics once two blades of adjacent rotors are seen to rub together.

211 Younger leaf blades of aposymbiotic plants (no endophyte present) had

212 as 2-fold elevated in BdWRI1-expressing leaf blades of B. distachyon.

213 tmosphere, which was assimilated into canopy blades of Macrocystis pyrifera sampled from coastal Cali

214 ns by torsional interconversion of the three blades of the BCO units break space-inversion symmetry i

215 ing anatomical pathways must project to both blades of the dentate gyrus as even a mild decrease in t

216 CA1, CA2 and CA3 and the medial and lateral blades of the dentate gyrus, as early as 1day after ADX,

217 he outermost strands of the first and fourth blades of the MMP-9 PEX domain were designed.

218 while distinct insertions within or between blades of the sema domains determine binding specificity

219 t debridement with the help of a sterile #15 blade on a Bard-Parker handle, whereas only conjunctival

220 of the basal region of shoot organs, such as BLADE ON PETIOLE 2 and the GROWTH REGULATORY FACTOR path

221 fluid flow using a microstructured printing blade, on the basis of the hypothesis of flow-induced po

222 Here, we present evidence that the BLADE-ON-PETIOLE (BOP) genes, which have previously been

223 ts together with homologs of the Arabidopsis BLADE-ON-PETIOLE (BOP) transcriptional cofactors, define

224 NOOT and COCH are Arabidopsis thaliana BLADE-ON-PETIOLE orthologs, and we have shown that their

225 -shaped cotyledon, lateral organ boundaries, blade-on-petiole, asymmetric leaves, and lateral organ f

226 The transcriptional activators BLADE-ON-PETIOLE1 (BOP1) and BOP2 are known to control A

227 t the organ-specific BTB-POZ domain proteins BLADE-ON-PETIOLE1 (BOP1) and BOP2 function as transcript

228 r analyses showed that ectopic expression of BLADE-ON-PETIOLE1 (BOP1) and BOP2, which encode transcri

229 sition, and the lateral organ boundary genes BLADE-ON-PETIOLE1 (BOP1) and BOP2, whose expression is r

230 elated to Arabidopsis (Arabidopsis thaliana) BLADE-ON-PETIOLE1 (BOP1) and BOP2.

231 lorescence deficient in abscission (ida) and blade-on-petiole1 (bop1)/bop2 and an IDA-overexpressing

232 ices misexpress lateral organ boundary genes BLADE-ON-PETIOLE1/2 (BOP1/2) and KNOTTED-LIKE FROM ARABI

233 s in the cell wall composition of csld1 leaf blades or epidermal peels, yet a greater abundance of th

234 by Sl-miR160 is essential for auxin-mediated blade outgrowth and early fruit development.

235 d Nicotiana sylvestris are required for leaf blade outgrowth and floral organ development as demonstr

236 n Medicago truncatula, which is required for blade outgrowth and leaf vascular patterning.

237 , STENOFOLIA (STF), plays a key role in leaf blade outgrowth by promoting cell proliferation at the a

238 lopment, but LFL has no obvious role in leaf blade outgrowth in M. truncatula on its own or in combin

239 etion of these two domains (STFdel) impaired blade outgrowth whereas fusing Mt-TPL to STFdel restored

240 accumulation specifically inhibited leaflet blade outgrowth without affecting other auxin-driven pro

241 -lobed framework exhibit diverse patterns of blade outgrowth, hirsuteness, and venation patterning.

242 gain-of-function ability to complement lam1 blade outgrowth.

243 gene, STENOFOLIA (STF), in controlling leaf blade outgrowth.

244 diated by the WUS-box of STF acts to promote blade outgrowth.

245 , expression of Alx1, an effector of scapula blade patterning, is absent in all compound mutants.

246 The use of a single razor blade per candidate instead of the traditional knife was

247 In this work, we propose a spiral blade plasmonic vortex lens (SBPVL) that offers unique o

248 Surprisingly, however, third-instar wing blade primordia devoid of compartmental dpp expression m

249 ansverse rachis on the trunk segments; these blades probably functioned as gills.

250 that spontaneously collapse to compact three-blade propeller geometry of either (P)- or (M)-handednes

251 osylation pathways, generating compact three-blade propeller-shaped trimers.

252 , a scaffold protein that folds into a seven-blade propeller.

253 Each monomer contains a five-bladed propeller domain with a cavity that could accommo

254 of the Vps15 WD domain that reveals a seven-bladed propeller resembling that of typical Gbeta subuni

255 detergent-solubilized complex adopts a three-bladed propeller shape with a curved transmembrane regio

256 of WD40 repeat proteins with a circular beta-bladed propeller structure.

257 of Sp-Nup120(1-950) also folds into a seven-bladed propeller with a markedly protruding 6D-7A insert

258 c (E+) vs endophyte-free (E-) clones in leaf blades, pseudostems, crowns and roots.

259 atissima, measured as the size of the annual blade, ranged up to sevenfold among sites.

260 sting between the contacting surfaces of the blade root.

261 we tested the hypotheses that wind speed and blade rotation speed influenced the way that bats intera

262 shifts, which are linearly dependent on the blade's rotating frequency.

263 version (mSlARF10) developed narrow leaflet blades, sepals and petals, and abnormally shaped fruit.

264 ere, we quantitatively account for this wing-blade shape change on the basis of cell divisions, cell

265 MrNV particles have pronounced dimeric blade-shaped spikes extending up to 6 nm from the outer

266 The blade-sheath boundary disruption, shorter ligule, and di

267 ed ligule and auricle structures form at the blade-sheath boundary.

268 pts that are specifically upregulated at the blade-sheath boundary.

269 Moreover, blade size was inversely correlated with mSlARF10 transc

270 in young (center) versus older (outer) leaf blades, so LOL gene expression was compared in these tis

271 Coated blade spray (CBS) is a mue technology engineered for ext

272 Coated blade spray (CBS) is a solid-phase microextraction based

273 celle assisted TF-SPME protocol using the 96-blade system requires only 30 min of extraction and 15 m

274 n; considering the advantage of using the 96-blade system, if all the blades in the brush are used, t

275 tation and the spacing of the ridges of this bladed terrain.

276 eivably cryovolcanic and ridges with complex bladed textures.

277 d on genes that were up-regulated toward the blade than on down-regulated genes and specifically, pho

278 s misexpressed in two different parts of the blade that correlate with the different phenotypes obser

279 he corpus callosum with sparing of the outer blades, the basis pontis, middle cerebellar peduncles, a

280 When applied by doctor-blading, they form membranes having three-dimensionally

281 The blade tilts back to photosynthesize and the sheath wraps

282 demonstrate that the development of ectopic blade tissue along bop1 bop2 leaf petioles is strongly s

283 ng the future body wall tissue from the wing blade tissue.

284 We used BLADE to build 113 circuits in human embryonic kidney an

285 ng a plastic sheet during delivery, a boiled blade to cut the cord, a boiled thread to tie the cord,

286 63.7%, 95% CI 4.4%-86.2%), use of a sterile blade to cut the umbilical cord (1.88, 1.25-2.82; 67.6%,

287 We designed a micropillar-patterned printing blade to induce recirculation in the ink for enhancing c

288 hanging gene expression from the distal leaf blade to its base.

289 e auricles act as a hinge, allowing the leaf blade to project at an angle from the stem, while the li

290 logic and arithmetic through DNA excision' (BLADE), to engineer genetic circuits with multiple input

291 MVR blade treatment across 170.0 +/- 14.1 degrees of TM resu

292 of astigmatism as compared with conventional blade trephination penetrating keratoplasty.

293 s in which a ribbon is drawn steadily over a blade under a fixed load show that the ribbon curvature

294 rd approaches increased with wind speed when blades were prevented from turning, yet decreased when b

295 division and expansion at the bases of leaf blades, where cytokinesis and cross-wall formation were

296 ession was similar in younger and older leaf blades, whereas expression of N. uncinatum LOL genes and

297 imulates dovetail joints for turbo machinery blades, which can fine tune the normal contact load exis

298 d origami design formed by eight MFC modular blades, which is retractable from sharp shuriken (closed

299 mon precipitate, occurred early as elongated blades with striations, and served as substrates for oth

300 phenyl tricarboxylate (UMCM-151) and a three-bladed zinc paddlewheel metal cluster in an MCP derived