ライフサイエンスコーパス: blade

1 r abrasion by sandpaper and by a sharp steel blade.

2 isotropic tissue flows that reshape the wing blade.

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

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

5 cave surface, including part of the atypical blade.

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

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

8 which extends from the N-terminal propeller blade.

9 the developing epithelium and the adult wing blade.

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

11 distinguishable from the rest of the turbine blade.

12 a supersecondary structure element called a blade.

13 ighting the inherent flexibility of the WD40 blade.

14 microelectronics or superalloys for turbine blades.

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

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

17 in sorghum and Johnsongrass but not in leaf blades.

18 derstanding durability of jet engine turbine blades.

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

20 developed for potential use in wind turbine blades.

21 speed particle impact for jet engine turbine blades.

22 drical structure composed of nine MT triplet blades.

23 ions such as aircraft cabins or wind turbine blades.

24 properly positioning the triplet microtubule blades.

25 ve continuously by amplification from single blades.

26 03-0.43; P = .001) compared with nonelectric blades.

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

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

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

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

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

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

33 4 binds a hydrophobic groove located between blades 4 and 5 of the hemagglutinin beta-propeller head.

34 Our structure identifies blades 4-6 of the beta-propeller of CyRPA as contact sit

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

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

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

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

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

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

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

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

43 ation, ab-interno trabeculectomy-Kahook Dual Blade and Endocyclophotocoagulation at Instituto de ojos

44 on technique, ab-interno trabeculectomy dual blade and endoscopic cyclophotocoagulation (ECP) surgeri

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

46 generations), Hydrus microstent, Kahook Dual Blade and gonioscopy-assisted transluminal trabeculotomy

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

48 Thickness of leaf blade and midrib were recorded separately.

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

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

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

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

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

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

55 ed an unusable marker for clones in the wing blade and therefore we reexamined the matter.

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

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

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

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

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

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

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

63 opulations lived successfully, using biface, blade, and osseous technologies, in multiple places in N

64 or tetramers of two blades, trimers of three blades, and dimers of four and five blades, respectively

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

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

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

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

69 e repressor STF/LAM1 is required for correct blade architecture and patterning in M. truncatula and N

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 6 are proteins predicted to contain four six-bladed beta-propeller domains and both bind the bone-spe

89 otein presents a classical paramyxoviral six-bladed beta-propeller fold and structurally classifies i

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

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

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

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

94 at 2.3 angstrom resolution revealed a seven-bladed beta-propeller fold with an iron cofactor coordin

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

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

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

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

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

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

101 ed a two-domain assembly made up of an eight-bladed beta-propeller interrupted by a beta-prism domain

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

103 as well as one distantly related dual seven-bladed beta-propeller protein from a marine bacterium, h

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

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

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

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

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

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

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

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

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

113 resence in the binding cleft shared by inter-bladed binding grooves of beta-propeller.

114 One- to six-bladed building blocks derived from two seven-bladed WD4

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

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

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

118 FTAZ:IT-M) that broke the 10% benchmark when blade-coated in air, a second donor material (PBDB-T) is

119 Currently, blade-coated perovskite solar cells (PSCs) with high pow

120 The blade-coated polyethylenimine cathode interlayer and act

121 ciency of 22.0% under 1 sun illumination for blade-coated PSCs is demonstrated with an open-circuit v

122 oss, yielding a high efficiency of 21.9% for blade-coated PSCs with an open-circuit voltage of 1.20 V

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

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

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

126 known attempt to print multiple materials by blade coating.

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

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

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

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

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

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

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

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

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

136 elded stable homo-oligomers with six to nine blades, depending on the size of the building block.

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

138 de distortions, indicating important role in blade development.

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

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

141 onistically to STF and LAM1 to regulate leaf blade development.

142 as a transcriptional coactivator during leaf blade development.

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

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

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

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

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

148 ylvestris resulted in a range of severe leaf blade distortions, indicating important role in blade de

149 ld sensitivity of Piezo2 is dependent on its blade domains, which render the channel resistant to col

150 e whether video laryngoscopy with a standard blade done by anaesthesia clinicians improves the first-

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

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

153 BLADE enables execution of sophisticated cellular comput

154 ancer has co-opted the sequences of the wing blade enhancer.

155 e novel spot enhancer and the ancestral wing blade enhancer.

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

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

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

159 , including shoestring leaves that lack leaf blade expansion.

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

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

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

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

164 ic stages along the developmental maize leaf blade gradient.

165 mutants also exhibited chlorosis in the leaf blades, greatly diminished plant growth, and reduced fer

166 d Ni-based superalloy single-crystal turbine blades has been a long-standing challenge.

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

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

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

170 ts, using video laryngoscopy with a standard blade improves the first-attempt success rate and reduce

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

172 four other species with narrow and thin leaf blades, including wheat (Triticum aestivum L.), maize (Z

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

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

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

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

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

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

179 n logic and arithmetic through DNA excision (BLADE) is a recently developed platform for implementing

180 ) annotation of partial sections of the leaf blade (LB).

181 were detected in different concentrations in blade leaf and petiole extracts, indicating celery parts

182 n the metabolic profile of its edible parts (blade leaves and petioles) also related to quality, fres

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

184 s high as that of the standard mooring, with blade length surrounding the modified mooring also found

185 istency in dicing performance and extend the blade lifespan.

186 ture possess dense population with sharp saw-blade like morphological features that can support subst

187 s composed of a rotator with three molecular blades linked via a ruthenium atom to a ratchet-shaped m

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

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

190 defined size and thickness using a vibrating blade microtome.

191 As such, a "razor-and-blades" model that couples the acoustic energy of the SA

192 criptionally repress its targets during leaf blade morphogenesis.

193 metal-binding sites within canonical calcium blade motifs, which appear to have structural rather tha

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

209 Arabidopsis (Arabidopsis thaliana) BLADE-ON-PETIOLE1 (BOP1) and BOP2 represent a class of g

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

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

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

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

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

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

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

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

218 nal coactivator play important roles in leaf blade outgrowth and flower development, but how these fa

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

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

221 nd LAM1 are WOX1 orthologs required for leaf blade outgrowth in Medicago truncatula and Nicotiana syl

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

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

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

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

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

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

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

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

230 predict excellent performance of the 2-input BLADE platform across the range of possible circuits.

231 echanistic mathematical model of the 2-input BLADE platform based on Cre- and Flp-mediated DNA excisi

232 experimentally constructed using the 2-input BLADE platform.

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

234 films made by both spin-coating and scalable blading process.

235 ubstituted quinolizinone 20 to a novel "four-blade propeller" shaped 1,2,3-trisubstituted quinolizino

236 ribe a systematic transformation of a "three-blade propeller" shaped lead, 2,3-disubstituted quinoliz

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

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

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

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

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

242 using breath-hold and respiratory triggered BLADE (proprietary name for periodically rotated overlap

243 also have a rigid body with triangular bony blades protruding from the back.

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

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

246 of three blades, and dimers of four and five blades, respectively, show structurally diverse propelle

247 sting between the contacting surfaces of the blade root.

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

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

250 F) associated with SCTG harvested by: double blade scalpel (DBS) and de-epithelialized (DE) SCTG.

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

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

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

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

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

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

257 ss of loop structure, helix unwinding, and a blade shift.

258 Moreover, blade size was inversely correlated with mSlARF10 transc

259 Coated blade spray (CBS) extraction/ionization is a technology

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

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

262 In this work, coated blade spray (CBS) was used to provide freedom of instrum

263 In this report, a suitable automated coated blade spray (CBS) workflow is proposed for the screening

264 A novel magnetic blade spray-tandem mass spectrometry (MBS-MS/MS) assay w

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

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

267 Pluto and help explain the appearance of the bladed terrain of Tartarus Dorsa.

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

269 eivably cryovolcanic and ridges with complex bladed textures.

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

271 rtion of the uncoated stainless-steel of the blade that is normally exposed to the matrix, consequent

272 finities, by thorough choice of the aromatic blades that interact through homoconjugation.

273 Compared to the bare blade, the MG coating provided the following reductions

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

275 The blade tilts back to photosynthesize and the sheath wraps

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

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

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

279 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%,

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

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

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

283 logies ranging from high-performance turbine blades to solder alloys.

284 dary (GB) sliding, which works like a "wiper blade" to correct all metastable phases into thermodynam

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

286 om the intracellular side of the "propeller" blade toward the inner vestibule of the channel-and the

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

288 h-resolution structures for tetramers of two blades, trimers of three blades, and dimers of four and

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

290 -friction (CoF) of Zr-based MG-coated dicing blades was shown to reduce the number and size of chips,

291 - angstrom resolution, which reveals a seven-bladed WD40 fold.

292 laded building blocks derived from two seven-bladed WD40 propellers yielded stable homo-oligomers wit

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

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

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

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

297 pth demonstrate the durability of the coated blades, which would no doubt enhance consistency in dici

298 d cell size and reduced cell number per leaf blade with incrementing ploidy.

299 irst report on the coating of diamond dicing blades with metallic glass (MG) coating to reduce chippi

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