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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.
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
38 lose to a hydrophobic groove located between blades 4 and 5 (beta4-beta5 groove) of the H protein bet
40 4 binds a hydrophobic groove located between blades 4 and 5 of the hemagglutinin beta-propeller head.
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
47 th membrane binding by a hydrophobic loop in blade 6, explaining the specificity of the PROPPINs for
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
52 and can substitute for STF function in leaf blade and flower development if expressed under the STF
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
63 addressed in the contents of the kit (boiled blade and thread, plastic sheet, gloves, hand washing, a
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
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
76 hereas the dorsal flaps and associated setal blades are homologous with the flaps of gilled lobopodia
79 m the presence of a dorsal array of flexible blades attached to a transverse rachis on the trunk segm
81 ated forms of GST-PEX9 containing structural blades B1B2 or B3B4, we have identified B3B4 as the prim
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
91 nserved contacts of the amino-terminal seven-bladed beta-propeller (sema) domains of both semaphorin
93 Here, we show that Vps18 indeed has a seven-bladed beta-propeller as its N-terminal domain by reveal
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
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
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
108 Nup157 (residues 70-893), folds into a seven-bladed beta-propeller followed by an alpha-helical domai
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
114 , folds into an extensively decorated, seven-bladed beta-propeller that forms the centerpiece of this
120 se proximity by the formation of a novel six-bladed beta-propeller, where the first blade is not form
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
131 al in reducing the amount of ink used during blade coating and improving the reproducibility of print
135 e sequenced four cDNA libraries created from blades collected at the sea surface and at 18 m depth du
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
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
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
148 To help understand regulation of maize leaf blade development, including sink-source transitions and
155 incised using 3 instruments: (1) novel dual-blade device; (2) microvitreoretinal (MVR) blade; and (3
157 bdivided into a proximal sheath and a distal blade, each with distinct developmental patterning.
163 trotransposon insertion leads to abortion of blade expansion in the mediolateral axis and disruption
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
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
173 ants and their submarine counterparts, algal blades, have a typical, saddle-like midsurface and rippl
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.
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
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
189 s can be described as simple, where the leaf blade is entire, or dissected, where the blade is divide
191 segmentation of the somitic component of the blade is partially lost; and third, there are striking d
193 and the somitic contribution to the scapular blade is significantly smaller than in previous models.
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
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
202 nt the development of a new diminutive stone blade (microlithic) technology beginning at 35-30 ka, th
205 d for trimers that yielded the expected "fan blade" motifs when visualized by cryoelectron microscopy
207 ZCD is an N-truncated CCD4 form, lacking one blade of the beta-propeller structure conserved in all C
210 n abrupt change in their kinematics once two blades of adjacent rotors are seen to rub together.
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,
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
223 ts together with homologs of the Arabidopsis BLADE-ON-PETIOLE (BOP) transcriptional cofactors, define
225 -shaped cotyledon, lateral organ boundaries, blade-on-petiole, asymmetric leaves, and lateral organ f
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
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
235 d Nicotiana sylvestris are required for leaf blade outgrowth and floral organ development as demonstr
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.
245 , expression of Alx1, an effector of scapula blade patterning, is absent in all compound mutants.
248 Surprisingly, however, third-instar wing blade primordia devoid of compartmental dpp expression m
250 that spontaneously collapse to compact three-blade propeller geometry of either (P)- or (M)-handednes
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
257 of Sp-Nup120(1-950) also folds into a seven-bladed propeller with a markedly protruding 6D-7A insert
261 we tested the hypotheses that wind speed and blade rotation speed influenced the way that bats intera
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
270 in young (center) versus older (outer) leaf blades, so LOL gene expression was compared in these tis
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
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
282 demonstrate that the development of ectopic blade tissue along bop1 bop2 leaf petioles is strongly s
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
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
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
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