ライフサイエンスコーパス: lamella

1 K (9-mm anterior lamella with 6-mm posterior lamella).

2 specialized extracellular matrix, the neural lamella.

3 that the event of interest is present in the lamella.

4 layer is constrained to within an individual lamella.

5 ited higher affinity for disk rims than disk lamella.

6 through the protrusion of the actin-enriched lamella.

7 esions at localized regions of the advancing lamella.

8 the sensory epithelium within each olfactory lamella.

9 ic organization more typical of a fibroblast lamella.

10 ll periphery and at dynamic spots within the lamella.

11 ars to cause MT buckling and breaking in the lamella.

12 o depolymerize into the field of view at the lamella.

13 .4 mircon/min rate of retrograde flow in the lamella.

14 y diffuses through the intercorneocyte lipid lamella.

15 identified plane; and (6) suturing of donor lamella.

16 anes, and loss of differentiation of retinal lamella.

17 obotic fabrication was typically an hour per lamella.

18 ransmission electron microscopy image of the lamella.

19 olocalizes with actinin4, is present at each lamella.

20 chains of pectin in the cell wall and middle lamella.

21 lls and is especially abundant in the middle lamella.

22 tion of FA growth at the leading edge of the lamella.

23 myosin activity and absence of a contractile lamella.

24 be generated about focal adhesions in a thin lamella.

25 d style, most likely by weakening the middle lamella.

26 s in the cell body but bind along MTs in the lamella.

27 assembly of the primary cell wall and middle lamella.

28 myosin phosphorylation within the spreading lamella.

29 F-actin) networks, the lamellipodium and the lamella.

30 ngate shape with narrow protrusions and wide lamellas.

31 09 hours (range, 96-630 hours) for posterior lamellas.

32 ior lamella 9 mm in diameter and a posterior lamella 6 mm in diameter.

33 iece mushroom graft consisted of an anterior lamella 9 mm in diameter and a posterior lamella 6 mm in

34 graft consisted of a large anterior stromal lamella (9.0 mm in diameter and +/- 250 mum in thickness

35 rlecan predominantly localizes to the neural lamella, a specialized ECM surrounding nerve bundles.

36 ce of the cell, indicating continuity of the lamella across the outer wall.

37 In the lamella, all marked and observed actin filaments remain

38 On the dorsal surface of the lamella, an optical gradient trap measured rearward forc

39 lly in the control of both the angle between lamella and backbone axes and the angle between surface

40 imate boundary between the lamellipodium and lamella and continued to grow as they were swept back to

41 sults show MLCK is a myosin regulator in the lamella and contractile ring, and pinpoints sites where

42 cans in the formation of cotton fiber middle lamella and contributing to fiber plasticity and elongat

43 t structures besides lamellipodia, including lamella and filopodia, may have unappreciated roles in c

44 cells were more motile and had more abundant lamella and filopodia.

45 lear region generates rearward forces in the lamella and forward forces in the cell rear.

46 terally within the septotemporally organized lamella and inhibitory trans-lamellar connections in the

47 ct but integrated actin populations, such as lamella and lamellipodia in migrating cells(13) or media

48 ing edge ruffling and retrograde flow in the lamella and lamellipodia.

49 tire microtubule lattice in the leading edge lamella and lamellipodium.

50 ow that distribution of most proteins in the lamella and PM domains is preserved even in the absence

51 from different regions of a single olfactory lamella and simultaneously from widely separated lamella

52 istinct accumulations of LFA-1-ICAM-1 in the lamella and TCR-MHC in the uropod, consistent with a mot

53 n the transition zone between the peripheral lamella and the cell body, a subset of MTs remains stati

54 esponsible for the degradation of the middle lamella and the loosening of the primary cell wall surro

55 in mechanical stiffening of both the leading lamella and the perinuclear region of motile cells.

56 ced in the root and stem cortex and the leaf lamella and trichomes in response to heavy metal stress.

57 at previously unknown sites, like the middle lamella and, most prominently, at an intracellular matri

58 08 hours (range, 108-678 hours) for anterior lamellas and 339 +/- 109 hours (range, 96-630 hours) for

59 a function resulted in significantly smaller lamellas and decreased process number, length, and branc

60 their growth cones had significantly smaller lamellas and reduced levels of F-actin in vitro.

61 periphery as extended by smaller individual lamella, and a newly discovered whole-interface actin-dr

62 in the outer segment: plasma membrane, disk lamella, and disk rim.

63 trengthens pectin cohesion within the middle lamella, and possibly the mucilage of wild-type seed coa

64 ontributes to the construction of the neural lamella, and resolve the transcriptomic differences amon

65 template-directed partitioning of coexisting lamella- and cylinder-like subdomains at the template pe

66 , our results suggest that the unique folded lamella architecture of the cone OS may maximize density

67 and that approximately 80% of the MTs in the lamella are not centrosome bound.

68 re more concentrated in the cell wall-middle lamella area of the parenchyma cells.

69 ted motoneurones had RER with a more ordered lamella arrangement than controls.

70 or MLCK-mediated myosin contractility in the lamella as a driving force for migration.

71 rence of the microtubule cytoskeleton in the lamella as compared with the cell body and provide the f

72 ain its localization just behind the leading lamella as PMNs migrate, indicating that membrane recycl

73 sfer of buccal mucosal membrane to posterior lamella as spacer graft, and canthal tightening.

74 reate the proximal surface of an evaginating lamella, as well as membrane protrusions that extend bet

75 e the acquisition of cryo-ET data within FIB-lamellas at specific locations, unambiguously identified

76 local chain overcrowding-induced asymmetric lamella bending, which is further confirmed by correlati

77 s to produce enzymes that degrade the middle lamella between cells in the AZ.

78 ction is limited by mass transfer across the lamella boundaries.

79 lusters at the mucosal tip of each olfactory lamella but scattered in the neuroepithelial region.

80 rils oriented in a common direction within a lamella but varying by ~30 to 90 degrees between adjacen

81 nt from the highly lignified compound middle lamella, but xylan occurred throughout the cell walls of

82 In the lamella, cell body, and tail there are two observable ty

83 lidated by adhesion of a cotton fiber middle lamella (CFML).

84 s were small and rearward directed under the lamella, changed direction in front of the nucleus, and

85 , such adhesion is mediated through a middle lamella composed primarily of pectic polysaccharides.

86 the volume represented within a typical FIB lamella constitutes a small fraction of the biological s

87 ) transplantation of a 9-mm anterior corneal lamella cut by microkeratome-assisted dissection (400-mu

88 The leading lamella develops no detectable propulsive traction, even

89 Microfibril direction within a lamella did not change gradually or abruptly across the

90 bition of Paks abolished F-actin flow in the lamella, displaced myosin IIA from the cell edge, and de

91 scence in Kanzi apples was not due to middle lamella dissolution, as tissue failure still occurred by

92 The ability to check the lamella during and after the milling process results in

93 MTs are excluded from the leading lamella during polarization and motility, but treatment

94 its function in modulating lamellipodium and lamella dynamics, and the implications of these dynamics

95 e observations indicate disruption of neural lamella ECM function triggers axonal destabilization and

96 ion dependence on particle distance from the lamella edge.

97 w manipulating curvature in an elastic fluid lamella enables the reversible relative positioning of f

98 tions of Arp2/3 and ADF/cofilin, whereas the lamella exhibits spatially random punctae of F-actin ass

99 d RSK promote myosin II-mediated tension for lamella expansion and optimal edge dynamics for cell mig

100 We propose that the coupling of lamella extensions to fluctuating rearward tractions in

101 detail, we created a microbridge from a thin lamella extracted by Focused Ion Beam (FIB) and measured

102 olled targeting at every milling step in the lamella fabrication process, validated with transmission

103 lasmas can be examined to further streamline lamella fabrication.

104 mall gold nanoparticles (AuNPs), and prepare lamella for cryo-electron tomography studies.

105 neous nanoscale medium-entropy intermetallic lamella form in the as-printed Al alloy.

106 y and reversibly blocked protrusion-mediated lamella formation and chemotaxis.

107 f proteins involved in actin dynamics during lamella formation in Drosophila S2 cells.

108 90 proteins implicated in actin function on lamella formation in Drosophila S2 cells.

109 ent properties, beta-actin localization, and lamella formation in motile cells.

110 Actin arginylation regulates lamella formation in motile fibroblasts, but the underly

111 We propose that lamella formation may reduce tension building at cell-ce

112 r the rho kinase inhibitor, Y-27632, blocked lamella formation, myosin phosphorylation within the pro

113 d filopodial formation and stabilization and lamella formation.

114 locity, the compressibility affects also the lamella formed and changes its ejection velocity observe

115 Top coats were applied to the lamella-forming block copolymers poly(styrene-block-trim

116 So far, the preparation of the high-quality lamella from a bulk largely depends on manual processes

117 This method produces magic size lamella, having a well-spaced discrete melting point, Tm

118 on that paved the way for an adhesive middle lamella in multicellular land plants.

119 spatial interaction of the lamellipodium and lamella in response to upstream signals.

120 chining) out 100-250-nm-thin regions (called lamella) in the intact frozen cells.

121 rabeculae on the dorsal surface of each gill lamella indicate eurypterids were capable of subaerial b

122 blasts in the body correlates with epidermal lamella invasion and subsequent adult skin differentiati

123 Indeed, the neural lamella is disrupted in the absence of Perlecan, with ax

124 cated at the corner of the impact, where the lamella is ejected, not in the centre, and it is influen

125 ted imaging of glutamatergic synapses in the lamella is facilitated by fluorescent pre- and postsynap

126 of living cells, whereas ER removal from the lamella is powered by actomyosin-based retrograde flow o

127 very thin amorphous layer on the crystalline lamella, just sufficient to accommodate a loop, but like

128 FA-1 that includes talin and encompasses the lamella/lamellipodial interface as well as further back

129 sed by oligodendrocytes and localizes to the lamella leading edge where actin polymerization is activ

130 CLEM-guided lamella preparation and in situ lamella lift-out procedures.

131 Hexagonally packed columnar structure or lamella-like columnar structure was obtained, depending

132 of wound healing, with reduced appearance of lamella-like membrane protrusions at the cell leading ed

133 Among them, the lamella-like structure with a diacetylene unit closer to

134 Lamella micromachining by focused ion beam milling at cr

135 MTs in the leading lamella move rearward relative to the substrate, as has

136 GSK3beta-induced lamella MT destabilization was partially rescued by expr

137 constitutively active GSK3beta destabilizes lamella MTs by disrupting lateral MT interactions with t

138 The plus ends of lamella MTs persist in growth perpendicular to the leadi

139 both plus end tracking and association along lamella MTs, we show that partial phosphorylation of the

140 sed spatial overlap of the lamellipodium and lamella networks and reduced cell-edge protrusion effici

141 al surface),7.0 mm in diameter, with a donor lamella obtained by microkeratome-assisted dissection, p

142 anism by which caspase 8 is recruited to the lamella of a migrating cell, promoting cell migration in

143 icate that ColXVII-actinin4 complexes at the lamella of a moving keratinocyte regulate actin dynamics

144 eal-space observation of skyrmion tubes in a lamella of FeGe using resonant magnetic x-ray imaging an

145 lls, MT turnover is increased twofold in the lamella of HGF-treated cells but unchanged in the retrac

146 ase (MRCK) has been shown to localize to the lamella of mammalian cells through its interaction with

147 This contrasts MTs in the lamella of migrating cells at the noncontacted leading e

148 MLCK is highly active in the lamella of migrating cells, but not at the retracting ta

149 flow rearward as occurs in the leading edge lamella of migrating cells.

150 olic distribution, caspase 8 is recruited to lamella of migrating cells.

151 radial (dorsal) stress fibers at the leading lamella of migrating renal epithelia.

152 apparent apoptosis in and under the cornoid lamella of PMVK-deficient lesional tissues, with incompl

153 ort a systematic study of melting of layered lamella of silver alkanethiolates (AgSCn).

154 Dividing the posterior lamella of the internal oblique aponeurosis and TAR was

155 rectus dissection, division of the posterior lamella of the internal oblique aponeurosis, and transve

156 f -82.56% (0.68%), incision of the posterior lamella of the internal oblique with a change of -17.67%

157 of -3.04% (2.42%), incision of the posterior lamella of the internal oblique with a change of -58.78%

158 ting the nucleus by envelopment at the inner lamella of the nuclear membrane.

159 lamella of the principal olive, the ventral lamella of the principal olive, and the rostral half of

160 ents from parts of, respectively, the dorsal lamella of the principal olive, the ventral lamella of t

161 termined scintigraphically ex vivo in a 1-cm lamella of the resected tumorous kidney.

162 omposite has been developed, wherein stacked lamellas of 1D vanadium pentoxide nanofibres, intercalat

163 ropulsive forces generated by the keratocyte lamella on both the ventral and the dorsal surfaces.

164 integrates the trajectories and dynamics of lamella open margin lattice components.

165 in the bulk of the film, consistent with the lamella orientation observed by GIWAXS, a more "edge-on"

166 organ shedding depends on the loss of middle lamella pectin in the abscission zone (AZ).

167 aulic response through size change of middle-lamella pectins.

168 ols such as multi-modal imaging, CLEM-guided lamella preparation and in situ lamella lift-out procedu

169 nce our method reduces the time required for lamella preparation and minimizes the need for user inpu

170 Cryo focused ion beam lamella preparation is a potent tool for in situ structu

171 s labour-intensive and can require both cryo-lamella preparation through cryo-focused ion beam (FIB)

172 ted endothelial keratoplasty using posterior lamella prepared with a 300-mum head microkeratome (Mori

173 retrograde fluxes at focal adhesions in the lamella region.

174 rites by forming soft-hard organic-inorganic lamella reminiscent of the natural sea-shell material na

175 2) is critical for the formation of the disc/lamella rim in photoreceptor outer segments (OSs), but p

176 t because bubbles are thought to coalesce by lamella rupture as the "limiting capillary pressure" is

177 spectroscopic analysis that is performed on lamella samples.

178 IB) micromachining is used to prepare a thin lamella-shaped sample out of a frozen-hydrated cell for

179 iate in fruiting bodies illuminated from the lamella side, in sliced fruiting bodies, and in the stip

180 llagen XVII (ColXVII) is found in actin-rich lamella, situated behind the lamellipodium.

181 lls showed altered localization of a leading lamella-specific marker, talin, and a uropod-specific ma

182 Importantly, we discover that the lamella structure can be fine-tuned using organic ligand

183 eserved even in the absence of RDS, rim, and lamella structures.

184 the notochord and lie beneath the epidermal lamella (subepidermal fibroblasts).

185 in bundle retrograde movement at the site of lamella, such that actin bundle movement is enhanced mor

186 he dorsal (0.4 nN/microm(2)) surfaces of the lamella, suggesting that dorsal matrix contacts are as e

187 which are regularly connected by pillars as lamella support.

188 e that extends to a depth of 60 nm from each lamella surface.

189 mbly at adhesions but retained a contractile lamella that generated large tension on adhesions.

190 ary cell wall and are abundant in the middle lamella that holds plant cells together.

191 ely fluorescently labeled lipid droplets, in lamellas that are 300 nm thick.

192 ion of the corresponding "twin" granule cell lamella, thereby lateralizing and amplifying the influen

193 can move through the crystal as evidenced by lamella thickening without disturbing the crystalline or

194 Between 1 and 12 months postoperatively, the lamella thickness (mean +/- SD) changed from 112 +/- 27

195 ly after preparation at the cornea bank, the lamella thickness decreased by 12% after 12 months.

196 mated endothelial keratoplasty (DSAEK) donor lamella thickness during the first postoperative year an

197 Donor lamella thickness in 41 eyes undergoing DSAEK for Fuchs

198 metry shows stepwise increases in Tm, as the lamella thickness increases by integer increments of cha

199 repeatability of the spatial resolution and lamella thickness.

200 will negate the potential improvements from lamella thinning beyond 90 nm.

201 -guided FIB fabrication of a frozen-hydrated lamella to address this problem: we built a coincident t

202 the cortical actin network feeds back on the lamella to help regulate actin flow speed and leading-ed

203 Here, we show a lamella-to-toroid transition, captured through the disso

204 ide an excellent thermal stability for these lamellas up to 350 degrees C.

205 Anterior and posterior lamella was obtained using 60 kHz and 150 kHz FS laser.

206 n in the apical cortex is transmitted to the lamella where force-sensitive FAs start to grow.

207 ead increased in the thickened region of the lamella where myosin condensation has been observed.

208 h stimulation both within and outside of the lamella where the mossy cell ablation took place.

209 ction of the second colocalized network, the lamella, where actomyosin contraction was integrated wit

210 ium lying along the proximal portion of each lamella, where it attaches to the midline raphe.

211 proteins affect the integrity of the middle lamella, which controls cell-to-cell adhesion and thus i

212 and elaborate architecture of equally spaced lamellas, which are regularly connected by pillars as la

213 ed by an elongate cell body with an anterior lamella whose cell edge is divided into protrusion-formi

214 consisted of 9-mm DALK and MK (9-mm anterior lamella with 6-mm posterior lamella).

215 reorganizes into a concentric lamellipod and lamella with retrograde actin flow that helps regulate t