ライフサイエンスコーパス: lamellae

1 tecture (e.g., parallel fibers, intertwined, lamellae).

2 alized collagen fibrils arranged in distinct lamellae.

3 s denoted glycodendrimercubosomes, and solid lamellae.

4 ial elongation via the addition of new basal lamellae.

5 the ratio of components recycled from older lamellae.

6 s are only detectable in nuclei and annulate lamellae.

7 es and concentrates solute molecules between lamellae.

8 onships, including disruption of the elastic lamellae.

9 d functional domains called grana and stroma lamellae.

10 ion on myosin II assembled into leading-edge lamellae.

11 an syndrome: fragmentation of aortic elastic lamellae.

12 rotypic GJs with oligodendrocytic somata and lamellae.

13 erlaid normal orthogonally arranged collagen lamellae.

14 parallel arrays similar to those of stromal lamellae.

15 f dysmorphic membranous structures devoid of lamellae.

16 lGAP abrogates ROCK-dependent suppression of lamellae.

17 in CNS oligodendrocytes and outermost myelin lamellae.

18 arrangement to the linear system of parallel lamellae.

19 ribution of total and preferentially aligned lamellae.

20 g virion de-envelopment at the outer nuclear lamellae.

21 nts had straight thylakoids but lacked grana lamellae.

22 eaviest caudally in laterally placed, curved lamellae.

23 ption of stratum corneum intercellular lipid lamellae.

24 growth factor-induced extension of membrane lamellae.

25 ilient framework for the intercellular lipid lamellae.

26 netration of microtubules into highly active lamellae.

27 esent throughout the stroma between collagen lamellae.

28 ich are composed of multiple, closely packed lamellae.

29 arying by ~30 to 90 degrees between adjacent lamellae.

30 compression machine localized to the base of lamellae.

31 at the same time, a continued production of lamellae.

32 ere prominently associated with the annulate lamellae.

33 ss a lipid bilayer located between two water lamellae.

34 roscopy of up to six distinct microfibrillar lamellae.

35 , and progressive destruction of the elastic lamellae.

36 ng in the formation of curved and concentric lamellae.

37 integrin also reduce the size and number of lamellae.

38 cm(2)) are approximately 70-fold softer than lamellae.

39 ed initially by actin purse strings and then lamellae.

40 f large, flat, cytoplasmic extensions termed lamellae.

41 and the formation of the extracellular lipid lamellae.

42 rrays, sheets with solvent-filled pores, and lamellae.

43 e in inter-planar spacing of the crystalline lamellae.

44 by a change in morphology of semicrystalline lamellae.

45 s the space between adjacent surfaces of two lamellae.

46 rotational intergrowths of single-unit-cell lamellae.

47 hexagonally packed cylinders and alternating lamellae.

48 of crystallographically co-oriented calcite lamellae.

49 e novo protein synthesis in unstacked stroma lamellae.

50 as smooth with mild scarring of the anterior lamellae.

51 on of iridescent color through microribs and lamellae.

52 ated to simultaneous twisting of anisometric lamellae.

53 Nrl(-/-)) exhibit balloon-like OSs devoid of lamellae.

54 rage, these vesicles are 49nm in radius with lamellae 8nm in thickness.

55 e of their ability to assemble into annulate lamellae, a cytoplasmic mimic of nuclear pores.

56 ence of misoriented, overlapping anisotropic lamellae, a kind of optical activity associated with the

57 sts (CEFs) localize beta-actin mRNA to their lamellae, a process important for the maintenance of cel

58 In filopodia and lamellae, a striking colocalization of the alpha6beta4 i

59 y, Xper5A11, labeled the closed rims of cone lamellae adjacent to the ciliary axoneme and the rims of

60 The formation of pseudopods and lamellae after ligation of chemoattractant sensitive G-p

61 Annulate lamellae (AL) are stacked ER-derived membranes containin

62 ynamics of an ER subdomain known as annulate lamellae (AL), a cytoplasmic nucleoporin-containing orga

63 specialized ER substructures called annulate lamellae (AL), where Ca(2+) release activity is attenuat

64 orm oversized and disorganized outer segment lamellae; although outer limiting membrane associations

65 gressive fragmentation of the aortic elastic lamellae and also display fragmentation of microfibrils

66 periodic structures consisting of undulating lamellae and alternating cylinders, with well-defined de

67 P96, and NUP93, had no affinity for annulate lamellae and assembled normally into nuclear pores.

68 eceded by extensive fragmentation of elastic lamellae and associated with elevated serine elastase ac

69 Electron microscopy revealed the lamellae and central core of the liposomes.

70 d particles were often associated with Golgi lamellae and cytoplasmic endomembrannes, but were rarely

71 ly be caused by the adherence of respiratory lamellae and epithelial proliferation obstructing respir

72 rial diseases are characterized by defective lamellae and excess SMCs; however, a mechanism linking t

73 e A colon carcinoma cells develop fan-shaped lamellae and exhibit random migration when plated on lam

74 nes form dysmorphic outer segments that lack lamellae and fail to associate properly with the cone ma

75 ich impaired adhesiveness of PLP-null myelin lamellae and fluctuations in osmolality in vivo might un

76 tegrins along the leading edge of fibroblast lamellae and growth cone filopodia.

77 These tubular OSs lack any stacked lamellae and have reduced phototransduction efficiency.

78 ipheral thylakoid protein enriched in stroma lamellae and is also present in grana.

79 py revealed the presence of CD63 on internal lamellae and of LAMP1 on the membrane surrounding the in

80 o-dimensional maps of the orientation of the lamellae and of the distribution of total and preferenti

81 cytosol to membrane ruffles at the edges of lamellae and promoted its colocalization with beta1 inte

82 PLIC-1 colocalized with G proteins in lamellae and pseudopods, and precipitated Gbetagamma in

83 onsists of circumferential layers of elastic lamellae and smooth muscle cells (SMCs), and many arteri

84 y increase in the number of rings of elastic lamellae and smooth muscle during arterial development.

85 cal increase of 35% in the number of elastic lamellae and smooth muscle in ELN +/- arteries.

86 individual demonstrated disorganized stromal lamellae and stromal staining with colloidal iron.

87 ce the appearance of PS on the outer bilayer lamellae and suggests that increases in intracellular Ca

88 ecreasing Rac activity suppressed peripheral lamellae and switched the cell migration patterns of fib

89 The eyelid lamellae and tarsal attachments of the levator aponeuros

90 crystallography, and microstructures of the lamellae and the phase relationships in this system is t

91 he invading solute is organized in stretched lamellae and the reaction is limited by mass transfer ac

92 orresponds with a reduction in the number of lamellae and the regularity of their ordering.

93 2/3 complex redistributes to the edge of the lamellae and to the Triton X-100-insoluble actin cytoske

94 entiation by stiffness of individual elastic lamellae and vascular smooth muscle.

95 ow is applicable to filter-feeding duck beak lamellae and whale baleen plates, as well as the fluid m

96 e alignment of collagen bundles and emergent lamellae and, we propose, plays a fundamental role in di

97 mouse platelets elaborate filopodia, spread lamellae, and assemble actin, identical to control WASp-

98 s pulposus, annulus fibrosus and constituent lamellae, and finer structures including collagen bundle

99 e further suggest that the striation-defined lamellae are a structural feature of a liquid crystallin

100 The self-supporting lamellae are apparently free of distortions or other art

101 The lamellae are derived from disk-like lipid membranes extr

102 lammation in vivo and show that Rac-mediated lamellae are essential for hemocyte motility and Rho sig

103 Thus, in normal animals, fixed CNS myelin lamellae are firmly adherent and resist separation; PLP-

104 Suberin lamellae are glycerolipid polymers covering the endoderm

105 Lamellae are initiated by parallel and partially redunda

106 ctron microscopy demonstrate that AD and ADA lamellae are made of a double layer of co-oligomers with

107 eys, thick myelin sheaths with more than ten lamellae are more common than in the young monkeys.

108 time that the dimensions and organisation of lamellae are responsible for the blue structural coloura

109 The single-layer AgSC10 lamellae are two-dimensional crystals and have uniform t

110 amic, actin-based protrusions (filopodia and lamellae) are critical, both in the mechanics of epithel

111 ayers of mineralized tissue are organized in lamellae around a central blood vessel.

112 In lamellae, Arp2/3 accumulation and polymerization correla

113 de their neighboring epidermal and notochord lamellae as part of the resorption process.

114 remodeling required to generate the barrier lamellae as well as for the reactions that result in des

115 However, cone lamellae assembly, albeit disorganized, concomitantly pe

116 ae of cone outer segments (COS) and the open lamellae at the base of rod outer segments (ROS).

117 he formation of Casparian strips and suberin lamellae at the endodermis limits the free diffusion of

118 The number of collagen lamellae between Descemet's membrane and most posterior

119 ree of through-plane interlacing of collagen lamellae between normal and mutant corneas.

120 rces and mechanical failure in regions where lamellae bifurcate.

121 cted by first an actin purse string and then lamellae, both of which serve to pull the surrounding ce

122 ectional area and straightens medial elastic lamellae but also induces profound remodelling of the ad

123 The stroma was organized into lamellae but lacked the anterior branching and interweav

124 ession is also required for the extension of lamellae, but not for the formation of filopodia.

125 ber of water molecules per headgroup for the lamellae, but they slow somewhat in the BC phase.

126 The thickness of the lamellae can be manipulated and systematically reduced t

127 the front evolves into a second regime where lamellae coalesce and form a mixing zone whose temporal

128 KL(4) to differentially partition into lipid lamellae containing varying levels of monounsaturation a

129 Membrane lamellae decorated with ribosomes were observed inside a

130 doing so, preserves the integrity of elastic lamellae despite the presence of high levels of proteina

131 Lamellae disassembled at low rates from the front to the

132 ence of myeloid bodies and peeling of myelin lamellae during the demyelination process.

133 ations for microfibrils motions in different lamellae during uniaxial and biaxial extensions.

134 K activity was required for the formation of lamellae, dynamic sites of motility, in carcinoma cells.

135 The epidermal wall contains ~100 lamellae, each ~40 nm thick, containing 3.5-nm wide cell

136 lesions and mineral deposition along elastin lamellae (elastocalcinosis).

137 alignment between the bacteria and collagen lamellae ex vivo (p < 0.001).

138 Water passing over the secondary lamellae exchanges gases with blood passing through the

139 This integrin's contribution to lamellae extension is most likely related to its localiz

140 o stacked grana regions and unstacked stroma lamellae for diffusion-based processes of the photosynth

141 PDE activities are both required to promote lamellae formation and chemotactic migration, our data i

142 t is regulated by cAMP and that functions in lamellae formation and migration.

143 interference RNA (siRNA) induce spontaneous lamellae formation and stimulate cell spreading on fibro

144 GF-stimulated chemotaxis and is required for lamellae formation on laminin-1.

145 actin-based Listeria movement, we find that lamellae formation requires a relatively small set of pr

146 ted alpha6beta4-dependent membrane ruffling, lamellae formation, and migration.

147 directed against the alpha6 subunit inhibit lamellae formation, indicating that redistribution of th

148 idently with the presence of Rds and partial lamellae formation.

149 grins and alpha3beta1 integrin contribute to lamellae formation.

150 ntains an extracellular matrix of orthogonal lamellae formed by parallel and equidistant fibrils with

151 ses with blood passing through the secondary lamellae, forming a system that has served as a classic

152 This control was demonstrated in a lamellae-forming poly(styrene-b-2-vinylpyridine) (PS-b-P

153 ome decompaction, i.e., separation of myelin lamellae from one another.

154 active index, cytoplasmic protein-containing lamellae from the low-index channels that are continuous

155 ing for the preparation of thin (200-500 nm) lamellae from vitrified cells grown on electron microsco

156 that included: a decreased number of elastic lamellae (from 6 to 4); altered area fraction of elastin

157 analysis of the mutants showed that suberin lamellae function as an apoplastic diffusion barrier to

158 rectal gland, stomach, intestine, olfactory lamellae, gill, and brain.

159 sted plywood) arrangement of collagen fibril lamellae has a key role in developing their unique prote

160 For pure n-C60H122 lamellae, however, suggestions of regular bands containi

161 contact with the ventral surface of the disc lamellae implies functional importance associated with t

162 osition of cell wall-associated suberin-like lamellae in both Arabidopsis thaliana and Nicotiana bent

163 ression led to the formation of suberin-like lamellae in both epidermal and mesophyll cells of leaves

164 vidence for the assembly of stacked annulate lamellae in Caenorhabditis.

165 gion of outer segment (OS) discs in rods and lamellae in cones requires functional retinal degenerati

166 in the altered organization of extracellular lamellae in epidermal cysts where the ester-linked chain

167 he collagen-rich adventitia and elastin-rich lamellae in intact rat arteries) which in turn can be se

168 nd projections are in medially placed curved lamellae in mid- and caudal pons.

169 eshadow the partitioning of PSI into stromal lamellae in plants, similarly sustained by long-distance

170 e for the mechanical collapse of the elastic lamellae in the aortic wall is also unknown.

171 /-) mice have an increased number of elastic lamellae in the ascending aorta and progressive aortic r

172 osa exploits the precise spacing of collagen lamellae in the central cornea to facilitate spread thro

173 rees ) but systematic splaying of individual lamellae in the film.

174 ith age, although the mean numbers of myelin lamellae in the sheaths increased from 5.6 in the young

175 al water loss, decreased intercellular lipid lamellae in the stratum corneum, and aberrant keratinocy

176 s, the diameters of axons and the numbers of lamellae in their myelin sheaths were determined.

177 erent and resist separation; PLP-null myelin lamellae, in contrast, are poorly adherent and more read

178 d N-terminus of SP-B in the packing of lipid lamellae into surfactant lamellar bodies or in stabilizi

179 issolution of homogalacturonan in the middle lamellae is augmented by an active biophysical process o

180 Fragmentation of the aortic elastic lamellae is characteristic of TAA.

181 small gap between the tips of the secondary lamellae is found to have a similarly strong effect on t

182 completely split so that one set of compact lamellae is surrounded by another set.

183 utational model of flow around the secondary lamellae is used to examine the hydrodynamic consequence

184 consistent with the hypothesis that suberin lamellae isolate the endodermal cell protoplast from the

185 ty, in contrast to conventional three-domain lamellae (LAM3) with ABCB periods.

186 in grana and its repair machinery in stroma lamellae: lateral shrinkage of grana diameter and increa

187 ctivity and decreased synthesis of the lipid lamellae lead to exacerbated breakdown of the epidermal

188 skin, which removes all of the extracellular lamellae, leaving the covalently attached lipids, showed

189 -density outer shell and lower-density inner lamellae-like layers that divide the core into compartme

190 ion in cell morphology with the formation of lamellae-like processes.

191 oretinal interface, which often consisted of lamellae-like structures of the condensed cortical vitre

192 ar membrane tubules and cytoplasmic annulate lamellae-like structures.

193 ratum corneum is provided by patterned lipid lamellae localized to the extracellular spaces between c

194 tion was due to intrusion of very thin glial lamellae (<0.3 microm in cross section).

195 the amorphous region between two crystalline lamellae M unit apart are modeled as random walks with o

196 quid-crystalline states in which crystalline lamellae made up of the coassembled proteorhodopsin and

197 , 94 (17.8%) were performed with young donor lamellae (mean donor age 49.31 +/- 6.35 years; range: 17

198 Therefore, F-actin is necessary for lamellae mechanics, but not sufficient.

199 d bilayer phase, i.e., plasmalemma and older lamellae (membrane recycling).

200 weeks); and a decreased area between elastic lamellae (minimum reached at 4 weeks).

201 Upon eyelid eversion, the 2 lamellae move as a unit and the postaponeurotic space re

202 a wealth of distinct morphologies, including lamellae, multi-lamellar vesicles, unilamellar vesicles,

203 ough endoplasmic reticulum containing linear lamellae of alternating electron-dense and electron-luce

204 re patterns in free-standing, single-crystal lamellae of BaTiO(3).

205 calization of beta-actin mRNA to the leading lamellae of chicken fibroblasts and neurite growth cones

206 y transmission electron microscopy show that lamellae of clinoenstatite are present in diopside grain

207 use sclera consisted of irregularly arranged lamellae of collagen fibrils with an average diameter of

208 ini of xlProminin-1 labeled the open rims of lamellae of cone outer segments (COS) and the open lamel

209 the trailing ends of Listeria moving in the lamellae of COS7 cells.

210 mposition of ECM materials in the trabecular lamellae of CS meshwork.

211 h, and cone outer segments were curved, with lamellae of heterogeneous sizes, defects also observed u

212 ogonal network of shorter actin filaments in lamellae of identically treated FLNa-expressing cells ca

213 Immediately distal to this initiation site, lamellae of increasing diameter are evident, indicating

214 issue, a three-dimensional reconstruction of lamellae of intervertebral disk is presented.

215 n beam milled defects in thin single crystal lamellae of KTiOPO4 (KTP).

216 The short-lived lamellae of M2 cells contain a dense mat of long actin f

217 measured actin turnover in lamellipodia and lamellae of migrating cells, using quantitative Fluoresc

218 nascent, focal complexlike structures in the lamellae of motile endothelial cells.

219 lin-specific molecule expressed on the outer lamellae of myelin.

220 PBTTT crystallizes with lamellae of pi-stacked polymer chains on both surfaces.

221 red VSMC as well as VSMC between the elastic lamellae of pig thoracic aorta were positive for polycys

222 red 10.15 +/- 3.6 microns composed of 5 to 8 lamellae of predominantly type-1 collagen bundles arrang

223 ing of endodermal cells that are enclosed by lamellae of suberin.

224 aortic medial ruptures, in which all elastic lamellae of the media were degraded and infiltrated with

225 staining was particularly strong between the lamellae of the spine apparatus.

226 led keratocytes, which reside in the fibrous lamellae of the stroma.

227 c antibodies localize throughout the leading lamellae of these cells at junctions between orthogonall

228 (POPC) lipid bilayer and placed between two lamellae of water.

229 a very limited set of morphologies, such as lamellae or hexagonally packed cylinders.

230 l to create specific specimen shapes such as lamellae or needles that can be analyzed further by tran

231 m) of nacre's building blocks, the aragonite lamellae (or platelets), and (ii) the imbricated, or sta

232 ase relationships in this system is that the lamellae originally exsolved as the high-pressure C-cent

233 mutants was significantly thinner with fewer lamellae (P < 0.05).

234 bacteria showed good alignment with collagen lamellae (P = 0.002).

235 agent, latrunculin A, softens and liquefies lamellae, physiological levels of F-actin, alone (11 +/-

236 Purse strings and lamellae produce a pulling force on surrounding cells, i

237 pling propagates across hundreds of membrane lamellae, producing long-range alignment of phase-separa

238 a indicate that mature disks are formed once lamellae reach full diameter, and the growth of a rim en

239 d number of FAs, their redistribution toward lamellae region, and an increase in cell tail length.

240 i of decompaction, but the great majority of lamellae remained compact.

241 to the loading environment; remarkably, most lamellae reorient towards the tensile axis and deform in

242 The extension of lamellae requires net actin assembly and an exposure of

243 r pore complexes from the cytosolic annulate lamellae reservoir, and expressed a set of nucleoporins,

244 nd corresponds to the gradient of interwoven lamellae seen in imaging of stromal cross-sections.

245 Stabilization occurs only for the mobile lamellae situated close to the free surface, and thus 2-

246 Lamellae splay as a consequence of space constraints rel

247 and the roles of PI 3-kinase and gelsolin in lamellae spreading.

248 elongated particles with an axially stacked lamellae structure are selectively prepared by utilizing

249 bles, suggesting defects in disassembly from lamellae subsequent to initial recruitment.

250 Lamellae subsequently spread between the projections.

251 ha6 integrins appear evenly distributed over lamellae surfaces.

252 stretching/sliding mechanisms, whereas other lamellae sympathetically rotate away from the tensile ax

253 proximately 5-fold more cytoplasmic annulate lamellae than control cells.

254 d or polygonal cells having broad, flattened lamellae that did not form long lamellar extensions.

255 dial extension and stabilization followed by lamellae that extend in the direction of stabilized filo

256 tacked grana thylakoids and unstacked stroma lamellae that is challenged by the tight stacking and lo

257 ctivity promoted the formation of peripheral lamellae that mediated random migration.

258 EO crystallizes as single, high-aspect-ratio lamellae that resemble single crystals.

259 -fold), and was composed of 5 to 11 collagen lamellae that revealed keratocytes on their anterior sur

260 ading in which oligodendrocytes extend large lamellae that spiral around axons to form myelin.

261 The PC is comprised of lamellae that surround the nerve fiber at its core.

262 ered by plate-like structures, the secondary lamellae, that provide the bulk of the respiratory surfa

263 As marginal cells produce lamellae, their basal type II hemidesmosomes disappear a

264 ane protrusions that extend between adjacent lamellae, thereby initiating a disk rim.

265 ks, control the sizing of rod disks and cone lamellae throughout their daily renewal.

266 f the reflectin-containing subcellular Bragg lamellae to change the brightness and color of reflected

267 ical layering of micro- and nanoscale silica lamellae to create a high-surface-area and low-shear sub

268 lly, the Bouligand-type structure allows the lamellae to reorient in response to the loading environm

269 h-velocity stretching of engineered arterial lamellae to simulate the mechanical forces of a blast pu

270 ceeds from a collection of water-poor planar lamellae, to a water-rich interconnected layer-phase and

271 ed by the Casparian strip and by the suberin lamellae, two hydrophobic barriers that restrict the fre

272 fuse to form a giant syncytium, which sends lamellae under the scab to re-epithelialize the damaged

273 te and subsequently anchored in chain-folded lamellae upon crystallization, are responsible for this

274 The periodicity of the polymer lamellae varies from 20 to 150 nm.

275 layer-phase and then a collection of closed lamellae (vesicles) that form a close-packed gel.

276 spheres, cylinders, bicontinuous structures, lamellae, vesicles, and many other complex or hierarchic

277 The ability of SP-B(1-25) to fuse lipid lamellae via this mechanism, particularly those enriched

278 oconus the gross organization of the stromal lamellae was dramatically changed, and the collagen fibr

279 Spontaneous formation of concentric lamellae was observed in self-assembling giant surfactan

280 the adhesiveness of PLP-null compact myelin lamellae we soaked aldehyde-fixed CNS specimens from PLP

281 In the case of lamellae, we detected actin suspension cables that appea

282 These curved/concentric lamellae were observed in FPOSS-based giant surfactants

283 In this study, in which posterior lamellae were prepared using a 300-mum head microkeratom

284 hus drive their aggregation into the stacked lamellae, where the residual hydrophobic mismatch betwee

285 tic wall characterized by fragmented elastic lamellae, whereas mice homozygous for the human allele d

286 ption of fibril spacing within the posterior lamellae, whereas the mid and anterior regions appeared

287 ponents of the stratum corneum extracellular lamellae, which regulate cutaneous permeability barrier

288 became thicker overall and were comprised of lamellae widely separated from one another by irregular

289 llular electron-lucent material and parallel lamellae with an undulated course.

290 Profiles obtained from lamellae with cholesterol sulfate partially substituted

291 PLA and PnBA, the side chains segregate into lamellae with domain spacing of 14 nm as measured by SAX

292 these MMs self-assembled into highly ordered lamellae with domain spacing over 100 nm.

293 c trans-membrane peptide localized in stroma lamellae with its highly conserved C terminus exposed to

294 embrane rupture and dilaceration of collagen lamellae with large fluid-filled intrastromal cysts; 5b,

295 Whereas wild-type cells extend lamellae within 30 min after plating, all of the calpast

296 e of the extensive network of photosynthetic lamellae within Prochlorococcus and the potential pathwa

297 causes the LMOGs to aggregate, probably into lamellae within the fibrils that constitute the basic un

298 lla and simultaneously from widely separated lamellae within the olfactory organ suggest that PWs are

299 ot been synthesized previously, most pack in lamellae within their solid phases.

300 identical cone-like morphology of stacks of lamellae without a continuous surrounding plasma membran