ライフサイエンスコーパス: meshwork

1 e in the Schlemm's canal (SC) and trabecular meshwork.

2 links on the nuclear envelope and the lamin meshwork.

3 ate at the Golgi and form a dense non-radial meshwork.

4 s performed to 360 degrees of the trabecular meshwork.

5 in combination with a model keratocyte actin meshwork.

6 ncapsulate agarose in the form of a gel-like meshwork.

7 outflow obstruction distal to the trabecular meshwork.

8 ior cornea initiating beneath the trabecular meshwork.

9 acaques by laser treatment to the trabecular meshwork.

10 ctility of the cortical membrane-bound actin meshwork.

11 pigmentary dispersion within the trabecular meshwork.

12 nal with no visible damage to the trabecular meshwork.

13 acaques by laser treatment to the trabecular meshwork.

14 e gelled into a tightly linked, low mobility meshwork.

15 single lamin filaments in three-dimensional meshwork.

16 res, Schlemm's canal (SC) and the trabecular meshwork.

17 ility of the break to traverse the chromatin meshwork.

18 tile stress generated by the platelet-fibrin meshwork.

19 ciliary muscle (46 +/- 5.6%) and trabecular meshwork (37 +/- 8.3%) of treated eyes relative to vehic

20 ose found in normal (5 kPa) and glaucomatous meshworks (75 kPa), or tissue culture polystyrene (TCP;

21 These lamin meshworks additionally play a role in gene expression.

22 The actin meshwork also positions an actin bundle network that org

23 -dependent adhesion organizes the microvilli meshwork and ensures the proper attachment of RCs to the

24 oplasmic giantin-based intermediate filament meshwork and in cytoplasmic bodies.

25 rats was associated with fibrotic trabecular meshwork and increased levels of F-actin, phosphorylated

26 lating DN-Ts are trapped within stromal cell meshwork and interfere with correct localization of MZ B

27 link the plasma membrane and cortical actin meshwork and mediate the dynamic nature of the membrane-

28 showed that chromatin decondensation, lamin meshwork and NE rupture and extracellular DNA release re

29 dversely affect the health of the trabecular meshwork and outflow resistance.

30 aqueous humor outflow through the trabecular meshwork and Schlemm's canal (SC) is the most important

31 hin human retina, optic nerve and trabecular meshwork and that ABCA1 and AFAP1 are also expressed in

32 sicles are enmeshed in an apical cytokeratin meshwork and that Rab11a likely acts upstream of Rab8a t

33 nvelope (NE) permeabilization, nuclear lamin meshwork and then NE rupture to release DNA into the cyt

34 actin cytoskeleton is organized into diverse meshworks and bundles that support many aspects of cell

35 to the anterior chamber angle and trabecular meshwork, and reduced postoperative use of steroids.

36 ams, plate-like structures and fibers of the meshwork, and within tissue gaps and pores.

37 reconfigurations of macromolecules, fibers, meshworks, and membranes.

38 bjects were analyzed to determine trabecular meshwork anteroposterior length and 3 anterior chamber a

39 cant positive association between trabecular meshwork anteroposterior length and all anterior chamber

40 cant positive association between trabecular meshwork anteroposterior length and all anterior chamber

41 evaluate the association between trabecular meshwork anteroposterior length and anterior chamber ang

42 Mean trabecular meshwork anteroposterior length was 824.86 +/- 181.77 mu

43 angle is associated with greater trabecular meshwork anteroposterior length.

44 ng, en face choriocapillaris images showed a meshwork appearance.

45 heral smooth muscle layers to form a tubular meshwork arborizing the gut wall.

46 Amoeboid microglia and disrupted astrocyte meshwork are consistent traits in aged CNS.

47 lamins A/C or lamin B1, the remaining lamin meshworks are altered compared with the lamin meshworks

48 The model, which approximates the actin meshwork as a visco-active gel exerting forces on a rigi

49 in ionically cross-linked MDP into a fibrous meshwork as determined by scanning and transmission elec

50 utilize graphene, a single-atom-thick carbon meshwork, as the thinnest possible impermeable and condu

51 y hypomorphic Schlemm's canal and trabecular meshwork, as well as elevated IOP, demonstrating that an

52 Successive reorganization of an F-actin meshwork, associated with microtubular structures, is ac

53 e perpendicular distance from the trabecular meshwork at 500 mum and 750 mum anterior to the scleral

54 to SMLM, in the context of the fibrous actin meshwork at the T cell immunological synapse, whose stru

55 data showed a crucial role for a contractile meshwork at the top of the cell, which is composed of ac

56 define the architecture of the nuclear lamin meshworks at molecular resolution, providing insights in

57 (w/v) readily diffused through the vitreous meshwork; at higher concentrations (~0.1% w/v), these na

58 How a tubular axonal meshwork becomes established without invading centrally

59 Lamin proteins form a meshwork beneath the nuclear envelope and contribute to

60 nt proteins that assemble into a filamentous meshwork, bridging the nuclear envelope and chromatin.

61 ntain the high density of actin filaments in meshwork by keeping actin filaments close enough for cro

62 le, or mechanical blockade of the trabecular meshwork by protein aggregates or contaminant particles

63 A disrupted the formation of the microfibril meshwork by the cells.

64 restructuring and constraining the spectrin meshwork can fully account for the observed changes in d

65 structures that resemble clumps, stars, and meshworks can appear in the process of ring assembly.

66 stic forces transmitted by the peptidoglycan meshwork cause the moving dislocations to interact not o

67 primary cultures of living human trabecular meshwork cells (hTMC) without the application of exogeno

68 vitro by infecting primary human trabecular meshwork cells and in vivo by injecting living rats intr

69 ork, which is a scenario toxic to trabecular meshwork cells and leads to early onset of ocular hypert

70 d several other ECM components in trabecular meshwork cells from the anterior segment of the eye was

71 By visual inspection, human trabecular meshwork cells infected with scAAV2.dnRhoA showed dimini

72 misfolding and aggregation within trabecular meshwork cells, and ultimately, ER stress-induced cell d

73 increase oxidative damage to the trabecular meshwork cells, resulting in elevation of intraocular pr

74 yocilin toxicity in primary human trabecular meshwork cells.

75 d TAZ are both expressed in human trabecular meshwork cells.

76 of NTRs, penetrate more readily into the FG-meshwork compared to their globular counterparts of iden

77 Our data suggest that a perinuclear actin meshwork connects actin cables to nuclei via actin-cross

78 Mammalian lamin meshworks consist of two types of lamin proteins, A type

79 rround themselves with a cell wall, a strong meshwork consisting primarily of the polymerized aminosu

80 dicted that actin filaments of the endocytic meshwork continually polymerize and disassemble, turning

81 tracellular matrix expression and trabecular meshwork contractility appears to coordinately impact ou

82 n silico model of two-dimensional actomyosin meshwork contraction, demonstrating that actomyosin mesh

83 When the meshwork contracts, it pulls the dorsal fibers away from

84 Thus, preventing this opening of the meshwork could be a route to prevent bleb formation, whi

85 t we use to investigate which aspects of the meshwork could be responsible for bleb formation.

86 aterial consisting of a porous elastic solid meshwork (cytoskeleton, organelles, macromolecules) bath

87 , which move faster as the surrounding actin meshwork decreases in size over time.

88 Our study also suggests that these MyosinII meshworks drive cell shape changes in response to extern

89 rization of cellular fibronectin (FN) into a meshwork drives endothelial cell (EC) polarity and vascu

90 agination and because of entanglement of the meshwork due to its dendritic structure and cross-linkin

91 tide crosslinks to allow expansion of the PG meshwork during growth.

92 k contraction, demonstrating that actomyosin meshworks exhibit an inherent force orienting mechanism

93 yocilin is a protein found in the trabecular meshwork extracellular matrix tissue of the eye that pla

94 uclei lacking LA/C exhibit slightly enlarged meshwork faces and some shape changes, whereas LB1-defic

95 ientation, we can distinguish between fibril meshworks, fibril bundles, and amyloid stars.

96 ned as nonvisibility of posterior trabecular meshwork for at least 2 quadrants.

97 m regions within the uveal and corneoscleral meshwork for image acquisition pairs of AF-SHG (without

98 oA knockout reduced fibroblast branching and meshwork formation and resulted in more compactly cluste

99 ture medium not only rescued the microfibril meshwork formation in LTBP2-suppressed ciliary epithelia

100 rane microdomains induce actin-microfilament meshwork formation, anchoring microtubules that grow rad

101 The filamentous meshwork formed by the lamin nucleoskeleton provides a s

102 mber of edges per face, suggesting that each meshwork has somewhat unique assembly characteristics.

103 ted in regions where the fibers in the lamin meshwork have a greater separation, and we find that thi

104 In this clinic-based population, trabecular meshwork height is shorter in PACG patients compared to

105 Trabecular meshwork height was measured from the scleral spur to th

106 Unexpectedly, an F-actin meshwork helps to tear down the large nucleus of starfis

107 rin red staining in primary human trabecular meshwork (HTM) cells and alkaline phosphatase (ALP) acti

108 ed from primary cultures of human trabecular meshwork (HTM) cells has confirmed secretion of ATX and

109 mine if oxidative stress on human trabecular meshwork (HTM) cells influences the stability of key mRN

110 Human trabecular meshwork (HTM) cells were cultured on hydrogels possessi

111 humor outflow and a stiffer human trabecular meshwork (HTM).

112 human cortical neuronal (HCN-1A), trabecular meshwork (HTMC), and pulmonary artery smooth muscle (PAS

113 egrity, leads to the collapse of the laminB2 meshwork, impairs neuronal survival, and markedly reduce

114 inability to visualize pigmented trabecular meshwork in 3 or more quadrants.

115 istance to AH outflow through the trabecular meshwork in ocular hypertension patients.

116 emonstrated a fully developed parietal actin meshwork in SEs.

117 Oxidative stress/damage to the trabecular meshwork in such post-vitrectomy cases may contribute to

118 ereas the MT cytoskeleton resembles a random meshwork in the cells' interior, MTs near the cell surfa

119 enriched in the smooth muscle and trabecular meshwork in the eye.

120 mbly, before the appearance of a dense actin meshwork in the initial segment, and before dendrites ac

121 el for modulation of a dynamic actin-vesicle meshwork in the oocyte at the origin of asymmetric posit

122 ther polarized actin arrays, nor dense actin meshworks in the AIS.

123 eshworks are altered compared with the lamin meshworks in wild-type nuclei or nuclei lacking lamin B2

124 n cross-members and the size of the skeletal meshwork increase in developing gametocytes, then decrea

125 fication inducer BMP2 gene to the trabecular meshwork induces elevated IOP in living rats without alt

126 rstood but has been attributed to trabecular meshwork injury from repeated injections, a potential to

127 ed rat hippocampus are affected by astrocyte meshwork integrity: evidence of a novel cell-cell interg

128 Although a simple neuronal meshwork interconnects the developing islet clusters as

129 us humor (AH) outflow through the trabecular meshwork is a primary risk factor for open-angle glaucom

130 re and open up after electroporation and the meshwork is expelled through a macropore.

131 The FG-meshwork is locally disrupted upon interacting with NTR-

132 Graph theory analysis shows that the lamin meshwork is not a random arrangement of filaments but ex

133 The contractile actin meshwork is organized like muscle sarcomeres, with repea

134 quantitative analysis reveals that the actin meshwork is organized radially and is compacted by the c

135 aqueous drainage tract distal to trabecular meshwork is potentially an important determinant of intr

136 nced glaucoma suggesting that the trabecular meshwork is the primary impediment to outflow and its ab

137 r crosslinking to the existing peptidoglycan meshwork is unclear.

138 ng showed that EPL1 assembles into irregular meshwork-like substructures.

139 blocks of the nuclear lamina, a filamentous meshwork lining the nucleoplasmic side of the inner nucl

140 d above the cuticular plate, a dense F-actin meshwork located underneath the apical plasma membrane.

141 ting fibrotic activity within the trabecular meshwork may result in ocular hypertension, we investiga

142 tion in native NPCs over the porous hydrogel meshwork model.

143 it is difficult to dissect mouse trabecular meshwork (MTM) tissues and establish MTM cell strains.

144 Metabolism of this PG meshwork must be spatially and temporally regulated in o

145 angles were defined as posterior trabecular meshwork not visible for >/=2 quadrants on non-indentati

146 e aligned in tightly bundled chains within a meshwork of astrocytes; however, the cell-cell cues that

147 ) makes it possible to investigate the dense meshwork of axons, dendrites, and synapses that form neu

148 oplasmic astrocytes develop a dense ramified meshwork of cellular processes to form intimate contacts

149 llular matrix (ECM) is a complex and dynamic meshwork of cross-linked proteins that supports cell pol

150 pulation, the astroglia, which forms a dense meshwork of cytoplasmic projections.

151 of neutrophil extracellular traps (NETs), a meshwork of decondensed chromatin lined with histones an

152 largely consisting of T cells embedded in a meshwork of epithelial cells, with no direct resemblance

153 bound compartments, which accumulate a dense meshwork of F-actin through the kinase activity of the S

154 clots develop a remarkable structure, with a meshwork of fibrin and platelet aggregates on the exteri

155 components of the nuclear lamina, a dynamic meshwork of intermediate filaments lining the nuclear en

156 The nuclear lamina-a meshwork of intermediate filaments termed lamins-is prim

157 ssociated with a novel cytoplasmic reticular meshwork of intermediate filaments.

158 nuclear morphology is the nuclear lamina, a meshwork of intermediate lamin filaments that lines the

159 cal effects pertaining to the formation of a meshwork of interpenetrating HA polymer chains are respo

160 Our work thus identifies the K-fiber meshwork of linked multipolar connectors as a key integr

161 The cell wall, composed of a simple meshwork of long glycan strands crosslinked by short pep

162 n of mechanical stress along the protein/DNA meshwork of meiotic chromosome axes, with topoisomerase

163 sin-1 are initially directed by a disordered meshwork of microtubules, generating minor slow cytoplas

164 agulation was then applied to the trabecular meshwork of one eye to induce chronic elevation of intra

165 agulation was then applied to the trabecular meshwork of one eye to induce chronic elevation of IOP a

166 agulation then was applied to the trabecular meshwork of one eye to induce chronic unilateral IOP ele

167 tensive colocalization of both proteins in a meshwork of perinuclear filamentous structures.

168 The skin is also innervated by a meshwork of peripheral nerves consisting of relatively s

169 The peptidoglycan (PG) sacculus, a meshwork of polysaccharide strands cross-linked by short

170 al extracellular matrix (ECM), an interwoven meshwork of proteins, glycoproteins, proteoglycans, and

171 osterior zonular fibers consisted of a dense meshwork of radially oriented microfibrils that we terme

172 vealed that RPMs are embedded in a reticular meshwork of red pulp fibroblasts characterized by the ex

173 lel bundles with low connectivity to a tight meshwork of short filaments.

174 erved in large fish and amphibian eggs are a meshwork of short, unstable microtubules maintained by a

175 We show that the quality of the BM stromal meshwork of SMZL infiltrates correlates with time to pro

176 cell membrane skeleton is a pseudohexagonal meshwork of spectrin, actin, protein 4.1R, ankyrin, and

177 Because the endothelial surface layer, a meshwork of surface-bound and loosely adherent glycosami

178 n levels in the aqueous humor and trabecular meshwork of Tg-MYOC(Y437H) mice.

179 arrest of compaction of the loose interwoven meshwork of the fetal myocardial primordium and subseque

180 t spanin-mediated fusion is regulated by the meshwork of the PG, thus coupling fusion to murein degra

181 atial boundaries within the dense astroglial meshwork of the SVZ and rostral migratory stream (RMS),

182 Biological networks are composed of a meshwork of thin filaments that span large volumes of ti

183 f ERK1/2 was also observed in the trabecular meshwork of transgenic mice expressing 6-fold higher lev

184 -bundling activities; the formation of large meshworks of Coro1A(E26K)-decorated filaments endowed wi

185 ructural stability of the nucleus comes from meshworks of intermediate filament proteins known as lam

186 e-it module is illustrated by application to meshworks of nuclear lamin A, minifilaments of myosin II

187 imate forces exerted by a polymerizing actin meshwork on an invagination of the plasma membrane durin

188 st 180 degrees (visible posterior trabecular meshwork on gonioscopy) after laser iridotomy.

189 ent on filopodial protrusions appearing as a meshwork on the cell surface, which colocalized with CXC

190 directly study proposed effects of an actin meshwork on the diffusion in a well-defined system.

191 Visualization of the actin meshwork openings at the immunologic synapse revealed th

192 CA1 and PMM2 are expressed in the trabecular meshwork, optic nerve and other ocular tissues.

193 attice-like) gluing within the extracellular meshwork or synaptogenesis.

194 ace lies close to regions leading to clumps, meshworks or double rings, and stars/cables.

195 types of insoluble organic matrices: chitin meshworks, organic microrings, and organic microplates,

196 a crescent interest in increasing trabecular meshwork outflow by extracellular matrix remodeling and/

197 of new agents that act mainly on trabecular meshwork outflow may be the future hypotensive treatment

198 citatory synapses and in other dense protein meshworks, owing to an impeded diffusion of the ~3,000-k

199 ormality, pupil edge pigment, and trabecular meshwork pigment.

200 t of missing ruff (P = 0.001) and trabecular meshwork pigmentation (P = 0.006).

201 s (8/10) showed moderate to heavy trabecular meshwork pigmentation and either Krukenberg spindle or t

202 llumination defects, and/or heavy trabecular meshwork pigmentation.

203 y increasing the connectivity of the F-actin meshwork, plastin enables the cortex to generate stronge

204 scent TM structures and filled corneoscleral meshwork pores.

205 of glaucoma, pigmentation of the trabecular meshwork (PTM), total energy delivered, and baseline int

206 inted-end rootlets anchored in a filamentous meshwork referred to as the "terminal web." Although cla

207 How such intricate meshwork relates to function and gives rise to a transpo

208 d bilayer that is strengthened by an elastic meshwork representing the cytoskeleton.

209 e uveal (UV), CS, and juxtacanalicular (JCT) meshwork, respectively, were captured at different depth

210 complication may be injury to the trabecular meshwork resulting from rapid elevations in IOP.

211 d a network of domains behaves rather like a meshwork, resulting in hop diffusion.

212 The trabecular meshwork's (TM) physiological role is to maintain normal

213 Trabecular meshwork size may play a role in ethnic differences of g

214 Human trabecular meshwork stem cells (TMSCs) were isolated as side popula

215 azole-sensitive clusters of the cytoskeletal meshwork surrounding SG.

216 red for formation of the cytoplasmic F-actin meshwork that controls the central position of the spind

217 late assembly of a dynamic cytoplasmic actin meshwork that facilitates translocation of the meiotic s

218 s the basic constituent of the proteinaceous meshwork that is localized between adjacent cytoplasmic

219 tically organize a dynamic cytoplasmic actin meshwork that mediates translocation of the spindle towa

220 F-actin imaging revealed a cytoplasmic meshwork that might restrict transport in a size-depende

221 protein (ARP)2/3 complex generates an actin meshwork that operates within a tip-localized, microtubu

222 ermediate filaments (DIFs) form an intricate meshwork that organizes myofibers within striated muscle

223 orming a porous and highly dynamic polymeric meshwork that percolates in radial and axial directions

224 mutant of FAK led to disruption of the actin meshwork that resulted in sequestration of IAV at the ce

225 lular matrix (ECM) provides an architectural meshwork that surrounds and supports cells.

226 s typically defined as a thin layer of actin meshwork that uniformly underlies the plasma membrane of

227 rA family assembles into a three-dimensional meshwork that uses the nucleoid as a scaffold and period

228 from Def(++) mice were composed of a fibrin meshwork that was denser and contained a higher proporti

229 a minimal continuum elastic model of a lamin meshwork that we use to investigate which aspects of the

230 f molecular processes (expansions of protein meshworks) that are required for degradation of protein

231 of the most abundant genes in the trabecular meshwork, the eye tissue responsible for maintenance of

232 ents may be more localized to the trabecular meshwork, therefore making GATT a particularly suitable

233 Immunostaining of trabecular meshwork tissue after exposure to 4MU showed an altered

234 Trabecular meshwork tissue showed moderate ALP activity at 13 days

235 luation revealed a well-organized trabecular meshwork tissue, exhibiting denser matrix in the treated

236 nd in the extracellular matrix of trabecular meshwork tissue, the anatomical region of the eye involv

237 sed in most tissues including the trabecular meshwork (TM) and heterozygous Sod2 knockout mice exhibi

238 tors in primary cultures of human trabecular meshwork (TM) and Schlemm's canal (SC) cells were determ

239 al outflow pathway comprising the trabecular meshwork (TM) and Schlemm's canal (SC).

240 The IOP is maintained by the trabecular meshwork (TM) and the elevation of IOP in open-angle gla

241 Various changes in the trabecular meshwork (TM) are responsible for elevated IOP.

242 Primary cultures of human trabecular meshwork (TM) cell monolayers were treated with dexameth

243 n and distribution of MRP4 in the trabecular meshwork (TM) cells and its role in homeostasis of IOP.

244 n the modulation of the volume of trabecular meshwork (TM) cells and, in turn, the aqueous humour (AH

245 (ECM) proteins were evaluated in trabecular meshwork (TM) cells by cDNA microarray, q-PCR, fluoresce

246 determine whether cultured human trabecular meshwork (TM) cells express BMP1, BMP1 expression is reg

247 s by compromising the function of trabecular meshwork (TM) cells in the anterior eye, but how these c

248 hyme-like transition (Endo-MT) of trabecular meshwork (TM) cells is known to be associated with prima

249 We have previously shown that trabecular meshwork (TM) cells might detect aqueous humor fluid she

250 age of the phagocytic property of trabecular meshwork (TM) cells, and developed a novel magnetic bead

251 expression and secretion by human trabecular meshwork (TM) cells.

252 ogical mechanisms of glaucomatous trabecular meshwork (TM) damage and elevation of intraocular pressu

253 open angle glaucoma and is due to trabecular meshwork (TM) damage, which leads to impaired aqueous hu

254 files of control and glaucomatous trabecular meshwork (TM) derived from human donors.

255 Aberrant remodeling of trabecular meshwork (TM) extracellular matrix (ECM) may induce ocul

256 nduced myocilin expression in the trabecular meshwork (TM) has been suggested to play an important ro

257 To determine if trabecular meshwork (TM) height differs between primary open-angle

258 ever, their potential role in the trabecular meshwork (TM) in the eye, which regulates intraocular pr

259 Trabecular meshwork (TM) is a highly mechanosensitive tissue in the

260 The trabecular meshwork (TM) is a specialized ocular tissue, which is r

261 The trabecular meshwork (TM) is an ocular tissue that maintains intraoc

262 ular matrix (ECM) proteins in the trabecular meshwork (TM) is associated with TM dysfunction and intr

263 ip between SPARC and TGF-beta2 in trabecular meshwork (TM) is unknown.

264 nges in the unlasered portions of trabecular meshwork (TM) of laser-treated primate eyes are understu

265 Because the trabecular meshwork (TM) plays an important role in aqueous outflow

266 Given that the trabecular meshwork (TM) provides most of aqueous humor outflow res

267 fluorescence (TPEF) of the human trabecular meshwork (TM) reveals beams of heterogeneous autofluores

268 e study was designed to determine trabecular meshwork (TM) stiffness and its relationship to outflow

269 ermine the localization of TNC in trabecular meshwork (TM) tissue and to analyze the effects of TNC o

270 The trabecular meshwork (TM) tissue controls drainage of aqueous humor

271 Trabecular meshwork (TM) tissue in the eye is under constant mechan

272 e biomechanical properties of the trabecular meshwork (TM), including the inner wall of Schlemm's can

273 t-like) from cells located in the trabecular meshwork (TM), the primary structural component of the c

274 smic reticulum (ER) stress in the trabecular meshwork (TM), the tissue that regulates IOP.

275 ted with chronic ER stress of the trabecular meshwork (TM).

276 synthesis and/or turnover in the trabecular meshwork (TM).

277 issues and is highly expressed in trabecular meshwork (TM).

278 th TSP1 and TSP2 are found in the trabecular meshwork (TM).

279 e to aqueous humor outflow in the trabecular meshwork (TM).

280 (CB) and its drainage through the trabecular meshwork (TM).

281 gle opening (all 4 quadrants with trabecular meshwork [TM] visible on gonioscopy after LPI).

282 olases must break peptide cross-links in the meshwork to allow insertion of new glycan strands betwee

283 ond to elevated IOP through softening of the meshwork to increase outflow.

284 is unclear whether rapsyn first forms a wide meshwork to which receptors can subsequently dock or whe

285 alicular connective tissue of the trabecular meshwork together with inner wall endothelium of Schlemm

286 The quantitative insights imply a role of meshwork topology in laminopathies.

287 diate filament proteins that assemble into a meshwork underneath the inner nuclear membrane, the nucl

288 ly assess the structure and dynamics of this meshwork using live-cell superresolution fluorescence mi

289 of PG and crosslink them into the cell wall meshwork via attached peptides.

290 classified as narrow if posterior trabecular meshwork was not visible and open if the angle was open

291 -like structures embedded in a collagen-rich meshwork where nutrients and oxygen are scarce.

292 instead of being secreted to the trabecular meshwork, which is a scenario toxic to trabecular meshwo

293 s present contractile apical-medial MyosinII meshworks, which control the apical area and junctional

294 the honeycomb-like extracellular DNA (eDNA) meshwork whilst also preventing its formation.

295 lamin filaments arrange to form an emergent meshwork whose topology dictates the mechanical properti

296 In summary, DCs respond to the LL mucin meshwork with a "semimature" activation phenotype, both

297 o generate a stable and compact pore-filling meshwork with a small mesh size.

298 Each isoform forms a distinct fiber meshwork, with comparable physical characteristics with

299 Thus, an interdependent meshwork within the CCAN underlies the centromere specif

300 tailed view of the organization of the lamin meshwork within the lamina.