ライフサイエンスコーパス: meshwork

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

2 ior cornea initiating beneath the trabecular meshwork.

3 acaques by laser treatment to the trabecular meshwork.

4 ctility of the cortical membrane-bound actin meshwork.

5 pigmentary dispersion within the trabecular meshwork.

6 nal with no visible damage to the trabecular meshwork.

7 acaques by laser treatment to the trabecular meshwork.

8 cted venules (10-50 mum) forming a hexagonal meshwork.

9 ormation or promote formation of a gauzelike meshwork.

10 (ATP) channels are present in the trabecular meshwork.

11 in both the ciliary body and the trabecular meshwork.

12 by laser photocoagulation of the trabecular meshwork.

13 ved laser photocoagulation of the trabecular meshwork.

14 ility of the break to traverse the chromatin meshwork.

15 of cochlin in human glaucomatous trabecular meshwork.

16 tile stress generated by the platelet-fibrin meshwork.

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

18 links on the nuclear envelope and the lamin meshwork.

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

20 s performed to 360 degrees of the trabecular meshwork.

21 in combination with a model keratocyte actin meshwork.

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

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

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

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

26 The morphology of the bovine trabecular meshwork after perfusion culture was similar to that of

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

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

29 induced by laser cauterization of trabecular meshwork and episcleral veins in rat eyes.

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

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

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

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

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

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

36 nt enzyme in protecting the lens, trabecular meshwork, and cornea against oxidative damage.

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

38 ing lamina, the lens capsule, the trabecular meshwork, and the iris.

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

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

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

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

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

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

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

46 angle is associated with greater trabecular meshwork anteroposterior length.

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

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

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

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

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

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

53 sin II-dependent contraction of the cortical meshwork asymmetrically distributes the highly conserved

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

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

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

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

58 uorescent protein fusions show that At SEOR1 meshworks at the margins and clots in the lumen are a ge

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

60 How a tubular axonal meshwork becomes established without invading centrally

61 INF2-non-CAAX is loosely attached to this meshwork, being extracted by brief digitonin treatment.

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

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

64 RhoA signaling and diminishes actin cortical meshwork by down-regulating Rac1 activity.

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

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

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

68 nd retraction simultaneously in MSP filament meshworks, called fibers, that assemble behind plasma me

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

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

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

72 junction (AJ) levels or ablating actomyosin meshworks causes tissue-wide epithelial tears, which rel

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

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

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

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

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

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

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

80 yocilin toxicity in primary human trabecular meshwork cells.

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

82 These tissues include the trabecular meshwork, ciliary body, ciliary epithelium, Muller cells

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

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

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

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

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

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

89 OPN was present in the trabecular meshwork, corneal epithelium and endothelium, iris, cili

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

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

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

93 NETs, consisting of a chromatin meshwork decorated with antimicrobial peptides, play an

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

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

96 Since precise regulation of the trabecular meshwork ECM composition and organization is required to

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

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

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

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

101 long-term gene expression in the trabecular meshwork following intracameral delivery of adeno-associ

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

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

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

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

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

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

108 ay inhibitor, in the glaucomatous trabecular meshwork (GTM), and found that key canonical Wnt signali

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

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

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

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

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

114 r in the human eye is through the trabecular meshwork (HTM) and Schlemm's canal (SC).

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

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

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

118 and ELISA, respectively, in human trabecular meshwork (HTM) cells transfected with miR-29b or scrambl

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

120 gene expression profile in human trabecular meshwork (HTM) cells.

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

122 ted ciliary epithelial (NPCE) and trabecular meshwork (HTM-3) cells were treated with spiradoline (SP

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

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

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

126 emonstrated a fully developed parietal actin meshwork in SEs.

127 bal laser photocoagulation of the trabecular meshwork in Sprague-Dawley rats.

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

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

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

131 ssion of transgenes in the murine trabecular meshwork in vivo.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

152 sections and primary normal human trabecular meshwork (NTM) cells were studied by Western blot and im

153 primary cultures of normal human trabecular meshwork (NTM) cells.

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

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

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

157 uter granular matrix covering the underlying meshwork of cellulose fibrils.

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

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

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

161 th glaucoma may be altered in the trabecular meshwork of glaucoma patients.

162 ia, the peptidoglycan (murein) sacculus is a meshwork of glycan strands joined by peptide crosslinks.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

197 ters obstacles within the actin cytoskeletal meshwork or when other motors are attached to the same c

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

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

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

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

202 ituent of the bacterial cell wall, forming a meshwork outside the cytoplasmic membrane that maintains

203 NF2-non-CAAX localizes in an actin-dependent meshwork pattern distinct from ER.

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

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

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

207 scent TM structures and filled corneoscleral meshwork pores.

208 te (AMP) and adenosine in porcine trabecular meshwork (PTM) cells treated with adenosine triphosphate

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

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

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

212 ven with unilateral laser-induced trabecular meshwork scarification and ocular hypertension, were obs

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

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

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

228 Trabecular meshwork tissue showed moderate ALP activity at 13 days

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

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

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

232 The trabecular meshwork (TM) and Schlemm's canal (SC) cells expressed P

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

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

235 its segmental distribution in the trabecular meshwork (TM) and the effect on outflow facility of sile

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

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

238 solated and purified from porcine trabecular meshwork (TM) cell culture media.

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

240 c oxide (NO)-induced decreases in trabecular meshwork (TM) cell volume and NO-induced increases in ou

241 to-ATPases from transformed human trabecular meshwork (TM) cells (TM5) and explant-derived TM cells w

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

243 emlin is elevated in glaucomatous trabecular meshwork (TM) cells and tissues and elevates intraocular

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

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

246 Elevated cAMP in the trabecular meshwork (TM) cells increases the aqueous humor outflow

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

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

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

250 ion and contractility in cultured trabecular meshwork (TM) cells.

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

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

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

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

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

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

257 The function of hevin in trabecular meshwork (TM) is unknown.

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

259 ted in the aqueous humor (AH) and trabecular meshwork (TM) of patients with primary open-angle glauco

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

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

262 were used to obtain images of the trabecular meshwork (TM) region within an intact mouse eye.

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

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

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

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

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

268 d inside-out patch clamp in human trabecular meshwork (TM) tissue or primary cultures of normal human

269 egulation of ECM synthesis in the trabecular meshwork (TM) under basal and TGF-beta2 stimulatory cond

270 ic and biochemical changes in the trabecular meshwork (TM), an ocular tissue involved in regulating I

271 tion in primary cultures of human trabecular meshwork (TM), Schlemm's canal (SC), and ciliary smooth

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

273 but accumulated in the ER of the trabecular meshwork (TM), thereby inducing ER stress in the TM of T

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

275 (CB) and its drainage through 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 athway genes are expressed in the trabecular meshwork (TM).

281 cellular matrix metabolism in the trabecular meshwork (TM).

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

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

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

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

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

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 ma with laser photocoagulation of trabecular meshwork was used.

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

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

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

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

296 ng of collagen type I in areas of trabecular meshwork with high MMP1 transgene expression.

297 cient transgene activation in the trabecular meshwork, with additional sites of transgene activation

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.