ライフサイエンスコーパス: extracellular matrix

1 re primarily regulated by growth factors and extracellular matrix.

2 ace and illustrate how integrins can remodel extracellular matrix.

3 r non-collagenous proteins to the developing extracellular matrix.

4 in producing and remodeling molecules in the extracellular matrix.

5 perties of mouse optic nerve gliomas and the extracellular matrix.

6 secretory pathway, and released to generate extracellular matrix.

7 ltidomain peroxidase that is secreted to the extracellular matrix.

8 o crosslink insoluble collagen IV within the extracellular matrix.

9 ell tryptase resulting in a proproliferative extracellular matrix.

10 ding neurons, glial cells, blood vessels and extracellular matrix.

11 ional (3-D) systems, and is modulated by the extracellular matrix.

12 , environmental sensing, and adhesion to the extracellular matrix.

13 roteins, immune and vascular wall cells, and extracellular matrix.

14 tic cavities are bridged by fibronectin-rich extracellular matrix.

15 rowth factors, and decreased accumulation of extracellular matrix.

16 interaction with alpha-dystroglycan and the extracellular matrix.

17 lagens, the main components of the cartilage extracellular matrix.

18 ibers like collagen, all of which makeup the extracellular matrix.

19 hor the intracellular keratin network to the extracellular matrix.

20 , surface-attached communities encased in an extracellular matrix.

21 cell interactions with the mineralized bone extracellular matrix.

22 crobial communities surrounded by a secreted extracellular matrix.

23 n is promoted by increasing stiffness of the extracellular matrix.

24 e composition and physical properties of the extracellular matrix.

25 ormation, remodeling, and the destruction of extracellular matrix.

26 responsiveness to mechanical stimulation and extracellular matrix accumulation with the progression o

27 lmark of chronic kidney disease and leads to extracellular matrix accumulation, organ scarring, and l

28 kocyte infiltration, cell proliferation, and extracellular matrix accumulation.

29 Extracellular matrix adhesion is required for normal epi

30 rane blebs, as well as on cell-cell and cell-extracellular matrix adhesions.

31 n, as well as the exquisitely organized bone extracellular matrix, also depend upon perilacunar remod

32 d, preserving simultaneously a cell-friendly extracellular matrix and a perfusable vascular tree.

33 are extracellular proteases that can cleave extracellular matrix and alter signaling pathways.

34 Healthy tissue is replaced by altered extracellular matrix and alveolar architecture is destro

35 rmed a proteomics comparison of the vascular extracellular matrix and associated molecules in human c

36 edge of migrating cells, linking them to the extracellular matrix and enabling force sensing and tran

37 proteins required for interactions with the extracellular matrix and for proteolysis.

38 non-lymphoid tissue sites, maneuver through extracellular matrix and form lasting inflammatory micro

39 nterstitial fluid pressure, regions of dense extracellular matrix and high cell density, and overall

40 of heterogeneously leaky microvessels, dense extracellular matrix and high interstitial pressure gene

41 the organization of fibrotic skeletal muscle extracellular matrix and identify novel structures that

42 It forms a network of fibers within the extracellular matrix and impacts intracellular processes

43 nic acid-binding proteoglycan present in the extracellular matrix and in ocular vitreous body.

44 The cellular organisation, extracellular matrix and microvascular network mimic hum

45 vbeta3, is activated through HSC adhesion to extracellular matrix and niche cells.

46 sis and cancer progression by processing the extracellular matrix and promoting angiogenesis.

47 ndrance of NP diffusion imposed by the brain extracellular matrix and reduces NP confinement within t

48 to activate protease-mediated degradation of extracellular matrix and reverse fibrosis.

49 ng specifically with components of the human extracellular matrix and serum.

50 der described by an anisotropic model of the extracellular matrix and, to our knowledge, novel model

51 ronments with distinct communities of cells, extracellular matrix, and nutrients that may differ from

52 expression of proteins responsible for core extracellular matrix architectures.

53 xtracellular impermeant anions ([A]o) of the extracellular matrix are both proposed to be important r

54 , major components of connective tissues and extracellular matrix, are significantly and irreversibly

55 is laxa syndromes and further link defective extracellular matrix assembly to faulty protein processi

56 PME and TME, focusing on myofibroblast- and extracellular matrix-associated growth factors, fibrosis

57 hoton-excited 3D printing technique produces extracellular matrix-based scaffolds with exceptional re

58 A new study, however, demonstrates that an extracellular-matrix-based stiffness gradient in the Dro

59 ibited elevated expression of genes encoding extracellular matrix, basement membrane proteins, and me

60 Despite its relevant role in extracellular matrix biosynthesis, little is known about

61 ggregates were more often encountered in the extracellular matrix but could also be observed within c

62 Thus, binding to GAGs in the extracellular matrix can direct and regulate vaspin inte

63 elies on the microscale juxtaposition of two extracellular matrix-coated surfaces.

64 A1 gene that codes for type VII collagen, an extracellular matrix component of the basement membrane

65 e functions including cell death regulation, extracellular matrix component synthesis, and pancreatic

66 intermediate filaments (GFAP, vimentin) and extracellular matrix components (laminin, collagen IV) c

67 on and probably involve an imbalance of host extracellular matrix components and their regulators suc

68 iverse genes encoding secreted molecules and extracellular matrix components to modulate the secretom

69 revealed remodelling and degradation of core extracellular matrix components.

70 ed coat mucilage, a specialized layer of the extracellular matrix composed of plant cell wall carbohy

71 ocesses including inflammatory signaling and extracellular matrix composition.

72 ent of A549 cells by targeting cell integrin-extracellular matrix connections (matrilysis) as well as

73 l structural proteins derived from the liver extracellular matrix, connective tissue and epithelium,

74 coli and other Enterobacteriaceae produce an extracellular matrix consisting of curli amyloid fibers

75 hesized that the presence of fibrin in tumor extracellular matrix contributes to hindered intratumora

76 iated fibroblasts (CAFs) and self-sustaining extracellular matrix (D-ECM), is a puzzling feature of p

77 l gene tight junction, pericyte coverage and extracellular-matrix deficits.

78 Integrin-mediated contact with the extracellular matrix defines the basal surface, setting

79 f GPR124 promotes cell adhesion, additive to extracellular matrix-dependent effect, coupled with filo

80 omal trafficking of microRNA-206 to regulate extracellular matrix deposition and muscle tissue remode

81 onary fibrosis model in mice and in reducing extracellular matrix deposition in the lung while also r

82 y regulating smooth muscle proliferation and extracellular matrix deposition.

83 es to show that mechanical compaction of the extracellular matrix during mesenchymal condensation is

84 ctin networks, cell-cell adhesions, and cell-extracellular matrix (ECM) adhesions.

85 d tumour growth, aberrant remodelling of the extracellular matrix (ECM) and increased local invasion

86 way remodelling with excessive deposition of extracellular matrix (ECM) and larger smooth muscle mass

87 the effect of migrating cells on underlying extracellular matrix (ECM) and test possible therapeutic

88 VEGF) each have different affinities for the extracellular matrix (ECM) and the coreceptor NRP1, whic

89 tly linked to strong deposition of fibrillar extracellular matrix (ECM) components and high expressio

90 sensing switches by sensing modifications in extracellular matrix (ECM) composition and mechanics.

91 on, we used mouse models to characterize the extracellular matrix (ECM) composition of normal lung, f

92 Here, we observed that the extracellular matrix (ECM) constructed by AKAP12+ colon

93 mechanical stimuli such as stiffness of the extracellular matrix (ECM) contribute to MSC phenotype i

94 astatic process is heavily influenced by the extracellular matrix (ECM) density and composition of th

95 In addition, extracellular matrix (ECM) detachment is a physiologic t

96 The liver extracellular matrix (ECM) expands with high-fat (HF) fe

97 hich is partially responsible for defects in extracellular matrix (ECM) formation and mineralization.

98 scales in wood, fungal hyphae with the dried extracellular matrix (ECM) from the fungus, and Ca oxala

99 - cytoplasmic impermeant anions, polyanionic extracellular matrix (ECM) glycoproteins, and plasmalemm

100 The remodeling of the stromal extracellular matrix (ECM) has a crucial, but incomplete

101 ean vessel density and poorly differentiated extracellular matrix (ECM) in MDA-MB-231 tumors relative

102 We investigated the physical role of the extracellular matrix (ECM) in vascular homeostasis in th

103 n by contact guidance in aligned collagenous extracellular matrix (ECM) is a critical enabler of brea

104 emergence onto damaged or organized fibrous extracellular matrix (ECM) is a crucial precursor to col

105 The extracellular matrix (ECM) is a fibrillar protein-based

106 The extracellular matrix (ECM) is an oft-overlooked componen

107 Integrin-mediated attachment to the extracellular matrix (ECM) is required to combat the ind

108 the biological fibrous architectures in the extracellular matrix (ECM) is the strong and directional

109 lude mesangial expansion and accumulation of extracellular matrix (ECM) leading to glomerulosclerosis

110 cal role of PHEX in a 3-dimensional model of extracellular matrix (ECM) mineralization.

111 Interactions with the extracellular matrix (ECM) occur through focal adhesions

112 Proteoglycans (PGs) in the extracellular matrix (ECM) play vital roles in axon grow

113 or fluid shear stress via interaction of the extracellular matrix (ECM) protein cochlin with the cell

114 1-CTGF-NOV (CCN)1 is a dynamically expressed extracellular matrix (ECM) protein with critical functio

115 Increased synthesis and deposition of extracellular matrix (ECM) proteins in the trabecular me

116 s characterised by excessive accumulation of extracellular matrix (ECM) proteins.

117 tor cells of fibrosis that produce excessive extracellular matrix (ECM) proteins.

118 s characterized by excessive accumulation of extracellular matrix (ECM) proteins.

119 The extracellular matrix (ECM) regulates cell migration and

120 ir surroundings underlies cell migration and extracellular matrix (ECM) remodeling and is thus an ess

121 Extracellular matrix (ECM) remodeling contributes to in-

122 Localized extracellular matrix (ECM) remodeling is thought to stab

123 Fibronectin (FN) is a critical regulator of extracellular matrix (ECM) remodeling through its availa

124 oproteinase 9 (MMP-9), an enzyme involved in extracellular matrix (ECM) remodelling and synaptic plas

125 e displayed reduced collagen arrangement and extracellular matrix (ECM) stiffness.

126 ABSTRACT: Skeletal muscle extracellular matrix (ECM) structure and organization ar

127 r conditional knockout mice showed decreased extracellular matrix (ECM) structure-related gene expres

128 y act as a mechanotransduction signal in the extracellular matrix (ECM) to coordinate the cross-talk

129 pends on a cross-talk with basement membrane extracellular matrix (ECM) via beta1 integrins which act

130 tegrating the adhesion of invadopodia to the extracellular matrix (ECM) with their ability to degrade

131 but relatively little is known about how the extracellular matrix (ECM), and particularly the mechani

132 onic acid synthesis and the formation of the extracellular matrix (ECM), and stimulates reepitheliali

133 h cells sense the physical attributes of the extracellular matrix (ECM), are known to drive cell bran

134 , major components of connective tissues and extracellular matrix (ECM), are significantly and irreve

135 stimulates lung fibroblasts to accumulate an extracellular matrix (ECM), enriched in hyaluronan (HA)

136 As a cell migrates through its extracellular matrix (ECM), lamellipod growth increases

137 Variants were assigned to the complement, extracellular matrix (ECM), lipid, cell survival, immune

138 e cancer cells interact with the surrounding extracellular matrix (ECM), remodeling ECM fiber network

139 s can expose epithelial cells to the stromal extracellular matrix (ECM), which is distinct from the E

140 f GBM cells with unique aspects of the brain extracellular matrix (ECM), which is relatively enriched

141 ion of cells and relevant biomolecules on an extracellular matrix (ECM)-like substrate with arbitrary

142 RNA-Seq analysis revealed that extracellular matrix (ECM)-receptor interaction and meta

143 mbrane assemblies that connect a cell to its extracellular matrix (ECM).

144 ity, and the physical characteristics of the extracellular matrix (ECM).

145 uronic acid (HA), the major component of the extracellular matrix (ECM).

146 tissues, adapts to mechanical strains in the extracellular matrix (ECM).

147 tterning anisotropic resistance within their extracellular matrix (ECM).

148 mediated cell attachments to the surrounding extracellular matrix (ECM).

149 which is the near-neuron domain of a brain's extracellular matrix (ECM).

150 etween the cell contents and the surrounding extracellular matrix (ECM).

151 ed of hematopoietic cells, stromal cells and extracellular matrix (ECM).

152 ght to target the proteins that comprise the extracellular matrix (ECM).

153 ts and the interaction between cells and the extracellular matrix (ECM).

154 zation of elastin, indicating defects in the extracellular matrix (ECM).

155 nterplay of multiple types of cells with the extracellular matrix (ECM).

156 lved in lipid synthesis and formation of the extracellular matrix) exhibited little change in their a

157 sly unrecognized mechanism for regulation of extracellular matrix formation and wound repair.

158 are microbial communities embedded within an extracellular matrix, forming a highly organized structu

159 t cardiac fibroblasts for fibrotic excessive extracellular matrix gene expression and binds Col3a1 an

160 ige differentiation marker and a decrease in extracellular matrix gene expression.

161 BLM-induced-fibrosis in mice, down regulate extracellular matrix genes expression, and reduce collag

162 gnificance: These results illuminate how the extracellular matrix glycoprotein tenascin-C in the tumo

163 This integrative approach nominated an extracellular matrix glycoprotein, fibulin-3 (FBLN3, als

164 mulation of hyaluronic acid-a high molecular extracellular matrix glycosaminoglycan implicated in pla

165 les in asthma and atopy and genes related to extracellular matrix, immunity, cell adhesion, epigeneti

166 stence of cancer cell migration through a 3D extracellular matrix in a matrix metalloproteinases (MMP

167 ation and highlight fundamental roles of the extracellular matrix in cardiac repair.

168 de of cell traction forces on the underlying extracellular matrix in culture is almost impossible to

169 The higher amount of extracellular matrix in MED12-LM than HMGA2-LM was parti

170 s in the microstructural organization of the extracellular matrix in peripheral nerve tissue in MS.

171 ophils remodel and migrate on periostin-rich extracellular matrix in the asthmatic airway in an ADAM8

172 ammary clock is controlled by the periductal extracellular matrix in vivo, which contributes to a dam

173 In contrast, the extracellular matrix in zebrafish allows substantial axo

174 rough the synthesis of connective tissue and extracellular matrix, inducing local pancreatic fibrosis

175 Engagement of integrins by the extracellular matrix initiates signaling cascades that d

176 ression levels of genes affecting tumor cell-extracellular matrix interaction, including loxl3, itga2

177 ved ejection fraction (HFpEF), cardiomyocyte-extracellular matrix interactions from excess collagen m

178 development requires integrin-dependent cell-extracellular matrix interactions.

179 cell viability but reduced cell motility and extracellular matrix invasion, as well as extravasation

180 It is a key regulator of the extracellular matrix, involved in the degradation of var

181 The native extracellular matrix is a space in which signals can be

182 A complex extracellular matrix is used for the maturation of CLCs;

183 These features included cartilage extracellular matrix loss without proteoglycan replaceme

184 composition and explored PEG and islet-like extracellular matrix (Matrigel; MG) islet encapsulation

185 gp120 and alpha4beta7 This suggests that the extracellular matrix may be an important mediator of HIV

186 major role in the establishment of the actin-extracellular matrix mechanical coupling.

187 chanistic studies of immunity, inflammation, extracellular matrix mechanics, epigenetic or transcript

188 uding tissue morphogenesis and architecture, extracellular matrix-mediated tissue remodeling, cytoske

189 ion of local and systemic factors regulating extracellular matrix mineralization can be possible ther

190 cm1, Syna and Synb, and in patterning of the extracellular matrix, Mmrn1, were temporally dysregulate

191 enesis of fibrosis, including WNT signaling, extracellular matrix modulation, and inflammation.

192 Tenascin-C is an extracellular matrix molecule that drives progression of

193 u on the cell surface, and interact with the extracellular matrix molecules and effectively abolish c

194 nclude secreted growth factors (angiokines), extracellular matrix molecules, and transmembrane protei

195 ng heterogeneous mechanical signaling in the extracellular matrix of developing and regenerating tiss

196 Curli is a functional amyloid protein in the extracellular matrix of enteric Gram-negative bacteria.

197 ns specifically recognized each other in the extracellular matrix of fibroblasts.

198 igands (e.g. fibronectin; Fn) present in the extracellular matrix of tissue or coatings on cardiac im

199 cant part of secreted vaspin is bound in the extracellular matrix on the cell surface.

200 oration of bioactive factors to either mimic extracellular matrix or to deliver a payload to diseased

201 Cell adhesion to the extracellular matrix or to surrounding cells plays a key

202 integrins bind macromolecular ligands in the extracellular matrix or transmit force to them.

203 According to our results, extracellular matrix organization and immune response ar

204 ssociated proteomics analysis indicated that extracellular matrix organization, small molecule metabo

205 ay between tumour cells and their neoplastic extracellular matrix plays a decisive role in malignant

206 ss, this isoform stimulates invasion through extracellular matrix, pointing to a critical role in sec

207 roblast differentiation into contractile and extracellular matrix-producing myofibroblasts.

208 or parathyroid hormone 2 receptor (PTH2R) in extracellular matrix production in wounds.

209 athological scars characterized by excessive extracellular matrix production that are prone to form i

210 Ileal genes controlling extracellular matrix production were upregulated at diag

211 f fibroblast proliferation, differentiation, extracellular matrix production, and apoptosis.

212 adipocyte differentiation, while increasing extracellular matrix production.

213 identify a novel role for PTH2R signaling in extracellular matrix production.

214 livery of a bispecific molecule targeting an extracellular matrix protein and delivering a TGF-beta m

215 Here, we identified the secreted extracellular matrix protein Del-1 as a component and re

216 simple coacervation of proteins, such as the extracellular matrix protein elastin, have not been repo

217 ing a significant impact on inflammatory and extracellular matrix protein expression.

218 used by mutations in FBN1, which encodes the extracellular matrix protein fibrillin-1.

219 served that proteolytic cleavage of the host extracellular matrix protein fibronectin by peritoneal c

220 s an environmental factor, aggregates of the extracellular matrix protein fibronectin perturb the mat

221 ted migration signaling pathways and reduced extracellular matrix protein production, and blocked myo

222 e provide evidence that tenascin-C (TNC), an extracellular matrix protein prominent in malignant glio

223 We previously found that the extracellular matrix protein secreted protein acidic and

224 The myofibroblasts, responsible for extracellular matrix protein synthesis, and the macropha

225 irulence factor interacting with laminin, an extracellular matrix protein ubiquitously expressed in t

226 phil adhesion and migration on periostin, an extracellular matrix protein upregulated in asthma by ty

227 We designed an approach to target an extracellular matrix protein, the fibronectin extra doma

228 duced by transforming growth factor-beta1 or extracellular matrix protein.

229 Dentin sialoprotein (DSP) is a dentin extracellular matrix protein.

230 The main extracellular matrix proteins and associated cytokines w

231 dystroglycan that is responsible for binding extracellular matrix proteins and certain arenaviruses.

232 oglycan functions as a receptor for multiple extracellular matrix proteins and its dysfunction leads

233 n, inflammatory cytokines, immune mediators, extracellular matrix proteins and oncogene expression.

234 wound healing, where excessive collagen and extracellular matrix proteins are deposited within the w

235 and acute inflammation not only by degrading extracellular matrix proteins but also by controlling th

236 In this study, we demonstrate that extracellular matrix proteins can mediate interactions b

237 ced mesangial expansion, accumulation of the extracellular matrix proteins fibronectin and type IV co

238 ue culture, TNC was superior amongst several extracellular matrix proteins in enhancing the sphere-fo

239 the potential role of fibronectin and other extracellular matrix proteins in HIV-1 biology.IMPORTANC

240 Fibrosis involves the production of extracellular matrix proteins in tissues and is often pr

241 nt HSCs to HSC myofibroblasts, which secrete extracellular matrix proteins responsible for the fibrot

242 mation of mineralized tissues is governed by extracellular matrix proteins that assemble into a 3D or

243 binant gp120 produced fibronectins and other extracellular matrix proteins that copurified with gp120

244 evelop contractile functions and secrete the extracellular matrix proteins that form this fibrous sca

245 e thought to be linked by several additional extracellular matrix proteins, including nidogen and per

246 Raman spectral changes related to extracellular matrix proteins, lipids, and nucleic acids

247 so increasing expression of cartilage tissue extracellular matrix proteins.

248 f different integrin subtypes and sensing of extracellular matrix proteins.

249 trix, involved in the degradation of various extracellular matrix proteins.

250 PSC) and is characterized by accumulation of extracellular matrix proteins.

251 pha/beta integrins, osteopontin, and related extracellular matrix proteins; (2) clastic cell fusion a

252 s for the detection and transduction of cell-extracellular matrix recognition events in a real time,

253 ls induces a transient alkalinization of the extracellular matrix, reducing cellular elongation.

254 anscriptome analyses show that expression of extracellular matrix-related genes changes dramatically

255 ptor for TIP39, suppressed the expression of extracellular matrix-related genes, including decorin, c

256 actin-positive blood vessels, and 5) of key extracellular matrix remodeling (CD44, Col1a1, integrins

257 RATIONALE: Cardiac fibroblasts (CFs) drive extracellular matrix remodeling after pressure overload,

258 scriptional regulation of genes critical for extracellular matrix remodeling and cell cycle progressi

259 oteomics from WS revealed an upregulation of extracellular matrix remodeling and focal adhesion proce

260 d that WNT2-mediated fibroblast motility and extracellular matrix remodeling enhanced cancer cell inv

261 Micu2(-/-) mice had increased expression of extracellular matrix remodeling genes, while single-cell

262 d on previous studies implicating changes in extracellular matrix remodeling in other, related optic

263 inhibited the gene program for fibrosis and extracellular matrix remodeling, although deletion of Tg

264 othelial cells, with decreased expression of extracellular matrix remodeling-enzyme coding genes and

265 in part, from ongoing inflammation and poor extracellular matrix remodeling.

266 ral airways, fluticasone/salmeterol reversed extracellular matrix remodelling after 12 weeks, both wi

267 bryonic fibroblasts growing on two different extracellular matrix-representing substrates (i.e., fibr

268 Collectively, our results indicate that PDAC extracellular matrix represents a nutrient reservoir for

269 xcited 3D printing to generate a native-like extracellular matrix scaffold with submicron resolution

270 populate different nephron portions of renal extracellular matrix scaffolds obtained after decellular

271 cells self-assembled inside acellular liver extracellular matrix scaffolds to form three-dimensional

272 L, we show that the treatment with synthetic extracellular matrix (sECM) encapsulated SC-ENb-TRAIL al

273 aling pathways, as well as downregulation of extracellular matrix signaling pathways.

274 In response to extracellular matrix signalling, these cells undergo epi

275 Extracellular matrix signals from the microenvironment r

276 ultured to produce connective tissue rich in extracellular matrix (stage 2), onto which LECs are seed

277 Increased extracellular matrix stiffness and application of mechan

278 ellular renal scaffold while maintaining the extracellular matrix structure and composition in terms

279 ore stable molecular components, such as the extracellular matrix structure of perineuronal nets (PNN

280 the skin of PTH2R(-/-) mice showed abnormal extracellular matrix structure, decreased decorin expres

281 et tenascin C retention in connective tissue extracellular matrix suggests the rigidity laid down for

282 k generated through enzymatic changes in the extracellular matrix surrounding the egg [2].

283 ms associated with collagen proteins and the extracellular matrix; terms associated with the anatomy

284 en cultured in a stiffened three-dimensional extracellular matrix that recapitulates the primary tumo

285 dense sheets of specialized, self-assembled extracellular matrix that surround most animal tissues (

286 e relationships between the pancreatic tumor extracellular matrix, the vasculature, the immune system

287 uPAR mediates degradation of the extracellular matrix through protease recruitment and en

288 extrinsic signals from the axon and from the extracellular matrix to first sort and ensheathe a singl

289 y defined synthetic hydrogel that mimics the extracellular matrix to support in vitro growth of intes

290 down-regulation of genes associated with the extracellular matrix was followed by a shift to genes as

291 Extracellular matrix was prepared from decellularized ai

292 Static platelet aggregate formation on extracellular matrix was similarly reduced in GF WT, Tlr

293 ts of genes whose proteins have roles in the extracellular matrix were amongst the top 300 genes with

294 drocyte loss and diminishment of specialised extracellular matrix, which can progress to an osteoarth

295 th activated mast cell supernatants produced extracellular matrix, which enhanced subsequent airway s

296 atriptase, induces potent destruction of the extracellular matrix whilst displaying distinct efficien

297 Notably, treatment of the extracellular matrix with ACM led to even more significa

298 normal fibroblasts, CAFs produce an Fn-rich extracellular matrix with anisotropic fiber orientation,

299 action coupling of hiPSC-CM when cultured on extracellular matrix with physiological stiffness (Matri

300 f a cancer cell to migrate through the dense extracellular matrix within and surrounding the solid tu