ライフサイエンスコーパス: extracellular matrix

1 , migration, adhesion, and remodeling of the extracellular matrix.

2 diseases associated with a remodeling of the extracellular matrix.

3 coagulation and complement processes and to extracellular matrix.

4 chondroitin sulfate proteoglycans of the SVZ extracellular matrix.

5 contribute to pathogenesis by overproducing extracellular matrix.

6 tion of hyaluronan in the pulmonary vascular extracellular matrix.

7 ration, spreading, migration and adhesion to extracellular matrix.

8 typic ligands on neighboring cells or in the extracellular matrix.

9 asts (tenocytes) embedded in a collagen-rich extracellular matrix.

10 functionally distinct layers, cell types and extracellular matrix.

11 roenvironment, such as the stiffening of the extracellular matrix.

12 ructure by adhering to each other and to the extracellular matrix.

13 nd stiffness due to alteration of myocardial extracellular matrix.

14 une cells, stromal cells, blood vessels, and extracellular matrix.

15 pling between the actin cytoskeleton and the extracellular matrix.

16 ity to locally secrete proteases and remodel extracellular matrix.

17 d as biofilms, which are held together by an extracellular matrix.

18 lly burst, releasing their contents into the extracellular matrix.

19 nt astroglial processes and the perisynaptic extracellular matrix.

20 growth, migration, and the formation of the extracellular matrix.

21 gene discovery using platforms targeting the extracellular matrix.

22 and functional properties in regulating the extracellular matrix.

23 rogressive scarring disease characterized by extracellular matrix accumulation and altered mechanical

24 ogether, these data demonstrate that altered extracellular matrix accumulation of HA occurs following

25 on cue-induced changes in astrocytes and the extracellular matrix adjacent to the synapse.

26 By examining the apical extracellular matrix (aECM), we also uncovered a vast ma

27 ing mechanisms used by the cell to sense its extracellular matrix also play a role in intercellular i

28 ury leads to podocyte loss or an increase of extracellular matrix, altering glomerular cellular compo

29 sis while the ovary exhibited enrichments in extracellular matrix and adhesion proteins.

30 al forces and regulatory signals between the extracellular matrix and an interacting cell.

31 s, which provide anchorage to the pancreatic extracellular matrix and are the origin of intracellular

32 well as genes associated with inflammation, extracellular matrix and cell cycle.

33 l tethering to the surrounding cytoskeleton, extracellular matrix and cells, and tissue-level archite

34 cells, fibroblasts, signaling molecules, and extracellular matrix and has a crucial role in tumor ini

35 ycan abundant on the cell surface and in the extracellular matrix and has several biological activiti

36 (-/-) compared with WT mice, whereas several extracellular matrix and inflammation genes were up-regu

37 In addition to producing the extracellular matrix and joint lubricants, FLS in RA pro

38 increase in levels of proteins involved with extracellular matrix and laminin interactions, and a dec

39 ive disease, characterized by alterations in extracellular matrix and loss of smooth muscle cells (SM

40 ove through an environment filled with dense extracellular matrix and mesoderm to reach targets throu

41 develop in a specialized niche that includes extracellular matrix and supporting stromal and endothel

42 ocal adhesions linking signaling between the extracellular matrix and the actin cytoskeleton.

43 cell response causing the overproduction of extracellular matrix and tissue dysfunction.

44 otic areas mainly consist of type I collagen extracellular matrix and, only to a lesser extent, mesen

45 yosin-generated forces, nuclear positioning, extracellular matrix, and cell-cell adhesion in shaping

46 s signaling, cell migration, adhesion to the extracellular matrix, and leukocyte function.

47 xpression of genes involved in inflammation, extracellular matrix, and lipid metabolism.

48 olved in ion channel signaling, development, extracellular matrix, and metabolism.

49 lent HC.HA complexes, thereby stabilizing an extracellular matrix around the oocyte required for fert

50 posed that this phenomenon defines the plant extracellular matrix as a 'democratic space' for collect

51 es and signal molecules, plant cells use the extracellular matrix as an alternative route for cell-ce

52 of proteins associated with inflammation and extracellular matrix as well as senescence-associated se

53 igned a tool to extract the thickness of the extracellular matrix at and outside of plasmodesmata pos

54 The use of extracellular matrix based injectable hydrogels has gain

55 tin (FN) is an essential glycoprotein of the extracellular matrix; binds integrins, syndecans, collag

56 xtracellular deposits that accumulate in the extracellular matrix (Bruch's membrane (BrM)) adjacent t

57 ion complexes link the glial membrane to the extracellular matrix, but little is known about integrin

58 dothelial cells proliferate and move over an extracellular matrix by following external gradients of

59 ion/modification of the dense adipose tissue extracellular matrix by MMP14, thereby releasing the mec

60 Photoreceptor neurons are surrounded by an extracellular matrix, called the interphotoreceptor matr

61 Wound healing is characterized by cell and extracellular matrix changes mediating cell migration, f

62 iterature has demonstrated the importance of extracellular matrix changes such as the accumulation of

63 s: metabolism, signaling, electrophysiology, extracellular matrix, clotting, and inflammation.

64 ene expression profile, referred to as ECM3 (Extracellular Matrix Cluster 3), indicated poorer surviv

65 ientation of reinforcing fibers representing extracellular matrix collagen.

66 d organoid substructure that reorganized the extracellular matrix compartment and recruited endotheli

67 pted by heparin, used as a surrogate for the extracellular matrix component, heparan sulfate.

68 a broad spectrum of substrates ranging from extracellular matrix components and adhesion molecules t

69 , imaging analysis show that CXCL13 binds to extracellular matrix components in situ, constraining it

70 controlling the synthesis and processing of extracellular matrix components in the palatal mesenchym

71 s UGDH as a key player for the production of extracellular matrix components that are essential for h

72 Periostin functions by interacting with extracellular matrix components to drive collagen fibril

73 Secreted extracellular matrix components which regulate craniofac

74 the effects of age on PV leaflet thickness, extracellular matrix components, and mechanical properti

75 is characterized by exuberant deposition of extracellular matrix components, leading to the deterior

76 l shelf elevation with reduced expression of extracellular matrix components.

77 reflecting differences in the expression of extracellular matrix components.

78 phocytes and associated cytokines; decreased extracellular matrix components; and reductions in marke

79 thus targeted integrin beta1, a mediator of extracellular matrix contact, and found that combined ME

80 ed organization of the cytoskeleton and cell-extracellular matrix contacts and modulated the trabecul

81 d medial tympaniform membranes consist of an extracellular matrix containing hyaluronic acid, collage

82 How extracellular matrix contributes to tissue morphogenesis

83 r, as well as potential neuronal, glial, and extracellular matrix contributions to functional changes

84 gically, growth factor interactions with the extracellular matrix control their bioavailability and s

85 O1, or Protrudin inhibited MT1-MMP-dependent extracellular matrix degradation and cancer cell invasio

86 ion effect of TMPRSS2 on pro-HGF activation, extracellular matrix degradation and prostate cancer cel

87 pression of MMPs associated with periodontal extracellular matrix degradation.

88 re the major cellular contributors to excess extracellular matrix deposition in the diseased liver an

89 CDH11 promotes immunosuppression and extracellular matrix deposition, and might be developed

90 Here, we sought to determine how the extracellular matrix directs synapse formation and regul

91 tissues mechanically deform the surrounding extracellular matrix during embryonic development, wound

92 es the composition of and signaling from the extracellular matrix during homeostatic plasticity.

93 , Nog) and the deposition of the provisional extracellular matrix (ECM) (Tnc, Postn, Spon2, Thbs2) as

94 NCH-1 is a cytoplasmic component of the cell-extracellular matrix (ECM) adhesion machine that is freq

95 ganization is mediated by cell-cell and cell-extracellular matrix (ECM) adhesions and is modulated by

96 d (HA) is a highly abundant component in the extracellular matrix (ECM) and a fundamental element to

97 Both the extracellular matrix (ECM) and DNA epigenetic regulation

98 Contralateral invasion is suppressed by extracellular matrix (ECM) and programmed cell death (PC

99 OFTs exhibit increased EC numbers as well as extracellular matrix (ECM) and SMC disorganization.

100 IL-33 instructs microglial engulfment of the extracellular matrix (ECM) and that its loss leads to im

101 rrying mutations affecting links between the extracellular matrix (ECM) and the TRNs but could not de

102 central to the molecular organization of the extracellular matrix (ECM) and to defining the cellular

103 usions that were important for breaching the extracellular matrix (ECM) and visceral muscle.

104 The native extracellular matrix (ECM) can exhibit heterogeneous nan

105 onse to tissue injury, stromal cells secrete extracellular matrix (ECM) components that remodel the t

106 d for their ability to adhere to immobilized extracellular matrix (ECM) components, exhibited a diver

107 uroinflammatory signaling and non-permissive extracellular matrix (ECM) components.

108 e composition and physical properties of the extracellular matrix (ECM) critically influence tumor pr

109 x metalloproteinases (MMPs), that are key in extracellular matrix (ECM) degradation.

110 Aberrant extracellular matrix (ECM) deposition and stiffening is

111 Hypoxia-induced extracellular matrix (ECM) deposition is an important ca

112 between normal and retracting vessels under extracellular matrix (ECM) disruption.

113 er the past two decades has established that extracellular matrix (ECM) elasticity, or stiffness, aff

114 mor-stroma co-cultures consisting of aligned extracellular matrix (ECM) fibers and ordered micro-arch

115 ng process, eCRT induces abundant neo-dermal extracellular matrix (ECM) formation by 3 days post-woun

116 yeloid cells (PyMT/TGFbetaRII(LysM)) affects extracellular matrix (ECM) formation in tumor tissue, sp

117 The extracellular matrix (ECM) has force-responsive (i.e., m

118 The abundant extracellular matrix (ECM) in PDAC comprises a major fra

119 The extracellular matrix (ECM) is a complex and dynamic mesh

120 The extracellular matrix (ECM) is a polymer network hypothes

121 enetration of theranostic nanoparticles, the extracellular matrix (ECM) is of crucial importance beca

122 rrant remodeling of trabecular meshwork (TM) extracellular matrix (ECM) may induce ocular hypertensiv

123 terodimeric transmembrane proteins that bind extracellular matrix (ECM) molecules on one side and con

124 erstitial cells and a natural decellularised extracellular matrix (ECM) obtained by whole thymus perf

125 elied on materials that do not represent the extracellular matrix (ECM) of brain tissue.

126 chanical interactions between tumors and the extracellular matrix (ECM) of the surrounding tissues ha

127 tand the effects of non-neoplastic cells and extracellular matrix (ECM) on drug resistance in gliobla

128 nt of CAC by measuring proteomic changes and extracellular matrix (ECM) organization over time in a m

129 gned to the complement, lipid metabolism, or extracellular matrix (ECM) pathways and ARMS2 also were

130 , including myofibroblast contractile force, extracellular matrix (ECM) production, chemotaxis, and w

131 hesis that human perinatal stem cell derived extracellular matrix (ECM) promotes hiPSC-CM maturation

132 Basement membrane and extracellular matrix (ECM) proteins were significantly d

133 s) are inducible endopeptidases that degrade extracellular matrix (ECM) proteins, and reveal tripepti

134 lular enzymes involved in the degradation of extracellular matrix (ECM) proteins.

135 shock proteins (HSPs), through regulation of extracellular matrix (ECM) remodeling and epithelial mes

136 egulation, inflammatory/repair response, and extracellular matrix (ECM) remodeling in the partially r

137 Extracellular matrix (ECM) remodeling is a hallmark of t

138 n fibrillar elastin and collagens leading to extracellular matrix (ECM) stabilization.

139 objective of this study is to elucidate the extracellular matrix (ECM) structure, composition, and b

140 obules demonstrated increased decorin in the extracellular matrix (ECM) surrounding epithelial cells,

141 Here, we present a tumour extracellular matrix (ECM) targeting ROS nanoscavenger m

142 properties and indications of scaffold-based extracellular matrix (ECM) technologies as alternatives

143 ting cells move across diverse assemblies of extracellular matrix (ECM) that can be separated by micr

144 desmoplastic stroma, along with an extensive extracellular matrix (ECM) that is rich in hyaluronan, p

145 s on matrix metalloprotease signaling in the extracellular matrix (ECM) through beta3-integrin to act

146 communication between resident cells and the extracellular matrix (ECM) through cell-matrix interacti

147 from hyperplasic to hypertrophic growth, the extracellular matrix (ECM) undergoes remodeling, and the

148 l migration through a three-dimensional (3D) extracellular matrix (ECM) underlies important physiolog

149 s also phosphorylated upon engagement of the extracellular matrix (ECM) via focal adhesion kinase.

150 vation protein (FAP) and accumulation of the extracellular matrix (ECM) was notably impaired in tumor

151 egrin signaling and cellular adhesion to the extracellular matrix (ECM) with inhibition of ciliation

152 uantitative mass spectrometry to analyze the extracellular matrix (ECM), a critical component of meta

153 ating how the mechanical cues exerted by the extracellular matrix (ECM), cell-ECM and cell-cell adhes

154 e characterized by excessive accumulation of extracellular matrix (ECM), is a leading cause of mortal

155 iveness to environment, including changes in extracellular matrix (ECM), is critical for normal proce

156 of cancer-associated fibroblasts (CAFs) and extracellular matrix (ECM), which plays a critical role

157 The delivery of stem cells on an extracellular matrix (ECM)-based platform alters cell be

158 investigate the potential of MRL/MpJ tendon extracellular matrix (ECM)-derived coatings to regulate

159 in the link between the cytoskeleton and the extracellular matrix (ECM).

160 iple involving extracellular tethers and the extracellular matrix (ECM).

161 prevalent glycosaminoglycans of the vascular extracellular matrix (ECM).

162 yte loss and dramatic changes in the cardiac extracellular matrix (ECM).

163 ordinated attachment and detachment from the extracellular matrix (ECM).

164 od vessel and tumor spheroids embedded in an extracellular matrix (ECM).

165 istances, which requires EVs to traverse the extracellular matrix (ECM).

166 and glycoprotein phases of connective tissue extracellular matrix (ECM).

167 The extracellular matrix encompasses a reservoir of bioactiv

168 rin in the glia, supporting proper glial and extracellular matrix ensheathment of the nervous system.

169 ted with expression of genes involved in the extracellular matrix (false discovery rate <0.25; NES, 2

170 gaps and pores, including those found within extracellular matrix fiber networks, between tightly pac

171 nalyses identified enrichment of Rho GTPase, extracellular matrix, focal adhesion and cytoskeleton pa

172 modification required for protein secretion, extracellular matrix formation, and organ growth.

173 cible factor-mediated adaptation to hypoxia, extracellular matrix formation, epigenetic regulation of

174 in regulation of oxidative phosphorylation, extracellular matrix formation, oocyte meiosis, choleste

175 soluble, low immunogenic (DNA-free), tendon extracellular matrix fraction (tECM) by urea extraction

176 essive H3K9me3 and H3K27me3 histone marks on extracellular matrix gene promoters and active H3K4me3 m

177 lammation-induced repression of chromatin on extracellular matrix gene promoters presents a therapeut

178 rk analysis revealed a structured network of extracellular matrix genes in NP compartments.

179 Extracellular matrix genes involved in epithelial-mesenc

180 lent transcriptional changes particularly in extracellular matrix genes, and this was accompanied by

181 r caused by mutations in the calcium binding extracellular matrix glycoprotein fibrillin-1.

182 ne antibiotic with off-target effects on the extracellular matrix, has demonstrated antifibrotic effe

183 ing growth factor-beta and the deposition of extracellular matrix - have metabolic implications.

184 ers reflecting the mechanisms that determine extracellular matrix homeostasis are altered by sacubitr

185 Biomarkers reflecting extracellular matrix homeostasis are elevated in heart f

186 How they control the extracellular matrix, important to breast physiology and

187 lted in lower accumulation of cartilage-like extracellular matrix in a pellet assay, while GRASLND ov

188 thway is critical for the development of the extracellular matrix in cartilage by regulating both ana

189 wed LOXL2 promotes proteoglycan networks and extracellular matrix in human TMJ-OA cartilage implants

190 ein linkage between the cytoskeleton and the extracellular matrix in skeletal muscle may contribute t

191 ein linkage between the cytoskeleton and the extracellular matrix in skeletal muscle may contribute t

192 Extracellular matrix in solid tumors has emerged as a sp

193 orchestrated by molecular signaling and the extracellular matrix in the mesenchyme.

194 ncludes genes involved in focal adhesion and extracellular matrix interactions, such as LAMB3 and CTN

195 Cell-ECM (extracellular matrix) interactions play essential roles

196 zing nanoparticle interaction with the tumor extracellular matrix is critical for developing strategi

197 The extracellular matrix is essential for brain development,

198 Drug cue-induced signaling in the extracellular matrix is regulated by catalytic activity

199 The tumor extracellular matrix is the main factor driving these in

200 , a ubiquitous glycosaminoglycan of the lung extracellular matrix, is rapidly recycled at sites of ve

201 llent model to study the mechanisms by which extracellular matrix macromolecules control collagen min

202 Extracellular matrix materials known as perineuronal net

203 way remodelling including alpha-SMA, HSP-47, extracellular matrix (MMP7, 9 and TIMP-1), angiogenesis

204 ncluding co-encapsulation of the injury site extracellular matrix modifier chondroitinase ABC (chABC)

205 g transcription factors and several encoding extracellular matrix-modifying proteins, were specifical

206 a prominent role in cell-matrix adhesion via extracellular matrix molecule fibronectin-induced alpha5

207 However, there has been no report that any extracellular matrix molecules expressed in periodontal

208 Perineuronal nets (PNNs) are assemblies of extracellular matrix molecules, which surround the cell

209 ells, depends on intricate interactions with extracellular matrix molecules.

210 pathogens, such as mammalian reovirus, mimic extracellular matrix motifs to specifically interact wit

211 An extracellular matrix of Fibronectin adheres the neural t

212 e lipoproteins already deposited in both the extracellular matrix of RPE cells and aged donor BrM tis

213 sition of amyloid-beta (Abeta) fibers in the extracellular matrix of the brain is a ubiquitous featur

214 ous neuron-specific substructures within the extracellular matrix of the central nervous system that

215 contribute to pathological remodeling of the extracellular matrix of the heart.

216 ls that efficiently create and negotiate the extracellular matrix of the mesoderm in order to migrate

217 These activated cells deposited extracellular matrix on the glomerular tuft which are al

218 The genes are enriched for functions in extracellular matrix organization and angiogenesis.

219 es in tumor tissues, while expression of the extracellular matrix organization pathway positively cor

220 pathogenesis, such as complement activation, extracellular matrix organization, platelet activation a

221 feration, differentiation, angiogenesis, and extracellular matrix organization.

222 m.SIGNIFICANCE STATEMENT The glial cells and extracellular matrix play important roles in supporting

223 nt, raltegravir were associated with greater extracellular matrix production and lipid accumulation i

224 00 is a major regulator of contractility and extracellular matrix production via control of H3K27 ace

225 e previously reported that a fragment of the extracellular matrix protein agrin promotes cardiac rege

226 tions in eyes shut homolog (EYS), a secreted extracellular matrix protein containing multiple laminin

227 Punctin/MADD-4, a member of the ADAMTSL extracellular matrix protein family, was identified as a

228 se-like protein (ACLP) is a collagen-binding extracellular matrix protein that has important roles in

229 Here, we identified an extracellular matrix protein that is released by these e

230 l density, and enhanced glycosylation of the extracellular matrix protein, alpha-dystroglycan, all co

231 taneous wound healing with discussion on how extracellular matrix proteins and hypoxia can be utilize

232 new approaches to MSC transplantation using extracellular matrix proteins and hypoxia preconditionin

233 omic analysis shows extensive alterations in extracellular matrix proteins and pathways related to fi

234 ion of inert heat-derived HSA hydrogels with extracellular matrix proteins and these may be used as a

235 The level of 3-bromotyrosine in extracellular matrix proteins from normally cultured cel

236 ATEMENT Emerging evidence supports roles for extracellular matrix proteins in boosting synapse format

237 merging evidence supports roles for secreted extracellular matrix proteins in boosting synaptogenesis

238 ive synthesis, deposition and remodelling of extracellular matrix proteins in fibrosis.

239 c pathway proteins and a higher abundance of extracellular matrix proteins in SAGN.

240 l junction-related proteins in squamous, and extracellular matrix proteins in sarcomatoid subtypes.

241 in regulating synaptic formation by clearing extracellular matrix proteins that embed neurons.

242 sm, unfolded protein responses, secretion of extracellular matrix proteins, and cell proliferation.

243 MV receptor integrin beta 1 dissociates from extracellular matrix proteins, becoming internalized wit

244 decreased the TGFbeta-dependent induction of extracellular matrix proteins, including collagen Ialpha

245 blast-like cells that secrete high levels of extracellular matrix proteins, resulting in fibrosis.

246 cells resulted in a decrease in adhesion to extracellular matrix proteins.

247 cretion of extracellular vesicles containing extracellular matrix proteins.

248 ps was assessed after treatment with various extracellular matrix proteins.

249 control their proliferation and secretion of extracellular matrix proteins.

250 oto-crosslinkable formulation of native ECM (extracellular matrix) proteins and used this bioink to 3

251 in pathways linked to insulin secretion and extracellular matrix-receptor interaction.

252 1 and alphaVbeta3/beta5 integrins, essential extracellular matrix receptors in mesenchymal tumors, wh

253 d a selective activation of inflammatory and extracellular matrix related gene sets.

254 cell migration, with increased expression of extracellular matrix-related genes, including MMP7 and M

255 simultaneous assessment of collagen-related extracellular matrix remodeling and inflammatory activit

256 al programs but also in subtypes involved in extracellular matrix remodeling and vascularization.

257 aled suppression of contractile SMC markers, extracellular matrix remodeling enzymes, and cytokines/r

258 t be caused by biophysical processes such as extracellular matrix remodeling in the case of mesenchym

259 e, we identify metabolic enzymes involved in extracellular matrix remodeling that are upregulated dur

260 e severity of pulmonary fibrotic lesions and extracellular matrix remodeling, and improved pulmonary

261 mune avoidance, increased lymphatic network, extracellular matrix remodeling, and increased seeding t

262 th smooth muscle cells (SMCs), inflammation, extracellular matrix remodeling, and mitogens.

263 cells revealed a gene signature dominated by extracellular matrix remodeling, notably affecting STMN3

264 osage influenced gene expression involved in extracellular matrix remodeling, which is critical for a

265 to a unique stem cell marker gene-positive, extracellular matrix-remodeling, "pioneer" cell phenotyp

266 ses in the haltere, which prevents the basal extracellular matrix remodelling necessary for wing morp

267 moting inflammation by driving angiogenesis, extracellular matrix remodelling, metastasis and immunos

268 ified multiple biological roles ranging from extracellular matrix reorganization to modulation of the

269 y the excessive deposition of a disorganized extracellular matrix, resulting in rigid benign tumors.

270 dhesions to uphold the structure of the glia-extracellular matrix sheath.

271 Further characterization of the extracellular matrix showed strong aggrecan and collagen

272 ubstantial dysregulation of inflammatory and extracellular matrix-signaling pathways with AF and AF+A

273 arkedly from normal brain in upregulation of extracellular matrix structural components including col

274 ts that most enriched proteins play roles in extracellular matrix structure and remodeling.

275 Perineuronal nets (PNNs) are an extracellular matrix structure rich in chondroitin sulfa

276 ibril surface charge on the integrity of the extracellular matrix structure surrounding glycated coll

277 lated to methylation, protein glycosylation, extracellular matrix structure, sugars, Krebs cycle inte

278 These results establish that the hyaluronan extracellular matrix surrounds developing excitatory syn

279 isms for mechanical hemostasis regulation in extracellular matrix that are pathologically activated i

280 feature in biological systems is texture in extracellular matrix that gains functions when hardened,

281 and its binding proteins to form bridges of extracellular matrix that ligate the severed ends of the

282 The zona pellucida (ZP) is an extracellular matrix that surrounds all mammalian oocyte

283 ese cells are organized and surrounded by an extracellular matrix, the interphotoreceptor matrix (IPM

284 lls, the perineurial glia, and a specialized extracellular matrix, the neural lamella.

285 ons are surrounded by specializations of the extracellular matrix, the perineuronal nets (PNNs).

286 endon cells to increase the stiffness of the extracellular matrix; this adaptation may occur in part

287 linking responses to the Shh mitogen and the extracellular matrix to control cerebellar granule neuro

288 lex targeting materials that penetrate brain extracellular matrix to increase transfection efficiency

289 nsmembrane proteases that remodel the apical extracellular matrix to promote wing morphogenesis.

290 Cells sense mechanical cues from the extracellular matrix to regulate cellular behavior and m

291 in transmitting mechanical stimuli from the extracellular matrix to tendon cells, thereby triggering

292 ability of spheroid cancer cells deprived of extracellular matrix to undergo ferroptosis.

293 n American patient group showed increases in extracellular matrix transcripts that may be due to unde

294 sis), matrix metalloproteinase-7 (related to extracellular matrix turnover), ST-2, and N-terminal pro

295 delling, junction dissolution, migration and extracellular matrix turnover.

296 ) is a phosphoglycoprotein secreted into the extracellular matrix upon liver injury, acting as a cyto

297 ed in bone, able to modify their surrounding extracellular matrix via specialized molecular remodelin

298 ations indicated that: (i) stiffening of the extracellular matrix was a prerequisite for cells overac

299 Fibrosis is the abnormal deposition of extracellular matrix, which can lead to organ dysfunctio

300 valuate the association of alteration in the extracellular matrix with diabetic status and its implic