ライフサイエンスコーパス: extracellular matrix protein

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

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

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

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

5 oduction of collagen type I (COL1) and other extracellular matrix proteins.

6 occal adhesins interacts with a multitude of extracellular matrix proteins.

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

8 erentiation into myofibroblasts that secrete extracellular matrix proteins.

9 cretion of extracellular vesicles containing extracellular matrix proteins.

10 s and to RGD motifs present in loops in many extracellular matrix proteins.

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

12 y stabilizing fibrin clots and cross-linking extracellular matrix proteins.

13 s endothelial function via interactions with extracellular matrix proteins.

14 pression of bone-related gene regulators and extracellular matrix proteins.

15 ofibroblasts, which secrete large amounts of extracellular matrix proteins.

16 oepicardial organ and aberrant deposition of extracellular matrix proteins.

17 tory proteins and enhances the production of extracellular matrix proteins.

18 f SMC contractile genes and up-regulation of extracellular matrix proteins.

19 differentiation with resulting deposition of extracellular matrix proteins.

20 st-derived MVs including calcium-binding and extracellular matrix proteins.

21 x metalloproteinase (MMP) degradation of the extracellular matrix proteins.

22 l cell surface where it promotes adhesion to extracellular matrix proteins.

23 control their proliferation and secretion of extracellular matrix proteins.

24 integrin receptors and subsequently degrades extracellular matrix proteins.

25 by an extensive network of stromal cells and extracellular matrix proteins.

26 ired cell spreading and adhesion to selected extracellular matrix proteins.

27 MicroRNA29 (miR29) targets extracellular matrix proteins.

28 collagen IX-deficient cartilage included 15 extracellular matrix proteins.

29 ion with adenosine deaminase (ADA) and other extracellular matrix proteins.

30 tes, endothelial and neuronal cells, and the extracellular matrix proteins.

31 ase-beta expression, indicative of increased extracellular matrix proteins.

32 mineralization process that is controlled by extracellular matrix proteins.

33 roteomics revealed a significant increase in extracellular matrix proteins.

34 metalloproteinase) family, known to process extracellular matrix proteins.

35 ng its ability to function as a receptor for extracellular matrix proteins.

36 kinase (AKT) signaling and up-regulation of extracellular matrix proteins.

37 (63%) were plasma membrane, cell surface or extracellular matrix proteins.

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

39 so increasing expression of cartilage tissue extracellular matrix proteins.

40 esembles structures found in many eukaryotic extracellular-matrix proteins.

41 Here, we report that extracellular matrix protein 1 (ECM1) is a previously un

42 345W mutation in EGF-containing fibulin-like extracellular matrix protein 1 (EFEMP1) to investigate t

43 Extracellular matrix protein 1, a direct targeting molec

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

45 duced fibrogenic gene expression, release of extracellular matrix proteins, activation of hepatic myo

46 d phenotypes, including enhanced adhesion to extracellular matrix proteins, activation of intracellul

47 ur study unveils netrin-4 as a non-enzymatic extracellular matrix protein actively disrupting pre-exi

48 Extracellular matrix proteins adsorbed onto mineral surf

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

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

51 anced adherence to human enterocytes through extracellular matrix protein and bacterial aggregation.

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

53 tent TGF-beta binding protein 1 (LTBP-1), an extracellular matrix protein and key regulator of TGF-be

54 re muscle centric followed by cell adhesion, extracellular matrix proteins and a few pro-inflammatory

55 ssion of alpha-smooth muscle actin (SMA) and extracellular matrix proteins and activated AMP-activate

56 g to an increased level of cell-junction and extracellular matrix proteins and an altered cytokine se

57 ucine-rich proteoglycans interact with other extracellular matrix proteins and are important regulato

58 The main extracellular matrix proteins and associated cytokines w

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

60 nned by a network of stromal cells producing extracellular matrix proteins and chemokines, enabling l

61 ent mesangial cells, increased production of extracellular matrix proteins and cytokines, and ultimat

62 cruited and activated to lay a foundation of extracellular matrix proteins and glycosaminoglycans tha

63 eric antigen receptor (CAR) T cells, reduced extracellular matrix proteins and glycosaminoglycans.

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

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

66 ing, and the effect of collagen I and fibrin extracellular matrix proteins and insulin-like growth fa

67 expression of alpha-smooth muscle actin and extracellular matrix proteins and is dependent on metabo

68 roglycan (DG) is a cell surface receptor for extracellular matrix proteins and is involved in cell po

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

70 r observed that Pneumocystis binding to host extracellular matrix proteins and lung epithelial cells

71 le pro-fibrotic molecules, including several extracellular matrix proteins and myofibroblast and cell

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

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

74 cle cell migration and adhesion to different extracellular matrix proteins and regulate cellular stif

75 lysaccharide that decorates cell surface and extracellular matrix proteins and regulates the biologic

76 and characterized by increased deposition of extracellular matrix proteins and scar formation in the

77 t, through proper assembly of RGD-containing extracellular matrix proteins and the correct incorporat

78 ed silica nanoparticle monolayer coated with extracellular matrix proteins and the desired siRNA.

79 sulted in 2-4 folds increase in secretion of extracellular matrix proteins and the reorganization of

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

81 olved in the synaptic plasticity by cleaving extracellular matrix proteins and, thus, is associated w

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

83 sections with collagen-I, fibronectin (major extracellular-matrix proteins), and alpha-SMA (well-char

84 rs, potentiation of growth factor signals by extracellular matrix proteins, and activation of self-re

85 HTRA1 has the capacity to degrade numerous extracellular matrix proteins, and as such, its potentia

86 actor beta-1-SMAD3 activation, production of extracellular matrix proteins, and cell contractility.

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

88 d chemokines, enzymes and enzyme inhibitors, extracellular matrix proteins, and membrane receptors, b

89 These include cell surface proteins, extracellular matrix proteins, and soluble ligands.

90 Extracellular matrix proteins are biosynthesized in the

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

92 des that cell surface, soluble-secreted, and extracellular matrix proteins are generally rich in disu

93 ngs demonstrate the direct involvement of an extracellular matrix protein as a receptor for TeNT at t

94 eered to display active enzymes that promote extracellular matrix protein assembly.

95 nt TGF-beta-binding protein-2 (LTBP-2) is an extracellular matrix protein associated with microfibril

96 novel candidates were identified, including extracellular matrix proteins associated with the baseme

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

98 repeating disaccharide that is necessary for extracellular matrix protein binding to O-mannosylated a

99 pport cells, gap junctions, soluble factors, extracellular matrix proteins, blood vessels and neural

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

101 ations in the primary amino acid sequence of extracellular matrix proteins can have profound effects

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

103 stribution was dependent on induction of the extracellular matrix protein collagen type V alpha 1 (co

104 clinical spectrum caused by mutations in the extracellular matrix protein collagen VI.

105 Here, we show that, similar to the extracellular matrix protein collagen, amyloids of vario

106 stronger response to TGF-beta1 in producing extracellular matrix protein (collagen and fibronectin)

107 lasts correlated with gene expression of the extracellular matrix proteins, collagen (Col)1a1, Col1a2

108 h Muscle Actin, Vimentin, and beta-catenin), extracellular matrix proteins (Collagens, Fibronectin, a

109 panied by key tumor-promoting changes in the extracellular matrix protein composition.

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

111 An extracellular matrix protein containing VWA-like domains

112 thermore, we found that CD157 binds to other extracellular matrix proteins containing heparin-binding

113 hanisms, in part through upregulation of the extracellular matrix protein decorin.

114 cers more invasive by increasing proteolytic extracellular matrix protein degradation fostering colle

115 minantly responsible for A549 cell rounding, extracellular matrix protein degradation, and IL-8 degra

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

117 hage activation to decrease TGF-beta-induced extracellular matrix protein deposition in the kidney in

118 ion of candidate molecules revealed that the extracellular matrix protein dermatopontin (Dpt) is invo

119 the epithelium to the cuticle via the apical extracellular-matrix protein Dumpy (Dp).

120 roperties in vitro Thus, Fgfbp1 is a crucial extracellular matrix protein during BBB maturation that

121 Bacterial adherence to extracellular matrix proteins (ECMp) plays important rol

122 , which execute tissue fibrosis by producing extracellular matrix proteins, efficiently engulf dead c

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

124 ted interaction between cancer cells and the extracellular matrix proteins, enhancing cell detachment

125 exhibited defective adhesion to a variety of extracellular matrix proteins, especially laminin-1 and

126 Our findings unravel a mechanism by which an extracellular matrix protein evokes stress signaling in

127 Affinity for these extracellular matrix proteins explains the striking abil

128 h factor beta-induced protein (TGFBIp) is an extracellular matrix protein expressed in several cell t

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

130 ac development and the regulation of cardiac extracellular matrix protein expression.

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

132 materials that mimic the nanoscale order of extracellular matrix protein fibers and yield suitable e

133 FBN1 encodes the extracellular matrix protein fibrillin 1, which is a maj

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

135 1 (PAR-1) expressed by stromal cells and the extracellular matrix protein, fibrinogen.

136 mponent, and, separately have shown that the extracellular matrix protein fibronectin (FN) contribute

137 The mechanism of assembly of the extracellular matrix protein fibronectin (FN) into elast

138 evels significantly reduced secretion of the extracellular matrix protein fibronectin (FN).

139 e this vasodilatation, we show here that the extracellular matrix protein fibronectin also contribute

140 des are known to mimic the binding domain of extracellular matrix protein fibronectin and selectively

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

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

143 Coating the detector surface with the extracellular matrix protein fibronectin resulted in cel

144 icated post-array detectors printed with the extracellular matrix protein fibronectin.

145 adhesion of vascular smooth muscle cells to extracellular matrix proteins fibronectin and collagen.

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

147 of these peptides further delineated how the extracellular matrix protein FN can support cell surviva

148 Bone sialoprotein (BSP) is an extracellular matrix protein found in mineralized tissue

149 ed by endogenous alarmins such as fragmented extracellular matrix proteins found in degenerating disc

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

151 Extracellular matrix proteins from the thrombospondin (T

152 ltistep process in which adhesion molecules, extracellular matrix proteins, growth factors, and their

153 ions, such as collagenous and noncollagenous extracellular matrix proteins, growth factors, proteases

154 This extracellular matrix protein has been described to be in

155 Osteopontin (OPN), an extracellular matrix protein, has a functional arginine-

156 Periostin, a secreted extracellular matrix protein, has been localized to depo

157 s growth factors, cytokines, chemokines, and extracellular matrix proteins have been limited yet prov

158 Extracellular matrix proteins have been shown to modulat

159 factor-binding domains identified in various extracellular matrix proteins have been shown to regulat

160 Dentin sialophosphoprotein (DSPP) is an extracellular matrix protein highly expressed by odontob

161 TNC is an extracellular matrix protein important in fetal developm

162 type 1 collagen expression (COL1A1), a major extracellular matrix protein important in liver fibrosis

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

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

165 en also identified widespread involvement of extracellular matrix proteins in DBL-1 regulation of bod

166 hat induction of Ctgf mediates expression of extracellular matrix proteins in diabetic kidney.

167 tion upon stimulation with growth factors or extracellular matrix proteins in different tumor cells.

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

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

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

171 ofibroblast proliferation and mRNA levels of extracellular matrix proteins in mice and attenuated myo

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

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

174 size and maintain collagen fibrils and other extracellular matrix proteins in tendon.

175 f proinflammatory cytokines, chemokines, and extracellular matrix proteins in the heart.

176 atment altered the expression of a subset of extracellular matrix proteins in the skin, including upr

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

178 Elastin is an important ECM (extracellular matrix) protein in large and small arterie

179 We investigated the role of periostin, an extracellular matrix protein, in the pathophysiology of

180 models to explain the observed enrichment of extracellular matrix proteins include both increased pro

181 , we identify copy number alterations in key extracellular matrix proteins including collagen 1 type

182 develops in a microenvironment enriched with extracellular matrix proteins including laminin (Ln)-332

183 Multiple extracellular matrix proteins, including collagen 1 and

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

185 on, revealed that miR-195 targets a cadre of extracellular matrix proteins, including collagens, prot

186 cells failed to express normal levels of key extracellular matrix proteins, including laminin alpha2.

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

188 Extracellular matrix proteins, including those of the la

189 ECM (Extracellular matrix) proteins, including basement-membr

190 ngth and diminishes the capacity of specific extracellular matrix proteins-including collagen I, coll

191 Neutrophil activation by FN, but not other extracellular matrix proteins, induces the release of th

192 four cell polarity, cell junction and apical extracellular matrix proteins involved in tracheal tube

193 rneuron-derived Collagen XIX, a synaptogenic extracellular matrix protein, is required for the format

194 Tenascin-C (TnC), an extracellular matrix protein, is transiently expressed d

195 Animal studies showed COL13A1, a synaptic extracellular-matrix protein, is involved in the formati

196 tin is one of the most highly phosphorylated extracellular matrix proteins known in nature with uniqu

197 tem provides a mechanism for the delivery of extracellular matrix proteins known to be important for

198 ts a new perspective on how mutations in the extracellular matrix protein laminin cause severe conseq

199 The extracellular matrix protein laminin conveys spatial inf

200 inoglycans such as heparan sulfate (HS), the extracellular matrix protein laminin, and/or integrin be

201 sclA allele restored the ability to bind the extracellular matrix proteins laminin and cellular fibro

202 ecular-weight kininogen (HK), as well as the extracellular matrix proteins laminin and collagen V.

203 ecrosis, and apoptosis and the generation of extracellular matrix proteins leading to fibrosis/cirrho

204 Extracellular matrix protein levels and contractile func

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

206 ifferentiation, and deposit large amounts of extracellular matrix proteins maintaining the structural

207 e used the EAE model and determined that the extracellular matrix protein matrilin-2 (MATN2) is an en

208 of the matrix metalloprotease MMP-10 and the extracellular matrix protein mindin (encoded by Spon2) i

209 at catalyzes the formation of cross-links in extracellular matrix proteins, namely, collagen and elas

210 Neural crest cells produce the extracellular matrix protein nidogen: impairing nidogen

211 nd factor A domain-containing protein 5a, an extracellular matrix protein of the brain.

212 Cells remove extracellular matrix proteins off the surface of gels co

213 ut did not significantly drive production of extracellular matrix proteins or alpha-smooth muscle act

214 Extracellular matrix proteins play an integral role in m

215 Periostin, an extracellular matrix protein, plays key role in cell adh

216 CXCL16 deficiency attenuated extracellular matrix protein production and suppressed b

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

218 processes, such as mucus hypersecretion and extracellular matrix protein production, are also direct

219 naling enhanced fibroblast proliferation and extracellular matrix protein production, effects relevan

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

221 include Vibrio polysaccharide (VPS) and the extracellular matrix proteins RbmA, RbmC, and Bap1.

222 The cell adhesion molecule L1 and the extracellular matrix protein Reelin play crucial roles i

223 Here, we report that the extracellular matrix protein Reelin, acting through its

224 e cellular and molecular mechanisms by which extracellular matrix proteins regulate left-right organ

225 ombospondin repeats)-like family, a class of extracellular matrix proteins related to the ADAM protea

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

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

228 E-glycan of dystroglycan serves as a tunable extracellular matrix protein scaffold, the extension of

229 Thrombospondin-1 (TSP-1) is a large extracellular matrix protein secreted by astrocytes duri

230 c carboxypeptidase-like protein (ACLP) is an extracellular matrix protein secreted by fibroblasts and

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

232 a multifunctional scaffold that coordinates extracellular matrix proteins, secreted cues, and transm

233 Cochlin, an extracellular matrix protein, shares homologies with the

234 characterized by luminal markers such as the extracellular matrix protein Slit.

235 mbinant WxL proteins from locus A bind human extracellular matrix proteins, specifically type I colla

236 amatically reduces lymphoma cell adhesion to extracellular matrix proteins, subcutaneous tumor size i

237 ustained fibrosis, excessive accumulation of extracellular matrix proteins substantially dampens the

238 yocardial fibrosis (ie, deposition of excess extracellular matrix proteins such as collagen).

239 The expression of extracellular matrix proteins such as Laminin and Fibron

240 r the interaction of alpha-dystroglycan with extracellular matrix proteins such as laminin-alpha2.

241 ils were activated in vitro with immobilized extracellular matrix proteins, such as fibronectin (FN),

242 Collagen and extracellular matrix proteins, such as heat shock protei

243 The presence of extracellular matrix proteins suggested increased produc

244 n with integrin beta1 were also required for extracellular matrix protein synthesis in response to HG

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

246 imulate fibroblast activation, inducing ECM (extracellular matrix) protein synthesis and promoting fi

247 CD47 KO increased tumor-associated extracellular matrix protein tenascin C (TNC) in xenogra

248 , diminishing expression of the desmoplastic extracellular matrix protein tenascin C, suppressing tum

249 SC derived from either PDLN or mPIN used the extracellular matrix protein Tenascin-C (TNC) to inhibit

250 Deposition of the extracellular matrix protein tenascin-C is part of the r

251 ed injury and attenuated upregulation of the extracellular matrix protein, tenascin C, which affords

252 Tropoelastin is an extracellular matrix protein that assembles into elastic

253 Fibronectin (FN) is an extracellular matrix protein that can be assembled by ce

254 Fibronectin (FN) is an extracellular matrix protein that can be assembled by ce

255 CCN6 (WISP3) is an extracellular matrix protein that exerts tumor suppressi

256 h factor-beta-induced protein (TGFBIp) is an extracellular matrix protein that has a role in a wide r

257 n-2 (MMRN2) is a unique endothelial specific extracellular matrix protein that has been implicated in

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

259 treatment reduced fibronectin expression, an extracellular matrix protein that is increased in diabet

260 entin sialophosphoprotein (DSPP) is a dentin extracellular matrix protein that is processed into dent

261 ility to angiogenic diseases and identify an extracellular matrix protein that is regulated by melano

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

263 gamma90 and the secretion of fibronectin, an extracellular matrix protein that regulates cell migrati

264 TIMP3 and vitronectin are 2 extracellular matrix proteins that abnormally accumulate

265 Amelogenin and ameloblastin are 2 extracellular matrix proteins that are essential for the

266 ause senescent erythrocytes to interact with extracellular matrix proteins that are exposed within th

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

268 ortant sources of inflammatory molecules and extracellular matrix proteins that contribute to disease

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

270 In many cases, natural aGPCR ligands are extracellular matrix proteins that dissociate the NTF to

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

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

273 s regulated by factors including enzymes and extracellular matrix proteins that promote or inhibit hy

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

275 d virus infectivity in vitro by proteolyzing extracellular matrix proteins, thereby increasing viral

276 selective peptides have been identified from extracellular matrix proteins; these peptides have prove

277 e of marked downregulation of genes encoding extracellular matrix proteins, those involving matrix de

278 This peptide interacts with the extracellular matrix protein thrombospondin 4 (TSP4), an

279 or-1 alpha (HIF-1alpha) and the synthesis of extracellular matrix proteins through a mechanical mecha

280 ated myofibroblasts that excessively deposit extracellular matrix proteins, thus compromising lung ar

281 Given the perceived difficulty in modifying extracellular matrix proteins to create aGPCR probes, we

282 gated in 96-well plates in medium containing extracellular matrix proteins to promote epithelializati

283 basis included enzymes, regulatory proteins, extracellular matrix proteins, transcription factors, an

284 The extracellular matrix protein tropoelastin is classically

285 Further, MMP12-mediated degradation of the extracellular matrix proteins tropoelastin and fibronect

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

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

288 t interactions and proteolytic processing of extracellular matrix proteins via MMP20.

289 ance of the interaction between uPAR and the extracellular matrix protein vitronectin (VN) for the si

290 novel role as a receptor for the plasma and extracellular matrix protein vitronectin (Vn).

291 approach to pattern the presentation of the extracellular matrix protein vitronectin, we accomplishe

292 n the levels of cytoskeletal, signaling, and extracellular matrix proteins were associated with CXCL8

293 The mRNA levels of inflammatory and extracellular matrix proteins were attenuated in the inf

294 s as well as the expression of cytokines and extracellular matrix proteins were evaluated by immunofl

295 Collagen and fibronectin (Fn) are two key extracellular matrix proteins, which are known to intera

296 PK increased the expression of alpha-SMA and extracellular matrix proteins, while inhibition of AMPK

297 Agrin is a large extracellular matrix protein whose isoforms differ in th

298 Laminins are extracellular matrix proteins, widely expressed but also

299 ions in fibrillin-1 (FBN1), which encodes an extracellular matrix protein with homology to latent TGF

300 Collagens are a group of extracellular matrix proteins with essential functions f