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 n the gene coding for FIBRILLIN-1 (FBN1), an extracellular matrix protein.

4 n that interferes with cell adhesion to this extracellular matrix protein.

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

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

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

8 differentiation with resulting deposition of extracellular matrix proteins.

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

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

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

12 integrin receptors and subsequently degrades extracellular matrix proteins.

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

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

15 MicroRNA29 (miR29) targets extracellular matrix proteins.

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

17 so increasing expression of cartilage tissue extracellular matrix proteins.

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

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

20 mineralization process that is controlled by extracellular matrix proteins.

21 rtic arch, aneurysms and failure to assemble extracellular matrix proteins.

22 ell characterized cell surface receptors for extracellular matrix proteins.

23 genes encoding proinflammatory cytokines and extracellular matrix proteins.

24 t necessary to mediate interaction with host extracellular matrix proteins.

25 reted serine protease that degrades numerous extracellular matrix proteins.

26 pe I collagen, and reduced the deposition of extracellular matrix proteins.

27 tion and increases adherence to several host extracellular matrix proteins.

28 s, cell-surface molecules on other cells and extracellular matrix proteins.

29 miR-29 regulates expression of extracellular matrix proteins.

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

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

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

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

34 erentiation into myofibroblasts that secrete extracellular matrix proteins.

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

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

37 s endothelial function via interactions with extracellular matrix proteins.

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

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

40 oepicardial organ and aberrant deposition of extracellular matrix proteins.

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

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

43 ermal growth factor-containing, fibulin-like extracellular matrix protein 1 (EFEMP1) causes its ineff

44 345W mutation in EGF-containing fibulin-like extracellular matrix protein 1 (EFEMP1) to investigate t

45 Extracellular matrix protein 1, a direct targeting molec

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

47 miR-29c induces cell apoptosis and increases extracellular matrix protein accumulation.

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

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

50 The extracellular matrix protein adhesin A (EmaA) of the Gra

51 Extracellular matrix proteins adsorbed onto mineral surf

52 ascin-C, a proproliferative and promigratory extracellular matrix protein, after injury was attenuate

53 ctivity on a number of substrates, including extracellular matrix proteins, although its role in neut

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

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

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

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

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

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

60 The main extracellular matrix proteins and associated cytokines w

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

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

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

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

65 growth and transcription factors, as well as extracellular matrix proteins and immune response protei

66 ithelium, as well as increasing adherence to extracellular matrix proteins and increasing biofilm for

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

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

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

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

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

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

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

74 and suppressed the expression of TGF-beta1, extracellular matrix proteins and p21 both in vivo and i

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

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

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

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

79 Gene set enrichment analysis identified extracellular matrix proteins and those with immunologic

80 a-dystroglycan to coordinate the assembly of extracellular matrix proteins and to bind arenaviruses o

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

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

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

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

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

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

87 Extracellular matrix proteins are biosynthesized in the

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

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

90 Because certain extracellular matrix proteins are known to modulate cell

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

92 d migration and adhesion of myeloid cells on extracellular matrix proteins, as well as impaired activ

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

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

95 Agrin, an extracellular matrix protein belonging to the heterogene

96 The extracellular matrix protein biglycan (Bgn) is a leucine

97 Here we examine a novel role for the extracellular matrix protein biglycan in synapse stabili

98 ed TMJ OA genetic mouse model deficient in 2 extracellular matrix proteins, biglycan and fibromodulin

99 rginine-glycine-aspartate (RGD)] that mimics extracellular matrix protein binding to integrins was mi

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

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

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

103 the increase in DNA content and adhesion to extracellular matrix proteins by TLR2-dependent stimulat

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

105 Recently, we discovered that the extracellular matrix protein collagen IV is important fo

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

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

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

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

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

111 ciated with an increase in the expression of extracellular matrix proteins: collagen I, tenascin, and

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

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

114 Type I collagen is a heterotrimeric extracellular matrix protein consisting of two alpha1(I)

115 An extracellular matrix protein containing VWA-like domains

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

117 omain present in the nidogen or entactin (an extracellular matrix protein), contributes to the protei

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

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

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

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

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

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

124 Two main proteases cleave enamel extracellular matrix proteins during amelogenesis.

125 Tenascin-C (Tnc) is an extracellular matrix protein (ECM) involved in various a

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

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

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

129 cupancy" of alphavbeta3 (i.e. the binding of extracellular matrix proteins) enhances signaling induce

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

131 Affinity for these extracellular matrix proteins explains the striking abil

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

133 interstitial nephritis antigen (TINag) is an extracellular matrix protein expressed in tubular baseme

134 ation in hippocampal explants, and TNR is an extracellular matrix protein expressed primarily in the

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

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

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

138 on within the fbn2b locus, which encodes the extracellular matrix protein Fibrillin 2b (OMIM ID: 1210

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

140 1 (PAR-1) expressed by stromal cells and the extracellular matrix protein, fibrinogen.

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

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

143 stis adhesin molecule Ail interacts with the extracellular matrix protein fibronectin (Fn) on host ce

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

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

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

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

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

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

150 In addition, adhesion of PASMC to the extracellular matrix protein fibronectin was critically

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

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

153 vivo and in vitro after cell culture on the extracellular matrix protein, fibronectin.

154 ntially expressed genes encoding interactive extracellular matrix proteins, fibronectin, integrins, a

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

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

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

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

159 This extracellular matrix protein has been described to be in

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

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

162 Tgfbi, a fasciclin family extracellular matrix protein, has various roles in human

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

164 ough several mutations in the genes encoding extracellular matrix proteins have been recognized, more

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

166 rt, evidence is presented that the conserved extracellular matrix protein hemicentin(HIM-4) is requir

167 Anosmin is an extracellular matrix protein implicated in FGF signaling

168 TNC is an extracellular matrix protein important in fetal developm

169 Elastin is the extracellular matrix protein in vertebrates that provide

170 ional analysis by relative quantification of extracellular matrix proteins in articular cartilages, m

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

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

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

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

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

176 eam gene expression profiles of major dentin extracellular matrix proteins in response to Nma/BAMBI,

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

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

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

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

181 f stromal syndecan-1, a receptor for several extracellular matrix proteins including collagens.

182 nalysis revealed circumferentially organized extracellular matrix proteins including elastin and the

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

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

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

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

187 Extracellular matrix proteins, including those of the la

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

189 ocystis carinii to lung epithelial cells and extracellular matrix proteins induces mRNA expression of

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

191 methods for identifying receptor-ligand and extracellular matrix protein interactions will greatly a

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

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

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

195 he C-terminal globular domains (LG45) of the extracellular matrix protein laminin 332.

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

197 The extracellular matrix protein laminin conveys spatial inf

198 he cytoskeletal marker beta-catenin, and the extracellular matrix protein laminin V.

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

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

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

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

203 hed activation of latent TGFbetas, which are extracellular matrix protein ligands for beta8 integrin.

204 s also induced hESCs to deposit and organize extracellular matrix proteins like laminin such that the

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 herin cdh-3, and two genes encoding secreted extracellular matrix proteins, mig-6/papilin and him-4/h

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

210 Amelogenin, the major extracellular matrix protein of dental enamel, regulates

211 We find that the expression of TNC, an extracellular matrix protein of stem cell niches, is ass

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

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

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

215 Here we show that, on cell adhesion to extracellular matrix proteins or stimulation by platelet

216 hat expression of Postn that encodes for the extracellular matrix protein periostin dramatically redu

217 Extracellular matrix proteins play an integral role in m

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

219 CXCL16 deficiency attenuated extracellular matrix protein production and suppressed b

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

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

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

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

224 expands our knowledge of calcium binding in extracellular matrix proteins; provides new clues into d

225 Immunoreactivity against the extracellular matrix protein Reelin in a region directly

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

242 les such as Cox-2 and PGE2 and expression of extracellular matrix proteins such as MMP2, vimentin, uP

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

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

245 Dystroglycan is an important receptor for extracellular matrix proteins, such as laminin, in the b

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

247 attenuated TGF-beta1-induced upregulation of extracellular matrix protein synthesis.

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 The extracellular matrix protein TGFBI enhances the cytotoxi

253 Tropoelastin is an extracellular matrix protein that assembles into elastic

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

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

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

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

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

259 Fibronectin (FN) is an extracellular matrix protein that is assembled into fibr

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

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

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

263 Reelin is an extracellular matrix protein that is vital for neuronal

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

267 ing affinity to the SDF-1 receptor CXCR4 and extracellular matrix proteins that become exposed after

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

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

273 nregulated in the mutant embryos and several extracellular matrix proteins that were upregulated in t

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

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

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

282 vitro results indicate that the presence of extracellular matrix proteins together with a mixture of

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

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

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

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

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

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

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

290 Deposition of extracellular matrix proteins was lower in the KD3010-tr

291 ogical cofactors that play numerous roles in extracellular matrix proteins, we examined the calcium b

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 channels and scaffolding, cell adhesion, and extracellular matrix proteins, which may hold the ion ch

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

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