コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 scribe a clot Treg population that forms the matricellular acid- and cysteine-rich protein SPARC (sec
6 GF and NOV) family of proteins is a group of matricellular biomolecules involved in both physiologica
7 lting from cardiomyocyte-TrkA recognition by matricellular connective tissue growth factor (CTGF/CCN2
8 eft ventricular size and function, including matricellular (e.g. SPON1, MFAP4), senescence-associated
11 epithelial STAT3 activity and develop stiff, matricellular-enriched fibrosis associated with high epi
14 he findings implicate epithelial tension and matricellular fibrosis in the aggressiveness of SMAD4 mu
15 r lesion formation, we examined whether this matricellular gene cluster was also coordinately regulat
16 nectin, collagen IV, collagen VI, myocilin), matricellular genes (connective tissue growth factor [CT
19 f angiogenesis is thrombospondin-1 (TSP1), a matricellular glycoprotein known to influence adhesion,
22 e (SPARC) is an extracellular Ca(2+)-binding matricellular glycoprotein that associates with cell pop
23 in, acidic and rich in cysteine (SPARC) is a matricellular glycoprotein that is capable of inhibiting
24 d Protein Acidic and Rich in Cysteine), is a matricellular glycoprotein that is produced by tumor and
26 hibition of some angiogenic responses by the matricellular glycoprotein thrombospondin-1 and is there
30 at SPARC/osteonectin, a small ECM-associated matricellular glycoprotein, can induce MMP-2 activation
32 tential role for thrombospondin-2 (TSP-2), a matricellular glycoprotein, in the regulation of primary
34 ted protein, acidic and rich in cysteine), a matricellular glycoprotein, modulates the interaction of
36 pondins (Thbs) are a family of five secreted matricellular glycoproteins in vertebrates that broadly
39 f Eomes-dependent genes encode intercellular/matricellular interaction and cytoskeletal components, l
42 ealing in skin fibroblasts and establish its matricellular mode of action through integrin receptors.
43 uch as CCN1, an immediate-early gene-encoded matricellular molecule critical for vascular development
47 ficantly, we found that the TGF-beta-induced matricellular protein (TGFBI) was similarly biphasically
50 ed, cooperative interaction between the CCN1 matricellular protein and canonical TGF-beta1/SMAD3 sign
52 ed protein acidic and rich in cysteine) is a matricellular protein associated with the extracellular
63 titative mass spectrometry, we find that the matricellular protein CCN1/CYR61 is highly regulated by
64 ecently provided the first evidence that the matricellular protein CCN3 (official symbol NOV) functio
65 re, we determined that the expression of the matricellular protein CCN3 is strongly reduced in rodent
70 cytes with keratinocytes upregulates CCN3, a matricellular protein critical to maintenance of normal
71 everal microarray databases suggest that the matricellular protein Cyr61 is highly induced by LPA.
72 tion by these agonists and revealed that the matricellular protein cysteine-rich 61 (Cyr61/CCN1) is s
73 lammatory mediator cyclooxygenase 2, and the matricellular protein cysteine-rich angiogenic inducer 6
75 ive tissue growth factor (CTGF or CCN2) is a matricellular protein expressed by multiple cell types i
77 Mechanistically, CA19-9 modification of the matricellular protein fibulin-3 increased its interactio
79 vel downstream target Sparc, which encodes a matricellular protein found in PDAC stroma that has been
80 ervations suggest an important role for this matricellular protein in the local regulation of inflamm
81 pression project pinpoints POSTN, encoding a matricellular protein involved in bone formation and bon
84 th factor (CTGF) is a cysteine-rich secreted matricellular protein involved in wound healing and tiss
85 bospondin-1 (TSP) is a transiently expressed matricellular protein known to promote chemotaxis of leu
86 Thrombospondin-1 (TSP1) is a multifunctional matricellular protein known to promote progression of ch
87 ein acidic and rich in cysteine (SPARC) is a matricellular protein known to regulate extracellular ma
88 m, we have uncovered a critical role for the matricellular protein Mindin (SPON2) in fibrogenesis.
90 Here we show that CCN6 (WISP3), a secreted matricellular protein of the CCN (CYR61/CTGF/NOV) family
92 r CCN1 (cysteine-rich 61, CYR61), a secreted matricellular protein of the CCN family, is a ligand of
93 CN3 (NOV, nephroblastoma overexpressed) is a matricellular protein of the CCN family, which also incl
98 are the first to show that induction of the matricellular protein osteopontin facilitates DMBA/TPA-i
99 hat Wnt-1 strongly induced the expression of matricellular protein osteopontin, and modestly enhanced
102 -and the quantification of its levels of the matricellular protein periostin, which cannot be accurat
105 Connective tissue growth factor (CTGF) is a matricellular protein presumed to be involved in the pat
107 ers of fibrinolysis, endothelial activation, matricellular protein release, and tissue damage and wit
108 , fibrinolysis, endothelial cell activation, matricellular protein release, and tissue damage were me
109 ered the role of thrombospondin-1 (TSP-1), a matricellular protein released in abundance from activat
110 otein 61 (Cyr61) is a dynamically expressed, matricellular protein required for proper angiogenesis a
111 secreted cysteine-rich and integrin-binding matricellular protein required for proper cardiovascular
112 factor 1 (CCN1) is a dynamically expressed, matricellular protein required for vascular development
115 le of which was the evolutionarily conserved matricellular protein Secreted Protein Acidic and Rich i
117 and rich in cysteine)/BM 40/osteonectin is a matricellular protein shown to function as a counteradhe
119 r-activation of the small GTPase Ran and the matricellular protein SMOC-2 that has important conseque
120 ient with a loss-of-function of the secreted matricellular protein SMOC2 (SPARC related modular calci
121 Arntl2 partner and functionally validate the matricellular protein Smoc2 as a pro-metastatic secreted
123 observed in the presence and absence of the matricellular protein SPARC (secreted protein, acidic an
124 This study identifies the stromal-derived matricellular protein SPARC as a novel regulator of isle
129 In addition, interstitial deposition of the matricellular protein tenascin, a marker of active remod
131 rowth factor (CCN2, also known as CTGF) is a matricellular protein that appears to play an important
133 We show that CCN1 (also known as CYR61), a matricellular protein that dampens and resolves liver fi
138 d Protein, Acidic and Rich in Cysteine) is a matricellular protein that inhibits mesangial cell proli
139 reported that fibulin-5, an integrin-binding matricellular protein that is essential for elastic fibe
142 ed connective tissue growth factor (CTGF), a matricellular protein that is highly expressed in the br
143 ein acidic and rich in cysteine (SPARC) is a matricellular protein that is important for the regulati
145 Connective tissue growth factor (CCN2) is a matricellular protein that is up-regulated in many fibro
147 Connective tissue growth factor (CTGF) is a matricellular protein that mediates cell-matrix interact
148 d protein, acidic and rich in cysteine) is a matricellular protein that modulates cell adhesion and p
149 protein acidic rich in cysteine (SPARC) is a matricellular protein that modulates the activity of gro
150 (osteonectin) (SPARC) gene, which encodes a matricellular protein that participates in normal tissue
151 ue growth factor (CTGF/CCN2) is an inducible matricellular protein that plays a major role in fibropr
153 ytes with keratinocytes up-regulated CCN3, a matricellular protein that we subsequently found to be c
155 to test the hypothesis that the prototypical matricellular protein thrombospondin (TSP)-1, a potent a
159 undertook a systematic study focused on the matricellular protein Thrombospondin-1 (THBS1) to uncove
162 ere found to contain excessive levels of the matricellular protein thrombospondin-2 (TSP2) and geneti
164 ng Protein-2 (Smoc-2) is a broadly-expressed matricellular protein which contributes to mitogenesis v
165 naling pathway protein 1 (WISP1), a secreted matricellular protein whose expression is elevated in se
168 the expression of thrombospondin 2 (TSP2), a matricellular protein with a demonstrated role in respon
171 otein acidic and rich in cysteine (SPARC), a matricellular protein with counteradhesive properties, i
173 orted that Olfactomedin-like 3 (Olfml3) is a matricellular protein with proangiogenic properties.
176 l Communication Network factor 4, a secreted matricellular protein, alters the tumor microenvironment
177 include Thrombospondin 2 (THBS2), encoding a matricellular protein, and cellular proteins, GAS1, CASR
178 bospondin-1 (TSP-1), a potent proatherogenic matricellular protein, as a putative link between hyperg
181 , acidic and rich in cysteine (SPARC) family matricellular protein, during invasive phases of prostat
182 ests that CYR61 (now named CCN1), a secreted matricellular protein, has a role in the pathogenesis of
183 ne), although primarily known as a secreted, matricellular protein, has also been identified in uroth
185 Periostin (PN), a novel fasciclin-related matricellular protein, has been implicated in cardiac de
186 , a secreted extracellular matrix-associated matricellular protein, is elevated in dermal fibroblasts
187 eport that expression of Sparcl1, a secreted matricellular protein, is upregulated in pulmonary capil
191 in 1 (SMOC1) is an osteonectin/SPARC-related matricellular protein, whose expression is regulated by
192 lved in extracellular matrix remodeling, and matricellular protein-protein and protein-cholangiocarci
198 ster analysis, we identified a subset of six matricellular proteins (eg, osteopontin and plasminogen
200 small leucin-rich repeat proteoglycans, and matricellular proteins affecting both the composition an
201 tuates secretion of structural collagens and matricellular proteins and markedly increases MMP2 secre
202 lecular signature composed of an ensemble of matricellular proteins and remodeling enzymes they provi
206 The thrombospondin (Thbs) family of secreted matricellular proteins are stress- and injury-induced me
207 ated that NELL1 loss skews the expression of matricellular proteins associated with reduced FAK signa
208 e combined effects of the fibroblast-derived matricellular proteins CD5L (CD5 antigen-like), SPARC (s
210 ediated pathways, neurohumoral cascades, and matricellular proteins deposited in the provisional matr
211 lcium-binding proteins (SMOCs) are conserved matricellular proteins found in organisms from Caenorhab
212 d by the excess deposition of structural and matricellular proteins in the extracellular space, under
216 y, we demonstrate that the presence of these matricellular proteins results in significantly stiffer
217 ckout sarcoma cells on wild-type OS-enriched matricellular proteins reversed the phenotypic and signa
221 e 1 (SC1) is a member of the SPARC family of matricellular proteins that has been implicated in the r
223 1) is a member of the CCN family of secreted matricellular proteins that includes connective tissue g
224 -adhesion is induced by the highly regulated matricellular proteins TSP1 and 2, tenascin-C, and SPARC
225 e we show that CCN1 (CYR61) and CCN2 (CTGF), matricellular proteins upregulated at sites of inflammat
228 ediators of extracellular matrix remodeling, matricellular proteins, and cardiac integrins compared w
229 ls of extracellular matrix genes, integrins, matricellular proteins, and growth factors, when compare
230 d SPARC, two homologs of the SPARC family of matricellular proteins, in the foreign body response.
231 ndly decreased gene expression of a group of matricellular proteins, of which periostin was prominent
241 incubation (8 h) of UCB CD34+ cells with the matricellular regulator Nov (CCN3) increases the frequen
245 Ab) that is directed against the pleiotropic matricellular signaling protein connective tissue growth