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5 GF and NOV) family of proteins is a group of matricellular biomolecules involved in both physiologica
6 lting from cardiomyocyte-TrkA recognition by matricellular connective tissue growth factor (CTGF/CCN2
8 epithelial STAT3 activity and develop stiff, matricellular-enriched fibrosis associated with high epi
10 he findings implicate epithelial tension and matricellular fibrosis in the aggressiveness of SMAD4 mu
11 r lesion formation, we examined whether this matricellular gene cluster was also coordinately regulat
13 f angiogenesis is thrombospondin-1 (TSP1), a matricellular glycoprotein known to influence adhesion,
16 e (SPARC) is an extracellular Ca(2+)-binding matricellular glycoprotein that associates with cell pop
17 in, acidic and rich in cysteine (SPARC) is a matricellular glycoprotein that is capable of inhibiting
18 d Protein Acidic and Rich in Cysteine), is a matricellular glycoprotein that is produced by tumor and
20 hibition of some angiogenic responses by the matricellular glycoprotein thrombospondin-1 and is there
24 at SPARC/osteonectin, a small ECM-associated matricellular glycoprotein, can induce MMP-2 activation
25 tential role for thrombospondin-2 (TSP-2), a matricellular glycoprotein, in the regulation of primary
27 ted protein, acidic and rich in cysteine), a matricellular glycoprotein, modulates the interaction of
32 ealing in skin fibroblasts and establish its matricellular mode of action through integrin receptors.
33 uch as CCN1, an immediate-early gene-encoded matricellular molecule critical for vascular development
35 ficantly, we found that the TGF-beta-induced matricellular protein (TGFBI) was similarly biphasically
38 ed, cooperative interaction between the CCN1 matricellular protein and canonical TGF-beta1/SMAD3 sign
40 ed protein acidic and rich in cysteine) is a matricellular protein associated with the extracellular
46 titative mass spectrometry, we find that the matricellular protein CCN1/CYR61 is highly regulated by
47 ecently provided the first evidence that the matricellular protein CCN3 (official symbol NOV) functio
48 re, we determined that the expression of the matricellular protein CCN3 is strongly reduced in rodent
53 cytes with keratinocytes upregulates CCN3, a matricellular protein critical to maintenance of normal
54 everal microarray databases suggest that the matricellular protein Cyr61 is highly induced by LPA.
55 tion by these agonists and revealed that the matricellular protein cysteine-rich 61 (Cyr61/CCN1) is s
56 lammatory mediator cyclooxygenase 2, and the matricellular protein cysteine-rich angiogenic inducer 6
59 vel downstream target Sparc, which encodes a matricellular protein found in PDAC stroma that has been
60 ervations suggest an important role for this matricellular protein in the local regulation of inflamm
63 th factor (CTGF) is a cysteine-rich secreted matricellular protein involved in wound healing and tiss
64 bospondin-1 (TSP) is a transiently expressed matricellular protein known to promote chemotaxis of leu
65 Thrombospondin-1 (TSP1) is a multifunctional matricellular protein known to promote progression of ch
66 ein acidic and rich in cysteine (SPARC) is a matricellular protein known to regulate extracellular ma
68 Here we show that CCN6 (WISP3), a secreted matricellular protein of the CCN (CYR61/CTGF/NOV) family
70 r CCN1 (cysteine-rich 61, CYR61), a secreted matricellular protein of the CCN family, is a ligand of
71 CN3 (NOV, nephroblastoma overexpressed) is a matricellular protein of the CCN family, which also incl
76 are the first to show that induction of the matricellular protein osteopontin facilitates DMBA/TPA-i
77 hat Wnt-1 strongly induced the expression of matricellular protein osteopontin, and modestly enhanced
80 Connective tissue growth factor (CTGF) is a matricellular protein presumed to be involved in the pat
81 ers of fibrinolysis, endothelial activation, matricellular protein release, and tissue damage and wit
82 , fibrinolysis, endothelial cell activation, matricellular protein release, and tissue damage were me
83 ered the role of thrombospondin-1 (TSP-1), a matricellular protein released in abundance from activat
84 otein 61 (Cyr61) is a dynamically expressed, matricellular protein required for proper angiogenesis a
85 secreted cysteine-rich and integrin-binding matricellular protein required for proper cardiovascular
87 le of which was the evolutionarily conserved matricellular protein Secreted Protein Acidic and Rich i
88 and rich in cysteine)/BM 40/osteonectin is a matricellular protein shown to function as a counteradhe
90 r-activation of the small GTPase Ran and the matricellular protein SMOC-2 that has important conseque
91 Arntl2 partner and functionally validate the matricellular protein Smoc2 as a pro-metastatic secreted
93 observed in the presence and absence of the matricellular protein SPARC (secreted protein, acidic an
94 This study identifies the stromal-derived matricellular protein SPARC as a novel regulator of isle
98 In addition, interstitial deposition of the matricellular protein tenascin, a marker of active remod
100 rowth factor (CCN2, also known as CTGF) is a matricellular protein that appears to play an important
102 We show that CCN1 (also known as CYR61), a matricellular protein that dampens and resolves liver fi
107 d Protein, Acidic and Rich in Cysteine) is a matricellular protein that inhibits mesangial cell proli
108 reported that fibulin-5, an integrin-binding matricellular protein that is essential for elastic fibe
111 ed connective tissue growth factor (CTGF), a matricellular protein that is highly expressed in the br
112 ein acidic and rich in cysteine (SPARC) is a matricellular protein that is important for the regulati
114 Connective tissue growth factor (CCN2) is a matricellular protein that is up-regulated in many fibro
115 Connective tissue growth factor (CTGF) is a matricellular protein that mediates cell-matrix interact
116 d protein, acidic and rich in cysteine) is a matricellular protein that modulates cell adhesion and p
117 protein acidic rich in cysteine (SPARC) is a matricellular protein that modulates the activity of gro
118 (osteonectin) (SPARC) gene, which encodes a matricellular protein that participates in normal tissue
119 ue growth factor (CTGF/CCN2) is an inducible matricellular protein that plays a major role in fibropr
120 ytes with keratinocytes up-regulated CCN3, a matricellular protein that we subsequently found to be c
122 to test the hypothesis that the prototypical matricellular protein thrombospondin (TSP)-1, a potent a
129 ng Protein-2 (Smoc-2) is a broadly-expressed matricellular protein which contributes to mitogenesis v
133 otein acidic and rich in cysteine (SPARC), a matricellular protein with counteradhesive properties, i
137 bospondin-1 (TSP-1), a potent proatherogenic matricellular protein, as a putative link between hyperg
139 , acidic and rich in cysteine (SPARC) family matricellular protein, during invasive phases of prostat
140 ests that CYR61 (now named CCN1), a secreted matricellular protein, has a role in the pathogenesis of
141 ne), although primarily known as a secreted, matricellular protein, has also been identified in uroth
143 Periostin (PN), a novel fasciclin-related matricellular protein, has been implicated in cardiac de
146 lved in extracellular matrix remodeling, and matricellular protein-protein and protein-cholangiocarci
149 ster analysis, we identified a subset of six matricellular proteins (eg, osteopontin and plasminogen
150 small leucin-rich repeat proteoglycans, and matricellular proteins affecting both the composition an
151 lecular signature composed of an ensemble of matricellular proteins and remodeling enzymes they provi
159 y, we demonstrate that the presence of these matricellular proteins results in significantly stiffer
162 e 1 (SC1) is a member of the SPARC family of matricellular proteins that has been implicated in the r
164 1) is a member of the CCN family of secreted matricellular proteins that includes connective tissue g
165 -adhesion is induced by the highly regulated matricellular proteins TSP1 and 2, tenascin-C, and SPARC
166 e we show that CCN1 (CYR61) and CCN2 (CTGF), matricellular proteins upregulated at sites of inflammat
167 ediators of extracellular matrix remodeling, matricellular proteins, and cardiac integrins compared w
168 d SPARC, two homologs of the SPARC family of matricellular proteins, in the foreign body response.
169 ndly decreased gene expression of a group of matricellular proteins, of which periostin was prominent
178 Ab) that is directed against the pleiotropic matricellular signaling protein connective tissue growth
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