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1 helial growth factor, PDGF, TGF-beta(1), and type 1 collagen).
2 sion of the major component of fibrotic ECM, type 1 collagen.
3 utes to their increased production of FN and type 1 collagen.
4 duced by vitronectin and fibronectin but not type 1 collagen.
5 1 also can detach cells from fibronectin and type-1 collagen.
6 dronate: 55.6% (P<.001) for C-telopeptide of type 1 collagen, 59.5% (P < .001) for serum n = propepti
7 the constitutively exposed binding motif of type 1 collagen and its receptor integrin alpha2 was sur
8 s through a microfluidic channel coated with type 1 collagen and observe the rate at which platelets
9 iation and progression, including depositing type 1 collagen and other extracellular matrix (ECM) com
10 phatase (ALP), osteocalcin (OCN), alpha 2(1)(type 1) collagen and osteonectin (ON), were performed.
12 ssue injury (e.g., NGAL, SOD, caspase 3, and type 1 collagen) and systemic expression of pro-inflamma
13 59.5% (P < .001) for serum n = propeptide of type 1 collagen, and 28.1% (P<.001) for bone-specific al
14 nducing increased production of fibronectin, type 1 collagen, and a-smooth muscle actin by fibroblast
15 nducing increased production of fibronectin, type 1 collagen, and alpha-smooth muscle actin by fibrob
16 Markers of bone turnover, N-telopeptides of type 1 collagen, and bone alkaline phosphatase decreased
17 er, it remains unclear how fibronectin (FN), type 1 collagen, and their receptor integrin subtypes di
18 A and protein expressions of fibronectin and type 1 collagen associated with the activation of p38 mi
19 ally distinct collagenases (Western blot), a type-1 collagen breakdown product/bone resorption marker
20 composed of 5 to 8 lamellae of predominantly type-1 collagen bundles arranged in transverse, longitud
22 ven platelet deposition in vitro on purified type 1 collagen by video phase-contrast microscopy at 22
23 These results demonstrate that fibrillar type 1 collagen can actively disrupt cell cycle progress
26 peptide (P1NP) and C-terminal telopeptide of type 1 collagen (CTX) at 0 (baseline), 13, and 26 weeks.
27 ) and resorption (C-terminal telopeptides of type 1 collagen (CTX)), and the K59N polymorphism in the
28 resorption marker C-terminal telopeptide of type 1 collagen (CTx), did not differ between groups (me
30 mes revealed molecular mimicry between human type 1 collagen epitope and bacterial collagen-like prot
31 the relationship between SM alpha-actin and type 1 collagen expression (COL1A1), a major extracellul
33 also inhibits osteoblast differentiation and type 1 collagen expression in a Runx-2- and osterix-inde
34 vitro, CLDH exhibited increased vimentin and type 1 collagen expression within cellular extensions co
35 oxia also upregulated VEGF, fibronectin, and type 1 collagen expressions associated with HIF-1alpha a
36 omains of matrix metalloprotease-1 (MMP1) on type 1 collagen fibrils correlate with its activity.
38 nd cultured monocyte/derived Mphi adhered to type 1 collagen gels, but not to nongelled collagen-, fi
39 atic stellate cells as well as expression of type 1 collagen genes and tissue inhibitor of matrix met
41 inal propeptide (PICP), amino-telopeptide of type 1 collagen (ICTP), collagen VI, desmosine, matrix m
42 switching NIH3T3 fibroblasts from growth on type 1 collagen in monolayer to a collagen gel might inf
43 addition, mixing recombinant periostin with type 1 collagen in solution caused a dramatic increase i
44 ited increased deposition of fibronectin and type 1 collagen, increased chemotaxis, and decreased pro
45 rms, if their increased expression of FN and type 1 collagen is under autocrine TGF beta control.
46 oculture with chloroquine or by adherence to type 1 collagen matrices was not reversed by bafilomycin
47 monocyte-derived macrophages that adhered to type 1 collagen matrices, but not to fibronectin, vitron
49 oth alpha-smooth muscle actin expression and Type 1 collagen mRNA levels in livers of mice fed a West
50 depositing basement membrane materials onto type 1 collagen nanofibers only in a region adjacent to
52 ne (fDPD/Cr), serum N-terminal propeptide of type 1 collagen, or beta C-terminal telopeptide, althoug
53 arathyroid hormone, cross-linked telopeptide type 1 collagen, osteocalcin, and bone-specific alkaline
54 r = 0.003) as well as FN (P < or = 0.04) and type 1 collagen (P < or = 0.03) (measured by specific EL
55 alone, the neutralizing antibodies decreased type 1 collagen production by the HGF fibroblasts by up
57 cell MCT1KO (AAV-Lrat-Cre) attenuated liver type 1 collagen protein expression and caused a downward
59 colorectal cancer cells in three-dimensional type 1 collagen reverts the invasive phenotype and resto
61 one formation) and C-terminal telopeptide of type 1 collagen (sCTX) (marker of bone resorption), were
62 ment, mitochondrial dysfunction, and reduced type 1 collagen secretion and alkaline phosphatase activ
63 3 ng/mL; P=0.22) and C-terminal crosslink of type 1 collagen (soy-fed: 0.944 +/- 0.06 and 0.89 +/- 0.
66 oth studies, the animals were administered a type 1 collagen-targeted gadolinium-based probe (surroga
67 oterminal propeptide of type III procollagen/type 1 collagen telopeptide ratio </=1 (odds ratio [95%
68 oterminal propeptide of type III procollagen/type 1 collagen telopeptide ratio </=1, measured 1 month
69 oterminal propeptide of type III procollagen/type 1 collagen telopeptide ratio (</=1) at 1 month is p
70 s well as biomarkers of myocardial fibrosis (type 1 collagen telopeptide, aminoterminal propeptide of
71 s of the ECM components fibronectin (FN) and type 1 collagen than normal human gingival (GN) fibrobla
72 of alpha smooth muscle actin (alpha-SMA) and type 1 collagen, the markers of HSCs activation and prol
73 o of urinary cross-linked N:-telopeptides of type 1 collagen to creatinine with alcohol consumption,
74 protein, cytochrome P4502E1, cytokeratin-18, type-1 collagen, transforming growth factor-beta 1, matr
75 rosslinks and serum N-terminal propeptide of type 1 collagen) were measured, 3199 women completed a f
76 tion, FimC and FimD bound to fibronectin and type 1 collagen, whereas FimE failed to interact with th
77 when it is responsible for the production of type 1 collagen, which causes scar formation in liver fi