ライフサイエンスコーパス: collagen III

1 lation of collagen I, and down-regulation of collagen III.

2 en III levels and the ratio of Collagen I to Collagen III.

3 f collagen III was similar to that of native collagen III.

4 r T3-SCI, the MCA had more collagen I (42%), collagen III (24%), transforming growth factor beta (47%

5 (33%, P < 0.02), collagen I (28%, P < 0.01), collagen III (34%, P < 0.01), fibronectin (48%, P < 0.01

6 renal expression of fibronectin, collagen I, collagen III, alpha-SMA, PAI-1, fibroblast-specific prot

7 xpression of fibrosis markers collagen I and collagen III also increased in 15-mo LP offspring.

8 However, corneal fibrosis markers, Collagen III and alpha-smooth muscle actin, were signifi

9 ccumulation of collagen III in the liver and collagen III and collagen IV in the heart; this is induc

10 immunolocalization of cellular fibronectin, collagen III and collagen IV.

11 splayed a reduced deposition of interstitial collagen III and fibronectin as well as total tissue col

12 Furthermore, ASM collagen III and laminin in asthma were correlated with

13 f Matrix Metalloproteinase (TIMP-3, TIMP-4), collagen-III and elastin levels were measured in whole b

14 ulation and immunohistochemical staining for collagens III and IV and attenuated glomerular and tubul

15 (total lung collagen content, peribronchial collagens III and V) and significantly less peribronchia

16 tin, beta-myosin heavy chain), and fibrosis (collagen III), and increased LV prosurvival signaling (a

17 GF-beta-stimulated expression of collagen I, collagen III, and alpha-smooth muscle actin.

18 tial infiltrates and fibrosis, deposition of collagen III, and apoptosis of tubular epithelial cells.

19 disease progression, including fibronectin, collagen III, and chemoattractants that were identified

20 by decreasing the expression of collagen I, collagen III, and fibronectin mRNA and protein.

21 rix-associated genes, including collagen VI, collagen III, and tissue inhibitor of metalloproteases-1

22 Immunohistochemical staining with collagen III antibody demonstrates an abundance of colla

23 ellular matrix, we identified collagen I and collagen III as well as mixtures of collagen I/collagen

24 d postradiation accumulation of interstitial collagen III but less myocardial degeneration in hearts

25 as alpha-smooth muscle actin (alpha-SMA) and Collagen III (Col III), in both HCFs and HKCs.

26 Collagen I (COL1A1), collagen III (COL3A1), hyaluronan synthase (HAS) 2, and

27 , cysteine-rich 61, collagen I (COL1A2), and collagen III (COL3A1).

28 g of 32 distinct combinations of collagen I, collagen III, collagen IV, fibronectin, and laminin.

29 extracellular matrix molecules (collagen I, collagen III, collagen IV, laminin and fibronectin) on c

30 than in control tendons (p=0.0079), whereas collagen III content was not different (p=1.0).

31 ntracutaneous fibrillin-rich microfibril and collagen III deposition and decreased mammalian target o

32 While collagen III deposition was not affected by the transgen

33 immunoreactive inflammation area, endomysial collagen III deposition, and hind limb grip strength.

34 c macrophages and was associated with excess collagen III deposition.

35 c alterations, with significant reduction in collagen III expression and deposition.

36 We tested whether TGF-beta mediates collagen III expression by treating animals with TGF-bet

37 en III antibody demonstrates an abundance of collagen III expression in this ECM.

38 Collagen III expression is seen in apposition to gels at

39 ptor on the activation of human platelets by collagen; (iii) generated low-GPVI mice in which the alp

40 gh affinity integrin-binding motifs in human collagen III (GROGER and GLOGEN) and a third motif (GLKG

41 methods included whole-slide digital images: collagen III immunohistochemistry and a new technique us

42 alysis, an approximately twofold increase in collagen III immunolabeling within the interstitial comp

43 Loss of LAP paralleled induction of collagen III immunoreactivity in this tissue compartment

44 in intervention reverses the accumulation of collagen III in the liver and collagen III and collagen

45 protein connective tissue growth factor and collagen III in vitro and decreased pulmonary vascular f

46 ow that AMPK activation by metformin reduced collagen III levels and the ratio of Collagen I to Colla

47 as potentially the best for clinical trials: collagen III morphometry and visual assessment of trichr

48 sion of collagen I mRNA lagged expression of collagen III mRNA and peaked at day 42 after PRK with a

49 .003), whereas collagen I did not change and collagen III mRNA increased 1.5-fold (P=0.02).

50 Collagen III mRNA levels peaked on day 21 with a 700-fol

51 t radiation-induced elevation of total gland collagen III mRNA was also blocked by neutralizing antib

52 n in previously published referent controls; collagen III N-terminal propeptide (5.6 [4.3-6.9] ng/mL)

53 galectin-3, matrix metalloproteinase-2, and collagen III N-terminal propeptide were measured in the

54 n content (P<0.0001), collagen I (P<0.0001), collagen III (P<0.0001), and myocyte size (P<0.0001).

55 ICP) and the amino terminal peptide from pro-collagen III (PIIINP), correlate with left atrial (LA) f

56 Serum YKL-40, N-terminal propeptide of collagen III (PIIINP), TGF-beta, and TNF-alpha were meas

57 (WT) mice, associated with lower collagen I, collagen III, plasminogen activator inhibitor (PAI-1), a

58 were validated for CCL2 and CXCL10 mRNA and collagen III protein.

59 -alpha2 integrin-subunit antibody and type I collagen, (iii) recombinant alpha2-I domain bound the wi

60 Thus, collagen III regulates the proper lamination of the cere

61 The proportion of collagen III relative to collagen I increased significan

62 the expression pattern of the GPR56 ligand, collagen III, revealed no visible gradient pattern.

63 Collagen III secretion was reduced 80% in both HCFs and

64 Collagen III, Sirius Red unpolarized, and visual scores

65 Radiation-induced collagen III staining in the adipose stroma was blocked

66 by trypsin, a property also seen for native collagen III, supporting a local structural relaxation o

67 The ratio of collagen III to collagen I was significantly lower in PR

68 to 6 months, at which time the proportion of collagen III was 70% above baseline values.

69 chimera containing six triplets (P7-P11') of collagen III was similar to that of native collagen III.

70 ing the entire triplehelical domain of human collagen III was used to locate binding sites for the co

71 titial area stained with picrosirius red and collagen III) was significantly increased 14 d after UUO

72 onal studies suggest that the interaction of collagen III with its receptor GPR56 inhibits neural mig