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1 4) mineralization evaluated by von Kossa and Alizarin-red.
5 formed mineralized nodules, and stained for alizarin red and alkaline phosphatase, while expressing
7 smooth muscle cells in culture, as shown by Alizarin red and van Kossa stain and increased alkaline
12 rum: re-calcification can be demonstrated by Alizarin Red and von Kossa stains, by depletion of serum
13 issue deposits, which reacted positively for alizarin red and von Kossa, and demonstrated increased e
14 ated by alkaline phosphatase (ALP) activity, Alizarin Red, and Von Kossa staining followed by scannin
15 (osteopontin, alkaline phosphatase activity, Alizarin red, and Von Kossa) compared with the control g
17 ent pups double stained with alcian blue and alizarin red exhibited generalized, pronounced skeletal
20 h before re-calcification can be detected by Alizarin Red or von Kossa staining and before the subseq
22 er numbers of von Kossa-positive nodules and alizarin red-positive nodules compared with WT cells wit
23 he interaction of the commercially available alizarin red S (ARS) chemosensor with the nanomaterial,
28 ipogenic differentiation were analyzed using alizarin red S and oil red O staining, respectively.
30 cell line was confirmed histologically using alizarin red S and von Kossa staining as well as Raman m
31 printed carbon electrodes modified with poly Alizarin Red S are employed as electrochemical sensors i
32 on, alkaline phosphatase (ALP) staining, and Alizarin Red S biomineralization assays were performed t
36 rphologically, staining with trypan blue and alizarin red S showed an apparently intact endothelial m
37 uration/mineralization), von Kossa stain and alizarin red S stain for mineralization, and enzyme assa
38 nt, real-time polymerase chain reaction, and alizarin red S staining and calcium content analysis wer
39 d fewer false-positive test results than did alizarin red S staining and could provide estimates of t
40 Histochemical analyses using Von Kossa and Alizarin red S staining of kidney sections confirmed the
43 osphatase (ALP) activity/staining as well as alizarin red S staining when compared with DPSCs of thei
49 d for 4 to 7 wks, formed toluidine-blue- and alizarin-red-stainable nodules, indicative of chondrogen
52 t reduced calcium deposition, as assessed by alizarin red staining (VICs: p < 0.0001; AV leaflets: p
55 ed enhanced mineralization, as determined by alizarin red staining and mineralized marker expression.
56 MM, as measured by ALP activity at d 14 and Alizarin Red staining at d 21 (by 1.57+/-0.03- and 1.71+
61 uantitative histopathologic evaluations with Alizarin Red staining independently confirmed the respec
67 used to interveneosteoblasts (OBs).CCK-8 and Alizarin Red staining were used to investigate the proli
68 ne phosphatase activity) and mineralization (alizarin red staining) compared with cells treated with
70 line phosphatase (ALP) activity measurement, alizarin red staining, and electron-dispersive x-ray spe
73 assess, by immunofluorescence microscopy and Alizarin red staining, the potential impact of intraleaf
74 ification was assessed using micro-CT scans, Alizarin Red staining, Von Kossa staining, and calcium a
83 y electron microscopy, whereas von Kossa and alizarin red stains showed no evidence of calcification.
85 sirius red to demonstrate collage type 1 and Alizarin red to demonstrate calcium/mineralisation furth
86 s that stained with the calcium deposit dye, Alizarin red, were abundant in the insoluble fraction fr