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1 lin is expressed by immature osteoblasts and chondroblasts.
2 into osteoblasts, adipocytes, myoblasts, or chondroblasts.
3 n to myoblasts, adipocytes, osteoblasts, and chondroblasts.
6 profile of MPCs induced to differentiate to chondroblasts and osteoblasts, significant differences i
8 evelopment of a highly proliferating pool of chondroblasts between the epiphyses and metaphyses of fu
9 ss of BMP5 does not prevent specification of chondroblasts, but does impair chondroblast proliferatio
10 duction of c-Fos in vitro in osteoblasts and chondroblasts caused an increase in Fgfr1 RNA and FGFR1
11 everal molecular markers required for normal chondroblast differentiation (&agr; 1(II) collagen, Fgfr
12 tion factors that act redundantly to promote chondroblast differentiation in all cartilages of the mo
15 hypertrophic chondrocyte markers, epiphyseal chondroblasts ectopically activate hypertrophic chondroc
16 Sox6 are thus redundant, potent enhancers of chondroblast functions, thereby essential for endochondr
20 Ps) induce differentiation of osteoblast and chondroblast lineage cells from uncommitted mesenchymal
23 on of growth plate columnar zones by keeping chondroblasts proliferating and by delaying chondrocyte
27 of other cell types such as preadipocytes or chondroblasts, the effect of hypoxia on myogenesis is in