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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
7 evelopment of a highly proliferating pool of chondroblasts between the epiphyses and metaphyses of fu
8 duction of c-Fos in vitro in osteoblasts and chondroblasts caused an increase in Fgfr1 RNA and FGFR1
9 everal molecular markers required for normal chondroblast differentiation (&agr; 1(II) collagen, Fgfr
10 tion factors that act redundantly to promote chondroblast differentiation in all cartilages of the mo
13 hypertrophic chondrocyte markers, epiphyseal chondroblasts ectopically activate hypertrophic chondroc
14 Sox6 are thus redundant, potent enhancers of chondroblast functions, thereby essential for endochondr
18 Ps) induce differentiation of osteoblast and chondroblast lineage cells from uncommitted mesenchymal
21 on of growth plate columnar zones by keeping chondroblasts proliferating and by delaying chondrocyte
23 of other cell types such as preadipocytes or chondroblasts, the effect of hypoxia on myogenesis is in
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