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1 ynthesis of type I collagen, the predominant bone matrix protein.
2 ding type I collagen, osteopontin, and other bone matrix proteins.
3 ssential cofactor for gamma-carboxylation of bone matrix proteins.
4 e phosphatase activity and the deposition of bone matrix proteins.
5 in and osteocalcin (osteoblast endochrondral bone matrix proteins), and proliferating cell nuclear an
6 d by vascularization and the presence of the bone matrix proteins, BSP and BAG-75.
7          Unlike ALP, expression of the major bone matrix proteins by the osteoblasts was only minimal
8                       DMP1, a key regulatory bone matrix protein, can be endocytosed by preosteoblast
9 associated with lysosomes in osteoclasts and bone matrix protein-containing vesicles in osteoblasts.
10                                          The bone matrix proteins dentin sialoprotein and osteopontin
11 ion of the ruffled border in osteoclasts and bone matrix protein deposition in osteoblasts, without a
12 protein are the most abundant noncollagenous bone matrix proteins expressed by osteoblasts.
13  ERK and p38 inhibitors on the regulation of bone matrix protein expression and JunB and JunD levels
14 th delayed maturation indicated by decreased bone matrix protein expression.
15 p junctional communication and production of bone matrix proteins in osteoblastic cells.
16 s of increased macrophages, PCNA levels, and bone matrix proteins in the aortic valve during experime
17           Osteocalcin (OC), a noncollagenous bone matrix protein, is expressed in high levels by oste
18 C-E1a was constructed using a noncollagenous bone matrix protein osteocalcin (OC) promoter to drive t
19 d the fact that plasmin specifically cleaves bone matrix protein osteocalcin (OC).
20 nifested by under-gamma-carboxylation of the bone matrix protein osteocalcin, may be common.
21 ity of Lrp5-/- osteoblasts to synthesize the bone matrix protein osteopontin after a mechanical stimu
22 ppresses bone formation in vivo and disrupts bone matrix protein synthesis by osteoblasts in vitro.
23  to expose osteoinductive or osteoconductive bone matrix proteins that should facilitate osteogenesis

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