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1 atrix gla protein was found predominantly in undercarboxylated form and was associated with the miner
2 ting vitamin K and inactive proteins such as undercarboxylated forms of factor II and osteocalcin to
5 resulted in decreased circulating levels of undercarboxylated OCN, impaired glucose tolerance, and r
7 ce in plasma phylloquinone, percentage serum undercarboxylated osteocalcin (%ucOC), and urinary gamma
8 plasma phylloquinone and serum percentage of undercarboxylated osteocalcin (%ucOC)] and IL-6, osteopr
9 hylloquinone concentration and percentage of undercarboxylated osteocalcin (%ucOC)] was measured at b
10 between circulating osteoblast (OB)-derived undercarboxylated osteocalcin (Glu-OCN) and pancreatic b
12 -factor II, PIVKA-II), and the percentage of undercarboxylated osteocalcin (ucOC), was determined in
13 es, serum osteocalcin [total osteocalcin and undercarboxylated osteocalcin (ucOC)], plasma phylloquin
15 cking IR in osteoblasts have low circulating undercarboxylated osteocalcin and reduced bone acquisiti
17 min K1-2,3-epoxide, PIVKA-II, and percentage undercarboxylated osteocalcin increased significantly be
18 e SPI-fed rats was associated with increased undercarboxylated osteocalcin secretion and altered JNK/
19 appear to result from chronic elevations in undercarboxylated osteocalcin that lead to downregulatio
23 ast insulin signaling reduce serum levels of undercarboxylated osteocalcin, which in turn exacerbate
27 rin led to the accumulation of intracellular undercarboxylated protein S forms that were rapidly secr
28 inary gamma-carboxyglutamic acid, and plasma undercarboxylated prothrombin (PIVKA-II) were measured.
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