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1 cient cells were generated by treatment with sodium chlorate.
6 ls is inhibited if cells are pretreated with sodium chlorate, an inhibitor of sulfate incorporation,
7 E fragment include heparin, heparan sulfate, sodium chlorate and heparinase, the low-density lipoprot
9 t study, inhibition of tyrosine sulfation by sodium chlorate decreased the secretion of processed CCK
10 lumbelliferyl-beta-D-xyloside) or sulfation (sodium chlorate) enhanced the release of apoE from cells
11 eased glycosaminoglycan chain sulfation with sodium chlorate enhances BMP2 morpho-genetic bioactivity
12 xylopyranoside or by the sulfation inhibitor sodium chlorate, indicating that SR-BI-mediated LDL-CE u
13 m with heparinase III, or growth of cells in sodium chlorate, indicating that sulfated heparan sulfat
14 in embryonic stem cells with heparinases or sodium chlorate inhibited differentiation of embryonic s
15 tion of the endothelial cell's glycocalyx or sodium chlorate inhibition of endothelial cell sulfated
17 antibody, suramin, or treatment with either sodium chlorate or heparitinase, demonstrating an autocr
20 er treatment of MEF cell lines with heparin, sodium chlorate, or heparinase II, demonstrating that he
21 rowth of expressing cells in the presence of sodium chlorate, significantly reduced the potency for M
22 were treated with various concentrations of sodium chlorate, so as to express a range of endogenous
23 alb/c3T3 fibroblasts were treated with 50 mM sodium chlorate to completely inhibit (99%) sulfation of
28 cholerae neuraminidase, tunicamycin, or 5 mM sodium chlorate, which blocks sulfation of surface prote
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