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1 duce apoptosis in the presence of high (10%) serum-containing medium.
2 deprivation and then began to proliferate in serum-containing medium.
3 the supernatant of mouse ECs incubated with serum-containing medium.
4 are viable but defective in filamentation on serum-containing medium.
5 into multilayered epithelia with addition of serum-containing medium.
6 when cells were cultured with vitamin D3 in serum-containing medium.
7 ilar to that in RA-treated cells cultured in serum-containing medium.
8 ed rat RPE cells maintained either in HDM or serum-containing medium.
9 ocess of hormonally defined medium (HDM) and serum-containing medium.
10 e when stimulated with retinoic acid (RA) in serum-containing medium.
11 sine, were only slightly decreased by NGF in serum-containing medium.
12 Calu-1 cells in serum-free medium but not in serum-containing medium.
13 d cyclodextrin for 1 h, followed by chase in serum-containing medium.
14 l phenotype while continuously expanded in a serum-containing medium.
15 d when cells were placed on collagen I or in serum-containing medium.
16 edium, but expression was lost on plastic in serum-containing medium.
17 inued to express CD34 when cultured on AM in serum-containing medium and on plastic in serum-free med
18 yte differentiation and extends life span in serum-containing medium but does not lead to immortaliza
19 rd to their circular dichroism, stability in serum-containing medium, cellular uptake, protein bindin
21 e was elevated in viable VSMCs maintained in serum-containing medium, declined significantly in respo
22 Addition of recombinant GDNF to cultures in serum-containing medium did not significantly affect DPC
26 t to nuclease degradation in the presence of serum-containing medium, indicating that secondary struc
27 e conjugates were illuminated in solution in serum containing medium, suggesting a switch in photoche
28 x target and, in addition are more stable in serum-containing medium than standard oligopyrimidine-de
29 ratinocytes of the epidermis are cultured in serum-containing medium using a fibroblast feeder layer.
30 Normal human skin fibroblasts maintained in serum-containing medium were synchronized with aphidicol
31 Culture of the intermediate progenitors in serum-containing medium with macrophage CSF resulted in
32 ratinocytes were grown in 1.2 mM calcium and serum-containing medium with vitamin C (50 microg per ml
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