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1 , and on confluent primary cultures and late-passage cultures.
2 stained in confluent primary through fourth-passage cultures.
3 observed in high passage as compared to low passage cultures.
4 the edges of wounds made in confluent early passage cultures also coexpressed p16 and gamma2, accomp
6 In contrast, LipL45 was not detected in high-passage, culture-attenuated strains, suggesting that Lip
7 u mice, all neural stem cells, regardless of passages, culture conditions, and donors, are able to es
10 on of MAGE-C2 in A375 melanoma cells and low-passage cultures from human metastatic melanomas (MRA ce
14 ession of NT and Trk receptor mRNAs in early-passaged, cultured HTM cells from donors of several ages
15 ous growth factor receptor mRNAs using early passaged, cultured HTM cells from donors of several ages
16 strain, displayed reduced adherence to early-passage cultured human keratinocytes, but adherence of t
17 tize both established cancer cells and a low-passage cultured human pancreatic tumor cell line using
18 ONYX-015 on a panel (n = 7) of primary first-passage cultures made from freshly resected lung cancers
20 cultures of corneal stromal cells and early passage cultures of corneal fibroblasts was used in thes
21 n synthesis of IL-8 and collagenase in early-passage cultures of corneal fibroblasts, demonstrating t
27 s (MSNP) to profile DNA methylation in early-passage cultures of stromal myofibroblasts isolated from
28 in and mRNA were also studied in primary and passaged cultures of corneal stromal cells using Western
32 neous at the single-cell level and, in early passage culture, yielded a range of cellular clones, all
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