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1 to IV ovarian, fallopian tube, or peritoneal epithelial carcinoma.
2 ontributes to stem cell markers and CXCR4 in epithelial carcinoma.
3 r stroma and are present in more than 90% of epithelial carcinomas.
4 expressed on reactive stromal fibroblasts of epithelial carcinomas.
5 itical step in the metastatic progression of epithelial carcinomas.
6 trum of p53 mutant mice from lymphoma toward epithelial carcinomas.
7 er and is aberrantly expressed in many other epithelial carcinomas.
8 fusions have not been well characterized in epithelial carcinomas.
9 wn to be highly expressed in colon and other epithelial carcinomas.
10 utor to genotoxin-induced apoptosis in human epithelial carcinomas.
11 ly associated with loss of heterozygosity in epithelial carcinomas.
14 population in a mouse model of transitional epithelial carcinoma and uncover a novel mechanism by wh
15 carcinogen-induced sarcomas and spontaneous epithelial carcinomas and also to select for tumour cell
17 he complex process of invasion-metastasis in epithelial carcinomas and cell trafficking in hematopoie
18 ly expressed on tumor stromal fibroblasts in epithelial carcinomas and is important in cancer growth,
19 ntly enter the bloodstream in the setting of epithelial carcinomas and possibly during injury or infl
20 r/hepatocyte growth factor (HGF/SF) protects epithelial, carcinoma, and other cell types against cyto
22 d in a wide range of solid tumors, including epithelial carcinomas, but causal linkage has only been
23 ly expressed by tumor stromal fibroblasts in epithelial carcinomas, but not by epithelial carcinoma c
24 expression is frequently low in human breast epithelial carcinoma cell lines and tissue, but is expre
25 e that mammary tumor cells arising from more epithelial carcinoma cell lines expressed high levels of
26 n breast (MDA-MB-231) and prostate (TSU-Pr1) epithelial carcinoma cell lines using a tetracycline-ind
27 n E-cadherin complexes in the A431 and MCF-7 epithelial carcinoma cell lines, which express alpha-cat
28 , desmocollin-2 (Dsc2) loss promotes colonic epithelial carcinoma cell proliferation and tumor format
29 a(2+) dynamics and concentration among human epithelial carcinoma cells (HeLa), human embryonic kidne
30 rated by inhibition of NMII activity in A431 epithelial carcinoma cells either directly with blebbist
31 The invasive transformation of A-459 lung epithelial carcinoma cells has been linked to the autocr
32 umor metastasis often involves detachment of epithelial carcinoma cells into the vasculature or lymph
33 prepared from [35S]methionine-labeled human epithelial carcinoma cells persistently infected with me
34 gest a paradigm of tumor metastasis: primary epithelial carcinoma cells that lose chromosomes harbori
35 tors (EGFRs) in a lysate solution from human epithelial carcinoma cells were immobilized into the hol
37 oblasts in epithelial carcinomas, but not by epithelial carcinoma cells, normal fibroblasts, or other
38 lycoprotein of 110 kDa in MDA-MB-468 mammary epithelial carcinoma cells, which can be cell surface-bi
42 e protease matriptase is widely expressed by epithelial/carcinoma cells in which its proteolytic acti
44 prognosis and metastatic progression of many epithelial carcinomas has been correlated independently
45 oxygenase (COX)-2 is up-regulated in several epithelial carcinomas including colon, breast, and lung.
46 at is overexpressed in the majority of human epithelial carcinomas, including breast and colorectal c
48 nts, including HPV, as observed in different epithelial carcinomas, may also play a role in melanoma
49 cell cycle kinetics of several human ovarian epithelial carcinoma (OEC) cell lines were evaluated.
51 y of tumor histologies were noted, including epithelial carcinomas, soft tissue sarcomas, and hematop
55 (LMP1) has been identified as an oncogene in epithelial carcinomas such as nasopharyngeal carcinoma (