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1 were visualized and measured with the aid of cytokeratin 8.
2 includes other cytoskeletal proteins such as cytokeratins 8, 13, and 18 and neurofilament proteins NF
3  approximately 9 microm in diameter, express cytokeratins 8, 18, and 19, CD133/1, telomerase, CD44H,
4 ith monoclonal antibody CAM5.2, specific for cytokeratins 8, 18, and 19, gave typical strong staining
5  of several cytoskeletal proteins, including cytokeratins 8, 18, and 19.
6 d found to be CD45 negative and positive for cytokeratins 8, 18, and/or 19 and 4',6-diamidino-2-pheny
7 ased placental glutathione S-transferase and cytokeratin 8-18 activity; starting at 12 wk).
8 and by the specific expression of epithelial cytokeratin 8.18, proximal tubular CD10, distal tubular
9  adhesions and a reduction in E-cadherin and cytokeratins 8/18 and 19.
10 t kinase 4 (CDK4), and Bcl2 and up-regulated cytokeratins 8/18, Bad, and Bax.
11 liferation of epithelial cells co-expressing cytokeratin 8 and 14, lack of luminal/basal layer segreg
12 d between bystin and tastin is enhanced when cytokeratin 8 and 18 are present as the third molecule.
13 tion of the secreted plasminogen activators (cytokeratin 8 and alpha-enolase).
14  of basal (p63, cytokeratin 14) and luminal (cytokeratin 8 and androgen receptor) epithelial cells, a
15 increase in expression of liver cell markers cytokeratin 8 and carcinoembryonic antigen, and in some
16 color immunofluorescent labeling of TLR2 and cytokeratins 8 and 15 revealed that TLR2 is coexpressed
17 tify two major ERalpha-interacting proteins, cytokeratins 8 and 18 (CK8.CK18).
18 this system, the columnar epithelial markers cytokeratins 8 and 18 (K8, 18) were strongly expressed a
19 iptase-PCR experiments to identify and clone cytokeratins 8 and 19 (K8 and K19) from cardiac muscle o
20                                              Cytokeratins 8 and 19 concentrate at costameres of stria
21  squamous differentiation, and antibodies to cytokeratins 8 and 19 were used as markers for glandular
22 of these tumors is supported by detection of cytokeratins 8 and 19, and the absence of alpha-inhibin,
23 ng immunocytochemical staining reactions for cytokeratins 8 and 19, for glutathione S-transferase pi
24 c cells coexpress luminal epithelium markers cytokeratin 8, androgen receptor, and neuroendocrine mar
25  gene NKX3.1 and an epithelial cell-specific cytokeratin 8, but not prostate specific antigen or andr
26                                              Cytokeratin 8 (CK 8) has been identified on the external
27 specific gene NKX3.1 and epithelial specific cytokeratin 8 (CK8) but not prostate specific antigen (P
28  that p50 and p57 correspond to two forms of cytokeratin 8 (CK8) on the basis of the following result
29            In subsequent stages until birth, cytokeratin 8 continues to be expressed in embryonic tas
30 complex as cytoskeletal filaments: vimentin, cytokeratin 8, cytokeratin 18, actin, and hair type II b
31 solated four differentially expressed genes: cytokeratin 8, cytokeratin 18, Hsp27 and GPCR -Br.
32   Expression of epithelial markers including cytokeratin-8, E-cadherin, and prosurfactant protein B d
33 pithelial regeneration propose that distinct cytokeratin 8-expressing progenitor cells, arising from
34 artially rescued Twist1-silenced ERalpha and cytokeratin 8 expression and reduced Twist1-induced inte
35 bust gustatory innervation, markedly reduced cytokeratin 8 expression in taste cells, and a high inci
36 ular morphology, ultrastructure, albumin, or cytokeratin-8 expression.
37 inantly consists of heterotypic complexes of cytokeratin 8 (K8) and cytokeratin 18 (K18).
38 ste bud primordia as discrete collections of cytokeratin 8-positive and elongated cells in epithelial
39                             In contrast, the cytokeratin 8-positive mammary cell population with prog
40  (cloned twice), fructose-1,6-biphosphatase, cytokeratin 8, TGFbeta1 binding protein, elongation fact
41  IL-8 by targeting its 3' UTR, and inhibited cytokeratin 8 via the cell cycle control protein cyclin
42  cytokeratins, including several isoforms of cytokeratin 8, were overexpressed in apparently normal m

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