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1 examined by immunohistochemistry for p63 and cytokeratin 14.
3 owed thinning of skin epithelium and loss of cytokeratin 14, an early marker of skin differentiation.
4 mitant with known basal cell markers p63 and cytokeratin 14 and was high in the proliferative human p
5 umor cells expressing markers of basal (p63, cytokeratin 14) and luminal (cytokeratin 8 and androgen
6 uently stained for pimonidazole, sirius red, cytokeratin 14, and hematoxylin-eosin for quantitative a
10 ssion of androgen receptor, ERalpha, ERbeta, cytokeratin 14 (basal cells), cytokeratin 18 (luminal ce
12 sitively for alpha-fetoprotein, albumin, and cytokeratin 14 (CK-14), protein markers expressed by the
13 pithelia that express nestin: one expressing cytokeratin 14 (CK14) and DeltaN-p63 and another express
14 d of stem cells, which were characterized by cytokeratin 14 (CK14) staining and enhanced tumor sphere
16 ferentiation during palate fusion, we bred a cytokeratin 14-Cre transgenic line into the R26R backgro
17 , cyclin D1, cyclin-dependent kinase 4, p53, cytokeratin 14, epidermal growth factor receptor, and by
20 dings and revealed a significant increase in cytokeratin 14 expression in the urothelium of the femal
25 binase (CreER(tam)) under the control of the cytokeratin 14 (K14) promoter (K14-CreER(tam)) and mice
26 t, the stratified squamous epithelial marker cytokeratin 14 (K14) was absent at the beginning, and ce
28 n genes identified a 5-fold up-regulation of cytokeratin 14 mRNA expression in ZD:p53-/- versus ZS:p5
29 he GMp motif in the N-terminal region of the cytokeratin 14 of ameloblasts binds to trityrosyl motif
30 microtubules in mesenchymal cells increased cytokeratin 14-positive (K14+) progenitors and their dif
31 ders and additionally revealed enrichment of cytokeratin 14-positive basal cells in the hyperplastic
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