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1 compared them with Sox2(-) (GFP(-)) CD133(+) dermal papilla cells.
2 duce potentially novel signaling pathways in dermal papilla cells.
3 ibulin-1d, was slightly upregulated in beard dermal papilla cells.
4 ssed at significantly higher levels in beard dermal papilla cells.
5 ivity is a direct effect of Wnt signaling to dermal papilla cells.
6 e, primary keratinocytes, preadipocytes, and dermal papilla cells.
7 in the inner root sheath, matrix cells, and dermal papilla cells.
8 in the inner root sheath, matrix cells, and dermal papilla cells.
9 s of the VDR status of the keratinocytes and dermal papilla cells.
10 nocytes of the outer root sheath, but not by dermal papilla cells.
11 that the comparison of the mRNA of cultured dermal papilla cells and fibroblasts can lead to the ide
12 d a previously unrecognised heterogeneity in dermal papilla cells and shown that Sox2-positive cells
14 in large quantities in cultured rat vibrissa dermal papilla cells but undetectable in cultured rat sk
15 this study was designed to determine whether dermal papilla cells cultured from human hair follicles
17 ptor and/or aromatase expression in cultured dermal papilla cells derived from human hair follicles.
20 P-1 expression was absent from hair bulb and dermal papilla cells during early to mid-anagen but was
21 show that Blimp1 is dynamically regulated in dermal papilla cells during hair follicle (HF) morphogen
22 from neonatal foreskins and cultured murine dermal papilla cells from adult GFP transgenic mice and
24 ggregated dermal papilla, and/or protect the dermal papilla cells from apoptosis induced by cytokines
27 med global gene expression analysis of human dermal papilla cells in culture and discovered very rapi
28 apitulate this process in humans using human dermal papilla cells in human skin have failed, suggesti
30 imulated and androgen-treated cultured human dermal papilla cells isolated from beard (androgen-sensi
31 uman skin have failed, suggesting that human dermal papilla cells lose key inductive properties upon
33 ed that the osteopontin gene is expressed in dermal papilla cells of pelage follicles during catagen
35 addition, this study supports that cultured dermal papilla cells provide a cell-based model system t
36 n of these genes in cultured beard and scalp dermal papilla cells reflected similar differences in mi
38 y skin keratinocytes and fibroblasts without dermal papilla cells served as positive and negative con
39 ens do not stimulate mitogenesis in cultured dermal papilla cells, this study was designed to determi
42 reased [3H] thymidine incorporation by other dermal papilla cells; trypsin treatment significantly re
43 inductive capability, and we show that human dermal papilla cells, when grown as spheroids, are capab
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