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1 native skin, fibroblasts, keratinocytes, and cultured skin.
2 n of HB-EGF-like growth factor mRNA in organ-cultured skin.
4 e 5'-phosphate hydrolase activity (pH 10) in cultured skin cells (normal and cancerous) ranged from 2
5 o conventional healing, and treatments using cultured skin cells have been devised to restart the wou
9 ht, mimics many effects of UV irradiation in cultured skin-derived cells, at least in part through th
10 e, yet the skin was unaffected, although the cultured skin epithelial cells from Tg mice expressed E7
13 neurons expressing APP(V642I) or APP-BP1, in cultured skin fibroblast cells from Down syndrome subjec
14 dulating the level of PPIX, in human primary cultured skin fibroblasts (FEK4) maintained either in ex
15 sion levels of TGF-beta system components in cultured skin fibroblasts (SFs) from type 1 diabetic pat
20 the net loss of GCase catalytic activity in cultured skin fibroblasts derived from patients with the
22 altered lamin A/C expression/organization in cultured skin fibroblasts from 11 male carriers of premu
23 ultured resident peritoneal macrophages, and cultured skin fibroblasts from Delta 18 COX-2 mice overe
28 xidative stress, and antioxidant defenses in cultured skin fibroblasts harboring COQ2 and PDSS2 mutat
29 previously that severe CoQ(10) deficiency in cultured skin fibroblasts harboring COQ2 and PDSS2 mutat
31 d ERalpha expression levels was confirmed in cultured skin fibroblasts obtained from Fli1(+/-) mice a
33 f biotin-dependent carboxylases in PBMCs and cultured skin fibroblasts were normal, excluding biotin
34 vity of L-3-hydroxyacyl-CoA dehydrogenase in cultured skin fibroblasts with acetoacetyl-CoA substrate
36 -containing extracellular matrix produced by cultured skin fibroblasts, whereas beads coated with Osp
37 eir telomeres were shorter than those in non-cultured skin from the same individuals, and than those
40 MEC transplantation in a clinically relevant cultured skin model, persistence of HDMEC after grafting
41 ization showed that the epidermal and dermal cultured skin substitute components express insulin-like
42 insulin-like growth factor I exhibited poor cultured skin substitute epidermal morphology throughout
48 trical capacitance (SEC) of the epidermis in cultured skin substitutes (CSS) in vitro and after graft
51 factor I were similar to the insulin-treated cultured skin substitutes at day 14, but by day 28 had d
52 ad MTT values similar to the insulin-treated cultured skin substitutes at day 14, but were significan
54 microscopy agreed with MTT data showing that cultured skin substitutes grown with insulin media had m
58 These results suggest that incubation of cultured skin substitutes in medium containing vitamin C
60 assays showed significantly higher values in cultured skin substitutes incubated with insulin at incu
61 factor I by keratinocytes and fibroblasts in cultured skin substitutes is not sufficient to fully rep
63 in supports greater physiologic stability in cultured skin substitutes over time, and that expression
65 ificantly higher for 5 microg per ml insulin cultured skin substitutes versus all other treatment gro
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