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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.
3                       Expression analysis of cultured skin biopsies from strains of mice with opposin
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
6  growth factor-I (IGF-I) and its receptor in cultured skin cells or in whole skin.
7 s not been described in normal human skin or cultured skin cells, however.
8 nduced or increased expression of CRH-R1a in cultured skin cells.
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
11 thylases and increased demethylases mRNAs in cultured skin epithelial cells.
12    This inhibitory activity was confirmed in cultured skin explants of atopic dermatitis lesions.
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
16                                              Cultured skin fibroblasts (XP22BE) showed decreased post
17 lpha-galactosidase A in white blood cells or cultured skin fibroblasts confirms the diagnosis.
18                                              Cultured skin fibroblasts demonstrated a 55% reduction i
19                                              Cultured skin fibroblasts derived from gelsolin-null mic
20  the net loss of GCase catalytic activity in cultured skin fibroblasts derived from patients with the
21                                              Cultured skin fibroblasts exhibited the accumulation of
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
24                   The power of proteomics in cultured skin fibroblasts from individuals with either s
25             Calcium signaling was altered in cultured skin fibroblasts from PSEN1 and PSEN2 mutation
26                                              Cultured skin fibroblasts from the patient had a coenzym
27 ne has been demonstrated in erythrocytes and cultured skin fibroblasts from TRMA patients.
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
30 nic pathways, in skeletal muscle as it is in cultured skin fibroblasts in PCOS.
31 d ERalpha expression levels was confirmed in cultured skin fibroblasts obtained from Fli1(+/-) mice a
32 +/+) and Npc1(-/-)) mice and in heterozygous cultured skin fibroblasts of NPC1 carriers.
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
35 rols in blood lymphocytes, and 11 and 14% in cultured skin fibroblasts, respectively.
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
38 bination of fibroblasts and keratinocytes in cultured skin grafts.
39                                              Cultured skin isolates were classified into 3 groups by
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
43                                Subsequently, cultured skin substitute grafts consisting of cultured h
44                                              Cultured skin substitute inserts were evaluated at 2 and
45  titrated at 0.0, 0.01, 0.1, and 1.0 mM in a cultured skin substitute model on filter inserts.
46                                Comparison of cultured skin substitutes (CSS) and split-thickness skin
47                                              Cultured skin substitutes (CSS) consisting of autologous
48 trical capacitance (SEC) of the epidermis in cultured skin substitutes (CSS) in vitro and after graft
49                                              Cultured skin substitutes (CSS), prepared using keratino
50                                              Cultured skin substitutes (n = 3 per group) were evaluat
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
53                                              Cultured skin substitutes consisting of collagen-glycosa
54 microscopy agreed with MTT data showing that cultured skin substitutes grown with insulin media had m
55                                              Cultured skin substitutes have become useful as adjuncti
56                             In contrast, the cultured skin substitutes in 50 ng per ml insulin-like g
57             The data show that incubation of cultured skin substitutes in medium containing vitamin C
58     These results suggest that incubation of cultured skin substitutes in medium containing vitamin C
59                                              Cultured skin substitutes incubated in 50 ng per ml insu
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
62                         Clinical efficacy of cultured skin substitutes may be increased if their carb
63 in supports greater physiologic stability in cultured skin substitutes over time, and that expression
64           Improved anatomy and physiology of cultured skin substitutes that result from nutritional f
65 ificantly higher for 5 microg per ml insulin cultured skin substitutes versus all other treatment gro
66                                              Cultured skin substitutes were grafted on full-thickness
67                                              Cultured skin substitutes were grafted to full-thickness
68                                              Cultured skin substitutes were prepared and incubated at
69                              After grafting, cultured skin substitutes with vitamin C developed funct
70 y the human keratinocytes and fibroblasts in cultured skin substitutes.
71 arrier during healing of wounds treated with cultured skin substitutes.

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