ライフサイエンスコーパス: cultured skin

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 Blood plasma and cultured skin biopsy samples, keratinocytes, dermal fibr

5 e 5'-phosphate hydrolase activity (pH 10) in cultured skin cells (normal and cancerous) ranged from 2

6 o conventional healing, and treatments using cultured skin cells have been devised to restart the wou

7 growth factor-I (IGF-I) and its receptor in cultured skin cells or in whole skin.

8 The toxic response of cultured skin cells to these compounds was measured by e

9 s not been described in normal human skin or cultured skin cells, however.

10 nduced or increased expression of CRH-R1a in cultured skin cells.

11 ht, mimics many effects of UV irradiation in cultured skin-derived cells, at least in part through th

12 e, yet the skin was unaffected, although the cultured skin epithelial cells from Tg mice expressed E7

13 thylases and increased demethylases mRNAs in cultured skin epithelial cells.

14 This inhibitory activity was confirmed in cultured skin explants of atopic dermatitis lesions.

15 neurons expressing APP(V642I) or APP-BP1, in cultured skin fibroblast cells from Down syndrome subjec

16 dulating the level of PPIX, in human primary cultured skin fibroblasts (FEK4) maintained either in ex

17 sion levels of TGF-beta system components in cultured skin fibroblasts (SFs) from type 1 diabetic pat

18 Cultured skin fibroblasts (XP22BE) showed decreased post

19 lpha-galactosidase A in white blood cells or cultured skin fibroblasts confirms the diagnosis.

20 Cultured skin fibroblasts demonstrated a 55% reduction i

21 Cultured skin fibroblasts derived from gelsolin-null mic

22 the net loss of GCase catalytic activity in cultured skin fibroblasts derived from patients with the

23 Cultured skin fibroblasts exhibited the accumulation of

24 altered lamin A/C expression/organization in cultured skin fibroblasts from 11 male carriers of premu

25 Cultured skin fibroblasts from A-T patients exhibit prem

26 ultured resident peritoneal macrophages, and cultured skin fibroblasts from Delta 18 COX-2 mice overe

27 The power of proteomics in cultured skin fibroblasts from individuals with either s

28 Calcium signaling was altered in cultured skin fibroblasts from PSEN1 and PSEN2 mutation

29 Cultured skin fibroblasts from the patient had a coenzym

30 ne has been demonstrated in erythrocytes and cultured skin fibroblasts from TRMA patients.

31 xidative stress, and antioxidant defenses in cultured skin fibroblasts harboring COQ2 and PDSS2 mutat

32 previously that severe CoQ(10) deficiency in cultured skin fibroblasts harboring COQ2 and PDSS2 mutat

33 nic pathways, in skeletal muscle as it is in cultured skin fibroblasts in PCOS.

34 d ERalpha expression levels was confirmed in cultured skin fibroblasts obtained from Fli1(+/-) mice a

35 +/+) and Npc1(-/-)) mice and in heterozygous cultured skin fibroblasts of NPC1 carriers.

36 f biotin-dependent carboxylases in PBMCs and cultured skin fibroblasts were normal, excluding biotin

37 vity of L-3-hydroxyacyl-CoA dehydrogenase in cultured skin fibroblasts with acetoacetyl-CoA substrate

38 rols in blood lymphocytes, and 11 and 14% in cultured skin fibroblasts, respectively.

39 rker, the Morphometric Imaging (MI) assay on cultured skin fibroblasts, was used in a double-blind, a

40 -containing extracellular matrix produced by cultured skin fibroblasts, whereas beads coated with Osp

41 eir telomeres were shorter than those in non-cultured skin from the same individuals, and than those

42 bination of fibroblasts and keratinocytes in cultured skin grafts.

43 Cultured skin isolates were classified into 3 groups by

44 MEC transplantation in a clinically relevant cultured skin model, persistence of HDMEC after grafting

45 ization showed that the epidermal and dermal cultured skin substitute components express insulin-like

46 insulin-like growth factor I exhibited poor cultured skin substitute epidermal morphology throughout

47 Subsequently, cultured skin substitute grafts consisting of cultured h

48 Cultured skin substitute inserts were evaluated at 2 and

49 titrated at 0.0, 0.01, 0.1, and 1.0 mM in a cultured skin substitute model on filter inserts.

50 Comparison of cultured skin substitutes (CSS) and split-thickness skin

51 Cultured skin substitutes (CSS) consisting of autologous

52 trical capacitance (SEC) of the epidermis in cultured skin substitutes (CSS) in vitro and after graft

53 Cultured skin substitutes (CSS), prepared using keratino

54 Cultured skin substitutes (n = 3 per group) were evaluat

55 factor I were similar to the insulin-treated cultured skin substitutes at day 14, but by day 28 had d

56 ad MTT values similar to the insulin-treated cultured skin substitutes at day 14, but were significan

57 Cultured skin substitutes consisting of collagen-glycosa

58 microscopy agreed with MTT data showing that cultured skin substitutes grown with insulin media had m

59 Cultured skin substitutes have become useful as adjuncti

60 In contrast, the cultured skin substitutes in 50 ng per ml insulin-like g

61 The data show that incubation of cultured skin substitutes in medium containing vitamin C

62 These results suggest that incubation of cultured skin substitutes in medium containing vitamin C

63 Cultured skin substitutes incubated in 50 ng per ml insu

64 assays showed significantly higher values in cultured skin substitutes incubated with insulin at incu

65 factor I by keratinocytes and fibroblasts in cultured skin substitutes is not sufficient to fully rep

66 Clinical efficacy of cultured skin substitutes may be increased if their carb

67 in supports greater physiologic stability in cultured skin substitutes over time, and that expression

68 Improved anatomy and physiology of cultured skin substitutes that result from nutritional f

69 ificantly higher for 5 microg per ml insulin cultured skin substitutes versus all other treatment gro

70 Cultured skin substitutes were grafted on full-thickness

71 Cultured skin substitutes were grafted to full-thickness

72 Cultured skin substitutes were prepared and incubated at

73 After grafting, cultured skin substitutes with vitamin C developed funct

74 y the human keratinocytes and fibroblasts in cultured skin substitutes.

75 arrier during healing of wounds treated with cultured skin substitutes.

76 nt responses between tension and non-tension cultured skin were also observed during the evaluation o