ライフサイエンスコーパス: osteoblast-like

1 growth factor treatment or with the state of osteoblast-like activity and appears to determine the na

2 antimigratory effects of zoledronic acid in osteoblast-like and endothelial cells.

3 The identification of osteoblast-like and osteoclast-like cells in human tissu

4 Sp3 sites act as enhancers in both MC3T3-E1 (osteoblast-like) and J774 (macrophage-like) cell lines,

5 d cell proliferation were analysed to assess osteoblast-like behaviour in the presence of Asc, Dex an

6 These include the presence of osteoblast-like calcifying vascular cells in the artery

7 We have demonstrated that both the UMR-106 osteoblast-like cell line and human osteoblasts in prima

8 bone formation within osteoblasts and in the osteoblast-like cell line MC3T3-E1, a finding consistent

9 In the human osteoblast-like cell line MG-63, 1,25-(OH)(2)D(3) and 19

10 estosterone with calcium channels in the rat osteoblast-like cell line ROS 17/2.8 was investigated.

11 Furthermore, in an osteoblast-like cell line, uroporphyrin-I decreased mine

12 Three different human osteoblast-like cell lines (MG-63, HOS, and SaOS-2) and

13 Osteoblast-like cell lines 2T3 and Oct-1 also show incre

14 well as murine (MC3T3-E1) and human (MG-63) osteoblast-like cell lines displayed all the previously

15 element that drives human SOST expression in osteoblast-like cell lines in vitro and in the skeletal

16 CRISPR-Cas9 editing of CD109 in SaOS-2 osteoblast-like cell lines showed that partial CD109 kno

17 steocalcin expression, we used rat and human osteoblast-like cell lines to generate stably transfecte

18 , whose expression is controlled by CBFA1 in osteoblast-like cell lines.

19 cell processes of Saos-2 when using it as an osteoblast-like cell model.

20 We found that UTY modulates the osteoblast-like cell phenotype in response to nanoscale

21 cale extracellular matrix cues to promote an osteoblast-like cell phenotype.

22 with inflammatory changes and expression of osteoblast-like cell phenotypes, but the cellular mechan

23 lar matrix remodelling and myofibroblast and osteoblast-like cell proliferation.

24 muscle cells to change into a chondrocyte or osteoblast-like cell; high total body burden of calcium

25 tion, RANKL upregulation in human mandibular osteoblast-like cells (HMOBs) were stimulated with PGE2.

26 simple, reproducible method to isolate human osteoblast-like cells (HOBs) and to evaluate in vitro ce

27 y was to examine the expression of CaMKII in osteoblast-like cells (MC4) and to elucidate its role in

28 nesis, nonosseous calcification, and ectopic osteoblast-like cells (that appear to function different

29 and cultured with fetal calf serum (10% for osteoblast-like cells and 2% for osteoclast-like cells).

30 anism of action of applied tensile forces in osteoblast-like cells and have critical implications in

31 The promoters are active in both osteoblast-like cells and in the M12 B-lymphocyte cell l

32 ation of the balance between the activity of osteoblast-like cells and OLCs.

33 In the present study MG63 osteoblast-like cells and primary bone marrow stromal ce

34 Myofibroblasts further differentiate into osteoblast-like cells and produce calcium nanoparticles,

35 ot analysis, we have demonstrated that human osteoblast-like cells as well as primary human osteoblas

36 is verified the differentiation of DFCs into osteoblast-like cells because clusters of mineralization

37 target gene expression were up-regulated in osteoblast-like cells derived from cortical bone of fema

38 ng vascular cells (CVCs), a subpopulation of osteoblast-like cells derived from the artery wall, were

39 ate that Gli1(+) cells are a major source of osteoblast-like cells during calcification in the media

40 These osteoblast-like cells from ALSKO mice failed to induce o

41 signals colocalized with calcified areas or osteoblast-like cells in human vascular lesions.

42 ADAM19 is also highly expressed in osteoblast-like cells in the bone, yet it does not appea

43 ted in the present study using UMR106-01 rat osteoblast-like cells in vitro.

44 at [Ca2+]o-stimulated chemotaxis of MC3T3-E1 osteoblast-like cells involves a G-protein-linked calciu

45 of the murine osteocyte cell line MLO-Y4 and osteoblast-like cells MC3T3-E1 and in primary rat osteob

46 vular leaflets may promote the generation of osteoblast-like cells through enhanced type I IFN signal

47 ses of primary mouse osteoblasts and UMR-106 osteoblast-like cells to a single period of dynamic stra

48 Delivering pediatric human bone-derived osteoblast-like cells to an in vivo murine bone loss mod

49 MG63 osteoblast-like cells were cultured on the 3 different s

50 Stably alpha2-silenced MG63 human osteoblast-like cells were used to test whether alpha2be

51 only been shown in some, but not all, clonal osteoblast-like cells, and the molecular mechanisms unde

52 compatibility of the Mg-Zn-Mn alloy on MG-63 osteoblast-like cells, further substantiating its safety

53 AK can target human primary chondrocytes and osteoblast-like cells, in addition to synovial fibroblas

54 al stress and selective differentiation into osteoblast-like cells, offering a promising nanotechnolo

55 sed by stimulation of proliferation of MG-63 osteoblast-like cells, was used to monitor purification

56 human and mouse osteoblasts and mouse MC3T3 osteoblast-like cells, we found that Akt activation by F

57 tiation of vascular smooth muscle cells into osteoblast-like cells, we investigated whether miRs impl

58 ansforming vascular smooth muscle cells into osteoblast-like cells, which can produce a matrix of bon

59 e beta(5) gene expression in macrophages and osteoblast-like cells, with each element exhibiting cell

60 tes in VICs activating to myofibroblasts and osteoblast-like cells.

61 tometry validated the target specifically in osteoblast-like cells.

62 organized extracellular matrix deposition by osteoblast-like cells.

63 in human microvascular endothelial and human osteoblast-like cells.

64 oses of PTH attenuated P(1)/P(2) activity in osteoblast-like cells.

65 ma cells and in adhesion of myeloma cells to osteoblast-like cells.

66 s of MEK(SP) were specific to Cbfa1-positive osteoblast-like cells.

67 n macrophage (osteoclast precursor)-like and osteoblast-like cells.

68 uent transdifferentiation of PAH-PASMCs into osteoblast-like cells.

69 with TGF-beta 1, PDGF-BB, and bFGF in bovine osteoblast-like cells.

70 PTH-stimulated adenylyl cyclase activity in osteoblast-like cells.

71 tive stress, uremia, and hyperphosphatemia, "osteoblast-like" cells form in the vessel wall.

72 cultures resulted in reacquisition of their osteoblast-like characteristics and lack of LPS responsi

73 l significance of the loss of the PDL cell's osteoblast-like characteristics during inflammation.

74 we observed that IL-1beta down-regulates the osteoblast-like characteristics of PDL cells in vitro.

75 th IL-1beta inhibits the expression of their osteoblast-like characteristics, as assessed by the fail

76 orskolin treatment of CVC for 3 days induced osteoblast-like "cuboidal" morphology, inhibited prolife

77 In MC3T3-E1 osteoblast-like cultures, dexamethasone (DEX) activates

78 in vitro vascular calcification by enhancing osteoblast-like differentiation of CVC.

79 nesis in PDL cells while down-regulating its osteoblast-like features and simultaneously reducing the

80 ed the levels of p21 mRNA and protein in the osteoblast-like human osteosarcoma cell line MG63 and st

81 ted gene transcription and mineralization in osteoblast-like MC3T3-E1 cells (WT) via a mechanism invo

82 Immunocytochemical studies performed with osteoblast-like MC3T3-E1 cells and other mammalian cell

83 Osteoblast-like MC3T3-E1 cells were allowed to attach to

84 steogenesis, as evidenced by increased human osteoblast-like MG-63 cell proliferation in vitro and ca

85 eaks (DSBs), in human cervix cancer HeLa and osteoblast-like MG-63 cells.

86 have found that a lipid fraction from human osteoblast-like MG63 cell-conditioned medium (MG63CM) co

87 r cells with TNF-alpha for 3 days induced an osteoblast-like morphology.

88 We show here that differentiated osteoblasts, like neurons, express the norepinephrine tr

89 , the MC3T3-E1(MC3T3) pre-osteoblast and rat osteoblast-like osteosarcoma 17/2.8 cell.

90 The fully differentiated rat osteoblast-like osteosarcoma 17/2.8 cells responded rapi

91 morphogenetic protein-2 [BMP-2]), MG63 human osteoblast-like osteosarcoma cells, and normal human ost

92 ulture undergo a phenotypic conversion to an osteoblast-like pattern of gene expression.

93 e profiles in three separate clones of human osteoblast-like PDL cells.

94 ed at the interface of bone and teeth, where osteoblast-like periodontal ligament (PDL) cells constan

95 a healthy periodontium PDL cells exhibit an osteoblast-like phenotype and are unresponsive to gram-n

96 -Luc assay in HepG2 cells as well as induced osteoblast-like phenotype in C2C12 cells expressing alka

97 Cells exhibiting an osteoblast-like phenotype in the vessel wall may be impo

98 Furthermore, TGF-beta1 down-regulated the osteoblast-like phenotype of PDL cells, i.e., alkaline p

99 lve associated with the transformation to an osteoblast-like phenotype that is inhibited by atorvasta

100 An osteoblast-like phenotype was in part verified for these

101 mal fibroblasts lacking Smad3 can acquire an osteoblast-like phenotype, including activation of Runx2

102 f vascular smooth muscle cells (VSMCs) to an osteoblast-like phenotype.

103 ence on differentiation of the cells into an osteoblast-like phenotype.

104 tion and that this process is mediated by an osteoblast-like phenotype.

105 active regulated process associated with an osteoblast-like phenotype.

106 To further determine the osteoblast-like properties of PDL cells, human PDL cells

107 erstitial cells increasingly adopt myofibro-/osteoblast-like properties, thereby fostering fibro-calc

108 d, phenotypically unstable chondrocytes with osteoblast-like properties.

109 TGF-L inhibits osteocalcin production in rat osteoblast-like Ros 17/2.8 cells.

110 receptor-mediated increases in ECAR in human osteoblast-like SaOS-2 cells.

111 vity of stretch-activated cation channels of osteoblast-like UMR-106.01 cells.

112 F)-alpha-induced NF-kappaB activation in rat osteoblast-like UMR106 cells.

113 ALDH1A1 inhibition promotes an osteoblast-like VIC phenotype and increases calcium depo