ライフサイエンスコーパス: glomerular mesangial cell

1 t proinflammatory cytokine expression in rat glomerular mesangial cells.

2 up-regulate the expression of lipocalin-2 in glomerular mesangial cells.

3 the ability of collagen IV to interact with glomerular mesangial cells.

4 with proliferation and apoptosis of resident glomerular mesangial cells.

5 COL1A2 gene activation by TGF-beta1 in human glomerular mesangial cells.

6 phospholipase C-dependent, pathway in human glomerular mesangial cells.

7 al growth factor-induced Ca2+ entry in human glomerular mesangial cells.

8 ad signaling in collagen production by human glomerular mesangial cells.

9 cipate in the development and maintenance of glomerular mesangial cells.

10 cells have the ability to differentiate into glomerular mesangial cells.

11 ition and, H3 and H4- acetylation in primary glomerular mesangial cells.

12 ; also called capacitative calcium entry) in glomerular mesangial cells.

13 by platelet-derived growth factor (PDGF) in glomerular mesangial cells.

14 oncomitant release of nitric oxide (NO) from glomerular mesangial cells.

15 a concomitant release of prostaglandins from glomerular mesangial cells.

16 staglandins (PGs) and nitric oxide (NO) from glomerular mesangial cells.

17 on, bradykinin (BK) is mitogenic in cultured glomerular mesangial cells.

18 fic transactivator of MMP-2 transcription by glomerular mesangial cells.

19 duces a biphasic activation of p21ras in rat glomerular mesangial cells.

20 rix accumulation was explored in vitro using glomerular mesangial cells.

21 racellular matrix turnover, was evaluated in glomerular mesangial cells.

22 We investigated the origin of the glomerular mesangial cell, a smooth muscle-like cell tha

23 Overexpression of this component in glomerular mesangial cells, a model perivascular myofibr

24 , we investigated the effects of 9-cis-RA on glomerular mesangial cell activation induced by transfor

25 iposomes were detected in the glomerulus and glomerular mesangial cells after tail vein injection in

26 ctivation and transient proliferation of the glomerular mesangial cells and by a prominent glomerular

27 regulates microRNA-192 (miR-192) in cultured glomerular mesangial cells and in glomeruli from diabeti

28 tubular epithelial cells (HKC-8) but not in glomerular mesangial cells and interstitial fibroblasts.

29 rate that GATA3 is specifically expressed in glomerular mesangial cells and plays a critical role in

30 g pathway is present and functional in human glomerular mesangial cells and plays a role in activatin

31 creases angiotensin II (AngII) levels in rat glomerular mesangial cells and that AngII mediates the i

32 stem cell is capable of differentiating into glomerular mesangial cells and that the process does not

33 to interact physically with NF-kappaB p65 in glomerular mesangial cells and thereby to inhibit NF-kap

34 Similarly, SPARC was increased in glomerular mesangial cells and visceral epithelial cells

35 We find that kidney beta8 is localized to glomerular mesangial cells, and expression is decreased

36 lipopolysaccharide treatment in vitro induce glomerular mesangial cell apoptosis by hitherto incomple

37 Glomerular mesangial cells are active participants in th

38 Glomerular mesangial cells are exposed to pulsatile capi

39 Glomerular mesangial cells are key modulators of the inf

40 quires the removal of proliferating resident glomerular mesangial cells, but excessive loss of glomer

41 Here, we show that TGF-beta activates Akt in glomerular mesangial cells by inducing miR-200b and miR-

42 TNF-restricted M(phi)-directed apoptosis of glomerular mesangial cells can be down-regulated by M(ph

43 In this study, a line of glomerular mesangial cells derived from normal mice was

44 oth muscle actin is known to be expressed in glomerular mesangial cells exclusively in pathologic sit

45 itioned by several cell lines and found that glomerular mesangial cells exclusively secrete a factor

46 ERK) pathway was inhibited in HMC and in rat glomerular mesangial cells expressing the dominant-negat

47 We first isolated glomerular mesangial cells from MKK3-null (Mkk3-/-) and

48 hat TGF-beta1 induces autophagy and protects glomerular mesangial cells from undergoing apoptosis dur

49 High glucose (HG) causes glomerular mesangial cell (GMC) growth, production of tr

50 Glomerular mesangial cell (GMC) proliferation and death

51 Glomerular mesangial cell (GMC) proliferation and matrix

52 COX-2 expression also has been described in glomerular mesangial cells (GMC), where COX-2 is not exp

53 inhibiting the activation of p38 in cultured glomerular mesangial cells (GMC).

54 Alteration in renal glomerular mesangial cell growth and fibronectin matrix

55 Human glomerular mesangial cells (HMC) are embedded in the mes

56 uced a rapid activation of p21(ras) in human glomerular mesangial cells (HMC).

57 ly decreased PEDF secretion in primary human glomerular mesangial cells (HMCs), suggesting that hyper

58 ized by in situ hybridization to vessels and glomerular mesangial cells in allogeneic and syngeneic (

59 scular smooth muscle cells and pericytes and glomerular mesangial cells in the kidney and that Tbx18-

60 tion in approximately 5000 gene promoters in glomerular mesangial cells, including those of Tgfb1, Tg

61 is study we examined the mechanisms by which glomerular mesangial cells ingest apoptotic cells and th

62 hysiologically activated human monocytes and glomerular mesangial cells (MC) by employing a cell cult

63 Activation of glomerular mesangial cells (MCs) by angiotensin II (Ang

64 Activation of glomerular mesangial cells (MCs) by angiotensin II (Ang

65 Here, we demonstrate that, in glomerular mesangial cells (MCs), endothelial nitric oxi

66 n rate (GFR) and the contractile function of glomerular mesangial cells (MCs).

67 s in fibronectin synthesis in cultured renal glomerular mesangial cells (MCs).

68 I) exerts contractile and trophic effects in glomerular mesangial cells (MCs).

69 high glucose (HG)- or TGF-beta-treated mouse glomerular mesangial cells (MMCs).

70 activated by 1 microm thapsigargin in human glomerular mesangial cells or A431 cells.

71 ) collagen gene (COL1A2) activation in human glomerular mesangial cells, potentially contributing to

72 Glomerular mesangial cells produce reactive oxygen inter

73 These data show that glomerular mesangial cell progenitors are derived from t

74 F-B plays a pivotal role in the mediation of glomerular mesangial cell proliferation.

75 These findings demonstrate that in glomerular mesangial cells, repeated cycles of stretchin

76 In human glomerular mesangial cells, Smad3 protein levels were sp

77 a hyperglycemic-induced hypocontractility of glomerular mesangial cells that may be associated with d

78 -kappaB selectively sensitizes primary adult glomerular mesangial cells to TNF-induced apoptosis but

79 alpha8 integrin expressed on the surface of glomerular mesangial cells was selected as a target mole

80 tion, and collagen synthesis in isolated rat glomerular mesangial cells were evaluated in vitro.

81 might regulate HK activity and expression in glomerular mesangial cells, which constitute the princip

82 the G3YR mice showed degenerative changes in glomerular mesangial cells, which deteriorated progressi

83 f NF-kappaB on cytokine-induced apoptosis of glomerular mesangial cells, which is important in determ

84 eport we demonstrate that conditioning human glomerular mesangial cells with IL-1beta results in the

85 Clones of recipient glomerular mesangial cells with the donor genotype were

86 scular pericytes, liver fat-storing cells or glomerular mesangial cells, with IFN-gamma dramatically