ライフサイエンスコーパス: mononuclear leukocyte

1 tein-coupled receptor kinase 2 expression in mononuclear leukocytes.

2 sured by real-time PCR from blood and tissue mononuclear leukocytes.

3 elatively sparing of normal peripheral blood mononuclear leukocytes.

4 TLR agonists, in the presence or absence of mononuclear leukocytes.

5 CCR3, and produced a normal calcium flux in mononuclear leukocytes.

6 ression in rodent cardiomyocytes and patient mononuclear leukocytes.

7 ells (SMC), extracellular matrix and admixed mononuclear leukocytes.

8 chemotactic activity for various subsets of mononuclear leukocytes.

9 CR4 expression was localized to infiltrating mononuclear leukocytes.

10 s investigated, except polymorphonuclear and mononuclear leukocytes.

11 disease is the perivascular accumulation of mononuclear leukocytes.

12 ed on the majority of human peripheral blood mononuclear leukocytes.

13 sulted in the presence of erythorbic acid in mononuclear leukocytes.

14 WMSKVKRFM (DcPLA2) was cloned from PMNLs and mononuclear leukocytes.

15 ear stress per se is sufficient to stimulate mononuclear leukocyte adhesion and, presumptively, migra

16 These data suggest that mononuclear leukocyte adhesion-dependent pathologies con

17 Mononuclear leukocytes also bound to poly(I.C)-treated M

18 nt protein-1 (MCP-1) is a potent agonist for mononuclear leukocytes and has been implicated in the pa

19 se include an increase in intestinal mucosal mononuclear leukocytes and hyperplasia of the muscularis

20 DPP4 was also found in a subset of mononuclear leukocytes and in serous cells of submucosal

21 injection stimulated OPGL expression in both mononuclear leukocytes and osteoblastic cells.

22 proteoglycans are both secreted by activated mononuclear leukocytes and released as a consequence of

23 therosclerosis is interaction of circulating mononuclear leukocytes and the endothelium.

24 and JFL relative to normal peripheral blood mononuclear leukocytes and the other cell lines.

25 Peripheral blood mononuclear leukocytes and U937 monocytic cells adhered

26 cle, colon, testes, bone marrow cells, blood mononuclear leukocytes, and blood erythrocytes of mrp(-/

27 The recruitment of mononuclear leukocytes, and the migration, growth and ac

28 This study demonstrates that mononuclear leukocytes are markedly more sensitive than

29 These mononuclear leukocytes are mostly monocyte-derived, but

30 potent chemotactic and activating factor for mononuclear leukocytes, are mediated by specific binding

31 receptor ligands inhibited TNF-alpha-induced mononuclear leukocyte arrest by 60-65%.

32 e activated than those incubated with normal mononuclear leukocytes, as judged by the increased endot

33 Proliferation of mononuclear leukocytes (assessed by expression of Ki-67,

34 Naive mononuclear leukocytes bind specifically to inflammation

35 ll surface hyaluronan (HA), and nonactivated mononuclear leukocytes bind to virus-induced HA structur

36 ere measured in 24-h culture supernatants of mononuclear leukocytes by immunoassays.

37 or T(H)1-type T cells (CXCL9 and CXCL10) and mononuclear leukocytes (CCL2, CCL3) among others.

38 We have reported that human mononuclear leukocytes contain large amounts of angioten

39 This accumulation of mononuclear leukocytes could be reversed by the administ

40 transgenic mice show cardiac infiltration by mononuclear leukocytes, culminating in dilated cardiomyo

41 The addition of Ags to mononuclear leukocyte cultures typically elicits modest

42 din E2, IL-10, and IL-4 production in atopic mononuclear leukocyte cultures.

43 livers of IL-12-treated mice were primarily mononuclear leukocytes expressing LFA-1, VLA-4, MAC-1, a

44 ood lipids and HMG CoA reductase activity in mononuclear leukocytes fell at week 8 during both diets,

45 the total infectivity was recovered from the mononuclear leukocyte fraction.

46 phox mRNA was less than 10% of normal in the mononuclear leukocytes from 3 of the 4 patients analyzed

47 Although mononuclear leukocytes from DKO mice did not mount a pro

48 respectively, and the cytosolic fraction of mononuclear leukocytes from NAT1*4/*4 and NAT1*10/*10 ho

49 Mononuclear leukocytes frozen at the baseline investigat

50 genotyping was performed on peripheral blood mononuclear leukocyte genomic DNA.

51 a albicans by Toll-like receptors 2 and 4 on mononuclear leukocytes has recently been discovered to d

52 Previous studies using mononuclear leukocytes have shown that the lipopolysacch

53 AL2 cleaves HA into fragments that stimulate mononuclear leukocytes in the immediate microenvironment

54 as the major quantitative adduct detected in mononuclear leukocytes in vivo and tumour cell lines in

55 In circulating mononuclear leukocytes, in stark contrast, no inflammato

56 The expression of BST-2 was increased on mononuclear leukocytes, including CD4-positive T lymphoc

57 al pneumonia associated with a predominantly mononuclear leukocyte infiltrate.

58 he development of an atherosclerotic plaque, mononuclear leukocytes infiltrate the artery wall throug

59 In vivo, DDR1 mRNA was detectable in mononuclear leukocytes infiltrating human renal tumor ti

60 Synovial tissue analysis confirmed mononuclear leukocyte infiltration in response to MSU cr

61 cular degeneration (AMD) is characterized by mononuclear leukocyte infiltration of the outer blood-re

62 eutropenia resulted in significantly reduced mononuclear leukocyte infiltration possibly due to reduc

63 lectin, and VCAM-1, particularly in areas of mononuclear leukocyte infiltration.

64 istic pathological changes include increased mononuclear leukocyte influx into the intestinal mucosa

65 Isolated autologous 99mTc-labeled mononuclear leukocytes injected into the left atrium loc

66 ver, they exhibited defective recruitment of mononuclear leukocytes into thioglycollate-induced perit

67 at transfusions of purified peripheral blood mononuclear leukocytes irradiated with 1,200 mJ/cm2 UVB

68 The accumulation of mononuclear leukocytes is an early and persistent findin

69 cular mechanisms that mediate recruitment of mononuclear leukocytes (lymphocytes and monocytes) and d

70 Less is known about placental patterns of mononuclear leukocyte (MNL) density and PTD.

71 It has been shown that peripheral-blood mononuclear leukocytes (MNL) are responsible for transfu

72 died the transendothelial migration of blood mononuclear leukocytes (MNL) from 76 HIV+ patients and 4

73 ge of tolerant mixed chimeras with 5 million mononuclear leukocytes (MNL) from naive syngeneic mice w

74 raviolet B (UVB)-irradiated peripheral blood mononuclear leukocytes (MNL) have been shown to induce h

75 ll cytotoxic activities in the population of mononuclear leukocytes (MNL) in the liver, but not in MN

76 o produce proinflammatory cytokines, promote mononuclear leukocytes (MNL) transendothelial migration,

77 Endogenous polymorphonuclear (PMNs) and mononuclear leukocytes (MNLs) attached and rolled in HEV

78 ring polymorphonuclear leukocytes (PMNs) and mononuclear leukocytes (MNLs) from diluted human blood (

79 To further identify which subset of spleen mononuclear leukocytes (MNLs) in the tolerant CBA mice i

80 ers ex vivo and transmit infectious virus to mononuclear leukocytes (MNLs) lodged beneath this endoth

81 drocytes were cultured with autologous blood mononuclear leukocytes (MNLs).

82 By contrast, the patients' mononuclear leukocytes, particularly monocytes, were hyp

83 tential of adenovirus vectors for studies of mononuclear leukocyte recruitment in vitro, we studied t

84 f retinoid X receptor (RXR)alpha on arterial mononuclear leukocyte recruitment is poorly understood,

85 a4 integrin signaling can selectively impair mononuclear leukocyte recruitment to sites of inflammati

86 elial cells and induces a temporal switch to mononuclear leukocyte recruitment.

87 ortant than the epithelium in recruitment of mononuclear leukocytes responsible for cell-mediated imm

88 -1) is a surface molecule expressed on human mononuclear leukocytes that functions as an inhibitory r

89 al intima as a result of the infiltration of mononuclear leukocytes, the proliferation of vascular sm

90 pound to mice led to impaired recruitment of mononuclear leukocytes to a site of inflammation in vivo

91 ar factor-kappa B activation was measured in mononuclear leukocytes using electrophoretic mobility sh

92 anism and recruitment of bone marrow-derived mononuclear leukocytes were evident in uterine tissue 1

93 othelial cells (MVEC) with sickle and normal mononuclear leukocytes were incubated, and endothelial a

94 Endothelial cells incubated with sickle mononuclear leukocytes were more activated than those in