ライフサイエンスコーパス: leukocyte adhesion molecule

1 but under inflammatory conditions acts as a leukocyte adhesion molecule.

2 thelial cells to express at least one of the leukocyte adhesion molecules.

3 After X-irradiation, the endothelial leukocyte adhesion molecule 1 (ELAM-1; E-selectin) was p

4 (TNF) activates transcription of endothelial leukocyte adhesion molecule-1 (CD62E) in endothelial cel

5 ll adhesion molecule-1 (VCAM-1), endothelial-leukocyte adhesion molecule-1 (E-selectin), and intercel

6 dy 7A9 binds specifically to the endothelial leukocyte adhesion molecule-1 (E-selectin), inhibiting t

7 on of adhesion molecules such as endothelial-leukocyte adhesion molecule-1 (E-selectin), intercellula

8 We found that endothelial leukocyte adhesion molecule-1 (ELAM-1), the earliest mar

9 hesion molecule (ICAM)-1 but not endothelial leukocyte adhesion molecule-1 expression on hepatic endo

10 higher doses required to inhibit endothelial-leukocyte adhesion molecule-1 expression.

11 ar cell adhesion molecule-1, and endothelial leukocyte adhesion molecule-1 in a time- and dose-depend

12 ar cell adhesion molecule-1, and endothelial leukocyte adhesion molecule-1 mRNA were detected by reve

13 appaB and an element, NF-ELAM-1 (endothelial leukocyte adhesion molecule-1), constitutively occupied

14 observed elevated expression of endothelial leukocyte adhesion molecule-1, a human glaucoma marker,

15 alpha (TNFalpha), tissue factor, endothelial leukocyte adhesion molecule-1, and vascular cell adhesio

16 This induction of endothelial-leukocyte adhesion molecule-1, vascular cell adhesion mo

17 sitive than changes in VCAM-1 or endothelial leukocyte adhesion molecule-1.

18 dose of natalizumab, an antibody against the leukocyte adhesion molecule alpha4 integrin, in patients

19 These alterations include expression of leukocyte adhesion molecules and decreased bioavailabili

20 tumor necrosis factor-induced expression of leukocyte adhesion molecules and procoagulant tissue fac

21 Therefore, the expression of leukocyte adhesion molecules and secretion of proinflamm

22 elial cells, their expression of ligands for leukocyte adhesion molecules, and vaso-occlusion.

23 Leukocyte adhesion molecules are critically involved at

24 proinflammatory cytokines and expression of leukocyte adhesion molecules by endothelial cells in res

25 lated the normal change in expression of the leukocyte adhesion molecules CD11b and CD62L.

26 aB-dependent reporter construct, endothelial leukocyte adhesion molecule CD25 (the 3E10 clone), were

27 mediated rolling of hard spheres coated with leukocyte adhesion molecules (cell-free system).

28 beta(2)-Integrins are leukocyte adhesion molecules composed of alpha (CD11a, -

29 Many mutant mice deficient in leukocyte adhesion molecules display altered hematopoies

30 this report, we have determined that the EC-leukocyte adhesion molecule E-selectin is a key target f

31 may "superinduce" expression of an important leukocyte adhesion molecule, E-selectin (ELAM-1, CD62E).

32 nucleotide (ASO) targeting human endothelial leukocyte adhesion molecule, E-selectin.

33 ulatory role in cytokine induction of the EC-leukocyte adhesion molecules (ELAM) E-selectin and vascu

34 Endothelial leukocyte-adhesion molecule (ELAM)-1 was not detected in

35 integrin alphaMbeta2 (Mac-1, CD11bCD18) are leukocyte adhesion molecules essential for innate immuni

36 E-selectin, a leukocyte adhesion molecule expressed on endothelium, is

37 eta2 integrins (CD11/CD18) are heterodimeric leukocyte adhesion molecules expressed on hematopoietic

38 irectly suppressed endothelial activation of leukocyte adhesion molecule expression and inflammation.

39 Preclinical investigations examining leukocyte adhesion molecules in I/R provided overwhelmin

40 anges with local expression of cytokines and leukocyte adhesion molecules in mice with disseminated c

41 othelial cell expression of cytokine-induced leukocyte adhesion molecules in vitro.

42 roke, and to study the potential role of the leukocyte adhesion molecule intercellular adhesion molec

43 ere to investigate the immunostaining of the leukocyte adhesion molecules intercellular adhesion mole

44 s that inhibit the expression of endothelial-leukocyte adhesion molecules intercellular adhesion mole

45 Leukocyte adhesion molecules involved in this process ha

46 A recent study shows that the leukocyte adhesion molecules known as selectins form 'ca

47 The leukocyte adhesion molecule L-selectin mediates lymphocy

48 orate in the biosynthesis of ligands for the leukocyte adhesion molecule L-selectin.

49 ry modification that promotes binding of the leukocyte adhesion molecule L-selectin.

50 thelium in a process mediated in part by the leukocyte adhesion molecule L-selectin.

51 The leukocyte adhesion molecule, L-selectin, mediates the re

52 al vascular endothelial cell ligands for the leukocyte adhesion molecule, L-selectin.

53 udy, we found that TXA(2) mimetics stimulate leukocyte adhesion molecule (LAM) expression on endothel

54 ncreased endothelial cell (EC) expression of leukocyte adhesion molecules (LAMs), which mediate monoc

55 or the synthesis of functional selectin-type leukocyte adhesion molecule ligands.

56 Reduced expression of MHC antigens and leukocyte adhesion molecules may contribute to the lack

57 E-selectin, an endothelial-cell-specific leukocyte adhesion molecule, may also function in angiog

58 whether the CD18 family (beta2-integrin) of leukocyte adhesion molecules mediates initial passage of

59 ulation of the endothelial cell cytokine and leukocyte adhesion molecule mRNAs in response to C. albi

60 ate the expression of any of the cytokine or leukocyte adhesion molecule mRNAs.

61 TNF-alpha induces leukocyte adhesion molecules on endothelial cells (ECs),

62 The expression of leukocyte adhesion molecules on endothelial cells is ind

63 t, Rho GTPases affect the expression of some leukocyte adhesion molecules on endothelial cells, such

64 ir ability to regulate the expression of key leukocyte adhesion molecules, on both leukocytes and end

65 ample, sulfation of tyrosine residues in the leukocyte adhesion molecule P-selectin glycoprotein liga

66 ical surface, where JAM-A played a role as a leukocyte adhesion molecule participating in transendoth

67 h AMD, there is increased immunostaining for leukocyte adhesion molecules, particularly in the periph

68 The L-selectin leukocyte adhesion molecule plays an important role in c

69 All three leukocyte adhesion molecule proteins were expressed on t

70 In contrast, the genes for leukocyte adhesion molecules showed a significant upregu

71 E-selectin, an inducible leukocyte adhesion molecule specifically expressed by en

72 capillaries enlarged into venules expressing leukocyte adhesion molecules, sprouting angiogenesis and

73 esion, and extravasation by up-regulation of leukocyte adhesion molecules such as E-selectin and P-se

74 n and extravasation through the induction of leukocyte adhesion molecules such as ICAM-1.

75 ription or surface expression of endothelial leukocyte adhesion molecules that are readily induced by

76 e-inducible, NF-kappaB-dependent endothelial-leukocyte adhesion molecules that participate in the leu

77 tigated the role of p75 in TNF-alpha-induced leukocyte adhesion molecules using cultured ECs derived

78 Increased leukocyte adhesion molecule VCAM-1 expression and leukoc

79 that the phenolic content of RW may modulate leukocyte adhesion molecules, whereas both ethanol and p

80 tress induces expression of endothelial cell leukocyte adhesion molecules, which are centrally import

81 T cells (Tn) are expanded in mice that lack leukocyte adhesion molecules, which have neutrophilia an

82 associated with endothelial upregulation of leukocyte adhesion molecules, which persist even after i

83 lming evidence that blocking the function of leukocyte adhesion molecules would be highly effective i