ライフサイエンスコーパス: lymphatic endothelium

1 cilitating their adhesion and transit across lymphatic endothelium.

2 ce of angiopoietin ligand cooperation in the lymphatic endothelium.

3 ascular endothelium and D2-40 negativity for lymphatic endothelium.

4 ctivating integrin alpha4beta1 on lymph node lymphatic endothelium.

5 hly and specifically expressed GPCR in mouse lymphatic endothelium.

6 AM-1 and DC-expressed ROCK in DC crawling on lymphatic endothelium.

7 ontribution of microRNAs in the induction of lymphatic endothelium.

8 rker because of its continuous expression in lymphatic endothelium.

9 quent crawling along the luminal side of the lymphatic endothelium.

10 re novel functional markers of proliferative lymphatic endothelium.

11 r studying cancer cell transmigration across lymphatic endothelium.

12 cient recombination of loxP-flanked genes in lymphatic endothelium.

13 target for Fiaf signaling in the intestinal lymphatic endothelium.

14 e of individual cells incorporating into the lymphatic endothelium.

15 lumen with a micropipette is blocked by the lymphatic endothelium.

16 becomes restricted during development to the lymphatic endothelium.

17 eaving only an SLC gene that is expressed in lymphatic endothelium and an ELC pseudogene.

18 pha6beta1 integrin is a netrin-4 receptor in lymphatic endothelium and consequently represents a pote

19 rosine kinase that is expressed in the adult lymphatic endothelium and high endothelial venules.

20 overns both neutrophil migration through the lymphatic endothelium and luminal crawling.

21 sufficient to promote tumor cell adhesion to lymphatic endothelium and lymph node metastasis in vivo,

22 , a 90-kDa cell-surface protein expressed in lymphatic endothelium and stromal cells of spleen and th

23 nts favouring the activation of pre-existing lymphatic endothelium and the de novo formation of lymph

24 echanisms of interaction between DCs and the lymphatic endothelium and the potential implications of

25 Spindle cells express markers of lymphatic endothelium and, interestingly, KSHV infection

26 reatment blocks passage through the cortical lymphatic endothelium, and argues against a functional r

27 pha/podoplanin is predominantly expressed by lymphatic endothelium, and recent studies have shown tha

28 cell tissue egress and migration across the lymphatic endothelium are not well defined.

29 vessels range, in their simplest form, from lymphatic endothelium attached to the interstitial matri

30 endritic cells, mast cells, fibroblasts, and lymphatic endothelium, but keratinocytes were the earlie

31 Stimulation of lymphatic endothelium by acetylcholine or a TRPV4 channe

32 and show that HA binding may be elicited in lymphatic endothelium by surface clustering with divalen

33 e inflammatory leukocyte accumulation around lymphatic endothelium congests the lymphatic system, imp

34 LYVE-1(-) lymphatic endothelium could serve as microvalves, suppor

35 Curiously, however, LYVE-1 in lymphatic endothelium displays little if any binding to

36 imics their migration across vascular and/or lymphatic endothelium during atherosclerosis and resolut

37 High endothelial venules and lymphatic endothelium expressed high levels of S1P1, and

38 The lymphatic endothelium expresses intercellular adhesion m

39 lar characteristics of blood vascular versus lymphatic endothelium have remained poorly defined.

40 s thought to be expressed exclusively on the lymphatic endothelium, high endothelial venules, and rar

41 (EGFP) chimeric mice were immunostained for lymphatic endothelium hyaluronan receptor (LYVE-1, a rou

42 levated expression in both the epidermis and lymphatic endothelium in "uninvolved" psoriatic skin (ie

43 neutrophils to crawl along the lumen of the lymphatic endothelium in an ICAM-1/MAC-1-dependent manne

44 esion was increased by cytokine treatment of lymphatic endothelium in association with increased expr

45 tegrin alpha4beta1 promotes expansion of the lymphatic endothelium in lymph nodes and serves as an ad

46 mmune response and suggest a function of the lymphatic endothelium in preventing undesired immune rea

47 Virus replicated in glandular epithelium and lymphatic endothelium in the decidua, cytotrophoblasts,

48 on the role played by the microvascular and lymphatic endothelium in the pathogenesis of IBD.

49 (CCR)7 ligands are selectively presented on lymphatic endothelium in the presence of inflammatory ch

50 , that NF-kappaB is constitutively active in lymphatic endothelium in the urinary bladder, uterus, in

51 , and integrin alpha4beta1 is a biomarker of lymphatic endothelium in tumor-draining lymph nodes from

52 rafficking, indicating a more active role of lymphatic endothelium in uptake and transport of molecul

53 hibit the expression of VEGFR3 in uninfected lymphatic endothelium, indicating that Ets-1 is a novel

54 Kaposi sarcoma is considered a neoplasm of lymphatic endothelium infected with Kaposi sarcoma-assoc

55 chemokine binding molecule expressed on the lymphatic endothelium, internalizes and degrades CC chem

56 lls emigrate from inflamed tissue across the lymphatic endothelium into the lymphatic vasculature and

57 The lymphatic endothelium is the preferred route for the dra

58 Whether complementary signalling occurs in lymphatic endothelium is unknown.

59 ine kinase receptor FLT-4, present on normal lymphatic endothelium, is robustly expressed in KS cells

60 = 21), confirming that synovium, not initial lymphatic endothelium, is the reflection site.

61 us endothelium is also specialized to become lymphatic endothelium later in development.

62 Using a novel marker for lymphatic endothelium, LYVE-1, we demonstrate here the o

63 nes that are preferentially expressed in the lymphatic endothelium (matrix Gla protein, apolipoprotei

64 n, signal transduction, or function in tumor lymphatic endothelium not only inhibits tumor lymphangio

65 elial cells and that Notch1 was activated in lymphatic endothelium of invasive mammary micropapillary

66 lymph nodes, and Peyer's patches, and in the lymphatic endothelium of multiple organs.

67 velop, despite the normal development of the lymphatic endothelium of the lymph heart, and embryos de

68 by squeezing through apparent portals in the lymphatic endothelium of these sinusoids.

69 Importantly, the suppressive effects of the lymphatic endothelium on DCs were observed only in the a

70 We found that, in addition to lymphatic endothelium, podoplanin was also expressed by

71 d DCs with an inflamed, TNF-alpha-stimulated lymphatic endothelium reduced expression of the costimul

72 The molecular profile of lymphatic endothelium seems to reflect characteristic fu

73 rge number of genes selectively expressed by lymphatic endothelium should facilitate the discovery of

74 be-like structures that expressed markers of lymphatic endothelium such as LYVE-1 and podoplanin.

75 leled by a strong up-regulation of ICAM-1 in lymphatic endothelium, suggesting that during inflammati

76 In addition, the expression of SLC in lymphatic endothelium suggests that the migration of lym

77 edge of the roles played by the vascular and lymphatic endothelium throughout the gut in the pathogen

78 , enhances the responsiveness of preexisting lymphatic endothelium to VEGFR-3 binding factors, VEGF-C

79 t of a dynamic and complex interplay between lymphatic endothelium, tumor cells, secreted growth fact

80 tions were immunostained for the presence of lymphatic endothelium using podoplanin (D2-40 antibody)

81 onal consequences, as lymphocyte adhesion to lymphatic endothelium was blocked by 10.1.1 Ab bound to

82 intracellular Ca(2+) signalling dynamics in lymphatic endothelium, we excised collecting lymphatic v

83 en localized to high endothelial venules and lymphatic endothelium, we propose that they may play an

84 n expression was gradually down-regulated on lymphatic endothelium whereas vascular endothelial growt

85 receptors Cxcr4a and Cxcr4b are expressed in lymphatic endothelium, whereas chemokine ligands Cxcl12a

86 new molecular markers for blood vascular and lymphatic endothelium with important implications for fu

87 Nevertheless, puncture of the initial lymphatic endothelium with the micropipette leads to rap