ライフサイエンスコーパス: lymphatic endothelium

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

2 r studying cancer cell transmigration across lymphatic endothelium.

3 cilitating their adhesion and transit across lymphatic endothelium.

4 cle by PCR, but only Kir6.1 was expressed in lymphatic endothelium.

5 ce of angiopoietin ligand cooperation in the lymphatic endothelium.

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

7 ctivating integrin alpha4beta1 on lymph node lymphatic endothelium.

8 hly and specifically expressed GPCR in mouse lymphatic endothelium.

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

10 ontribution of microRNAs in the induction of lymphatic endothelium.

11 rker because of its continuous expression in lymphatic endothelium.

12 re novel functional markers of proliferative lymphatic endothelium.

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

14 target for Fiaf signaling in the intestinal lymphatic endothelium.

15 e of individual cells incorporating into the lymphatic endothelium.

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

17 becomes restricted during development to the lymphatic endothelium.

18 ssential functions in the remodelling of the lymphatic endothelium.

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

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

21 functional differences between vascular and lymphatic endothelium and describes current understandin

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

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

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

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

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

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

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

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

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

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

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

33 tains more than 167K cells, representing the lymphatic endothelium, blood endothelium, stromal, cilia

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

35 Stimulation of lymphatic endothelium by acetylcholine or a TRPV4 channe

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

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

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

39 The drivers of lymphatic endothelium development, SOX18 and PROX1, regu

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

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

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

43 The lymphatic endothelium expresses intercellular adhesion m

44 Microarray analyses of isolated lymphatic endothelium from CLNs of ischemic mice confirm

45 cell identity but also demonstrate that the lymphatic endothelium has haemogenic capacity, ordinaril

46 n brain based on imaging specific markers of lymphatic endothelium has not been described.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

65 The lymphatic endothelium is the preferred route for the dra

66 Whether complementary signalling occurs in lymphatic endothelium is unknown.

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

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

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

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

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

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

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

74 We show that PXM-derived cells form the lymphatic endothelium of multiple organs and tissues, wi

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

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

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

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

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

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

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

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

83 In contrast, lymphatic endothelium-specific expression of Kir6.1 GoF

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

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

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

87 -mediated constraint on LYVE-1 clustering in lymphatic endothelium that tunes the receptor for select

88 f cells that express the cardinal marker for lymphatic endothelium-the lymphatic vessel hyaluronan re

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

90 uch less is known about the responses of the lymphatic endothelium to S1P and the functions of S1PRs

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

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

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

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

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

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

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

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

99 ncover Col2(+) lineage cells as an origin of lymphatic endothelium, which regulates local inflammator

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

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