ライフサイエンスコーパス: immunocyte

1 ates intercellular adhesion of coelomocytes (immunocytes).

2 oducing beta-cells are destroyed by invading immunocytes.

3 raft mucosa undergoes repopulation with host immunocytes.

4 ith aberrant regulation of keratinocytes and immunocytes.

5 ay cells have been proposed to be the sponge immunocytes.

6 relevant direction for attraction of mucosal immunocytes.

7 mitantly reduce repopulation by autoreactive immunocytes.

8 s (n = 8), did not contain such NKR positive immunocytes.

9 kin by injection of autologous blood-derived immunocytes.

10 ation of knockout mouse strains and specific immunocyte ablation techniques.

11 on in xenografts composed of human PHKCs and immunocytes abolished psoriasiform hyperplasia and infla

12 a(2+)-permeable cation channel essential for immunocyte activation, insulin secretion, and postischem

13 nological synapse," the membrane assembly of immunocyte adhesion and signaling.

14 in the distribution and function of splenic immunocytes and a significant reduction in suppressive a

15 s that direct cell- cell interaction between immunocytes and airway smooth muscle may also modulate a

16 sses that include inflammatory activation of immunocytes and macrophages, spillage of intracellular c

17 ow clear that molecular interactions between immunocytes and microbes are mediated largely by Toll-li

18 noid substance, can be found in invertebrate immunocytes and microglia.

19 arterial endothelial cells and invertebrate immunocytes and microglia.

20 are hyperplastic keratinocytes, infiltrating immunocytes, and activated endothelial cells.

21 sease, continuously fed by a mixed influx of immunocytes, and thus susceptible to evolve over time in

22 In sea urchin embryos, pigmented immunocytes are specified in vegetal epithelium, transit

23 ur current understanding of how these unique immunocytes arise, traffic to various sites, and may or

24 In addition, infected mice given primed immunocytes at 4 d.p.i. showed a significant increase in

25 ctional trafficking of lymphocytes and other immunocytes begins as soon as the vascular clamp is rele

26 Antiviral responses, neuroinflammation and immunocyte blood-brain barrier (BBB) trafficking follow

27 ated during HCV infection, and LPA activates immunocytes, but whether this contributes to immune acti

28 lerotic changes in the absence of detectable immunocytes by acting on VSMCs to potentiate growth-fact

29 cavity, the coelom, containing four types of immunocytes called coelomocytes.

30 nism of treatment response in tumor spheroid/immunocyte co-cultures.

31 sults from a blockade of the infiltration of immunocytes containing beta-endorphin and the consequent

32 our NN skin samples injected with autologous immunocytes converted to psoriatic plaques.

33 modulation of the keratinocyte phenotype by immunocyte-derived cytokines, in which induction of CDw6

34 that promise site-specific actions affecting immunocyte differentiation and proliferation are feasibl

35 that promise site-specific actions affecting immunocyte differentiation and proliferation are now fea

36 inferred from transcriptional changes during immunocyte differentiation.

37 As well, we propose that immunocytes disperse when Sp-Eph enhances adhesion, caus

38 ion or function of Sp-Eph results in rounded immunocytes entering ectoderm but not adopting a dendrit

39 nflammation or persistent changes in mucosal immunocytes, enterochromaffin and mast cells, enteric ne

40 Some immunocytes express proteins homologous to the Drosophil

41 Immunocytes express Sp-Eph and Sp-Efn is expressed throu

42 put in vivo analysis of the transcriptome of immunocytes from an invertebrate.

43 e the breadth and underpinning of changes in immunocyte gene expression due to genetic variation in m

44 We showed imaging of infiltrating immunocytes in BLT mice that spontaneously developed a g

45 serve to inhibit the pathogenetic ability of immunocytes in psoriasis.

46 ermine the role of I kappa B-alpha deficient immunocytes in the pathogenesis of the skin disease in a

47 specifically in coelomocytes, which are the immunocytes in the sea urchin.

48 tocompatibility complex class II+, or CD11b+ immunocytes in the skin mesenchyme was increased, and es

49 lly, video microscopic tracing of GFP-tagged immunocytes in the skin of mouse ears reveals that motil

50 Circulating immunocytes including CD4(+) and CD8(+) T cells, regulat

51 iferation, we discovered that intraepidermal immunocytes, including both CD4 and CD8+ T cells, expres

52 mal keratinocytes and dermal infiltration of immunocytes, including lymphocytes.

53 lti-layered capsule, which reduced allograft immunocyte infiltrates by enhancement of apoptotic death

54 In mosaic embryos, immunocytes insert preferentially in ectoderm expressing

55 Expressing Sp-Efn throughout embryos permits immunocyte insertion in ventral ectoderm.

56 Injection of activated immunocytes into symptomless psoriatic skin grafts, chan

57 l role of keratinocytes in the regulation of immunocytes is poorly understood.

58 and acanthosis and introduce targeting nerve-immunocyte/KC interactions as potential psoriasis therap

59 are important in the development of several immunocyte lineages and modulating the immune response.

60 f the IFN-induced response across a range of immunocyte lineages.

61 As the main immunocytes lining pulmonary alveoli, alveolar macrophag

62 m and host immune cells and demonstrate that immunocytes may influence the ability of C. albicans to

63 -alpha-syn and vasoactive intestinal peptide immunocytes or natural Tregs administered to MPTP mice a

64 SMO deficiency also substantially altered immunocyte phenotype and in vitro function.

65 nal mucosa is capable of developing a mature immunocyte population and that exposure to luminal stimu

66 Intraepithelial and lamina propria immunocyte population densities and subset distributions

67 Mucosal immunocyte population densities were lower in AN cysts h

68 y to develop a mucosal immune system with an immunocyte population similar to that of native small in

69 by unfavorably altering effector:suppressor immunocyte ratios and upregulating PD-1 expression on CD

70 t, we prevented treatment-induced peripheral immunocyte recruitment and, surprisingly, largely ablate

71 Immunocyte recruitment is a multistep, sequential engage

72 Glial cells orchestrate immunocyte recruitment to focal areas of viral infection

73 tation (ITx) on the basis of altered mucosal immunocytes, rejecting and rejection-free ITx allografts

74 In all but one psoriatic patient, the immunocytes required preactivation with IL-2 and superan

75 Coculture of PHKCs with immunocytes resulted in the upregulation of RAC1-depende

76 Because they occur in the immunocyte-rich lymphoid tissues, they are easily access

77 ller cell activity was observed, and splenic immunocytes secreted copious quantities of IFN-gamma.

78 d defined novel phenotypic markers for these immunocytes (see the related article beginning on page 2

79 However, critical changes within key immunocyte subsets are not known.

80 ovides evidence for the presence of specific immunocyte subsets in mixed tissues.

81 Mast cells are granular immunocytes that reside in the body's barrier tissues.

82 r lavage fluids after challenge, and splenic immunocytes that secreted IL-5 but not gamma interferon

83 driven by proinflammatory cytokines from the immunocytes, the functional role of keratinocytes in the

84 d molecular patterns (PAMPs) activate innate immunocytes through pattern recognition receptors.

85 by the ability of pathogenetic blood-derived immunocytes to induce secondary activation and disordere

86 invasive labeling and subsequent tracking of immunocytes, to investigate pancreatic infiltrate dynami

87 and HBD2 in mucosal inflammation to include immunocyte trafficking and killing of microbes with the

88 The presence of NKR bearing immunocytes was also observed in 10 of 15 different biop

89 In contrast, if activated immunocytes were exposed to 1alpha, 25-dihydroxycholecal

90 re combined immunodeficient mice, autologous immunocytes were injected into dermis, and the resultant

91 servations in which autologous blood-derived immunocytes were injected into PN skin engrafted onto SC

92 e pancreatic islets by a mixed population of immunocytes, which results in the impairment and eventua