ライフサイエンスコーパス: gastrointestinal mucosa

1 moting the resolution of inflammation in the gastrointestinal mucosa.

2 ecreted CA and exists in both saliva and the gastrointestinal mucosa.

3 course), which occurs across the oral and/or gastrointestinal mucosa.

4 virulence factor in EAEC colonization of the gastrointestinal mucosa.

5 mbryo, to turnover in the homeostasis of the gastrointestinal mucosa.

6 nic infection, few have explored Treg in the gastrointestinal mucosa.

7 ortion of intraepithelial lymphocytes in the gastrointestinal mucosa.

8 the interactions between EAEC and the human gastrointestinal mucosa.

9 rologists to obtain in-vivo histology of the gastrointestinal mucosa.

10 uch as the skin, respiratory tract, and oral/gastrointestinal mucosa.

11 e of inducing growth in normal and malignant gastrointestinal mucosa.

12 ities, including growth-promoting actions on gastrointestinal mucosa.

13 or, and the number of tumors per 1000 mm2 of gastrointestinal mucosa.

14 ns in terminally differentiated cells in the gastrointestinal mucosa.

15 Aminobiphosphonates can irritate the upper gastrointestinal mucosa.

16 real-time, microscopic visualization of the gastrointestinal mucosa, allowing an endoscopic approach

17 olvement in lymphocyte recruitment to normal gastrointestinal mucosa and associated lymphoid tissue.

18 A-producing plasma cell populations in human gastrointestinal mucosa and bone marrow and the specific

19 ine and etoposide in the bone marrow and the gastrointestinal mucosa and emphasize the potential for

20 ing of vaccine-elicited T lymphocytes to the gastrointestinal mucosa and for vaccine protective effic

21 6 appears to be most highly expressed in the gastrointestinal mucosa and in kidney and lung.

22 so reduced proviral DNA in peripheral blood, gastrointestinal mucosa and lymph nodes without the deve

23 ressing endings were seen clearly within the gastrointestinal mucosa and myenteric plexus, respective

24 ammadelta T cells are primarily found in the gastrointestinal mucosa and play an important role in th

25 and function in blood, spleen, lymph nodes, gastrointestinal mucosa, and bronchoalveolar lavage of u

26 eptor (EGFR) triggers mitogenic signaling in gastrointestinal mucosa, and its expression is also upre

27 ed levels of proviral DNA in lymph nodes and gastrointestinal mucosa as compared with treatment at la

28 Galpha(t)-(2), also was demonstrated in the gastrointestinal mucosa as well as in STC-1 cells, as re

29 e sites of origin include the oral, lung and gastrointestinal mucosa, as data consistent with this hy

30 viding a point-of-care diagnostic method for gastrointestinal mucosa associated illnesses.

31 Functional analysis of the gastrointestinal mucosa-associated lymphoid tissue revea

32 The organisms penetrate the gastrointestinal mucosa by unknown mechanisms and are ph

33 gnificant accumulation of eosinophils in the gastrointestinal mucosa compared with control mice.

34 The gastrointestinal mucosa contains a complex network of ly

35 The gastrointestinal mucosa contains an intact immune system

36 umor size, the proportion of the area of the gastrointestinal mucosa covered with tumor, and the numb

37 are rapidly depleted from the periphery and gastrointestinal mucosa during acute HIV-1 infection.

38 of rhIL-11 to preserve the integrity of the gastrointestinal mucosa during cancer treatment regimens

39 the poor bioavailability of 2-MeOE2, as the gastrointestinal mucosa expresses high levels of 17beta-

40 protein contributes to the protection of the gastrointestinal mucosa from injury by strengthening and

41 The gastrointestinal mucosa harbors the majority of the body

42 The gastrointestinal mucosa has proven to be an interesting

43 ary, we demonstrate that UGTs are located in gastrointestinal mucosa, have vast overlapping activitie

44 glands, lymphoid organs, bone, bone marrow, gastrointestinal mucosa, heart, and kidneys.

45 IV-specific cellular immune responses to the gastrointestinal mucosa in a primate model.

46 The gastrointestinal mucosa is a major lymphoid tissue reser

47 Gastrointestinal mucosa is an early target of HIV and a

48 As the gastrointestinal mucosa is an important site of HIV tran

49 c stem cell transplantation (allo-HSCT), the gastrointestinal mucosa is damaged, and colonizing bacte

50 The human gastrointestinal mucosa is exposed to a diverse normal m

51 The upper gastrointestinal mucosa is exposed to endogenous and exo

52 The gastrointestinal mucosa is exposed to numerous chemical

53 The gastrointestinal mucosa is the primary site where human

54 (HIV) in peripheral blood, but the effect in gastrointestinal mucosa is uncertain.

55 emokine receptor expression in the blood and gastrointestinal mucosa; mucosal cells are predominantly

56 samples of normal pancreas (n = 11), normal gastrointestinal mucosa (n = 22), resected pancreas canc

57 Imaging of the gastrointestinal mucosa of mice infected with differenti

58 on was also seen on organisms colonizing the gastrointestinal mucosa of mice, indicating that the ant

59 etabolism of SCFAs affected apoptosis in the gastrointestinal mucosa of the mouse, and whether this a

60 d tissue-resident Vdelta1 T cells within the gastrointestinal mucosa of virally suppressed people wit

61 ockade involve either barrier tissues (e.g., gastrointestinal mucosa or skin) or endocrine organs, al

62 Therefore, the metabolism of SCFAs by the gastrointestinal mucosa plays a role in modulating apopt

63 Epithelial and other cells of the gastrointestinal mucosa rely on both luminal and bloodst

64 conclude that, based on these findings, the gastrointestinal mucosa represents a favored target for

65 (BaP) and the MCP in the bone marrow and the gastrointestinal mucosa, respectively.

66 may be a common mechanism by which the upper gastrointestinal mucosa responds to noxious insults.

67 bout the effects of individual NSAIDs on the gastrointestinal mucosa, risk factors for sustaining an

68 The gastrointestinal mucosa, structurally formed by the epit

69 e chemokine receptor CCR9 to localize to the gastrointestinal mucosa; their respective ligands, mucos

70 In the gastrointestinal mucosa they provide the priming cytokin

71 responsible for the unique tolerance of the gastrointestinal mucosa to proinflammatory stimuli.

72 d stability of CD25(+) FOXP3(+) cells in the gastrointestinal mucosa to support immunoregulation and

73 (renal proximal tubular epithelial cells and gastrointestinal mucosa) to damage to renal glomerular t

74 press toxicity to the bone marrow and to the gastrointestinal mucosa when used at therapeutic doses,

75 owever, these neurons are not present in the gastrointestinal mucosa, where 5-HT initiates peristalti

76 the host-toxin response at the level of the gastrointestinal mucosa, where STEC infection begins.

77 understanding of prorepair mechanisms in the gastrointestinal mucosa will aid in the development of n

78 that induces potent immune responses in the gastrointestinal mucosa would be highly desirable.