ライフサイエンスコーパス: granulomatous inflammation

1 and necroses, intravascular coagulation, and granulomatous inflammation.

2 e or after the onset of experimental chronic granulomatous inflammation.

3 m albumin reflected mainly lung cellular and granulomatous inflammation.

4 h fibrosis, crypt abscesses, crypt loss, and granulomatous inflammation.

5 but these may include carcinogenic change or granulomatous inflammation.

6 intravenously into eight mice bearing local granulomatous inflammation.

7 nocytes, and macrophages and produce typical granulomatous inflammation.

8 necrotizing vasculitis, and eosinophil-rich granulomatous inflammation.

9 attenuated P. acnes-induced ear swelling and granulomatous inflammation.

10 relieving P. acnes-induced ear swelling and granulomatous inflammation.

11 lium-specific CD4(+) T cells in the lung and granulomatous inflammation.

12 ng anti-IL-17 mAb markedly inhibited hepatic granulomatous inflammation.

13 also resulted in significant exacerbation of granulomatous inflammation.

14 aggregates within poorly organized areas of granulomatous inflammation.

15 ics of T cell influx and mobilization during granulomatous inflammation.

16 4 days but were associated with considerable granulomatous inflammation.

17 o multiple facets of type-2 hypersensitivity granulomatous inflammation.

18 odulate T cell recruitment and activation in granulomatous inflammation.

19 nd Th2 cells participate in the ovum-induced granulomatous inflammation.

20 14-amino acid cyclic peptide that regulates granulomatous inflammation.

21 the predominant finding (42.2%), followed by granulomatous inflammation (29%), steatosis/steatohepati

22 With granulomatous inflammation, 52% met the criteria for tub

23 i develop severe CD4 T cell-mediated hepatic granulomatous inflammation against parasite eggs associa

24 e displaying diminished type 2 responses and granulomatous inflammation, also do not fully default to

25 embedded tissue specimens studied, 57 showed granulomatous inflammation and 53 had been cultured for

26 nonhematopoietic cells may partly facilitate granulomatous inflammation and bacterial dissemination.

27 a from the tissues, leading to local chronic granulomatous inflammation and compensatory adaptive imm

28 icited a late xenograft reaction, leading to granulomatous inflammation and dissolution of the membra

29 humans is attributed to parasite egg-induced granulomatous inflammation and fibrosis in the host live

30 ansoni, parasite eggs cause hepatointestinal granulomatous inflammation and fibrosis mediated by CD4

31 thermore, a significant reduction of hepatic granulomatous inflammation and IL-17 production in inter

32 We showed that granulomatous inflammation and liver fibrosis were signi

33 Crohn disease (CD) are both characterized by granulomatous inflammation and related to nucleotide oli

34 yllium (Be) exposure and is characterized by granulomatous inflammation and the accumulation of Be-re

35 occupational lung disorder characterized by granulomatous inflammation and the accumulation of beryl

36 ure in the workplace and is characterized by granulomatous inflammation and the accumulation of beryl

37 beryllium disease (CBD) is characterized by granulomatous inflammation and the accumulation of CD4(+

38 crotizing vasculitis that is associated with granulomatous inflammation and the presence of anti-neut

39 at while a reduction in IL-4/IL-13-dependent granulomatous inflammation and tissue eosinophilia was o

40 Aspiration biopsy of the vertebra revealed granulomatous inflammation and yeast forms; culture yiel

41 crotizing and crescentic glomerulonephritis, granulomatous inflammation, and systemic necrotizing vas

42 tant role for CCR5, MIP-1 alpha, and CCR2 in granulomatous inflammation, and that CCR5 and MIP-1 alph

43 nsure that any further complications such as granulomatous inflammation are managed and documented.

44 The tissue Ags that drive this granulomatous inflammation are uncertain.

45 osure to antigen, WT mice developed a marked granulomatous inflammation associated with an increase i

46 The symptoms result from granulomatous inflammation associated with dying cyst fo

47 CBA/J (CBA) mice develop severe hepatic granulomatous inflammation associated with prominent Th1

48 llmark of Mycobacterium-induced pathology is granulomatous inflammation at the site of infection.

49 administration was associated with enhanced granulomatous inflammation, but did not prevent infectio

50 ught to elucidate the role of osteopontin in granulomatous inflammation by characterizing its express

51 Exserohilum provokes robust neutrophilic and granulomatous inflammation capable of thwarting fungal g

52 understanding of the pathways underlying the granulomatous inflammation characteristic of sarcoidosis

53 ysis of all 3 cases revealed elastolysis and granulomatous inflammation characterized by multinucleat

54 -->TLR2KO) exhibited a marked attenuation in granulomatous inflammation compared with WT mice.

55 Granulomatous inflammation consistent with Crohn's disea

56 osin-stained sections revealed non-caseating granulomatous inflammation consistent with skeletal sarc

57 t studies support the concept that pulmonary granulomatous inflammation directed by interferon (IFN)-

58 ains had similar degrees of interstitial and granulomatous inflammation during the first 12 weeks of

59 The granulomatous inflammation elicited by i.t. challenge pr

60 exclude infectious and autoimmune causes of granulomatous inflammation, followed by dermatologic wor

61 racterized by pronounced hepatic egg-induced granulomatous inflammation in a proinflammatory cytokine

62 These results suggest that exuberant granulomatous inflammation in CGD is probably not the re

63 The granulomatous inflammation in infection with the helmint

64 to chronic beryllium disease as evidenced by granulomatous inflammation in lung tissue.

65 d cannot substitute for the demonstration of granulomatous inflammation in lung tissue.

66 tory for macrophages and induced less severe granulomatous inflammation in mice, demonstrating that t

67 hogenic antigens relevant to immune-mediated granulomatous inflammation in sarcoidosis, we used a lim

68 rget of the adaptive immune response driving granulomatous inflammation in sarcoidosis.

69 Granulomatous inflammation in schistosomiasis is strictl

70 The granulomatous inflammation in the bowel of patients with

71 itical for protecting mice from a Th1-driven granulomatous inflammation in the ileum.

72 with schistosomiasis mansoni, where chronic granulomatous inflammation in the liver causes portal hy

73 ritical for the development of Th17-mediated granulomatous inflammation in the lung in response to S.

74 dritic cell-mediated development of a type 1 granulomatous inflammation in the lung in response to SC

75 CD4(+) T cells play a key role in granulomatous inflammation in the lung of patients with

76 eplacement IFN-gamma, the GKO mice developed granulomatous inflammation in the lung.

77 haracterized by a CD4+ T cell alveolitis and granulomatous inflammation in the lung.

78 D patients with beryllium sulfate results in granulomatous inflammation in the skin.

79 characterized by an increase in the area of granulomatous inflammation, increased numbers of resisti

80 type 1 (TH1) lymphocytes, attenuates chronic granulomatous inflammation induced by bacterial cell wal

81 responses are required for the generation of granulomatous inflammation induced by inhaled S. chartar

82 responses are required for the generation of granulomatous inflammation induced by inhaled SC.

83 Granulomatous inflammation is a typical feature of Takay

84 Granulomatous inflammation is characteristic of many aut

85 such as periprosthetic osteolysis, in which granulomatous inflammation is initiated by particle phag

86 Granulomatous inflammation is key to the pathogenesis of

87 y infections on CD4 T-cell-regulated chronic granulomatous inflammation is not well understood.

88 plays an important role in controlling acute granulomatous inflammation, it plays no essential role i

89 lation of silica into adult rats resulted in granulomatous inflammation leading to fibrosis and alveo

90 Extravascular granulomatous inflammation may be initiated by ANCA-indu

91 of monocyte chemotactic protein-1 (MCP-1) to granulomatous inflammation mediated by Th1- and Th2-rela

92 Pulmonary granulomatous inflammation modulated by IFN-gamma and IL

93 d suppression in Th2 cytokine expression and granulomatous inflammation observed in egg/CpG-sensitize

94 lated mainly to the egg stage, which induces granulomatous inflammation of affected tissues.

95 ase of ROS, as occurs in the immune-specific granulomatous inflammation of chronic beryllium disease

96 pportunistic pathogenic bacterium, developed granulomatous inflammation of the ileum, characterized b

97 se resulting from lymphocytic and frequently granulomatous inflammation of the peripheral airways, al

98 is (GPA; or Wegener's granulomatosis) is the granulomatous inflammation of the upper respiratory trac

99 hese mice in exacerbated hepatic egg-induced granulomatous inflammation or in the levels of IL-17 ind

100 is syndrome had chronic active colitis, with granulomatous inflammation present in 7 of 11 patients (

101 SC-mediated granulomatous inflammation required IFN-gamma and was TL

102 S. chartarum-mediated granulomatous inflammation required intact IL-23 or IL-1

103 iency with recurrent pyogenic infections and granulomatous inflammation, results from loss of phagocy

104 ciation with bioaerosols and the presence of granulomatous inflammation support consideration of myco

105 In schistosomiasis mansoni, hepatic granulomatous inflammation surrounding parasite eggs is

106 in 2 patients and demonstrated noncaseating granulomatous inflammation surrounding tattoo ink in the

107 ith schistosome helminths is associated with granulomatous inflammation that forms around parasite eg

108 asite eggs elicit a Th cell-mediated hepatic granulomatous inflammation that leads to scarring, porta

109 . parvum in sensitized rats caused pulmonary granulomatous inflammation that was histologically simil

110 s granulomatous lesions are detected, severe granulomatous inflammation was detected in only one of t

111 Surprisingly, although granulomatous inflammation was enhanced at the acute sta

112 Since both responses usually correlate with granulomatous inflammation, we tested six prominently ex

113 mma/TNF-dominant) and 2 (IL-4/IL-5-dominant) granulomatous inflammation were analyzed in mice with kn

114 Severe diffuse inflammation and granulomatous inflammation were evident in the livers of

115 though the soluble and cellular mediators of granulomatous inflammation were qualitatively similar in

116 y beryllium exposure and is characterized by granulomatous inflammation with accumulation of CD4+ T c

117 Pulmonary tuberculosis is characterized by granulomatous inflammation with an extensive infiltratio

118 Pulmonary tuberculosis is characterized by granulomatous inflammation with an extensive infiltratio

119 C57BL/6 mice, but not DBA/2 mice, developed granulomatous inflammation with an increase in lung inde

120 and C was C > S > W and ranged from intense granulomatous inflammation with caseous necrosis for inf

121 nge with 10(6) S. chartarum spores developed granulomatous inflammation with multinucleate giant cell

122 and challenged with 10(6) SC spores develop granulomatous inflammation with multinucleate giant cell

123 e inflammation early progressing to chronic, granulomatous inflammation with necrosis later that spre

124 opathological examination revealed extensive granulomatous inflammation within the dermis and subcuta

125 worms produce ova that incite focal Th2-type granulomatous inflammation within the liver and intestin

126 ry infection prolonged survival and enhanced granulomatous inflammation without reducing lung CFU.