ライフサイエンスコーパス: thymic stromal lymphopoietin

1 leased by the skin affected by AD (including thymic stromal lymphopoietin).

2 inflammatory markers IL-1, IL-4, IL-13, and thymic stromal lymphopoietin.

3 moderate affinity for IL-7 but does not bind thymic stromal lymphopoietin.

4 prostaglandin E(2), interleukin (IL)-10, and thymic stromal lymphopoietin.

5 feron gamma, tumor necrosis factor alpha, or thymic stromal lymphopoietin.

6 production by activating dendritic cells via thymic stromal lymphopoietin.

7 , IL-1alpha, IL-1beta, CCL20/MIP-3alpha, and thymic stromal lymphopoietin.

8 BLIN-4L could also respond to human thymic stromal lymphopoietin.

9 the interplay with dendritic cells primed by thymic stromal lymphopoietin.

10 Thymic stromal lymphopoietin, a cytokine skewing the imm

11 Thymic stromal lymphopoietin, a four helix-bundle cytoki

12 als expressed significantly higher levels of thymic stromal lymphopoietin, a major proinflammatory cy

13 Injection of recombinant thymic stromal lymphopoietin also induced scratching beh

14 Recent studies of TSLP (thymic stromal lymphopoietin), an epithelial cell-derive

15 e resulting class switching was amplified by thymic stromal lymphopoietin, an epithelial interleukin

16 in(-)CD45R(lo-neg)CD19(+) cells responded to thymic stromal lymphopoietin and 'preferentially' recons

17 ry cytokines and chemokines, including IL-5, thymic stromal lymphopoietin and CCL11, that help to ini

18 on house dust mite (HDM)-induced release of thymic stromal lymphopoietin and GM-CSF from tracheal ep

19 ed production of CCL17 and CCL22, but not of thymic stromal lymphopoietin and IL-33, in vitro.

20 Thymic stromal lymphopoietin and osteopontin expression

21 However, thymic stromal lymphopoietin and OX40 ligand were not re

22 the receptor for the Th2-promoting cytokine thymic stromal lymphopoietin and the high-affinity IgE r

23 cteristics of receptors for IL-4, IL-13, and thymic stromal lymphopoietin and their respective ligand

24 ion of ATP receptor P2X7R, and production of thymic stromal lymphopoietin and type 1, type 2, and typ

25 L-18 receptor 1 (IL1RL1-IL18R1), RAD50-IL13, thymic stromal lymphopoietin and WD repeat domain 36 reg

26 f CCL20/macrophage-inducible protein 3alpha, thymic stromal lymphopoietin, and CCL3-like 1 because of

27 Basophilia was promoted by thymic stromal lymphopoietin, and depletion of basophils

28 lease cytokines, such as IL-1, IL-25, IL-33, thymic stromal lymphopoietin, and GM-CSF, and endogenous

29 and a reduction in AD-related cytokine IL-8, thymic stromal lymphopoietin, and IL-10 secretion were o

30 ounding, migratory epithelia produce CXCL10, thymic stromal lymphopoietin, and IL-1beta and its antag

31 mulation with a combination of IL-25, IL-33, thymic stromal lymphopoietin, and IL-2.

32 increased expression of IL-4, IL-13, IL-22, thymic stromal lymphopoietin, and other cytokines associ

33 were those noted in TH2 (IL13, CCL18, CCL26, thymic stromal lymphopoietin, and periostin), TH9/IL-9,

34 the proallergic cytokines IL-1alpha, IL-33, thymic stromal lymphopoietin, and the growth factor amph

35 n of chemokine and cytokine genes, including thymic stromal lymphopoietin; and skin remodeling with f

36 g antibodies against IL-5, IL-13, IL-33, and thymic stromal lymphopoietin, as well as oral chemoattra

37 serum markers (CCL2, CCL5, CCL11, IL-3, and thymic stromal lymphopoietin) at 3 time points (ie, duri

38 of cytokines (interleukin [IL] 25, IL33, and thymic stromal lymphopoietin) by colon tissues, which ac

39 k the function of relevant molecules such as thymic stromal lymphopoietin, chemoattractant-receptor h

40 Thymic stromal lymphopoietin combined with IL-33 increas

41 thymic stromal lymphopoietin directly stimulates eosinop

42 identified genetic perturbations (eotaxin-3, thymic stromal lymphopoietin, IL-13, and filaggrin) that

43 cells preferentially expressed receptors for thymic stromal lymphopoietin, IL-25, and IL-33 and demon

44 outcomes, with an emphasis on the actions of thymic stromal lymphopoietin, IL-25, and IL-33 at the ep

45 r biologics similarly inhibit TH2 cytokines (thymic stromal lymphopoietin, IL-4, IL-5, IL-13, and the

46 2-associated cytokines (interleukin (IL)-33, thymic stromal lymphopoietin, IL-5 and IL-13), serum imm

47 y inflammatory mediators from AECs including thymic stromal lymphopoietin, IL-6, and PGE2, in part th

48 MCT feeding stimulated jejunal-epithelial thymic stromal lymphopoietin, Il25, and Il33 expression

49 he non-haematopoietic-cell-derived cytokines thymic stromal lymphopoietin, IL33 and IL25 (also known

50 -CSF and chemokines such as CCL2, CCL20, and thymic stromal lymphopoietin in epithelial cells through

51 Furthermore, airway SCs upregulate thymic stromal lymphopoietin in response to exposure to

52 n of the epithelial-cell-restricted cytokine thymic stromal lymphopoietin in the intestine and, after

53 cytokine expression in response to IL-33 and thymic stromal lymphopoietin in vitro.

54 ion for the Th2-inducing cytokines IL-33 and thymic stromal lymphopoietin in WT mice with colitis, wh

55 and stimulated secretion of IL-8, IL-10, and thymic stromal lymphopoietin independent of PAR2 activit

56 1, VCAM-1, E-selectin, RANTES, IL-17, IL-33, thymic stromal lymphopoietin, inducible NO synthase, and

57 ar destruction, which results in lower serum thymic stromal lymphopoietin levels, milder B-cell lymph

58 itic cells (that have been "educated" by the thymic stromal lymphopoietin molecule produced by a thym

59 esponses and airway pathology, and IL-33 and thymic stromal lymphopoietin most likely play key roles

60 atitis via the protease-activated receptor 2-thymic stromal lymphopoietin pathway.

61 The cytokines IL-4, IL-13, and thymic stromal lymphopoietin play a key role in allergic

62 Thymic stromal lymphopoietin plays divergent roles in th

63 Thymic stromal lymphopoietin production and dermatitis i

64 lial IL-25 and proangiogenic progenitor cell thymic stromal lymphopoietin production.

65 Mice deficient in IL-33R (Il1rl1(-/-)) and thymic stromal lymphopoietin receptor (Tslpr(-/-)) showe

66 ession profiling and to assess the effect of thymic stromal lymphopoietin receptor (TSLPR) blockade i

67 dependently of IL-3 by increasing functional thymic stromal lymphopoietin receptor (TSLPR) expression

68 Binding of TSLP to the thymic stromal lymphopoietin receptor (TSLPR) is increas

69 Wild-type (WT) BALB/c, thymic stromal lymphopoietin receptor (TSLPR) knockout (

70 Thymic stromal lymphopoietin receptor (TSLPR) signaling

71 Overexpression of the thymic stromal lymphopoietin receptor (TSLPR; encoded by

72 on expression levels of receptors for TSLP (thymic stromal lymphopoietin receptor [TSLPR] and CD127)

73 Thymic stromal lymphopoietin receptor expression on bloo

74 Thymic stromal lymphopoietin receptor was observed on pe

75 rface-activating receptors, such as CD48 and thymic stromal lymphopoietin receptors, as well as inhib

76 f autocrine/paracrine IL-10, IL-4, IL-22 and thymic stromal lymphopoietin regulated these JAK-depende

77 protease-activated receptor 2, resulting in thymic stromal lymphopoietin secretion and a cutaneous T

78 IL-33 and thymic stromal lymphopoietin sensitized naive animals to

79 ckout (FcRgamma(-/-)) mice were crossed with thymic stromal lymphopoietin transgenic (TSLPtg) mice, w

80 sin II type 1 receptor blocker (losartan) in thymic stromal lymphopoietin transgenic (TSLPtg) mice, w

81 In addition, administration of imatinib to thymic stromal lymphopoietin transgenic mice with establ

82 tested the protective effects of imatinib in thymic stromal lymphopoietin transgenic mice, a model of

83 P = 0.01), higher mRNA transcript numbers of thymic stromal lymphopoietin (TSLP) (1.6-fold, P = 0.009

84 l roles in allergic inflammation mediated by thymic stromal lymphopoietin (TSLP) (see the related art

85 We evaluated the role of the innate cytokine thymic stromal lymphopoietin (TSLP) acting on mast cells

86 ls that was dependent on the innate cytokine thymic stromal lymphopoietin (TSLP) and also induced ano

87 hat have been epicutaneously sensitized with thymic stromal lymphopoietin (TSLP) and antigen to repea

88 Thymic stromal lymphopoietin (TSLP) and calpain 14 (CAPN

89 ptors share components of the IL-7 receptor: thymic stromal lymphopoietin (TSLP) and IL-15.

90 nses are developed simultaneously, driven by thymic stromal lymphopoietin (TSLP) and IL-23, respectiv

91 irements for the epithelial cytokines IL-33, thymic stromal lymphopoietin (TSLP) and IL-25 in the act

92 Thymic stromal lymphopoietin (TSLP) and IL-33 are consid

93 Both thymic stromal lymphopoietin (TSLP) and IL-33 levels wer

94 eosinophilia, as well as increased levels of thymic stromal lymphopoietin (TSLP) and IL-5 in the skin

95 Thymic stromal lymphopoietin (TSLP) and IL-7 are related

96 We also treated mice with recombinant thymic stromal lymphopoietin (TSLP) and TRAIL.

97 in the blood myeloid compartment as well as thymic stromal lymphopoietin (TSLP) and transforming gro

98 licating hepatic epithelial-derived cytokine thymic stromal lymphopoietin (TSLP) and type 2 immunity,

99 cells was suppressed by anti-IL-1 and anti- thymic stromal lymphopoietin (TSLP) and was enhanced by

100 ymorphisms in the gene encoding the cytokine thymic stromal lymphopoietin (TSLP) are associated with

101 The pro-TH2 cytokines IL-25, IL-33, and thymic stromal lymphopoietin (TSLP) are associated with

102 OX40-OX40L interactions and thymic stromal lymphopoietin (TSLP) are important in the

103 CRLF2 binds its ligand thymic stromal lymphopoietin (TSLP) as a heterodimer wit

104 that both genetic and chemical induction of thymic stromal lymphopoietin (TSLP) at a distant site le

105 Thymic stromal lymphopoietin (TSLP) became important onl

106 onstrate that the overproduction of cytokine thymic stromal lymphopoietin (TSLP) by AD skin promotes

107 dized lipids that triggered the induction of thymic stromal lymphopoietin (TSLP) by epithelial cells

108 mice were associated with overproduction of thymic stromal lymphopoietin (TSLP) by IECs, which negat

109 Only dendritic cells (DCs) activated by thymic stromal lymphopoietin (TSLP) can induce a robust

110 ial cell-derived cytokines IL-25, IL-33, and thymic stromal lymphopoietin (TSLP) can promote CD4(+) T

111 Thymic stromal lymphopoietin (TSLP) controls allergic TH

112 Whether thymic stromal lymphopoietin (TSLP) directly induces pot

113 The cytokine thymic stromal lymphopoietin (TSLP) drives immature B ce

114 Lung-specific thymic stromal lymphopoietin (TSLP) expression is suffic

115 rotease inhibitor Kazal-type 5 (SPINK5), and thymic stromal lymphopoietin (TSLP) gene variants and ch

116 ct sensitization pattern was associated with thymic stromal lymphopoietin (TSLP) genotype.

117 Furthermore, thymic stromal lymphopoietin (TSLP) has also been sugges

118 The epithelial-derived cytokine thymic stromal lymphopoietin (TSLP) has been associated

119 The cytokine thymic stromal lymphopoietin (TSLP) has been implicated

120 Thymic stromal lymphopoietin (TSLP) has been implicated

121 The cytokine thymic stromal lymphopoietin (TSLP) has been implicated

122 The cytokine thymic stromal lymphopoietin (TSLP) has been linked to h

123 Thymic stromal lymphopoietin (TSLP) has emerged as an im

124 The epithelial-derived cytokine thymic stromal lymphopoietin (TSLP) has important roles

125 The cytokine thymic stromal lymphopoietin (TSLP) has recently been im

126 Elevated IL-13 and thymic stromal lymphopoietin (TSLP) have been found in t

127 monstrate a previously unrecognized role for thymic stromal lymphopoietin (TSLP) in promoting the pop

128 However, the role of thymic stromal lymphopoietin (TSLP) in the development o

129 the role of the epithelial-derived cytokine thymic stromal lymphopoietin (TSLP) in the response to R

130 Mice overexpressing the proallergic cytokine thymic stromal lymphopoietin (TSLP) in the skin develop

131 We show that human DCs activated by thymic stromal lymphopoietin (TSLP) induced a robust exp

132 Thymic stromal lymphopoietin (TSLP) is a cytokine expres

133 Thymic stromal lymphopoietin (TSLP) is a cytokine implic

134 Thymic stromal lymphopoietin (TSLP) is a cytokine primar

135 Thymic stromal lymphopoietin (TSLP) is a cytokine produc

136 Thymic stromal lymphopoietin (TSLP) is a cytokine produc

137 Thymic stromal lymphopoietin (TSLP) is a cytokine produc

138 Thymic stromal lymphopoietin (TSLP) is a cytokine produc

139 Thymic stromal lymphopoietin (TSLP) is a cytokine that f

140 Thymic stromal lymphopoietin (TSLP) is a cytokine that p

141 Thymic stromal lymphopoietin (TSLP) is a cytokine that p

142 Thymic stromal lymphopoietin (TSLP) is a cytokine that t

143 Thymic stromal lymphopoietin (TSLP) is a cytokine with p

144 Thymic stromal lymphopoietin (TSLP) is a major proallerg

145 Thymic stromal lymphopoietin (TSLP) is a newly identifie

146 Thymic stromal lymphopoietin (TSLP) is a newly identifie

147 Human thymic stromal lymphopoietin (TSLP) is a novel epithelia

148 Thymic stromal lymphopoietin (TSLP) is a pivotal cytokin

149 Thymic stromal lymphopoietin (TSLP) is a pro-allergic cy

150 Thymic stromal lymphopoietin (TSLP) is a recently cloned

151 Thymic stromal lymphopoietin (TSLP) is a type 1 cytokine

152 Thymic stromal lymphopoietin (TSLP) is a type I cytokine

153 Thymic stromal lymphopoietin (TSLP) is a type I cytokine

154 Thymic stromal lymphopoietin (TSLP) is an epithelial cel

155 Thymic stromal lymphopoietin (TSLP) is an epithelial-cel

156 Thymic stromal lymphopoietin (TSLP) is an epithelial-der

157 Thymic stromal lymphopoietin (TSLP) is an epithelium-der

158 Thymic stromal lymphopoietin (TSLP) is an essential cyto

159 Thymic stromal lymphopoietin (TSLP) is an IL-7-related c

160 Thymic stromal lymphopoietin (TSLP) is an interleukin (I

161 Thymic stromal lymphopoietin (TSLP) is an interleukin 7

162 Thymic stromal lymphopoietin (TSLP) is crucial for the d

163 Thymic stromal lymphopoietin (TSLP) is elevated in asthm

164 The epithelial-derived cytokine thymic stromal lymphopoietin (TSLP) is important for the

165 Thymic stromal lymphopoietin (TSLP) is induced in allerg

166 RATIONALE: Thymic stromal lymphopoietin (TSLP) is known to be eleva

167 Thymic stromal lymphopoietin (TSLP) is known to be eleva

168 romote the growth and activation of B cells, thymic stromal lymphopoietin (TSLP) is now known to have

169 The cytokine thymic stromal lymphopoietin (TSLP) is produced by epith

170 Thymic stromal lymphopoietin (TSLP) is produced by epith

171 Thymic stromal lymphopoietin (TSLP) is said to increase

172 The epithelial-derived cytokine thymic stromal lymphopoietin (TSLP) is sufficient to ind

173 lls and innate immune cells via the cytokine thymic stromal lymphopoietin (TSLP) is thought to drive

174 ic march suggest that systemic, skin-derived thymic stromal lymphopoietin (TSLP) mediates progression

175 Thymic stromal lymphopoietin (TSLP) pathway blockade is

176 We show here that human thymic stromal lymphopoietin (TSLP) potently activated C

177 Thymic stromal lymphopoietin (TSLP) potently induces der

178 owed that dendritic cells (DCs) activated by thymic stromal lymphopoietin (TSLP) prime naive CD4(+) T

179 We previously showed that mDCs, educated by thymic stromal lymphopoietin (TSLP) produced by the epit

180 triggered by an increased expression of the thymic stromal lymphopoietin (TSLP) proinflammatory cyto

181 The cytokine thymic stromal lymphopoietin (TSLP) promotes differentia

182 Thymic stromal lymphopoietin (TSLP) recently has emerged

183 CRLF2 encodes the thymic stromal lymphopoietin (TSLP) receptor, which acti

184 Mucosally produced thymic stromal lymphopoietin (TSLP) regulates Th2 respon

185 Thymic stromal lymphopoietin (TSLP) released after antig

186 Recent studies revealed a critical role for thymic stromal lymphopoietin (TSLP) released from epithe

187 se-activated receptor 2 (PAR2), resulting in thymic stromal lymphopoietin (TSLP) secretion and a cuta

188 Thymic stromal lymphopoietin (TSLP) signals via a recept

189 component of the receptors for both IL-7 and thymic stromal lymphopoietin (TSLP) suggests that IL-2 c

190 genomic databases, and its homology to mouse thymic stromal lymphopoietin (TSLP) suggests that it is

191 The murine cytokine thymic stromal lymphopoietin (TSLP) supports the develop

192 Thymic stromal lymphopoietin (TSLP) that is released by

193 nemia in the development of liver disease in thymic stromal lymphopoietin (TSLP) transgenic mice that

194 genital mucosal epithelial cells to produce thymic stromal lymphopoietin (TSLP) via activation of th

195 The cellular receptor for murine thymic stromal lymphopoietin (TSLP) was detected in a va

196 e tissue-derived cytokines IL-25, IL-33, and thymic stromal lymphopoietin (TSLP) was significantly di

197 el cytokine from a thymic stromal cell line (thymic stromal lymphopoietin (TSLP)) promotes the develo

198 so when ILC2s were stimulated with IL-7 and thymic stromal lymphopoietin (TSLP), 2 ligands of IL-7 r

199 s also proposed to control the activation of thymic stromal lymphopoietin (TSLP), a cytokine implicat

200 Thymic Stromal Lymphopoietin (TSLP), a cytokine implicat

201 with polymorphisms in the gene that encodes thymic stromal lymphopoietin (TSLP), a cytokine that pro

202 Here we report that thymic stromal lymphopoietin (TSLP), a keratinocyte-deri

203 Moreover, thymic stromal lymphopoietin (TSLP), an epithelial-deriv

204 In this study, we report that thymic stromal lymphopoietin (TSLP), an IL-7-like type 1

205 rus infection or dsRNA stimulation increased thymic stromal lymphopoietin (TSLP), an upstream pro-all

206 in association with induction of Il33, Csf2, thymic stromal lymphopoietin (Tslp), and Ccl20 transcrip

207 several cytokines (e.g., IL-4, IL-12, IL-23, thymic stromal lymphopoietin (TSLP), and IFNgamma) impli

208 ain innate factors, namely IL-25, IL-33, and thymic stromal lymphopoietin (TSLP), are elaborated by s

209 nd mast cells, a higher expression levels of thymic stromal lymphopoietin (TSLP), cathelicidin, prote

210 We previously showed that human thymic stromal lymphopoietin (TSLP), highly expressed by

211 The epithelium-associated cytokines thymic stromal lymphopoietin (TSLP), IL-25, and IL-33 ar

212 s known to activate ILCs (IL-2, IL-7, IL-12, thymic stromal lymphopoietin (TSLP), IL-25, and IL-33).

213 at epithelial cell-derived cytokines such as thymic stromal lymphopoietin (TSLP), IL-33, and IL-25 ma

214 was associated with an increase in levels of thymic stromal lymphopoietin (TSLP), IL-9, and IL-13, bu

215 ative PCR was used to measure mRNA for sHBEC thymic stromal lymphopoietin (TSLP), IL33, POSTN, and IL

216 fic for the epithelial-cell-derived cytokine thymic stromal lymphopoietin (TSLP), in patients whose a

217 This factor, termed thymic stromal lymphopoietin (TSLP), is a protein of 140

218 rtinez-Cingolani et al identified that human thymic stromal lymphopoietin (TSLP), previously shown to

219 ns in receptors for interleukin-7 (IL-7) and thymic stromal lymphopoietin (TSLP), resulting in a nove

220 ons of the other innate cytokines, IL-33 and thymic stromal lymphopoietin (TSLP), to the observed ast

221 ytokines, interleukin-25 (IL-25), IL-33, and thymic stromal lymphopoietin (TSLP), which nonredundantl

222 Th2 central memory cells are stimulated with thymic stromal lymphopoietin (TSLP)-activated dendritic

223 etween classical IL-3-elicited basophils and thymic stromal lymphopoietin (TSLP)-elicited basophils.

224 r kappa B (NFkappaB)-dependent production of thymic stromal lymphopoietin (TSLP).

225 T5 in DCs led to the inability to respond to thymic stromal lymphopoietin (TSLP).

226 ratinocytes is the pro-inflammatory cytokine thymic stromal lymphopoietin (TSLP).

227 One such product is thymic stromal lymphopoietin (TSLP).

228 show that human breast cancer cells produce thymic stromal lymphopoietin (TSLP).

229 c cell interactions via cytokines, including thymic stromal lymphopoietin (TSLP).

230 produce a wide range of cytokines including thymic stromal lymphopoietin (TSLP).

231 y dendritic cells that were activated by the thymic stromal lymphopoietin (TSLP).

232 nown ligands for IL-7Ralpha: IL-7 itself and thymic stromal lymphopoietin (TSLP).

233 port that human Hassall's corpuscles express thymic stromal lymphopoietin (TSLP).

234 merulonephritis induced by overexpression of thymic stromal lymphopoietin (TSLP).

235 described interleukin 7 (IL-7)-like factor, thymic stromal lymphopoietin (TSLP).

236 cytokines interleukin 33 (IL-33), IL-25 and thymic stromal lymphopoietin (TSLP).

237 cytokines interleukin 25 (IL-25), IL-33 and thymic stromal lymphopoietin (TSLP).

238 Intestinal epithelial cells (IECs) produce thymic stromal lymphopoietin (TSLP); however, the in viv

239 ukin-4 (IL-4), IL-5, IL-9, IL-13, IL-31, and thymic stromal lymphopoietin (TSLP); pro-inflammatory cy

240 pithelial cell (EC)-derived cytokines (e.g., thymic stromal lymphopoietin [TSLP]) activating human ba

241 Epithelial cytokines (IL-33, IL-25, and thymic stromal lymphopoietin [TSLP]) and mast cell media

242 es usually undetectable on arrays (ie, IL22, thymic stromal lymphopoietin [TSLP], CCL22, and CCL26).

243 B cell progenitors seeded in the presence of thymic stromal lymphopoietin undergo significant expansi

244 Thymic stromal lymphopoietin was recently identified as

245 helial expression of IL-25, but not IL-33 or thymic stromal lymphopoietin, was increased in a subset

246 In addition, IL-7 or thymic stromal lymphopoietin were able to replace IL-2.

247 Furthermore, both CXCL10 and thymic stromal lymphopoietin were localized in migratory

248 In this article, we report that IL-33 and thymic stromal lymphopoietin were produced quickly in th

249 ucing cytokines, including interleukin 4 and thymic stromal lymphopoietin, which are involved in TH2

250 ucing cytokines, including interleukin 4 and thymic stromal lymphopoietin, which are involved in TH2

251 vitro scratch wound initiated the release of thymic stromal lymphopoietin, which was greater in epith