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 al keratinocytes increased the production of 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 inflammatory markers IL-1, IL-4, IL-13, and thymic stromal lymphopoietin.

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

11 Thymic stromal lymphopoietin, a cytokine skewing the imm

12 Thymic stromal lymphopoietin, a four helix-bundle cytoki

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

14 Injection of recombinant thymic stromal lymphopoietin also induced scratching beh

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

16 Low temperature exposure induced thymic stromal lymphopoietin, an alarmin implicated in e

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

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

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

20 ed nearly all the cytokine release including thymic stromal lymphopoietin and endothelin-1.

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

22 Thymic stromal lymphopoietin and IL-33 signaling recipro

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

24 Thymic stromal lymphopoietin and osteopontin expression

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

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

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

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

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

30 )2-stimulating epithelial factors (IL-33 and thymic stromal lymphopoietin) and T(H)2 cytokines (IL-4,

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

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

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

34 hology, including IL-4, IL-13, IL-22, IL-31, thymic stromal lymphopoietin, and IFN-gamma, signal thro

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

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

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

38 olecules, such as OX40, OX40 ligand (OX40L), thymic stromal lymphopoietin, and IL-33.

39 cytokine responses such as IL-25, IL-33, and thymic stromal lymphopoietin, and increasing the epithel

40 Their persistence in skin required IL-7 and thymic stromal lymphopoietin, and localization was depen

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

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

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

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

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

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

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

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

49 Thymic stromal lymphopoietin combined with IL-33 increas

50 thymic stromal lymphopoietin directly stimulates eosinop

51 AD-related cytokines thymic stromal lymphopoietin, endothelin-1, and inflamma

52 epithelial layer, such as IL-25, IL-33, and thymic stromal lymphopoietin, engage and activate each o

53 sinophils, mast cell activation, increase of thymic stromal lymphopoietin, eotaxin-1 and type 2 cytok

54 miR-1 recruited P-selectin, thymic stromal lymphopoietin, eotaxin-3, and thrombopoie

55 17 responses, along with increased IL-36 and thymic stromal lymphopoietin expression, which were furt

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

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

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

59 d cells (ILC2s); dendritic cells primed with thymic stromal lymphopoietin, IL-25, and IL-33; and B an

60 e, we provide a brief review of the roles of thymic stromal lymphopoietin, IL-33, and IL-25 in divers

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

62 2-associated cytokines (interleukin (IL)-33, thymic stromal lymphopoietin, IL-5 and IL-13), serum imm

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

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

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

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

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

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

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

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

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

72 IL-1beta and thymic stromal lymphopoietin induced by low temperature

73 two-step mechanism has been hypothesized: a thymic stromal lymphopoietin-induced allergic sensitizat

74 Tumor necrosis factor-alpha potentiated thymic stromal lymphopoietin-induced Ca(2+)-influx, wher

75 1, VCAM-1, E-selectin, RANTES, IL-17, IL-33, thymic stromal lymphopoietin, inducible NO synthase, and

76 nd activation-regulated chemokine, IL-5, and thymic stromal lymphopoietin levels were significantly i

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

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

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

80 nide (iLNP(BUD5)) to deliver mRNA encoding a thymic stromal lymphopoietin nanobody (mnbTSLP) for the

81 ytokines (eg, IL-4, IL-13, IL-31, IL-33, and thymic stromal lymphopoietin), neurotransmitters (eg, su

82 ured in the presence of IL-3, IL-33, GM-CSF, thymic stromal lymphopoietin, or IL-25.

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

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

85 Thymic stromal lymphopoietin plays divergent roles in th

86 Thymic stromal lymphopoietin production and dermatitis i

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

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

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

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

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

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

93 Thymic stromal lymphopoietin receptor (TSLPR) signaling

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

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

96 Thymic stromal lymphopoietin receptor deficient mice had

97 Thymic stromal lymphopoietin receptor expression on bloo

98 Thymic stromal lymphopoietin receptor was observed on pe

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

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

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

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

103 ulate COX-2 upon IL-2, IL-25, and IL-33 plus thymic stromal lymphopoietin stimulation.

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

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

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

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

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

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

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

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

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

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

114 decreased the IL-1beta-mediated increases in thymic stromal lymphopoietin (TSLP) and GM-CSF in primar

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

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

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

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

119 thelial cell-derived danger signal mediators thymic stromal lymphopoietin (TSLP) and IL-33 are consis

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

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

122 Here, we show that thymic stromal lymphopoietin (TSLP) and IL-5(+) type 2 i

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

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

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

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

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

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

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

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

131 IL-4, IL-25, and thymic stromal lymphopoietin (TSLP) are overexpressed in

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

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

134 Thymic stromal lymphopoietin (TSLP) became important onl

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

136 ted that this was the result of secretion of thymic stromal lymphopoietin (TSLP) by cancer cells.

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

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

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

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

141 Thymic stromal lymphopoietin (TSLP) controls allergic TH

142 Whether thymic stromal lymphopoietin (TSLP) directly induces pot

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

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

145 resembling atopic dermatitis and relying on thymic stromal lymphopoietin (TSLP) from keratinocytes a

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

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

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

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

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

151 Thymic stromal lymphopoietin (TSLP) has been implicated

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

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

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

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

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

157 Further, the cytokine thymic stromal lymphopoietin (TSLP) has recently been sh

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

159 IL-33 and thymic stromal lymphopoietin (TSLP) have both been impli

160 Inhibition of thymic stromal lymphopoietin (TSLP) improves asthma cont

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

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

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

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

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

166 Thymic stromal lymphopoietin (TSLP) is a cytokine expres

167 Thymic stromal lymphopoietin (TSLP) is a cytokine implic

168 Thymic stromal lymphopoietin (TSLP) is a cytokine primar

169 Thymic stromal lymphopoietin (TSLP) is a cytokine produc

170 Thymic stromal lymphopoietin (TSLP) is a cytokine produc

171 Thymic stromal lymphopoietin (TSLP) is a cytokine produc

172 Thymic stromal lymphopoietin (TSLP) is a cytokine produc

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

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

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

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

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

178 Thymic stromal lymphopoietin (TSLP) is a major proallerg

179 Thymic stromal lymphopoietin (TSLP) is a newly identifie

180 Thymic stromal lymphopoietin (TSLP) is a newly identifie

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

182 Thymic stromal lymphopoietin (TSLP) is a pivotal cytokin

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

184 Thymic stromal lymphopoietin (TSLP) is a recently cloned

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

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

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

188 Thymic stromal lymphopoietin (TSLP) is an epithelial cel

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

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

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

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

193 Thymic stromal lymphopoietin (TSLP) is an essential cyto

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

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

196 Thymic stromal lymphopoietin (TSLP) is an interleukin 7

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

198 Thymic stromal lymphopoietin (TSLP) is elevated in asthm

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

200 Thymic stromal lymphopoietin (TSLP) is induced in allerg

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

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

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

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

205 Thymic stromal lymphopoietin (TSLP) is produced by epith

206 Thymic stromal lymphopoietin (TSLP) is said to increase

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

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

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

210 Thymic stromal lymphopoietin (TSLP) pathway blockade is

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

212 Thymic stromal lymphopoietin (TSLP) potently induces der

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

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

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

216 The cytokine thymic stromal lymphopoietin (TSLP) promotes differentia

217 Thymic stromal lymphopoietin (TSLP) recently has emerged

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

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

220 Thymic stromal lymphopoietin (TSLP) released after antig

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

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

223 Thymic stromal lymphopoietin (TSLP) signals via a recept

224 Here, we show that thymic stromal lymphopoietin (TSLP) stimulates T cells t

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

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

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

228 Thymic stromal lymphopoietin (TSLP) that is released by

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

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

231 2 balance by downregulating the secretion of thymic stromal lymphopoietin (TSLP) via inactivation of

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

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

234 not different between the mouse strains, but thymic stromal lymphopoietin (TSLP) was significantly in

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

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

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

238 Thymic Stromal Lymphopoietin (TSLP), a cytokine implicat

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

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

241 Concurrently, gene expression of Thymic Stromal Lymphopoietin (TSLP), a type-III IFN-indu

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

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

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

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

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

247 40, tumor necrosis factor-alpha (TNF-alpha), Thymic stromal lymphopoietin (TSLP), and macrophage-deri

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

249 alarmins, such as interleukin-33 (IL-33) and thymic stromal lymphopoietin (TSLP), are major players i

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

251 IL13, C-C motif chemokine ligand 26 (CCL26), thymic stromal lymphopoietin (TSLP), Charcot-Leyden crys

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

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

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

255 The epithelial cell-derived cytokines thymic stromal lymphopoietin (TSLP), IL-33, and IL-25 ar

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

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

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

259 ht to dissect its role, also in synergy with thymic stromal lymphopoietin (TSLP), in airway inflammat

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

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

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

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

264 expression of keratinocyte-derived cytokine, Thymic Stromal Lymphopoietin (TSLP), the key gene in AD

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

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

267 Here we show that thymic stromal lymphopoietin (TSLP)-a cytokine implicate

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

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

270 et that expresses interleukin-33 (IL-33) and thymic stromal lymphopoietin (TSLP).

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

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

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

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

275 triggering inflammation via the induction of thymic stromal lymphopoietin (TSLP).

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

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

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

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

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

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

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

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

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

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

286 re recruited to inflamed skin via CXCL12 and thymic stromal lymphopoietin (TSLP)/IL-3-dependent upreg

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

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

289 -6, and soluble IL-6R), epithelial alarmins (thymic stromal lymphopoietin [TSLP] and IL-33), and neut

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

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

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

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

294 Thymic stromal lymphopoietin was recently identified as

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

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

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

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

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

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