ライフサイエンスコーパス: epithelium

1 issue-specific genes in the thymic medullary epithelium.

2 hroughout the cornified layers of the tongue epithelium.

3 omain in developing and postnatal intestinal epithelium.

4 pically visible lesions on the adventitia or epithelium.

5 nt non-sensory cells of the cochlear sensory epithelium.

6 une cells that reside outside the intestinal epithelium.

7 be conditionally deleted from the intestinal epithelium.

8 cteria to adhere and colonize the intestinal epithelium.

9 ce of goblet cell metaplasia in the prostate epithelium.

10 ate into a monolayer of polarized intestinal epithelium.

11 ired for maintenance of the gastrointestinal epithelium.

12 tate dehydrogenase A occurring in the airway epithelium.

13 localized within the basal layer of the skin epithelium.

14 illary epithelium in contact with mandibular epithelium.

15 thin EC cells of human and mouse small bowel epithelium.

16 thereby leading to atrophy of the esophageal epithelium.

17 r hormone receptor expression in the mammary epithelium.

18 a source of progenitors for the transitional epithelium.

19 ury to the lung endothelium and the alveolar epithelium.

20 cilia define an additional uniciliated (E3) epithelium.

21 ease of the expression of CXCR7 in pulmonary epithelium.

22 dium promoted the differentiation toward the epithelium.

23 the hematopoietic lineage and the intestinal epithelium.

24 ltiple mature cell lineages in the olfactory epithelium.

25 pic hepatic differentiation in the pulmonary epithelium.

26 rrant DNA retention is tolerated in the oral epithelium.

27 n high-turnover tissues including intestinal epithelium.

28 pathological events in the retinal pigmented epithelium.

29 d cystic fibrosis (CF) cultured human airway epithelium.

30 in the hyper-proliferation of mammary gland epithelium.

31 r of host-commensal interactions in the oral epithelium.

32 ure studies of neurogenesis in the olfactory epithelium.

33 ity that is capable of disrupting the airway epithelium.

34 creases replicative activity in the prostate epithelium.

35 ression proper, cells leave a single-layered epithelium.

36 ral stem cells to reconstitute the olfactory epithelium.

37 e vasculature has instructive effects on the epithelium.

38 expression in the intestine: the intestinal epithelium.

39 igration during homoeostatic turnover of the epithelium.

40 imits their absorption across the intestinal epithelium.

41 nd inhibited cell proliferation in the wound epithelium.

42 onsumption of glucose by the retinal pigment epithelium.

43 long as the toxins exert their action on the epithelium.

44 the receptors are highly expressed in airway epithelium.

45 ir barrier function in differentiated airway epithelium.

46 nal barrier by inhibiting necroptosis in the epithelium.

47 germ cell exfoliation from the seminiferous epithelium.

48 tracing in the regenerating mouse olfactory epithelium.

49 an 20%, displacing surrounding BM and vulval epithelium.

50 plex host-microbe interactions in this naive epithelium.

51 ion and cytodifferentiation of the prostatic epithelium.

52 all of the cell types found within the nasal epithelium.

53 mation only in the neighboring, non-infected epithelium.

54 significantly enhanced binding to oviductal epithelium.

55 ized in basal layer of entire murine corneal epithelium.

56 widely prevalent diseases that afflict this epithelium.

57 rface of the eye, consisting of a stratified epithelium, a collagenous stroma and an innermost single

58 In human airway epithelium air-liquid interface (HAE-ALI) cultures, HBoV

59 he interface of the implant and the adjacent epithelium allows for bacterial invasion, which may lead

60 both in vitro and in vivo and that the crypt epithelium also expressed IL-6.

61 led homeostatic phenotypes in the intestinal epithelium-an archetypal canonical, Wnt pathway-dependen

62 " cells to be enriched within the intestinal epithelium and among lamina propria lymphocytes.

63 ne are the cells of origin for multi-layered epithelium and Barrett's oesophagus.

64 od at delivery, in fetal lung, and in buccal epithelium and blood during childhood.

65 t a major energy source for the host colonic epithelium and enhance epithelial barrier function throu

66 Quantifying preserved retinal pigment epithelium and EZ areas on FAF and OCT images, respectiv

67 the lactate as fuel for the retinal pigment epithelium and for neighboring Muller glial cells.

68 In addition to the effect of THP on the epithelium and granulopoiesis, this new immunomodulatory

69 ris (Tm) infected mice, tuft cells, IL-25 in epithelium and IL-13 in the mesenchyme were significantl

70 atidylcholine can be detected in the uterine epithelium and in pre-implantation-stage embryos, respec

71 ange factor (GEF) expressed in the olfactory epithelium and in the striatum.

72 O. formigenes interacts with colonic epithelium and induces colonic oxalate secretion, thereb

73 (Irf4) is highly expressed in murine thymic epithelium and is required to prime thymic epithelial ce

74 f multiprotein complexes to regulate mammary epithelium and keratinocyte differentiation and prolifer

75 It is composed of rabbit conjunctival epithelium and lacrimal gland cell spheroids, and recapi

76 MMP-28 is expressed by the pulmonary epithelium and macrophage, and we have found that it reg

77 the distinct roles of YAP/TAZ in endodermal epithelium and mesenchyme and find that, although dispen

78 e present when interactions between both the epithelium and mesenchyme are required for normal morpho

79 Primary cilia are located in the dental epithelium and mesenchyme at early stages of tooth devel

80 xpressed genes (DEGs) were found between the epithelium and mesenchyme in the base of oral cavity as

81 Compared with normal epithelium and noninflammation-induced tumors, inflammat

82 tor was predominantly expressed on pulmonary epithelium and on polymorphonuclear neutrophil (PMNs) af

83 n with a predominant effect on the pulmonary epithelium and PMNs.

84 atery diarrhoea, which was caused by a leaky epithelium and reduced bile re-absorption in the intesti

85 ess signaling pathways in the ocular surface epithelium and resident immune cells.

86 cells in protection against retinal pigment epithelium and retinal injury.

87 on in laser-captured regions of the cervical epithelium and stroma of untreated or estrogen-treated n

88 t cell types of the mouse jejunal intestinal epithelium and that miRNAs respond to microbiota in a hi

89 gion- and lineage-specific crosstalk between epithelium and their neighboring mesenchymal partners pr

90 omodulatory cross-talk between the bronchial epithelium and tissue-resident immune cells controls the

91 l study revealed minimal hepatocyte, biliary epithelium and vascular endothelium injury during preser

92 ds is globally similar to the immature human epithelium and we utilize HIOs to investigate complex ho

93 passage of live bacteria through the colonic epithelium, and determine the role of mast cells (MCs) a

94 cluding the epithelium of lips and olfactory epithelium, and ii) mechanosensory cells of neuromasts b

95 extracellular matrix, connective tissue and epithelium, and proteins related to the immune system.

96 side in the basal compartment of the mammary epithelium, and their neoplastic counterparts, mammary T

97 inantly present within the intestine and the epithelium, and they were not colocalized with Zn granul

98 The expression of epithelium- and neutrophil-derived host defense peptides

99 proliferation of goblet cells in the airway epithelium; and the production of antigen-specific IgE a

100 residing in the basal layer of the olfactory epithelium are capable of reconstituting the neuroepithe

101 onnections to the intrinsic mechanics of the epithelium are largely unexplored.

102 ctions between microbiota and the intestinal epithelium are not fully understood.

103 eptor agonist (LABA) on GCM in the bronchial epithelium are unknown.

104 l domains of suprabasal keratins of the skin epithelium are very resistant to evidence-based structur

105 Using normal colonic crypt epithelium as a comparator, we identify enhancers with r

106 eratectomy, in which surgical removal of the epithelium, basement membrane, and anterior stroma was p

107 xpands more than the right wall, as the left epithelium becomes more polarized and undergoes radial r

108 of asthma exacerbations, with the bronchial epithelium being the major site of HRV infection and rep

109 Retinal pigment epithelium-BM thickness, as measured by SD OCT segmentat

110 auses retention of nuclear DNA in the tongue epithelium but not in the skin.

111 t required for maintenance of the intestinal epithelium, but are required for regulation of intestina

112 Breast cancer originates from this epithelium, but the molecular mechanisms that underlie b

113 exposure to acrolein affects the intestinal epithelium by decrease/redistribution of tight junction

114 Cs) into gastric organoids containing fundic epithelium by first identifying and then recapitulating

115 lates branching morphogenesis in the mammary epithelium by modulating the response of the FGFR signal

116 Both the compounds improved the gut epithelium by promoting goblet and Paneth cells populati

117 endent inflammatory signaling in the mucosal epithelium can be therapeutically targeted by the pharma

118 zes in infection of the ciliated respiratory epithelium, causing disease of variable severity with li

119 ally, in primary human fetal retinal pigment epithelium cells, ligand binding to TLR2 induced robust

120 rizontal, photoreceptor, and retinal pigment epithelium cells, thus exposing the anatomical substrate

121 hamartoma of the retina and retinal pigment epithelium (CHRRPE) involving the macula.

122 The mammary gland epithelium consists of differentiated luminal epithelial

123 PCa model, WHSC1 overexpression in prostate epithelium cooperated with Pten deletion to produce a me

124 by COUP-TFII, which suppresses a mesenchyme-epithelium cross-talk responsible for Wolffian duct main

125 elevance of promoting the healing of corneal epithelium debridement.

126 transport of miR-133b-3p from mesenchyme to epithelium decreases DIP2B, which may function as an epi

127 cription factor and are dependent on pigment epithelium-derived factor (PEDF) on the outer surface of

128 the known neuroprotective molecule, pigment epithelium-derived factor (PEDF) plus docosahexaenoic ac

129 MLL and MLL-fusions form a complex with lens epithelium-derived growth factor (LEDGF/p75; encoded by

130 However, how transcriptional regulation of epithelium-derived signaling controls morphogenesis of t

131 ision, presence of atrophy/fibrosis, pigment epithelium detachment, and geographic atrophy/fibrotic s

132 opment, the vasculature co-develops with the epithelium during branching morphogenesis; however, it i

133 terning information initially resides in the epithelium during development.

134 ening of Bruchs membrane and retinal pigment epithelium dysfunction.

135 HPV oncogene expression in the cervical epithelium elicited significant gene-expression changes

136 nd in turn NGF overexpression within gastric epithelium expanded enteric nerves and promoted carcinog

137 ken up by M cells in the follicle-associated epithelium (FAE) region of Peyer's patches.

138 Expression of CRABP2 was found in epithelium, fibroblasts, and tumor Schwann cells of skin

139 xidant and prooxidant enzymes in the corneal epithelium, followed by the imbalance between metallopro

140 al stress of embryo elongation; mistiming of epithelium formation leads to defects in morphogenesis.

141 s the progression of the disease in salivary epithelium from female mice as follows: (a) improves sec

142 3 as a novel molecular determinant of thymic epithelium function throughout life.

143 visualization of areas where the intestinal epithelium had been compromised and demonstrated the pot

144 The adult mammalian cochlear sensory epithelium houses two major types of cells, mechanosenso

145 namic crosstalk between immune cells and the epithelium; however, the mechanisms involved remain inco

146 changes in germ-free mice, affecting the gut epithelium, immune system and enteric nervous system.

147 1 gene was highly upregulated in colon tumor epithelium in a HIF-2alpha-dependent manner.

148 e used to investigate injury to the ciliated epithelium in a multi-contrast setting.

149 IL-17RA-positive cells in the submucosa and epithelium in children with STRA compared with controls

150 significantly higher percentage of maxillary epithelium in contact with mandibular epithelium.

151 microbiota exert important influences on the epithelium in health and disease.

152 established primary cultures from follicular epithelium in human homeostatic conditions (h7H medium).

153 as robustly expressed by the retinal pigment epithelium in mouse and human eyes, both normal and with

154 Twist expression was generalised in the epithelium in normal but become more basal and nuclear w

155 h precursor lesions (STICs) in the fallopian epithelium in only half of the cases.

156 Whereas benign epithelium in prostates with and without tumor were simi

157 role of Wnt7b signaling and the ureteric bud epithelium in renal medullary capillary development.

158 l progenitor cells to repair the bronchiolar epithelium in response to lung damage.

159 Disruption of the epithelium in the female reproductive tract (FRT) is hyp

160 nd Fgfr4 are expressed in the mesenchyme and epithelium, inactivation in the mesenchyme, but not the

161 ogenitors differentiate into intestinal-like epithelium (including goblet cells) and thereby reproduc

162 combinase-mediated Ptch1 ablation in mammary epithelium increased proliferation and branching, but di

163 Cholinergic stimulation of the gastric epithelium induced nerve growth factor (NGF) expression,

164 the OTC significantly affected the overlying epithelium, inducing a regenerative response marked by i

165 ngement in neighboring cells that maintained epithelium integrity but did not absolutely require Casp

166 enhanced upon destruction of the respiratory epithelium integrity with EGTA or N-acetylcysteine.

167 Indeed, the proliferative response of the epithelium involves expression of several pathways previ

168 LP gene Irf6 only in the late embryonic oral epithelium ( Irf6 cKO), bypassing the role of the gene i

169 The intestinal epithelium is a functional barrier that secludes luminal

170 The intestinal epithelium is a major site for the conversion of dietary

171 The gut epithelium is a principal site for detecting such agents

172 We hypothesized that the human distal tip epithelium is an analogous progenitor population and tes

173 The bronchial epithelium is continuously exposed to a multitude of nox

174 The intestinal epithelium is continuously renewed by intestinal epithel

175 Repair of the alveolar epithelium is critical for clinical recovery; however, m

176 emonstrate that integrity of the respiratory epithelium is crucial in the host's innate defence again

177 Integrity of the airway epithelium is essential for normal lung function.

178 The arcade cell epithelium is generated after the epidermis and digestiv

179 er-relationship of capillaries and the renal epithelium is key to renal physiology, but how renal tub

180 that temporal regulation of the arcade cell epithelium is mediated by the pioneer transcription fact

181 Adult neurogenesis in the olfactory epithelium is often depicted as a unidirectional pathway

182 A similar transitional columnar epithelium is present at the transitional zones of other

183 nstrate that beta2AR signaling in the airway epithelium is sufficient to mediate key features of the

184 sgenic expression of beta2ARs only in airway epithelium is sufficient to rescue IL-13-induced AHR, in

185 The intestinal epithelium is the first physiological barrier breached b

186 tion from conducting airways to the alveolar epithelium is therefore a pivotal event in influenza pat

187 ) colitis model, and we demonstrate that the epithelium is transiently reprogrammed into a primitive

188 nd induced MET, arguing that HCMV induces an epithelium-like cellular environment during infection.

189 Precisely how this primary epithelium maintains continuous integrity during rapid a

190 ng from the expansion of the extra-embryonic epithelium, mediated by cell membrane adhesion and tensi

191 roach to knock out Nedd4L in mice intestinal epithelium (Nedd4L(f/f) ;Vil-Cre(ERT2) ) we show here th

192 EGs between gustatory (GE) and non-gustatory epithelium (NGE), and between GE and the underlying mese

193 The capacity of the olfactory epithelium (OE) for lifelong neurogenesis and regenerati

194 e remarkable capacity of the adult olfactory epithelium (OE) to regenerate fully both neurosensory an

195 e expression of this marker in the olfactory epithelium of adult mice.

196 Previously we showed that the epithelium of healthy mouse corneas becomes vulnerable t

197 , Runx2 was induced by 6.2-fold in pulmonary epithelium of house dust mite-challenged mice.

198 Here, we demonstrate that the epithelium of human pluripotent stem-cell-derived human

199 The respiratory epithelium of humans and animals is frequently exposed t

200 emosensory cells of taste buds including the epithelium of lips and olfactory epithelium, and ii) mec

201 al epithelium of the fly and in the tracheal epithelium of mice exhibit transient activation of TOR s

202 ic changes within the pre-neoplastic mammary epithelium of mice with and without stromal PTEN express

203 FoxO) in colon cancer cells and in the colon epithelium of mice.

204 with increased Il33 expression in the airway epithelium of Scnn1b-Tg mice.

205 testinal tract, particularly in the squamous epithelium of the esophagus.

206 regenerative stimuli, SCs in the intestinal epithelium of the fly and in the tracheal epithelium of

207 adequate models in which to study the fundus epithelium of the human stomach.

208 iously unidentified transitional zone in the epithelium of the upper gastrointestinal tract and provi

209 tracellular deposition of C3d in the corneal epithelium of vaccinated animals following challenge and

210 lial-mesenchymal transformations of the lens epithelium or, less likely, of the disorganized adjacent

211 c infarction of the choroid, retinal pigment epithelium, outer part of the retina and the optic nerve

212 Insults to the airway epithelium play a key role in constrictive bronchiolitis

213 ted the gp130/IL6/Stat3 signaling in colonic epithelium potentially assisted by infiltrating immune c

214 e of neuroblasts' delamination from the otic epithelium prefigure their position within the SAG.

215 inactivation in the mesenchyme, but not the epithelium, recapitulated the defects.

216 tes that autocrine IL-6 signaling in the gut epithelium regulates crypt homeostasis through the Panet

217 The proximal tubule epithelium relies on mitochondrial function for energy,

218 entiate human pluripotent stem cells to lung epithelium rely on passing through progenitor states tha

219 ibility to bacterial adhesion (>3-fold), the epithelium remained resistant to bacterial penetration.

220 is not strictly essential, it contributes to epithelium remodeling in the posterior midgut and thereb

221 of recipient mice that had their endogenous epithelium removed.

222 The mouse gut epithelium represents a constitutively challenged enviro

223 tion of both mPot1a and p53 in mouse mammary epithelium resulted in development of highly invasive br

224 nscript levels specifically in the bronchial epithelium resulted in reinstatement of susceptibility t

225 ne a detailed map of the postnatal olfactory epithelium, revealing cell fate potentials and branchpoi

226 including the occurrence of retinal pigment epithelium (RPE) abnormalities, choroidal neovasculariza

227 an important function of the retinal pigment epithelium (RPE) and it is essential for retinal homeost

228 boring epithelial cells, the retinal pigment epithelium (RPE) and podocytes, respectively.

229 or atrophy can occur without retinal pigment epithelium (RPE) atrophy and that atrophy can undergo an

230 zed to the apical aspects of retinal pigment epithelium (RPE) cells and contributes to a delayed c-wa

231 ntraretinal migration of the retinal pigment epithelium (RPE) cells in age-related macular degenerati

232 rol accumulation beneath the retinal pigment epithelium (RPE) cells is supposed to contribute the pat

233 ssion in the endothelium and retinal pigment epithelium (RPE) components of the BRB, and that TRPV4-s

234 eneration characterized by retinal pigmented epithelium (RPE) death; the RPE also exhibits DICER1 def

235 eration and atypical central retinal pigment epithelium (RPE) defects not attributable to geographic

236 aracterised by extensive sub-retinal pigment epithelium (RPE) deposits, RPE atrophy, choroidal neovas

237 otent stem cells to generate retinal pigment epithelium (RPE) from an individual suffering from retin

238 To report on the presence of retinal pigment epithelium (RPE) humps in high myopia, and to describe t

239 pecifically localized to the retinal pigment epithelium (RPE) in Abca4 (-/-) Stargardt model mice com

240 Daily, the retinal pigment epithelium (RPE) ingests a bolus of lipid and protein in

241 AMD histopathology involves retinal pigment epithelium (RPE) injury associated with immune cell infi

242 en the neural retina and the retinal pigment epithelium (RPE) is critical for several processes, incl

243 iological functions of the retinal pigmented epithelium (RPE) is the clearance of shed photoreceptor

244 m the SD-OCT and the area of retinal pigment epithelium (RPE) loss from the FAF.

245 (ERK1/2) is increased in the retinal pigment epithelium (RPE) of age-related macular degeneration (AR

246 ed a wild-type Mfrp to the retinal pigmented epithelium (RPE) of Mfrp (rd6) /Mfrp (rd6) mice via aden

247 To investigate when retinal pigment epithelium (RPE) tears occur and their associated treatm

248 rement parameters, including retinal pigment epithelium (RPE) thickness, central macular thickness, a

249 t is a major function of the retinal pigment epithelium (RPE) to support the neural retina.

250 ions with normally appearing retinal pigment epithelium (RPE) were the loss of the POS and ellipsoid

251 generation (AMD) affects the retinal pigment epithelium (RPE), a cell monolayer essential for photore

252 the photoreceptor-supporting retinal pigment epithelium (RPE), especially in a zone corresponding to

253 d terminal maturation of the retinal pigment epithelium (RPE), fenestrated choroid endothelial cells

254 g lipofuscin pigments in the retinal pigment epithelium (RPE), increased oxidative stress, augmented

255 aling in the entire eye, the retinal pigment epithelium (RPE), or the vascular endothelium.

256 ar and systemic factors with retinal pigment epithelium (RPE)-Bruch's membrane (BM) complex thickness

257 nzyme DICER1 in the mature retinal pigmented epithelium (RPE).

258 ciliary margin (CM), and the retinal pigment epithelium (RPE).

259 enchymal transition (EMT) of retinal pigment epithelium (RPE).

260 e phagocytosis of OSs by the retinal pigment epithelium (RPE).

261 chronic degeneration of the retinal pigment epithelium (RPE).

262 manner in chicken embryonic retinal pigment epithelium (RPE)/choroid in the absence of light.

263 cells in the human and mouse small bowel GI epithelium selectively express the mechanosensitive ion

264 The epithelium showed no evidence of canonical hedgehog sign

265 tion of Sirt1 specifically in the intestinal epithelium (SIRT1 iKO, villin-Cre+, Sirt1(flox/flox) mic

266 Intestinal epithelium-specific HuR knockout not only decreased Cdc4

267 , we studied mice with conditional global or epithelium-specific Smo deletions and observed similar e

268 acter must translocate across the intestinal epithelium, spread systemically in the circulation, and

269 m 20 fresh OSCC biopsies (cases) and 20 deep-epithelium swabs (matched control subjects) was sequence

270 Retinal pigment epithelium tears act differently depending on when they

271 al taste organs are papillae, composed of an epithelium that includes specialized taste buds, the bas

272 itor cell population in the mouse esophageal epithelium that is characterized by expression of kerati

273 In the intestinal epithelium, the aberrant regulation of cell/cell junctio

274 Loss of retinal pigment epithelium, the presence of a thin choroid, a perivascul

275 eased the barrier function of the intestinal epithelium, thus preventing the translocation of lipopol

276 The ability of the bronchial epithelium to control the balance of inhibitory and acti

277 vates the C3a receptor in the choroid plexus epithelium to disrupt the blood-CSF barrier.

278 preoperative anterior chamber depth (corneal epithelium to lens), and horizontal corneal diameter.

279 portant for early responses of the bronchial epithelium to Th2-stimuli.

280 dal blood passes through the retinal pigment epithelium to the retina where photoreceptors convert it

281 f the temporal peripapillary retinal pigment epithelium (tRPE) from its position in central gaze reac

282 s in the cell orientation field in different epithelium types.

283 is particularly important as the intestinal epithelium undergoes self-renewal every 4-7 days through

284 Specific factors from the corneal epithelium underlying the stimulation of stromal fibrosi

285 expression was observed in human asthma lung epithelium, underlying the potential clinical importance

286 models lacking p53 expression in the breast epithelium unleashes a torrent of DNA damage responses (

287 ) replicate their genomes in differentiating epithelium using the viral proteins E1 and E2 in associa

288 C1 domain peptide was transported across the epithelium via a microtubule-dependent mechanism and is

289 (mTORC1), was acutely deleted in intestinal epithelium via Tamoxifen injection in Tritrichomonas mur

290 s whereas intracellular Clusterin maintained epithelium viability during lung repair.

291 Damage of the pigment epithelium was also confirmed.

292 tational model of guinea-pig pancreatic duct epithelium was developed to determine the transport mech

293 -regulated kinase signaling in Wolffian duct epithelium was responsible for the retention of male str

294 RNA-Seq data from corneal epithelium were compared to epidermal hair follicle stem

295 vo roles of TFEB in the mammalian intestinal epithelium were not known.

296 Typhimurium penetrating the epithelium were significantly higher.

297 ntify a novel signaling pathway in the colon epithelium, where FoxO tumor suppressors could provide p

298 f wound healing is the generation of a basal epithelium wholly replacing the epidermis of the wound.

299 buting to IL-8 secretion in the CF bronchial epithelium with KL functioning as an endocrine and local

300 readily taken up into or through respiratory epithelium, with very low silver levels found in blood a