ライフサイエンスコーパス: epithelial

1 Preclinical studies have demonstrated epithelial ablation followed by regeneration of normaliz

2 PAG1 deficiency increased airway epithelial activation, ILC2 expansion, and T(H) 2 differ

3 ce, "Origins of allergic disease: Microbial, epithelial and immune interactions" were to present and

4 Epithelial and mast cell interactions, leading to the sy

5 strated by coordinated signals from adjacent epithelial and mesenchymal cells.

6 ed chromatin interactions in normal prostate epithelial and prostate cancer cells.

7 , and barrier function and identify dietary, epithelial, and immune checkpoints along this axis to be

8 in western diet (WD)-induced loss of colonic epithelial barrier (CEB) function in mice with a genetic

9 sbiosis, resulting in compromised intestinal epithelial barrier and chronic mucosal inflammation.

10 C-BMP can measure ABCC1 activity at the lung epithelial barrier and may be applicable in humans to as

11 different approaches to diagnose and target epithelial barrier defects are currently being developed

12 Epithelial barrier dysfunction facilitates transepitheli

13 mice with a genetic impairment in intestinal epithelial barrier function, junctional adhesion molecul

14 ting epithelial regeneration, which prolongs epithelial barrier impairment and creates an environment

15 By putting the epithelial barrier to the forefront of the pathophysiolo

16 [ABCC1]) is abundantly expressed at the lung epithelial barrier, where it may influence the pulmonary

17 he most abundant T-lymphocyte subset in some epithelial barriers such as mouse skin.

18 nerating a conducive microenvironment on the epithelial boundary, which becomes further dysbiotic by

19 Whereas its effect on epithelial branching and alveologenesis are likely causa

20 e structures, reminiscent of those formed by epithelial breast cells.

21 s. air) with a published data set from human epithelial brushes (smoker vs. non-smoker) revealed a hi

22 HOTAIR is a lncRNA overexpressed in several epithelial cancers and strongly correlated with invasion

23 he development of many types of lymphoid and epithelial cancers.

24 Using mice with inducible intestinal epithelial cell (IEC)-specific deletion of Phb1 (Phb1(iD

25 Here we examine medullary thymic epithelial cell (mTEC) heterogeneity and its influence o

26 IR-AF) provided evidence for retinal pigment epithelial cell (RPE) involvement.

27 d a gene and protein signature similar to an epithelial cell and gained chromatin accessibility sites

28 ST6Gal-I expression in blocking homeostatic epithelial cell apoptosis in gastric cancer pathogenesis

29 application initiates changes in intestinal epithelial cell characteristics relative to those of sta

30 uman intestinal enteroids (HIEs) are primary epithelial cell cultures that can provide insights into

31 al thickness (34%; P < 0.001), and increased epithelial cell density (13%; P < 0.001).

32 in IL-13 biology to determine whether airway epithelial cell expression of 2 key mediators critical f

33 alignancy cascade, indicating that increased epithelial cell expression of ST6Gal-I is associated wit

34 outgrowth forms through extreme increases in epithelial cell height.

35 chnique to measure the tension in individual epithelial cell junctions of cells in various locations

36 A recombinant human corneal limbal epithelial cell line expressing a LC3-GFP fusion protein

37 ed that hypothesis by infecting an oviductal epithelial cell line with C muridarum, followed by immun

38 nd tryptamine toxicity on a human intestinal epithelial cell line.

39 g of cytotoxic T cells to mediate intestinal epithelial cell lysis.

40 report in Science that type III IFNs disrupt epithelial cell proliferation and differentiation in the

41 f macrophages in obese mice enhanced mammary epithelial cell stem/progenitor activity, elevated expre

42 y activating the p62-NRF2 axis, resulting in epithelial cell transformation.

43 gment epithelium (RPE) is a highly polarized epithelial cell type maintained at a senescence state, a

44 ution representation of the multiple mammary epithelial cell types in the organoids, and demonstrate

45 ron progenitor cells (NPCs) give rise to all epithelial cell types of the nephron, the filtering unit

46 The epithelial cell-derived danger signal mediators thymic s

47 mpare the role of myeloid- versus intestinal epithelial cell-derived IL-33 during dextran sodium sulf

48 treated HO-exposed mice and primary alveolar epithelial cells (AECs) with the novel TREK-1 activators

49 silico and in vitro using human endometrial epithelial cells (EEC) grown as monolayers or a 3-dimens

50 -culture on patient-derived human intestinal epithelial cells (HIECs), and incorporate perfused vascu

51 Here, we integrated intestinal epithelial cells (IEC) derived from human intestinal org

52 ells as a model, we observed that intestinal epithelial cells (IECs) were permissive to EV-A71 infect

53 not GT-I) invaded bovine and murine mammary epithelial cells (MECs) and induced apoptosis, as determ

54 e marrow chimeras, GILT expression in thymic epithelial cells (TECs), but not hematopoietic cells, wa

55 17 and miR-548b were upregulated in alveolar epithelial cells after CI/EVR, which merit further explo

56 is present in nasal, tracheal, and bronchial epithelial cells and constitutes a central element of th

57 of fungal metabolites, which can be toxic to epithelial cells and lead to barrier dysfunction.

58 it alters nutrient metabolism in intestinal epithelial cells and microbiome, leading to increased la

59 larity (PCP) pathway is required in alveolar epithelial cells and myofibroblasts for alveologenesis i

60 it enhances viral replication in human lung epithelial cells and primary human airway tissues by inc

61 Although epithelial cells are among the first to encounter pneumo

62 g mesenchymal neighbors, while its overlying epithelial cells become WNT-restricted.

63 tic and epigenetic alterations in colorectal epithelial cells but also affect the gut microbiota and

64 demonstrate viral tropism for choroid plexus epithelial cells but little to no infection of neurons o

65 R2) is strongly upregulated on renal tubular epithelial cells by acute cell-mediated rejection (ACR.

66 SCCs were distinguished from the surrounding epithelial cells by calretinin and phospholipase C140 im

67 vival factor for functionally differentiated epithelial cells by expressing a hyperactive STAT5 mutan

68 innate immune signaling, in HT-29 intestinal epithelial cells challenged with TNF-alpha or STS.

69 Here we review recent studies on how colon epithelial cells communicate directly with colon afferen

70 n of MNV receptor (CD300lf) in human HEK293T epithelial cells conferred susceptibility to MNV infecti

71 levels of ST6GAL-I and SOX9 in human gastric epithelial cells correlated positively with one another

72 pendent H33258 uptake was rarely observed in epithelial cells derived from the ectocervix and transfo

73 of selected Par proteins in blastomeres and epithelial cells during the embryogenesis of the ctenoph

74 Here, we show that intestinal epithelial cells expressing IRE1beta have an attenuated

75 Strikingly, medullary thymic epithelial cells expressing the autoimmune regulator wer

76 Gingival epithelial cells form an anatomic architecture that conf

77 elium to define transcriptomes of individual epithelial cells from healthy BALB/c mice (controls) and

78 -ATPase mRNA were determined in the cultured epithelial cells from lenses of the two types of mice.

79 table for the study of any kind of monolayer epithelial cells growth.

80 ggest that promoting the survival of gastric epithelial cells has implications not only for H. pylori

81 that TGFbeta1 activity is reduced in breast epithelial cells in obesity.

82 Cytokine production by vaginal epithelial cells in response to lactobacilli in the pres

83 y expressed in neutrophils, macrophages, and epithelial cells in response to wounding.

84 chromatin remodeling machinery in intestinal epithelial cells in the colitis response and shows how a

85 ow two extragenic CREs that are prominent in epithelial cells in the lung, regulate expression of the

86 ifferentiation of the human prostate luminal epithelial cells induced by caAKT1 and c-Myc and reveals

87 How intestinal epithelial cells interact with the microbiota and how th

88 splaying characteristic conversion of planar epithelial cells into multipolar and invasive mesenchyma

89 However, when proliferation of resident epithelial cells is impaired, alternative regeneration m

90 behavior, but how this signal is received by epithelial cells is unknown.

91 Epithelial cells kept their original levels of prolifera

92 sion of miR-183 cluster in the human retinal epithelial cells leads to the reprogramming and transfor

93 is an ER stress sensor uniquely expressed in epithelial cells lining mucosal surfaces.

94 human pathogen Chlamydia trachomatis targets epithelial cells lining the genital mucosa.

95 at constitutive AKT activation in intestinal epithelial cells markedly enhances tumor invasion and me

96 PRRSV-induced autophagy in thymic epithelial cells modulates the development of T cells, a

97 activity was sharply increased in intestinal epithelial cells of microbiota-replete mice compared wit

98 cells that surround the biliary tree but not epithelial cells of the canals of Hering.

99 The virus naturally infects epithelial cells of the feather follicle epithelium from

100 ts role has not been investigated in gastric epithelial cells or gastric tumorigenesis.

101 hypothesized that Chlamydia-infected DCs and epithelial cells present overlapping sets of Chlamydia-M

102 w that ablation of HNF-1beta in mIMCD3 renal epithelial cells results in activation of beta-catenin a

103 While endocervical epithelial cells secreted large amounts of several cytok

104 Tubular epithelial cells showed strong production of periostin d

105 Epithelial cells spontaneously form acini (also known as

106 emonstrate a novel mechanism by which cystic epithelial cells stimulate myofibroblasts in the pericys

107 estinal mucosa is lined by a single layer of epithelial cells that forms a tight barrier, separating

108 ed of a monolayer of diverse and specialized epithelial cells that perform functions ranging from nut

109 ry mediators) that feed back to regulate the epithelial cells themselves.

110 been shown to stimulate DNA damage in breast epithelial cells through mechanisms mediated by estrogen

111 n induced pluripotent stem cell-derived lung epithelial cells to model early-stage lung adenocarcinom

112 ge outlined here demonstrates the ability of epithelial cells to possess highly organized defense mac

113 , the cellular processes and contribution of epithelial cells to the host response are poorly underst

114 ch in turn facilitates the movement of tumor epithelial cells toward nutrient-rich territories.

115 type and TP53 knockout human retinal pigment epithelial cells using a focused dual guide RNA library

116 econd, when Xist is conditionally deleted in epithelial cells using Keratin14-Cre or in B cells using

117 HSV-1 enters epithelial cells via an endocytosis mechanism that is lo

118 g to and subsequent infection of respiratory epithelial cells were increased upon preincubation of th

119 PBMCs from healthy donors and/or respiratory epithelial cells were stimulated with soluble antigens o

120 rticipants underwent bronchoscopy to collect epithelial cells whose DNA methylation was measured usin

121 el: the fusion was faster for spheroids from epithelial cells with lower apparent surface tension tha

122 c Pg-strains to invade human-retinal pigment epithelial cells(ARPE-19), their survival, intracellular

123 CE2 suggests tongue keratinocytes, olfactory epithelial cells, airway club cells and respiratory cili

124 These are gut sensory epithelial cells, and those that form synapses are refer

125 (AKI) with adaptive proliferation of tubular epithelial cells, but repair can also lead to fibrosis a

126 herapeutically relevant cell types including epithelial cells, endothelial cells, B cells, T cells an

127 In epithelial cells, ME spread more efficiently, consistent

128 asthma pathophysiology, including on airway epithelial cells, mucus hypersecretion, and airway remod

129 lung microvascular endothelial and alveolar epithelial cells, we demonstrated that N-WASP downregula

130 tion factor TFIIH, in both B lymphocytes and epithelial cells, we hypothesized that SM utilizes XPB t

131 LT also promotes ETEC adhesion to intestinal epithelial cells, we postulated that increases in cAMP,

132 ss I and II molecules in endothelial but not epithelial cells, which exhibited constitutive expressio

133 cation, is found predominantly in intestinal epithelial cells, with chromogranin A-positive enteroend

134 maze-like patterns on the surface of mucosal epithelial cells.

135 he population level in human retinal pigment epithelial cells.

136 ncogene activation on this process in normal epithelial cells.

137 nd muc5ac mRNA expression in cultured airway epithelial cells.

138 that block EBV and KSHV infection of target epithelial cells.

139 ALOX15 was predominantly expressed by epithelial cells.

140 the cortical cytoskeleton in normal mammary epithelial cells.

141 primary ADPKD and normal human kidney (NHK) epithelial cells.

142 o the binding to integrins on the surface of epithelial cells.

143 , IL-1beta and Cxcl-1) and also apoptosis of epithelial cells.

144 ) and 'non-professional' phagocytes, such as epithelial cells.

145 facilitated by the synthetic TAR RNA in oral epithelial cells.

146 fibroblasts moved at an increased speed over epithelial cells.

147 y and invasiveness of TNBC and benign breast epithelial cells.

148 olarization and zonula adherens formation in epithelial cells.

149 internalization and endosomal trafficking in epithelial cells.

150 nto autophagosomes for degradation in airway epithelial cells.

151 itself and ST2 protein expression in airway epithelial cells.

152 intracellular bacterial pathogens of mucosal epithelial cells.

153 he presentation of HLA-B, -C, and -E on lung epithelial cells.

154 eterogeneous by clustering analysis than the epithelial cells.

155 human-specific mediator of pluripotency and epithelial character in hPSCs.

156 n multiple environments - abscess formation; epithelial colonization; and cigarette smoke toxin expos

157 the cytotoxicity of so-obtained BRJ to human epithelial colorectal adenocarcinoma (Caco-2) and human

158 We now provide conclusive evidence that the epithelial component of pharyngeal teeth in zebrafish (t

159 patients with microdissected sarcomatoid and epithelial components.

160 N-511-E8 resulted in multilayered stratified epithelial constructs within ten days.

161 Six episodes of reticular bullous epithelial corneal edema were identified in 5 eyes of 5

162 is pathophysiological biomarker of alveolar epithelial damage.

163 cluded 18 patients with NK with a persistent epithelial defect or corneal ulcer, treated with topical

164 ry outcome measures included the size of the epithelial defect overlying the Intacs body, the intende

165 dry eye disease and 4 studies of persistent epithelial defect.

166 ignancy that has been attributed to a higher epithelial density.

167 OCT was used to evaluate pigmented epithelial detachments, SMH, and subretinal fluid before

168 d immune homeostasis but also enhancing skin epithelial differentiation.

169 ice toward the development of severe corneal epithelial disease after exposure to a dry environment.

170 Genome-wide nasal epithelial DNAm and gene expression were measured.

171 This study aimed to identify nasal epithelial DNAm differences between severe and nonsevere

172 rt a causal role for ER stress and resulting epithelial dysfunction in PF and suggest ER stress as a

173 of a particular pattern of reticular bullous epithelial edema in a series of patients treated with ne

174 influenza severity by damaging the pulmonary epithelial-endothelial barrier and increasing pulmonary

175 = 0.79, P = .007) and an association between epithelial eosinophils and IL-5 concentrations in nasal

176 Enhancing the activity of TMEM16A increases epithelial fluid secretion and enhances mucus clearance

177 on measures of hyperinflation, and the nasal epithelial gene-expression profile in severe COPD.

178 wards absorptive enterocyte lineage ensuring epithelial growth.

179 locks aberrant splicing in primary bronchial epithelial (hBE) cells from CF patients with the mutatio

180 und repair are active processes that mediate epithelial healing at mucosal surfaces.

181 Epithelial Hh ligands not only regulate a variety of mes

182 pathway with key roles in organ development, epithelial homeostasis, tissue regeneration, wound heali

183 leukin-22 (IL-22) is a critical regulator of epithelial homeostasis.

184 ta provide critical insight into the initial epithelial host response to Aspergillus.

185 This work illustrates how epithelial host responses intersect with gut microbial m

186 More importantly, we observed biliary epithelial hyperplasia, which is an indicator of a high-

187 Paneth cells (PCs) are crucial for epithelial immune defense and highly vulnerable to ische

188 e to present and discuss potential microbial-epithelial-immune interactions underlying the early-life

189 and epithelial restitution after intestinal epithelial injury.

190 regulates energy balance in IECs and thereby epithelial integrity and barrier function.

191 otypes that can be linked to p120-catenin in epithelial integrity and turnover, and additional phenot

192 intestinal syndrome, spared gut function and epithelial integrity, and spared cell death in crypt bas

193 ance of the early life window for microbiota-epithelial interactions in the presence of inflammatory

194 Epithelial signaling centers control epithelial invagination and organ development, but how t

195 ditional changes in aging, as glandular-like epithelial invaginations (GLEIs) derived from ABSCs emer

196 kinase-mediated redistribution of the major epithelial junctional proteins.

197 ributed to intrinsic differences between the epithelial lineages, we find that single cells of all li

198 ncentrations measured in plasma, lung/airway epithelial lining fluid, and alveolar cells.

199 pectedly, mRNA and protein expression of the epithelial marker E-cadherin either remained unaltered o

200 ures; these CTCs expressed proliferation and epithelial markers and correlated with poor clinical out

201 tissue types, specifically in regard to the epithelial mesenchymal transition (EMT) structural compo

202 f the most fundamental functions for various epithelial, mesenchymal, and immune cells.

203 lls to identify the key players establishing epithelial-mesenchymal cell plasticity during reversible

204 the known roles of ILF3 in immune response, epithelial-mesenchymal differential editing sites are en

205 ed as one of the key ECM markers in the lung epithelial-mesenchymal interface both at the RNA and pro

206 redict how factors known to promote a hybrid epithelial-mesenchymal phenotype can alter the phenotypi

207 survival, but also induced an AKT-dependent epithelial-mesenchymal transition (EMT) and beta-catenin

208 ecular pathways, both cytokines also induced epithelial-mesenchymal transition (EMT) in lung cancer c

209 engulfment, Schwann cell (SC) demyelination, epithelial-mesenchymal transition (EMT), loss of sensati

210 AKT in LAD cells, although unable to induce epithelial-mesenchymal transition (EMT), VAL exerts pote

211 These data demonstrate the induction of epithelial-mesenchymal transition (EMT), which included

212 rotein stimulates differential expression of epithelial-mesenchymal transition (EMT)-associated genes

213 consequently potentiates Pi triggered lethal epithelial-mesenchymal transition (EMT).

214 n, migration, invasion, drug resistance, and epithelial-mesenchymal transition (EMT).

215 g the process of cell invasion, adhesion and epithelial-mesenchymal transition (EMT).

216 es mesoderm and endoderm germ layers through epithelial-mesenchymal transition (EMT).

217 regions, identifying E-box motifs common to epithelial-mesenchymal transition driver transcription f

218 22, phosphorylated STAT3, and markers of the epithelial-mesenchymal transition than nonneoplastic tis

219 and NCI-H1944 cells, accompanied by reduced epithelial-mesenchymal transition.

220 d adenocarcinoma, characterized by extensive epithelial-mesenchymal transition.

221 ulations enriched with highly plastic hybrid epithelial/mesenchymal cells, which display invasive fea

222 ignaling pathway, as well as conservation of epithelial/mesenchymal cross talk in the intestine, has

223 n bacteria associated with a primary colonic epithelial monolayer in an in vitro human gut model syst

224 gy to enhance delivery across endothelial or epithelial monolayers is conjugation to cell-penetrating

225 Despite displaying an epithelial morphology, sEOC maintains a high expression

226 bacteria having evolved traits to invade the epithelial mucus layer and reside deep within the intest

227 ess advantage was absent in mice that lacked epithelial NADPH oxidase 1 (NOX1) activity.

228 the branch geometry of the embryonic kidney epithelial network.

229 maturation and regenerative function of the epithelial niche in ST2(-/-) mice.

230 h pre-malignant and malignant nasopharyngeal epithelial (NPE) cells.

231 ECM prestrain and actomyosin tension during epithelial organogenesis and homeostasis.

232 in accessibility sites correlated with other epithelial originating TCGA tumors.

233 potential chemopreventive role of statins in epithelial ovarian cancer risk.

234 All women diagnosed with epithelial ovarian cancer should have germline genetic t

235 25 responses to neoadjuvant chemotherapy for epithelial ovarian cancer should not be used as individu

236 BRCA testing for all women with non-mucinous epithelial ovarian cancer, there is significant variabil

237 r women with newly diagnosed, advanced-stage epithelial ovarian cancer.

238 significantly associated with lower odds of epithelial ovarian cancer.

239 , acts as a guidance cue to orchestrate this epithelial pathfinding behavior, but how this signal is

240 rs and ordered micro-architecture induced an epithelial phenotype in CRC cells while disordered ECM d

241 ive role of YAP1 in maintenance of the adult epithelial phenotype.

242 s is implemented in a specialized way during epithelial polarization and that Aurora B has a role in

243 of regionally specified primary human airway epithelial progenitor and smooth muscle cells.

244 all cells in 2D cultures of a human bladder epithelial progenitor cell line in a dose-dependent mann

245 tified CD177 as a novel regulator of mammary epithelial proliferation and breast cancer pathogenesis

246 l infiltration into the ileum was increased; epithelial proliferation was decreased along with signif

247 observed in the bile duct, including ductal epithelial proliferation, micropapillary growth of bilia

248 iency, which also induced a delay in cryptal epithelial proliferation.

249 ation, and acetylated KLF5 is known to alter epithelial proliferation.

250 g stem cells during infection and preventing epithelial regeneration, which prolongs epithelial barri

251 We hypothesized that epithelial remodeling during diseases characterized by c

252 Epithelial remodeling involves ratcheting behavior where

253 erapeutic approaches to restore the impaired epithelial repair mechanisms in COPD, which is still a h

254 The bladder epithelial repair response is cumulative and aberrant as

255 its immunomodulatory actions, while abnormal epithelial repair responses may contribute to remodellin

256 function for the IL-33-ST2 axis in bronchial epithelial repair, and implicate ST2 in myeloid cell dif

257 t promotes CD8 T cell activation, as well as epithelial repair.

258 both necessary and sufficient to induce the epithelial response, which is mediated by activation of

259 s an important regulator of inflammation and epithelial responses in the prostate.

260 the regulation of cellular proliferation and epithelial restitution after intestinal epithelial injur

261 e centrosomes of immortalized retina pigment epithelial (RPE1) cells.

262 Contrarily in the mouse incisors, epithelial SCs are maintained throughout life and endles

263 Many animal embryos pull and close an epithelial sheet around the ellipsoidal egg surface duri

264 Here, we propose a mechanistic theory of epithelial shells which resemble small-organoid morpholo

265 Epithelial signaling centers control epithelial invagina

266 etween acid-sensing ion channels (ASICs) and epithelial sodium channel (ENaCs), these channel familie

267 he CCD and indirectly reduces principal cell epithelial sodium channel abundance and function.

268 ultivation of limbal melanocytes with limbal epithelial stem/progenitor cells on fibrin hydrogels pre

269 Epithelial structure is generated by the dynamic reorgan

270 porting the notion that events at the airway epithelial surface are critical for the development of t

271 lled from the discussions was that damage to epithelial surfaces lies at the origin of the various ma

272 lowing the generation of two opposing apical epithelial surfaces within the centre of an initially un

273 nderstanding apical morphogenesis in diverse epithelial systems.

274 r H3K27me3/EZH2-mediated repression of Snail epithelial target genes.

275 thin that environment, and indeed throughout epithelial tissues, cells experience competition with th

276 cancers arise from mutations in cells within epithelial tissues.

277 ation of T654 EGFR correlates with increased epithelial to mesenchymal, migration and invasion, and m

278 a stimulation downregulated SOX2 and induced epithelial-to-mesenchymal transdifferentiation accompani

279 Epithelial-to-mesenchymal transition (EMT) has been asso

280 Modulators of epithelial-to-mesenchymal transition (EMT) have recently

281 In human breast carcinomas, epithelial-to-mesenchymal transition (EMT) upregulates L

282 ast cancer, increased ECM stiffness promotes epithelial-to-mesenchymal transition (EMT), cell invasio

283 rogenitor cells emanating from epithelia via epithelial-to-mesenchymal transition (EMT).

284 Vimentin is a classic marker of epithelial-to-mesenchymal transition and is therefore an

285 They undergo epithelial-to-mesenchymal transition and migrate through

286 population of progenitor cells that undergo epithelial-to-mesenchymal transition displaying characte

287 ed CD133-mediated cancer stemness and hybrid epithelial-to-mesenchymal transition features in advance

288 tory: initiated in basal cells exhibiting an epithelial-to-mesenchymal transition signature, tumorige

289 YAP/TEAD engage the epithelial-to-mesenchymal transition transcription facto

290 ic cells were used to evaluate the CSC, EMT (epithelial-to-mesenchymal transition), and metabolic pro

291 XCL11 significantly induced tumor migration, epithelial-to-mesenchymal transition, and matrix remodel

292 tes several key oncogenic processes, such as epithelial-to-mesenchymal transition, cellular migration

293 ression of twist1b-a well-known regulator of epithelial-to-mesenchymal transition.

294 Topological data analysis using human epithelial transcriptomic data from the U-BIOPRED cohort

295 beta-depleted cells undergo a mesenchymal to epithelial transition (MET) and re-organise into acini-l

296 all protein is required to promote the early epithelial transmigration of human neutrophils into the

297 c spatial locations in which ~50 um-diameter epithelial tubules form by cell coalescence and structur

298 olangiocarcinoma (CCA) is a highly malignant epithelial tumor of the biliary tree with poor prognosis

299 small-cell lung cancer, mesothelioma, thymic epithelial tumours, and other pulmonary neuroendocrine n

300 -) and VDD significantly reduce both corneal epithelial wound healing and nerve density in diabetic m