ライフサイエンスコーパス: epithelial cell

1 block membrane fusion with both B cells and epithelial cells.

2 hymic epithelial cells, and medullary thymic epithelial cells.

3 n rescues F508del-CFTR function in bronchial epithelial cells.

4 s and proliferation rate in cultured corneal epithelial cells.

5 in miR-143 and miR-145 transfected cervical epithelial cells.

6 , and preventing bacterial adherence to lung epithelial cells.

7 communities within the cytoplasm of bladder epithelial cells.

8 d not affect the integrity of the intestinal epithelial cells.

9 innate immune response in human small airway epithelial cells.

10 blet cell differentiation of human bronchial epithelial cells.

11 DUB to deubiquitinate and stabilize TRAF2 in epithelial cells.

12 cell death and a reduced number of secretory epithelial cells.

13 reast cancer cells compared to normal breast epithelial cells.

14 invading another cell, is typical for tumor epithelial cells.

15 adherin expression and cell-cell junction in epithelial cells.

16 e properties to ErbB2-positive human mammary epithelial cells.

17 C3-STING interaction in the cytosol of human epithelial cells.

18 yonic fibroblasts and normal human bronchial epithelial cells.

19 d Nupr1 expression in cultured human tubular epithelial cells.

20 ation and caspase-3 activation in intestinal epithelial cells.

21 discrete population of multiciliated airway epithelial cells.

22 zation of Staphylococcus aureus by A549 lung epithelial cells.

23 there are few reports on PSMA expression in epithelial cells.

24 n three times in differentiated swine airway epithelial cells.

25 the posttranscriptional level in intestinal epithelial cells.

26 lored using CB1-knockdown (CB1Kd) intestinal epithelial cells.

27 icro RNA (miRNA) transcriptome in human lung epithelial cells.

28 ed in either fibroblasts or modified retinal epithelial cells.

29 e of a novel SENP7 isoform SENP7S in mammary epithelial cells.

30 tein levels in human breast milk and mammary epithelial cells.

31 romal lymphopoietin and GM-CSF from tracheal epithelial cells.

32 al enhancers active in primary human corneal epithelial cells.

33 e model of COPD, and primary human bronchial epithelial cells.

34 induces profound autophagy in cultured renal epithelial cells.

35 a protrude from the basal surfaces of somite epithelial cells.

36 ed by the loss and aberrant function of lung epithelial cells.

37 ns 1 and 10 and adhered to keratinocytes and epithelial cells.

38 P protein expression in both mesenchymal and epithelial cells.

39 immune cells (8-12) , other studies detected epithelial cells (13) , and still others detected immune

40 (13) , and still others detected immune and epithelial cells (14-16) .

41 In human primary corneal epithelial cells, 24,25(OH)2D3 stimulated migration.

42 as a major factor VAT releases to transform epithelial cells-a novel, potential pathway of VAT-enhan

43 In epithelial cells, abundance changes for more than 400 S.

44 Binding of C. albicans to EphA2 on oral epithelial cells activates signal transducer and activat

45 g MP types: endothelial MPs, epithelial MPs (epithelial cell adhesion molecule [EpCAM](+)MPs, E-cadhe

46 Their induced target genes encode diverse epithelial cell adhesion molecules, while mesenchymal ge

47 Alveolar epithelial cell (AEC) mitochondrial dysfunction and apop

48 3a) in normal primary human alveolar type II epithelial cells (AECs).

49 nd higher, are toxic for the human bronchial epithelial cells after 4-day exposure.

50 TP2 localized exclusively to proximal tubule epithelial cells along the apical but not the basolatera

51 of CuO NPs induced IL-8 release in the lung epithelial cells already at subtoxic concentrations (1-1

52 ted strain specificity, and neutralized both epithelial cell and fibroblast entry.

53 ithelial cell entry also inhibited spread in epithelial cells and a correlation existed between the p

54 kinase receptor ErbB2/HER2 in normal mammary epithelial cells and breast cancer cells.

55 osomes mediate communication between corneal epithelial cells and corneal keratocytes as well as vasc

56 nduced pluripotent stem cell-derived foregut epithelial cells and hypothalamic neurons.

57 o the intracellular niche in human bronchial epithelial cells and in a murine pneumonia model.

58 nalling pathway that functions in intestinal epithelial cells and may present useful targets in the m

59 release of HbetaD1 and HbetaD2 from colonic epithelial cells and mucosal tissues.

60 mplex virus (HSV) infection is restricted to epithelial cells and neurons and is controlled by CD8 T

61 f a transgene increased growth of intestinal epithelial cells and organoids.

62 in distribution and sphingosine levels in CF epithelial cells and prevents P. aeruginosa infection in

63 that is specifically expressed in intestinal epithelial cells and restricts rotavirus infection.

64 that coordinates actomyosin dynamics between epithelial cells and sustains the remodelling of the adh

65 We investigated how cgt affects gastric epithelial cells and the host immune response.

66 ide a unique perspective on and insight into epithelial cells and tissues, whether normal or diseased

67 hered mucin is expressed in nasal polyp (NP) epithelial cells and upregulated under inflammatory cond

68 PIK3R1 knockdown transforms human mammary epithelial cells, and genetic ablation of Pik3r1 acceler

69 ateral polarity is a fundamental property of epithelial cells, and its loss is a hallmark of cancer.

70 of B cells, dendritic cells, cortical thymic epithelial cells, and medullary thymic epithelial cells.

71 s involved in meningococcal interaction with epithelial cells, and suggests new insights into the rol

72 hibition of STAT3 phosphorylation in uterine epithelial cells, and the antitumor effects of P4 are me

73 wn about how LMP1 expression is regulated in epithelial cells, and there are conflicting reports abou

74 report that extracellular Clusterin promoted epithelial cell apoptosis whereas intracellular Clusteri

75 TAF accumulated inside genital epithelial cells as TFV-DP, the active drug form.

76 myosin accumulation at the apical surface of epithelial cells, as seen in the vertebrate neural tube

77 primary blood leukocytes or retinal pigment epithelial cells at effective concentrations; protects h

78 Alveolar type II epithelial cells (ATII) are instrumental in early wound

79 With knockdown of SENP7S in mammary epithelial cells, Axin1-beta-catenin interaction is lost

80 prene SOA on gene expression in human airway epithelial cells (BEAS-2B) through an air-liquid interfa

81 Human bronchial epithelial cells, BEAS-2B, directly exposed to house dus

82 When epithelial cells become too crowded, they activate the s

83 orchestrated trafficking circuits in bladder epithelial cells (BECs) that expels intracellular uropat

84 d three-dimensional network lined by biliary epithelial cells, but how its branching patterns are pre

85 increased proliferation of intestinal tumour epithelial cells by almost two-fold in primary culture o

86 efficient lytic reactivation in EBV-infected epithelial cells by enhancing expression of the Z and R

87 and BLIMP1 induce lytic EBV reactivation in epithelial cells by synergistically activating the two E

88 Intestinal epithelial cells (Caco-2 and IEC-6 lines) were transfect

89 Moreover, the epithelial cells can be propagated indefinitely in vitro

90 coordinated but poorly understood changes in epithelial cell-cell adhesion and cell motility.

91 hasone to modulate gene expression in airway epithelial cells coincided with its potency to resolve A

92 by driving the energy metabolism of colonic epithelial cells (colonocytes) toward beta-oxidation.

93 to dysplastic hyperproliferation of tubular epithelial cells, confirming the procarcinogenic role of

94 Epithelial cells connect via cell-cell junctions to form

95 Epithelial cells constitutively released IFN-gamma, whic

96 Using an adaptation of our in vitro primary epithelial cell culture system, we found that prostaglan

97 nsulin deprivation in normal human bronchial epithelial cells cultured in organotypic conditions clos

98 7 fully blocked CFTR chloride conductance in epithelial cell cultures and intestine after cAMP agonis

99 red for regulation of TNF-induced intestinal epithelial cell death and survival.

100 We elaborate on how cross-talk between epithelial cells, dendritic cells, and innate lymphoid c

101 p had significantly higher OSDI score, basal epithelial cells density, stromal reflectivity and sub-b

102 tophagic flux, which was conserved in kidney epithelial cells derived from both Pkd1-null mice and AD

103 Epithelial cells derived from ERG transgenic mouse prost

104 Emerging data now suggest that epithelial cell-derived cytokines such as thymic stromal

105 Our results indicate that epithelial cell-derived exosomes mediate communication b

106 a human monoclonal antibody specific for the epithelial-cell-derived cytokine thymic stromal lymphopo

107 ay inform mechanisms underlying pathological epithelial cell detachment.

108 Deletion of EGFR from intestinal epithelial cells did not affect tumor growth.

109 er, genetic inactivation of the GR in kidney epithelial cells did not induce the immunosuppressive ef

110 genes were reproduced in vitro in esophageal epithelial cells differentiated in the presence of IL-13

111 Here we show that epithelial cell differentiation also induces LMP1 expres

112 In this study, we show that epithelial cell differentiation induces LMP1 expression

113 ole for KLF7 as a KLF4 antagonist in corneal epithelial cell differentiation, and explains how two SN

114 (HPV) replication cycle is tightly linked to epithelial cell differentiation.

115 production of IL-17A which acts on bronchial epithelial cells directly and in concert with other envi

116 on microscopy confirmed that the surrounding epithelial cells directly closed lesions up to six cells

117 of genomic architecture in mouse intestinal epithelial cells disclosed that microbiota colonization

118 Although both epithelial cell division and cell extrusion require Piez

119 However, it is unclear how epithelial cell division is controlled to balance cell d

120 However, epithelial cell division must be tightly linked to cell

121 n alternative mechanism for entosis in human epithelial cells, driven by mitosis.

122 dative stress, and subsequently apoptosis in epithelial cells during ischemia-reperfusion injury.

123 a human three-dimensional (3-D) endometrial epithelial cell (EEC) model using the HEC-1A cell line a

124 merous different cell types, such as tubular epithelial cells, endothelial cells, and podocytes, work

125 entry, while all antibodies that neutralized epithelial cell entry also inhibited spread in epithelia

126 osal explants and primary equine respiratory epithelial cells (EREC), grown at the air-liquid interfa

127 We argue instead that the epithelial cells-especially in the luminal compartment-s

128 ng these intercellular networks that connect epithelial cells, evading immune and antiviral defenses

129 human epithelial cell lines or primary human epithelial cells exposed to IL-13, IL-17A, or both.

130 show that both human and murine endometrial epithelial cells express the high affinity Na(+)-coupled

131 Pulmonary and LP-derived epithelial cells expressed at best minor levels of C3aR.

132 trix that are differentiated from follicular epithelial cells expressing transcription factor KROX20.

133 re noncytotoxic and protected A549 pulmonary epithelial cells from A. fumigatus-induced cell damage f

134 Primary human bronchial epithelial cells from asthma patients and controls were

135 cycle-promoting proteins, thereby preventing epithelial cells from exiting the cell cycle and enterin

136 the most extensive analysis of primary renal epithelial cells from JBTS patients to date.

137 fluid leukocytes, cytokines, mediators, and epithelial cell function for these asthma subgroups.

138 anisms by which these miRNAs modify cervical epithelial cell function.

139 ution of cytoplasmic Esrp1 in maintenance of epithelial cell functions.

140 In growing follicles, lower bulb epithelial cells had high viability, and mitochondria we

141 signaling changes across six human bronchial epithelial cell (HBEC) strains that were systematically

142 Here, data from human bronchial epithelial cells (HBEC) confirm that cigarette smoke not

143 the lower airways to examine human bronchial epithelial cells (HBEC) is essential for understanding n

144 ontrol and asthmatic primary human bronchial epithelial cells (HBECs) by means of analysis of transep

145 We used primary human bronchial epithelial cells (HBECs) from asthmatics and healthy con

146 (0.1 muM to 100 muM) increased human corneal epithelial cell (HCEC) viability and migration.

147 immunohistochemistry study of human corneal epithelial cells (HCECs) and human keratocytes (HKs) cul

148 work defines regulatory enhancers in corneal epithelial cells, highlights global gene-regulatory rela

149 r airways represented by primary human nasal epithelial cells (HNECs) and murine nasal epithelial cel

150 cellularized dTBs seeded with porcine dental epithelial cells, human dental pulp cells, and human umb

151 ulatory relationships shared among different epithelial cells, identifies a role for KLF7 as a KLF4 a

152 ential for buffering Nkx2.1 expression, lung epithelial cell identity, and tissue homeostasis.

153 TNF exerts beneficial effects on intestinal epithelial cell (IEC) responses to injury.

154 rns and transcriptomes of primary intestinal epithelial cells (IEC) of children newly diagnosed with

155 oid cells that reside between the intestinal epithelial cells (IECs) that form the intestinal mucosal

156 eport that, unlike non-metastatic intestinal epithelial cells (IECs), metastatic IECs express TLR3 an

157 2 expansion, airway hyperresponsiveness, and epithelial cell IL-25 expression were attenuated by anti

158 Abundantly expressed in lung epithelial cells, IL-33 plays critical roles in both inn

159 Drebrin expression is restricted to basal epithelial cells in benign human prostate but is upregul

160 human prostate but is upregulated in luminal epithelial cells in foci of prostatic malignancy.

161 ates with the actin cytoskeleton in prostate epithelial cells in normal tissues, but not in prostate

162 ic action of IGF1R-PI3K-Akt-Tor signaling in epithelial cells in real-time.

163 ssion data from a study on human respiratory epithelial cells in response to influenza A virus (IAV)

164 2+-permeable pores in the membrane, damaging epithelial cells in small intestine and colon.

165 shed that HIV-1 can infect kidney transplant epithelial cells in the absence of detectable viremia.

166 of a sortable population of multipotent non-epithelial cells in the adult pancreas that can commit t

167 a barrier on the apical side of neighboring epithelial cells in the bronchial mucosa.

168 Epithelial cells in tissues use their actin cytoskeleton

169 n molecules, CD44 and annexin II, in tubular epithelial cells in vitro and in vivo, and treatment wit

170 ffects of rapamycin on primary human corneal epithelial cells in vitro.

171 ith IRF6 in the cytoplasm of primary palatal epithelial cells in vivo, and their interaction with IRF

172 some transcription factors in the context of epithelial cell infection by IAV.

173 blind viruses demonstrated the importance of epithelial cell infection for clinical disease, highligh

174 In conclusion, lung epithelial cells influence the efficacy of most antimicr

175 roliferation and differentiation of prostate epithelial cells, inhibiting prostate development.

176 of RNE cells, active migration of connected epithelial cells into the RNE is a crucial player in its

177 reasingly stiff collagen promoted dispersive epithelial cell invasion.

178 P2X7R-mediated IL-1beta release in SMG epithelial cells is dependent on transmembrane Na(+) and

179 Epstein-Barr virus (EBV) entry into epithelial cells is mediated by the conserved core fusio

180 functioning at the apical plasma membrane of epithelial cells, is required for epithelial polarity.

181 asymmetrically partitioned during mitosis in epithelial cells just before delamination and selection

182 In VDR knockout mouse epithelial cells (KO), 1,25(OH)2D3 increased CYP24A1 and

183 otein lysates from a nontumorigenic prostate epithelial cell line (NMVP cells).

184 regulation of CBS in an adenoma-like colonic epithelial cell line is sufficient to induce metabolic a

185 cell lines and primary fibroblasts and human epithelial cell lines or primary human epithelial cells

186 of TTP in both endometriotic and endometrial epithelial cell lines.

187 e recombinant HIV-1 did not infect the renal epithelial cell lines.

188 Thus, in EBV-infected epithelial cells, LMP1 expression is promoted by differe

189 ge occurs through decline in stem/clonogenic epithelial cell loss mediated by microvascular protectio

190 IL-13 levels were increased in airway epithelial cells, macrophages, type 2 innate lymphoid ce

191 tic inactivation of KRas(G12D) in mouse lung epithelial cells markedly impairs the progression of KRa

192 rferon response to viral infection by airway epithelial cells may be a mechanism leading to lung func

193 s of AZD4547 on mammary development, mammary epithelial cell (MEC) populations, and oncogenic signali

194 motes lactational differentiation of mammary epithelial cells (MECs) via its cognate receptor and the

195 tors are recruited to the surface of mammary epithelial cells (MECs), and the vesicle transport syste

196 or deleterious consequences for the colonic epithelial cell metabolism and physiology in terms of mi

197 romotes lung fibrosis by augmenting alveolar epithelial cell mitochondrial DNA damage and apoptosis.

198 al epithelial cells (HNECs) and murine nasal epithelial cells (MNECs) and isolated murine trigeminal

199 small intestine and translocate through the epithelial cell monolayer by an intracellular pathway to

200 uctance measurement in polymer membranes and epithelial cell monolayers at discrete points in a sampl

201 ic membranes and then demonstrated in living epithelial cell monolayers under physiological condition

202 ifferentiation model of the medullary thymic epithelial cell (mTEC) lineage from immature MHC class I

203 clinical relevance in normal human bronchial epithelial cells (NHBEs) and nasal polyp tissues.

204 accumulate preferentially in breast luminal epithelial cells, not in basal epithelial or stromal cel

205 Treatment of rat kidney epithelial cells (NRK-52E) with the mitochondrial-target

206 In contrast, the rate of decline in thymic epithelial cell numbers with age was radiation-sensitive

207 t may act as a homeostatic sensor to control epithelial cell numbers, triggering extrusion and apopto

208 xpression of IL-36alpha in the renal tubular epithelial cells of a mouse model of unilateral ureteral

209 ore, tamoxifen-induced deletion of EGFR from epithelial cells of established intestinal tumors in mic

210 to reconstitute ORMDL3 expression in airway epithelial cells of Ormdl3 knockout mice.

211 cus, which is observed in blood and squamous epithelial cells of smokers, but not in lung cancer.

212 It was expressed mainly in the epithelial cells of the crypts and only marginally in th

213 lpha defensin HD5 is produced by specialized epithelial cells of the gastrointestinal and genito-urin

214 t in primary mouse submandibular gland (SMG) epithelial cells, P2X7R activation also induces the asse

215 Epithelial cell permeability was increased in miR-143 an

216 ofound changes in stem cell differentiation, epithelial cell phenotypes and fibroblast proliferation.

217 and immunofluorescent staining of glomerular epithelial cells (podocytes) indicated that VtE ameliora

218 /PRDM1 is essential for the establishment of epithelial cell polarity and functional maturation of al

219 an undifferentiated, non-dividing esophageal epithelial cell population in patients with active EoE.

220 Microfold (M) cells are epithelial cells present in mucosal tissues and speciali

221 ture experiments with primary human T cells, epithelial cells pretreated with 1,25D suppressed activa

222 ing the acute respiratory distress syndrome, epithelial cells, primarily alveolar type (AT) I cells,

223 ly unrecognized role for IL-27 in regulating epithelial cell proliferation and antiviral host defense

224 und repair requires a coordinated program of epithelial cell proliferation and differentiation as wel

225 e mice and littermate controls, and analyzed epithelial cell proliferation and ultrastructure from th

226 xosomes released by bronchial fibroblasts on epithelial cell proliferation in severe asthma.

227 However, the factors that trigger epithelial cell proliferation in this inflammatory proce

228 of TGF-beta2 and significantly increased the epithelial cell proliferation of both healthy and severe

229 intracellular superoxide and inhibited cyst epithelial cell proliferation through extracellular sign

230 Bronchial epithelial cell proliferation was evaluated by BrdU inco

231 of 1,25(OH)2D3 and 24R,25(OH)2D3 on corneal epithelial cell proliferation, migration, and on the vit

232 er, these results suggest beta2ARs on airway epithelial cells promote the asthma phenotype and that t

233 vides a molecular pathway that could control epithelial cell properties required for proper morphogen

234 This suggests that YAP controls local epithelial cell properties.

235 Comparative infection with wild-type and epithelial cell receptor-blind viruses demonstrated the

236 n of Clusterin leads to divergent effects on epithelial cell regeneration and lung repair during fibr

237 This shows that epithelial cells respond to minimal wounds in a collecti

238 tion by FGF2, and Ptprb knockdown in mammary epithelial cells resulted in a higher level of fibroblas

239 cing of TTP in endometriotic and endometrial epithelial cells revealed differential response to infla

240 initiated by C. muridarum infection of tubal epithelial cells (serving as the first hit) - into patho

241 enchyme, which modulate GREM1 expression and epithelial cell shapes.

242 In response to injury, AQP3-depleted colonic epithelial cells showed defective lamellipodia, focal ad

243 ignificantly reduces survival in co-cultured epithelial cells, signifying an important role of CAF ex

244 d effects upon gene expression in human lung epithelial cells, some of which are epigenetically progr

245 roach, we expanded minor clones and obtained epithelial cell-specific DNA/RNA for quantitative NGS an

246 the gL glycosylation mutant N69L/S71V had an epithelial cell-specific hyperfusogenic phenotype.

247 The proliferation of primary epithelial cells stimulated by IL-17A or TGF-beta2 was a

248 C3/C3 fragments primarily in the intestinal epithelial cells, suggesting local involvement of comple

249 , via induction of interleukin 6 (IL-6) from epithelial cells, tailored effector T cell function, pro

250 Resident fibroblasts that contact tumor epithelial cells (TEC) can become irreversibly activated

251 c epithelium and is required to prime thymic epithelial cells (TEC) for effective Treg induction.

252 on of cytokines and chemokines from tracheal epithelial cells (TECs) in vitro and tracheal tissue ex

253 The importance of thymic epithelial cells (TECs) is evidenced by clear links betw

254 abled us to discover a population of tubular epithelial cells that expresses CD11C, a marker typicall

255 The pattern recognition receptors (PRRs) in epithelial cells that mediate this differential response

256 and anti-inflammatory properties of IL-20 on epithelial cells, the current study provides evidence th

257 In human lung epithelial cells, the microRNA-150 (miR-150) was identif

258 ined by VEGF that is produced by neighboring epithelial cells, the retinal pigment epithelium (RPE) a

259 lectrically non-excitable cells, for example epithelial cells, this is achieved by primary release of

260 tally new roles of TMEM16A in differentiated epithelial cells: TMEM16A provides a mechanism for enhan

261 rom androgen receptor (AR)-dependent luminal epithelial cells to AR-independent basal-like cells.

262 Indeed, exposure of mouse tracheal epithelial cells to IL-1beta or IL-1alpha resulted in in

263 ey's urine-concentrating function, instructs epithelial cells to produce chemokines that localize mon

264 Notably, this process can expose epithelial cells to the stromal extracellular matrix (EC

265 We previously reported that HCA2 in A431 epithelial cells transduced Gbetagamma-protein kinase C-

266 specific biomarkers of early fallopian tube epithelial cell transformation.

267 vation in an in vitro model of human mammary epithelial cell transformation.

268 Environmental challenges to epithelial cells trigger gene expression changes that el

269 ing as a barrier for the organs they encase, epithelial cells turn over at some of the fastest rates

270 The aim of this study was to evaluate the epithelial cell turnover and expression of proliferation

271 lar signatures such as their non-tumorigenic epithelial cell type, three-dimensional growth, latruncu

272 ions and restrictions of the mesenchymal and epithelial cell types in the developing and mature mouse

273 lls and/or progenitors that can generate all epithelial cell types of a given tissue.

274 It has been reported that lens epithelial cells undergo EMT during cataract formation,

275 Collective migration of epithelial cells underlies diverse tissue-remodeling eve

276 is decreased, matrix-attached human mammary epithelial cells upregulate and internalize beta4-integr

277 granules in differentiated primary bronchial epithelial cells using fluorescence lifetime imaging mic

278 Depletion of CAF1 in untransformed epithelial cells using siRNA was sufficient to recapitul

279 ich we specifically ablated Mig-6 in uterine epithelial cells using Sprr2f-cre mice (Sprr2f(cre+)Mig-

280 tion, ROS disassembles adherens junctions in epithelial cells via posttranslational mechanisms, that

281 lled bacillary dysentery, and invade colonic epithelial cells via the T3SS.

282 periments in mice lacking EGFR in intestinal epithelial cells (Villin-Cre; Egfr(f/f) and Villin-CreER

283 Bacterial fitness in abscesses and in epithelial cells was studied, by comparing the parental

284 As proof of concept, cultured renal epithelial cells were exposed to urinary exosomes and ce

285 1 knockout, and wild-type mouse nasal septal epithelial cells were grown at an air-liquid interface (

286 current study, primary human fallopian tube epithelial cells were infected with N. gonorrhoeae, and

287 TAM expression and shedding by tubular epithelial cells were investigated by PCR and enzyme-lin

288 e specificity for islet beta cells and renal epithelial cells were reliably characterized in recipien

289 Primary bronchial epithelial cells were stimulated with IL-17A and/or IL-2

290 Human retinal pigment epithelial cells were treated with various combinations

291 r-liquid interface cultures of primary nasal epithelial cells were used to measure transepithelial el

292 is a major contributor to actin assembly in epithelial cells, where it works with the Ena/VASP famil

293 doplasmic reticulum stress-mediated death of epithelial cells, which is an important mechanism contri

294 targeting Stard7 to mitochondria or treating epithelial cells with a mitochondrial-targeted antioxida

295 , NY/108 virus replicated in human bronchial epithelial cells with an increased efficiency compared w

296 es of these cell lines demonstrated that the epithelial cells with surface expression of PD-L1, E-cad

297 By in vitro infection of gastric epithelial cells with wild-type and VacA-deficient H. py

298 hat TGFbeta can induce purified primary lens epithelial cells within the same culture to undergo diff

299 -5A attenuated canonical WNT-driven alveolar epithelial cell wound healing and transdifferentiation i

300 In VDR wildtype mouse corneal epithelial cells (WT), 1,25(OH)2D3 increased CYP24A1 pro