ライフサイエンスコーパス: epithelial

1 c kidney), Vero (African-green monkey kidney epithelial), 3T12 (mouse fibroblast), and RAW 264.7 (mou

2 pithelium consists of differentiated luminal epithelial and basal myoepithelial cells, as well as und

3 The alpha6beta4 integrin protects adherent epithelial and carcinoma cells from ferroptosis induced

4 EMT that correlate with accessibility of key epithelial and EMT transcription factor binding sites.

5 onitored on genes with a pivotal function in epithelial and hepatic morphogenesis, differentiation an

6 olon, as well as normal human MCF10A mammary epithelial and human peripheral blood mononuclear cells

7 expression of ERBB genes with genes encoding epithelial and mesenchymal proteins.

8 he life of the animal due to the presence of epithelial and mesenchymal stem cells-provides a model f

9 entified a ferrireductase: six-transmembrane epithelial antigen of prostate 4 (STEAP4) was highly ind

10 ffect of miR-143 and miR-145 on the cervical epithelial barrier and to elucidate the mechanisms by wh

11 gammadelta T cells located near the epithelial barrier are integral components of local infl

12 Loss of claudin-18 was sufficient to impair epithelial barrier function in 16HBE cells and in mouse

13 for the host colonic epithelium and enhance epithelial barrier function through unclear mechanisms.

14 (GI) (patho)physiology; from GI motility and epithelial barrier function to enteric neuroinflammation

15 MSC-Ex recovered the destruction of the epithelial barrier in the differentiated Caco-2 cells in

16 1 plays a significant role in maintenance of epithelial barrier in the intestine via regulation of ap

17 Mast cells and TH2 cells might decrease epithelial barrier integrity in AR, maintaining a leaky

18 nal relevance of this strong collecting duct epithelial barrier is unresolved.

19 merous gastrointestinal functions, including epithelial barrier permeability and motility.

20 barrier integrity in AR, maintaining a leaky epithelial barrier.

21 he secretion of immunoglobulins (Igs) across epithelial barriers, which is achieved via the polymeric

22 of histone modifications in human bronchial epithelial BEAS-2B cells and human nasal RPMI2650 cells

23 din-18.1 mRNA levels were measured in airway epithelial brushings from healthy controls and patients

24 Epithelial cadherin (Ecadherin) is responsible for the i

25 Alveolar epithelial cell (AEC) mitochondrial dysfunction and apop

26 (0.1 muM to 100 muM) increased human corneal epithelial cell (HCEC) viability and migration.

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

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

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

30 7 fully blocked CFTR chloride conductance in epithelial cell cultures and intestine after cAMP agonis

31 ay inform mechanisms underlying pathological epithelial cell detachment.

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

33 Although both epithelial cell division and cell extrusion require Piez

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

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

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

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

38 reasingly stiff collagen promoted dispersive epithelial cell invasion.

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

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

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

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

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

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

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

46 Epithelial cell permeability was increased in miR-143 an

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

90 Epithelial cells connect via cell-cell junctions to form

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

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

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

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

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

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

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

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

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

100 2+-permeable pores in the membrane, damaging epithelial cells in small intestine and colon.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

121 1 knockout, and wild-type mouse nasal septal epithelial cells were grown at an air-liquid interface (

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

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

124 Human retinal pigment epithelial cells were treated with various combinations

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

152 P protein expression in both mesenchymal and epithelial cells.

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

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

155 hymic epithelial cells, and medullary thymic epithelial cells.

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

157 s and proliferation rate in cultured corneal epithelial cells.

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

159 , and preventing bacterial adherence to lung epithelial cells.

160 communities within the cytoplasm of bladder epithelial cells.

161 blet cell differentiation of human bronchial epithelial cells.

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

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

164 induces profound autophagy in cultured renal epithelial cells.

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

166 ronic inflammation, such as products of lung epithelial cellular breakdown and arachidonic acid casca

167 Epithelial chemokine CXCL14 synergizes with CXCL12 via a

168 ned in mice lacking a tectorin-based matrix, epithelial cilia or the planar cell polarity genes Vangl

169 Here, we reveal that the breast epithelial clock is regulated by the mechano-chemical st

170 For instance, the two adult lung epithelial compartments (airways and alveoli) are separa

171 rease in the number of blood vessels and sub-epithelial connective tissue matrix components within th

172 adhesion to the scaffold and well-stratified epithelial constructs, with maintenance of a progenitor

173 We exposed human bronchial epithelial cultures (HBECs) to air or whole tobacco smok

174 Primary human airway basal stem cell-derived epithelial cultures and micro-optical coherence tomograp

175 , reducing recurrence presumably by limiting epithelial damage and facilitating microbiome recovery.

176 roorganisms and form EETs at sites of airway epithelial damage to protect the host from infections in

177 recombinant human interferon (IFN)-gamma or epithelial-derived IFN-gamma in constitutively released

178 Presence of epithelial desquamation, erythema, and erosions on gingi

179 raphy angiograhy (OCTA) of drusenoid pigment epithelial detachments (PEDs) in a woman affected by Com

180 embranes as retinal complications of pigment epithelial detachments.

181 rs and genes, which are involved in alveolar epithelial differentiation, was demonstrated.

182 of proinflammatory cytokines, and subsequent epithelial disorders and mitochondrial dysfunction.

183 ogy can be applied to interrogate intestinal epithelial dynamics and characterize situations in which

184 cover function in an animal model of corneal epithelial dysfunction after surgical transplantation.

185 Epithelial dysfunction is critical in the pathology of m

186 bility to severe intestinal inflammation and epithelial dysregulation, accompanied by excessive necro

187 4 disrupts the mucosal barrier, resulting in epithelial expression of the IL-6-like cytokine Upd3, le

188 oride channel, resulting in dysregulation of epithelial fluid transport in the lung, pancreas and oth

189 tivates mRNA expression of a broad cohort of epithelial genes, including junctional factor dlg-1 Accu

190 he molecular mechanisms that underlie breast epithelial hierarchy remain ill-defined.

191 cruitment was a direct response to increased epithelial HIF-2alpha signaling.

192 Intestinal epithelial HIF-2alpha-overexpressing mice demonstrated t

193 of Jagged1 neither interferes with prostate epithelial homeostasis nor significantly accelerates tum

194 More recently, the presence of epithelial injury and inflammation in the airways of ath

195 l host defense against pathogen exposure and epithelial injury, yet little is known about how enterop

196 re reserve stem cells that respond to severe epithelial injury.

197 of proinflammatory cytokines and influences epithelial integrity of cholangiocytes.

198 ealing in response to lung injury, restoring epithelial integrity through spreading and migration.

199 effect of nasal secretions of AR patients on epithelial integrity.

200 Epithelial invasion required matrix anchorage as well as

201 an be expanded and differentiated to form an epithelial layer expressing K12 and PAX6, and able to re

202 nd FACS sorting into a population of corneal epithelial-like progenitor cells.

203 hod to separately derive lung versus thyroid epithelial lineages, as these two cell types each origin

204 of the proximal lung endoderm with complete epithelial loss at later stages of development.

205 ity and objective responses in patients with epithelial malignancies.

206 tuzumab, and the TGFbeta inhibitor expressed epithelial markers and were more differentiated.

207 that overexpression of the oncogenic protein epithelial membrane protein-2 (EMP2) correlates with end

208 use lung mesenchyme, the cells recapitulated epithelial-mesenchymal developing lung interactions.

209 re lung, inflammation and injury disrupt the epithelial-mesenchymal interactions required for normal

210 osomes are mobile genetic signals regulating epithelial-mesenchymal interactions.

211 Twist-mediated oncogenic functions including epithelial-mesenchymal transition (EMT) and cancer stem

212 e (RTK) AXL has been intrinsically linked to epithelial-mesenchymal transition (EMT) and promoting ce

213 Epithelial-mesenchymal transition (EMT) has been recogni

214 related to cancer stem cells (CSCs) markers, epithelial-mesenchymal transition (EMT) inducers and bas

215 FPR2 knock-down, implying the involvement of epithelial-mesenchymal transition (EMT).

216 dial cells were highly adipogenic through an epithelial-mesenchymal transition both in vitro and in v

217 miR-194 stimulated migration, invasion, and epithelial-mesenchymal transition in human prostate canc

218 RHAMM by the RB/E2F pathway was critical for epithelial-mesenchymal transition, motility, and invasio

219 ivation of peritoneal fibroblasts, mitigated epithelial-mesenchymal-transition (EMT), as well as enha

220 Moreover, GRHL2 suppresses the oncogenic epithelial-mesencyhmal transition, thereby acting as a t

221 h is distinct from the ECM within the normal epithelial microenvironment.

222 chanisms that connect gene regulation and 3D epithelial morphogenesis.

223 in organization and AJ protein levels during epithelial morphogenesis.

224 inar lineage that has broad implications for epithelial morphogenesis.

225 ize the following MP types: endothelial MPs, epithelial MPs (epithelial cell adhesion molecule [EpCAM

226 Mechanistically, acid-induced epithelial MV miR-17/221 promoted beta1 integrin recycli

227 Acid-induced epithelial MV release promoted macrophage migration in v

228 tion of p38, prevented TGFbeta from inducing epithelial-myofibroblast transition and cell migration b

229 type 2 airway inflammation in juvenile beta-epithelial Na(+) channel (Scnn1b)-transgenic (Tg) mice.

230 Treatment with the epithelial Na(+) channel blocker amiloride, improving ai

231 Epithelial Na(+) channels (ENaCs) are members of the ENa

232 there was a significant increase in corneal epithelial nerve regeneration and substance P-positive n

233 d in M-ILK-deficient mice, and activation of epithelial NF-kappaB and PI3K signaling pathways are res

234 ontribution of innate receptor engagement on epithelial or dendritic cells by HDMs that ultimately me

235 reast luminal epithelial cells, not in basal epithelial or stromal cells, of BRCA1 mutation carriers.

236 e signaling network controls cell migration, epithelial organization, axon patterning and other aspec

237 elimination of integrin alpha5 abrogates the epithelial-organizing effects of P4G11.

238 ate cells, PCa xenografts and fresh prostate epithelial organoids.

239 Epithelial ovarian cancer is a leading cause of death in

240 Perfusion-independent regulation of epithelial pattern formation by the vasculature during o

241 xins that eliminate glia in mice, intestinal epithelial permeability and proliferation increase; this

242 The epithelial permeability, determined by fluorescently lab

243 ce of trastuzumab, caused cells to regain an epithelial phenotype.

244 identified originally in flies to coordinate epithelial planar cell polarity (PCP).

245 some and dense EVs preparations suggest that epithelial polarity impacts directional release.

246 trinsic tumor-suppressive mechanism, whereby epithelial polarity proteins dictate the cytoarchitectur

247 lls is necessary for proper establishment of epithelial polarity.

248 embrane of epithelial cells, is required for epithelial polarity.

249 te: (i) ADMA-mediated NOS uncoupling reduces epithelial production of NO and increases oxygen and nit

250 signature component specifically produced by epithelial progenitor cells.

251 d large intestines, but caused no defects in epithelial proliferation, barrier integrity, or ultrastr

252 Rapid epithelial renewal occurs, but the specific cell of orig

253 AK) and the chemokine receptor CXCR4 promote epithelial repair mechanisms.

254 importance of postmitotic cell growth in gut epithelial repair.

255 enic signaling produced by retinal pigmented epithelial (RPE) cells under different conditions simula

256 A1 locus with subretinal/sub-retinal pigment epithelial (RPE) hemorrhage related to neovascular AMD (

257 The lack of functional peri-implant epithelial sealing with basal lamina (BL) attachment at

258 te responses and regional differences in the epithelial secretome participating in RSV lower respirat

259 ative proteomics analysis of the RSV-induced epithelial secretory response in cells representative of

260 Hemidesmosomes (HDs) are epithelial-specific cell-matrix adhesions that stably an

261 mitantly exhibit an expansion of the mammary epithelial stem cell (MaSC) enriched basal/myoepithelial

262 as a central intrinsic regulator of mammary epithelial stem cell quiescence and exhaustion and is ne

263 This review focuses on the epithelial stem cells of skin, where they come from, whe

264 For patients with the epithelial subtype who underwent trimodality therapy, me

265 ivalis lipopolysaccharide (PgLPS)-stimulated epithelial supernatant was investigated in HMOBs.

266 tion of theory and experiments, we show that epithelial surface cells not only trigger blastoderm exp

267 on between these bacteria and the intestinal epithelial surface.

268 mbryo dynamics of the actomyosin-rich apical epithelial surface.

269 broblasts may not fully recapitulate that of epithelial tight junction strands, this is the first dir

270 Rab protein distributions during Drosophila epithelial tissue remodeling and show that Rab35 is dyna

271 junctions that provide adhesive strength in epithelial tissue.

272 dback sequelae of mTORC1 loss of function in epithelial tissue.

273 In studies of intestinal epithelial tissues from patients with CD and embryonic f

274 productive area of study is on single layer epithelial tissues in which the adherence junctions of c

275 esponsible for the intercellular cohesion of epithelial tissues.

276 The regulation of bronchial epithelial TJs by TH2 cells and their cytokines and thei

277 a (HCC), a highly metastatic cancer, undergo epithelial to amoeboid transition in physiological envir

278 tion with canonical Wnt signaling during the epithelial to mesenchymal transition (EMT) from NMP to m

279 dherens junctions, dedifferentiation, and an epithelial to mesenchymal transition (EMT) transcription

280 We found that it induces reversion of epithelial to mesenchymal transition.

281 -3 supports the TIC/CSC state and induces an epithelial-to-mesenchymal transition (EMT) by driving ex

282 Reversing epithelial-to-mesenchymal transition (EMT) in cancer cel

283 Depletion of NatD suppresses the epithelial-to-mesenchymal transition (EMT) of lung cance

284 oor prognosis owing to its role in promoting epithelial-to-mesenchymal transition (EMT), invasiveness

285 3K27me3), and inhibition of genes related to epithelial-to-mesenchymal transition (EMT).

286 henotypes were also affected at the level of epithelial-to-mesenchymal transition and the ERK1/2 sign

287 n the proliferation, survival, migration and epithelial-to-mesenchymal transition of cancer cells.

288 and differentiation, resistance to anoikis, epithelial-to-mesenchymal transition, tumor cell dormanc

289 proteins and with an increased expression of epithelial-to-mesenchymal transition-related genes.

290 ll types and opens new research avenues into epithelial trafficking.

291 Aberrant mesenchymal-epithelial transition factor (MET) expression has been r

292 nsive analysis indicates that mesenchymal-to-epithelial transition is requisite to initiate SMCs repr

293 uption of cell polarity is a prerequisite in epithelial tumor initiation, the roles of CDC42 in tumor

294 Then, chemically-induced epithelial tumors in the hamster cheek pouch were treate

295 Finally, epithelial tumors were more susceptible to elimination b

296 Here we report the generation of alveolar epithelial type 2 cells (AEC2s), the facultative progeni

297 delicate regulation of colonic pH, including epithelial water absorption, nutrient inflow, and lumina

298 nded colonic mucosa was sufficient to impair epithelial wound healing in vivo.

299 th factor-1 are shown to promote the corneal epithelial wound healing.

300 al functional effects for these ROCKs at the epithelial zonula adherens (ZA).