ライフサイエンスコーパス: epithelial tissue

1 ntained throughout cytokinesis in vertebrate epithelial tissue.

2 in metastatic cancer cells and low in normal epithelial tissue.

3 that occur during cytokinesis in vertebrate epithelial tissue.

4 rmal postnatal development of a non-lymphoid epithelial tissue.

5 us that persistently replicates in glandular epithelial tissue.

6 l to study directed cell migration within an epithelial tissue.

7 ession profile of a human prostate glandular epithelial tissue.

8 of HBO1-JADE1S/L in injured and regenerating epithelial tissue.

9 e study of cell polarity within an organized epithelial tissue.

10 of stem cell behaviour in regenerative adult epithelial tissue.

11 dity to their receptors and the infection of epithelial tissue.

12 ffered between benign and preinvasive breast epithelial tissue.

13 junctions that provide adhesive strength in epithelial tissue.

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

15 both mice and humans into robust intestinal epithelial tissue.

16 ferative growth of the partially transformed epithelial tissue.

17 t can trigger complement activation in renal epithelial tissue.

18 cancers arise from mutations in cells within epithelial tissues.

19 ls play a critical role in calcium uptake in epithelial tissues.

20 signaling is poorly understood in developing epithelial tissues.

21 ellular dynamics within multiscale models of epithelial tissues.

22 promoting geometry and mechanical sensing in epithelial tissues.

23 ium homeostasis as Ca(2+) uptake channels in epithelial tissues.

24 s of recent lineage tracing assays involving epithelial tissues.

25 l geometric property of TCJ distributions in epithelial tissues.

26 al morphogenesis in transporting and sensory epithelial tissues.

27 s expressed abundantly and constitutively in epithelial tissues.

28 hannel, regulates ion and fluid transport in epithelial tissues.

29 rectly quantify infection rates in bronchial epithelial tissues.

30 e a wide range of morphogenetic processes in epithelial tissues.

31 us, trypsin IV may regulate ENaC function in epithelial tissues.

32 ial mediator of electrolyte transport across epithelial tissues.

33 rostate tumors compared with adjacent normal epithelial tissues.

34 ncy and then spread from infected neurons to epithelial tissues.

35 engineered normal and precancerous squamous epithelial tissues.

36 MP) are ubiquitous innate immune elements in epithelial tissues.

37 cts that provide a vital barrier function in epithelial tissues.

38 programs promote SC and CSC stemness in many epithelial tissues.

39 he major gammadelta lymphocyte population in epithelial tissues.

40 vation of regenerative stasis within diverse epithelial tissues.

41 te immune events occurring within peripheral epithelial tissues.

42 manageable tumors might also arise in other epithelial tissues.

43 and the resultant migration of cells within epithelial tissues.

44 that are shaped by coordinated migration of epithelial tissues.

45 ntenance of the cellular architecture of all epithelial tissues.

46 emerged as a central regulator of growth in epithelial tissues.

47 rine prostate adenocarcinoma in the adjacent epithelial tissues.

48 erm and are unable to migrate through intact epithelial tissues.

49 chanism by which TAK1 kinase is activated in epithelial tissues.

50 ctions between B. anthracis and lymphoid and epithelial tissues.

51 n vivo and causes accumulation of ROS in the epithelial tissues.

52 lifespan, and reduced cell proliferation in epithelial tissues.

53 al processes in nervous, muscular, and renal epithelial tissues.

54 cterized by fragility of specific subsets of epithelial tissues.

55 morphogenesis and postnatal regeneration of epithelial tissues.

56 lial cancer and gene/drug delivery to normal epithelial tissues.

57 mechanism that likely is conserved in other epithelial tissues.

58 om individual animals, germinal centers, and epithelial tissues.

59 underlies the morphogenesis and functions of epithelial tissues.

60 scriptome analysis were done using the rumen epithelial tissues.

61 on of the nuclear-cytoplasmic ratio (N/C) of epithelial tissues.

62 ted between cells are critical for sculpting epithelial tissues.

63 es compared with noncancerous nasopharyngeal epithelial tissues.

64 xis and planar division orientation in other epithelial tissues.

65 l role in the development and maintenance of epithelial tissues.

66 esponsible for the intercellular cohesion of epithelial tissues.

67 ance of stem cell (SC) pools in regenerating epithelial tissues.

68 neration of bioelectric gradients in mammary epithelial tissues.

69 mensional cell morphology and packing within epithelial tissues.

70 ysis of cell shape, polarity and behavior in epithelial tissues.

71 ent membrane, an ECM barrier surrounding all epithelial tissues.

72 nar polarity, is a characteristic feature of epithelial tissues [1].

73 -deficient pancreas has defects in all three epithelial tissues: a partial loss of endocrine cells, a

74 This model represents two key epithelial tissues-amnioserosa and germband-as adjacent

75 specific genes (FBXL7, ITPR3 and RAD51B from epithelial tissue and ALOX15 from blood) and one female-

76 icrodissected normal non-neoplastic prostate epithelial tissue and compared it to non-transformed and

77 were similarly coordinated in normal breast epithelial tissue and hormone-negative ductal carcinoma

78 The base simulation of a simplified patch of epithelial tissue and immune response exhibits distinct

79 detected in the goblet cells of human colon epithelial tissue and primary culture of colonic epithel

80 at the Ecad:Fc MTM stably integrated into an epithelial tissue and reduced migration at the interface

81 Bacteroides-derived lipids transfer to host epithelial tissue and the hepatic portal vein.

82 re, this gene was predominantly expressed in epithelial tissues and encoded by multiple haplotypes in

83 g of how adenoviruses establish infection in epithelial tissues and has implications for cancer thera

84 CP proteins maintain planar polarity in many epithelial tissues and have been implicated in cilia dev

85 omal cadherins mediate cell-cell adhesion in epithelial tissues and have been known to be altered in

86 osis were regulated by phenytoin in gingival epithelial tissues and in connective tissues similar to

87 L2 is induced during development in multiple epithelial tissues and localizes to the apical and junct

88 n 1 (CUGBP1) and HuR are highly expressed in epithelial tissues and modulate the stability and transl

89 ibes the ability of migrating cells to cross epithelial tissues and occurs during development, infect

90 gammadeltaT cells are a major component of epithelial tissues and play a role in tissue homeostasis

91 Lymphocyte infiltration into epithelial tissues and proinflammatory cytokine release

92 o Fraser syndrome (FS), in which cohesion of epithelial tissues and stroma is perturbed.

93 rane is restricted to the basal periphery of epithelial tissues and the basement membrane-mediated si

94 totic errors trigger apoptosis in Drosophila epithelial tissue, and blocking this apoptotic response

95 at confer mechanical strength to cardiac and epithelial tissue, and may also participate in signaling

96 atory response in immune cells cultured with epithelial tissue, and more so following incubation with

97 tivity and geometry information of deforming epithelial tissues, and computational tools to interroga

98 rol mechanical stress homeostasis in dynamic epithelial tissues, and highlight our methods as a resou

99 erplay may contribute towards conserving the epithelial tissue architecture at steady-state and in di

100 The integrity of epithelial tissue architecture is maintained through adh

101 ell-cell cooperation that normally maintains epithelial tissue architecture, individual subclones wit

102 (eAGR2) is a microenvironmental regulator of epithelial tissue architecture, which plays a role in th

103 Epithelial tissues are composed of polarized cells with

104 Epithelial tissues are highly organized systems with a r

105 eage-restricted differentiation in committed epithelial tissues are poorly understood.

106 ll lineage determination and regeneration in epithelial tissues are poorly understood.

107 Epithelial tissues are protective barriers that display

108 However, their physiological roles in epithelial tissues are unknown.

109 nd Lgr6, well-known markers of stem cells in epithelial tissues, are markers of mesenchymal cells in

110 tion of the aECM in a growing and remodeling epithelial tissue as an outermost barrier.

111 xisting knowledge of the behavior of enteric epithelial tissue as influenced by inflammation with the

112 innate properties, preferentially reside in epithelial tissues as the first line of defense.

113 ll subsets preferentially reside in specific epithelial tissues as the first line of defense.

114 ssion of Hoxa1 and Hoxc13 in oral and dental epithelial tissues as well as in the epidermis of skin d

115 or alpha 1 (IL-22Ra1), which is expressed on epithelial tissues, as well as hepatocytes.

116 To deconstruct regenerating adult epithelial tissue at single-cell resolution, we created

117 al retinoic acid metabolism and maintain the epithelial tissue barrier by generating airway cells ins

118 i-cellular model representing the human lung epithelial tissue barrier via multi-colour flow cytometr

119 Animal epithelial tissue becomes reproducibly colonized by spec

120 xperiments indicate a partial requirement in epithelial tissue, but confirm the essential role of Pvr

121 e amplification in a naturally proliferative epithelial tissue by elevating Polo-like kinase 4 (Plk4)

122 tate future application of the code to other epithelial tissue by inputting different transporters, c

123 derived signals control the morphogenesis of epithelial tissues by controlling the collective orienta

124 requirement in the genesis and evolution of epithelial tissues by determining its occurrence and evo

125 Solid tumors derived from epithelial tissues (carcinomas) are responsible for 90%

126 in networks in Drosophila epithelial and non-epithelial tissues, causing no overt phenotype.

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

128 In epithelial tissues, cells expressing oncogenic Ras (here

129 lution studies of the mechanics of confluent epithelial tissues consisting of tens of thousands of ce

130 The formation of epithelial tissues containing lumens requires not only t

131 st in some tumors compared with their normal epithelial tissue counterparts.

132 d mucosal trafficking of PMNs and associated epithelial tissue damage is a pathological hallmark of n

133 As epithelial tissues develop, groups of cells related by d

134 Consequently, the epithelial tissues display excessive proliferation, inad

135 l stromal compartment that produce long-term epithelial tissue during postpartum endometrial regenera

136 mplications for the mechanical regulation of epithelial tissues during development, homeostasis, and

137 t cobl shows enriched expression in ciliated epithelial tissues during zebrafish organogenesis.

138 e capabilities, must tear a hole through its epithelial tissue each time it opens its mouth.

139 onvergent-extension (CE), a planar-polarized epithelial tissue elongates (extends) in-plane in one di

140 s a promising approach for xeno-free corneal epithelial tissue engineering for ocular surface reconst

141 in the limbal niche as culture matrices for epithelial tissue engineering.

142 Epithelial tissues (epithelia) remove excess cells throu

143 r approach can aid in mechanical analysis of epithelial tissues, especially when local changes in cel

144 Many epithelial tissues expand rapidly during embryonic devel

145 S. aureus can form polymicrobial biofilms on epithelial tissue, facilitated by the C. albicans adhesi

146 C populations that are resident within other epithelial tissues for cancer.

147 Epithelial tissues form the boundaries of organs, where

148 icrodissection was used to obtain neoplastic epithelial tissue from 17 tumors which were examined usi

149 neoplastic low-grade and high-grade prostate epithelial tissue from radical prostatectomies, each wit

150 an cells and for basal cell populations from epithelial tissues from all three germ layers and theref

151 eterozygous clones and nontumorigenic breast epithelial tissues from BRCA mutation carriers, FISH rev

152 E-cadherin function, ablation experiments in epithelial tissues from different organ systems reveal m

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

154 ntrast, HCC was detected in all extension of epithelial tissue, from apical to basal cells in pterygi

155 control local mechanical forces to elongate epithelial tissues, genes controlling global forces in e

156 Yap1 and its paralogue Taz largely control epithelial tissue growth.

157 In epithelial tissues, growth control depends on the mainte

158 Recent studies of epithelial tissues have revealed the presence of tissue-

159 This resistance was coupled with a faster epithelial tissue healing response.

160 Following infection of epithelial tissues, herpes simplex virus 1 (HSV-1) virio

161 e extracellular matrix (ECM) is critical for epithelial tissue homeostasis and function.

162 ranging from germline stem cell division to epithelial tissue homeostasis and regeneration.

163 sed to play an important role in maintaining epithelial tissue homeostasis in many systems.

164 egulation of cell proliferation is vital for epithelial tissue homeostasis, and uncontrolled prolifer

165 on to maintain overall stem cell numbers and epithelial tissue homeostasis.

166 and compare it with transcriptomes of other epithelial tissues, identifying cornea-enriched genes, p

167 issection was used to isolate the neoplastic epithelial tissue in 20 cases.

168 iption during development and maintenance of epithelial tissue in organisms.

169 The visceral endoderm (VE) is an epithelial tissue in the early postimplantation mouse em

170 oth in cultured mammary acini and in mammary epithelial tissues in a mouse model of deregulated cycli

171 Using time-lapse confocal imaging of epithelial tissues in living zebrafish larvae, we provid

172 c density reflects the amount of stromal and epithelial tissues in relation to adipose tissue in the

173 g antipathogen responses and regeneration of epithelial tissues in the gut.

174 umnar epithelial transitions seen in complex epithelial tissues in vivo.

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

176 form of collective oscillations in confined epithelial tissues in which the oscillatory motion is th

177 Epithelial tissue, in which cells adhere tightly to each

178 uctural characteristics of human endometrial epithelial tissue, including cell differentiation, the p

179 e are distinct cell subpopulations in normal epithelial tissue, including stem cells, progenitor cell

180 d Wnt signals maintain stem cells in various epithelial tissues, including in lung development and re

181 s required for normal development of several epithelial tissues, including the bladder and prostate g

182 th commensal microbes in various mucosal and epithelial tissues, including the intestinal tract.

183 gainst many solid tumors that originate from epithelial tissues, including triple-negative breast can

184 Regulated spindle orientation maintains epithelial tissue integrity and stem cell asymmetric cel

185 e that p63 is a crucial gene for maintaining epithelial tissue integrity and support the deregulation

186 Innate lymphoid cells (ILCs) guard epithelial tissue integrity during homeostasis, but can

187 -mediated cell-cell adhesion is required for epithelial tissue integrity in homeostasis, during devel

188 Maintenance of epithelial tissue integrity requires coordination betwee

189 ll morphology defects in mitosis and impairs epithelial tissue integrity.

190 in developing epithelial tissues to promote epithelial tissue integrity.

191 he zonula adherens (za) is crucial to ensure epithelial tissue integrity.

192 of how TJ assembly sets the permeability of epithelial tissue is lacking.

193 The most fundamental function of an epithelial tissue is to act as a barrier, regulating int

194 The skin as the outmost epithelial tissue is under frequent physical, chemical,

195 dysregulated migration of PMNs into mucosal epithelial tissues is characteristic of chronic inflamma

196 e predominate connexin in the myocardium and epithelial tissues, is phosphorylated on more than a doz

197 When willin is expressed in D. melanogaster epithelial tissues, it has the same subcellular localiza

198 al Wnt-signaling drives cell polarization in epithelial tissues, it remains unclear whether such inst

199 ic DSG3 epitopes and autoantibody binding to epithelial tissues, leading to clinical and histologic r

200 tional rearrangements in actively remodeling epithelial tissues like the retina and tracheal system.

201 gammadelta T cells preferentially reside in epithelial tissues like the skin.

202 Mature fibroblasts in epithelial tissues live in the interstitial spaces betwe

203 constitute a conserved mechanism underlying epithelial tissue maintenance.

204 Epithelial tissues mechanically deform the surrounding e

205 ponents around the cell periphery is key for epithelial tissue morphogenesis and homeostasis.

206 ithin epithelial apical junctions, mediating epithelial tissue morphogenesis and tensional homeostasi

207 amental cellular process that contributes to epithelial tissue morphogenesis during normal developmen

208 culture provides an innovative tool to study epithelial tissue morphogenesis in a large field of view

209 During epithelial tissue morphogenesis, developmental progenito

210 te the dynamics and biomechanical control of epithelial tissue morphogenesis.

211 e apical cell constriction in the context of epithelial tissue morphogenesis.

212 a fide marker of adult stem cells in several epithelial tissues, most notably in the intestinal crypt

213 rapeutic agents damage rapidly proliferating epithelial tissue, namely via the cell population-specif

214 ession during branching morphogenesis in the epithelial tissue of an early embryonic salivary gland a

215 significantly higher in biopsies from sinus epithelial tissue of CRS patients with nasal polyps comp

216 as it colonizes the colonic lumen, mucus or epithelial tissue of mice.

217 rdinating extracellular matrix protection in epithelial tissues of chitinous invertebrates.

218 e used computational modeling and engineered epithelial tissues of precise geometry to define the exp

219 nervous, hemopoietic, endocrine, and certain epithelial tissues of Tg[CerPrP] mice.

220 ated in the developing brain, in contrast to epithelial tissues of the imaginal discs.

221 sensitive ion channel primarily expressed in epithelial tissues of the skin, nose, and tongue.

222 Myc expression in epithelial tissues of transgenic mice (K5-Myc) led to in

223 r, we study the development and migration of epithelial tissues on glass wires of well-defined radii

224 l as be used as tools for gene delivery into epithelial tissues or epithelial tumors.

225 The basement membrane is crucial for epithelial tissue organization and function.

226 eling and single cell migration, its role in epithelial tissue organization and mammary gland morphog

227 cription of E-cadherin, a key determinant of epithelial tissue organization.

228 ntribute to the molecular network regulating epithelial tissue organization.

229 oth Mus musculus (stromal) and Homo sapiens (epithelial) tissue origins.

230 step of the pathway enhances Ras(V12)-driven epithelial tissue overgrowth via the accumulation of rea

231 cellular matrix contacting the basal side of epithelial tissues, plays an important role in the contr

232 ved cells resident within cancer susceptible epithelial tissues principally by influencing early even

233 CP), the long-range in-plane polarization of epithelial tissues, provides directional information tha

234 Plasticity in epithelial tissues relates to processes of embryonic dev

235 Morphogenesis of epithelial tissues relies on the interplay between cell

236 phogenesis, homeostasis, and regeneration of epithelial tissues rely on the accurate orientation of c

237 ce, Btbd7 is a regulatory gene that promotes epithelial tissue remodeling and formation of branched o

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

239 eviously unknown, multilayered regulation of epithelial tissue remodeling coordinated by the microRNA

240 t state associated with senescence in normal epithelial tissue repair and its abnormal persistence in

241 ury, inhibit inflammation, and contribute to epithelial tissue repair, their use has been suggested a

242 olled growth and morphogenesis of developing epithelial tissues require coordination of multiple fact

243 Epithelial tissues require the removal and replacement o

244 The development and maintenance of polarized epithelial tissue requires a tightly controlled orientat

245 Extrusion of apoptotic cells from epithelial tissues requires orchestrated morphological r

246 The propagation of force in epithelial tissues requires that the contractile cytoske

247 Morphogenesis of epithelial tissues requires tight spatiotemporal coordin

248 obust and universal mechanism to explain how epithelial tissues restore their integrity.

249 RNA concentration the area of ocular surface epithelial tissue sample processed for the Gene 1.0 ST a

250 ve effectively collected ocular surface (OS) epithelial tissue samples from the Limbal Epithelial Cry

251 For epithelial tissues, some of that coordination is accompl

252 knockout (KO) mouse model, which allows for epithelial tissue-specific Grhl2 KO in an inducible mann

253 thelial-mesenchymal transition (EMT) in both epithelial tissue stem cells and breast cancer cells.

254 ereas others have been shown to originate in epithelial tissue stem cells.

255 ssembly, the multiprotein complex regulating epithelial tissue structure and function following de no

256 mine the dynamics of stem cells within human epithelial tissues such as colonic crypts.

257 In a wide range of epithelial tissues such as kidney tubules or breast acin

258 tomography method for 3-D reconstruction of epithelial tissues such as mammary gland, cornea and the

259 y for deriving and sustaining organoids from epithelial tissues such as prostate, colon, gastric, liv

260 In epithelial tissues such as the kidney and gut, microvill

261 ut does not have detectable effects in other epithelial tissues such as the related mucosa of the lar

262 to the epithelial keratins of soft and hard epithelial tissues such as: skin, cornea, hair and nail.

263 nce shows that unlike other endoderm-derived epithelial tissues, such as the intestine, Wnt/beta-cate

264 ocesses involve mechanical rearrangements of epithelial tissues that are driven by precisely regulate

265 es in intestinal stem cell dynamics in human epithelial tissues that might be used to study premalign

266 and one female-specific gene (HLA-DQA1 from epithelial tissue) that are disregulated during asthma.

267 In many epithelial tissues, the cells' contractile network is po

268 Unlike many epithelial tissues, the corneal epithelium is insulin in

269 In epithelial tissues, the Hippo pathway is regulated by fu

270 In epithelial tissues, the shape of the interphase cell is

271 esion and unidirectional drug release toward epithelial tissue, thereby prolonging drug exposure and

272 In epithelial tissues, this process has been shown to be cr

273 on during branching morphogenesis of mammary epithelial tissues through key regulators of EMT.

274 odel developed to describe the biophysics of epithelial tissue to explore this problem.

275 Although HPV16 transforms infected epithelial tissues to cancer in the presence of several

276 The ability of epithelial tissues to heal after injury is essential for

277 tional analysis of high resolution images of epithelial tissues to infer relative magnitude of forces

278 ty may have evolved as a general strategy in epithelial tissues to maximize energy efficiency.

279 horylates and activates Moesin in developing epithelial tissues to promote epithelial tissue integrit

280 orce-activated mechanotransducer, in mammary epithelial tissue transformation and invasion.

281 portant for the viral life cycle in specific epithelial tissue types and contribute to cellular trans

282 Epithelial tissues undergo extensive collective movement

283 oteome in branching morphogenesis of mammary epithelial tissues using a three-dimensional organotypic

284 We have studied dysregulated cyclin E in epithelial tissues using organotypic cultures of human m

285 r multiscale spatiotemporal simulation of an epithelial tissue, viral infection, cellular immune resp

286 To investigate the roles of Acvr1b in the epithelial tissues, we created mice with a conditional d

287 lar Notch receptor trafficking in Drosophila epithelial tissues, we recovered mutations that disrupt

288 Epithelial tissues were collected and analyzed by immuno

289 Rumen epithelial tissues were collected at necropsy at 17 week

290 Liver and rumen epithelial tissues were collected at necropsy at 17 week

291 in Vero E6 cells and primary human alveolar epithelial tissues were not affected.

292 rm distinct cell fate decisions to Notch1 in epithelial tissues, where carcinomas such as SCC arise.

293 e localized to neuronal, cardiovascular, and epithelial tissues, where they play critical roles in co

294 ing spread from latently infected ganglia to epithelial tissues, where viral progeny are produced in

295 function as voltage-independent channels in epithelial tissues, whereas KCNQ1 function as voltage-ac

296 shape to achieve robust mitotic rounding in epithelial tissues, which is where most cancers initiate

297 This includes epithelial tissues, which often narrow and elongate in c

298 ansmembrane glycoprotein widely expressed in epithelial tissues whose functions are just beginning to

299 AVM combines the Vertex Model for confluent epithelial tissues with active matter dynamics.

300 entration (THC) and scattering properties of epithelial tissues with mean errors of 4.7% and 6.9%, re