ライフサイエンスコーパス: epidermal cell

1 ighly anisotropic expansion of a single seed epidermal cell.

2 pectin that extend above the center of each epidermal cell.

3 acid transporter primarily expressed in root epidermal cells.

4 namics during axial cell expansion of living epidermal cells.

5 embly and motility of cilia in multiciliated epidermal cells.

6 ion assay in tobacco (Nicotiana benthamiana) epidermal cells.

7 Plant trichomes are defensive specialized epidermal cells.

8 polyethyleneimine (PEI) - especially on skin epidermal cells.

9 tinuous proliferation and differentiation of epidermal cells.

10 ient uptake and O2/CO2 exchange through leaf epidermal cells.

11 robably through the biosynthetic activity of epidermal cells.

12 l distinct MAMP signalling pathways in plant epidermal cells.

13 ly through an additional autocrine effect on epidermal cells.

14 specialized secondary cell wall of seed coat epidermal cells.

15 s displayed defects in patterning of conical epidermal cells.

16 thesis of highly branched xylan in seed coat epidermal cells.

17 FT) 20 (Ift20) during polarized migration of epidermal cells.

18 response that maintains genome integrity of epidermal cells.

19 se and more bundled actin filament arrays in epidermal cells.

20 fection, which prevented fungal ingress into epidermal cells.

21 larity from the basal to apical side of root epidermal cells.

22 1 expression and defence suppression in rice epidermal cells.

23 ses the cortical actin cytoskeleton in plant epidermal cells.

24 protein-tagged OsCPK4 in onion (Allium cepa) epidermal cells.

25 duced MMC and centriole numbers in embryonic epidermal cells.

26 in of the plasma membrane and EE/TGN in root epidermal cells.

27 the formation of fungal haustoria in barley epidermal cells.

28 nd a range of variation in relative sizes of epidermal cells.

29 ally activates BMP signaling in leading edge epidermal cells.

30 less cytotoxic effects against normal mouse epidermal cells.

31 fied by the outer domain of Arabidopsis root epidermal cells.

32 ast late in the differentiation of seed coat epidermal cells.

33 sion altered the outer wall diameter of leaf epidermal cells.

34 ry for the efficient movement of CPC between epidermal cells.

35 ns, produced in the endoplasmic reticulum of epidermal cells.

36 We find that ATML1 is expressed in all epidermal cells.

37 dopsis plants and Nicotiana benthamiana leaf epidermal cells.

38 taneous squamous cell carcinoma, cSCC) human epidermal cells.

39 ariations in wall stiffness between adjacent epidermal cells.

40 rmination of cell division of the underlying epidermal cells.

41 ne comprising pObs and adjacent motile basal epidermal cells.

42 e it elongates invasive hyphae in underlying epidermal cells(5).

43 (HSPGs) Dally and Syndecan on the surface of epidermal cells act as local permissive signals for the

44 Epidermal cells act via Draper-mediated recognition to f

45 ALT1 was expressed specifically in stem epidermal cells and flower petals.

46 d for optimal proliferation of E7-transgenic epidermal cells and for the growth of HNSCC tumors.

47 in were significantly upregulated by IL-4 in epidermal cells and keratinocytes.

48 WS1 is responsible for cuticle deposition on epidermal cells and organization of the endomembrane sys

49 based on light-dependent morphology of leaf epidermal cells and phytoliths derived from them.

50 growth behavior was carried out by culturing epidermal cells and proliferation was quantified via via

51 hocyte antigen-positive T cells activated by epidermal cells and S pyogenes in patients with GP.

52 hin the epidermis and FBN-1 was expressed in epidermal cells and secreted to the apical surface as a

53 a functional, excitatory connection between epidermal cells and sensory neurons.

54 In a translational model of human psoriatic epidermal cells and skin-homing T cells, JNJ-54271074 se

55 associated with asymmetric division of young epidermal cells and stomatal opening, respectively, and

56 atory cytokines in resident IL-4R-expressing epidermal cells and thereby alters the psoriatic skin ph

57 in most plants are separated by at least one epidermal cell, and this spacing is thought to enhance s

58 o an abundant postmitotic lineage, including epidermal cells, and are not required for regeneration.

59 s of the stress sensor FoxO than neighboring epidermal cells, and hence exhibit no marked induction o

60 sion of genes associated with keratinocytes, epidermal cells, and monocytes, versus ustekinumab.

61 al axis in Drosophila melanogaster embryonic epidermal cells, and thus more frequently contact E-cadh

62 rstitial-type DCs and inflammatory dendritic epidermal cells appearing in dermatitis/eczema lesions,

63 ther than being randomly distributed, p53(+) epidermal cells are enriched only in areas overlying thi

64 Specialized epidermal cells are essential for the complex tissue reg

65 rocess of tissue replacement in which larval epidermal cells are replaced by adult cells.

66 elled cotton fibers, produced from seed coat epidermal cells are the largest natural source of textil

67 s and it is commonly believed that embryonic epidermal cells are the only cells that can respond to h

68 displacement of guard cells into neighboring epidermal cells, are crucial for facilitating high rates

69 Together, these results identify vertebrate epidermal cells as broad-specificity phagocytes that lik

70 During wound repair, epidermal cells at the edge of an injury establish front

71 , we show that upon damage in a mouse model, epidermal cells at the wound edge convert to an embryoni

72 In epidermal cells, BAF and p63 mutually recruit each other

73 iotroph in intimate contact with living rice epidermal cells before necrotic lesions develop.

74 stomata and enforce a minimum spacing of one epidermal cell between stomata.

75 stomata and enforce a minimum spacing of one epidermal cell between stomata.

76 Cutaneous injuries damage not only epidermal cells but also the axonal endings of somatosen

77 initially at the three-way junctions between epidermal cells but develop most rapidly in the anisocyt

78 A precursors (iridoids) are localised in the epidermal cells, but major TIAs including serpentine and

79 The TEX1 protein was present in epidermal cells, but not in the germline, and, through T

80 which is displayed at the surface of stigma epidermal cells, by its even more polymorphic pollen coa

81 CHCs are synthesised in sub-epidermal cells called oenocytes that are very difficult

82 ntegrin-based adhesion in suppressing larval epidermal cell-cell fusion--a role that may be conserved

83 pathogen showing direct penetration of leaf epidermal cells comparable to G. orontii.

84 e Notch pathway plays a key role in limiting epidermal cell competency to respond to Atoh1 expression

85 duce new Merkel cells in the epidermis, that epidermal cell competency to respond to Atoh1 varies by

86 tion in the AtGATL5 gene generates seed coat epidermal cell defects both in mucilage synthesis and ce

87 mation in M. lewisii flowers, which involves epidermal cell development and carotenoid pigmentation.

88 To examine the relationship between epidermal cell development and cuticle assembly in the c

89 Individual human epidermal cells differ in their self-renewal ability.

90 importance of post-translational controls in epidermal cell differentiation and flavonoid metabolism.

91 In this study, we survey the epidermal cell differentiation in a systematic manner by

92 anthocyanin and anthocyanin biosynthesis and epidermal cell differentiation in plants.

93 Epidermal cell differentiation is a paramount and conser

94 hinum majus) petals, are known regulators of epidermal cell differentiation.

95 ondary cell wall structures during seed coat epidermal cell differentiation.

96 erived dendritic cell/inflammatory dendritic epidermal cell differentiation.

97 ther that stomatal formation is inhibited in epidermal cells directly in contact with the vein or tha

98 Strikingly, DeltaNp63(-/-) epidermal cells display profound defects in terminal dif

99 The epidermal cells displayed a decreased tangential cell wi

100 normal in bulliform cell differentiation and epidermal cell division.

101 In vivo tracking of leaf epidermal cell divisions, combined with marker lines and

102 omata are produced by a controlled series of epidermal cell divisions.

103 Arabidopsis (Arabidopsis thaliana) hypocotyl epidermal cells, dynamic cortical microtubules labeled w

104 During development, epidermal cell elongation and microtubule alignment occu

105 Vertebrate and invertebrate epidermal cells ensheath peripheral arbors of somatosens

106 otransmitters; however, direct evidence that epidermal cells excite tactile afferents is lacking.

107 re, we find that RHM1 is required to promote epidermal cell expansion.

108 that in photosynthetic Nicotiana benthamiana epidermal cells, exposure to high light increases H2O2 p

109 ctions and biological processes reveals that epidermal cells express genes involved in pathogen defen

110 passive has been recently challenged because epidermal cells express sensory ion channels and neurotr

111 asis lesions attacking melanocytes, the only epidermal cells expressing ADAMTSL5.

112 muno-electron microscopy analyses of tobacco epidermal cells expressing BdCSLF6, we demonstrate that

113 xplained on the basis of a reduced number of epidermal cells facilitating ion supply to the guard cel

114 e seed coat of the apetala2 mutant where the epidermal cells fail to differentiate.

115 We show that Ovol1/Ovol2-deficient epidermal cells fail to undertake alpha-catenin-driven a

116 A similar MBW complex regulates epidermal cell fate by activating the transcription of G

117 role for post-transcriptional regulation of epidermal cell fate decisions.

118 TCP proteins couple leaf morphogenesis with epidermal cell fate determination.

119 and uterine masses that express neuronal and epidermal cell fate markers.

120 he appropriate spatial expression of several epidermal cell fate regulators in a similar manner as SC

121 dy provides a molecular explanation for root epidermal cell fate switch in response to ribosomal defe

122 te environmental signals to control immature epidermal cell fate, and ultimately stomatal density, ar

123 localization and its function in regulating epidermal cell fate.

124 ene regulatory network that establishes root epidermal cell fate.

125 ost-transcriptional regulators of plant root epidermal cell fate.

126 ODERMAL FACTOR2 (PDF2) are indispensable for epidermal cell-fate specification in Arabidopsis embryos

127 sitive regulator of both cuticle and conical epidermal cell formation in tomato fruit, acting as a me

128 Moreci and Lechler follow the lifetime of an epidermal cell from its birth to its ultimate death, and

129 Genome-wide DNA methylation profiling of epidermal cells from 12 patients undergoing narrow-band

130 t a large population of jigsaw-puzzle shaped epidermal cells from Arabidopsis thaliana leaves.

131 Epidermal cells from healthy skin were analyzed for thei

132 rocess of axial cell expansion; for example, epidermal cells from hypocotyls with reduced CP are long

133 Circulating memory T cells and autologous epidermal cells from samples from either patients with G

134 are potentially mutagenic and detrimental to epidermal cell function.

135 UX1 in lateral root cap (LRC) and elongating epidermal cells greatly enhance auxin's shootward flux,

136 ative spectroscopy showed that, in the PM of epidermal cells, H2O2 treatment induces an increase in l

137 persicum) fruit, the thick cuticle embedding epidermal cells has crucial roles in the control of path

138 naling in Arabidopsis (Arabidopsis thaliana) epidermal cells; however, the immune signals that imping

139 Langerhans cells and inflammatory dendritic epidermal cells (IDEC) are located in the epidermis of A

140 me analysis to investigate the site-specific epidermal cell identity on volar skin.

141 ucture that is capable of maintaining robust epidermal cell identity post-germination.

142 insights into the regulation and function of epidermal cell-immune cell interactions and into how com

143 n increase in NADH fluorescence in the basal epidermal cells, implying a reduction in basal cell oxid

144 airs are tubular extensions of specific root epidermal cells important in plant nutrition and water a

145 ly reproducing plants, a single somatic, sub-epidermal cell in an ovule is selected to differentiate

146 Expansion of ARF3 expression into lateral epidermal cells in a TAS3 ta-siRNA-insensitive mutant le

147 cle is laid down at the cell wall surface of epidermal cells in a wide variety of structures, but the

148 However, the mutant had shorter epidermal cells in comparison with wild-type Hwayoung (H

149 All aerial epidermal cells in land plants are covered by the cuticl

150 racellular matrix constituents in developing epidermal cells in particular, involves a dephosphorylat

151 likely underlie the loss of adhesion between epidermal cells in plants with reduced levels of DEK1 an

152 RNAi impaired the function of multiciliated epidermal cells in propelling planarian movement, as wel

153 evelopment of structures derived from single epidermal cells in the common ancestor of the land plant

154 Most epidermal cells in the distal part of the leg stump prol

155 he lateral cell-cell junctions of wound-edge epidermal cells in the early healing stages.

156 Tip-growing rhizoid cells develop among flat epidermal cells in the epidermis of the early-diverging

157 touch dome stem cells that are unique among epidermal cells in their activated Hedgehog signaling an

158 During larval growth each epidermal cell increases manyfold in size but neither di

159 f silver precipitation were observed in some epidermal cells, indicating moderate cuticular uptake.

160 luding pauci-cellular infiltration with rare epidermal cell infiltration or necrosis, were accounted

161 cluding paucicellular infiltration with rare epidermal cell infiltration or necrosis, were accounted

162 itive activation of beta-catenin in adjacent epidermal cells, initiating the follicle gene expression

163 ateral branches arise by re-specification of epidermal cells into branch initials.

164 ntiation of the maternally derived seed coat epidermal cells into mucilage secretory cells is a commo

165 Arabidopsis thaliana (Arabidopsis) seed coat epidermal cells involves pronounced changes highlighted

166 trolled absorption of soil nutrients by root epidermal cells is critical for growth and development.

167 ransformation, and colony formation of mouse epidermal cells JB6 Cl41, human colon cancer DLD-1, brea

168 nesis strain that expresses markers labeling epidermal cell junctions and the neuronal cell surface.

169 Our cell sorting-based study of the epidermal cell layer transcriptome confirms that core UV

170 gulate bacterial passage through the plant's epidermal cell layer.

171 ulates bacterial passage through the plant's epidermal cell layer.

172 more, cell morphology and the arrangement of epidermal cell layers, on whose activity cuticle formati

173 the inner part of the cell wall of the outer epidermal cell layers.

174 predominantly basally localized PIN1 in root epidermal cells, leading to agravitropic root growth.

175 dramatic left-handed helical growth of petal epidermal cells, leading to left-handed twisted petals.

176 rganized in nests and the surrounding larval epidermal cells (LECs).

177 We analyzed the growth of epidermal cell lineages in the Arabidopsis (Arabidopsis

178 Wound-edge epidermal cells migrate as a sheet to close the wound.

179 We find that as dorsal epidermal cells migrate past one another they produce F-

180 tissues, where it is responsible for proper epidermal cell morphology and overall plant growth.

181 interaction, E2F target gene expression, and epidermal cell number and shape in e2fb mutant and overe

182 and (4) dull mutants display alterations in epidermal cell number and shape.

183 ell division as indicated by the higher leaf epidermal cell number in SlP4H1- and SlP4H9-silenced pla

184 with its cognate SRK receptor in the stigma epidermal cells of Arabidopsis (Arabidopsis thaliana) pl

185 ary for seed mucilage adherence to seed coat epidermal cells of Arabidopsis (Arabidopsis thaliana).

186 rescent protein-tagged phyB (phyB-FP) in the epidermal cells of Arabidopsis hypocotyl and cotyledon.

187 Guard cells and epidermal cells of hornworts show striking similarities

188 Epidermal cells of leaves are diverse: tabular pavement

189 pores formed appressoria and penetrated into epidermal cells of M. truncatula, P. pachyrhizi failed t

190 The ablation of HS in the interfollicular epidermal cells of mature skin led to the spontaneous fo

191 with resultant calcium oscillations in root epidermal cells of Medicago truncatula and Lotus japonic

192 The gene was only expressed in the epidermal cells of stems, primordial leaves, and young l

193 DeltaNp63 using transcriptomes derived from epidermal cells of TAp63(-/-) and DeltaNp63(-/-) mice.

194 ose microfibrils were disordered only in the epidermal cells of the any1 inflorescence stem, whereas

195 We analyze the epidermal cells of the Arabidopsis sepal, focusing on co

196 BR-induced genes were primarily detected in epidermal cells of the basal meristem zone and were enri

197 ccumulates in hypocotyl cortex cells and sub-epidermal cells of the embryonic cotyledons, but rather

198 cuticle is a protective layer synthesized by epidermal cells of the plants and consisting of cutin co

199 ribute to sugar secretion, specifically from epidermal cells of the root apex.

200 sion and phospholipid uptake are high in the epidermal cells of the root tip and in guard cells, the

201 The thick cuticle covering and embedding the epidermal cells of tomato (Solanum lycopersicum) fruit a

202 automated cell-pressure-probe (ACPP) on leaf epidermal cells of Tradescantia virginiana, the validity

203 predominantly through the LRC, entering the epidermal cells only as they enter the elongation zone.

204 Both epidermal cell optogenetic inhibition and interruption o

205 ipeline and applied it to track and quantify epidermal cells over 3-4 d in Arabidopsis thaliana shoot

206 ques, making large-scale characterization of epidermal cell parameters impractical.

207 As part of a larger regulatory network of epidermal cell patterning and L1-layer identity, we foun

208 nstrated that brassinosteroid-regulated root epidermal cell patterning is dependent on the WER-GL3/EG

209 ession in ros1 is restored and the defective epidermal cell patterning is suppressed by mutations in

210 structure-function relationship in hypocotyl epidermal cell patterning through global topological ana

211 tin polymer formation, cuticle assembly, and epidermal cell patterning.

212 80B1 mutants, underscoring the aberrant root epidermal cell patterning.

213 fessional phagocytes, but we have found that epidermal cells phagocytose somatosensory axon debris in

214 Epidermal cells phagocytosed not only somatosensory axon

215 ellular traits, such as stomatal density and epidermal cell phenotypes.

216 ence imaging that cdc-42 is not required for epidermal cell polarization or junction assembly, but ra

217 Recent work in Xenopus has identified an epidermal cell population critical for tail regeneration

218 Arabidopsis (Arabidopsis thaliana) seed coat epidermal cells produce large amounts of mucilage that i

219 nduced ear swelling, leukocyte infiltration, epidermal cell proliferation, and dermal angiogenesis.

220 c plaques by inducing epidermal hyperplasia, epidermal cell proliferation, and recruitment of leukocy

221 tion drives tumor development by stimulating epidermal cell proliferation.

222 myosin purse strings in the leading edges of epidermal cells promote closure, whereas the bulk of the

223 PAT6-generated cutin monomers in influencing epidermal cell properties that are integral to leaf-micr

224 Live imaging revealed that epidermal cells rapidly internalize debris into dynamic

225 ndrite injury of Drosophila sensory neurons, epidermal cells rather than hemocytes are the primary ph

226 Remarkably, epidermal cells rather than professional phagocytes are

227 SSc epidermis and asked whether SSc-injured epidermal cells release factors capable of promoting fib

228 hanisms underlying nuclear movements in root epidermal cells remains limited.

229 Iron absorption in Arabidopsis root epidermal cells requires the IRT1 transporter that also

230 L17F in wounds and control immunological and epidermal cell responses.

231 onstitutively active MEK1 in differentiating epidermal cells results in chronic inflammation (InvEE m

232 Perturb-ATAC in primary human epidermal cells revealed three sequential modules of cis

233 Epidermal cells secrete proteins and enzymes that assemb

234 o elongation, a process driven by asymmetric epidermal cell shape changes.

235 Cultured epidermal cell sheets (CES) containing undifferentiated

236 organ growth and in the morphology of petal epidermal cells, showing that the interaction between JA

237 s including above-ground biomass, leaf size, epidermal cell size and number and stomatal density and

238 tin synthesis with cell wall development and epidermal cell size has been identified.

239 n per stoma was dependent on maintaining one epidermal cell spacing and the physiological parameters

240 Knockdown of HAX1 and EB2 in skin epidermal cells stabilizes focal adhesions and impairs e

241 s activation of many wound response genes in epidermal cells surrounding wound sites.

242 Arabidopsis thaliana seed coat epidermal cells synthesize and secrete large quantities

243 tomatal guard cells are pairs of specialized epidermal cells that control water and CO2 exchange betw

244 haped structure surrounds an opening between epidermal cells that facilitates the exchange of gases b

245 na) seeds release polysaccharides from their epidermal cells that form a two-layered hydrogel, termed

246 cell transformation in pathologically normal epidermal cells that have been exposed to carcinogens is

247 nd elicited robust defence responses in rice epidermal cells that included elevated pathogenesis-rela

248 cell fate regulators in the differentiating epidermal cells that ultimately generate the abnormal ce

249 Secreted by epidermal cells, the Obst-A protein is specifically enri

250 other regulator of PME activity in seed coat epidermal cells, the subtilisin-like Ser protease SBT1.7

251 In epidermal cells, the yellow fluorescent protein-tagged M

252 possibly the mucilage of wild-type seed coat epidermal cells, through oxidation of RG-I Gal side-chai

253 y active state seen in the basal and spinous epidermal cells to a fully inactive state in the keratin

254 t receptor-like kinase, is required for root epidermal cells to appropriately interpret their locatio

255 t epidermis, causing a greater proportion of epidermal cells to be specified as root hair cells rathe

256 n neurons but rather functions in the nearby epidermal cells to correctly position glia during postla

257 pplied to individual Tradescantia virginiana epidermal cells to determine both exosmotic and endosmot

258 on factor ATML1 pattern a field of identical epidermal cells to differentiate into giant cells inters

259 AM fungi colonize root epidermal cells to gain access to the root cortex, and t

260 complex facilitates CPC movement between the epidermal cells to help establish the cell-type pattern

261 ists at the cell surface of Arabidopsis root epidermal cells to optimize iron uptake.

262 Although the response of epidermal cells to stretching has been studied in vitro(

263 Lipid secretion from epidermal cells to the plant surface is essential to cre

264 However, the ability of epidermal cells to utilize TNTs remains a mystery.

265 omponent of desmosome complexes that mediate epidermal cell-to-cell adhesion and tissue integrity.

266 A focused analysis of root epidermal cell transcriptomes defined developmental traj

267 Moreover, DeltaNp63(-/-) epidermal cells transduced with an inducible DGCR8 plasm

268 In addition to protoplasts, leaf epidermal cells transiently transformed by biolistic par

269 changes to single actin filament turnover in epidermal cells treated with bacterial and fungal MAMPs.

270 Our data show that melanocytes are the only epidermal cell type to express the senescence marker p16

271 dy completes the characterisation of all the epidermal cell types in the early tadpole epidermis and

272 recursors that differentiate into one of two epidermal cell types, guard cells or pavement cells.

273 thway has the potential to similarly pattern epidermal cell types, we expanded the expression domain

274 inated individual filament behaviors in root epidermal cells under control conditions and after indol

275 By analyzing imaging data of tobacco leaf epidermal cells under two different conditions, i.e., na

276 The leaf outer epidermal cell wall acts as a barrier against pathogen a

277 h a new role for DEK1 in pathways regulating epidermal cell wall deposition and remodeling.

278 n the cuticle and the main components of the epidermal cell wall during tomato fruit development.

279 the changes observed in the cuticle and the epidermal cell wall indicate a deep interaction between

280 ovel role for DEK1 in the regulation of leaf epidermal cell wall structure.

281 stops the fungal hyphae from penetrating the epidermal cell wall.

282 advance our understanding of the role of the epidermal cell walls in growth regulation and establish

283 These PRPs are absent from root epidermal cell walls, and PRP accumulation is highly loc

284 increased levels of cellulose and pectins in epidermal cell walls, and this is correlated with the ex

285 mping froghoppers perforated the cuticle and epidermal cell walls, and wounds could be visualized aft

286 secretion of IL-1beta and IL-6 by psoriatic epidermal cells was inhibited by IL-4 via transcriptiona

287 ith microbes that do not directly enter leaf epidermal cells were seemingly unaltered or showed even

288 Recently, seed coat epidermal cells were shown to provide an excellent syste

289 In leaf epidermal cells where a polygonal ER network can be reso

290 nsporter in the leaf phloem and in cotyledon epidermal cells where import into the embryo occurs.

291 zed to the cytosol and the nucleus of barley epidermal cells, whereas Hsp16.9 and Hsp17.5 are cytosol

292 maintains biotrophic nutrition within living epidermal cells, whereas in barley the symbiont undergoe

293 ed, bulge HF-SCs begin to differentiate into epidermal cells, which naturally lack SOX9.

294 We cultured freshly isolated psoriatic epidermal cells, whole psoriatic and healthy skin biopsi

295 This mutation decreases epidermal cell width but not length, and probably also r

296 , mice remained viable and healthy, although epidermal cells with centrosome amplification were still

297 icrotubule array architecture in light-grown epidermal cells with explicit reference to array pattern

298 Treatment of wild-type epidermal cells with SMIFH2 mimicked the phenotype of pr

299 nase (ILK) caused formation of multinucleate epidermal cells within the Drosophila larval epidermis.

300 Expression of Epr3 in epidermal cells within the susceptible root zone shows t