ライフサイエンスコーパス: epidermal cell

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

2 ustorium to extract nutrition from the plant epidermal cell.

3 ighly anisotropic expansion of a single seed epidermal cell.

4 robably through the biosynthetic activity of epidermal cells.

5 l distinct MAMP signalling pathways in plant epidermal cells.

6 ly through an additional autocrine effect on epidermal cells.

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

8 specialized secondary cell wall of seed coat epidermal cells.

9 s displayed defects in patterning of conical epidermal cells.

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

11 ariations in wall stiffness between adjacent epidermal cells.

12 response that maintains genome integrity of epidermal cells.

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

14 fection, which prevented fungal ingress into epidermal cells.

15 1 expression and defence suppression in rice epidermal cells.

16 ses the cortical actin cytoskeleton in plant epidermal cells.

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

18 duced MMC and centriole numbers in embryonic epidermal cells.

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

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

21 ally activates BMP signaling in leading edge epidermal cells.

22 less cytotoxic effects against normal mouse epidermal cells.

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

24 affected in mucilage release from seed coat epidermal cells.

25 erization in the PM of live Arabidopsis root epidermal cells.

26 uorescence complementation analysis in onion epidermal cells.

27 could derive data for up to 11k PDs from 3k epidermal cells.

28 ymes in the endomembrane system of seed coat epidermal cells.

29 rmination of cell division of the underlying epidermal cells.

30 y so for chloroplast production in cotyledon epidermal cells.

31 ne comprising pObs and adjacent motile basal epidermal cells.

32 stability of cortical microtubules in barley epidermal cells.

33 tin network is reoriented in elongating root epidermal cells.

34 ays and in particular, those associated with epidermal cells.

35 cells gained characteristics of motor organ epidermal cells.

36 e reorganization of microtubules in cultured epidermal cells.

37 (MTs) on the outer tangential wall (OTW) of epidermal cells.

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

39 acid transporter primarily expressed in root epidermal cells.

40 dopsis plants and Nicotiana benthamiana leaf epidermal cells.

41 namics during axial cell expansion of living epidermal cells.

42 embly and motility of cilia in multiciliated epidermal cells.

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

44 Plant trichomes are defensive specialized epidermal cells.

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

46 tinuous proliferation and differentiation of epidermal cells.

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

48 Force application to epidermal cells above root primordia caused cell death i

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

50 Epidermal cells act via Draper-mediated recognition to f

51 Localized clusters of misdivided epidermal cells also led to the formation of warty lesio

52 ability during expansion stages of cotyledon epidermal cells, an exquisite model system for vegetativ

53 ignalling and depend on interactions between epidermal cells and a population of fibroblasts at the b

54 bit elevated cuticle membrane thickness over epidermal cells and cuticular ledges with increased occl

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

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

57 ure studies on MT dynamics in other faces of epidermal cells and in cells deeper within the hypocotyl

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

59 n cell wall biochemistry, morphology of leaf epidermal cells and lower structural integrity via diffe

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

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

62 The cuticle is synthesized by epidermal cells and predominantly consists of an aliphat

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

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

65 terized paralog, SYM-1, is also expressed in epidermal cells and secreted into the apical ECM.

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

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

68 n, PIN2 is depleted from apical membranes of epidermal cells and shows basal to apical relocalization

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

70 that are expressed on the apical surfaces of epidermal cells and some tubular epithelia, including th

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

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

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

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

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

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

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

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

79 UVA1- and UVB-induced TTs were repaired in epidermal cells at a similar rate.

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

81 (PMEI6), specifically expressed in seed coat epidermal cells at the time when mucilage polysaccharide

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

83 Large numbers of FITC(+) epidermal cells became detectable 12-24 hours after inje

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

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

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

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

88 inactivation is tolerated by interfollicular epidermal cells but results in depletion of hair follicl

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

90 "self"-pollen is triggered within the stigma epidermal cell by allele-specific interaction between tw

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

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

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

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

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

96 Epidermal cell death correlated with the proximity to ro

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

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

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

100 release was delayed and outer cell walls of epidermal cells did not fragment.

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

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

103 Epidermal cell differentiation and skin tumor suppressio

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

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

106 Epidermal cell differentiation is a paramount and conser

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

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

109 erived dendritic cell/inflammatory dendritic epidermal cell differentiation.

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

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

112 The epidermal cells displayed a decreased tangential cell wi

113 normal in bulliform cell differentiation and epidermal cell division.

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

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

116 ne dinucleotide (NADH) fluorescence of human epidermal cells during arterial occlusion.

117 relates with changes in PIN1 polarization in epidermal cells during development.

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

119 During development, epidermal cell elongation and microtubule alignment occu

120 Selective lack of IL-15Ralpha on stromal epidermal cells exacerbated psoriasiform inflammation in

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

122 expressed Langerin, and >95% of Langerin(+) epidermal cells exhibited significant FITC signals.

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

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

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

126 mice in which non-dividing, differentiating epidermal cells express oncogenically activated MAPK kin

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

128 Most (>90%) of the FITC(+) epidermal cells expressed Langerin, and >95% of Langerin

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

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

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

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

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

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

135 Hence, reprogramming of epidermal cell fate by the volatile plant hormone ethyle

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

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

138 localization and its function in regulating epidermal cell fate.

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

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

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

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

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

144 Kdf1 is expressed in epidermal cells from early stages of epidermis formation

145 Epidermal cells from healthy skin were analyzed for thei

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

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

148 several phenotypes indicative of a defect in epidermal cell function, including reduced anthocyanin a

149 oles and rachises reduced in length, and the epidermal cells gained characteristics of motor organ ep

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

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

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

153 Plant epidermal cells have evolved specialist functions associ

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

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

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

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

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

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

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

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

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

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

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

165 changing the morphology and organization of epidermal cells in the leaf collar region.

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

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

168 s of fluorescently tagged AtGALT2 in tobacco epidermal cells indicated that AtGALT2 is probably local

169 Cytological analysis of internode epidermal cells indicates that SLs control cell number b

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

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

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

173 Instead, multiple cell types, including epidermal cells, intra-ray fibroblasts, and osteoblasts,

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

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

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

177 ature anther wall, which comprises the outer epidermal cell layer, whose turgor pressure is related t

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

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

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

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

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

183 2 fragment in maize mesophyll protoplasts or epidermal cells leads to a decrease in the delivery of P

184 usly down-regulate auxin responses in stigma epidermal cells, likely by regulating a mobile signal de

185 igenesis, pluripotent stem cell biology, and epidermal cell lineage decisions, labor and cost-intensi

186 eratinocytes are capable of committing to an epidermal cell lineage, but are likely to suffer from di

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

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

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

190 ranscription for plant cell pigmentation and epidermal cell morphology.

191 Exposure of epidermal cells not overlying a root to either force and

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

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

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

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

196 Guard cells and epidermal cells of hornworts show striking similarities

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

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

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

200 in pathways are spatially colocalized within epidermal cells of petals and temporally overlap in part

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

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

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

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

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

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

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

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

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

210 are able to induce stromule formation in the epidermal cells of tobacco hypocotyls and the root hairs

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

212 CD2 is preferentially expressed in epidermal cells of tomato stems and is a homolog of Arab

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

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

215 be positioned either at the basal surface of epidermal cells, or enclosed within epidermal invaginati

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

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

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

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

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

221 80B1 mutants, underscoring the aberrant root epidermal cell patterning.

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

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

224 Epidermal cells phagocytosed not only somatosensory axon

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

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

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

228 ns the circadian clock imposes regulation of epidermal cell proliferation so that skin is at a partic

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

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

231 tion drives tumor development by stimulating epidermal cell proliferation.

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

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

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

235 Remarkably, epidermal cells rather than professional phagocytes are

236 DP cells by interactions with hair follicle epidermal cells, rather than being derived from a distin

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

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

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

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

241 Epidermal cells secrete proteins and enzymes that assemb

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

243 Cultured epidermal cell sheets (CES) containing undifferentiated

244 vented through transplantation of autologous epidermal cell sheets or seeded decellularized biologica

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

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

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

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

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

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

251 y receptor cells within taste buds, and like epidermal cells, taste cells are regularly replaced thro

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

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

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

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

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

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

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

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

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

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

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

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

264 that the directional motile response of fish epidermal cells to the cathode in an electric field does

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

266 b), is a skin disease that exhibits impaired epidermal cell-to-cell adhesion and altered differentiat

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

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

269 Transient expression in onion epidermal cells, transformed with a 2x35S::ZmHyPRP-GFP c

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

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

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

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

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

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

276 t in vivo in transiently transformed tobacco epidermal cells using bimolecular fluorescence complemen

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

284 the cortex and during symmetric divisions of epidermal cells was constant and cells divided at a fair

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

286 Consequently, the number of epidermal cells was significantly reduced in these lines

287 ortical array of living Arabidopsis thaliana epidermal cells, we dissected the contribution of CP to

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

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

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

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

292 presence in stromules, not even in hypocotyl epidermal cells, which contain abundant stromules.

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