ライフサイエンスコーパス: cuticular

1 o such trends were observed for surficial or cuticular accumulation.

2 P4G102 provoked a decrease in the content of cuticular alkanes, which as an important fraction of cut

3 tent bias towards rapid loss of internal non-cuticular anatomy compared with recalcitrant cuticular a

4 cuticular anatomy compared with recalcitrant cuticular anatomy.

5 trast, engrailed RNAi in Oncopeltus produces cuticular and appendage defects similar to Drosophila.

6 portant components and organizers of the pre-cuticular and cuticular apical ECM, and adds to the smal

7 hese affected regions may have a role in the cuticular and the basement membrane extracellular matrix

8 ents and organizers of the pre-cuticular and cuticular apical ECM, and adds to the small but growing

9 Striking differences in cuticular architecture and quantities of cutin and waxes

10 acilitate the transmission of a GFP-labelled cuticular bacterium.

11 d in 80% ethanol, indicating a defect in the cuticular barrier.

12 oevolution of multiple mechanisms, including cuticular barriers, has occurred in highly pyrethroid-re

13 d spike surfaces, results from deposition of cuticular beta-diketone wax on their surfaces; this phen

14 th variants were more effective than hBF8 in cuticular bleeding and FeCl(3) carotid artery models.

15 However, in both a cuticular bleeding model and a cremaster laser arteriole

16 In a cuticular bleeding time study, these animals also had on

17 substrate for the synthesis of neuronal and cuticular catecholamines.

18 such as activation of ethylene biosynthesis, cuticular changes, and cell-wall loosening-changes that

19 ist of arthropods known to biosynthesize the cuticular chemicals of their deceived hosts to exploit t

20 Here, we show that the cuticular chemistry of Argentine ant workers, Linepithem

21 an eye to heeding the lessons of nature, the cuticular coatings of byssal threads from two species of

22 VAH and COX-2) and the other one was a novel cuticular collagen (Col-4).

23 served correlated response to selection upon cuticular colour and immune variables probably results f

24 Given that cuticular colour has a heritable component, we have take

25 Population level variation in cuticular colour has been linked to pathogen resistance

26 Cuticular colour in the mealworm beetle (Tenebrio molito

27 Cuticular colour is dependent upon melanin production, w

28 GA application increased levels of cuticular components but not trichome formation on gl1 p

29 defense such as biosynthetic precursors for cuticular components or the phytohormone jasmonic acid.

30 scripts revealed diminished cross-linking of cuticular components, further confirming the important r

31 ion tools, we tested the hypothesis that the cuticular compounds (Z)-10-tritriacontene and (Z)-6-pent

32 ration, reacting to and detoxifying specific cuticular compounds present on the host cuticle during t

33 at full turgor, turgor loss point (TLP), and cuticular conductance.

34 at night was on average 5 times greater than cuticular conductance.

35 e antibiotic-producing bacteria in elaborate cuticular crypts, supported by unique exocrine glands, a

36 ion of hb expression and results in variable cuticular defects in the mesothorax (T2) due to abnormal

37 This model also explains the cuticular demelanization effect resulting from AgNP sinc

38 -F1 is required for proper maturation of the cuticular denticles.

39 intact vs dried and ground leaves points to cuticular development - and not internal structural or b

40 tter understand species-level differences in cuticular development and composition.

41 ) through iridescent signals produced by its cuticular diffraction grating.

42 In the soft drusen (28 [70%]) and cuticular drusen (8 [20%]) groups, qAF8 levels within th

43 Drusen (LCD), Malattia Leventinese (ML), and Cuticular Drusen (CD).

44 drusen phenotype and 4 human donor eyes with cuticular drusen (n = 2), soft drusen (n = 1), and hard

45 hough the ultrastructural characteristics of cuticular drusen appear more similar to those of hard dr

46 Of eyes with more than 5 years of follow-up, cuticular drusen disappeared from view in 58.3% of eyes,

47 n multimodal imaging and the topography of a cuticular drusen distribution; age-dependent variations

48 um in 9 eyes (39.1%), SDD in 5 eyes (21.7%), cuticular drusen in 1 eye (4.3%) and no drusen were evid

49 drusenoid deposits (SDD) in 8 eyes (29.6%), cuticular drusen in 2 eye (7.4%) and no drusen were evid

50 Appearance of cuticular drusen in multimodal imaging and the topograph

51 atient characteristics, such as early onset, cuticular drusen on fluorescein angiography, and family

52 ants of final visual acuity in eyes with the cuticular drusen phenotype (both P < 0.015).

53 red forty eyes of 120 clinic patients with a cuticular drusen phenotype and 4 human donor eyes with c

54 Cuticular drusen phenotype may confer a unique risk for

55 d multimodal imaging data of patients with a cuticular drusen phenotype.

56 To define the range and life cycles of cuticular drusen phenotypes using multimodal imaging and

57 en distribution; age-dependent variations in cuticular drusen phenotypes, including the occurrence of

58 Small cuticular drusen typically demonstrated a homogenous ult

59 -17.1% [95% CI, -24.1% to -9.5%], P < .001; cuticular drusen, -19.6% [95% CI, -30.3% to -7.2%], P =

60 sis, drusen were categorized as soft drusen, cuticular drusen, and/or reticular pseudodrusen (RPD).

61 are commonly referred to as basal laminar or cuticular drusen.

62 basal contents was seen frequently in larger cuticular drusen.

63 to review the histologic characteristics of cuticular drusen.

64 ins contributing to the embryonic sheath and cuticular ECM.

65 val growth, despite being lined with a rigid cuticular ECM.

66 It is an important constituent of the cuticular exoskeleton that plays a key role in the insec

67 elegans to bacterial pathogens, revealing a cuticular function for AGMO-dependent lipid metabolism i

68 The nymphs, but not adults, have a row of cuticular gear (cog) teeth around the curved medial surf

69 o gene expression profiles revealed that the cuticular genes display biphasic expression during A. ga

70 The cuticular hairs and sensory bristles that decorate the a

71 manifested by an array of distally pointing cuticular hairs.

72 isolating individual MBCHs from the complex cuticular hydrocarbon (CHC) blends of insects, as well a

73 uticular layer and a significant increase in cuticular hydrocarbon (CHC) content ( approximately 29%)

74 eral mechanism for desiccation resistance is Cuticular Hydrocarbon (CHC) melting point.

75 ,11-C27 and -C29 dienes) and a change in the cuticular hydrocarbon blend.

76 Low volatility, lipid-like cuticular hydrocarbon pheromones produced by Drosophila

77 ed for a normal gustatory response to female cuticular hydrocarbon pheromones that modulate male cour

78 ith other males that secrete female-specific cuticular hydrocarbon pheromones, but not with females l

79 erine ant Harpegnathos saltator in detecting cuticular hydrocarbon pheromones.

80 spectrometry analyses reveal that the innate cuticular hydrocarbon profile of the mimic morph resembl

81 cVA is a major component of the male cuticular hydrocarbon profile, but it is not found on vi

82 ogue) caused workers to acquire a queen-like cuticular hydrocarbon profile, resulting in the overprod

83 Analysis of the female cuticular hydrocarbon profiles showed that corpora allat

84 onia giraulti with its own uniquely distinct cuticular hydrocarbon profiles, behavioral characteristi

85 found that (z)-7-tricosene, a male-enriched cuticular hydrocarbon that was previously shown to inhib

86 e genetic architecture of courtship song and cuticular hydrocarbon traits in two phygenetically disti

87 Cuticular hydrocarbons (CHC) have been successfully used

88 ns important in mediating eusocial behaviour.Cuticular hydrocarbons (CHC) mediate the interactions be

89 involving the transfer and homogenization of cuticular hydrocarbons (CHCs) across members of the colo

90 solution: females imbue males with their own cuticular hydrocarbons (CHCs) at mating and utilise chem

91 Drosophila cuticular hydrocarbons (CHCs) can function as pheromones

92 Cuticular hydrocarbons (CHCs) have two fundamental funct

93 Insect cuticular hydrocarbons (CHCs) prevent desiccation and se

94 The surface of insects is coated in cuticular hydrocarbons (CHCs); variations in the composi

95 Cuticular hydrocarbons (CHs) of species of the Drosophil

96 We show that methyl-branched cuticular hydrocarbons (mbCHCs) are a dual trait that af

97 of an aromatic compound (2-phenylundecane), cuticular hydrocarbons (pentacosane and heptacosane), fa

98 Six additional cuticular hydrocarbons also were identified.

99 o a broad array of compounds, including both cuticular hydrocarbons and general odorants that are lik

100 s of semiochemicals are described, including cuticular hydrocarbons and mandibular gland components t

101 By using the combined odors of forager cuticular hydrocarbons and of seeds, the colony captures

102 tory communication, such as the synthesis of cuticular hydrocarbons and the perception of environment

103 This provides the first direct evidence that cuticular hydrocarbons are the informational basis of po

104 Strong correlational evidence indicates that cuticular hydrocarbons are the means of identifying chea

105 Eusocial insects use cuticular hydrocarbons as components of pheromones that

106 their cuticle and the prevalence of smaller cuticular hydrocarbons compared with other species.

107 Decreasing sensillum responsiveness to cuticular hydrocarbons could potentially reduce mutually

108 resentative members and find they can detect cuticular hydrocarbons from different ant castes, with o

109 rward method for the isolation of individual cuticular hydrocarbons from the complex CHC blend.

110 r alkanes, which as an important fraction of cuticular hydrocarbons have been shown to confer desicca

111 to detection and discrimination of different cuticular hydrocarbons important in mediating eusocial b

112 sized that the accumulation of excess native cuticular hydrocarbons on the antennae would impair olfa

113 hila melanogaster, pheromones in the form of cuticular hydrocarbons play prominent roles in courtship

114 terproofing and that adult oenocytes produce cuticular hydrocarbons required for desiccation resistan

115 In many insect species, cuticular hydrocarbons serve as pheromones that can medi

116 ntennae accumulated three to four times more cuticular hydrocarbons than groomed antennae.

117 tive gustatory pheromone receptor for female cuticular hydrocarbons that stimulate male courtship.

118 ts employ specific, evolutionarily conserved cuticular hydrocarbons to signal their presence and inhi

119 reased courtship caused by depletion of male cuticular hydrocarbons was suppressed by a mutation in t

120 Cuticular hydrocarbons were sampled from the surface of

121 responses to general odors in comparison to cuticular hydrocarbons which can act as fertility signal

122 P450 reductase results in flies deficient in cuticular hydrocarbons, highly susceptible to desiccatio

123 nd spatial characterization of 28 species of cuticular hydrocarbons, including a new major class of o

124 oleic acid, the odor of the forager itself, cuticular hydrocarbons, or a combination of both with in

125 Ophrys exaltata employs chemical mimicry of cuticular hydrocarbons, particularly the 7-alkenes, in a

126 his reduction was associated with a shift in cuticular hydrocarbons, the chemical signatures used by

127 02 plays a critical role in the synthesis of cuticular hydrocarbons, which are important for cuticle

128 Moreover, these cells respond to cuticular hydrocarbons, with different cells selectively

129 ile hydrocarbon and non-volatile lipids with cuticular hydrocarbons.

130 o control females despite changes in certain cuticular hydrocarbons.

131 ical tool currently used to study Drosophila cuticular hydrocarbons.

132 ship behavior in response to female-specific cuticular hydrocarbons.

133 bon pheromones, but not with females lacking cuticular hydrocarbons.

134 on systems based on learned odors, typically cuticular hydrocarbons.

135 siological responses to several long-chained cuticular hydrocarbons.

136 ovide an excellent basis for future study of cuticular inflation function.

137 oscopy, we show for the first time that most cuticular inflations develop between the second and thir

138 acterise structure and suggest a function of cuticular inflations in the most tractable and widely-us

139 r-ventral projections of the cuticle termed "cuticular inflations", which are thought to be involved

140 icroscopy enabled ultrastructural imaging of cuticular inflations, and showed the presence of an addi

141 of building blocks forming the outer surface cuticular layer.

142 FOCL1-GFP localizes to the guard cell outer cuticular ledge and plants lacking FOCL1 produce stomata

143 ants lacking FOCL1 produce stomata without a cuticular ledge.

144 cts in stomata structure including a lack of cuticular ledges between guard cells, highlighting the i

145 membrane thickness over epidermal cells and cuticular ledges with increased occlusion of the stomata

146 s a strong pathogen barrier, regions lacking cuticular lining, such as the shrimp's excretory organ,

147 that antennal grooming removes excess native cuticular lipids and foreign chemicals that physically a

148 Within aggregations, however, cuticular lipids are disseminated by contact among group

149 and "contamination" of cockroaches with the cuticular lipids of another stage or sex may interfere w

150 Transcriptome and cuticular lipids profiling coupled with comprehensive mi

151 TRANSFERASE4, and the ATP-BINDING CASSETTE11 cuticular lipids transporter.

152 Cuticular lipids, both cutin monomers and cuticular waxe

153 a significant increase in the amount of leaf cuticular lipids.

154 ntact sex pheromone embedded in the female's cuticular lipids.

155 The cuticular mechanosensory neurons had only CsGABArdl and

156 monomer composition of the polyesters of the cuticular membrane has not been analyzed.

157 e therefore likely to be associated with the cuticular membrane.

158 of substantial amounts of dicarboxylates in cuticular membranes is unexpected.

159 on springtails presenting an overview on the cuticular morphology and chemistry and their biological

160 Its cuticular morphology and ultrastructure reject cycadalea

161 ects of the body plan, such as appendage and cuticular morphology.

162 gy for structural colouration in nature: the cuticular multilayer.

163 loss of nuclei in syncytial blastoderms, and cuticular pattern defects in late-stage embryos.

164 th) is needed to understand whether distinct cuticular patterns correlate with distinct chemical comp

165 orophyll-leaching assays, indicate increased cuticular permeability of pe leaves.

166 parent, and lacs1-1 lacs2-3 had much higher cuticular permeability than either parent.

167 ion, enhance drought tolerance, and modulate cuticular permeability when overexpressed in Arabidopsis

168 The cuticular phenotypes of cer9 are associated with delayed

169 0 lines for black and 10 lines for tan adult cuticular phenotypes over at least six generations and m

170 ecognizing group members via colony-specific cuticular pheromonal signatures.

171 Minor indications of stomatal and cuticular Pi uptake were also observed.

172 cribe, underlie, and are interwoven into the cuticular plate (CP), and they also encircle the basal b

173 eral wall and was not detected at the apical cuticular plate and basal region.

174 Prestin labeling was not found at the cuticular plate and stereocilia.

175 in 7 (LMO7) is specifically localized in the cuticular plate and the cell junction.

176 lower circumferences and separated from the cuticular plate by a dense cluster of exceptionally larg

177 In addition to the cuticular plate defects, older Lmo7 KO mice develop abno

178 Lmo7 KO mice suffer multiple cuticular plate deficiencies, including reduced filament

179 vely studied mechanosensory hair bundle, the cuticular plate is not as well understood.

180 the apical junctional complex and above the cuticular plate, a dense F-actin meshwork located undern

181 embrane of the hair cell from the underlying cuticular plate, and a severing of the hair-bundle's roo

182 arge mitochondria between its filaments, the cuticular plate, and plasma membrane--suggests that the

183 cell's apical membrane lifted away from the cuticular plate, and stereocilia elongated and fused.

184 n-rich structures in bundles, the underlying cuticular plate, and the circumferential actin belt.

185 ugh the ankle region to anchor them into the cuticular plate.

186 re embedded in a filamentous meshwork in the cuticular plate.

187 the apical surface, the hair bundle and the cuticular plate.

188 numbers of vesicles invaded the compromised cuticular plate.

189 In rda/rda mice, cuticular plates of utricle hair cells initially formed

190 ans in having a segmented body with repeated cuticular plates, longitudinal muscles, dorsoventral mus

191 odifications (e.g. preservation of esters or cuticular polysaccharides), which in combination with th

192 Cretaceous amber from Spain with specialized cuticular processes forming a dorsal basket that carry a

193 Fourteen types of sensilla and five types of cuticular processes were found on the mouthparts of nymp

194 larvae who nestle the trash among setigerous cuticular processes, known as trash-carrying, rendering

195 s of dpw3 plants exhibited unbalanced anther cuticular profile, abnormal Ubisch bodies, disrupted cal

196 emonstration that a mutation in a Drosophila cuticular protein gene alters overall morphology confirm

197 ected for rp2 P450s but not for a cluster of cuticular protein genes previously associated with resis

198 ion mechanism (consistent over-expression of cuticular protein genes) were associated with pyrethroid

199 explored in its microarchitecture and in the cuticular protein, mcfp-1.

200 s directly as a proteolytic enzyme degrading cuticular proteins before ecdysis and/or indirectly by p

201 in Anopheles gambiae that code for putative cuticular proteins in this CPR family, over 1% of the to

202 The most abundant family of insect cuticular proteins, the CPR family, is recognized by the

203 ntification of cellular growth, we find that cuticular ridge formation progresses down the sepal from

204 ::GFP-GUS reporter expression coincides with cuticular ridge formation, descending the sepal from tip

205 e acyltransferase6 (gpat6), and defective in cuticular ridges (dcr) were grouped in three separate cl

206 that CUS2 is crucial for the maintenance of cuticular ridges after they are formed.

207 Surprisingly, cuticular ridges at first form normally in the cus2 muta

208 2) mutant, which causes a great reduction in cuticular ridges on the mature sepal epidermis, but only

209 iled morphology and spatial relationships of cuticular sensilla and internal sensory receptors, are t

210 is fundamental for studying the relevance of cuticular strain information within the complex neuromus

211 While structural and/or cuticular structural functions were the only two enriche

212 ydration conditions, we demonstrate that the cuticular structure is highly porous and that the presen

213 In this study we examine the cuticular structure of the red alga Chondrus crispus (Ir

214 nce, we find that for all sexually dimorphic cuticular structures examined, ix and dsx are dependent

215 Numerous cuticular structures have been discovered this century;

216 a embryo and larva and provide templates for cuticular structures involved in larval locomotion.

217 ion is controlled by specialized, contiguous cuticular structures located at the junction between the

218 phila are the larval primordia for the adult cuticular structures of the adult fly.

219 re decorated with several types of polarized cuticular structures, such as hairs and bristles.

220 weedle proteins are incorporated into larval cuticular structures.

221 muli in the form of pigments, volatiles, and cuticular substances (hairs, waxes) derived from plant s

222 ability to bind to insect hemocytes and the cuticular surface of a nematode, H. bacteriophora.

223 the importance of two features of the outer cuticular surface of the beetle's wings: structural inte

224 scribed class of compounds on the Drosophila cuticular surface.

225 e expressed that bond the dorsal and ventral cuticular surfaces of the wing following migration of th

226 wn to have outcomes equivalent to those with cuticular suturing, it is unknown whether adhesive strip

227 The head capsule houses an anterior cuticular tentorium, a feature uniquely shared by myriap

228 ding for the formation of new epithelial and cuticular tissue.

229 We conclude that the cuticular transpiration barrier is primarily formed by t

230 racuticular waxes contributed equally to the cuticular transpiration barrier.

231 to compare water loss with and without added cuticular triterpenoids in Arabidopsis leaf waxes.

232 cavity that pull on and buckle stiff-ribbed cuticular tymbal membranes located beneath the folded wi

233 in some epidermal cells, indicating moderate cuticular uptake.

234 his phenotype is due to decreased amounts of cuticular water that is reported to modulate cuticle mec

235 Insects use hydrocarbons as cuticular waterproofing agents and as contact pheromones

236 ng important fruit quality traits, including cuticular wax accumulation and flavonoid biosynthesis, a

237 ow that this mutant is severely deficient in cuticular wax accumulation and has a reduced tolerance o

238 eover, the grooming behavior and presence of cuticular wax aids in the maintenance of superhydrophobi

239 These stress treatments led to increases in cuticular wax amount per unit area of 32% to 80%, due pr

240 the prevalence of C28 to C34 acyl lipids in cuticular wax and the pollen coat.

241 discovered a unique mechanism of regulating cuticular wax biosynthesis during Arabidopsis (Arabidops

242 exoribonuclease, is a positive regulator of cuticular wax biosynthesis in Arabidopsis (Arabidopsis t

243 e discovered a novel regulatory mechanism of cuticular wax biosynthesis that involves the ECERIFERUM7

244 aracterized clade of KCS enzymes involved in cuticular wax biosynthesis.

245 overlapping, if not redundant, functions in cuticular wax biosynthesis.

246 Cuticular wax composition greatly impacts plant response

247 Major cuticular wax compounds, such as very long-chain fatty a

248 Cuticular wax deposition and composition affects drought

249 implicating RNA silencing in the control of cuticular wax deposition during inflorescence stem devel

250 ype Columbia) led to significantly increased cuticular wax deposition on leaves of 4-week-old and 6-w

251 nt and we show that it exhibits reduced stem cuticular wax deposition, aberrant seed coat mucilage ex

252 ted light signaling during the regulation of cuticular wax deposition.

253 ry-long-chain fatty acids C24 and C26 in the cuticular wax fraction.

254 Cuticular wax is a mixture of aliphatic very-long-chain

255 genes affect the composition and quantity of cuticular wax is unclear.

256 During and after this elongation, the cuticular wax load and composition remain remarkably con

257 Total leaf cuticular wax load increased after each of three periods

258 5S promoter led to a significant increase in cuticular wax loading on leaves of transgenic alfalfa.

259 ehydration stress by characterizing the leaf cuticular wax of tree tobacco (Nicotiana glauca L. Graha

260 sense silencing of Arabidopsis REQUIRED FOR CUTICULAR WAX PRODUCTION1, the HvKCS6 ortholog, revealed

261 h cutin monomers and a dramatic shift in the cuticular wax profile (especially on leaves) toward the

262 The AtI-module is primarily involved with cuticular wax, the AtII-module with suberin and the AtII

263 he extracellular matrix for the formation of cuticular wax.

264 recruitment of unsaturated substrates to the cuticular wax.

265 ghly heritable traits, chaff color, and leaf cuticular wax.

266 In plants, the export of cuticular waxes and various cell wall components relies

267 opulus trichocarpa), revealing that the leaf cuticular waxes are predominantly composed of alkanes an

268 ituation on maize seedling leaves, where the cuticular waxes are primary alcohols and aldehydes.

269 Cuticular waxes are the major components of plant cuticl

270 Cuticular waxes are unusual secretory products, consisti

271 These findings highlight the crucial role of cuticular waxes as the first point of contact with the e

272 nfirmed variation in chemical composition of cuticular waxes between the berry species.

273 Cuticular waxes coat all primary aboveground plant organ

274 In addition, the silk cuticular waxes contain metabolically related unsaturate

275 The chemical composition of the cuticular waxes from gl8a and gl8b mutants indicates tha

276 e major components of flag leaf and peduncle cuticular waxes included primary alcohols, beta-diketone

277 ously shown to have a specific deficiency in cuticular waxes longer than 28 carbons, and heterologous

278 present study, composition and morphology of cuticular waxes of northern wild berry species bilberry

279 inally, metabolite profiling analyses of the cuticular waxes of two maize inbred lines (B73 and Mo17)

280 s) on the morphology and micro-structures of cuticular waxes on leaf surfaces was investigated.

281 are required for the normal accumulation of cuticular waxes on seedling leaves.

282 Plant cuticular waxes play a crucial role in limiting nonstoma

283 Transgenic alfalfa plants with increased cuticular waxes showed enhanced drought tolerance demons

284 ons constitute a large portion (>90%) of the cuticular waxes that coat this organ, which contrasts wi

285 -chain (VLC) alkanes are major components of cuticular waxes that cover aerial organs, mainly acting

286 minant compounds in bilberry and lingonberry cuticular waxes were triterpenoids, while fatty acids an

287 Plant aerial organs are coated with cuticular waxes, a hydrophobic layer that primarily serv

288 ain targeted metabolites were flavonoids and cuticular waxes, both of which are important in many asp

289 hain lengths of C(2)(8) or greater in flower cuticular waxes, but it has no impact on flower cuticle

290 Cuticular lipids, both cutin monomers and cuticular waxes, on rst1 leaves were significantly eleva

291 for LTPGs in the synthesis or deposition of cuticular waxes, suberin and sporopollenin.

292 ents of a variety of compounds, for example, cuticular waxes, suberin, and sphingolipids.

293 r composed of the cutin polyester matrix and cuticular waxes.

294 two major components, the polymer cutin and cuticular waxes.

295 -long-chain fatty acid (VLCFA) precursors of cuticular waxes.

296 ter matrix that is embedded and covered with cuticular waxes.

297 and free fatty acids as novel components of cuticular waxes.

298 enzyme may act in the synthesis of cutin or cuticular waxes.

299 had alterations in both cuticle membrane and cuticular waxes.

300 erences in the composition of leaf cutin and cuticular waxes.