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 lls called seam cells generates a pattern of cuticular alae in anterior body regions and neural sensi

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

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

5 cuticular anatomy compared with recalcitrant cuticular anatomy.

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

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

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

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

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

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

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

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

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

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

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

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

18 substrate for the synthesis of neuronal and cuticular catecholamines.

19 ding the heliotrope rash, Gottron's papules, cuticular changes including periungual telangiectasia, a

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

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

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

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

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

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

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

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

28 Cuticular colour in the mealworm beetle (Tenebrio molito

29 Cuticular colour is dependent upon melanin production, w

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

47 Appearance of cuticular drusen in multimodal imaging and the topograph

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

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

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

51 Cuticular drusen phenotype may confer a unique risk for

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

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

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

55 Small cuticular drusen typically demonstrated a homogenous ult

56 -17.1% [95% CI, -24.1% to -9.5%], P < .001; cuticular drusen, -19.6% [95% CI, -30.3% to -7.2%], P =

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

58 to review the histologic characteristics of cuticular drusen.

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

60 taining was evident in RPE cells adjacent to cuticular drusen.

61 basal contents was seen frequently in larger cuticular drusen.

62 ins contributing to the embryonic sheath and cuticular ECM.

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

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

65 ne residues involved in the stabilization of cuticular extracellular matrix.

66 abdominal pouches, densely packed with fine cuticular filaments, which in alkaloid-fed males are alk

67 We propose that the cuticular folding of the eye stalk as well as the coilin

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

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

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

71 The cuticular hairs and sensory bristles that decorate the a

72 cell outline, and in the size and number of cuticular hairs secreted by each cell.

73 manifested by an array of distally pointing cuticular hairs.

74 The cuticular hydrocarbon (CH) pheromones in Drosophila mela

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

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

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

78 ,11-C27 and -C29 dienes) and a change in the cuticular hydrocarbon blend.

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

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

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

82 erine ant Harpegnathos saltator in detecting cuticular hydrocarbon pheromones.

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

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

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

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

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

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

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

90 Cuticular hydrocarbons (CHC) have been successfully used

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

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

93 Drosophila cuticular hydrocarbons (CHCs) can function as pheromones

94 Insect cuticular hydrocarbons (CHCs) prevent desiccation and se

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 Six additional cuticular hydrocarbons also were identified.

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

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

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

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

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

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

104 Eusocial insects use cuticular hydrocarbons as components of pheromones that

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

106 Decreasing sensillum responsiveness to cuticular hydrocarbons could potentially reduce mutually

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

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

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

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

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

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

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

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

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

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

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

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

119 Cuticular hydrocarbons were sampled from the surface of

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

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

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

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

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

125 02 plays a critical role in the synthesis of cuticular hydrocarbons, which are important for cuticle

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

127 o control females despite changes in certain cuticular hydrocarbons.

128 siological responses to several long-chained cuticular hydrocarbons.

129 ical tool currently used to study Drosophila cuticular hydrocarbons.

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

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

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

133 sechellia and D. mauritiana differ in their cuticular hydrocarbons: the predominant compound in D. s

134 of building blocks forming the outer surface cuticular layer.

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

136 ants lacking FOCL1 produce stomata without a cuticular ledge.

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

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

139 pede's body cavity by the glands' impervious cuticular lining.

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

141 Transcriptome and cuticular lipids profiling coupled with comprehensive mi

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

143 Cuticular lipids, both cutin monomers and cuticular waxe

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

145 g T2 denticle pattern, and it can rescue the cuticular loss-of-function phenotype of Antp mutants.

146 etween the apical epithelial surface and the cuticular matrix.

147 The cuticular mechanosensory neurons had only CsGABArdl and

148 several genes are known to be necessary for cuticular melanization, but the involvement of these gen

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

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

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

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

153 zygotic embryonic lethal mutations affecting cuticular morphology in Nasonia vitripennis (Hymenoptera

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

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

156 We describe 74 of >100 lines with embryonic cuticular mutant phenotypes, including representatives o

157 ts and the plasma membrane bordering the sub-cuticular oil storage cavity, often contains densely sta

158 s with the separation and filling of the sub-cuticular oil storage space, the maturation of glandular

159 esised function of LTPs in the deposition of cuticular or epicuticular waxes.

160 ytic enzyme in the processing/degradation of cuticular or other proteins.

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

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

163 These results suggest that cell wall and cuticular permeability may be important determinants in

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

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

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

167 ne show significant changes in cell wall and cuticular permeability.

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

171 primarily localized in vesicles beneath the cuticular plate 27 h postinjection; (2) the number of ve

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

173 myosin XV protein is concentrated within the cuticular plate and stereocilia of cochlear sensory hair

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

175 tween (but not associated with) actin of the cuticular plate and the circumferential belt.

176 stic probe was attached to the cell near the cuticular plate and the other end of the cell was held w

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

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

179 In the cuticular plate, a meshwork of actin filaments, myosin-I

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

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

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

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

184 numbers of vesicles invaded the compromised cuticular plate.

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

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

187 occurred at stereocilia bases, close to the cuticular plate.

188 in adaptation; concentration of myosin-VI in cuticular plates and association with stereociliary root

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

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

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

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

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

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

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

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

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

200 -N cross-links between histidine residues in cuticular proteins, and both ring and side-chain carbons

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

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

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

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

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

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

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

208 ese faecal structures and preserves even the cuticular scale pattern on individual hair.

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

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

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

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

213 y and function during the various changes in cuticular structure which accompany nematode growth and

214 In Drosophila all adult epithelial cuticular structures are polarized within the plane, whe

215 These cuticular structures are produced by cytoskeletal-mediat

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

217 for drought, we present evidence that these cuticular structures function to maintain photosynthetic

218 Numerous cuticular structures have been discovered this century;

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

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

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

222 rtment cells to specify the various types of cuticular structures that they differentiate.

223 ferentiate properly: the alae, seam-specific cuticular structures, are generally absent and expressio

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

225 weedle proteins are incorporated into larval cuticular structures.

226 ontacts between neuronal sensory endings and cuticular structures.

227 in the altered polarity of adult Drosophila cuticular structures.

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

229 f aesthetascs that have yet to emerge on the cuticular surface and thereafter decreases gradually and

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

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

232 dermal hairs that decorate much of the adult cuticular surface, the shafts of the bristle sense organ

233 scribed class of compounds on the Drosophila cuticular surface.

234 ch wing has expanded, the dorsal and ventral cuticular surfaces bonding to one another to form the ma

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

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

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

238 racuticular waxes contributed equally to the cuticular transpiration barrier.

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

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

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

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

243 activity of the CER2 promoter in hypocotyls, cuticular wax accumulates on this organ in a CER2-depend

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

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

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

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

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

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

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

251 Cuticular wax composition greatly impacts plant response

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

253 Cuticular wax deposition and composition affects drought

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

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

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

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

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

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

260 5S promoter led to a significant increase in cuticular wax loading on leaves of transgenic alfalfa.

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

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

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

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

265 he extracellular matrix for the formation of cuticular wax.

266 recruitment of unsaturated substrates to the cuticular wax.

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

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

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

270 Cuticular waxes are the major components of plant cuticl

271 Cuticular waxes are unusual secretory products, consisti

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

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

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

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

281 y and qualitatively affect the deposition of cuticular waxes on the surface of 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 ain targeted metabolites were flavonoids and cuticular waxes, both of which are important in many asp

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

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

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

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

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

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

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

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

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

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

297 had alterations in both cuticle membrane and cuticular waxes.

298 mount and alters the composition of seedling cuticular waxes.

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

300 The adult cuticular wing of Drosophila is covered by an array of d