ライフサイエンスコーパス: cucumber

1 elon genome compared with the close relative cucumber.

2 involved in resistance to biotic stresses in cucumber.

3 chromosome occurred during domestication of cucumber.

4 ependent on whether models received grape or cucumber.

5 In Phases 2 and 4, both were offered cucumber.

6 of FP and EFP in two cucurbits, pumpkin and cucumber.

7 systemic acquired resistance in tobacco and cucumber.

8 antagonistic impact on arsenate toxicity to cucumber.

9 terized in several plant species, but not in cucumber.

10 eous solution, and a recovery of 82-110%, in cucumber.

11 e evolution and the domestication history of cucumber.

12 . hardwickii is the progenitor of cultivated cucumber.

13 differentiation between wild and cultivated cucumbers.

14 nal specificity in pea 9/13-lipoxygenase and cucumber 13/9-lipoxygenase are different.

15 ch controlled dual positional specificity in cucumber 13/9-lipoxygenase, strongly suggests that the m

16 pple (5 mg dry weight), spirulina (5 mg), or cucumber (5 mg) either in 0.5 ml water by oral gavage or

17 The witness was then offered a slice of cucumber, a less preferred food.

18 ty outside the Brassicaceae, the intron from cucumber AG has at least partial activity in A. thaliana

19 representatives from another species of sea cucumber and from a sea urchin species.

20 limits of detection for the two bacteria in cucumber and hamburger extracts were determined to be 57

21 eteroptera: Miridae) are pests of glasshouse cucumber and sweet pepper crops respectively.

22 each polypeptide, but highly conserved when cucumber and sweet potato sequences are compared.

23 cur during intestine regeneration in the sea cucumber and that the onset of these changes is correlat

24 While the concentration of most PCs in cucumber and tomato leaves were of similar order, their

25 C uptake and translocation were evaluated in cucumber and tomato plants to elucidate the effects of P

26 nes in two distantly related plant families, cucumber and tomato, produced low-acid, bland tasting fr

27 enous tissue (MCT) of echinoderms (e.g., sea cucumbers and starfish) is a remarkable example of a bio

28 cohol compounds associated with 'mushroom', 'cucumber', and 'fatty-grassy' aroma characteristics, the

29 the more bitter-tasting vegetables (olives, cucumber, and broccoli) by the nontaster children (P < 0

30 e are the main contributors to the metallic, cucumber, and mushroom notes of the samples.

31 mately 26% sequence identity with the mango, cucumber, and rat peroxisomal thiolases.

32 flow primarily from the fascicular phloem in cucumber, and several other cucurbit species, but primar

33 ion in different surface water, grape juice, cucumber, and tomato samples.

34 carrot, squash, eggplant, radish, mushroom, cucumber, and tomato).

35 sed on different genetic distances to melon, cucumber, and watermelon in the Benincaseae tribe.

36 loci on chromosome 7 of cultivated and wild cucumbers, and the syntenic melon chromosome I suggested

37 of fruits and vegetables, including bananas, cucumbers, and tomatoes.

38 dentification of SALMFamide genes in the sea cucumber Apostichopus japonicus (class Holothuroidea) an

39 contraction have been discovered in the sea cucumber Apostichopus japonicus (Phylum Echinodermata; C

40 ely related to SnRK1a sequences expressed in cucumber, Arabidopsis thaliana, tobacco and potato.

41 e colinearity surrounding the watermelon and cucumber atp9 coding regions, and the much smaller water

42 Cucumber basic protein (CBP) is a PLT which has a relati

43 isible, EPR, and paramagnetic NMR spectra of cucumber basic protein (CBP), which is a plantacyanin.

44 ical thermal maxima parameter (CTM50) of the cucumber beetle (Diabrotica undecimpunctata), wolf spide

45 ne, which had been isolated from the striped cucumber beetle Acalymma vittatum.

46 ctive to the several species of diabroticite cucumber beetles and corn rootworms and is considered a

47 Cucumber beetles and wolf spiders were equally heat tole

48 as the virus spread through the fields, the cucumber beetles became increasingly concentrated upon t

49 over, the VRT had no effect on resistance to cucumber beetles or the incidence of wilt disease before

50 al wilt disease (a fatal disease vectored by cucumber beetles).

51 of the transgene on fitness, on herbivory by cucumber beetles, on the incidence of mosaic viruses, an

52 xic-anoxic sediments supported a greater sea cucumber biomass.

53 obtained were similar to those of melon and cucumber, but the phenolic contents were much higher.

54 In the large Cucurbitaceae genus Cucumis, cucumber (C. sativus) is the only species with 2n = 2x =

55 ms, we investigated chromosome synteny among cucumber, C. hystrix and melon using integrated and comp

56 ng melon (C. melo) and the sister species of cucumber, C. hystrix, have 2n = 2x = 24 chromosomes, imp

57 Previous results showing that cucumber C7 stayed largely intact during the entire evol

58 m among 5 types of vegetables (black olives, cucumbers, carrots, red pepper, and raw broccoli) to con

59 ituted by addition of salt-extracted rice or cucumber cell wall proteins.

60 alyze the acid-induced extension of isolated cucumber cell walls.

61 of CsHMA5.1 and CsHMA5.2 in the tonoplast of cucumber cells.

62 fe genotype, the less mature giving a green, cucumber character and lacking the sweet, fruity charact

63 Broken and reconstituted cucumber chloroplasts were unable to maintain Mg-chelata

64 atase, as it has been assayed only in intact cucumber chloroplasts.

65 chloroplasts was 3- to 4-fold higher than in cucumber chloroplasts.

66 trikingly different evolutionary fates, with cucumber chromosome C1 apparently resulting from inserti

67 centromeric region of translocated AK2/AK8, cucumber chromosome C3 originating from a Robertsonian-l

68 -like translocation between AK4 and AK6, and cucumber chromosome C5 originating from fusion of AK9 an

69 f 53 C. hystrix syntenic blocks on the seven cucumber chromosomes, and allow us to infer at least 59

70 e rearrangement events that led to the seven cucumber chromosomes, including five fusions, four trans

71 Collagen fibrils from sea cucumber (class Holothuroidea) dermis were previously fo

72 ular and biochemical characterization of two cucumber copper ATPases, CsHMA5.1 and CsHMA5.2, indicati

73 Transient expression assays in etiolated cucumber cotyledons indicate that the 315 bp fragment (-

74 1 or a cell elongation-related expansin from cucumber (CsExp1).

75 al strength in the mutable dermis of the sea cucumber Cucumaria frondosa.

76 Two cucumber ( Cucumis sativus L.) proteins, PCI6 (PABP-CT-i

77 s with arsenate toxicity was investigated in cucumber (Cucumis sativa L) using 10 contrasting soils.

78 Cucumber (Cucumis sativa) leaves infiltrated with Pseudo

79 Extension of heat-inactivated walls from cucumber (Cucumis sativus cv Burpee Pickler) hypocotyls

80 Sex determination in cucumber (Cucumis sativus L.) is controlled largely by t

81 ss mitigated by exogenous glutathione (GSH), cucumber (Cucumis sativus L.) seedlings were exposed to

82 ng proteins were detected in phloem sap from cucumber (Cucumis sativus) and lupin (Lupinus albus).

83 One of the four FRO genes in the melon and cucumber (Cucumis sativus) genomes was Fe-regulated, and

84 d network" model, we assessed the ability of cucumber (Cucumis sativus) hypocotyl walls to undergo cr

85 measure in vivo phloem transport velocity in cucumber (Cucumis sativus) plants during early seedling

86 Experiments using cucumber (Cucumis sativus) plants show that the shoot gr

87 In this study, hydroponically grown cucumber (Cucumis sativus) plants were aerially treated

88 (NPs) were evaluated in hydroponically grown cucumber (Cucumis sativus) plants.

89 nship between IAA and OGA activity in intact cucumber (Cucumis sativus) seedlings.

90 ed studies on pumpkin (Cucurbita maxima) and cucumber (Cucumis sativus) to determine the origin and c

91 Cucumber (Cucumis sativus) was grown under an artificial

92 cinnamyl alcohol dehydrogenases (CADs) from cucumber (Cucumis sativus) with low activity toward p-co

93 e report the 1685-kb mitochondrial genome of cucumber (Cucumis sativus).

94 ed from a cDNA library from RNA of senescing cucumber (Cucumis sativus, L.) cotyledons.

95 t the germination and sugar responses of the cucumber (Cucumis sativus, L.) malate synthase (Ms) gene

96 Cucumber, Cucumis sativus L. is the only taxon with 2n =

97 Apple and spirulina but not cucumber decreased MDA levels in the aged rats.

98 zinon successfully from aqueous solution and cucumber, demonstrating the potential of MISPE for rapid

99 ucture during in situ tensile testing of sea cucumber dermis, we investigate the ultrastructural mech

100 ed on collagen fibrils isolated from the sea cucumber dermis.

101 hed new light on two important stages in sea cucumber development.

102 Southern blot analysis with cucumber DNA shows a simple hybridisation pattern indica

103 udy, we identified 36 CsDof members from the cucumber draft genomes which could be classified into ei

104 Cucumber expansin antibody recognized a single protein b

105 on are shown to be complimentary to those of cucumber expansin.

106 cross-reacts with an antibody raised against cucumber expansin.

107 tomato walls in a fashion characteristic of cucumber expansins.

108 he features of these fibrils, and of the sea cucumber fibrils that have been described, is one in whi

109 idal, similar to those of vertebrate and sea cucumber fibrils.

110 As sea cucumber fisheries throughout the world succumb to overe

111 one strategy applied to the multispecies sea cucumber fishery in Australia's Great Barrier Reef Marin

112 pivotal role in the determination of sex in cucumber flowers.

113 the tomato fruit were much lower than in the cucumber fruit.

114 es, suggesting macromolecule modification of cucumber fruit.

115 ot analysis shows that the expression of the cucumber gene increases in cotyledons as they expand and

116 enomics and biochemistry, we identified nine cucumber genes in the pathway for biosynthesis of cucurb

117 The cucumber genome has a novel structure for plant mitochon

118 Whole-genome sequencing of the cucumber genome provides a new opportunity to advance ou

119 ly comprising 193 Mbp, or 53% of the 367 Mbp cucumber genome.

120 Cucumber green mottle mosaic virus (CGMMV) was first des

121 crease in proinflammatory cytokines, whereas cucumber had no effect, suggesting that one mechanism by

122 droitin sulfate (fCS) extracted from the sea cucumber Holothuria forskali is composed of the followin

123 generating intestine cDNA library of the sea cucumber Holothuria glaberrima.

124 ion of the enteric nervous system in the sea cucumber Holothuria glaberrima.

125 The sea cucumber Holothuria scabra was cultured on sediments und

126 The sea cucumber, Holothuria glaberrima, has the capacity to reg

127 g of candidate genes for several diseases in cucumber; however, the exact defence mechanisms remain u

128 Transcription of the cucumber hpr-A gene is responsive to cytokinin and light

129 Frozen-thawed cucumber hypocotyl segments were strained by 20-30% by i

130 alls and by its similarity to expansins from cucumber hypocotyls.

131 characteristics the acid-growth activity of cucumber hypocotyls.

132 in the intestine is overexpressed during sea cucumber intestinal regeneration.

133 Cucumber is vulnerable to many foliage diseases.

134 s triggered significant metabolic changes in cucumber leaves and root exudates.

135 values were most often exceeded in arugula, cucumber, lemon, and grape commodities.

136 Sea cucumbers, like other echinoderms, have the ability to r

137 lar beta-adrenergic receptor physiology, and cucumber (low ORAC) had no effect, indicating that the r

138 ant species: alfalfa, Arabidopsis, Brassica, cucumber, maize, and rice.

139 CGMMV) was first described in 1935 infecting cucumber, making it one of the first plant viruses to be

140 By comparative analyses of the genomes of cucumber, melon and watermelon, we uncovered conserved s

141 t confer a bitter taste in cucurbits such as cucumber, melon, watermelon, squash, and pumpkin.

142 m a variety of homogenized foods (hamburger, cucumber, milk, and lettuce) even after covalent attachm

143 Our results demonstrate that the expanded cucumber mitochondrial genome is in part due to extensiv

144 NA motifs accounted for >13% (194 kb) of the cucumber mitochondrial genome, equaling >50% of the size

145 ning 71.4% of the sequence was unique to the cucumber mitochondrial genome.

146 Coexpression of each enzyme with cucumber monogalactosyldiacylglycerol (MGDG) synthase in

147 re either mock inoculated or inoculated with cucumber mosaic cucumovirus, oil seed rape tobamovirus,

148 The cucumber mosaic virus (CMV) 2b protein suppresses RNA si

149 dopsis thaliana targeted during infection by cucumber mosaic virus (CMV) 2b protein, known to suppres

150 ous analysis of replicase recognition of the Cucumber mosaic virus (CMV) and BMV SLCs indicates that

151 A system already under use in field tests is cucumber mosaic virus (CMV) and its satellite RNAs.

152 se gene sequence from RNA-2 of strain Fny of cucumber mosaic virus (CMV) are resistant to systemic CM

153 Cucumber mosaic virus (CMV) comprises numerous isolates

154 onse (systemic necrosis) to seven strains of Cucumber mosaic virus (CMV) from pepper or tomato, but n

155 Cucumber mosaic virus (CMV) has been divided into two su

156 Resistance to Cucumber mosaic virus (CMV) in tobacco lines transformed

157 istance to infection in cowpea by strains of cucumber mosaic virus (CMV) involves a local, hypersensi

158 minent feature on the surfaces of virions of Cucumber mosaic virus (CMV) is a negatively charged loop

159 Cucumber mosaic virus (CMV) is a tripartite RNA virus th

160 Cucumber mosaic virus (CMV) is an RNA plant virus with a

161 g of 12 restriction enzyme marker mutants of Cucumber mosaic virus (CMV) onto young leaves of squash

162 ucture and genetic diversity of a California Cucumber mosaic virus (CMV) population was assessed by s

163 inants were observed in the progenies of the Cucumber mosaic virus (CMV) reassortant L(1)L(2)F(3) con

164 D satellite RNA (satRNA) is a strain of cucumber mosaic virus (CMV) satRNA that induces an epide

165 a and N. clevelandii coexpressing wt BMV and Cucumber mosaic virus (CMV) showed that despite trans-en

166 r maize based on a naturally maize-infecting cucumber mosaic virus (CMV) strain, ZMBJ-CMV.

167 ble for efficient and accurate initiation of cucumber mosaic virus (CMV) subgenomic RNA4.

168 Cucumber mosaic virus (CMV) systemically infects both to

169 n and deletion mutations of the replicase of Cucumber mosaic virus (CMV) was determined in planta by

170 e plant viruses, Tobacco mosaic virus (TMV), Cucumber mosaic virus (CMV), and Cowpea chlorotic mottle

171 s infected with potato virus Y (PVY) or with cucumber mosaic virus (CMV), but not in plants infected

172 e 3a movement protein (MP) of a plant virus, Cucumber mosaic virus (CMV), forms ribonucleoprotein (RN

173 the effects of a widespread plant pathogen, Cucumber mosaic virus (CMV), on the quality and attracti

174 as detected in another tripartite RNA virus, cucumber mosaic virus (CMV), suggesting that the 1a-1a i

175 Cucumber mosaic virus (CMV), the type member of the genu

176 We previously devised a cucumber mosaic virus (CMV)-based vector system carrying

177 Cucumber mosaic virus (CMV)-encoded 2b protein was among

178 ridae family, alfalfa mosaic virus (AMV) and cucumber mosaic virus (CMV).

179 the tripartite positive-strand RNA genome of cucumber mosaic virus (CMV).

180 tatus challenged with a generalist pathogen, Cucumber mosaic virus (CMV).

181 ad significantly reduced symptom severity by Cucumber mosaic virus (CMV).

182 Here, we describe a mutant of Cucumber mosaic virus (CMV-Delta2b) that is silenced pre

183 The structure of cucumber mosaic virus (CMV; strain Fny) has been determi

184 acco plants infected with the Fny isolate of Cucumber mosaic virus (Fny-CMV) that will direct synthes

185 Notably, the Cucumber mosaic virus 2b protein, shown previously to fu

186 ypersusceptible to TMV, turnip mosaic virus, cucumber mosaic virus and cauliflower mosaic virus as we

187 ts were infected with two different viruses, cucumber mosaic virus and oilseed rape mosaic virus.

188 s (members of Tobamovirus genus), but not to Cucumber mosaic virus and Potato virus X (members of dif

189 umulation of two other heterologous viruses: cucumber mosaic virus and tobacco mosaic virus.

190 ports describe that the 2b suppressor of the Cucumber mosaic virus binds ARGONAUTE and that the P0 su

191 Finally, the structure of cucumber mosaic virus bound to a loop involved in aphid

192 SDE5 also results in hyper-susceptibility to cucumber mosaic virus but not turnip mosaic virus.

193 However, a mixed infection of TYLCV with cucumber mosaic virus compromised the resistance.

194 s study, we used an artificial population of Cucumber mosaic virus consisting of 12 restriction enzym

195 c infection with cauliflower mosaic virus or cucumber mosaic virus did not induce the tryptophan path

196 tobacco, the 3a movement protein (3a MP) of Cucumber mosaic virus fused to green fluorescent protein

197 he tripartite viruses Brome mosaic virus and Cucumber mosaic virus have been shown to induce VIGS in

198 of plant potyviruses and the 2b gene of the cucumber mosaic virus have been shown to interfere with

199 Previous work using Tobacco mosaic virus and Cucumber mosaic virus indicated that evolutionarily rela

200 Symptom enhancement by the satRNA of Cucumber mosaic virus is caused by minus-strand inductio

201 Replication of the satellite RNA (satRNA) of Cucumber Mosaic Virus is dependent on replicase proteins

202 ic plus-strand initiation was specific since cucumber mosaic virus minus-strand RNA templates were un

203 Here, KN1 and the cucumber mosaic virus movement protein (CMV-MP) were use

204 nts showed enhanced susceptibility to either cucumber mosaic virus or oilseed rape mosaic virus based

205 Tobamovirus, but not Cucumber mosaic virus or Potato virus X, infection of N.

206 in Arabidopsis induced by expression of the Cucumber mosaic virus silencing suppressor protein 2b kn

207 nt of satellite RNA (satRNA) associated with Cucumber mosaic virus strain Q (Q-satRNA) has a propensi

208 ber viroid (PSTVd), a satRNA associated with Cucumber Mosaic Virus strain Q (Q-satRNA) has the propen

209 ript profile for RCY1-mediated resistance to cucumber mosaic virus strain Y (CMV-Y) in Arabidopsis.

210 exhibited enhanced disease susceptibility to cucumber mosaic virus when the virus-encoded function to

211 RNA (satRNA) with its helper virus, namely, cucumber mosaic virus, causes systemic necrosis in tomat

212 One of these proteins, the 2b protein of cucumber mosaic virus, prevents systemic spread of the s

213 A viruses, cowpea chlorotic mottle virus and cucumber mosaic virus.

214 ents showing strong hybridization signals to cucumber mtDNA and little or no signal to watermelon mtD

215 The cucumber mtDNA clones carried short (30-53 bp), repetiti

216 Sequence analysis of 136 kb of cucumber mtDNA revealed only 11.2% with significant homo

217 ce of AIM1 shows extensive similarity to the cucumber multifunctional protein involved in beta-oxidat

218 To identify host proteins present in the cucumber necrosis tombusvirus (CNV) replicase, we affini

219 ive template-dependent replicase complex for Cucumber necrosis tombusvirus (CNV), which is a plus-str

220 or a partially purified RdRp preparation of Cucumber necrosis tombusvirus.

221 y related Tomato bushy stunt virus (TBSV) or Cucumber necrosis virus (CNV) in a yeast model or in pla

222 Cucumber necrosis virus (CNV) is a member of the genus T

223 Cucumber necrosis virus (CNV) is a member of the genus T

224 Cucumber Necrosis Virus (CNV) is a member of the genus T

225 The replicase of Cucumber necrosis virus (CNV), a tombusvirus, contains t

226 nip crinkle virus, Tomato bushy stunt virus, Cucumber necrosis virus, and Potato virus X.

227 equences from diverse sources, including the cucumber nuclear and chloroplast genomes, viruses, and b

228 ented nettle (wild host) and a salad leaf of cucumber or sweet pepper, where the salad leaves had hig

229 Seq data to study the development of the sea cucumber Parastichopus parvimensis.

230 verse was not true, which suggested that the cucumber pellet was the component that lost activity dur

231 e typical fruit vegetables including tomato, cucumber, pepper under the greenhouse environment.

232 ferent pesticides and metabolites in tomato, cucumber, pepper, spinach, zucchini, grape, cherry, peac

233 to a test chamber in which 1 monkey received cucumber pieces for 20 min and the other received apple

234 bioavailability of acidic PCs for uptake by cucumber plants as compared to fresh water irrigation.

235 Here, the response of cucumber plants in hydroponic culture at early developme

236 ion access period (IAP) to inoculate CCYV on cucumber plants showed a transmission efficiency rate of

237 In this research, cucumber plants were cultivated for 150 days in sandy lo

238 under conditions which may occur in nature, cucumber plants were subjected to reduced light intensit

239 y by heterograft studies between pumpkin and cucumber plants, in which CmNACP transcripts were shown

240 ped multiple reaction monitoring methods for cucumber proteins that are representative markers for FP

241 nins) that affect body wall stiffness in sea cucumbers, providing a novel perspective on mechanisms o

242 l genome possessed no significant amounts of cucumber repetitive DNAs.

243 Holothurians, or sea cucumbers, respond to adverse stimuli by autotomizing an

244 eased sequestration of copper in vacuoles of cucumber root cells under copper excess.

245 of the sugar response employed a transgenic cucumber root system.

246 When cucumber roots are excised and incubated without a carbo

247 emale L. rugulipennis spent more time on the cucumber salad host, and chose it first most often, but

248 , were obtained when strawberry, tomato, and cucumber samples spiked with trifloxystrobin were analys

249 and Salmonella sp. in complex hamburger and cucumber samples with extraordinary sensitivity and spec

250 NACP transcripts were shown to accumulate in cucumber scion phloem and apical tissues.

251 results suggest that exogenous GSH enhances cucumber seedling tolerance of HT stress by modulating t

252 otein extract from the cell walls of growing cucumber seedlings possessed the ability to induce the e

253 capuchin monkeys are more likely to reject a cucumber slice after seeing that another capuchin has re

254 led novel transcripts that are unique to sea cucumber, some of which we have experimentally validated

255 The possibility that the cucumber SPF1-type protein may be involved in carbohydra

256 The low reduction potential of cucumber stellacyanin is due mainly to a glutamine ligan

257 ction potentials of six type-1 copper sites (cucumber stellacyanin, P. aeruginosa azurin, poplar plas

258 es by 30-70% on tomato, rice, tea, broccoli, cucumber, strawberry, and other plants when treated exte

259 o 32-kD proteins in glyoxysomal membranes of cucumber, sunflower, castor bean, and cotton indicate th

260 However, the cucumber supernatant fraction was active when combined w

261 and intensive crops, such as tomato, potato, cucumber, sweet pepper, carrot, and grapevine.

262 re offered vegetables: either a single type (cucumber, sweet pepper, or tomato) or a variety of all 3

263 support the sub-species status of these two cucumber taxa, and suggest that C. sativus var. hardwick

264 Our experiments on cucumber tendrils demonstrate that tendril coiling occur

265 sea urchin), Holothuria forskali Chiaje (sea cucumber), the gastropod molluscs Aplysia fasciata Poire

266 When models were offered cucumber, they rejected it at higher rates than did witn

267 The acrosomal process of the sea cucumber Thyone briareus can extend 90 microm in 10 s, b

268 served in the acrosomal reactions of the sea cucumber Thyone, and the horseshoe crab Limulus.

269 example of the acrosomal reaction in the sea cucumber Thyone, whose filopodia can grow remarkably qui

270 entration of diazinon from aqueous media and cucumber tissue.

271 absorbed Ti was present as TiO(2) within the cucumber tissues, demonstrating that the TiO(2) NPs were

272 e the major pectins or hemicelluloses of the cucumber wall.

273 y, a high-density genetic map for cultivated cucumber was developed that contained 735 marker loci in

274 k region) and shoot-root junction regions of cucumber, watermelon and pumpkin.

275 Following pectinase treatment of cucumber, we observed the rapid accumulation of p-coumar

276 Witness rejections of cucumber were infrequent and were not dependent on wheth

277 il specimens isolated from the dermis of sea cucumbers were obtained in vitro.

278 howed root-to-fruit translocation of TiO2 in cucumber without biotransformation.