ライフサイエンスコーパス: cotton

1 hat regulates the drought stress response in cotton.

2 a reference-grade genome assembly for Upland cotton.

3 nate and define the leaf shape of cultivated cotton.

4 (G-LSR2) in Vd991 were less virulent only on cotton.

5 cloth, respectively, than when covered with cotton.

6 R express at various developmental stages of cotton.

7 1Ab/Cry2Ae/Vip3A, and the single-gene Cry2Ae cotton.

8 greater sorption of polar compounds to polar cotton.

9 wide characterization of this gene family in cotton.

10 erved in transgenic cotton than conventional cotton.

11 relative to separate blocks of Bt and non-Bt cotton.

12 concentrations in the roots of conventional cotton.

13 en and ruptured, especially in Bt-transgenic cotton.

14 in a seed mixture relative to a block of Bt cotton.

15 factor of 610 (0.055% w/w blood solids) for cotton.

16 is responsible for the major leaf shapes in cotton.

17 h eventually may compromise the future of Bt cotton.

18 we characterize AS in the polyploid species cotton.

19 egy for the management of plant bug pests of cotton.

20 ), is among the most devastating diseases in cotton.

21 COL2 is an epiallele in allotetraploid cottons.

22 nutrients on conventional and Bt-transgenic cottons.

23 a dual domestication processes in tetraploid cottons.

24 pended on the distance between GM and non-GM cottons; (3) total PGF to Shiyuan321 (8.61%) was higher

25 A and GhMYB25-like D, which were encoded by cotton A subgenome and the D subgenome, respectively, wa

26 Expression validation in different cotton accessions and coexpression network construction

27 We resequence the genomes of 147 cotton accessions, including diverse wild relatives, lan

28 variation map for 352 wild and domesticated cotton accessions.

29 both toxins could prolong the efficacy of Bt cotton against this pest in China.

30 ton lineage of an ancestral genome common to cotton and cacao, and proposed evolutionary models to sh

31 orm to support further studies in and beyond cotton and genomics communities.

32 derstanding of the disease and resistance in cotton and may facilitate the development cotton with im

33 ntributed significantly to its adaptation to cotton and may represent a significant mechanism in the

34 ally and refuges are scarce, as seen with Bt cotton and pink bollworm in India.

35 Over 30 days cotton and polyester fabrics accumulated 3475 and 1950 n

36 Chemical release from cotton and polyester to laundry water was >80% of alipha

37 Here, cotton and polyester-cotton fabrics were sonochemically

38 Analyses of cotton and rapeseed datasets showed that more additive-b

39 he reference-grade assembly of allopolyploid cotton and serve as a general strategy for sequencing ot

40 ted cytosines in domesticated allotetraploid cottons and their tetraploid and diploid relatives.

41 sub genome anchored physical maps of Upland cotton, and a new-generation approach to the whole-genom

42 ich is highly virulent on its original host, cotton, and performed comparisons with the reference gen

43 lter monopodial apices, implying that once a cotton apex is SP-determined, it cannot be reset by flor

44 In particular, many crop species such as cotton are difficult to regenerate.

45 Cotton attire worn by the Teotihuacan elite may have bee

46 63 eyes (22%) and divided into 3 categories: cotton ball sign (defined as a fuzzy hyperreflective are

47 l acuity was highest in association with the cotton ball sign and lowest in the acquired vitelliform

48 The cotton ball sign, foveolar detachment, and acquired vite

49 and domestication history of allotetraploid cottons based on the whole genomic variation between G.

50 (Xcm) are essential for bacterial blight of cotton (BBC).

51 nduced by hot pepper fruits and repressed by cotton bolls in H. assulta.

52 istant strain survived on field-collected Bt cotton bolls producing both toxins.

53 racteristics of cotton plants in response to cotton bollworm (CBW; Helicoverpa armigera) larvae infes

54 ng with data from a four-year field study of cotton bollworm (Helicoverpa armigera) resistance to tra

55 The cotton bollworm, Helicoverpa armigera, has developed str

56 nducted laboratory diet experiments with the cotton bollworm, Helicoverpa armigera, to evaluate cross

57 ific DNA mutation is the long-term dream for cotton breeding scientists.

58 er eyelids and sweeping of the fornices with cotton buds, and maintaining clinical suspicion of conta

59 ulted in significantly enhanced virulence on cotton but did not affect virulence on tomato or lettuce

60 d silenced, while COL2D is repressed in wild cottons but highly expressed due to methylation loss in

61 us is not only of agricultural importance in cotton, but through pioneering chimeric and morphometric

62 a systematic investigation, a novel graphene/cotton-carbon cathode is presented here that enables sul

63 The graphene/cotton-carbon cathodes deliver peak capacities of 926 an

64 isplayed strong ties to the Gulf Coast where cotton cloth was made.

65 Pyramided cotton containing Cry1Ac/Cry1F was effective against SS

66 iperda were all susceptible to the pyramided cotton containing Cry1Ac/Cry2Ab, Cry1Ac/Cry1F/Vip3A, Cry

67 eractions between two toxins in pyramided Bt cotton (Cry1Ac and Cry2Ab).

68 olerant cotton cultivars than in susceptible cotton cultivars after inoculation with V. dahliae.

69 s all showed higher accumulation in tolerant cotton cultivars than in susceptible cotton cultivars af

70 different fiber development stages in upland cotton cv BM-1.

71 5 putative R2R3-MYB genes were identified in cotton D genome (Gossypium raimondii), that are much lar

72 Gene loss following cotton decaploidy has largely just reduced gene copy num

73 ol-5-yl urea, TDZ), formerly registered as a cotton defoliant, is a well known inhibitor of cytokinin

74 xpression, and repressing COL2 in cultivated cotton delays flowering.

75 enabled unprecedented functional analysis of cotton development.

76 velop and map new CAPS and dCAPS markers for cotton developmental-regulatory genes that are important

77 SFT and SP influenced cotton domestication and are ideal targets for further a

78 GhDREB2, that is involved in controlling the cotton drought response.

79 porphyrin), which is detected as a bisignate Cotton Effect (ECCD).

80 Circular dichroism spectroscopy shows strong Cotton effects (Deltaepsilon = +/-100 M(-1) cm(-1) at 30

81 ution with the nonpolar solvent, the intense Cotton effects are recovered, thus proving a reversible

82 Cotton effects characteristic of the aryl groups organiz

83 could determine the signs of the individual Cotton effects has been considered.

84 substrate immediately gives rise to intense Cotton effects in the visible region.

85 The substrate binding yields characteristic Cotton effects that provide information about the target

86 ic signatures of domestication traits during cotton evolution.

87 Transgenic cotton expressing the variant protein, Cry51Aa2.834_16,

88 fuse reflection DLs for blood on acrylic and cotton fabrics were in the mid-IR spectral window corres

89 Here, cotton and polyester-cotton fabrics were sonochemically coated with zinc oxid

90 hemically modified starch sizes on polyester/cotton fabrics, and had relative weaving efficiency simi

91 uman plasma samples from orchard workers and cotton farmers with long-term exposure to organophosphor

92 cal data when planning strategies to improve cotton farming in India.

93 nvolvement of ethylene in the development of cotton fiber cells.

94 Mature cotton fiber consists of nearly pure cellulose.

95 the potential regulatory roles of miRNAs in cotton fiber development and the importance of miRNAs in

96 The role of microRNAs (miRNAs) during cotton fiber development remains unclear.

97 ta indicate significant roles of laccases in cotton fiber development, and presents an excellent oppo

98 s that TCP genes may play important roles in cotton fiber development.

99 se miRNAs, which are potentially involved in cotton fiber development.

100 s but little is known how microRNAs regulate cotton fiber development.

101 n factor genes are specifically expressed in cotton fiber during different developmental stages, incl

102 n wildtype Xu-142, 26 miRNAs are involved in cotton fiber initiation and 48 miRNAs are related to pri

103 ng different developmental stages, including cotton fiber initiation and early development.

104 Among 54 miRNAs, 18 miRNAs were involved in cotton fiber initiation and eight miRNAs were related to

105 nsights into regulatory processes underlying cotton fiber initiation.

106 The economic value of cotton fiber lies in its length and quality.

107 Further, analysis of cotton fiber phenolic compounds showed an overall decrea

108 and distinct supramolecular structure of the cotton fiber provided a favorable environment for the co

109 ion in plants and could play crucial role in cotton fiber quality.

110 g of allopolyploidy, which will help improve cotton fiber quality.

111 Overall, the results reveal diverse cotton fiber tip morphologies and support primary wall s

112 nanoparticles throughout an entire volume of cotton fiber.

113 nforced the multilayered architecture of the cotton fiber.

114 Using a well-studied cotton fiberless mutant Xu-142-fl, we compared 54 miRNAs

115 Cotton fibers arise through highly anisotropic expansion

116 be encouraged to 'self-fumigate' nests with cotton fibers that have been treated with permethrin.

117 ivity and biochemical analysis of developing cotton fibers was performed using G. arboreum species.

118 The single-celled cotton fibers, produced from seed coat epidermal cells a

119 mary and secondary cellulose biosynthesis of cotton fibre in a "relay race"-like fashion.

120 ral functional lncRNA candidates involved in cotton fibre initiation and elongation.

121 hirsutum contributes the most production of cotton fibre, but G. barbadense is valued for its better

122 lignin metabolism in domesticated tetraploid cotton fibres.

123 plex in Pakistan, CLCuD affected plants from cotton fields at Vehari were collected.

124 could have contributed to the suitability of cotton for cultivation worldwide.

125 raploid genome is one of major challenges in cotton for repressing gene expression.

126 , D-genome) of the allopolyploid (AD-genome) cottons, G. hirsutum and G. barbadense.

127 mbled to direct Cas9-mediated allotetraploid cotton genome editing.

128 rating DNA level mutations on allotetraploid cotton genome with high-efficiency and high-specificity.

129 targeted knockout of a gene residing in the cotton genome.

130 chromes and/or HY5 gene (s) into G. hirsutum cotton genotypes or vice versa.

131 tractive hybridisation and cDNA libraries of cotton genotypes tolerant to Verticillium wilt and was i

132 n levels were varied through manipulation of cotton Golgi-related (CGR) 2 or 3 genes encoding two fun

133 ins and an unrelated plant-specific protein, cotton Golgi-related 3 (CGR3), in pectin methylesterific

134 er farmers compared with growing the Asiatic cotton Gossypium arboreum L.

135 American cotton (Gossypium hirsutum L.), transformed with Bacillu

136 Here, we investigated the role of a cotton (Gossypium hirsutum) actin gene in the organizati

137 Domestication of upland cotton (Gossypium hirsutum) converted it from a lanky ph

138 We used cotton (Gossypium hirsutum) fibers that underwent robust

139 Upland cotton (Gossypium hirsutum) has long been an important e

140 pecies, including wheat (Triticum aestivum), cotton (Gossypium hirsutum), and soybean (Glycine max),

141 5, miRNVL5) with its target gene GhCHR from cotton (Gossypium hirsutum).

142 Drought is a key limiting factor for cotton (Gossypium spp.) production, as more than half of

143 The reference genome sequence for cotton (Gossypium spp.) revealed a ploidy change of a co

144 molecular mechanisms of fiber initiation in cotton (Gossypium spp.), an integrated approach combinin

145 entification of lncRNAs has been reported in cotton (Gossypium spp.).

146 the two cultivated species of allopolyploid cotton, Gossypium barbadense produces extra-long fibers

147 m, and concomitantly graded according to the Cotton grading system.

148 Cotton has been cultivated and used to make fabrics for

149 mically important plants including wheat and cotton have more than two copies of each chromosome.

150 for 26% of maize, 43% of soybean and 45% of cotton herbicide applications.

151 ng its use by breeders to produce a superior cotton ideotype.

152 Leaf shape played a unique role in cotton improvement, as breeders have selected for entire

153 ld serve as a rich resource for genome-based cotton improvement.

154 king insects, have emerged as major pests of cotton in China.

155 e emerged as economically important pests of cotton in the United States.

156 Vd991 were higher during the early stages of cotton infection, as compared with other hosts.

157 Upland cotton is a model for polyploid crop domestication and t

158 e of many agricultural crops, the cultivated cotton is an allotetraploid and has a large genome ( 2.5

159 Cotton is an important crop that is grown mainly for its

160 Cotton is one of the most important textile crops but li

161 Most of the commercially-grown cotton is tetraploid, thus making it much more difficult

162 an virus, Cotton leaf curl Kokhran virus and Cotton leaf curl Alabad virus, several distinct species

163 The first epidemic of cotton leaf curl disease (CLCuD) in early 1990's in the

164 Cotton leaf curl disease (CLCuD), caused by cotton leaf

165 rst epidemic; Cotton leaf curl Multan virus, Cotton leaf curl Kokhran virus and Cotton leaf curl Alab

166 mbinant begomovirus named Burewala strain of Cotton leaf curl Kokhran virus that lacks a full complem

167 eral distinct species of alphasatellites and cotton leaf curl Multan betasatellite were found associa

168 ruses characterized from the first epidemic; Cotton leaf curl Multan virus, Cotton leaf curl Kokhran

169 Cotton leaf curl disease (CLCuD), caused by cotton leaf curl viruses (CLCuVs), is among the most dev

170 In cotton leaves, simultaneous measurement of carbon and ox

171 PD was induced by cotton ligature around the maxillary left first molars (

172 , animals of groups EP and EP-HN019 received cotton ligatures around mandibular first molars (MFMs).

173 enome of cotton, we made use of a transgenic cotton line previously generated in our laboratory that

174 ches, we revealed a 5x multiplication in the cotton lineage of an ancestral genome common to cotton a

175 In contained field trials, the transgenic cotton lines significantly suppressed the development of

176 provides a resource for engineering superior cotton lines.

177 ngated single-celled trichomes that comprise cotton lint fibers.

178 u I dCAPS, and one HY5-specific Hinf I dCAPS cotton markers were developed.

179 tin are resistant to Phenacoccus solenopsis (cotton mealybug), Myzus persicae (green peach aphids) an

180 amples were prepared by dip-coating acrylic, cotton, nylon, and polyester fabrics from solutions of d

181 Ebola-positive body fluid-impregnated cotton pads were serially sampled.

182 phocoris suturalis, which is one of the main cotton pests found in the 31 locations in China and Japa

183 s study detailed the genome mapping of three cotton phytochrome genes with newly developed CAPS and d

184 help us target important native genes in the cotton plant in future.

185 any other genome editing technologies in the cotton plant.

186 exin were distinctly lower in GhPAO-silenced cotton plants after V. dahliae infection.

187 se response that insect herbivory trigger in cotton plants and how defense mechanisms are orchestrate

188 However, transgenic cotton plants expressing this protein did not exhibit ef

189 tome changes and volatile characteristics of cotton plants in response to cotton bollworm (CBW; Helic

190 The proportion of larvae on non-Bt cotton plants in the seed mixture was also significantly

191 for devastating wilt diseases in many crops) cotton plants increase production of microRNA 166 (miR16

192 s revealed that CBW infestation could induce cotton plants to release volatile compounds comprised li

193 Responding to CBW larvae infestation, cotton plants undergo drastic reprogramming of the trans

194 eaves of both conventional and Bt-transgenic cotton plants via xylem sap.

195 tion system for the generation of transgenic cotton plants with equal or higher transformation effici

196 ient and simple means to generate transgenic cotton plants, but also helps address many of the concer

197 of A. suturalis was expressed in transgenic cotton plants.

198 exhibited drastically enhanced virulence in cotton plants.

199 or transformed cells and generate transgenic cotton plants.

200 cytochrome P450 proteins in Arabidopsis and cotton plants.

201 Recombinant cotton polyamine oxidase (GhPAO) was found to catalyse t

202 gned to filter macromolecules, and the inner cotton portion was designed to absorb cervicovaginal flu

203 from greenhouse experiments with transgenic cotton producing Bt toxin Cry1Ac and the bollworm, Helic

204 licoverpa armigera) resistance to transgenic cotton producing Bt toxin Cry1Ac in six provinces of nor

205 but field-evolved practical resistance to Bt cotton producing Cry1Ac has occurred widely in India.

206 Switching to Bt cotton producing two or more toxins and integrating othe

207 results provide genomic bases for improving cotton production and for further evolution analysis of

208 e on three single-gene and five pyramided Bt cotton products.

209 SNPs of known genomic location in tetraploid cotton provided unique opportunities to characterize gen

210 ity of these loci to fiber quality and other cotton QTL was demonstrated in two A-subgenome and one D

211 otential for producing enhanced disease in a cotton rat (CR) model.

212 RSV F (PIV5/F) or G (PIV5/G) protein in the cotton rat and African green monkey models for their rep

213 r adjuvant) in a preclinical RSV susceptible cotton rat challenge model compared to formaldehyde inac

214 rvations are relevant to the validity of the cotton rat model itself and to safe development of nonli

215 enital herpes in the novel DMPA-synchronized cotton rat model of HSV-1 and HSV-2 infection.

216 and dose-dependent antiviral efficacy in the cotton rat model of RSV infection.

217 sion (SE) (GLA-SE) and alum adjuvants in the cotton rat model.

218 d tested their efficacies in both murine and cotton rat models of RSV infection.

219 al development over a wide dose range in the cotton rat RSV enhanced-disease model, as suboptimal dos

220 t medroxyprogesterone acetate (DMPA)-treated cotton rat Sigmodon hispidus model of HSV-2 and HSV-1 ge

221 Intranasal infection of cotton rats (Sigmodon hispidus) resulted in high numbers

222 ir immunogenicity and protective efficacy in cotton rats and African green monkeys, which are among t

223 DB1 was also highly immunogenic in cotton rats and elicited broadly neutralizing antibodies

224 The gD/AS04 vaccine was immunogenic in cotton rats and induced serum IgG directed against gD-2

225 ion RSV F elicits neutralizing antibodies in cotton rats and induces complete protection against vira

226 ive transfer of serum from gD/AS04-immunized cotton rats conferred stronger protection against HSV-1

227 SC-Ad-vaccinated cotton rats had markedly lower influenza titers than RD-

228 When vaccinated cotton rats were challenged with wild-type RSV A, DB1 re

229 Cotton rats were intramuscularly vaccinated using a prim

230 bust immunity against RSV infection in mice, cotton rats, and nonhuman primates.

231 as less than that of HSV-2 genital herpes in cotton rats, and yet the model allowed for comparative e

232 ministered intranasally or subcutaneously in cotton rats, the candidates were highly immunogenic and

233 In cotton rats, the vaccines elicited RSV F- or G-specific

234 ttenuation in the upper and lower airways of cotton rats.

235 s were highly attenuated in cell culture and cotton rats.

236 cells and in the upper and lower airways of cotton rats.

237 and triggered strong protective immunity in cotton rats.

238 nic, and protective against RSV challenge in cotton rats.

239 nic, and protective against RSV challenge in cotton rats.

240 n cell culture and were highly attenuated in cotton rats.

241 so triggered a strong protective immunity in cotton rats.

242 ivity, replicated as efficiently as rhMPV in cotton rats.

243 natural refuges were as effective as non-Bt cotton refuges.

244 as effective as an equivalent area of non-Bt cotton refuges.

245 , Apis mellifera and Pieris rapae) in one GM cotton (resistant to the insect Helicoverpa armigera and

246 ve to commercial Bacillus thuringiensis (Bt) cotton, resulting in significant economic losses and an

247 be chosen as regions become drier, and corn, cotton, rice and soybeans are more likely to be selected

248 y increased over the last 25 years in maize, cotton, rice and wheat.

249 icular, we find that when temperature rises, cotton, rice, sorghum and winter wheat are more likely t

250 ncreased in border cells of roots exposed to cotton root rot (Phymatotrichopsis omnivora), and the va

251 According to Cotton's criteria, 17 patients (80.9%) developed mild pa

252 ncreatitis severity was defined according to Cotton's criteria.

253 with concomitant high expression of GhCHR in cotton seedlings.

254 First, cotton shirts were exposed to air at an elevated concent

255 in diploid, allopolyploid, and domesticated cotton shows that despite most DNA methylation being con

256 GhPAO silencing in cotton significantly reduced the Spd level and increased

257 Cotton simultaneously maintains robust monopodial indete

258 ree skin flame burn and 48 breaths of cooled cotton smoke inhalation under deep anesthesia and analge

259 genes identified between wild and cultivated cottons, some contribute to domestication traits, includ

260 While the widely cultivated cotton species Gossypium hirsutum is generally susceptib

261 lies of a single datasets collected from the cotton species Gossypium raimondii.

262 nitor diploid (G. arboreum and G. raimondii) cotton species identified 84, 44 and 46 laccase genes, r

263 ive analysis of TCP gene family in a diploid cotton species, Gossypium arboreum, including phylogenet

264 dense, are the two cultivated allotetraploid cotton species.

265 ly conserved nature of laccases across three cotton species.

266 of these two important cultivated tetraploid cotton species.

267 production, as more than half of the global cotton supply is grown in regions with high water shorta

268 , whereas silencing of GhSWEET10 compromises cotton susceptibility to infections.

269 due to methylation loss in all domesticated cottons tested.

270 A high-performance, cotton-textile-enabled asymmetric supercapacitor is inte

271 , and more damage was observed in transgenic cotton than conventional cotton.

272 ght phthalates were significantly greater in cotton than polyester and similar for BFRs and high mole

273 relies on refuges of host plants other than cotton that do not make Bt toxins.

274 ra is the ancestral leaf shape of tetraploid cotton that gave rise to the okra allele and that normal

275 polyploid crop plants such as allotetraploid cotton that has A- and D-sub-genomes.

276 for delaying insect resistance to transgenic cotton that produces insecticidal proteins from Bacillus

277 The device is 1.5 cm x 1.0 cm and includes a cotton thread to transport the aqueous sample via capill

278 A complete characterization of the cotton thread used as well as the sensing element has be

279 icrofluidic device of easy assembly based on cotton threads, low cost materials and measurements by m

280 te, were detected in 50% examined transgenic cotton through PCR amplification assay and sequencing an

281 the underlying mechanism of the response of cotton to drought stress remains elusive.

282 n combination, on four crop plants (cabbage, cotton, tobacco and tomato) were analyzed, in comparison

283 as isolated from the intestines and feces of cotton-top tamarins (CTTs) with chronic colitis.

284 ate the efficacy of the system in recovering cotton transformants following Agrobacterium-mediated tr

285 R. felis was also found in the cotton used for sucrose feeding after the mosquitoes wer

286 ed by commercial Bacillus thuringiensis (Bt) cotton varieties resulting in economic losses and increa

287 has been selected for further development of cotton varieties that could potentially reduce or elimin

288 Resistant cotton varieties were introduced in late 1990's but soon

289 more, during infection of N. benthamiana and cotton, VdEG1 and VdEG3 acted as PAMPs and virulence fac

290 system to target a gene within the genome of cotton, we made use of a transgenic cotton line previous

291 The results revealed that the MYB genes in cotton were differentially expressed under salt and drou

292 in cotton and may facilitate the development cotton with improved resistance to BBC.

293 o cross-resistance occurs and integrating Bt cotton with other control tactics could also increase th

294 -crop monocultures of bean (annual herb) and cotton (woody shrub) would be globally an order of magni

295 opic examination revealed the development of cotton wool spot-like lesions in anti-VEGF treated Ins2(

296 iandrosterone was positively associated with cotton wool spots, and serum testosterone response durin

297 including choroidal folds, optic disc edema, cotton-wool spots, globe flattening, and refraction chan

298 morrhages, and nerve layer infarcts known as cotton-wool spots.

299 is a longitudinal study of endotoxin-exposed cotton workers and endotoxin-unexposed silk workers that

300 igh-speed weaving of polyester and polyester/cotton yarns to substantially decrease environmental pol