ライフサイエンスコーパス: cauliflower

1 members (i.e. radish, cabbage, broccoli, and cauliflower).

2 uble chlorophyll-binding protein (WSCP) from cauliflower.

3 ntity genes LEAFY (LFY), APETALA1 (AP1), and CAULIFLOWER.

4 ales are relevant for symptom development in cauliflower.

5 ize LAA: Cactus, Chicken Wing, Windsock, and Cauliflower.

6 topic accumulation of pigments in the purple cauliflower.

7 t by functional complementation in wild-type cauliflower.

8 oli, broccoli sprouts, Brussels sprouts, and cauliflower.

9 soy -2.47 lb (95% CI, -3.09 to -1.85 lb) and cauliflower -1.37 lb (95% CI -2.27, -0.47).

10 Wing (451 [48%]), Windsock (179 [19%]), and Cauliflower (24 [3%]).

11 vealed a splicing site mutation in the white cauliflower allele.

12 cosegregation was observed for broccoli and cauliflower alleles at the IPMS-Bo gene and 4C-GSL conte

13 of phenolic compounds and glucosinolates in cauliflower and broccoli byproduct purees after fermenta

14 The enlarged inflorescence (curd) of cauliflower and broccoli provide not only a popular vege

15 sed content of antioxidant compounds in both cauliflower and broccoli.

16 All pomegranate, cauliflower and cabbage samples were pesticides-free.

17 al purification of the COP9 signalosome from cauliflower and confirm its eight-subunit composition.

18 t, caffeine- and catechin-enriched broccoli, cauliflower and kale microgreens were produced.

19 DTA and Tween, as a donor plant on broccoli, cauliflower and kale sprouts was investigated.

20 tenoids and provitamin A and tocopherols, in cauliflowers and to verify the effect of the cooking pro

21 fixed in B. oleracea ssp. botrytis (domestic cauliflower) and B. oleracea ssp. italica (broccoli), bo

22 rassica species vegetables (such as cabbage, cauliflower, and brussels spouts), exhibits antitumor ef

23 s of the Brassica genus, including broccoli, cauliflower, and Brussels sprouts, exhibits promising ca

24 1-2 and apetala1, apetala2, leafy1, apetala1 cauliflower, and terminal flower1 showed that emf1-2 is

25 We have also found that in an apetala1 cauliflower (ap1 cal) background the ld mutation convert

26 Cauliflowers are generally associated with healthy diets

27 es such as garlic, onion, leek, broccoli and cauliflower, are the main advantages of IL-VA-LLME.

28 targets include the APETALA1-related factor, CAULIFLOWER, as well as three transcription factors and

29 al allele of the BoGSL-ELONG gene from white cauliflower, based on the absence of 4C GSL in this crop

30 affected by the treatment with broccoli and cauliflower biofortified with Cs or Cs combined with per

31 nsense mutation in exon 5 of the B. oleracea CAULIFLOWER (BoCAL) gene are segregating in both wild an

32 ting and unique Purple (Pr) gene mutation in cauliflower (Brassica oleracea var botrytis) confers an

33 The Orange (Or) gene mutation in cauliflower (Brassica oleracea var botrytis) confers the

34 The Or gene of cauliflower (Brassica oleracea var. botrytis) causes man

35 rate reductase (NR) was highly purified from cauliflower (Brassica oleracea var. botrytis) extracts.

36 be measured in intact plastids isolated from cauliflower (Brassica oleracea) buds.

37 tected proteolytic activity in extracts from cauliflower (Brassica oleracea) that process both CLV3 a

38 We report here on the detailed anatomy of cauliflower (Brassicaoleracea) and Arabidopsis (Arabidop

39 evolve from the common ancestor of kohlrabi, cauliflower, broccoli, and Chinese kale.

40 ettuce and the cruciferous family (broccoli, cauliflower, cabbage, etc.) (P(trend) < 0.005).

41 psis, the closely related APETALA1 (AP1) and CAULIFLOWER (CAL) MADS-box genes share overlapping roles

42 The closely related APETALA1 (AP1) and CAULIFLOWER (CAL) meristem identity genes are also impor

43 ntity genes LEAFY (LFY), APETALA1 (AP1), and CAULIFLOWER (CAL), and the floral organ identity genes A

44 PETALA1 (AP1), together with the AP1 paralog CAULIFLOWER (CAL), control the onset of flower developme

45 meristem identity genes, APETALA1 (AP1) and CAULIFLOWER (CAL).

46 maller fibrils and occasional fibrils with a cauliflower configuration.

47 of certain crucifers including broccoli and cauliflower contain 10-100 times higher levels of glucor

48 ferae and genus Brassica (e.g., broccoli and cauliflower) contain substantial quantities of isothiocy

49 a2 knockdown results in pathognomonic dermal cauliflower-contoured collagen fibril aggregates, but ab

50 hyperextensibility at low strain and dermal cauliflower-contoured collagen fibril aggregates, two cE

51 The cauliflower-derived plasma membrane vesicles are able to

52 i(R) edible parts by nanoencapsulation using cauliflower-derived plasma membrane vesicles.

53 More than 75% of CLV3 in cauliflower extracts is bound with CLV1, consistent with

54 14-3-3-binding proteins were purified from cauliflower extracts, in sufficient quantity for amino a

55 s, Arabidopsis lyrata and Brassica oleracea (cauliflower), fail to bind single-strand telomeric DNA i

56 In Arabidopsis seedlings and cauliflower florets, Rpn6 (a proteasome non-ATPase regul

57 The CAULIFLOWER gene, a floral regulatory locus, has been im

58 vely consumed Brassica vegetables (broccoli, cauliflower, green cabbage, Chinese cabbage, kale, and B

59 pv campestris (Xcc) during infection of the cauliflower host plant (Brassica oleracea).

60 s, carotenoids and vitamin A in broccoli and cauliflower inflorescences grown in an organic system.

61 d on myrosinases extracted from broccoli and cauliflower inflorescences, employing sinigrin and gluco

62 ity of six Brassica crops-broccoli, cabbage, cauliflower, kale, nabicol and tronchuda cabbage-was mea

63 sidues at trace levels in cabbage, broccoli, cauliflower, lettuce, celery, spinach, and mustard.

64 Fractal nanoplatinum with cauliflower-like morphology was formed on the reduced gr

65 rimental analyses in an Arabidopsis thaliana cauliflower-like mutant with modeling, we found that cur

66 f hedgehog-like shaped Pd nanoparticles into cauliflower-like nanoparticles with the particle size de

67 red with 15.0mM calcium gained an irregular, cauliflower-like structure, and at concentrations larger

68 ccurring alleles of the Arabidopsis thaliana CAULIFLOWER locus reveal considerable intraspecific dive

69 of partially purified mPDC from potato, pea, cauliflower, maize and barley, with [2-14C]pyruvate, sug

70 dopsis SAM by screening a Brassica oleracea (cauliflower) meristem cDNA library with the homeobox fra

71 Telomerase activity was abundant in cauliflower meristematic tissue and undifferentiated cel

72 Telomerase from cauliflower meristematic tissues exhibited relaxed DNA s

73 Merihb1 is highly expressed in mRNA from cauliflower meristems and also accumulates in stem and f

74 e/TIA in Cactus, Chicken Wing, Windsock, and Cauliflower morphologies was 12%, 4%, 10%, and 18%, resp

75 nce, in front of a minimal 35S promoter from cauliflower mosaic virus (-46 to +4), conferred specific

76 timerized transcriptional enhancers from the cauliflower mosaic virus (CaMV) 35S gene has been applie

77 Gene constructs consisting of the cauliflower mosaic virus (CaMV) 35S promoter driving a c

78 UGT1 antisense mRNA under the control of the cauliflower mosaic virus (CaMV) 35S promoter exhibited d

79 y expressing KAN under the regulation of the cauliflower mosaic virus (CAMV) 35S promoter indicate th

80 Frequently, the cauliflower mosaic virus (CaMV) 35S promoter is used to

81 n of chimeric gene constructs containing the cauliflower mosaic virus (CaMV) 35S promoter required th

82 six expression constructs, two utilized the cauliflower mosaic virus (CaMV) 35S promoter with duplic

83 thin the AGAMOUS second intron (AGI) and the Cauliflower Mosaic Virus (CaMV) 35S promoter, respective

84 nsgenic tobacco plants that express either a cauliflower mosaic virus (CaMV) 35S promoter-TTS2 transg

85 the GFP fusion proteins expressed under the cauliflower mosaic virus (CaMV) 35S promoter.

86 novel Arabidopsis cDNA library driven by the cauliflower mosaic virus (CaMV) 35S promoter.

87 anscribed at moderate levels compared to the cauliflower mosaic virus (CaMV) 35S promoter.

88 ne (LUC) driven by CREB fused with a minimal cauliflower mosaic virus (CaMV) 35S promoter.

89 ransactivator/viroplasmin (TAV) protein from Cauliflower mosaic virus (CaMV) can function as a suppre

90 he amount of CP produced by the constitutive cauliflower mosaic virus (CaMV) double 35S promoter.

91 Gene I of cauliflower mosaic virus (CaMV) encodes a protein that i

92 rtions of the large intergenic region of the Cauliflower mosaic virus (CaMV) genome for promoter acti

93 the role of Arabidopsis thaliana PBs during Cauliflower mosaic virus (CaMV) infection.

94 Cauliflower mosaic virus (CaMV) is a double-stranded DNA

95 The gene VI product (P6) of Cauliflower mosaic virus (CaMV) is a multifunctional pro

96 Cauliflower mosaic virus (CaMV) is aphid-transmitted, wi

97 The P6 protein of Cauliflower mosaic virus (CaMV) is responsible for the f

98 Here, we show that cauliflower mosaic virus (CaMV) MP contains three tyrosi

99 experiments directed towards development of cauliflower mosaic virus (CaMV) replicons for propagatio

100 dy, we report the first crystal structure of cauliflower mosaic virus (CaMV) RT in complex with a dup

101 r three defense pathways during infection by Cauliflower mosaic virus (CaMV), a compatible pathogen o

102 f autophagy in the compatible interaction of cauliflower mosaic virus (CaMV), a double-stranded DNA p

103 rotein P6 is the main symptom determinant of cauliflower mosaic virus (CaMV), and transgene-mediated

104 plify sequences flanking 35S transgenes from cauliflower mosaic virus (CaMV).

105 MPs of turnip vein clearing virus (TVCV) and cauliflower mosaic virus (CaMV).

106 T1;5, play important roles in infection with Cauliflower mosaic virus (CaMV).

107 pyogenes Cas9 (SpCas9) under the control of Cauliflower mosaic virus 35S (35S), S. lycopersicum ribo

108 curonidase (GUS) reporter gene driven by the cauliflower mosaic virus 35S (CaMV35S) promoter to stand

109 little effect on activity of the full-length cauliflower mosaic virus 35S and maize ubiquitin promote

110 driven by the strong constitutive promoters, cauliflower mosaic virus 35S and tCUP.

111 ted transformation with a T-DNA that carries cauliflower mosaic virus 35S enhancer sequences at its r

112 , EC 4.3.1.5) gene, modified by inclusion of cauliflower mosaic virus 35S enhancer sequences in its p

113 An activation tagging screen in which the cauliflower mosaic virus 35S enhancer was inserted rando

114 used activation tagging with T-DNA carrying cauliflower mosaic virus 35S enhancers to investigate th

115 onstitutive over-expression of MPL1 from the Cauliflower mosaic virus 35S gene promoter curtailed the

116 ssed constitutively from the promoter of the cauliflower mosaic virus 35S gene.

117 ld-type SHM1 under the control of either the cauliflower mosaic virus 35S or the SHM1 promoter in shm

118 entation upstream or downstream of a minimal cauliflower mosaic virus 35S promoter (-90 to +5).

119 ase (Nia) construct under the control of the cauliflower mosaic virus 35S promoter (35S-Nia2), one cl

120 S1/cad1-3) or ectopically expressed with the cauliflower mosaic virus 35S promoter (35S::TaPCS1/cad1-

121 e-specific detection of a transgene from the Cauliflower Mosaic Virus 35S Promoter (CaMV35S), inserte

122 xin transcribed region (Fed-1) driven by the cauliflower mosaic virus 35S promoter (P35S), light acts

123 nt expression of ACMV-[CM] AC4 driven by the Cauliflower mosaic virus 35S promoter (p35S-AC4) enhance

124 la gene under transcriptional control of the cauliflower mosaic virus 35S promoter accumulated ricino

125 Overexpression of Pto under the cauliflower mosaic virus 35S promoter activates spontane

126 Next, Tag1 was inserted between a cauliflower mosaic virus 35S promoter and a beta-glucuro

127 ctases) were placed under the control of the cauliflower mosaic virus 35S promoter and introduced int

128 When a fusion gene comprising the cauliflower mosaic virus 35S promoter and RF2a cDNA was

129 s (TBSV) cDNA, positioned between a modified cauliflower mosaic virus 35S promoter and the hepatitis

130 This fusion was placed downstream of the cauliflower mosaic virus 35S promoter and upstream of th

131 (Nicotiana tabacum) under the control of the cauliflower mosaic virus 35S promoter caused up to a 4-f

132 Overexpressing Pto under the control of the cauliflower mosaic virus 35S promoter constitutively act

133 ng the osmotin gene under the control of the cauliflower mosaic virus 35S promoter constitutively ove

134 dimer can confer light responsiveness of the cauliflower mosaic virus 35S promoter containing the -92

135 ression of DEK1-MEM under the control of the cauliflower mosaic virus 35S promoter gave a dominant ne

136 expressing UGT707B1 under the control of the cauliflower mosaic virus 35S promoter have been construc

137 e GCR1 under the control of the constitutive cauliflower mosaic virus 35S promoter have reduced sensi

138 the novel WAVE-DAMPENED2 (WVD2) gene by the cauliflower mosaic virus 35S promoter in mutant plants.

139 nsgene under the control of the constitutive cauliflower mosaic virus 35S promoter in order to suppre

140 th GIG1 cDNA under the constitutively active cauliflower mosaic virus 35S promoter in the gig1 backgr

141 Expression of des from the cauliflower mosaic virus 35S promoter in the plant speci

142 on of the same gene under the control of the cauliflower mosaic virus 35S promoter in transgenic plan

143 r-expression of F5H under the control of the cauliflower mosaic virus 35S promoter increased lignin s

144 either behind its own promoter or behind the cauliflower mosaic virus 35S promoter into Lotus cornicu

145 Overexpression of AtERF53 driven by the cauliflower mosaic virus 35S promoter resulted in an uns

146 or (LeETR1) under the control of an enhanced cauliflower mosaic virus 35S promoter resulted in some e

147 ants overexpressing CGS under control of the cauliflower mosaic virus 35S promoter show increased sol

148 ntaining a kanamycin resistance marker and a cauliflower mosaic virus 35S promoter to control express

149 ent, the gusA gene that was driven by the 2x Cauliflower mosaic virus 35S promoter was bombarded into

150 pecific unknown seed protein promoter or the Cauliflower mosaic virus 35S promoter were employed.

151 d antisense HEMA1 mRNA from the constitutive cauliflower mosaic virus 35S promoter were generated.

152 of antisense mRNA (under the control of the cauliflower mosaic virus 35S promoter) markedly retards

153 ed on the detection of a specific GM (P-35S (Cauliflower mosaic virus 35S promoter)) and non-GM DNA m

154 e was overexpressed under the control of the cauliflower mosaic virus 35S promoter, a guaiacyl-rich,

155 in Arabidopsis thaliana under control of the cauliflower mosaic virus 35S promoter, and the transcrip

156 essing DWF4 (AOD4) were generated, using the cauliflower mosaic virus 35S promoter, and their phenoty

157 lase promoter, but not the commonly employed cauliflower mosaic virus 35S promoter, generates a ligni

158 lation; when expressed from the constitutive cauliflower mosaic virus 35S promoter, IRT1 protein accu

159 and the other CYCA1;2/TAM-GFP driven by the cauliflower mosaic virus 35S promoter, the largest diffe

160 l line under the control of the constitutive cauliflower mosaic virus 35S promoter, was introduced in

161 The cauliflower mosaic virus 35S promoter-directed expressio

162 tation (PGbetaS-AS) under the control of the cauliflower mosaic virus 35S promoter.

163 is plants with AtWRKY18 under control of the cauliflower mosaic virus 35S promoter.

164 ta-galactosidase 4 (TBG4) cDNA driven by the cauliflower mosaic virus 35S promoter.

165 gal introns) clone, regulated by an enhanced cauliflower mosaic virus 35S promoter.

166 isoform, in leaf tissue under control of the cauliflower mosaic virus 35S promoter.

167 cDNAs under the control of the constitutive cauliflower mosaic virus 35S promoter.

168 rame is transcribed under the control of the cauliflower mosaic virus 35S promoter.

169 xpression of GFP-fusions was controlled by a cauliflower mosaic virus 35S promoter.

170 transketolase cDNA under the control of the cauliflower mosaic virus 35S promoter.

171 bidopsis lines expressing CCX3 driven by the cauliflower mosaic virus 35S promoter.

172 72a-1 (35S::MIR172) under the control of the cauliflower mosaic virus 35S promoter.

173 ith PHOT expression constructs driven by the cauliflower mosaic virus 35S promoter.

174 P)-4 in antisense conformation driven by the cauliflower mosaic virus 35S promoter.

175 To address this question, we introduced a Cauliflower mosaic virus 35S promoter:HSFA2 construct in

176 quence in the antisense orientation, and the cauliflower mosaic virus 35S RNA gene terminator.

177 ucted an expression cassette composed of the Cauliflower Mosaic Virus 35S RNA promoter, the A. thalia

178 Overexpression plants were generated using cauliflower mosaic virus 35S, and protein levels in the

179 compared with other commonly used promoters (cauliflower mosaic virus 35S, mas2', and maize ubiquitin

180 the WRINKLED1 cDNA under the control of the cauliflower mosaic virus 35S-promoter led to increased s

181 This was true for the autonomous element in cauliflower mosaic virus 35S-Tag1-beta-glucuronidase con

182 Surprisingly, cauliflower mosaic virus 35S::GL1 try plants contain a s

183 1-like homeobox gene, SHOOT MERISTEMLESS, in cauliflower mosaic virus 35S::KNAT1 transformants.

184 f three transgenic tomato lines carrying the cauliflower mosaic virus 35S::Pto transgene exhibited mi

185 In plants with a cauliflower mosaic virus 35S:HF-RPL18 transgene immunopu

186 rnip mosaic virus, cucumber mosaic virus and cauliflower mosaic virus as well as to the fungus Botryt

187 3 under the control of the 35S promoter from cauliflower mosaic virus consist of two outer whorls of

188 orescent protein (GFP) or with a similar 35S-cauliflower mosaic virus constitutive promoter construct

189 Two regions of cauliflower mosaic virus DNA were designed as markers to

190 es a Dissociation (Ds) element containing 4x cauliflower mosaic virus enhancers along with the Activa

191 Others have suggested that Cauliflower mosaic virus evolved in this manner and our

192 of the viral genome, it is possible that the Cauliflower mosaic virus genome is composed of genes fro

193 Transcription from the as-1 element of the cauliflower mosaic virus is induced by salicylic acid (S

194 on was examined for the seven genes of eight Cauliflower mosaic virus isolates.

195 shunting has only been observed to date on a cauliflower mosaic virus mRNA.

196 the response because systemic infection with cauliflower mosaic virus or cucumber mosaic virus did no

197 placed by either the C.fasciculata or by the cauliflower mosaic virus ORF VI sequence.

198 gene under the enhanced 355 promoter of the cauliflower mosaic virus produced green fluorescence tha

199 These were constitutively transcribed from a cauliflower mosaic virus promoter and assayed for posttr

200 Overexpression of AtPAP15 with the 35S cauliflower mosaic virus promoter produced mutants with

201 includes the bZIP motif to a minimal -50 35S cauliflower mosaic virus promoter, enhanced expression i

202 omato prosystemin gene, regulated by the 35S cauliflower mosaic virus promoter, resulted in constitut

203 of an internal control with an enhanced 35S cauliflower mosaic virus promoter.

204 omparable in strength of the full-length 35S cauliflower mosaic virus promoter.

205 Cauliflower mosaic virus replication complexes are conde

206 l to those required for ribosome shunting in cauliflower mosaic virus RNA and are well conserved in c

207 pe) to systemic infection with the DNA virus cauliflower mosaic virus was shown to result in enhancem

208 th overexpression (using the 35S promoter of Cauliflower mosaic virus) or suppression (using double-s

209 echnology, studying the molecular biology of Cauliflower mosaic virus, rice tungro viruses, and Banan

210 ing So KAS III when under the control of the cauliflower mosaic virus-35S promoter and in Arabidopsis

211 PDH45 overexpression driven by constitutive cauliflower mosaic virus-35S promoter in rice transgenic

212 sgenic pea lines (in a lele background) with cauliflower mosaic virus-35S-driven expression of PsGA3o

213 s clone of CMV RNA3 (LS strain) fused to the cauliflower mosaic virus-derived 35S promoter.

214 tible to the virulent pathogens Erisyphe and cauliflower mosaic virus.

215 s under the control of the 35S promoter from cauliflower mosaic virus.

216 SPY under the control of the 35S promoter of Cauliflower mosaic virus.

217 that at least four DNA binding proteins from cauliflower nuclear extracts are also calmodulin (CaM) b

218 t cells in orange tissues in melon fruit and cauliflower OR mutant have only one or two enlarged chro

219 transgenic potato tubers that expressed the cauliflower Orange (Or) gene.

220 eloping ATs for the regular and cosmopolitan cauliflower pests Brevicoryne brassicae, Plutella xylost

221 regulatory locus, has been implicated in the cauliflower phenotype in both Arabidopsis thaliana and B

222 genic Arabidopsis (Arabidopsis thaliana) and cauliflower plants expressing the Pr-D allele recapitula

223 Here, we report on the structures of cauliflower Pol V in the free and elongation conformatio

224 Cauliflowers present an unusual organ arrangement with a

225 identity genes, such as LEAFY, APETALA 1 and CAULIFLOWER, prevent TERMINAL FLOWER 1 transcription in

226 her Brassicaceae species including broccoli, cauliflower, radish and rapeseed.

227 ation of the theory to recombinant WSCP from cauliflower, reconstituted with chlorophyll a or chlorop

228 Far-Western overlays of soluble extracts of cauliflower revealed many proteins that bound to digoxyg

229 4 of 16 amino acids in the amino terminus of cauliflower RPB5 that was microsequenced, and shows 42 a

230 age and also at the adult plant stage, while cauliflower showed the highest antioxidant activity in s

231 ables (mushroom, brussels sprouts, broccoli, cauliflower, snow peas, tomato, and garlic) were employe

232 tected an activity in extracts from carrots, cauliflower, soybean, Arabidopsis, and rice with all the

233 Cauliflower sprouts had high total glucosinolate content

234 eans and green beans) and vegetable (potato, cauliflower, tomato, spinach, green beans, lettuce, egg

235 46), Windsock was 4.5 times (p = 0.038), and Cauliflower was 8.0 times (p = 0.056) more likely to hav

236 most permeable for catechins from Cs, while cauliflower was most permeable for caffeine.

237 To unravel the nature of the Pr mutation in cauliflower, we isolated the Pr gene via a combination o

238 the aliphatic GLs related to red cabbage and cauliflower were identified as discriminant markers amon

239 n, mushroom, brussels sprouts, broccoli, and cauliflower were superior to snow peas, garlic and tomat

240 d to any Pol II subunit in Pol purified from cauliflower, wheat or At.