ライフサイエンスコーパス: cauliflower

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

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

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

4 topic accumulation of pigments in the purple cauliflower.

5 t by functional complementation in wild-type cauliflower.

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

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

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

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

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

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

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

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

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

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

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

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

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

19 1-2 and apetala1, apetala2, leafy1, apetala1 cauliflower, and terminal flower1 showed that emf1-2 is

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

37 maller fibrils and occasional fibrils with a cauliflower configuration.

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

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

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

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

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

43 14-3-3-binding proteins were purified from cauliflower extracts, in sufficient quantity for amino a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

58 Telomerase from cauliflower meristematic tissues exhibited relaxed DNA s

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

140 The cauliflower mosaic virus 35S promoter-directed expressio

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

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

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

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

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

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

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

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

149 72a-1 (35S::MIR172) under the control of the cauliflower mosaic virus 35S promoter.

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

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

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

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

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

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

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

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

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

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

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

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

162 1-like homeobox gene, SHOOT MERISTEMLESS, in cauliflower mosaic virus 35S::KNAT1 transformants.

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

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

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

166 3 under the control of the 35S promoter from cauliflower mosaic virus consist of two outer whorls of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

203 4 of 16 amino acids in the amino terminus of cauliflower RPB5 that was microsequenced, and shows 42 a

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

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

206 Cauliflower sprouts had high total glucosinolate content

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

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

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

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