ライフサイエンスコーパス: Brassica

1 all tested Allium and Brussels sprouts from Brassica.

2 idopsis thaliana and important crops such as Brassica.

3 arious cruciferous plants belonging to genus Brassica.

4 l breeding target for P uptake efficiency in Brassica.

5 developmental stage, and quality of oilseed Brassicas.

6 l pathogen that causes black spot disease on Brassicas.

7 ou7 (Chinese) and their progenitors with the Brassica 60 K Illumina Infinium SNP array and mapped a t

8 of physically anchored SNP markers (Illumina Brassica 60K Infinium array).

9 genetic mapping of all 19 centromeres of the Brassica A and C genomes to the reference Brassica napus

10 These represent segments of the Brassica A genome as found in Brassica rapa and Brassica

11 Like Arabidopsis and Brassica AGL15, GmAGL15 was preferentially expressed in

12 adense), genetic complexity equalled only by Brassica among sequenced angiosperms.

13 When considering Brassica and plum consumption in Luxembourg, it is estim

14 nt varied considerably between the different Brassica and plum varieties, with highest concentrations

15 mbination, and genome evolution in the genus Brassica and will facilitate new applied breeding techno

16 to understand trichome gene function in the Brassicas and highlights the potential of B. villosa as

17 This inverse correlation is attributed to brassica anticarcinogenic components, especially isothio

18 reported previously between A. thaliana and Brassica (approximately 66%).

19 results suggest that the three C genomes in Brassica are more similar to each other than the three A

20 e evolutionary research such as Arabidopsis, Brassica, Boechera, Thellungiella, and Arabis species.

21 SRK for the self-incompatibility response in Brassica, but it has been suggested that ARC1 is not req

22 Brassica by-products could be used as sources of product

23 napus and the corresponding segments of the Brassica C genome as found in Brassica oleracea and B. n

24 Brassica villosa is a wild Brassica C genome species with very dense trichome cover

25 nfluence of Allium (garlic, onion, leek) and Brassica (cabbage, Brussels sprouts) plants juices, on j

26 ed and applied to selenium-enriched pakchoi (Brassica chinensis Jusl var parachinensis (Bailey) Tsen

27 d that the split between Arabidopsis and the Brassica complex (broccoli, cabbage, canola) occurred ab

28 ng target for altering the Ca composition of Brassica, consistent with prior knowledge from Arabidops

29 studies show an inverse association between Brassica consumption and chronic diseases.

30 The important crop genus Brassica contains self-incompatible outbreeding species

31 of glucosinolate profiles revealed that each Brassica crop accumulated different types and amounts of

32 Brassica crop diversification involves correlated evolut

33 Brassica crop species are prolific producers of indole-s

34 ve of Arabidopsis (Arabidopsis thaliana) and Brassica crop species, thrives on the shores of Lake Tuz

35 The hydrolytic products of glucosinolates in brassica crops are bioactive compounds.

36 Differences in antioxidant activity of Brassica crops were related to differences in total phen

37 Antioxidant activity of six Brassica crops-broccoli, cabbage, cauliflower, kale, nab

38 eloped multiple linear-regression-models for Brassica, flavonoids, anthocyanins, lutein and vitamin C

39 Increasing their levels into Brassica food is considered an expedient nutritional str

40 at the medial region of the fruits, whereas Brassica fruits lack this tissue.

41 d patterns of the triplicated regions in the Brassica genome are best explained by a two-step fractio

42 This study provides insights into Brassica genome evolution and will underpin research int

43 n between the different versions of the same Brassica genome, for gene fragments and annotated putati

44 Genes conserved across the Brassica genomes and the homoeologous segments of the ge

45 ted that the mesohexaploidization of the two Brassica genomes contributed to their diversification in

46 Brassica genomes have all undergone a whole-genome tripl

47 Homoeologous regions of Brassica genomes were analyzed at the sequence level.

48 be particularly appropriate when considering Brassica genomes.

49 between this stacked genotype and five other Brassica genotypes in constructed mesocosm plant communi

50 The Brassica genus encompasses three diploid and three allop

51 e morphological diversity--a hallmark of the Brassica genus.

52 In addition, transcriptome analyses of Brassica homologues of Arabidopsis genes linked to paren

53 We also show that, unlike reports in Brassica, inactivation of the MLPK ortholog AtAPK1b and

54 ons of half-tetrad-derived individuals (from Brassica interspecific hybrids) using a high-density arr

55 Brassica is an ideal model to increase knowledge of poly

56 study, we have isolated and characterized a Brassica juncea 'ERD' gene (BjERD4) which encodes a nove

57 a with the nonhyperaccumulators S. elata and Brassica juncea for selenate uptake in long- (9 d) and s

58 We assembled an allopolyploid Brassica juncea genome by shotgun and single-molecule re

59 distribution and speciation in the roots of Brassica juncea grown in Zn contaminated media (400 mg k

60 rying sulfur (S) supply on glucosinolates in Brassica juncea in order to reveal whether a partial roo

61 Fifty protein interactors of a Brassica juncea NRAMP protein was identified by a Split-

62 fect of Se (through soil) induced changes in Brassica juncea plants in the presence and absence of 24

63 A cDNA expression library from Brassica juncea was introduced into the fission yeast Sc

64 TuMV) has been found in a number of mustard (Brassica juncea) accessions.

65 In contrast, eukaryotic (Brassica juncea) HMGCS binds hymeglusin in a more solven

66 mustard (Brassica nigra) and brown mustard (Brassica juncea) in food.

67 mustard (Brassica nigra) and brown mustard (Brassica juncea).

68 , including Arabidopsis, Camelina sativa and Brassica juncea, neither has been produced in commercial

69 in Saccharomyces cerevisiae, Arabidopsis, or Brassica juncea.

70 etion of several key hallmarks of meiosis in Brassica napus (AACC), a young polyphyletic allotetraplo

71 cellular metabolism in developing embryos of Brassica napus (bna572) was used to predict biomass form

72 ost economically important Brassica species, Brassica napus (oilseed rape), and those of Brassica rap

73 maculans, the causal agent of stem canker in Brassica napus (oilseed rape), confers a dual specificit

74 netics studies in the polyploid crop species Brassica napus (oilseed rape).

75 ic interaction between the cultivated specie Brassica napus (rapeseed) and the parasitic weed Phelipa

76 ly, we demonstrated that the expression of a Brassica napus ACBP (BnACBP) complementary DNA in the de

77 foliar anion levels in a diversity panel of Brassica napus accessions, 84 of which had been genotype

78 as also identified in the omega-7 content of Brassica napus aleurone, with the highest level detected

79 ytological investigation of 50 resynthesized Brassica napus allopolyploids across generations S(0:1)

80 ibility in two diverse Brassicaceae species, Brassica napus and A. lyrata, and is frequently deleted

81 ground symptoms of Verticillium infection on Brassica napus and Arabidopsis thaliana are stunted grow

82 Further analyses (also in Brassica napus and Cucurbita maxima) employing complemen

83 upinus alba and Vicia faba, nonlegume dicots Brassica napus and Helianthus annus, and nonlegume cerea

84 Brassica napus and Helianthus annuus pollen were the var

85 ssica A genome as found in Brassica rapa and Brassica napus and the corresponding segments of the Bra

86 Here, a Brassica napus BBM (BnBBM) was used to investigate genet

87 A subsequent analysis of simulated Brassica napus chromosome 1A and 1C genotypes demonstrat

88 rides collected from 331 genetically diverse Brassica napus cultivars and used them to obtain detaile

89 nuclear male sterility, the coding region of Brassica napus cysteine protease1 (BnCysP1) was isolated

90 lity-restoration system in rice by combining Brassica napus cysteine-protease gene (BnCysP1) with ant

91 rt that the hydrophilic N-terminal domain of Brassica napus DGAT1 (BnaDGAT11-113) regulates activity

92 vered that the A subgenomes of B. juncea and Brassica napus each had independent origins.

93 ack regulation of fatty acid biosynthesis in Brassica napus embryo-derived cell cultures and to chara

94 ong chain fatty acid (VLCFA) biosynthesis in Brassica napus embryos.

95 zed the Arabidopsis ABI1 gene orthologue and Brassica napus gene paralogues encoding protein phosphat

96 The recent release of the Brassica napus genome supplies essential genetic informa

97 he Brassica A and C genomes to the reference Brassica napus genome.

98 Here we report metabolomic responses of Brassica napus guard cells to elevated CO2 using three h

99 In this study, Brassica napus guard-cell proteins altered by redox in r

100 her plant species, the cruciferin complex of Brassica napus has an octameric barrel-like structure, w

101 ing chromosome pairing in the allotetraploid Brassica napus has been hampered by the lack of chromoso

102 Brassica napus is an important oilseed crop for human co

103 enes, we developed a stacked line of canola (Brassica napus L.) from a segregating F(2) population th

104 Oilseed rape (Brassica napus L.) was formed ~7500 years ago by hybridi

105 t of seed yield and quality in oilseed rape (Brassica napus L.).

106 tin A (TSA) in cultured male gametophytes of Brassica napus leads to a large increase in the proporti

107 We investigated this using the Brassica napus microspore embryogenesis system, where th

108 Here, we used chemical and genetic tools on Brassica napus microspore-derived embryos and Arabidopsi

109 esis, is essential in Arabidopsis but not in Brassica napus or maize (Zea mays), where duplicated nuc

110 this study we analyzed the transcriptomes of Brassica napus parental lines and their F1 hybrids at th

111 revious map in the Tapidor x Ningyou7 (TNDH) Brassica napus population, giving a new map with a total

112 scription of GUS in a similar pattern in the Brassica napus seed coat.

113 ometric metabolic network model representing Brassica napus seed storage metabolism.

114 in this species and in Triticum aestivum and Brassica napus seeds.

115 he northern latitudes utilises oilseed rape (Brassica napus subsp. oleifera) and turnip rape (B. rapa

116 from Arabidopsis (Arabidopsis thaliana) and Brassica napus that accumulates to its highest amount in

117 t of homologous genes could be identified in Brassica napus that exhibited a similar expression patte

118 Using tomato (Solanum lycopersicum) and Brassica napus verified the potency of this combination

119 es in seeds from Bt-transgenic oilseed rape (Brassica napus) and its hybrids with wild mustard (B. ju

120 pulation of the polyploid crop oilseed rape (Brassica napus) and representative ancestors of the pare

121 rassicaceae species, including oilseed rape (Brassica napus) and the model plant Arabidopsis (Arabido

122 of the commercially important oilseed rape (Brassica napus) and turnip rape (Brassica rapa) were inv

123 fficiency is relatively low in oilseed rape (Brassica napus) due to weak nitrogen remobilization duri

124 pid accumulation in developing oilseed rape (Brassica napus) embryos.

125 Canola (Brassica napus) is a widely cultivated species and provi

126 Oilseed rape (Brassica napus) is the third most productive vegetable o

127 Transgenic oilseed rape (Brassica napus) lines were generated in which the E. col

128 Starting from isogenic canola (Brassica napus) lines, epilines were generated by select

129 etabolism in developing embryos of rapeseed (Brassica napus) oilseeds, we present an in silico approa

130 equired for this restarting in oilseed rape (Brassica napus) seed has been investigated.

131 ased imaging of the developing oilseed rape (Brassica napus) seed illustrates that, following embryo

132 peptides and an accessory enzyme, in canola (Brassica napus) seeds.

133 as compared to a parallel study of rapeseed (Brassica napus) to further understand the regulation of

134 (ACP) of protein hydrolysates from rapeseed (Brassica napus) was studied in 36 hydrolysates obtained

135 stably transformed tetraploid oilseed rape (Brassica napus) with a CRISPR-Cas9 construct targeting t

136 a vulgaris), raspberry (Rubus idaeus), rape (Brassica napus), alder buckthorn (Frangula alnus) and th

137 Canola (Brassica napus), an agriculturally important oilseed cro

138 elopment in soybean (Glycine max), rapeseed (Brassica napus), and Arabidopsis (Arabidopsis thaliana).

139 rabidopsis (Arabidopsis thaliana), rapeseed (Brassica napus), and barley (Hordeum vulgare), we observ

140 kwheat (Fagopyrum esculentum), oilseed rape (Brassica napus), and goldenrod (Solidago virgaurea).

141 uding Arabidopsis thaliana and oilseed rape (Brassica napus), produce dry fruits that open upon matur

142 rop plants soybean (Glycine max) and canola (Brassica napus), suggesting that TTM2 is involved in imm

143 From oilseed rape (Brassica napus), we cloned two orthologs of the Arabidop

144 es of TT16 in an important oil crop, canola (Brassica napus), were dissected by a loss-of-function ap

145 cultured developing embryos of oilseed rape (Brassica napus).

146 ments in seed oil yield (e.g. in canola-type Brassica napus).

147 ilseeds, soybean (Glycine max) and rapeseed (Brassica napus).

148 rated on Arabidopsis [Arabidopsis thaliana], Brassica napus, and rice [Oryza sativa]), and results ar

149 ma for self-incompatible pollen rejection in Brassica napus, Arabidopsis lyrata, and Arabidopsis thal

150 ges of developing seeds of Ricinus communis, Brassica napus, Euonymus alatus and Tropaeolum majus, wh

151 In the allopolyploid Brassica napus, we obtained a petal-closed flower mutati

152 isum sativum), which makes border cells, and Brassica napus, which makes border-like cells.

153 tructure of cruciferin, the 12 S globulin of Brassica napus.

154 I) oxidation state) in a plant cell model of Brassica napus.

155 enced species, including the closely related Brassica napus.

156 om the crystal structure of the protein from Brassica napus.

157 ct obtained after edible oil production from Brassica napus.

158 en in Arabidopsis (Arabidopsis thaliana) and Brassica napus.

159 tudy, we investigate the stress responses of Brassica nigra (wild black mustard) exposed consecutivel

160 We show in Arabidopsis thaliana and Brassica nigra that localized FR enrichment at the lamin

161 aneous detection of traces of black mustard (Brassica nigra) and brown mustard (Brassica juncea) in f

162 white mustard (Sinapis alba), black mustard (Brassica nigra) and brown mustard (Brassica juncea).

163 on glucosinolate concentrations of mustard (Brassica nigra) and collard (B. oleracea var. acephala)

164 h as oxazolidine-2-thione from progoitrin in brassica oilseed meal are toxic and detrimental to anima

165 nd strong resistance to many insect pests of Brassica oilseeds and vegetables.

166 Antioxidant capacity (AC) of Brassica oilseeds, white flakes and meal was determined

167 This investigation employed the cabbage Brassica oleracae and snail Otala lactea as models to de

168 genitor species Brassica rapa (A genome) and Brassica oleracea (C genome).

169 Brassicaceae species, Arabidopsis lyrata and Brassica oleracea (cauliflower), fail to bind single-str

170 nt sprouting conditions of four varieties of Brassica oleracea (red cabbage, broccoli, Galega kale an

171 We resequenced 199 Brassica rapa and 119 Brassica oleracea accessions representing various morpho

172 egments of the Brassica C genome as found in Brassica oleracea and B. napus.

173 he meiotic chromosome axis protein, ASY1, in Brassica oleracea anthers and meiocytes.

174 nome editing in barley (Hordeum vulgare) and Brassica oleracea by targeting multicopy genes.

175 bred open-pollinating genotypes of broccoli (Brassica oleracea convar.

176 tness costs increased on the better-defended Brassica oleracea cultivars.

177 Here we show that although Brassica oleracea displays strong parent-of-origin effec

178 Recent sequencing of the Brassica rapa and Brassica oleracea genomes revealed extremely contrasting

179 from the field and used to inoculate OSR and Brassica oleracea grown under controlled conditions in a

180 TPSs from A. thaliana, Capsella rubella, and Brassica oleracea in Nicotiana benthamiana yielded funga

181 jor determinant of heading date variation in Brassica oleracea is from variation in vernalization res

182 and glutathione content in broccoli florets (Brassica oleracea L. italica cv. Bellstar) during prolon

183 main polyphenol components from red cabbage (Brassica oleracea L. Var. Capitata f. Rubra) extracts th

184 ves all major carotenoids found in broccoli (Brassica oleracea L. var. italica), carrot (Daucus carot

185 olvent polarity on antioxidant properties of Brassica oleracea leaves were optimized by response surf

186 Here we show by analysis of the Brassica oleracea pangenome that nearly 20% of genes are

187 d to thermal GL degradation in a segregating Brassica oleracea population.

188 tural variation and fine mapping in the crop Brassica oleracea to show that allelic variation at thre

189 ue Purple (Pr) gene mutation in cauliflower (Brassica oleracea var botrytis) confers an abnormal patt

190 work were extracted bioactive compounds from Brassica oleracea var capitata using supercritical CO2 a

191 n Se volatilization from plants, a broccoli (Brassica oleracea var italica) cDNA encoding COQ5 methyl

192 Diets rich in broccoli (Brassica oleracea var italica) have been associated with

193 Broccoli (Brassica oleracea var. italica) is a vegetable that requ

194 Broccoli (Brassica oleracea var. italica) is associated with varie

195 Two Brassicaceae (Eruca sativa, Brassica oleracea var. sabauda) were stored in air and u

196 Kale (Brassica oleracea var. sabellica) reveals a great divers

197 he antioxidant activity of sprouts from four Brassica oleracea varieties was evaluated using "in vitr

198 human health found in edible sprouts of two Brassica oleracea varieties, broccoli and Tuscan black k

199 n intact plastids isolated from cauliflower (Brassica oleracea) buds.

200 Samples of cabbage (Brassica oleracea) grown in peat fortified with differen

201 the circadian clock of postharvest cabbage (Brassica oleracea) is entrainable by light-dark cycles a

202 Here we describe a draft genome sequence of Brassica oleracea, comparing it with that of its sister

203 s-wide allelic diversity within domesticated Brassica oleracea, including representation of wild rela

204 yzus persicae), maintained on the model crop Brassica oleracea, to different types of cues from aphid

205 of its progenitor species, Brassica rapa and Brassica oleracea.

206 f two major groups of vegetables and fruits, Brassica oleraceae and prunus spp., and estimated their

207 la has become the major lepidopteran pest of Brassica owing to its strong ability of resistance devel

208 ast, fitness costs were heterogeneous in the Brassica pekinensis studies: fitness costs in geneticall

209 Brassica plants accumulate selenium (Se) especially in s

210 tard oil) is a powerful irritant produced by Brassica plants as a defensive trait against herbivores

211 is, the causal agent of black rot disease of Brassica plants, possesses a specific system for GlcNAc

212 umulation of Se and glucosinolates in mature Brassica plants, Se supply generally did not affect gluc

213 yotypes developed for the progenitor species Brassica rapa (A genome) and Brassica oleracea (C genome

214 three eudicot species: Arabidopsis thaliana, Brassica rapa (extrastaminal nectaries) and Nicotiana at

215 in shoots of an inbred mapping population of Brassica rapa (IMB211 x R500); 23 cis- and 948 trans-eQT

216 he activity of superoxide dismutase (SOD) in Brassica rapa also displayed a growth-stage dependent re

217 We resequenced 199 Brassica rapa and 119 Brassica oleracea accessions repre

218 egments of the Brassica A genome as found in Brassica rapa and Brassica napus and the corresponding s

219 Recent sequencing of the Brassica rapa and Brassica oleracea genomes revealed ext

220 quence assemblies of its progenitor species, Brassica rapa and Brassica oleracea.

221 at WUE is important for drought tolerance in Brassica rapa and that artificial selection for increase

222 the beta-glucosidase BABG that is present in Brassica rapa but absent in Arabidopsis was shown to act

223 ranscriptomic changes that occur in the crop Brassica rapa during initial perception of drought, we a

224 floral whorls in recombinant inbred lines of Brassica rapa in multiple environments to characterize t

225 terns of trait integration and modularity in Brassica rapa in response to three simulated seasonal te

226 physiological and biochemical adjustments in Brassica rapa in soil growing conditions and (2) to dete

227 over ontogeny in recombinant inbred lines of Brassica rapa in the field and glasshouse.

228 dish (Raphanus sativus L.) (TBR) and Turnip (Brassica rapa L.) using a simple and effective single-st

229 ed three copies of eIF(iso)4E in a number of Brassica rapa lines.

230 Aux/IAA family, as well as in their putative Brassica rapa orthologs.

231 We measured leaf lengths and widths in Brassica rapa recombinant inbred lines (RILs) throughout

232 etative traits, and life history in a set of Brassica rapa recombinant inbred lines within and across

233 The genome sequence of the paleohexaploid Brassica rapa shows that fractionation is biased among t

234 GFP-CENH3 from the close relative Brassica rapa was targeted to centromeres, but did not c

235 lseed rape (Brassica napus) and turnip rape (Brassica rapa) were investigated with (1)H NMR metabolom

236 nd our study of the plant circadian clock to Brassica rapa, an agricultural crop.

237 influence of time on the drought response of Brassica rapa, an agriculturally important species of pl

238 Brassica napus (oilseed rape), and those of Brassica rapa, the genome of which is currently being se

239 Using recombinant inbred lines of Brassica rapa, we examined the quantitative-genetic arch

240 al profiling of the hypocotyl epidermis from Brassica rapa, we show that auxin acts in the epidermis

241 Using the oilseed and vegetable crop species Brassica rapa, we show that the perception of low red to

242 In Brassica rapa, we tested for physiological differentiati

243 e triplication event prior to diverging from Brassica rapa.

244 A. thaliana, A. lyrata, Capsella rubella and Brassica rapa.

245 an period was related to drought response in Brassica rapa.

246 ave investigated circadian clock function in Brassica rapa.

247 er size of CeO2 throughout the life cycle of Brassica rapa.

248 generated from whole genome triplication in Brassica rapa.

249 s occurred on chromosomes A06 and A01 within Brassica rapa; these were enriched with P metabolism-rel

250 he cis-element was sufficient to convert the Brassica replum to an Arabidopsis-like morphology.

251 Conversely, Brassica RPL containing the Arabidopsis version of the c

252 Dissection and analysis of Brassica seed coats showed that suberization is not spec

253 Polyester deposition was followed over Brassica seed development and distinct temporal patterns

254 We report a chemical analysis of Se in Brassica seeds (canola, Indian mustard, and white mustar

255 d conducted comparative analyses between the Brassica sequences and those of the orthologous region o

256 es of Arabidopsis and economically important Brassica species are being sequenced with whole-genome s

257 ession differences in an exceptionally hairy Brassica species compared with a glabrous species opens

258 nt trichome-related roles for these genes in Brassica species compared with Arabidopsis.

259 in, and difenoconazole was developed for the Brassica species pak choi and broccoli.

260 rom Arabidopsis to broccoli, the use of wild Brassica species to develop cultivars with potential con

261 cation of every chromosome among these three Brassica species utilized genetically mapped bacterial a

262 s consistent with previous results for other Brassica species, and 97.5 +/- 3.1% between the B. napus

263 he genome of the most economically important Brassica species, Brassica napus (oilseed rape), and tho

264 Brassica species, including crops such as cabbage, turni

265 Brassica species, particularly canola varieties, are cul

266 Based on studies in Brassica species, the membrane-tethered kinase MLPK, the

267 sts of resistance for insects feeding on two Brassica species.

268 cating that this phenomenon is widespread in Brassica species.

269 dopsis-specific POFs, and an Arabidopsis and Brassica-specific protein of unknown function, conferred

270 Based on work in Brassica spp., the thioredoxin h-like proteins THL1 and

271 We found that Se-biofortified Brassica sprouts all were able to synthesize significant

272 Brassica sprouts are considered a healthy food product,

273 Brassica sprouts are widely marketed as functional foods

274 The consumption of brassica sprouts as raw vegetables provides a fair amoun

275 The phenolic content of Brassica sprouts had a significant contribution to the a

276 al to the overall nutritional quality of the brassica sprouts studied.

277 did not affect glucosinolate accumulation in Brassica sprouts.

278 lenocysteine (SeMSCys) and glucosinolates in Brassica sprouts.

279 ctive compounds after the consumption of raw brassica sprouts.

280 ights into the relationships between various Brassica tetraploids and their diploid-progenitors at a

281 c comparison of IND genes in Arabidopsis and Brassica to identify conserved regulatory sequences that

282 Our results suggest that breeding of brassica varieties for commercially valuable variation i

283 For this purpose, 17 plum and 27 Brassica varieties were collected in Luxembourg, and ana

284 Among the traditional Portuguese brassica varieties, Penca cabbage sprouts produced under

285 al intensification and greater production of Brassica vegetable and oilseed crops over the past two d

286 considered in regards to cancer preventative Brassica vegetable related bioactivity.

287 Thus, Brassica vegetable sprouts can be biofortified with Se f

288 ivars from the six most extensively consumed Brassica vegetables (broccoli, cauliflower, green cabbag

289 As Brassica vegetables are mainly consumed cooked, the infl

290 Thermal processing of Brassica vegetables can lead to substantial loss of pote

291 Brassica vegetables have been shown to have antioxidant

292 tion, are decreased in populations consuming brassica vegetables regularly.

293 to overwintering has been exploited to breed brassica vegetables that can be harvested year-round.

294 ), a promising anticancer phytochemical from Brassica vegetables, ablates ERalpha expression, and we

295 atory control of anthocyanin biosynthesis in Brassica vegetables, and offers a genetic resource for d

296 f the cancer preventative isothiocyanates in Brassica vegetables, such as cabbage, broccoli, or pak c

297 ficial glucosinolates for producing improved brassica vegetables.

298 nd Se(VI)] speciation analysis in Allium and Brassica vegetables.

299 Brassica villosa is a wild Brassica C genome species wit

300 h genome introgression from the wild species Brassica villosa.