ライフサイエンスコーパス: Brassica napus

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

2 on that mimicked the nectar of oilseed rape (Brassica napus).

3 rieties of a globally important crop-canola (Brassica napus).

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

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

6 enced species, including the closely related Brassica napus.

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

8 xes were determined in developing embryos of Brassica napus.

9 evidence for a CBF cold-response pathway in Brassica napus.

10 12 homologues (BnSAG12-1 and BnSAG12-2) from Brassica napus.

11 mponents of the pollen coat, or tryphine, of Brassica napus.

12 in similar to the BGL4 beta-glucosidase from Brassica napus.

13 nhanced expression during leaf senescence in Brassica napus.

14 non-homologous crossovers in allotetraploid Brassica napus.

15 ature leaves and the developing pod walls of Brassica napus.

16 we characterized four BnaHB6 homologues from Brassica napus.

17 four paleologous copies in the oilseed crop Brassica napus.

18 linked NLR-ID/NLR pair: BnRPR1 and BnRPR2 in Brassica napus.

19 that it contributes to disease resistance in Brassica napus.

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

21 ct obtained after edible oil production from Brassica napus.

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

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

24 Brassica napus (2n = 4x = 38, AACC) is an important allo

25 3x = 29; AAC) resulting from a cross between Brassica napus (2n = 4x = 38; AACC) and Brassica rapa (2

26 In canola (Brassica napus), a major global oil seed crop, spontaneo

27 ximize oleic acid in the seed oil of canola (Brassica napus), a species that expresses three active F

28 e) occurs in at least two forms in rapeseed (Brassica napus): a homomeric (HO) and presumably cytosol

29 d, tuberous, and leafy) of the allopolyploid Brassica napus, a species that contains the economically

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

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

32 6 representative morphotypes of neopolyploid Brassica napus accessions and detected 258,865 SVs in 2,

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

34 association analyses of oilseed rape/canola (Brassica napus) accessions to identify genetic variation

35 Developing embryos of Brassica napus accumulate both triacylglycerols and prot

36 In Brassica napus, accurately initiated pre-rRNA transcript

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

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

39 ionary tape' with six isogenic resynthesised Brassica napus allopolyploid lines and investigated subg

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

41 43% and 76% identical to the rat, yeast and Brassica napus amino acid sequences, respectively.

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

43 Brassica napus, an allotetraploid crop, is hypothesized

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

45 Here, we isolated phloem sap from Brassica napus and analyzed it via size exclusion chroma

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

47 the A6 1,3-beta-glucanase gene products from Brassica napus and Arabidopsis thaliana, the predicted w

48 creased expression during leaf senescence in Brassica napus and Arabidopsis thaliana.

49 the complete gene family were isolated from Brassica napus and B. oleracea species.

50 een annual and biennial cultivars of oilseed Brassica napus and B. rapa is conferred by genes control

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

52 We biochemically fractionated PSVs from Brassica napus and defined a crystalloid-like fraction t

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

54 Brassica napus and Helianthus annuus pollen were the var

55 ological status of green oilseeds in planta, Brassica napus and soybean (Glycine max) seeds were rapi

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

57 munity into the nectar of NN-treated canola (Brassica napus) and assessed microbial survival and grow

58 ssessment of hybridization between rapeseed (Brassica napus) and B. rapa from a combination of source

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

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

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

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

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

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

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

66 ), microspore embryogenesis in oilseed rape (Brassica napus), and somatic embryogenesis in alfalfa (M

67 e well-studied cases of tobacco, cotton, and Brassica napus, and apply it to several cases: allotetra

68 BnGRP10 from Brassica napus, and GRRBP2 from Euphorbia esula) have id

69 CeO(2)) in the tissues of Triticum aestivum, Brassica napus, and Hordeum vulgare, after exposure to s

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

71 en related cDNA sequences were isolated from Brassica napus anther mRNA using RACE-PCR and compared w

72 In situ localization analyses of developing Brassica napus anthers revealed flavonoids present exclu

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

74 abidopsis thaliana PLANT U-BOX17 (PUB17) and Brassica napus ARC1 as the closest homologs of tobacco A

75 Mature pollen grains of Brassica napus are shown to contain three major acyl lip

76 PARCL) protein from Arabidopsis thaliana and Brassica napus at functional and structural levels.

77 ple PRB1 from Nicotiana tabacum and PR1 from Brassica napus, at 64% and 78% identity respectively.

78 study we expressed Trapaeolum majus LPAAT in Brassica napus (B. napus) cv 12075 to evaluate the effec

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

80 and 75% identity to a class of oilseed rape (Brassica napus) BCCPs.

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

82 genetic basis of natural variation in SOC of Brassica napus by genome- and transcriptome-wide associa

83 crops has been tested here in oilseed rape (Brassica napus) by analyzing the effect of suppressing k

84 To investigate the effects of temperature on Brassica napus (canola) resistance to Leptosphaeria macu

85 We tested these hypotheses using Brassica napus (canola), an allotetraploid derived from

86 isoform, AtMRP1, which transports the model Brassica napus chlorophyll catabolite transporter substr

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

88 ollen coatings of both Brassica oleracea and Brassica napus contain a small family of basic 6-8 kDa p

89 Mature seeds of Arabidopsis thaliana and Brassica napus contain complex mixtures of aliphatic mon

90 Here, we show that resistance of Brassica napus cotyledons against Leptosphaeria maculans

91 rds of flying insects found in oilseed rape (Brassica napus) crops, using an optical remote sensor an

92 Brassica napus (cultivar Reston) seed proteins were anal

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

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

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

96 of ROC1, 2 and 3 are 75% to 91% identical to Brassica napus cytosolic CyP, contain no leader peptides

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

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

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

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

101 Developing Brassica napus embryos were cultured with [U-13C6]glucos

102 h a value of over 80% previously observed in Brassica napus embryos, in which light and the RuBisCO b

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

104 ic efficiency in developing seeds, rapeseed (Brassica napus) embryos were cultured in media in which

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

106 We have isolated a gene and cDNA from Brassica napus encoding a hybrid-proline-rich protein.

107 ansformation of fab1 plants with a cDNA from Brassica napus encoding a KAS II enzyme resulted in comp

108 bition data, on the complexes of E. coli and Brassica napus ENR with triclosan and NAD(+) which revea

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

110 e E. coli FabG structure with the homologous Brassica napus FabG.NADP(+) binary complex reveals that

111 Arabidopsis thaliana and Brassica napus FAE1 KCS enzymes are highly homologous bu

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

113 ative tapetum oleosins encoded by two cloned Brassica napus genes were raised.

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

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

116 ion was identified in several annual oilseed Brassica napus genotypes used as parents in crosses to b

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

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

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

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

121 pairing between homoeologous chromosomes in Brassica napus has been identified.

122 sis (Arabidopsis thaliana) and oilseed rape (Brassica napus), indicating its potential usefulness in

123 transgenes from transplastomic oilseed rape (Brassica napus) into wild relatives will be avoided if c

124 MALE STERILITY 5 (MS5) in Brassica napus is a fertility-related new gene, which ha

125 Brassica napus is a recently formed polyploid resulting

126 Brassica napus is an important oilseed crop for human co

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

128 Oilseed rape (Brassica napus) is an important crop that is cultivated

129 Oilseed rape (Brassica napus) is an important global oil crop, with sp

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

131 Here we show that, in developing embryos of Brassica napus L.

132 wth, photosynthesis, and nutrient content of Brassica napus L.

133 expression of an isocitrate lyase gene from Brassica napus L. during late embryogenesis and during p

134 Herein, Brassica napus L. grown under Pb contaminated soil (300

135 L.) was transferred into the dicotyledonous Brassica napus L. using Agrobacterium-mediated transform

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

137 Rapeseed (Brassica napus L.) is an important oil-producing crop fo

138 Here, we isolated a rapeseed (Brassica napus L.) mutant named dwarf and compact archit

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

140 roccoli (Brassica oleracea L.), and mustard (Brassica napus L.).

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

142 accurate chromosome number of oilseed rape (Brassica napus L., 2n=38), we have developed a quantitat

143 n and a second open reading frame (ORFII) in Brassica napus (L.) is a divergent promoter, and also to

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

145 anatomical characteristics of oilseed rape (Brassica napus) leaves in different growth stages under

146 (BTE), in developing seeds of oilseed rape (Brassica napus) led to the production of oils containing

147 ic changes in approximately 50 resynthesized Brassica napus lines independently derived by hybridizin

148 Several Brassica napus lines transformed with genes responsible

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

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

151 e jojoba FAR cDNA is expressed in embryos of Brassica napus, long-chain alcohols can be detected in t

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

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

154 CA)) and an inactive (MPK4(IN)) version of a Brassica napus MPK4 (BnMPK4) in Nicotiana benthamiana le

155 Expression of the cDNA under control of the Brassica napus napin promoter in transgenic Arabidopsis

156 cDNA and genomic clones encoding Brassica napus non-specific lipid transfer proteins (LTP

157 ed than the average methylation level of the Brassica napus nuclear DNA.

158 es from a food industry side-stream, canola (Brassica napus) oil pressing residues.

159 Precociously germinating Brassica napus (oilseed rape) embryos produce extra coty

160 The response of Brassica napus (oilseed rape) to systemic infection with

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

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

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

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

165 ects of recent and ancient allopolyploidy in Brassica napus, on genes implicated in plastid protein c

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

167 .e. olives) with rapeseed oil (obtained from Brassica napus) or with corn oil (also named maize oil,

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

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

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

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

172 ecent characterization of DGAT2 enzymes from Brassica napus reveals that DGAT2 enzymes with similar a

173 Exemplary investigations of Brassica napus root exposed to nano-CeO(2) revealed no a

174 d K(3)SO(4)(+) NPs, could be observed within Brassica napus root tissue.

175 he protein was similar to ENR from the plant Brassica napus (root mean square for Calphas, 0.30 A).

176 Furthermore, in Brassica napus, rRNA genes silenced in vegetative tissue

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

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

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

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

181 CoA pool during lipid synthesis in maturing Brassica napus seeds and during storage lipid breakdown

182 C14-18 substrates in vitro and expression in Brassica napus seeds leads to an oil enriched in C14-18

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

184 mRNA isolated from developing oilseed rape (Brassica napus) seeds and expression patterns correlated

185 5S promoter and in Arabidopsis and rapeseed (Brassica napus) seeds overexpressing either of the Ch KA

186 nder normal field growth conditions, canola (Brassica napus) seeds produce chloroplasts during early

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

188 etal muscle, Arabidopsis thaliana, maize and Brassica napus showed that the catalytic subunit sequenc

189 We collected transcriptome time series for Brassica napus spring, winter, semi-winter, and Siberian

190 Rapeseed (Brassica napus subsp.

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

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

193 ed the interaction of U(VI) and Eu(III) with Brassica napus suspension plant cells as a model system.

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

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

196 expressed in embryos and flowers, tissues of Brassica napus that synthesize lipids at high rates.

197 In Brassica napus there are nine copies of FLC.

198 rative mapping of RPM1 and flanking genes in Brassica napus to determine the ancestral state of the R

199 ing time data from double haploid progeny of Brassica napus to illustrate the proposed method.

200 ons, xylem and phloem sap were obtained from Brassica napus to quantitatively analyze which thiol spe

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

202 lity of the conventional crop, oilseed rape (Brassica napus), to form hybrids with its wild relatives

203 pression of the endogenous extensin genes in Brassica napus, using northern hybridisation and dot blo

204 coring germination across a diverse panel of Brassica napus varieties, SeedGerm implicates a gene imp

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

206 In addition, NPC4 in Brassica napus was S-acylated and mutation of the S-acyl

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

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

209 metabolism and seed oil synthesis in canola (Brassica napus), we have characterized four canola homol

210 gulation of sugars in seeds of oilseed rape (Brassica napus), we measured relevant enzyme activities,

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

212 Genetic maps of Brassica napus were constructed from four segregating po

213 ely related proteins ("napin") isolated from Brassica napus were determined by mass spectrometry with

214 s study, four populations of IBLs of oilseed Brassica napus were developed and analyzed to map genomi

215 that are expressed during leaf senescence in Brassica napus were identified by the isolation of repre

216 Over 1000 genetically linked RFLP loci in Brassica napus were mapped to homologous positions in th

217 Cut leaves of Populus deltoides and Brassica napus were placed in either KCl or one of three

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

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

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

221 present in the important crop oilseed rape (Brassica napus), with each type having four isoforms.