ライフサイエンスコーパス: Brassica napus

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

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

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

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

5 12 homologues (BnSAG12-1 and BnSAG12-2) from Brassica napus.

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

7 ct obtained after edible oil production from Brassica napus.

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

9 nhanced expression during leaf senescence in Brassica napus.

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

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

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

13 enced species, including the closely related Brassica napus.

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

15 xes were determined in developing embryos of Brassica napus.

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

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

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

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

20 Developing embryos of Brassica napus accumulate both triacylglycerols and prot

21 In Brassica napus, accurately initiated pre-rRNA transcript

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

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

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

25 43% and 76% identical to the rat, yeast and Brassica napus amino acid sequences, respectively.

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

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

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

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

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

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

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

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

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

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

36 Brassica napus and Helianthus annuus pollen were the var

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

64 Brassica napus (cultivar Reston) seed proteins were anal

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

95 Brassica napus is a recently formed polyploid resulting

96 Brassica napus is an important oilseed crop for human co

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 Several Brassica napus lines transformed with genes responsible

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 5S promoter and in Arabidopsis and rapeseed (Brassica napus) seeds overexpressing either of the Ch KA

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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