ライフサイエンスコーパス: Brassica oleracea

1 rva from its normal food plant (the cabbage, Brassica oleracea).

2 holoenzyme activity purified from broccoli (Brassica oleracea).

3 ing infection of the cauliflower host plant (Brassica oleracea).

4 from unknown varieties of Brassica rapa and Brassica oleracea.

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

6 and present at approximately 2000 copies in Brassica oleracea.

7 anscriptase domains from retrotransposons in Brassica oleracea.

8 atmospheric H(2)S supply were manipulated in Brassica oleracea.

9 e 4 of Arabidopsis thaliana was sequenced in Brassica oleracea.

10 TL that control eight curd-related traits in Brassica oleracea.

11 r phenotype in both Arabidopsis thaliana and Brassica oleracea.

12 between 30 and 40 PCP genes in the genome of Brassica oleracea.

13 ted homology with the SLG and SRK genes from Brassica oleracea.

14 between Brassica rapa (2n = 2x = 20, AA) and Brassica oleracea (2n = 2x = 18, CC).

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

16 A detailed comparative map of Brassica oleracea and Arabidopsis thaliana has been esta

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

18 The pollen coatings of both Brassica oleracea and Brassica napus contain a small fam

19 ly derived by hybridizing double haploids of Brassica oleracea and Brassica rapa.

20 Here, we report the cloning of PCP-A1 from Brassica oleracea and demonstrate that it is unlinked to

21 ined by reads that mapped to the host plant, Brassica oleracea, and a facultative symbiont, Regiella.

22 actions among this herbivore, its host-plant Brassica oleracea, and its primary natural enemy Cotesia

23 sion of genes involved in their synthesis in Brassica oleracea, and perform functional analysis of Bo

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

25 eed Arabidopsis thaliana (125 megabases) and Brassica oleracea ( approximately 600 megabases), a spec

26 A genes inherited from the other progenitor, Brassica oleracea, are undetectable.

27 h isolated protoplasts from warm-grown kale (Brassica oleracea) as a model system, we tested protein

28 ive Brassicaceae species (Brassica carinata, Brassica oleracea, Brassica rapa, Eruca vesicaria and Si

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

30 transposon 1) CACTA transposable elements in Brassica oleracea, but were lost in the majority of the

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

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

33 ressed in the Arabidopsis SAM by screening a Brassica oleracea (cauliflower) meristem cDNA library wi

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

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

36 We show that the S2 and S13 haplotypes of Brassica oleracea contain extensive sequence divergence

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

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

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

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

41 Metabolomic analyses of Brassica oleracea, Glycine max, and Ipomoea aquatica pla

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

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

44 roteins (GRPs) from Arabidopsis thaliana and Brassica oleracea had diverged substantially, making ide

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

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

47 We report a cell-free system from broccoli (Brassica oleracea) inflorescence that supports promoter-

48 Brassica oleracea is closely related to the model plant,

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

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

51 Broccoli (Brassica oleracea L) sprouts are well known for their hi

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

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

54 Broccoli (Brassica oleracea L. var. italica) is largely cultivated

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

56 vegetative tissues of Arabidopsis, broccoli (Brassica oleracea L.), and mustard (Brassica napus L.).

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

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

59 um cepa, Beta vulgaris, Brassica campestris, Brassica oleracea, Pennisetum glaucum, Pinus elliottii,

60 lates the aliphatic glucosinolate pathway in Brassica oleracea plants increasing the production of th

61 hia coli and for partially purified cabbage (Brassica oleracea) PLD alpha.

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

63 promoter of a more closely related species, Brassica oleracea, programs both +1 and +29 transcriptio

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

65 Analysis of the syntenic region in Brassica oleracea revealed even greater divergence, but

66 Surprisingly, diploid Brassica oleracea segregating populations had a similar

67 A total of 595,321 Brassica oleracea shotgun reads were sequenced by TIGR (

68 ons and several biological functions for the Brassica oleracea subgenome biased pairs, but no enrichm

69 a suite of tropic stimulus-induced genes in Brassica oleracea that are responsive to an auxin gradie

70 lytic activity in extracts from cauliflower (Brassica oleracea) that process both CLV3 and CLE1 at th

71 total amounts ranging from 8.5 umol/g dw in Brassica oleracea to 32.9 umol/g dw in Sinapis alba.

72 we take advantage of the large seed size in Brassica oleracea to analyse effects of temperature on i

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

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

75 the TNP2-like transposase genes of the Bot1 (Brassica oleracea transposon 1) CACTA transposable eleme

76 tic glucosinolate (GSL) gene, BoGSL-ELONG in Brassica oleracea, using the Arabidopsis sequence databa

77 exchange in the cotyledons of Chinese kale (Brassica oleracea var alboglabra).

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

79 he Orange (Or) gene mutation in cauliflower (Brassica oleracea var botrytis) confers the accumulation

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

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

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

83 n factors for all the cultivars were >1 with Brassica oleracea var. acephala (kale) having the highes

84 binary BAC library (JBo) from genomic DNA of Brassica oleracea var. alboglabra, in order to underpin

85 The Or gene of cauliflower (Brassica oleracea var. botrytis) causes many tissues of

86 e (NR) was highly purified from cauliflower (Brassica oleracea var. botrytis) extracts.

87 dae)] to a host plant (white cabbage cabbage Brassica oleracea var. capitata f. alba cv. Castello L.)

88 ta (vegetable), Raphanus sativus L. (tuber), Brassica oleracea var. capitata L. (leaf), and Bixa orel

89 (ACSOs) and carotenoids in Brussels sprouts (Brassica oleracea var. gemmifera) and leek (Allium ampel

90 transcriptomic response of Brussels sprouts (Brassica oleracea var. gemmifera) primary roots to feedi

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

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

93 Broccoli (Brassica oleracea var. italica) is known for its ability

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

95 i (Brassica rapa subsp. chinensis) and kale (Brassica oleracea var. sabellica) differ in their SPM co

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

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

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

99 To optimize the nutritional value of Brassica oleracea vegetables, the outcome of these hydro

100 d the formation of VOSCs was investigated in Brassica oleracea vegetables.

101 infect the crop species Brassica juncea and Brassica oleracea We used transgressive segregation in r

102 Arabidopsis thaliana and its close relative Brassica oleracea, we have identified conserved regions

103 representing triplicated genome segments of Brassica oleracea, which are each paralogous with one an