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1 rva from its normal food plant (the cabbage, Brassica oleracea).
2  holoenzyme activity purified from broccoli (Brassica oleracea).
3 of its progenitor species, Brassica rapa and Brassica oleracea.
4  and present at approximately 2000 copies in Brassica oleracea.
5 anscriptase domains from retrotransposons in Brassica oleracea.
6 atmospheric H(2)S supply were manipulated in Brassica oleracea.
7 e 4 of Arabidopsis thaliana was sequenced in Brassica oleracea.
8 TL that control eight curd-related traits in Brassica oleracea.
9 r phenotype in both Arabidopsis thaliana and Brassica oleracea.
10 between 30 and 40 PCP genes in the genome of Brassica oleracea.
11 ted homology with the SLG and SRK genes from Brassica oleracea.
12     We resequenced 199 Brassica rapa and 119 Brassica oleracea accessions representing various morpho
13                A detailed comparative map of Brassica oleracea and Arabidopsis thaliana has been esta
14 egments of the Brassica C genome as found in Brassica oleracea and B. napus.
15                  The pollen coatings of both Brassica oleracea and Brassica napus contain a small fam
16 ly derived by hybridizing double haploids of Brassica oleracea and Brassica rapa.
17   Here, we report the cloning of PCP-A1 from Brassica oleracea and demonstrate that it is unlinked to
18 he meiotic chromosome axis protein, ASY1, in Brassica oleracea anthers and meiocytes.
19 eed Arabidopsis thaliana (125 megabases) and Brassica oleracea ( approximately 600 megabases), a spec
20 A genes inherited from the other progenitor, Brassica oleracea, are undetectable.
21 h isolated protoplasts from warm-grown kale (Brassica oleracea) as a model system, we tested protein
22 n intact plastids isolated from cauliflower (Brassica oleracea) buds.
23 nome editing in barley (Hordeum vulgare) and Brassica oleracea by targeting multicopy genes.
24 genitor species Brassica rapa (A genome) and Brassica oleracea (C genome).
25 ressed in the Arabidopsis SAM by screening a Brassica oleracea (cauliflower) meristem cDNA library wi
26 Brassicaceae species, Arabidopsis lyrata and Brassica oleracea (cauliflower), fail to bind single-str
27  Here we describe a draft genome sequence of Brassica oleracea, comparing it with that of its sister
28    We show that the S2 and S13 haplotypes of Brassica oleracea contain extensive sequence divergence
29 bred open-pollinating genotypes of broccoli (Brassica oleracea convar.
30 tness costs increased on the better-defended Brassica oleracea cultivars.
31                   Here we show that although Brassica oleracea displays strong parent-of-origin effec
32   Recent sequencing of the Brassica rapa and Brassica oleracea genomes revealed extremely contrasting
33 from the field and used to inoculate OSR and Brassica oleracea grown under controlled conditions in a
34                          Samples of cabbage (Brassica oleracea) grown in peat fortified with differen
35 roteins (GRPs) from Arabidopsis thaliana and Brassica oleracea had diverged substantially, making ide
36 TPSs from A. thaliana, Capsella rubella, and Brassica oleracea in Nicotiana benthamiana yielded funga
37 s-wide allelic diversity within domesticated Brassica oleracea, including representation of wild rela
38  We report a cell-free system from broccoli (Brassica oleracea) inflorescence that supports promoter-
39                                              Brassica oleracea is closely related to the model plant,
40 jor determinant of heading date variation in Brassica oleracea is from variation in vernalization res
41  the circadian clock of postharvest cabbage (Brassica oleracea) is entrainable by light-dark cycles a
42 and glutathione content in broccoli florets (Brassica oleracea L. italica cv. Bellstar) during prolon
43 main polyphenol components from red cabbage (Brassica oleracea L. Var. Capitata f. Rubra) extracts th
44 ves all major carotenoids found in broccoli (Brassica oleracea L. var. italica), carrot (Daucus carot
45 vegetative tissues of Arabidopsis, broccoli (Brassica oleracea L.), and mustard (Brassica napus L.).
46 olvent polarity on antioxidant properties of Brassica oleracea leaves were optimized by response surf
47              Here we show by analysis of the Brassica oleracea pangenome that nearly 20% of genes are
48 um cepa, Beta vulgaris, Brassica campestris, Brassica oleracea, Pennisetum glaucum, Pinus elliottii,
49 hia coli and for partially purified cabbage (Brassica oleracea) PLD alpha.
50 d to thermal GL degradation in a segregating Brassica oleracea population.
51  promoter of a more closely related species, Brassica oleracea, programs both +1 and +29 transcriptio
52 nt sprouting conditions of four varieties of Brassica oleracea (red cabbage, broccoli, Galega kale an
53           Analysis of the syntenic region in Brassica oleracea revealed even greater divergence, but
54                        Surprisingly, diploid Brassica oleracea segregating populations had a similar
55                           A total of 595,321 Brassica oleracea shotgun reads were sequenced by TIGR (
56  a suite of tropic stimulus-induced genes in Brassica oleracea that are responsive to an auxin gradie
57 lytic activity in extracts from cauliflower (Brassica oleracea) that process both CLV3 and CLE1 at th
58 tural variation and fine mapping in the crop Brassica oleracea to show that allelic variation at thre
59 yzus persicae), maintained on the model crop Brassica oleracea, to different types of cues from aphid
60 tic glucosinolate (GSL) gene, BoGSL-ELONG in Brassica oleracea, using the Arabidopsis sequence databa
61 ue Purple (Pr) gene mutation in cauliflower (Brassica oleracea var botrytis) confers an abnormal patt
62 he Orange (Or) gene mutation in cauliflower (Brassica oleracea var botrytis) confers the accumulation
63 work were extracted bioactive compounds from Brassica oleracea var capitata using supercritical CO2 a
64 n Se volatilization from plants, a broccoli (Brassica oleracea var italica) cDNA encoding COQ5 methyl
65                      Diets rich in broccoli (Brassica oleracea var italica) have been associated with
66 binary BAC library (JBo) from genomic DNA of Brassica oleracea var. alboglabra, in order to underpin
67                  The Or gene of cauliflower (Brassica oleracea var. botrytis) causes many tissues of
68 e (NR) was highly purified from cauliflower (Brassica oleracea var. botrytis) extracts.
69                                    Broccoli (Brassica oleracea var. italica) is a vegetable that requ
70                                    Broccoli (Brassica oleracea var. italica) is associated with varie
71                                    Broccoli (Brassica oleracea var. italica) is known for its ability
72              Two Brassicaceae (Eruca sativa, Brassica oleracea var. sabauda) were stored in air and u
73                                        Kale (Brassica oleracea var. sabellica) reveals a great divers
74 he antioxidant activity of sprouts from four Brassica oleracea varieties was evaluated using "in vitr
75  human health found in edible sprouts of two Brassica oleracea varieties, broccoli and Tuscan black k
76  Arabidopsis thaliana and its close relative Brassica oleracea, we have identified conserved regions
77  representing triplicated genome segments of Brassica oleracea, which are each paralogous with one an

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