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1 er size of CeO2 throughout the life cycle of Brassica rapa.
2  generated from whole genome triplication in Brassica rapa.
3 e triplication event prior to diverging from Brassica rapa.
4 A. thaliana, A. lyrata, Capsella rubella and Brassica rapa.
5 an period was related to drought response in Brassica rapa.
6 ircadian transcriptome in the polyploid crop Brassica rapa.
7 ave investigated circadian clock function in Brassica rapa.
8 lost in the majority of the Bot1 elements in Brassica rapa.
9 ing double haploids of Brassica oleracea and Brassica rapa.
10 system in the laboratory using rapid-cycling Brassica rapa.
11 cal mapping between Arabidopsis thaliana and Brassica rapa.
12 mily of the plant species studied, except in Brassica rapa.
13 mestication of the diverse crop varieties of Brassica rapa.
14 ed for reproduction in other plants, such as Brassica rapa.
15 NV4A is highly expressed in the nectaries of Brassica rapa.
16 p derived from interspecific crosses between Brassica rapa (2n = 2x = 20, AA) and Brassica oleracea (
17 ween Brassica napus (2n = 4x = 38; AACC) and Brassica rapa (2n = 2x = 20; AA).
18 yotypes developed for the progenitor species Brassica rapa (A genome) and Brassica oleracea (C genome
19 he activity of superoxide dismutase (SOD) in Brassica rapa also displayed a growth-stage dependent re
20 nd our study of the plant circadian clock to Brassica rapa, an agricultural crop.
21 influence of time on the drought response of Brassica rapa, an agriculturally important species of pl
22  genes as being "flexible." We construct the Brassica rapa ancestral genome and observe the continuin
23                           We resequenced 199 Brassica rapa and 119 Brassica oleracea accessions repre
24 egments of the Brassica A genome as found in Brassica rapa and Brassica napus and the corresponding s
25                     Recent sequencing of the Brassica rapa and Brassica oleracea genomes revealed ext
26 zed to be a hybrid from unknown varieties of Brassica rapa and Brassica oleracea.
27 quence assemblies of its progenitor species, Brassica rapa and Brassica oleracea.
28 ssicoraphanus, a synthetic allotetraploid of Brassica rapa and Raphanus sativus.
29 at WUE is important for drought tolerance in Brassica rapa and that artificial selection for increase
30 ceae: Arabidopsis thaliana, Camelina sativa, Brassica rapa, and Eutrema salsugineum.
31 ed pre-rRNA transcripts from one progenitor, Brassica rapa are detected readily, whereas transcripts
32  Here we report on a novel dwarf mutant from Brassica rapa (Brrga1-d) that is caused by substitution
33 the beta-glucosidase BABG that is present in Brassica rapa but absent in Arabidopsis was shown to act
34                      Because loss of RdDM in Brassica rapa causes seed abortion, embryo methylation m
35  as two important vegetable crops, Pak Choi (Brassica rapa chinensis) and Choy Sum (Brassica rapa var
36 ranscriptomic changes that occur in the crop Brassica rapa during initial perception of drought, we a
37 ecies (Brassica carinata, Brassica oleracea, Brassica rapa, Eruca vesicaria and Sinapis alba) were an
38 three eudicot species: Arabidopsis thaliana, Brassica rapa (extrastaminal nectaries) and Nicotiana at
39                An anthocyanin-less mutant of Brassica rapa ("fast plants") was compared with varietie
40                          We have cloned four Brassica rapa homologs (BrFLC) of the MADS-box flowering
41 in shoots of an inbred mapping population of Brassica rapa (IMB211 x R500); 23 cis- and 948 trans-eQT
42 floral whorls in recombinant inbred lines of Brassica rapa in multiple environments to characterize t
43 terns of trait integration and modularity in Brassica rapa in response to three simulated seasonal te
44 physiological and biochemical adjustments in Brassica rapa in soil growing conditions and (2) to dete
45 over ontogeny in recombinant inbred lines of Brassica rapa in the field and glasshouse.
46                                              Brassica rapa is a mesopolyploid species that is domesti
47 ls to mediate SI in heading Chinese cabbage (Brassica rapa L. ssp.
48   Two-season greenhouse pot experiments with Brassica rapa L. were performed with and without the coc
49 dish (Raphanus sativus L.) (TBR) and Turnip (Brassica rapa L.) using a simple and effective single-st
50 ngated to erucic acid in developing seeds of Brassica rapa L., embryos were labeled with [14C]acetate
51    The elongated internode (ein) mutation of Brassica rapa leads to a deficiency in immunochemically
52 ed three copies of eIF(iso)4E in a number of Brassica rapa lines.
53 Aux/IAA family, as well as in their putative Brassica rapa orthologs.
54 lowed us to expose the entire root system of Brassica rapa plants to a square array of water sources,
55                                           In Brassica rapa, RdDM is required in the maternal sporophy
56       We measured leaf lengths and widths in Brassica rapa recombinant inbred lines (RILs) throughout
57 etative traits, and life history in a set of Brassica rapa recombinant inbred lines within and across
58  and untreated soils, we transferred forward Brassica rapa root microbiomes (from high-biomass or ran
59    The genome sequence of the paleohexaploid Brassica rapa shows that fractionation is biased among t
60 sequence divergence between sequences from a Brassica rapa ssp. pekinensis EST library isolated from
61 and identified BrPGIP3 from Chinese cabbage (Brassica rapa ssp. pekinensis) as a candidate.
62                                              Brassica rapa) ssp.
63  pairs, but no enrichment was identified for Brassica rapa subgenome biased pairs.
64  stress-induced H(2)O(2) and SA signals when Brassica rapa subsp.
65  stages (microgreens or leaves) of pak choi (Brassica rapa subsp. chinensis) and kale (Brassica olera
66 nse to moderate drought in four genotypes of Brassica rapa The quantum yield of PSII ( (PSII) ) is he
67  Brassica napus (oilseed rape), and those of Brassica rapa, the genome of which is currently being se
68 ere we report three PAP genes in the diploid Brassica rapa; the three PAPs are associated with differ
69 s occurred on chromosomes A06 and A01 within Brassica rapa; these were enriched with P metabolism-rel
70 e between conventional oilseed rape and wild Brassica rapa to model the future behavior of transplast
71 he evolutionary response of an annual plant, Brassica rapa, to a recent climate fluctuation resulting
72  (Apis mellifera) and a mass-flowering crop (Brassica rapa var. oleifera) on pollinator communities,
73 Choi (Brassica rapa chinensis) and Choy Sum (Brassica rapa var. parachinensis).
74                             Experiments with Brassica rapa verified that that gravitropism-like induc
75            GFP-CENH3 from the close relative Brassica rapa was targeted to centromeres, but did not c
76            Using recombinant inbred lines of Brassica rapa, we examined the quantitative-genetic arch
77 al profiling of the hypocotyl epidermis from Brassica rapa, we show that auxin acts in the epidermis
78 Using the oilseed and vegetable crop species Brassica rapa, we show that the perception of low red to
79                                           In Brassica rapa, we tested for physiological differentiati
80 lseed rape (Brassica napus) and turnip rape (Brassica rapa) were investigated with (1)H NMR metabolom