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1 e triplication event prior to diverging from Brassica rapa.
2 A. thaliana, A. lyrata, Capsella rubella and Brassica rapa.
3 an period was related to drought response in Brassica rapa.
4 ave investigated circadian clock function in Brassica rapa.
5 ing double haploids of Brassica oleracea and Brassica rapa.
6 system in the laboratory using rapid-cycling Brassica rapa.
7 cal mapping between Arabidopsis thaliana and Brassica rapa.
8 er size of CeO2 throughout the life cycle of Brassica rapa.
9 generated from whole genome triplication in Brassica rapa.
10 yotypes developed for the progenitor species Brassica rapa (A genome) and Brassica oleracea (C genome
11 he activity of superoxide dismutase (SOD) in Brassica rapa also displayed a growth-stage dependent re
13 influence of time on the drought response of Brassica rapa, an agriculturally important species of pl
15 egments of the Brassica A genome as found in Brassica rapa and Brassica napus and the corresponding s
18 at WUE is important for drought tolerance in Brassica rapa and that artificial selection for increase
19 ed pre-rRNA transcripts from one progenitor, Brassica rapa are detected readily, whereas transcripts
20 Here we report on a novel dwarf mutant from Brassica rapa (Brrga1-d) that is caused by substitution
21 the beta-glucosidase BABG that is present in Brassica rapa but absent in Arabidopsis was shown to act
22 ranscriptomic changes that occur in the crop Brassica rapa during initial perception of drought, we a
23 three eudicot species: Arabidopsis thaliana, Brassica rapa (extrastaminal nectaries) and Nicotiana at
26 in shoots of an inbred mapping population of Brassica rapa (IMB211 x R500); 23 cis- and 948 trans-eQT
27 floral whorls in recombinant inbred lines of Brassica rapa in multiple environments to characterize t
28 terns of trait integration and modularity in Brassica rapa in response to three simulated seasonal te
29 physiological and biochemical adjustments in Brassica rapa in soil growing conditions and (2) to dete
31 dish (Raphanus sativus L.) (TBR) and Turnip (Brassica rapa L.) using a simple and effective single-st
32 ngated to erucic acid in developing seeds of Brassica rapa L., embryos were labeled with [14C]acetate
33 The elongated internode (ein) mutation of Brassica rapa leads to a deficiency in immunochemically
37 etative traits, and life history in a set of Brassica rapa recombinant inbred lines within and across
38 The genome sequence of the paleohexaploid Brassica rapa shows that fractionation is biased among t
39 sequence divergence between sequences from a Brassica rapa ssp. pekinensis EST library isolated from
40 Brassica napus (oilseed rape), and those of Brassica rapa, the genome of which is currently being se
41 ere we report three PAP genes in the diploid Brassica rapa; the three PAPs are associated with differ
42 s occurred on chromosomes A06 and A01 within Brassica rapa; these were enriched with P metabolism-rel
43 e between conventional oilseed rape and wild Brassica rapa to model the future behavior of transplast
44 he evolutionary response of an annual plant, Brassica rapa, to a recent climate fluctuation resulting
47 al profiling of the hypocotyl epidermis from Brassica rapa, we show that auxin acts in the epidermis
48 Using the oilseed and vegetable crop species Brassica rapa, we show that the perception of low red to
50 lseed rape (Brassica napus) and turnip rape (Brassica rapa) were investigated with (1)H NMR metabolom
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