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1 B. oleracea and B. rapa rRNA genes also competed equally
2 B. oleracea and B. rapa rRNA genes were active when tran
3 B. oleracea was able to utilize atmospheric H(2)S as S-s
4 ced Brassica loci with a known position on a B. oleracea genetic map to the positions of their putati
7 mutations in target genes of both barley and B. oleracea and show stable transmission of these mutati
9 cea ssp. botrytis (domestic cauliflower) and B. oleracea ssp. italica (broccoli), both of which show
13 , an allotetraploid derived from B. rapa and B. oleracea in which only B. rapa rRNA genes are transcr
15 idization events (ca. 20 Myr for B. rapa and B. oleracea relative to Arabidopsis), with an analysis o
16 .IND.a and BolC.IND.a genes from B. rapa and B. oleracea share identical function with Arabidopsis IN
17 ars ago by hybridization between B. rapa and B. oleracea, followed by chromosome doubling, a process
18 ypic configuration is more conserved between B. oleracea S13 and B. campestris S8, two haplotypes tha
20 lymorphism, however, is also present in both B. oleracea ssp. acephala (kale) and B. oleracea ssp. ol
21 ons of mustard (Brassica nigra) and collard (B. oleracea var. acephala) and the effects of leaf nitro
25 n caused the normally silent, under-dominant B. oleracea rRNA genes to become expressed to high level
26 and class 2 TEs is responsible, in part, for B. oleracea genome expansion since divergence from a com
27 binding activities in nuclear extracts from B. oleracea, partial purification and DNA cross-linking
29 s costs were higher on the low-quality host (B. oleracea); and experimental methodology did not influ
33 Based on 186 corresponding loci detected in B. oleracea and A. thaliana, at least 19 chromosome stru
34 g this nonsense mutation are nearly fixed in B. oleracea ssp. botrytis (domestic cauliflower) and B.
35 e identified the product of the SRK6 gene in B. oleracea stigmas and have shown that it has character
37 s have amplified to very high copy number in B. oleracea where they have contributed significantly to
39 of gene fragments, as previously reported in B. oleracea, were observed in B. rapa and B. napus, indi
47 extraction to obtain bioactive compounds of B. oleracea var capitata showed to be a promising altern
48 at most of the phytochemical constituents of B. oleracea leaves are polar and possess strong antioxid
50 uence of A. thaliana with a partial draft of B. oleracea has permitted an estimation of the patterns
59 gene content was observed, both between the B. oleracea paralogous segments and between them and the
64 arrying a nonsense mutation in exon 5 of the B. oleracea CAULIFLOWER (BoCAL) gene are segregating in
68 are consistent with the hypothesis that the B. oleracea genome has been highly rearranged since dive
70 e exclusive GL breakdown products in the two B. oleracea varieties, since nitriles were also produced
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