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1 the Arabidopsis (Arabidopsis thaliana) gene YUCCA.
2 down BT2 expression in the high-auxin mutant yucca.
3 by laying their eggs but not pollinating the yucca.
4 ollen, and the exclusion of copollinators by yuccas.
5 ation from an rbcL-based molecular clock for yuccas.
6 phylogenies and timelines for both moths and yuccas.
7 esis in transgenic plants overexpressing the YUCCA 1 (YUC1) auxin biosynthesis gene led to enhanced s
9 SA PROMOTER BINDING PROTEIN LIKE (SPL), NAC, YUCCA and AGAMOUS-LIKE genes associated with increases i
11 known obligate pollination mutualism between yuccas and yucca moths is a major model system for studi
13 suggests that evolution of mutualism between yuccas and yucca moths may have required few behavioral
14 ve been implicated in the diversification of yuccas and yucca moths, which exhibit ecological relatio
17 riments and biochemical assays indicate that YUCCA catalyzes hydroxylation of the amino group of tryp
23 dentify YUCCA6 as a functional member of the YUCCA family with unique roles in growth and development
24 it hyperactivation of genes belonging to the YUCCA family, encoding putative flavin monooxygenase enz
25 mediated induction of several members of the YUCCA gene family, leading to auxin production in the co
27 fied eight putative StYUC (Solanum tuberosum YUCCA) genes whose deduced amino acid sequences share 50
30 te pollinators inflict a heavy cost on their yucca hosts by laying their eggs but not pollinating the
32 eversal of an obligate mutualism: within the yucca moth complex, distinct cheater species derived fro
33 coloradensis (Lepidoptera: Prodoxidae) is a yucca moth, which feeds on the flowering stalks of three
34 o, and published data on legume-rhizobia and yucca-moth mutualisms are consistent with PFF and not wi
38 ate pollination mutualism between yuccas and yucca moths is a major model system for studies of coevo
39 The obligate mutualism between yuccas and yucca moths is a major model system for the study of coe
40 at evolution of mutualism between yuccas and yucca moths may have required few behavioral and life hi
41 licated in the diversification of yuccas and yucca moths, which exhibit ecological relationships that
46 System (GPS) surveys from 1991 to 1997 near Yucca Mountain, Nevada, indicate west-northwest crustal
51 which feeds on the flowering stalks of three Yucca species as larvae, but does not provide pollinatio
53 ariation among moths on different species of Yucca, the effect of host specificity on genetic distanc
54 expression is increased, particularly in the YUCCA/Tryptophan Aminotransferase of Arabidopsis1 pathwa
55 terization of a dominant Arabidopsis mutant, yucca, which contains elevated levels of free auxin.
56 phan to indole-3-pyruvate (IPA) and that the YUCCA (YUC) family of flavin monooxygenases participates
57 C2 encodes a previously identified member of YUCCA (YUC) flavin monooxygenase-like proteins (YUC8).
58 we demonstrate that auxin synthesized by the YUCCA (YUC) flavin monooxygenases is essential for the e
59 Previous genetic studies demonstrated that YUCCA (YUC) flavin-containing monooxygenases (FMOs) cata
60 ncodes a flavin monooxygenase similar to the YUCCA (YUC) genes of Arabidopsis, which are involved in
62 ilies, CYTOCHROME P450 79B2/B3 (CYP79B2/B3), YUCCA (YUC), and TRYPTOPHAN AMINOTRANSFERASE OF ARABIDOP
63 the promoter of the auxin biosynthesis gene YUCCA (YUC)4 and activates transcription of the genes YU
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