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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 e, out-of-season flowering in desert-adapted Yucca.
5 ollen, and the exclusion of copollinators by yuccas.
6 ation from an rbcL-based molecular clock for yuccas.
7 phylogenies and timelines for both moths and yuccas.
8 esis in transgenic plants overexpressing the YUCCA 1 (YUC1) auxin biosynthesis gene led to enhanced s
9 evealed that Indole-3-pyruvate monooxygenase YUCCA 10 (RhYUC10) and Auxin transporter-like protein 2
10 O-CYCLOPROPANE-1-CARBOXYLATE SYNTHASE 2, and YUCCA 5, in addition to genes encoding transcription fac
11               Together with previous work on YUCCA, a flavin monooxygenase also implicated in IAOx pr
12 SA PROMOTER BINDING PROTEIN LIKE (SPL), NAC, YUCCA and AGAMOUS-LIKE genes associated with increases i
13                                              Yucca and Beschorneria have CAM-like expression of PPC2,
14                The complex mutualism between yuccas and the moths that pollinate their flowers is reg
15 known obligate pollination mutualism between yuccas and yucca moths is a major model system for studi
16               The obligate mutualism between yuccas and yucca moths is a major model system for the s
17 suggests that evolution of mutualism between yuccas and yucca moths may have required few behavioral
18 ve been implicated in the diversification of yuccas and yucca moths, which exhibit ecological relatio
19 or mutualisms such as figs and fig wasps and yuccas and yucca moths.
20                Our study identifies PIFs and YUCCAs as novel molecular players promoting phototropism
21                                Flowering for Yucca brevifolia (Joshua tree) and Yucca schidigera (Moj
22                     Composed of two species, Yucca brevifolia and Y. jaegeriana (Asparagaceae), Joshu
23 e change effects on masting by Joshua trees (Yucca brevifolia and Y. jaegeriana), keystone perennials
24 riments and biochemical assays indicate that YUCCA catalyzes hydroxylation of the amino group of tryp
25 emergence of pollinators within 0-6 My after yucca colonization.
26                                              YUCCA encodes a flavin monooxygenase-like enzyme and bel
27 e non-purified oil and the saponins from the Yucca extract lead to the formation of nanostructured ad
28 ling and heat-induced auxin biosynthesis via YUCCA family genes are synergistically required to maint
29       We find Crispoid to be a member of the YUCCA family of auxin biosynthetic genes.
30 SUPER1 encodes YUCCA5, a novel member of the YUCCA family of flavin monooxygenases.
31 ndancy of multiple pathways that involve the YUCCA family of flavin-dependent mono-oxygenases.
32 dentify YUCCA6 as a functional member of the YUCCA family with unique roles in growth and development
33 it hyperactivation of genes belonging to the YUCCA family, encoding putative flavin monooxygenase enz
34 atens TRYPTOPHAN AMINO-TRANSFERASE (TAR) and YUCCA FLAVIN MONOOXYGENASE-LIKE (YUC) auxin biosynthesis
35 mediated induction of several members of the YUCCA gene family, leading to auxin production in the co
36        When exposed to shade, we found three YUCCA genes, YUC2, YUC5, and YUC8, to be transcriptional
37 fied eight putative StYUC (Solanum tuberosum YUCCA) genes whose deduced amino acid sequences share 50
38                                              Yucca GRAS-labelled saponins have been and are increasin
39                              Colonization of yuccas had occurred by 41.5 +/- 9.8 million years ago (M
40 te pollinators inflict a heavy cost on their yucca hosts by laying their eggs but not pollinating the
41                                              Yucca in the American desert Southwest typically flowers
42 a (Joshua tree) and Yucca schidigera (Mojave yucca) is driven by complex, nonlinear interactions betw
43 MF), yet the AMF of the Eastern Joshua tree (Yucca jaegeriana) remain completely uncharacterized.
44 anscriptional increase of auxin biosynthetic YUCCA-like genes.
45 eversal of an obligate mutualism: within the yucca moth complex, distinct cheater species derived fro
46  coloradensis (Lepidoptera: Prodoxidae) is a yucca moth, which feeds on the flowering stalks of three
47 o, and published data on legume-rhizobia and yucca-moth mutualisms are consistent with PFF and not wi
48              Major differences compared with yucca moths and their hosts are that G. politella only p
49 to have resulted from coevolved mutualism in yucca moths are plesiomorphic to the family.
50               Derived nonpollinating cheater yucca moths evolved 1.26 +/- 0.96 Mya.
51 ate pollination mutualism between yuccas and yucca moths is a major model system for studies of coevo
52    The obligate mutualism between yuccas and yucca moths is a major model system for the study of coe
53 at evolution of mutualism between yuccas and yucca moths may have required few behavioral and life hi
54 licated in the diversification of yuccas and yucca moths, which exhibit ecological relationships that
55 ms such as figs and fig wasps and yuccas and yucca moths.
56 tacle appears abruptly in female pollinating yucca moths.
57 nent of the oviposition behavior than in the yucca moths.
58 time of major life history events within the yucca moths.
59                                    Since the Yucca Mountain project in the U.S. was defunded in 2010,
60  System (GPS) surveys from 1991 to 1997 near Yucca Mountain, Nevada, indicate west-northwest crustal
61 y regulates auxin production by activating a YUCCA (MpYUC2) auxin biosynthetic enzyme in stem cells.
62             The results suggest a functional YUCCA pathway of auxin biosynthesis in potato that may b
63 e 50%-70% identity with those of Arabidopsis YUCCA proteins.
64 ting step converting IPA to IAA catalyzed by YUCCA proteins.
65 ering for Yucca brevifolia (Joshua tree) and Yucca schidigera (Mojave yucca) is driven by complex, no
66 -in-water emulsions (SFO-in-W) stabilized by Yucca Schidigera Roezl saponin extract, is by >50 times
67             All include canonical, conserved YUCCA sequences: FATGY motif, FMO signature sequence, an
68 which feeds on the flowering stalks of three Yucca species as larvae, but does not provide pollinatio
69       Existing techniques presently used for Yucca steroidal saponin quantification remain either ina
70 ariation among moths on different species of Yucca, the effect of host specificity on genetic distanc
71 expression is increased, particularly in the YUCCA/Tryptophan Aminotransferase of Arabidopsis1 pathwa
72 terization of a dominant Arabidopsis mutant, yucca, which contains elevated levels of free auxin.
73 could directly bind the GCC-box motif in the YUCCA (YUC) auxin biosynthesis genes FveYUC4 and FveYUC2
74 phan to indole-3-pyruvate (IPA) and that the YUCCA (YUC) family of flavin monooxygenases participates
75 elated to plant flavin monooxygenases of the YUCCA (YUC) family, which catalyze the final step in aux
76 C2 encodes a previously identified member of YUCCA (YUC) flavin monooxygenase-like proteins (YUC8).
77 we demonstrate that auxin synthesized by the YUCCA (YUC) flavin monooxygenases is essential for the e
78   Previous genetic studies demonstrated that YUCCA (YUC) flavin-containing monooxygenases (FMOs) cata
79                                          The YUCCA (YUC) genes encode flavin monooxygenases that cata
80 ncodes a flavin monooxygenase similar to the YUCCA (YUC) genes of Arabidopsis, which are involved in
81                                              YUCCA (YUC) proteins constitute a family of flavin monoo
82 ilies, CYTOCHROME P450 79B2/B3 (CYP79B2/B3), YUCCA (YUC), and TRYPTOPHAN AMINOTRANSFERASE OF ARABIDOP
83  the promoter of the auxin biosynthesis gene YUCCA (YUC)4 and activates transcription of the genes YU
84 anscriptional induction of STYLISH (STY) and YUCCAs (YUC).