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1 on (Antirrhinum majus), and petunia (Petunia hybrida).
2  in many flowers, including petunia (Petunia hybrida).
3 e distant asterid species petunia (Petunia x hybrida).
4 tolide biosynthesis in the stigma of Petunia hybrida.
5  the flavonoid-3',5'-hydroxylases of Petunia hybrida.
6 xillaris, one of the parental species of Pe. hybrida.
7 nabled in vivo directed evolution of Gerbera hybrida 2-pyrone synthase activity in E. coli .
8     Flowers of the artificial hybrid Petunia hybrida, a cross between P. integrifolia and P. axillari
9             By characterization of a Petunia hybrida adenosine triphosphate-binding cassette (ABC) tr
10 two MIXTA-related genes, PhMYB1 from Petunia hybrida and AtMYB16 from Arabidopsis thaliana, in petal
11 of CCRs from Medicago truncatula and Petunia hybrida and of an atypical CAD (CAD2) from M. truncatula
12                            SBP1 from Petunia hybrida and Solanum chacoense is a putative E3 ubiquitin
13 ated degradation (ERAD) pathway in both Rosa hybrida and Solanum lycopersicum.
14 to 61% sequence identity to petunia (Petunia hybrida) and potato (Solanum tuberosum) FLS.
15 s ANTHOCYANIN11 (AN11) from petunia (Petunia hybrida) and TRANSPARENT TESTA GLABRA1 (TTG1) from Arabi
16 ilobium hirsutum, Nicotiana tabacum, Petunia hybrida, and the cereal crop Setaria italica to a crucif
17 ns, faba bean [Vicia faba], petunia [Petunia hybrida], and tobacco [Nicotiana tabacum]).
18 that in the asterid species petunia (Petunia hybrida), AP2B/BLIND ENHANCER (BEN) confines the C-funct
19 howed that both isoeugenol and eugenol in P. hybrida are biosynthesized from coniferyl acetate in rea
20 tar-type bicolour petals of petunia (Petunia hybrida) are caused by post-transcriptional gene silenci
21                       Using petunia (Petunia hybrida) as a model for vegetative branching, we manipul
22  genomic DNA from the progenitors of Petunia hybrida, as well as from Nicotiana tabacum, indicated th
23 ve hypermethylated DNA fragment from Petunia hybrida, attracts DNA methylation when transferred into
24        Here, we observed that, in rose (Rosa hybrida), biologically active CK is accumulated during p
25 , suppressing the expression of PhIGS1 in P. hybrida by RNA interference also leads to a decrease in
26            We show that the petunia (Petunia hybrida) C-clade genes PETUNIA MADS BOX GENE3 and FLORAL
27  by RNAi suppression of the petunia (Petunia hybrida) cinnamoyl-CoA reductase 1 (PhCCR1), which catal
28 es whereas FNS II from the nonlegume Gerbera hybrida, converted flavanones to flavones directly.
29                                    Petunia x hybrida cv 'Mitchell Diploid' floral volatile benzenoid/
30 opulation from two diploid cultivars, Rosa x hybrida cv H190 and Rosa wichurana, which have contrasti
31  understanding of EIN2, a petunia (Petunia x hybrida cv Mitchell Diploid [MD]) homolog of the Arabido
32 as modified in transgenic petunia (Petunia x hybrida cv Mitchell).
33            We transformed petunia (Petunia x hybrida cv V26) with P(SAG12)-IPT.
34                                 In Petunia x hybrida cv. 'Mitchell Diploid' floral fragrance is compr
35 nthesis of FVBPs in the corolla of Petunia x hybrida cv. 'Mitchell Diploid'.
36 iphered spatial patterns of prickles on Rosa hybrida cv. 'Red Queen' stem.
37                                   In Petunia hybrida cv. Mitchell flowers, the biosynthesis and emiss
38   We have isolated and characterized Petunia hybrida cv. Mitchell phenylacetaldehyde synthase (PAAS),
39                             Petunia (Petunia hybrida cv. Mitchell) flowers, which emit large amounts
40 e the metabolic pathways in petunia (Petunia hybrida) cv Mitchell leading from Phe to benzenoid compo
41                          In petunia (Petunia hybrida), EMISSION OF BENZENOIDS II (EOBII) controls tra
42                    The Sho gene from Petunia hybrida encodes an enzyme responsible for the synthesis
43 flowering plants, such as petunia (Petunia x hybrida), ethylene produced in floral organs after polli
44  a putative ortholog of the petunia (Petunia hybrida) floral scent regulator ODORANT1 (ODO1), control
45 e based on the epicuticular waxes of Petunia hybrida flower petals was formulated to test the effect
46 petal senescence markedly reduces rose (Rosa hybrida) flower quality and value.
47 ure of eugenol and isoeugenol, while Petunia hybrida flowers emit mostly isoeugenol with small amount
48                        Here, we used Petunia hybrida flowers, which are rich in Phe-derived volatiles
49    The epidermal cells of petunia (Petunia x hybrida) flowers are the main site of volatile emission.
50 (isoeugenol and eugenol) in petunia (Petunia hybrida) flowers have the precursor 4-coumaryl coenzyme
51 of the benzenoid network in petunia (Petunia hybrida) flowers revealed that both pathways yield benze
52       Here, we show that in petunia (Petunia hybrida) flowers, which typically produce high phenylala
53 n a genetic mutant screen a petunia (Petunia hybrida) Gibberellic Acid Insensitive, Repressor of Gibb
54  morning, antiphasic to the expression of P. hybrida GIGANTEA (PhGI), the master scent regulator ODOR
55 A repetitive DNA sequence (RPS) from Petunia hybrida had previously been shown to enhance expression
56                   The plant species Medicago hybrida had the highest abundance in honey produced by A
57                                  The Petunia hybrida HAIRY MERISTEM (HAM) gene, a member of the GRAS
58 es anthocyanin synthesis in petunia (Petunia hybrida) has been characterized.
59  bourboniana and 8 h ethylene-treated AZ (R. hybrida) identified a core set of 255 genes uniquely reg
60                       Our studies in Gerbera hybrida indicate functional diversification for SEPALLAT
61                        Indeed, in rose (Rosa hybrida), inhibition of bud outgrowth by darkness is sup
62                                      Petunia hybrida is a popular bedding plant that has a long histo
63 protein is 59% identical to petunia (Petunia hybrida) isoeugenol synthase 1 and displays apparent Km
64 demonstrate that the circadian clock gene P. hybrida LATE ELONGATED HYPOCOTYL (LHY; PhLHY) regulates
65 e have isolated a cDNA from petunia (Petunia hybrida) leaves encoding a putative protein of 214 amino
66 ntly an R2R3-MYB was identified in Petunia x hybrida line P720 to have a role in the transcriptional
67                        In petunia (Petunia x hybrida), MADS-box homeotic genes dictate floral organ i
68 BII was isolated and characterized from P. x hybrida 'Mitchell Diploid' (MD) and Nicotiana attenuata.
69           This redundancy is lost in Petunia hybrida, not because of the inability of PhCUL1-B to int
70 ssion of a MYB transcription factor, Petunia hybrida ODORANT1, to alter Phe and phenylpropanoid metab
71  potential CoA-ligases from petunia (Petunia hybrida) petal-specific cDNA libraries.
72 ATA19, resulted in reduced fusion of Petunia hybrida petals, with silencing of both PhGATA19 and its
73          Here, we studied petunia (Petunia x hybrida) petals that form a limb and tube through congen
74 atory proteins ANTHOCYANIN11 (AN11) (Petunia hybrida [petunia]) and TRANSPARENT TESTA GLABRA1 (TTG1)
75  homology to the recently identified Petunia hybrida phenylacetaldehyde synthase involved in floral s
76 opersicum; SlpreproHypSys), petunia (Petunia hybrida; PhpreproHypSys), potato (Solanum tuberosum; Php
77 opersicon esculentum) and petunia (Petunia x hybrida) plants were conducted to determine if normal or
78 erium-mediated infection of petunia (Petunia hybrida) plants with tobacco rattle virus (TRV) bearing
79              Here, a gene encoding a Petunia hybrida plastidial cationic amino-acid transporter (PhpC
80 xperiments with germinating petunia (Petunia hybrida) pollen and boronate-affinity chromatography sho
81                             Petunia (Petunia hybrida) pollen requires flavonols (Fl) to germinate.
82  a spontaneous mutable Hf1 allele in Petunia hybrida provided an opportunity to isolate and character
83 anscription factor in woody plant rose (Rosa hybrida), regulates local auxin biosynthesis and auxin t
84 n of VvMYB4a and VvMYB4b in petunia (Petunia hybrida) repressed general phenylpropanoid biosynthetic
85 tathione S-transferase from petunia (Petunia hybrida) required for efficient anthocyanin export from
86 co (Nicotiana tabacum), and petunia (Petunia hybrida) resulted in plants with GA deficiency and typic
87 F) transcription factor family in rose (Rosa hybrida), RhERF1 and RhERF4 which play a role in petal a
88  a high degree of specificity to the Petunia hybrida S-ribonuclease.
89 tein1 (Pi SBP1), almost identical to Petunia hybrida SBP1, which interacts with Pi SLFs, S-RNases, Pi
90                                   In Petunia hybrida, SL transport within the plant and towards the r
91                                   In Petunia hybrida, volatile emissions are dominated by products of
92 lower head margin in the model plant Gerbera hybrida We discovered a previously unidentified expressi
93 nal models to explain phyllotaxis in Gerbera hybrida We show that phyllotactic patterning in gerbera
94 ) and UNUSUAL FLORAL ORGANS (UFO) in Gerbera hybrida, we show that GhUFO is the master regulator of f
95 the orthologous gene of PhEOBII from Petunia hybrida, which contributes to the regulation of eugenol