ライフサイエンスコーパス: hybrida

1 on (Antirrhinum majus), and petunia (Petunia hybrida).

2 in many flowers, including petunia (Petunia hybrida).

3 tolide biosynthesis in the stigma of Petunia hybrida.

4 the flavonoid-3',5'-hydroxylases of Petunia hybrida.

5 nabled in vivo directed evolution of Gerbera hybrida 2-pyrone synthase activity in E. coli .

6 Flowers of the artificial hybrid Petunia hybrida, a cross between P. integrifolia and P. axillari

7 By characterization of a Petunia hybrida adenosine triphosphate-binding cassette (ABC) tr

8 two MIXTA-related genes, PhMYB1 from Petunia hybrida and AtMYB16 from Arabidopsis thaliana, in petal

9 of CCRs from Medicago truncatula and Petunia hybrida and of an atypical CAD (CAD2) from M. truncatula

10 SBP1 from Petunia hybrida and Solanum chacoense is a putative E3 ubiquitin

11 to 61% sequence identity to petunia (Petunia hybrida) and potato (Solanum tuberosum) FLS.

12 s ANTHOCYANIN11 (AN11) from petunia (Petunia hybrida) and TRANSPARENT TESTA GLABRA1 (TTG1) from Arabi

13 ilobium hirsutum, Nicotiana tabacum, Petunia hybrida, and the cereal crop Setaria italica to a crucif

14 ns, faba bean [Vicia faba], petunia [Petunia hybrida], and tobacco [Nicotiana tabacum]).

15 that in the asterid species petunia (Petunia hybrida), AP2B/BLIND ENHANCER (BEN) confines the C-funct

16 howed that both isoeugenol and eugenol in P. hybrida are biosynthesized from coniferyl acetate in rea

17 Using petunia (Petunia hybrida) as a model for vegetative branching, we manipul

18 genomic DNA from the progenitors of Petunia hybrida, as well as from Nicotiana tabacum, indicated th

19 ve hypermethylated DNA fragment from Petunia hybrida, attracts DNA methylation when transferred into

20 , suppressing the expression of PhIGS1 in P. hybrida by RNA interference also leads to a decrease in

21 We show that the petunia (Petunia hybrida) C-clade genes PETUNIA MADS BOX GENE3 and FLORAL

22 by RNAi suppression of the petunia (Petunia hybrida) cinnamoyl-CoA reductase 1 (PhCCR1), which catal

23 es whereas FNS II from the nonlegume Gerbera hybrida, converted flavanones to flavones directly.

24 understanding of EIN2, a petunia (Petunia x hybrida cv Mitchell Diploid [MD]) homolog of the Arabido

25 as modified in transgenic petunia (Petunia x hybrida cv Mitchell).

26 We transformed petunia (Petunia x hybrida cv V26) with P(SAG12)-IPT.

27 In Petunia x hybrida cv. 'Mitchell Diploid' floral fragrance is compr

28 nthesis of FVBPs in the corolla of Petunia x hybrida cv. 'Mitchell Diploid'.

29 We have isolated and characterized Petunia hybrida cv. Mitchell phenylacetaldehyde synthase (PAAS),

30 Petunia (Petunia hybrida cv. Mitchell) flowers, which emit large amounts

31 e the metabolic pathways in petunia (Petunia hybrida) cv Mitchell leading from Phe to benzenoid compo

32 In petunia (Petunia hybrida), EMISSION OF BENZENOIDS II (EOBII) controls tra

33 The Sho gene from Petunia hybrida encodes an enzyme responsible for the synthesis

34 flowering plants, such as petunia (Petunia x hybrida), ethylene produced in floral organs after polli

35 ure of eugenol and isoeugenol, while Petunia hybrida flowers emit mostly isoeugenol with small amount

36 Here, we used Petunia hybrida flowers, which are rich in Phe-derived volatiles

37 (isoeugenol and eugenol) in petunia (Petunia hybrida) flowers have the precursor 4-coumaryl coenzyme

38 of the benzenoid network in petunia (Petunia hybrida) flowers revealed that both pathways yield benze

39 n a genetic mutant screen a petunia (Petunia hybrida) Gibberellic Acid Insensitive, Repressor of Gibb

40 morning, antiphasic to the expression of P. hybrida GIGANTEA (PhGI), the master scent regulator ODOR

41 A repetitive DNA sequence (RPS) from Petunia hybrida had previously been shown to enhance expression

42 The Petunia hybrida HAIRY MERISTEM (HAM) gene, a member of the GRAS

43 es anthocyanin synthesis in petunia (Petunia hybrida) has been characterized.

44 Our studies in Gerbera hybrida indicate functional diversification for SEPALLAT

45 Indeed, in rose (Rosa hybrida), inhibition of bud outgrowth by darkness is sup

46 Petunia hybrida is a popular bedding plant that has a long histo

47 protein is 59% identical to petunia (Petunia hybrida) isoeugenol synthase 1 and displays apparent Km

48 demonstrate that the circadian clock gene P. hybrida LATE ELONGATED HYPOCOTYL (LHY; PhLHY) regulates

49 e have isolated a cDNA from petunia (Petunia hybrida) leaves encoding a putative protein of 214 amino

50 ntly an R2R3-MYB was identified in Petunia x hybrida line P720 to have a role in the transcriptional

51 BII was isolated and characterized from P. x hybrida 'Mitchell Diploid' (MD) and Nicotiana attenuata.

52 ssion of a MYB transcription factor, Petunia hybrida ODORANT1, to alter Phe and phenylpropanoid metab

53 potential CoA-ligases from petunia (Petunia hybrida) petal-specific cDNA libraries.

54 atory proteins ANTHOCYANIN11 (AN11) (Petunia hybrida [petunia]) and TRANSPARENT TESTA GLABRA1 (TTG1)

55 homology to the recently identified Petunia hybrida phenylacetaldehyde synthase involved in floral s

56 opersicum; SlpreproHypSys), petunia (Petunia hybrida; PhpreproHypSys), potato (Solanum tuberosum; Php

57 opersicon esculentum) and petunia (Petunia x hybrida) plants were conducted to determine if normal or

58 erium-mediated infection of petunia (Petunia hybrida) plants with tobacco rattle virus (TRV) bearing

59 Here, a gene encoding a Petunia hybrida plastidial cationic amino-acid transporter (PhpC

60 xperiments with germinating petunia (Petunia hybrida) pollen and boronate-affinity chromatography sho

61 Petunia (Petunia hybrida) pollen requires flavonols (Fl) to germinate.

62 a spontaneous mutable Hf1 allele in Petunia hybrida provided an opportunity to isolate and character

63 n of VvMYB4a and VvMYB4b in petunia (Petunia hybrida) repressed general phenylpropanoid biosynthetic

64 tathione S-transferase from petunia (Petunia hybrida) required for efficient anthocyanin export from

65 co (Nicotiana tabacum), and petunia (Petunia hybrida) resulted in plants with GA deficiency and typic

66 a high degree of specificity to the Petunia hybrida S-ribonuclease.

67 tein1 (Pi SBP1), almost identical to Petunia hybrida SBP1, which interacts with Pi SLFs, S-RNases, Pi

68 In Petunia hybrida, SL transport within the plant and towards the r

69 In Petunia hybrida, volatile emissions are dominated by products of

70 ) and UNUSUAL FLORAL ORGANS (UFO) in Gerbera hybrida, we show that GhUFO is the master regulator of f

71 the orthologous gene of PhEOBII from Petunia hybrida, which contributes to the regulation of eugenol