ライフサイエンスコーパス: snapdragon

1 the vegetative and the reproductive phase in snapdragon.

2 otein with homology to the cycloidea gene of snapdragon.

3 a process that takes between 35 and 40 h in snapdragon and approximately 32 h in petunia.

4 Evidence from the Antirrhineae (snapdragon and relatives) indicates that several TCP gen

5 s in the leaf vascular responses of alyssum, snapdragon and tobacco plants suggest common functions o

6 of methyl benzoate production in diurnally (snapdragon) and nocturnally (tobacco and petunia) emitti

7 Here, snapdragon (Antirrhinum majus) GPPS-SSU was over-express

8 Here, we show that expression of snapdragon (Antirrhinum majus) GPPS.SSU in tobacco (Nico

9 /MIXTA-like proteins, initially described in snapdragon (Antirrhinum majus) petals, are known regulat

10 scent compounds detected in the majority of snapdragon (Antirrhinum majus) varieties.

11 model systems such as Arabidopsis thaliana, snapdragon (Antirrhinum majus), and petunia (Petunia hyb

12 a and Rosea1 transcription factor genes from snapdragon (Antirrhinum majus), paying particular attent

13 nd bHLH TFs, i.e. AmRosea1 and AmDelila from snapdragon (Antirrhinum majus).

14 ization observed in Arabidopsis thaliana and snapdragon (Antirrhinum majus).

15 instance, iridoids in the ornamental flower snapdragon (Antirrhinum majus, Plantaginaceae family) ar

16 enes of this class in Arabidopsis (TCP1) and snapdragon (Antirrhinum majus; CYCLOIDEA) have been show

17 Snapdragon (Antirrhinum) mutants lacking conical cells h

18 In the genus Antirrhinum (snapdragons), as in other plants, a suite of morphologic

19 pproach, we identified an Antirrhinum majus (snapdragon) BALDH, which exhibits 40% identity to bacter

20 Petunia and snapdragon both synthesize methylbenzoate from benzoic a

21 sea1 and AmDelila transcription factors from snapdragon can activate the anthocyanin pathway in orang

22 n floral scent emission were investigated in snapdragon cv Maryland True Pink and petunia cv Mitchell

23 We use the Snapdragon flower as a model system to address this prob

24 tent, in the cells of the outer epidermis of snapdragon flower petal lobes.

25 lation-wide differences in color patterns in snapdragon flowers are caused by an inverted duplication

26 Snapdragon flowers emit two monoterpene olefins, myrcene

27 Terpenoids emitted from snapdragon flowers include three monoterpenes derived fr

28 ssion of these monoterpene synthase genes in snapdragon flowers revealed coordinated regulation of ph

29 t abundant scent compounds of bee-pollinated snapdragon flowers, occurs in a rhythmic manner, with ma

30 In snapdragon flowers, the volatile ester methyl benzoate i

31 2,2-2H2]-mevalolactone) were supplied to cut snapdragon flowers, which emit both monoterpenes and the

32 is function of FSM1 differs from that of the snapdragon FSM1-like gene, RAD, which through an antagon

33 basilicum geraniol synthase (GES) gene with snapdragon GPPS-SSU led to a more than threefold increas

34 Co-expression of snapdragon GPPS-SSU with the O. basilicum alpha-zingiber

35 ncode bona fide GGPPS that can interact with snapdragon GPPS.SSU and form a functional GPPS enzyme in

36 model species Antirrhinum majus (the garden snapdragon) has over 20 close wild relatives that are mo

37 we expressed two transcription factors from snapdragon in tomato, the fruit of the plants accumulate

38 SnapDRAGON is a suite of programs developed to predict d

39 These newly isolated snapdragon monoterpene synthases, together with Arabidop

40 )-beta-Ocimene synthase is highly similar to snapdragon myrcene synthases (92% amino acid identity) a

41 illustrate these principles with a study of snapdragon petal growth.

42 thyl benzoate is produced in upper and lower snapdragon petal lobes by enzymatic methylation of benzo

43 acterized three closely related cDNAs from a snapdragon petal-specific library that encode two myrcen

44 squiterpene biosynthesis in the epidermis of snapdragon petals.

45 , to observe the development of Antirrhinum (snapdragon) petals.

46 regulate anthocyanin production in maize and snapdragon, respectively.

47 mes responsible for the terpenoid profile of snapdragon scent remaining to be characterized.

48 ences in leaf allometry between Antirrhinum (snapdragon) species, including variation in heteroblasty

49 odel developmental system Antirrhinum majus (snapdragon), the closely related genes CYCLOIDEA (CYC) a

50 In snapdragon, the decrease in methylbenzoate emission is t

51 essed in developing floral primordia, and in snapdragon, they are required for floral zygomorphy (bil

52 arge subunit partner(s) and formed an active snapdragon/tobacco GPPS in planta.

53 ural variation within the genus Antirrhinum (snapdragons), which has evolved hairy alpine-adapted spe