ライフサイエンスコーパス: Antirrhinum majus

1 i.e. AmRosea1 and AmDelila from snapdragon (Antirrhinum majus).

2 rved in Arabidopsis thaliana and snapdragon (Antirrhinum majus).

3 variation in 3000 leaves from 400 plants of Antirrhinum majus.

4 ment of conical epidermal cells in petals of Antirrhinum majus.

5 to the development of dorsal petal lobes of Antirrhinum majus.

6 ptide-encoding sequence from the oli gene of Antirrhinum majus.

7 ms such as Arabidopsis thaliana, snapdragon (Antirrhinum majus), and petunia (Petunia hybrida).

8 In the early 1900s, Erwin Baur established Antirrhinum majus as a model system, identifying and cha

9 Tam3 from Antirrhinum majus belongs to the Ac/Ds family of transpo

10 class in Arabidopsis (TCP1) and snapdragon (Antirrhinum majus; CYCLOIDEA) have been shown to be asym

11 An Antirrhinum majus dihydroflavonol reductase (DFR) cDNA w

12 Here we report the isolation of a gene from Antirrhinum majus encoding a protein from an entirely no

13 This observation extends previous reports in Antirrhinum majus, Epilobium hirsutum, Nicotiana tabacum

14 In Antirrhinum majus, floral zygomorphy is established by t

15 ne responsible for conferring dorsal fate in Antirrhinum majus flowers.

16 Here, snapdragon (Antirrhinum majus) GPPS-SSU was over-expressed in tomato

17 Here, we show that expression of snapdragon (Antirrhinum majus) GPPS.SSU in tobacco (Nicotiana tabacu

18 Ectopic expression of the MIXTA gene from Antirrhinum majus in S. dulcamara results in the formati

19 le) and Dicotyledonae (Nicotiana tabacum and Antirrhinum majus) indicating that LINEs are a universal

20 w that the growth and asymmetry of leaves in Antirrhinum majus involves the related YABBY transcripti

21 MIXTA, which in Antirrhinum majus is reported to regulate certain aspect

22 n the distantly related core eudicot species Antirrhinum majus L., paralogous SBP-box proteins SBP1 a

23 Investigation of two classic mutants in Antirrhinum majus, mutabilis and incolorata I, showed th

24 The identification of Antirrhinum majus mutants with ectopic petal spurs sugge

25 he reporter system is based on expression of Antirrhinum majus MYB-related Rosea1 (Ros1) transcriptio

26 i X N. sanderae) homolog of the antirrhinum (Antirrhinum majus) MYB305.

27 In Antirrhinum majus, one proposed role of the gene fimbria

28 transcription factor genes from snapdragon (Antirrhinum majus), paying particular attention to chang

29 proteins, initially described in snapdragon (Antirrhinum majus) petals, are known regulators of epide

30 lly symmetrical flowers of the model species Antirrhinum majus (Plantaginaceae) are highly specialize

31 ridoids in the ornamental flower snapdragon (Antirrhinum majus, Plantaginaceae family) are derived fr

32 In four Antirrhinum majus populations with different mating syst

33 ng bZIP proteins are expressed in flowers of Antirrhinum majus, predominantly in vascular tissues, ca

34 unctional genomic approach, we identified an Antirrhinum majus (snapdragon) BALDH, which exhibits 40%

35 In the model developmental system Antirrhinum majus (snapdragon), the closely related gene

36 ing mechanisms used by four such proteins in Antirrhinum majus, SQUA, PLE, DEF and GLO.

37 The model species Antirrhinum majus (the garden snapdragon) has over 20 cl

38 In Antirrhinum majus, the MIXTA protein directs the formati

39 unds detected in the majority of snapdragon (Antirrhinum majus) varieties.

40 ve identified a mutation at the DAG locus of Antirrhinum majus which blocks the development of chloro