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1 rved in Arabidopsis thaliana and snapdragon (Antirrhinum majus).
2 variation in 3000 leaves from 400 plants of Antirrhinum majus.
3 ment of conical epidermal cells in petals of Antirrhinum majus.
4 to the development of dorsal petal lobes of Antirrhinum majus.
5 ptide-encoding sequence from the oli gene of Antirrhinum majus.
8 class in Arabidopsis (TCP1) and snapdragon (Antirrhinum majus; CYCLOIDEA) have been shown to be asym
10 Here we report the isolation of a gene from Antirrhinum majus encoding a protein from an entirely no
11 This observation extends previous reports in Antirrhinum majus, Epilobium hirsutum, Nicotiana tabacum
15 Here, we show that expression of snapdragon (Antirrhinum majus) GPPS.SSU in tobacco (Nicotiana tabacu
16 Ectopic expression of the MIXTA gene from Antirrhinum majus in S. dulcamara results in the formati
17 le) and Dicotyledonae (Nicotiana tabacum and Antirrhinum majus) indicating that LINEs are a universal
18 w that the growth and asymmetry of leaves in Antirrhinum majus involves the related YABBY transcripti
20 n the distantly related core eudicot species Antirrhinum majus L., paralogous SBP-box proteins SBP1 a
22 he reporter system is based on expression of Antirrhinum majus MYB-related Rosea1 (Ros1) transcriptio
25 transcription factor genes from snapdragon (Antirrhinum majus), paying particular attention to chang
26 proteins, initially described in snapdragon (Antirrhinum majus) petals, are known regulators of epide
27 lly symmetrical flowers of the model species Antirrhinum majus (Plantaginaceae) are highly specialize
28 ridoids in the ornamental flower snapdragon (Antirrhinum majus, Plantaginaceae family) are derived fr
30 ng bZIP proteins are expressed in flowers of Antirrhinum majus, predominantly in vascular tissues, ca
31 unctional genomic approach, we identified an Antirrhinum majus (snapdragon) BALDH, which exhibits 40%
37 ve identified a mutation at the DAG locus of Antirrhinum majus which blocks the development of chloro
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