戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 opsis reflects greater genetic redundancy in Antirrhinum .
2 ene which controls dorsoventral asymmetry in Antirrhinum.
3 support for a model of parallel evolution in Antirrhinum.
4 ter the first described plant PEBP gene from Antirrhinum.
5  space separating two flower color morphs of Antirrhinum.
6 n a downstream target gene RADIALIS (RAD) in Antirrhinum.
7  in Arabidopsis, similar to the situation in Antirrhinum.
8  transformation in stamen number relative to Antirrhinum, aborting the lateral and adaxial stamens du
9                  The fimbriata (fim) gene of Antirrhinum affects both the identity and arrangement of
10 cture is conserved in relation to AG and the Antirrhinum AG orthologue, PLENA (PLE), and low-stringen
11             TEM orthologs were isolated from antirrhinum (AmTEM) and olive (OeTEM) and were expressed
12 rent, reflecting the diverse morphologies of Antirrhinum and Arabidopsis flowers.
13 ion is associated with petal identity, as in Antirrhinum and Arabidopsis, but this is achieved throug
14                                           In Antirrhinum and Arabidopsis, mutations in the floral mer
15 antly from weak C-function mutant alleles in Antirrhinum and Arabidopsis.
16 t three duplications since the divergence of Antirrhinum and Arabidopsis.
17 rgence among Antirrhinum species and between Antirrhinum and Digitalis is also low.
18 stinct from the expression pattern of RAD in Antirrhinum and from the endogenous RAD-like genes of Ar
19 or establishing petal and stamen identity in Antirrhinum and is expressed in all three layers of the
20 mologous transcription factors FLORICAULA of Antirrhinum and LEAFY of Arabidopsis share conserved rol
21 ibution of Tkn2 KNOX transcripts compared to Antirrhinum and maize suggests either a different spatia
22 f plants sampled from natural populations of Antirrhinum and Misopates species.
23 plains the biosynthesis of 7-epi-iridoids in Antirrhinum and related genera.
24 n protein, closely related to PHANTASTICA in Antirrhinum and ROUGH SHEATH2 in maize, both of which ne
25 a langsdorffii X N. sanderae) homolog of the antirrhinum (Antirrhinum majus) MYB305.
26 e have tested whether the model proposed for Antirrhinum applies to Arabidopsis, by creating transgen
27 red for the ABC functions in Arabidopsis and Antirrhinum are members of the MADS-box gene family, and
28 ogs AG from Arabidopsis and PLENA (PLE) from Antirrhinum are shown to be representatives of separate
29 -evolved with overall leaf shape and size in Antirrhinum because these characters are constrained by
30 ntity is based on studies of Arabidopsis and Antirrhinum, both of which are highly derived eudicots.
31    We tested for parallel trait evolution in Antirrhinum by investigating phylogenetic relationships
32                      This feature of the two Antirrhinum C-function-like genes is markedly different
33  We have determined the crystal structure of Antirrhinum CEN to 1.9 A resolution.
34 y a natural variant of the barley homolog of Antirrhinum CENTRORADIALIS (HvCEN) as a contributor to s
35                An allele of the DAG locus of Antirrhinum (dag::Tam3), which is required for chloropla
36 amiana using TRV-VIGS was similar to that of Antirrhinum def and Arabidopsis ap3 mutants and caused t
37 uggest that NbDEF is a functional homolog of Antirrhinum DEF.
38         Dorsoventral asymmetry in flowers of Antirrhinum depends on expression of the cycloidea gene
39 shape--petal asymmetry--in the petal lobe of Antirrhinum depends on the direction of growth rather th
40    The development of reproductive organs in Antirrhinum depends on the expression of an organ identi
41 cterize the phylogenetic orthologue of Ls in Antirrhinum, ERAMOSA (ERA).
42  identity in Arabidopsis; their orthologs in Antirrhinum exhibit similar functions.
43 r the presence of high-fitness ridges in the Antirrhinum floral-color adaptive landscape, their data
44 UPULIFORMIS (CUP) in formation of the ornate Antirrhinum flower shape.
45  lip, and characteristic folds of the closed Antirrhinum flower.
46                                           In Antirrhinum, flower asymmetry depends on activation of R
47                                          The Antirrhinum gene CENTRORADIALIS (CEN) and the Arabidopsi
48  revealed that Stp is the pea homolog of the Antirrhinum gene Fimbriata (Fim) and of UNUSUAL FLORAL O
49 that cyc and fil1 are among the least biased Antirrhinum genes, so that their low diversity is not du
50 gest either that these gene families (or the Antirrhinum genome) are unusually constrained or that th
51 e history of eudicots and that the ancestral Antirrhinum had an active H gene and restricted trichome
52  present in multiple groups, suggesting that Antirrhinum has repeatedly colonised alpine habitats.
53                                              Antirrhinum has two genes corresponding to AP2, termed L
54 e controlling floral asymmetry, cycloidea in Antirrhinum, has been isolated.
55 e used primers designed from three published Antirrhinum hispanicum S-allele sequences in PCR reactio
56 hese phenotypes resemble the Arabidopsis and Antirrhinum homeotic B-function mutants apetala3/deficie
57 ra (desert ghost flower), which differs from Antirrhinum in corolla (petal) symmetry and pollination
58 in Senecio versus dorsal petal elongation in Antirrhinum In S vulgaris, diversification of CYC genes
59 lower 1 in Arabidopsis and centroradialis in Antirrhinum, inflorescences that are normally indetermin
60     Introduction of a RAD genomic clone from Antirrhinum into Arabidopsis leads to a novel expression
61 ablishment and maintenance and, in maize and Antirrhinum, it has been proposed that PHAN acts as an e
62                    Dorsoventral asymmetry of Antirrhinum leaves requires activity of the Phantastica
63 umulation of knox gene products in maize and Antirrhinum leaves, respectively.
64  Eluta locus by transposon-tagging, using an Antirrhinum line that spontaneously lost the nonsuppress
65 the coupling of RAD to CYC regulation in the Antirrhinum lineage and hence the co-option of RAD had a
66 of RAD may have occurred specifically in the Antirrhinum lineage.
67 in an early divergence of alpine and lowland Antirrhinum lineages, and the alleles underlying this sp
68 etic replicas of petal surfaces and isogenic Antirrhinum lines differing only in petal epidermal cell
69                                Compared with Antirrhinum, little divergence is again observed.
70                We report the discovery of an Antirrhinum MADS-box gene, FARINELLI (FAR), and the isol
71 ble for model organisms such as Arabidopsis, Antirrhinum, maize, rice and wheat, a phylogenetic persp
72 lly symmetrical flowers of the model species Antirrhinum majus (Plantaginaceae) are highly specialize
73 unctional genomic approach, we identified an Antirrhinum majus (snapdragon) BALDH, which exhibits 40%
74            In the model developmental system Antirrhinum majus (snapdragon), the closely related gene
75                            The model species Antirrhinum majus (the garden snapdragon) has over 20 cl
76   In the early 1900s, Erwin Baur established Antirrhinum majus as a model system, identifying and cha
77                                    Tam3 from Antirrhinum majus belongs to the Ac/Ds family of transpo
78                                           An Antirrhinum majus dihydroflavonol reductase (DFR) cDNA w
79  Here we report the isolation of a gene from Antirrhinum majus encoding a protein from an entirely no
80 ne responsible for conferring dorsal fate in Antirrhinum majus flowers.
81    Ectopic expression of the MIXTA gene from Antirrhinum majus in S. dulcamara results in the formati
82 w that the growth and asymmetry of leaves in Antirrhinum majus involves the related YABBY transcripti
83                              MIXTA, which in Antirrhinum majus is reported to regulate certain aspect
84 n the distantly related core eudicot species Antirrhinum majus L., paralogous SBP-box proteins SBP1 a
85                        The identification of Antirrhinum majus mutants with ectopic petal spurs sugge
86 he reporter system is based on expression of Antirrhinum majus MYB-related Rosea1 (Ros1) transcriptio
87                                      In four Antirrhinum majus populations with different mating syst
88 ve identified a mutation at the DAG locus of Antirrhinum majus which blocks the development of chloro
89                            Here, snapdragon (Antirrhinum majus) GPPS-SSU was over-expressed in tomato
90 Here, we show that expression of snapdragon (Antirrhinum majus) GPPS.SSU in tobacco (Nicotiana tabacu
91 le) and Dicotyledonae (Nicotiana tabacum and Antirrhinum majus) indicating that LINEs are a universal
92 i X N. sanderae) homolog of the antirrhinum (Antirrhinum majus) MYB305.
93 proteins, initially described in snapdragon (Antirrhinum majus) petals, are known regulators of epide
94 unds detected in the majority of snapdragon (Antirrhinum majus) varieties.
95 ms such as Arabidopsis thaliana, snapdragon (Antirrhinum majus), and petunia (Petunia hybrida).
96  transcription factor genes from snapdragon (Antirrhinum majus), paying particular attention to chang
97 rved in Arabidopsis thaliana and snapdragon (Antirrhinum majus).
98  i.e. AmRosea1 and AmDelila from snapdragon (Antirrhinum majus).
99 This observation extends previous reports in Antirrhinum majus, Epilobium hirsutum, Nicotiana tabacum
100                                           In Antirrhinum majus, floral zygomorphy is established by t
101      Investigation of two classic mutants in Antirrhinum majus, mutabilis and incolorata I, showed th
102                                           In Antirrhinum majus, one proposed role of the gene fimbria
103 ridoids in the ornamental flower snapdragon (Antirrhinum majus, Plantaginaceae family) are derived fr
104 ng bZIP proteins are expressed in flowers of Antirrhinum majus, predominantly in vascular tissues, ca
105 ing mechanisms used by four such proteins in Antirrhinum majus, SQUA, PLE, DEF and GLO.
106                                           In Antirrhinum majus, the MIXTA protein directs the formati
107  variation in 3000 leaves from 400 plants of Antirrhinum majus.
108 ment of conical epidermal cells in petals of Antirrhinum majus.
109  to the development of dorsal petal lobes of Antirrhinum majus.
110 ptide-encoding sequence from the oli gene of Antirrhinum majus.
111  class in Arabidopsis (TCP1) and snapdragon (Antirrhinum majus; CYCLOIDEA) have been shown to be asym
112 e show that the previous inability to obtain Antirrhinum mutants corresponding to the A class gene AP
113                                  Snapdragon (Antirrhinum) mutants lacking conical cells have been sho
114                      Unlike the situation in Antirrhinum, none of the Arabidopsis RAD-like genes are
115 c tobacco lines, biolistic transformation of Antirrhinum petals and promoter activation/repression as
116  is expressed only in the inner epidermis of Antirrhinum petals.
117 gene sequence was found to be similar to the Antirrhinum PHANTASTICA (PHAN) gene sequence, which enco
118 ily conserved sequences in the intron of the Antirrhinum PLENA (PLE) gene to establish whether they r
119 ences, and one to a very similar unpublished Antirrhinum S-like RNase sequence.
120 red in Arabidopsis are therefore separate in Antirrhinum, showing that the genetic basis of some aspe
121 fied visually, to observe the development of Antirrhinum (snapdragon) petals.
122 antify differences in leaf allometry between Antirrhinum (snapdragon) species, including variation in
123                                 In the genus Antirrhinum (snapdragons), as in other plants, a suite o
124 rns using natural variation within the genus Antirrhinum (snapdragons), which has evolved hairy alpin
125                             Divergence among Antirrhinum species and between Antirrhinum and Digitali
126 mined the evolutionary relationships between Antirrhinum species and how these relate to geography an
127 s variation in trichome patterns between all Antirrhinum species except one.
128                              Hybrids between Antirrhinum species have been used successfully to ident
129                                              Antirrhinum species with diverse floral phenotypes forme
130 s, euAP1 (including Arabidopsis APETALA1 and Antirrhinum SQUAMOSA) and euFUL (including Arabidopsis F
131          It has previously been proposed for Antirrhinum that another gene, FIMBRIATA (FIM), mediates
132           A transcription factor couple from Antirrhinum that is known to control anthocyanin biosynt
133                                           In Antirrhinum, the inflorescence can be distinguished by i
134 ved role in petal growth in both Senecio and Antirrhinum, the regulatory relationships and expression
135  the normally indeterminate inflorescence of Antirrhinum to terminate in a flower.
136 ed an Impatiens homologue of the FIM gene of Antirrhinum (UFO in Arabidopsis), Imp-FIM, and analysed
137     zfl2, the maize homolog of FLORICAULA of Antirrhinum, was associated with plant height.
138 and FT were observed in both Arabidopsis and antirrhinum, which correlated with the length of the JVP
139 rsity studies revealed that the fil1 gene of Antirrhinum, which has been reported to be single copy,
140            We have studied the cin mutant of Antirrhinum, which has crinkly rather than flat leaves.

 
Page Top