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1 a flower primordium into a three-dimensional flower bud.
2 sses caused by frost injury to overwintering flower buds.
3 onent of essential oil from caper leaves and flower buds.
4 rgans, whereas LeGGH3 is expressed mainly in flower buds.
5 tile when jasmonate is applied to developing flower buds.
6 eproductive phase to be competent to produce flower buds.
7 n predominates in the reproductive organs of flower buds.
8  expression of the amino acid transporter in flower buds.
9 nnabinoids and terpenoids were quantified in flower buds.
10  growth of nascent roots, stems, leaves, and flower buds.
11      SGlu7 mRNA also accumulated in pods and flower buds.
12 e for the cytoplasmic isozyme are highest in flower buds.
13  plants in the laboratory and field increase flower bud abscisic acid levels and delay flowering in s
14 hat peach PpeS6PDH gene is down-regulated in flower buds after dormancy release, concomitantly with c
15 forms the boundary region between developing flower bud and the SAM.
16 frost has clear benefits for the survival of flower buds and flowers, such phenological advancement m
17 tes that MYC-146 is most highly expressed in flower buds and flowers.
18 pa ssp. pekinensis EST library isolated from flower buds and genomic sequences from Arabidopsis thali
19 tissue-specific expression in the tapetum of flower buds and in the anther filaments upon anthesis.
20 omologues are expressed at a higher level in flower buds and inflorescence stems than in rosette and
21 directly impacted by frost through damage to flower buds and reproductive structures.
22 med on total RNA from root, stem, leaf, pod, flower bud, and hypocotyl using DNA probes for the diffe
23 s and siliques, less abundant in flowers and flower buds, and barely detectable in roots.
24  and developing tissues, such as shoot tips, flower buds, and roots, but weakly in mature stem and le
25 d flowers 16 months after transformation and flower buds appeared 30-40 days on juvenile immature sci
26 ge its expression; conditions under which no flower buds are formed reduce this state and/or prevent
27  the wild type where developmentally typical flower buds are the terminal inflorescence structures ob
28 ficient photoperiodic stimulation results in flower bud arrest or even failure.
29 es, and roots and in the vascular bundles in flower buds but does not occur in the apical regions of
30  concentrated in young leaves and developing flower buds but not in the shoot meristem.
31 i) were highly branched; (iii) produced more flower buds, but most of these flowers did not mature, r
32 ar (Populus deltoides), are not able to form flower buds during the first several years of their life
33           The factors that regulate seasonal flower bud formation are also unknown.
34 ants were all in the flowering stage, and no flower-bud formation can be obtained in explants from st
35               Culture conditions that permit flower-bud formation in an explant are conditions that m
36                           In the Arabidopsis flower bud, four sepals robustly initiate and grow to a
37  which are the leaf-like organs that enclose flower buds, have consistent size and shape, indicating
38            The finding that capacity to form flower buds in explants is present in all Nicotiana biot
39   After this transition, trees begin to form flower buds in the spring of each growing season.
40                         The capacity to form flower buds in thin-layer explants was studied in flower
41 y be causally connected to the appearance of flower buds in thin-layer tobacco cultures.
42                         Expression of SSP in flower buds is developmentally regulated, with maximal l
43 he population of stem cells present in young flower buds is lost after the production of a fixed numb
44 f daphnane diterpene ester isolated from the flower buds of Daphne genkwa, has been reported to have
45                                        Dried flower buds of Japanese sophora (Sophora japonica) compr
46  postulated to mediate sorbitol synthesis in flower buds of peach concomitantly with specific chromat
47 ion of PpeS6PDH and sorbitol accumulation in flower buds of peach.
48 on in tolerance to environmental stresses in flower buds of peach.
49 e/early binucleate stages were isolated from flower buds of tobacco (Nicotiana tabacum L.) and in vit
50  metabolites and potential biomarkers in the flower buds of two contrasting chickpea genotypes: the h
51 workers collect phenological data (number of flower buds, open flowers and fruits) from specimens of
52 e of the winter/spring transition may damage flower buds or open flowers, limiting fruit and seed pro
53 ermal tissue of roots, petals, and sepals of flower buds, papillae cells of flowers, siliques, and en
54  fusion between aerial organs (especially in flower buds), reduced fertility under low humidity, incr
55 droxylase cDNAs were overexpressed in purple flower buds relative to the pink.
56       LNO1 is highly expressed in anthers of flower buds, stigma papilla of open flowers, and embryo
57  miR172 has a higher expression level in the flower bud than in any other organ, our results also sho
58  allowing plants to avoid winter injuries of flower buds that commonly occur in temperate regions.
59 aturity and impact their capacity to develop flower buds the following season.
60 nalyze small RNA (sRNA) sequencing data from flower buds to identify candidate dominance modifiers.
61  and specific expression in young leaves and flower buds using GUS reporters.
62 dic alpha-glucosidase activity from broccoli flower buds was purified using concanavalin A and ion-ex
63                            GUS expression in flower buds was specifically localized to GSTs.
64               Sepals enclose and protect the flower bud, while petals can be large and showy so as to