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1 a flower primordium into a three-dimensional flower bud.
2 onent of essential oil from caper leaves and flower buds.
3 rgans, whereas LeGGH3 is expressed mainly in flower buds.
4 tile when jasmonate is applied to developing flower buds.
5 eproductive phase to be competent to produce flower buds.
6 n predominates in the reproductive organs of flower buds.
7 expression of the amino acid transporter in flower buds.
8 growth of nascent roots, stems, leaves, and flower buds.
9 SGlu7 mRNA also accumulated in pods and flower buds.
10 e for the cytoplasmic isozyme are highest in flower buds.
11 sses caused by frost injury to overwintering flower buds.
12 hat peach PpeS6PDH gene is down-regulated in flower buds after dormancy release, concomitantly with c
15 pa ssp. pekinensis EST library isolated from flower buds and genomic sequences from Arabidopsis thali
16 tissue-specific expression in the tapetum of flower buds and in the anther filaments upon anthesis.
17 omologues are expressed at a higher level in flower buds and inflorescence stems than in rosette and
19 med on total RNA from root, stem, leaf, pod, flower bud, and hypocotyl using DNA probes for the diffe
21 and developing tissues, such as shoot tips, flower buds, and roots, but weakly in mature stem and le
22 ge its expression; conditions under which no flower buds are formed reduce this state and/or prevent
23 the wild type where developmentally typical flower buds are the terminal inflorescence structures ob
24 es, and roots and in the vascular bundles in flower buds but does not occur in the apical regions of
26 i) were highly branched; (iii) produced more flower buds, but most of these flowers did not mature, r
27 ar (Populus deltoides), are not able to form flower buds during the first several years of their life
29 ants were all in the flowering stage, and no flower-bud formation can be obtained in explants from st
36 he population of stem cells present in young flower buds is lost after the production of a fixed numb
37 f daphnane diterpene ester isolated from the flower buds of Daphne genkwa, has been reported to have
38 postulated to mediate sorbitol synthesis in flower buds of peach concomitantly with specific chromat
41 e/early binucleate stages were isolated from flower buds of tobacco (Nicotiana tabacum L.) and in vit
42 workers collect phenological data (number of flower buds, open flowers and fruits) from specimens of
43 ermal tissue of roots, petals, and sepals of flower buds, papillae cells of flowers, siliques, and en
44 fusion between aerial organs (especially in flower buds), reduced fertility under low humidity, incr
47 miR172 has a higher expression level in the flower bud than in any other organ, our results also sho
48 allowing plants to avoid winter injuries of flower buds that commonly occur in temperate regions.
50 dic alpha-glucosidase activity from broccoli flower buds was purified using concanavalin A and ion-ex
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