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1 ter the estimated divergence of host species Populus tremula and Populus balsamifera/Populus trichoca
2 bidopsis, Gossypium hirsutum, Populus alba x Populus tremula, corn (Zea mays), and Dictyostelium disc
3 nus Populus: Populus alba (white poplar) and Populus tremula (European aspen).
4 ascular cambium, and wood-forming tissues of Populus tremula The transcriptome comprised 28,294 expre
5                                   Transgenic Populus tremula x alba (717-1B4) plants with reduced exp
6 re of the mature leaves of the model species Populus tremula x alba across all seven hierarchical ord
7                    We report that transgenic Populus tremula x alba expressing a bacterial SA synthas
8 om leaves of Populus nigra and hybrid aspen (Populus tremula x P. tremuloides) in response to changes
9 opsis thaliana, and we consequently named it Populus tremula x Populus alba (Pta) LBD1.
10  poplar response to water stress, transgenic Populus tremula x Populus alba plants characterized by t
11 eling during 48 h following shoot removal in Populus tremula x Populus alba softwood cuttings in the
12 ent and composition were modified in poplar (Populus tremula x Populus alba) by specifically down-reg
13                                     Poplars (Populus tremula x Populus alba) down-regulated for cinna
14 y characterized an activation-tagged poplar (Populus tremula x Populus alba) mutant with enhanced woo
15 ield-grown, CCR-down-regulated poplar trees (Populus tremula x Populus alba) on the bacterial rhizosp
16 of catechin and PAs as well as hybrid aspen (Populus tremula x Populus alba) overexpressing the MYB13
17         We have developed transgenic poplar (Populus tremula x Populus alba) plants with greatly incr
18 tial in lignin biosynthesis in woody poplar (Populus tremula x Populus alba) plants.
19 hat down-regulation of CSE in hybrid poplar (Populus tremula x Populus alba) resulted in up to 25% re
20 sly poorly characterized response of poplar (Populus tremula x Populus alba) roots to low nitrogen (L
21  experimental evidence that, in gray poplar (Populus tremula x Populus alba), Suc enters the phloem t
22                         Using hybrid poplar (Populus tremula x Populus alba), we applied this strateg
23 ar-old high-density stands of hybrid poplar (Populus tremula x Populus alba).
24 ith contrasting wood anatomy (Quercus robur, Populus tremula x Populus alba, and Pinus pinaster).
25 t evolved with Populus trichocarpa (Ptr) and Populus tremula x Populus tremuloides (Ptt) were studied
26 in the strong isoprene emitter hybrid aspen (Populus tremula x Populus tremuloides), and used rapid c
27 ension wood and normal wood of hybrid aspen (Populus tremula x Populus tremuloides).
28 nhibition in isoprene-emitting hybrid aspen (Populus tremula x Populus tremuloides).
29 condary cell wall formation in hybrid aspen (Populus tremula x Populus tremuloides).
30 in the strong isoprene emitter hybrid aspen (Populus tremula x Populus tremuloides).
31 rification, and functional reconstitution of Populus tremula x tremuloides CesA8 (PttCesA8), implicat
32 ambial development, we engineered transgenic Populus tremula x tremuloides trees with an elevated cyt
33  PECTIN METHYLESTERASE1 (PtxtPME1) in aspen (Populus tremula x tremuloides) triggers the formation of
34 poration to developing wood of hybrid aspen (Populus tremula x tremuloides).

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