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1  whether proteasome activity is required for tracheary element (TE) differentiation, the proteasome i
2          Using a transformable Pinus radiata tracheary element (TE) system as an experimental platfor
3 oyl-CoA reductase (CCR) in the Pinus radiata tracheary element (TE) system impacted both the metaboli
4  determine whether XCP1 could be involved in tracheary element autolysis, promoter activity and local
5 ession of PrCCoAOMT expression in P. radiata tracheary element cultures affected lignin content and c
6 tand eudicot evolution, the genetic basis of tracheary element development, and the genetic diversity
7 ablish a tight linkage between the timing of tracheary element differentiation and rising SPS activit
8                                        Here, TRACHEARY ELEMENT DIFFERENTIATION FACTOR (TDIF) peptide
9 s as in other grasses, CLAVATA3-like but not TRACHEARY ELEMENT DIFFERENTIATION FACTOR (TDIF)-like pep
10 s regulated by a peptide signaling involving Tracheary Element Differentiation Inhibitory Factor (TDI
11 ule characterized by a peptide ligand called TRACHEARY ELEMENT DIFFERENTIATION INHIBITORY FACTOR (TDI
12                            Here we show that TRACHEARY ELEMENT DIFFERENTIATION INHIBITORY FACTOR (TDI
13 scriptomic analysis showed that genes of the tracheary element differentiation inhibitory factor-phlo
14                                              Tracheary element differentiation requires strict coordi
15 ammed cell death during organ senescence and tracheary element differentiation.
16                                            A tracheary element expression pattern was detected for XC
17 reds of the genes involved in the process of tracheary element formation.
18 er, these findings suggest that XND1 affects tracheary element growth through regulation of secondary
19 ncluded a reduction in both plant height and tracheary element length and an increase in metaxylem re
20 xylem vessels and little or no expression of tracheary element marker genes.
21 raulic conductivity (Ks ), wood density, and tracheary element size from natural populations.
22  patterning, we developed a method to induce tracheary element transdifferentiation of isolated proto
23 in, to reproducibly trans-differentiate into tracheary elements (TE) after 96 h, while in the presenc
24 sociated with lignification in both in vitro tracheary elements (TEs) and organs of zinnia (Zinnia el
25                                        Xylem tracheary elements (TEs) form hollow, sap-conducting tub
26            Postmortem lignification of xylem tracheary elements (TEs) has been debated for decades.
27 es, ZRNaseI and ZRNaseII, in differentiating tracheary elements (TEs) induced from isolated mesophyll
28 mechanisms regulating the autolysis of xylem tracheary elements (TEs) is important for understanding
29 , we characterize p48h-17 cDNA from in vitro tracheary elements (TEs) of Zinnia elegans which encodes
30                                        Xylem tracheary elements (TEs) synthesize patterned secondary
31 h ASL19 and ASL20 were expressed in immature tracheary elements (TEs), and the expression was depende
32                     Plant vascular cells, or tracheary elements (TEs), rely on circumferential second
33 ant cell wall was examined in Zinnia elegans tracheary elements (TEs), which specialize by developing
34                  The secondary cell walls of tracheary elements and fibers are rich in cellulose micr
35 re synthesized in specialized cells, such as tracheary elements and fibers, and their remarkable stre
36  characteristics with the secondary walls of tracheary elements and fibers.
37 cells can contribute to the lignification of tracheary elements and fibers.
38  wall modifications lead to the formation of tracheary elements and sieve tubes.
39 e key structural event in forming functional tracheary elements and we have identified over 50 partia
40                Secondary walls in fibers and tracheary elements constitute the most abundant biomass
41 uction in the Golgi of developing protoxylem tracheary elements in Arabidopsis (Arabidopsis thaliana)
42 ressed by mesophyll cells differentiating as tracheary elements in vitro.
43 three new ones identified in differentiating tracheary elements of Zinnia elegans.
44 not detected in the cytoplasm or vacuoles of tracheary elements or neighbors.
45  reveals that atao1 expression in developing tracheary elements precedes and overlaps with lignificat
46  Pits are regions in the cell walls of plant tracheary elements that lack secondary walls.
47 ell culture of synchronously differentiating tracheary elements was used to identify three new expans
48 f Zinnia elegans L. cv Envy differentiate to tracheary elements when cultured in inductive medium con
49 nveiling details about local interactions of tracheary elements with surrounding material, which vari
50 expression of XND1 blocks differentiation of tracheary elements.
51 M NAC DOMAIN1 (XND1) is upregulated in xylem tracheary elements.
52 aseolus vulgaris), contained differentiating tracheary elements.
53 interrupted the differentiation of the xylem tracheary elements.
54 erstanding ascending fluid transport and for tracheary mechanical strength relevant to potential appl
55                      Here we show that plant tracheary microfilaments, collected from Agapanthus afri
56                                          The tracheary system of plant leaves is composed of a cellul