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1 ns with cellulose microfibrils in the native primary wall.
2 istinguish two distinct domains in the grass primary wall.
3  which is often followed by digestion of the primary wall.
4 s, and inner pith parenchyma cells with thin primary walls.
5 interaction, suggesting a structural role in primary wall architecture.
6 t effectively formed a pit channel, with the primary wall being the pit channel membrane.
7 ry wall called a pit chamber, and a modified primary wall called the pit membrane.
8  adhesion modulated by an outer layer of the primary wall can coordinate the extensive growth of a la
9 ce suggests that the complex associated with primary wall cellulose deposition consists of CESA1, -3,
10 e synthase (CESA) genes that are involved in primary wall cellulose synthesis.
11 ty due to pollen defects, demonstrating that primary-wall cellulose synthesis is necessary for pollen
12 measurements, we aimed to understand how the primary wall CESA complex acts during shoot apical meris
13 t are coincident with the down-regulation of primary wall CesAs, several Csl genes, and GT8 glycosyl
14           Xyloglucan (XyG) is a load-bearing primary wall component in dicotyledonous and non-gramina
15 ayers: an outermost granular layer, a middle primary wall composed of a meshwork of cellulose fibrils
16 is thaliana seed coat mutant, which displays primary wall detachment, reduced mucilage extrusion, and
17 nt secondary wall thickenings underlying the primary wall during xylogenesis in vitro.
18 me cell walls are more like those of typical primary walls even though the wall becomes quite thick.
19 accharide hydrolysis occurs in parallel with primary wall expansion, morphological effects are subtle
20                       The molecular basis of primary wall extension endures as one of the central eni
21 o explore how xylan structure contributes to primary wall function.
22 ting an overall increase in secondary versus primary walls in mutants, indicative of higher xylem pro
23 functional AtHB15 is necessary for retaining primary walls in parenchyma pith cells.
24 support to the single-network model of plant primary walls in which a substantial fraction of the cel
25 ma is a useful model system for the study of primary wall microfibril structure because its microfibr
26 s peaks between pectins and cellulose in the primary wall of Arabidopsis (Arabidopsis thaliana), indi
27  three major types of polysaccharides in the primary wall of Arabidopsis form a single cohesive netwo
28       Pectic components were detected in the primary wall of the pollen mother cell.
29                     Xyloglucan is present in primary walls of all angiosperms.
30 ibly involved in the intrusive growth of the primary walls of differentiating xylem cells.
31  that comprise a significant fraction of the primary walls of eudicotyledonous plant cells.
32                   Pectin is most abundant in primary walls of expanding cells, but beta-1,4-galactan
33                                          The primary walls of grasses are composed of cellulose micro
34                                          The primary walls of grasses are composed of cellulose micro
35                                       In the primary walls of growing plant cells, the glucose polyme
36 yloglucan, an abundant polysaccharide in the primary walls of many plants.
37 ate NMR techniques to study the hydration of primary-wall polysaccharides of the model plant, Arabido
38                             Isolation of two primary wall related CesA genes from xylem tissues also
39 es a maximum identity of 86% with AtCESA2, a primary wall-related CesA member from Arabidopsis, a dic
40 genes and temporally prolonged expression of primary wall-related genes.
41 ely characterised, the structure of xylan in primary walls remains less well understood, particularly
42                  This modification, found in primary wall-rich tissues of diverse conifer species, in
43 p of cells and illustrate dynamic changes in primary wall structure and composition occurring during
44 iber initiation and 48 miRNAs are related to primary wall synthesis and secondary wall thickening.
45 se cotton fiber tip morphologies and support primary wall synthesis occurring at the apex and discret
46 NTERACTING PROTEIN1, already associated with primary wall synthesis, was enriched during secondary ce
47 thesis enabled by regulatory uncoupling from primary wall synthesis.
48                   Cells first elongate their primary wall, then lay down a lignified secondary wall,
49 ess and cellulose content but also decreased primary wall thickness and cell elongation.
50      Their protoxylem vessels consisted of a primary wall with helical thickenings that effectively f
51 tion, we now compare never-dried Arabidopsis primary walls with dehydrated and rehydrated samples.
52           These findings uncover a conserved primary wall xylan modification in seed plants and defin