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

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