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1 tiating xylem, young xylem fibers and phloem companion cells.
2 subsequent unloading at least into adjacent companion cells.
3 st NtFT3 expression was restricted to phloem companion cells.
4 Occasionally, PP1 was detected in companion cells.
5 appears to be maintained by the surrounding companion cells.
6 hat TEV-GUS entered the phloem parenchyma or companion cells adjacent to the sieve elements, suggesti
7 lem vessels in the root and the stem, phloem companion cells and a ring of cells around the phloem st
10 tion of mesophyll cells, guard cells, phloem companion cells and sieve elements are clearly described
14 e plasma membrane of sieve elements, but not companion cells, and accumulates at the earliest stages
15 desmatal frequencies leading into minor vein companion cells are higher than in species known to load
17 egulate flowering time, acting in the phloem companion cells, as previously described for CO and HOS1
18 oot cap, protophloem sieve elements, and the companion cells associated with metaphloem sieve element
19 NA was localized by in situ hybridization in companion cells at early stages of vascular differentiat
20 mplastic continuity appears to exist between companion cells (CCs) and sieve elements of the phloem,
24 Membrane proteins within the sieve element-companion cell complex have essential roles in the physi
25 fer from the apoplast into the sieve element-companion cell complex, so-called apoplastic loading.
29 at the plasma membrane of the sieve element-companion cell complexes functions as a synthase, and th
30 ransporter was targeted to the sieve element-companion cell complexes of the leaf phloem and to the e
31 , and in the phloem, including sieve-element/companion cell complexes, parenchyma, and in the exuding
32 cessory cells, whereas in both gametophytes, companion cells contribute non-cell-autonomously to the
33 600 mM sorbitol, whereas sieve elements and companion cells did not plasmolyze even in 1.2 M sorbito
35 s, is dependent upon protein import from the companion cells for maintenance of the phloem long-dista
37 ession in tobacco is limited to two of three companion cells in class-V veins, which are the most ext
38 a connect bundle sheath cells to specialized companion cells (intermediary cells) in the minor veins.
39 -GFP was mobile in the phloem; it moved from companion cells into sieve elements and into a previousl
41 s, or other phenotypes of phloem elements or companion cells, leading to localized cell responses and
43 The Arabidopsis thaliana central cell, the companion cell of the egg, undergoes DNA demethylation b
45 h clade were first expressed specifically in companion cells of Arabidopsis (Arabidopsis thaliana) an
46 lon drives gene expression in the minor-vein companion cells of both transgenic tobacco (Nicotiana ta
49 here show that BvSUT1 mRNA was localized to companion cells of the leaf's vascular system, which sup
51 crose transporter AtSUC2 is expressed in the companion cells of the phloem (specialized vascular tiss
55 as expressed from a promoter specific to the companion cells of the smallest veins of mature leaves.
56 omplementary DNAs were also expressed in the companion cells of wild-type Arabidopsis, with the aim o
57 :GFP was not able to move from either phloem companion cells or epidermal cells, both of which have b
58 lthough transcripts could be detected in the companion cells, peptide fingerprint analysis suggested
59 ur results demonstrate that demethylation in companion cells reinforces transposon methylation in pla
60 nt negative version of TPL (tpl-1) in phloem companion cells results in early flowering and a decreas
61 ented symplasmic domain is the sieve element-companion cell (SE-CC) complex in the phloem tissue.
62 smodesmal channels involved in sieve element/companion cell (SE/CC) unloading and post-phloem transpo
63 s revealed the presence of CmNACP RNA in the companion cell-sieve element complex of leaf, stem and r
68 conserved role for reprogramming in germline companion cells, such as nurse cells in insects and vege
69 mPP36 requires proteolytic processing in the companion cell to produce a soluble, movement-competent,
70 irulence factors into the phloem elements or companion cells to interfere with host targets (e.g., pr
71 nt and indicated that it functions in phloem companion cells to load Suc and also in other cell types
72 Thus, non-specific loss of proteins from companion cells to sieve elements may explain the pletho
73 truct provides a hitherto unique entree into companion cell-to-SE protein targeting, as well as a new
74 ere observed when NHL26 was overexpressed in companion cells, under the control of a companion cell-s
79 is expressed in the mitochondria of the root companion cells, where all three active GDH enzyme prote
80 the phloem sap traffic cell to cell from the companion cells, where they are synthesized, into the si
82 dicated a high level of RBP50 transcripts in companion cells, while immunolocalization experiments de
83 ility of plasmodesmata or sugar signaling in companion cells, with a specific effect on sugar export.
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