戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 auxin and cytokinin signaling domains in the stele.
2 ependent reactive oxygen species in the root stele.
3 cell spread through the cells of the central stele.
4 olism enzyme preferentially expressed in the stele.
5  auxin treatment increases expression in the stele.
6 , McHKT is mainly confined to endodermis and stele.
7 y affects the potassium concentration in the stele.
8 data suggest the asymmetry originated in the stele.
9 rmis, but only partially affected MFs in the stele.
10 -like arrangement of vascular bundles in the stele.
11 g the arrangement of vascular bundles in the stele.
12 cal/epidermal cells compared to cells of the stele.
13 , visible fluorescence was restricted to the stele.
14 d, have been a major focus in studies of the stele.
15  prevent absorbed Mn from leaking out of the stele.
16 localized at the root epidermis, cortex, and stele.
17 carbon cost of transporting nutrients to the stele.
18         Severe O2 deficiency occurred in the stele and apical regions of roots in stagnant solutions.
19 h SHR protein acts both as a signal from the stele and as an activator of endodermal cell fate and SC
20 s while ABA enhances ROP11 expression in the stele and broadens its distribution in the endodermis.
21 s present at similar levels in both the root stele and cortex of three Vitis spp. genotypes that exhi
22 ts in the exchange of macromolecules between stele and cortex.
23 rameters for cellular characteristics of the stele and cortex.
24 tem from the allometric relationship between stele and cortical tissues.
25 ment and maintenance of the boundary between stele and ground tissue.
26 tosis, and apoplastic sodium influx into the stele and hence the shoot.
27 epidermis and cortex, IRT3 from epidermis to stele and HMA2 in xylem parenchyma.
28 ntiated inner cortical cells adjacent to the stele and is preceded by a wave of autofluorescence that
29 ified HWS expression to be restricted to the stele and lateral root cap, cotyledonary margins, tip of
30 , strong expression was detected only in the stele and meristem region of roots and a dramatic decrea
31 s are coexpressed constitutively in the root stele and meristematic tissue.
32 thus may play a key role in Cd flux into the stele and root-to-shoot Cd transport.
33 lating the apoplastic movement of Lns in the stele and suggest that plants possess an uptake system w
34 ght the large importance of the width of the stele and the cortex.
35         Bidirectional cross-talk between the stele and the surrounding tissues involving a mobile tra
36 opetally through the root within the central stele and then, upon reaching the root apex, auxin is tr
37                               Root diameter, stele and xylem diameter, and xylem number were more res
38  in cells undergoing radial expansion in the stele and/or cell wall dissolution.
39  of roots, allometry between root cortex and stele, and independence between root cell wall thickness
40 ils (thick roots with a larger proportion of stele, and smaller distal cortical cells).
41  including root hairs, epidermis, cortex and stele, and to the leaf vasculature.
42 e is collateral, and vascular bundles in the stele are arranged in a ring.
43 on as an apoplastic diffusion barrier to the stele at sites of lateral root emergence where Casparian
44 n the epidermis, whereas BR signaling in the stele buffered this effect.
45 HR messenger RNA is found exclusively in the stele cells internal to the endodermis and cortex, indic
46 on is SHORT-ROOT (SHR), which moves from the stele cells into the endodermis and root tip of Arabidop
47 atterning genes to promote the production of stele cells, but might also indirectly feed into establi
48                                       In the stele, changes in aquaporin activity accounted for about
49   This gene was highly expressed in the root stele compared to the cortex, and its expression decreas
50 as always greatest in interior tissues (i.e. stele, endodermis, and/or vascular tissues) for all root
51       We identified 158 interactions with 13 stele-expressed promoters, many of which occur physicall
52 ts drive the cortical expression of SCR, and stele-expressed SHR protein accumulates in cortical cell
53 transcription factor resource of 92% of root stele-expressed transcription factors and 74.5% of root-
54 ity; but, these hypotheses often isolate the stele from a whole-plant developmental context, ignoring
55   The primary vascular system of plants (the stele) has attracted interest from paleobotanists, devel
56 stic space between the soil solution and the stele in roots [1-3].
57 highly specific manner from the cells of the stele in which it is synthesized outward.
58 d by the leakage of a small peptide from the stele into the cortex.
59 ORT-ROOT (SHR) protein, which moves from the stele into the neighboring ground tissue layer to specif
60  that subcellular localization of SHR in the stele is intrinsic to the SHR protein.
61               Ecologically, the dorsiventral stele is overrepresented in stem-climbing ferns, where i
62 and the radial hydraulic conductance for the stele (L(R, S)) of the distal root region by 32% and 41%
63 taxylem SCW pits, while ABA signaling in the stele limits this enlargement.
64 (Zea mays) primary root tissues, the cortex, stele, meristematic zone, and elongation zone, was gener
65 lucuronidase showed strong expression in the stele of hairy roots for all 4 PRP genes tested, with ad
66 rimarily found in the epidermis, cortex, and stele of mature primary and lateral roots, but not in th
67 ontrast, repressed BR genes prevailed in the stele of the apical meristem zone.
68         Free IAA occurs predominantly in the stele of the mesocotyl whereas esterified IAA is mainly
69                         O2 deficiency in the stele reduced the concentrations of K, Na and Cl in the
70 DR5::GUS expression in the root tips and the stele region proximal to the root tip.
71 the epidermis, and the innermost tissue, the stele, respectively.
72  expression was observed in the cells of the stele situated adjacent to the xylem poles.
73  expression is largely localized to the root stele, suggesting a centric and gradual release of its d
74  the plasma membrane and is expressed in the stele, suggesting a role in vascular loading; FPN2 local
75                                  Made in the stele, the SHR protein moves into an adjacent cell layer
76 EGT1 is expressed in elongating cortical and stele tissues, which are distinct from known root gravit
77 utative transcription factor, moves from the stele to a single layer of adjacent cells, where it ente
78 iffusive transport of these solutes from the stele to the cortex via endodermal plasmodesmata.
79  the cell fate regulator SHORT-ROOT from the stele to the ground tissue has been associated with tran
80                  With EDTA, Cu levels in the stele were higher than those in the cortex after 1 week
81 redominantly expressed in the endodermis and stele, ZIP3 and ZIP5 in the epidermis and cortex, IRT3 f