ライフサイエンスコーパス: stele

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 data suggest the asymmetry originated in the stele.

8 rmis, but only partially affected MFs in the stele.

9 -like arrangement of vascular bundles in the stele.

10 g the arrangement of vascular bundles in the stele.

11 cal/epidermal cells compared to cells of the stele.

12 , visible fluorescence was restricted to the stele.

13 Severe O2 deficiency occurred in the stele and apical regions of roots in stagnant solutions.

14 h SHR protein acts both as a signal from the stele and as an activator of endodermal cell fate and SC

15 s present at similar levels in both the root stele and cortex of three Vitis spp. genotypes that exhi

16 ts in the exchange of macromolecules between stele and cortex.

17 ment and maintenance of the boundary between stele and ground tissue.

18 tosis, and apoplastic sodium influx into the stele and hence the shoot.

19 ntiated inner cortical cells adjacent to the stele and is preceded by a wave of autofluorescence that

20 ified HWS expression to be restricted to the stele and lateral root cap, cotyledonary margins, tip of

21 , strong expression was detected only in the stele and meristem region of roots and a dramatic decrea

22 s are coexpressed constitutively in the root stele and meristematic tissue.

23 thus may play a key role in Cd flux into the stele and root-to-shoot Cd transport.

24 Bidirectional cross-talk between the stele and the surrounding tissues involving a mobile tra

25 opetally through the root within the central stele and then, upon reaching the root apex, auxin is tr

26 Root diameter, stele and xylem diameter, and xylem number were more res

27 in cells undergoing radial expansion in the stele and/or cell wall dissolution.

28 e is collateral, and vascular bundles in the stele are arranged in a ring.

29 on as an apoplastic diffusion barrier to the stele at sites of lateral root emergence where Casparian

30 n the epidermis, whereas BR signaling in the stele buffered this effect.

31 HR messenger RNA is found exclusively in the stele cells internal to the endodermis and cortex, indic

32 on is SHORT-ROOT (SHR), which moves from the stele cells into the endodermis and root tip of Arabidop

33 atterning genes to promote the production of stele cells, but might also indirectly feed into establi

34 In the stele, changes in aquaporin activity accounted for about

35 This gene was highly expressed in the root stele compared to the cortex, and its expression decreas

36 as always greatest in interior tissues (i.e. stele, endodermis, and/or vascular tissues) for all root

37 We identified 158 interactions with 13 stele-expressed promoters, many of which occur physicall

38 transcription factor resource of 92% of root stele-expressed transcription factors and 74.5% of root-

39 stic space between the soil solution and the stele in roots [1-3].

40 highly specific manner from the cells of the stele in which it is synthesized outward.

41 ORT-ROOT (SHR) protein, which moves from the stele into the neighboring ground tissue layer to specif

42 that subcellular localization of SHR in the stele is intrinsic to the SHR protein.

43 and the radial hydraulic conductance for the stele (L(R, S)) of the distal root region by 32% and 41%

44 (Zea mays) primary root tissues, the cortex, stele, meristematic zone, and elongation zone, was gener

45 rimarily found in the epidermis, cortex, and stele of mature primary and lateral roots, but not in th

46 ontrast, repressed BR genes prevailed in the stele of the apical meristem zone.

47 Free IAA occurs predominantly in the stele of the mesocotyl whereas esterified IAA is mainly

48 O2 deficiency in the stele reduced the concentrations of K, Na and Cl in the

49 DR5::GUS expression in the root tips and the stele region proximal to the root tip.

50 the epidermis, and the innermost tissue, the stele, respectively.

51 expression was observed in the cells of the stele situated adjacent to the xylem poles.

52 expression is largely localized to the root stele, suggesting a centric and gradual release of its d

53 the plasma membrane and is expressed in the stele, suggesting a role in vascular loading; FPN2 local

54 Made in the stele, the SHR protein moves into an adjacent cell layer

55 utative transcription factor, moves from the stele to a single layer of adjacent cells, where it ente

56 iffusive transport of these solutes from the stele to the cortex via endodermal plasmodesmata.

57 the cell fate regulator SHORT-ROOT from the stele to the ground tissue has been associated with tran

58 With EDTA, Cu levels in the stele were higher than those in the cortex after 1 week