ライフサイエンスコーパス: endodermis

1 in selected areas of the root epidermis and endodermis.

2 lature and the later steps in the cortex and endodermis.

3 the phloem of every vascular bundle and the endodermis.

4 division that normally generates cortex and endodermis.

5 ly (p < 0.01) higher than those in the inner endodermis.

6 and growth was present in the epidermis and endodermis.

7 from proliferation to differentiation in the endodermis.

8 t of the SHR homologs was not limited to the endodermis.

9 n between these two domains acts through the endodermis.

10 ith HSS being localized in cells of the root endodermis.

11 easing aquaporin densities in the phloem and endodermis.

12 regarding these two important aspects of the endodermis.

13 e neighboring ground tissue layer to specify endodermis.

14 stem for PEI-QDs) was likely limited by the endodermis.

15 signaling network operating primarily in the endodermis.

16 at blocks extracellular diffusion across the endodermis.

17 mulating in the root border cells and at the endodermis.

18 pression in nodule cortex cells and vascular endodermis.

19 ys 7 and 14 from periclinal divisions of the endodermis.

20 in the cortical parenchyma and close to the endodermis.

21 cell types of the ground tissue - cortex and endodermis.

22 why nearly all plants have a single layer of endodermis.

23 o cortical cells immediately adjacent to the endodermis.

24 epidermis and the vascular tissue inside the endodermis.

25 ributes to solute transport through the root endodermis.

26 ich in turn inhibit movement of SHR from the endodermis [11].

27 The endodermis acts as a "second skin" in plant roots by pro

28 idence in support of the hypothesis that the endodermis acts as a signaling center.

29 he highest tissue concentrations were in the endodermis and cortex approximately 4 mm or more behind

30 The endodermis and cortex arise continuously from the pericl

31 Roots of salt cress develop both an extra endodermis and cortex cell layer compared to Arabidopsis

32 responsible for formation of ground tissue (endodermis and cortex) as well as specification of endod

33 clusively in the stele cells internal to the endodermis and cortex, indicating that it has a non-cell

34 ground tissue into two separate layers: the endodermis and cortex.

35 tive periclinal asymmetric cell divisions in endodermis and cortex/endodermis initial daughters.

36 AHA4 is expressed most strongly in the root endodermis and flowers, as suggested by promoter-GUS rep

37 n has been detected in the cells of the root endodermis and in leaves directly underneath developing

38 ental concentrations in the epidermis, outer endodermis and inner endodermis are significantly (p < 0

39 beta GlcY penetrated roots as far as the endodermis and it is suggested that the interaction of b

40 In plants, such a barrier is provided by the endodermis and its Casparian strips--cell wall impregnat

41 In response to osmotic and salt stress, the endodermis and pericycle displayed prolonged oscillation

42 n phloem tissues for sucrose synthase or the endodermis and phloem for soluble acid invertase.

43 ized PvUPS1 to the nodule endodermis and the endodermis and phloem of the nodule vasculature.

44 We found that ABA accumulated in the endodermis and quiescent center of Arabidopsis thaliana

45 NPF3 is expressed in root endodermis and repressed by GA.

46 ), which moves from the stele cells into the endodermis and root tip of Arabidopsis, where it specifi

47 In roots, McHKT is mainly confined to endodermis and stele.

48 reproducibly found in specific cells of the endodermis and the adjacent cortex parenchyma of the roo

49 hybridization localized PvUPS1 to the nodule endodermis and the endodermis and phloem of the nodule v

50 anism for the longitudinal patterning of the endodermis, and represent the first example in plants of

51 the ABA pathway, also acts primarily in the endodermis, and we define the crosstalk between these tw

52 ys greatest in interior tissues (i.e. stele, endodermis, and/or vascular tissues) for all root zones.

53 in the epidermis, outer endodermis and inner endodermis are significantly (p < 0.01) different.

54 at the elemental concentrations in the outer endodermis are significantly (p < 0.01) higher than thos

55 cellular pathway and the roles played by the endodermis as a barrier.

56 Our results identify the endodermis as a gateway with an ABA-dependent guard, whi

57 athways of water across the root tissue, the endodermis as a layer with distinct transport properties

58 e that lead to extra cells in the cortex and endodermis, as well as additional cell layers.

59 damage and during normal growth in the root endodermis, bark, specialized organs (e.g., Solanum tube

60 centric layers of the epidermis, cortex, and endodermis before entering the central cylinder.

61 ce of these barriers and the position of the endodermis between the inner and outer parts of the root

62 protophloem was restricted to the pericycle-endodermis boundary, identifying plasmodesmata at this i

63 cinale, HSS is detected only in cells of the endodermis, but in a later developmental stage, addition

64 te the deposition of Casparian strips in the endodermis by recruiting the lignin polymerization machi

65 a common bean UPS1 transporter in cortex and endodermis cells of soybean nodules and found that deliv

66 within a contiguous cell layer that included endodermis, cortex/endodermis (joint) initial (CEI) cell

67 rts the idea that the neuronal properties of endodermis-derived endocrine pancreatic cells may find t

68 zation altogether, a suberized exodermis and endodermis developed in the maturation zone, which gave

69 results uncover a role for MYB36 outside the endodermis during LRP development through a mechanism an

70 The root endodermis has relatively higher concentrations of these

71 otropy identified the preferential growth of endodermis in response to this hormone.

72 rmis and cortex) as well as specification of endodermis in the Arabidopsis root.

73 the longitudinal cell division of the cortex/endodermis initial daughter cell, resulting in a single

74 tric cell divisions in endodermis and cortex/endodermis initial daughters.

75 The endodermis is also a unique mechanical barrier to organo

76 The root endodermis is characterized by the Casparian strip and b

77 that the pattern of cell division within the endodermis is sensitive to the dose of this protein: hig

78 na in which the ability to form a functional endodermis is spatially limited independently of SHR.

79 at DELLA activity in the vascular tissue and endodermis is sufficient to enable arbuscule formation i

80 The endodermis is the innermost cortical cell layer that fea

81 cell layer that included endodermis, cortex/endodermis (joint) initial (CEI) cells and the quiescent

82 Casparian strips and suberin lamellae at the endodermis limits the free diffusion of nutrients and ha

83 feration and differentiation generate mature endodermis, marked by the Casparian strip, a cell-wall m

84 As a gateway for solutes, the endodermis may also serve as an important site for sensi

85 g the formation of the Arabidopsis root, the endodermis, middle cortex (MC), and cortex are produced

86 In the endodermis, misexpression of the ABA insensitive1-1 muta

87 When ectopically expressed in the endodermis, most CASPLs were able to integrate the CASP

88 e present study demonstrates that the nodule endodermis of alfalfa (Medicago sativa) root nodules con

89 rmation of Casparian strips in the suberized endodermis of Arabidopsis roots.

90 step, was mainly localized in the cortex and endodermis of embryo axes in germinating seeds.

91 m parenchyma, and MIP-C in the epidermis and endodermis of immature roots.

92 S1 cDNA was expressed only in the cortex and endodermis of non-germinating ga1-3 seeds (deficient in

93 ease 5 (UPS5) is expressed in the cortex and endodermis of roots and its transcription is enhanced by

94 in the cell wall of certain tissues such as endodermis of roots, aerial and underground periderms, a

95 KT2;1 was mainly expressed in the cortex and endodermis of roots.

96 ssed in the meristematic zone, pericycle and endodermis of the Arabidopsis thaliana (Arabidopsis) roo

97 Analogous to its expression in the endodermis of the root, SCR is expressed in the starch s

98 ing-like cell-wall modifications in the root endodermis of vascular plants.

99 of mature roots but also are present in the endodermis of younger roots, where they are not extracte

100 ts that respiratory consumption of O2 in the endodermis or nodule parenchyma may be an essential comp

101 raction by facilitating transport across the endodermis, ostensibly by influencing both membrane inte

102 analysis of root cell walls showed that the endodermis presented a barrier (albeit partial) to the m

103 In the endodermis, SHR upregulates the transcription factors SC

104 a moving transcription factor essential for endodermis specification in the Arabidopsis root.

105 SHR is necessary for both cell division and endodermis specification.

106 nced root growth, increased number of cortex/endodermis stem cells and decreased number of columella

107 e further show that NO accumulates in cortex/endodermis stem cells and their precursor cells.

108 f Zn with cysteine-rich peptides in the root endodermis, suggesting enhanced synthesis of phytochelat

109 eas extra cortex cells are produced from the endodermis, suggesting the involvement of intercellular

110 sion and loss of SCARECROW expression in the endodermis, the ectopic accumulation of starch and lipid

111 ly expressed in the root epidermis, the root endodermis, the small parenchyma cells surrounding matur

112 ed in the inner layers of the skin, the root endodermis, the vascular cambium and the epidermis of th

113 Interestingly, the endodermis undergoes secondary differentiation, becoming

114 When exposed to arsenite, the endodermis was again a site of accumulation, although no

115 lation) and plastid size and position in the endodermis were measured in seedlings grown for 8 d in t

116 achieved in the Casparian strip of the root endodermis where a discrete band of lignin is crucial to

117 nals were localized to the epidermis and the endodermis, whereas lower transcript levels were detecte

118 W (SCR) revealed expression localized to the endodermis, which is similar to its expression in Arabid