ライフサイエンスコーパス: vascular bundle

1 KD prior to placement of an AVF in the iliac vascular bundle.

2 the skin surface approximately above a major vascular bundle.

3 ls, during systemic signaling, occurs at the vascular bundles.

4 y is detected in leaves, but only within the vascular bundles.

5 ts were localised to the phloem cells of the vascular bundles.

6 y marked by COL2 and BSP or RUNX2 within the vascular bundles.

7 ion domain VP16 (HVA-VP16) resulted in fewer vascular bundles.

8 eferentially in cells surrounding fibers and vascular bundles.

9 parenchyma while ShSUT1 was up-regulated in vascular bundles.

10 ular Patterning, and reduced cell numbers in vascular bundles.

11 to changes in both the number and pattern of vascular bundles.

12 gars, possibly through additional amphivasal vascular bundles.

13 omously, transport velocity can differ among vascular bundles.

14 outlines and a discontinuous distribution of vascular bundles.

15 ng produced stunted plants with disorganized vascular bundles.

16 ated in young cotyledons, green tissues, and vascular bundles.

17 ascicular region that normally separates the vascular bundles.

18 highest in the parenchymatous tissue around vascular bundles.

19 s and showed an unusual arrangement of small vascular bundles.

20 of the leaf and the isolated BSCs with their vascular bundle along the developmental gradient were de

21 ted, twisted leaves with small, disorganized vascular bundles, an enlarged sclerenchyma and large air

22 induced when L2 reached the differentiating vascular bundle and during early stages of the nematode-

23 n extended from contact cells throughout the vascular bundle and into extravascular cells, revealing

24 is involved in delivery of allantoin to the vascular bundle and loading into the nodule phloem.

25 -cells) situated between the phloem of every vascular bundle and the endodermis.

26 y possess both fascicular phloem (FP) within vascular bundles and additional extrafascicular phloem (

27 particles (NPs): destroying chloroplasts and vascular bundles and altering absorption of nutrients on

28 00) of epidermal cells and vascular tissues (vascular bundles and bundle sheath cells) from ethanol:a

29 tected only in the epidermal cell layer, the vascular bundles and bundle sheath cells.

30 s, a cortex, a ring of secondarily thickened vascular bundles and interfascicular cells, and inner pi

31 ay occur that are associated with misaligned vascular bundles and outgrowths of ectopic margins.

32 efined by the vertical growth pattern of its vascular bundles and parenchyma cell tissue, limits its

33 comparison of the levels of RBP50 present in vascular bundles and phloem sap indicated that this prot

34 expression profiling of storage parenchyma, vascular bundles and rind dissected from a maturing stal

35 r phloem (FP)] and another peripheral to the vascular bundles and scattered through stem and petiole

36 ultraviolet autofluorescence is observed in vascular bundles and sclerid layers.

37 how that ZePel expression is associated with vascular bundles and shoot primordia.

38 actuator relies on the radial arrangement of vascular bundles and surrounding tissues around a centra

39 o propagate at rapid rates through the plant vascular bundles and to regulate many of the systemic pr

40 he medullary interstitium, loss of medullary vascular bundles, and decreased urine concentrating abil

41 arley, the ptGRP1 homologue is found in leaf vascular bundles, and may also be present in the surroun

42 The outer periphery of the stalk has fewer vascular bundles, and the sclerids underlying the epider

43 D40 mRNA accumulated in the pericycle of the vascular bundle at 24 h after root inoculation with nod

44 Prior to leaf expansion, vascular bundles attached to the first developing leaf d

45 ression of all ZCN genes was associated with vascular bundles, but each gene had a specific spatial a

46 The syncytium is formed within the vascular bundle by partial degradation of cell walls and

47 gen species are generated near cell walls of vascular bundle cells by oligogalacturonide fragments pr

48 Root vascular bundle cells of light-grown mutant seedlings de

49 ry [Ca(2+)]i signals in spongy mesophyll and vascular bundle cells, but not other cell types, and det

50 MAP20 is expressed during the late stages of vascular bundle development and localizes around forming

51 pathway genes, jasmonic acid response genes, vascular bundle development genes, and K(+) transport ge

52 tion of MAP20 in different cell types during vascular bundle development.

53 icroscopy reveals that specific sites of the vascular bundle; either xylem or the phloem can be uniqu

54 ch GI is expressed exclusively in mesophyll, vascular bundles, epidermis, shoot apical meristem, or r

55 ifferent phloem systems, one within the main vascular bundles [fascicular phloem (FP)] and another pe

56 hemicellulose, and thinner sclerenchyma and vascular bundle fibre cells than wild-type plants; where

57 However, the regulation of vascular bundle formation is poorly understood in the Ar

58 anastomosis of the deep inferior epigastric vascular bundle from the donor muscle to the recipient n

59 ts, and Streptomyces can move into the plant vascular bundle from the flowers and from the rhizospher

60 dermis and a cell layer or two away from the vascular bundle in the rice leaf sheath.

61 ts showed crystals tend to accumulate around vascular bundles in all species, irrespective of size, i

62 , specifically disrupt the normal pattern of vascular bundles in cotyledons, mature leaves, and inflo

63 egion in stems, leaves, and roots and in the vascular bundles in flower buds but does not occur in th

64 Furthermore, branching vascular bundles in the avb1 stems abnormally penetrated

65 lar bundles seen in the wild-type stems, the vascular bundles in the avb1 stems were similar to amphi

66 expand, such as those residing inner to the vascular bundles in the fruit pericarp.

67 essential for entry of the viral genome into vascular bundles in the inoculated leaves in the absence

68 P4 was mainly expressed in phloem of diffuse vascular bundles in the nodes and the axillary meristem.

69 in transporting Zn to the phloem of diffuse vascular bundles in the nodes for subsequent distributio

70 acrophages infiltrated areas adjacent to the vascular bundles in the outer medulla within hours of re

71 mutant leaves and stalk, and deformation of vascular bundles in the stalk resulting in the loss of x

72 tissues within the bundle is collateral, and vascular bundles in the stele are arranged in a ring.

73 he mechanisms controlling the arrangement of vascular bundles in the stele.

74 a disruption in the ring-like arrangement of vascular bundles in the stele.

75 and alterations in the radial patterning of vascular bundles in the stem.

76 r, leaf size, root system, and the number of vascular bundles, indicating the enhancement of source s

77 lls are arranged in encircling layers around vascular bundles, is one of the major traits that differ

78 sues including the epidermis, mesophyll, and vascular bundle, its tissue-specific functions in thermo

79 tions, the McHAKs showed signals in the leaf vascular bundles, mesophyll, and epidermal cells as well

80 dopsis, we have isolated an avb1 (amphivasal vascular bundle) mutant with a novel vascular pattern.

81 an inhibitor that prevents the formation of vascular bundles near pre-existing bundles.

82 vascular activity, hva-d, showing increased vascular bundle number and enhanced cambium proliferatio

83 t a low basal level in the root tips and the vascular bundle of differentiated roots.

84 ith cavity, weak spiral growth but increased vascular bundle of the thick wall Moso.

85 role for RBOHD-driven ROS production at the vascular bundles of Arabidopsis in mediating light stres

86 for local and systemic ROS signaling at the vascular bundles of Arabidopsis.

87 e deposition of spot-like callose patches in vascular bundles of directly inoculated spikelets, while

88 lar cambium and xylem tissues as well as the vascular bundles of expanding catkins.

89 fibers and vessel elements is altered in the vascular bundles of ifl1 mutants.

90 are also concentrated in the differentiating vascular bundles of internodes.

91 e revealed that the gene is expressed in the vascular bundles of kernels, seedling roots, and coleopt

92 ent and evolutionary origins of the inverted vascular bundles of ovuliferous scales, (3) the role of

93 ) for precise delivery of agrochemicals into vascular bundles of plant tissue.

94 ics of C4 photosynthesis in cells around the vascular bundles of stems of C3 plants might explain why

95 antly accumulated Zn in enlarged and transit vascular bundles of the basal node, whereas in wild-type

96 The vascular bundles of the lamina form a nexus at the petio

97 that macrophages infiltrate the area of the vascular bundles of the outer medulla, these macrophages

98 , respectively, in microtissue strips of the vascular bundles of the outer medullary vasa recta.

99 The vascular bundles of the stem interconnect at the node, f

100 conducted a screen for mutants with altered vascular bundle organization in Arabidopsis cotyledons.

101 tagged SCL15 predominantly localizes to, the vascular bundles particularly in the phloem companion ce

102 nts indicated reduction of cell expansion in vascular bundles, particularly on their abaxial surface.

103 ther most of the evaporation occurs from the vascular bundles (perivascular), from the photosynthetic

104 es function in patterning lateral organs and vascular bundles produced from the shoot apical and vasc

105 :GUS staining appeared to predominate in the vascular bundles relative to surrounding cortex cells wh

106 und that GI expressed in either mesophyll or vascular bundles rescues the late-flowering phenotype of

107 Unlike the collateral vascular bundles seen in the wild-type stems, the vascul

108 We hypothesized that the AQPs of the vascular bundle sheath (BS) cells regulate K(leaf).

109 ty strongly increases when the proportion of vascular bundle sheath (BS) tissue is higher than 15%, w

110 synthesis is observed in infected tissue and vascular bundles show strong lignification.

111 companion cell vacuoles of the phloem in all vascular bundles, showing a strong co-localization with

112 lin-4 forms nodules with centrally located vascular bundles similar to that found in lateral roots

113 Mycorrhizas increased vascular bundle size, demonstrating that these fungi can

114 ectopic deposition of suberin around twisted vascular bundles, the de-etiolation phenotype, and conti

115 t aligned microchannels similar to a plant's vascular bundles through a uniaxial freeze-drying proces

116 orter gene analysis showed expression in the vascular bundle throughout the plant, except in the flow

117 Vascular bundles transport water and photosynthate to al

118 attributed to differential carbon flux into vascular bundles versus that into fiber cells.

119 ered through stomata and then transported to vascular bundles via apoplastic movement.

120 RIPC to the femoral vascular bundle was compared against direct ischemic pre

121 lique muscle and fascia with its independent vascular bundle was isolated and stored in cold Universi

122 artial hepatic IR and of RIPC to the femoral vascular bundle were applied.

123 The vascular bundles were destroyed by CeO2 nanoparticles, a

124 Additional amphivasal vascular bundles were identified in the pith of pedicels

125 ally, CO and FT are expressed exclusively in vascular bundles, whereas GI is expressed in various tis

126 ll bridge bordering the enlarged and diffuse vascular bundles, whereas iron and manganese were locali

127 preferentially affects carbon flux into the vascular bundles, whereas the adt3456 knock-out addition

128 rt of nutrients for aphids, and a network of vascular bundles which accompanying schizogenous ducts a

129 exhibit enhanced lignin deposition in their vascular bundles with altered S:G ratio under salt stres