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1 to changes in both the number and pattern of vascular bundles.
2 gars, possibly through additional amphivasal vascular bundles.
3 omously, transport velocity can differ among vascular bundles.
4 ng produced stunted plants with disorganized vascular bundles.
5 ated in young cotyledons, green tissues, and vascular bundles.
6 ascicular region that normally separates the vascular bundles.
7  highest in the parenchymatous tissue around vascular bundles.
8 s and showed an unusual arrangement of small vascular bundles.
9  parenchyma while ShSUT1 was up-regulated in vascular bundles.
10 y is detected in leaves, but only within the vascular bundles.
11 ts were localised to the phloem cells of the vascular bundles.
12 of the leaf and the isolated BSCs with their vascular bundle along the developmental gradient were de
13 ted, twisted leaves with small, disorganized vascular bundles, an enlarged sclerenchyma and large air
14  induced when L2 reached the differentiating vascular bundle and during early stages of the nematode-
15 n extended from contact cells throughout the vascular bundle and into extravascular cells, revealing
16  is involved in delivery of allantoin to the vascular bundle and loading into the nodule phloem.
17 -cells) situated between the phloem of every vascular bundle and the endodermis.
18 y possess both fascicular phloem (FP) within vascular bundles and additional extrafascicular phloem (
19 particles (NPs): destroying chloroplasts and vascular bundles and altering absorption of nutrients on
20 00) of epidermal cells and vascular tissues (vascular bundles and bundle sheath cells) from ethanol:a
21 tected only in the epidermal cell layer, the vascular bundles and bundle sheath cells.
22 s, a cortex, a ring of secondarily thickened vascular bundles and interfascicular cells, and inner pi
23 ay occur that are associated with misaligned vascular bundles and outgrowths of ectopic margins.
24 comparison of the levels of RBP50 present in vascular bundles and phloem sap indicated that this prot
25  expression profiling of storage parenchyma, vascular bundles and rind dissected from a maturing stal
26 r phloem (FP)] and another peripheral to the vascular bundles and scattered through stem and petiole
27  ultraviolet autofluorescence is observed in vascular bundles and sclerid layers.
28 how that ZePel expression is associated with vascular bundles and shoot primordia.
29 he medullary interstitium, loss of medullary vascular bundles, and decreased urine concentrating abil
30 arley, the ptGRP1 homologue is found in leaf vascular bundles, and may also be present in the surroun
31   The outer periphery of the stalk has fewer vascular bundles, and the sclerids underlying the epider
32 D40 mRNA accumulated in the pericycle of the vascular bundle at 24 h after root inoculation with nod
33                     Prior to leaf expansion, vascular bundles attached to the first developing leaf d
34 ression of all ZCN genes was associated with vascular bundles, but each gene had a specific spatial a
35           The syncytium is formed within the vascular bundle by partial degradation of cell walls and
36 gen species are generated near cell walls of vascular bundle cells by oligogalacturonide fragments pr
37                                         Root vascular bundle cells of light-grown mutant seedlings de
38 ry [Ca(2+)]i signals in spongy mesophyll and vascular bundle cells, but not other cell types, and det
39 ch GI is expressed exclusively in mesophyll, vascular bundles, epidermis, shoot apical meristem, or r
40 ifferent phloem systems, one within the main vascular bundles [fascicular phloem (FP)] and another pe
41  hemicellulose, and thinner sclerenchyma and vascular bundle fibre cells than wild-type plants; where
42  anastomosis of the deep inferior epigastric vascular bundle from the donor muscle to the recipient n
43 , specifically disrupt the normal pattern of vascular bundles in cotyledons, mature leaves, and inflo
44 egion in stems, leaves, and roots and in the vascular bundles in flower buds but does not occur in th
45                       Furthermore, branching vascular bundles in the avb1 stems abnormally penetrated
46 lar bundles seen in the wild-type stems, the vascular bundles in the avb1 stems were similar to amphi
47  expand, such as those residing inner to the vascular bundles in the fruit pericarp.
48 essential for entry of the viral genome into vascular bundles in the inoculated leaves in the absence
49 acrophages infiltrated areas adjacent to the vascular bundles in the outer medulla within hours of re
50 tissues within the bundle is collateral, and vascular bundles in the stele are arranged in a ring.
51 a disruption in the ring-like arrangement of vascular bundles in the stele.
52 he mechanisms controlling the arrangement of vascular bundles in the stele.
53  and alterations in the radial patterning of vascular bundles in the stem.
54 r, leaf size, root system, and the number of vascular bundles, indicating the enhancement of source s
55 lls are arranged in encircling layers around vascular bundles, is one of the major traits that differ
56 tions, the McHAKs showed signals in the leaf vascular bundles, mesophyll, and epidermal cells as well
57 dopsis, we have isolated an avb1 (amphivasal vascular bundle) mutant with a novel vascular pattern.
58  an inhibitor that prevents the formation of vascular bundles near pre-existing bundles.
59 t a low basal level in the root tips and the vascular bundle of differentiated roots.
60 ith cavity, weak spiral growth but increased vascular bundle of the thick wall Moso.
61 e deposition of spot-like callose patches in vascular bundles of directly inoculated spikelets, while
62 lar cambium and xylem tissues as well as the vascular bundles of expanding catkins.
63 fibers and vessel elements is altered in the vascular bundles of ifl1 mutants.
64 are also concentrated in the differentiating vascular bundles of internodes.
65 e revealed that the gene is expressed in the vascular bundles of kernels, seedling roots, and coleopt
66 ics of C4 photosynthesis in cells around the vascular bundles of stems of C3 plants might explain why
67  that macrophages infiltrate the area of the vascular bundles of the outer medulla, these macrophages
68 , respectively, in microtissue strips of the vascular bundles of the outer medullary vasa recta.
69  conducted a screen for mutants with altered vascular bundle organization in Arabidopsis cotyledons.
70 tagged SCL15 predominantly localizes to, the vascular bundles particularly in the phloem companion ce
71 nts indicated reduction of cell expansion in vascular bundles, particularly on their abaxial surface.
72 ther most of the evaporation occurs from the vascular bundles (perivascular), from the photosynthetic
73 es function in patterning lateral organs and vascular bundles produced from the shoot apical and vasc
74 :GUS staining appeared to predominate in the vascular bundles relative to surrounding cortex cells wh
75 und that GI expressed in either mesophyll or vascular bundles rescues the late-flowering phenotype of
76                        Unlike the collateral vascular bundles seen in the wild-type stems, the vascul
77         We hypothesized that the AQPs of the vascular bundle sheath (BS) cells regulate K(leaf).
78 ty strongly increases when the proportion of vascular bundle sheath (BS) tissue is higher than 15%, w
79 synthesis is observed in infected tissue and vascular bundles show strong lignification.
80 companion cell vacuoles of the phloem in all vascular bundles, showing a strong co-localization with
81   lin-4 forms nodules with centrally located vascular bundles similar to that found in lateral roots
82                        Mycorrhizas increased vascular bundle size, demonstrating that these fungi can
83 ectopic deposition of suberin around twisted vascular bundles, the de-etiolation phenotype, and conti
84 t aligned microchannels similar to a plant's vascular bundles through a uniaxial freeze-drying proces
85 orter gene analysis showed expression in the vascular bundle throughout the plant, except in the flow
86  attributed to differential carbon flux into vascular bundles versus that into fiber cells.
87                          RIPC to the femoral vascular bundle was compared against direct ischemic pre
88 lique muscle and fascia with its independent vascular bundle was isolated and stored in cold Universi
89 artial hepatic IR and of RIPC to the femoral vascular bundle were applied.
90                                          The vascular bundles were destroyed by CeO2 nanoparticles, a
91                        Additional amphivasal vascular bundles were identified in the pith of pedicels
92 ally, CO and FT are expressed exclusively in vascular bundles, whereas GI is expressed in various tis
93 ll bridge bordering the enlarged and diffuse vascular bundles, whereas iron and manganese were locali
94  preferentially affects carbon flux into the vascular bundles, whereas the adt3456 knock-out addition
95  exhibit enhanced lignin deposition in their vascular bundles with altered S:G ratio under salt stres

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