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1 structural colouration on the surface of the fronds.
2 to stromal cells near the regenerating nerve fronds.
3 d that CAI induced regression of neovascular fronds.
4 g the internal tissue of Psaronius tree-fern fronds.
5 m surface, and middle section of Lemna minor fronds.
6 soils had approximately 1.5 times more As in fronds (2540, 780, and 920 mg kg(-1)) than those from P-
7 evalence of mucilage ducts within stipes and fronds (absent in Lessonia) and fully developed unilocul
8 differentially expressed transcripts between frond and mature turion tissues revealed major pathways
9 rks, overfolded edges of Dickinsonia, felled fronds and drag structures generated by uprooted frond h
10 roduce a pool of cells from which individual frond apical initials are sequentially specified.
11 sts that the spores produced on Osmunda spp. fronds are probably asexual.
12  of three pinnae to half of the mediolateral frond axis.
13 ometric equations for palm (R(2) = 0.92) and frond biomass are developed and contrasted to existing a
14                                          Its frond biomass in PR-soils (52.2 g plant(-1) year(-1) or
15                             In addition, its frond biomass increased by 20% consecutively with each h
16 r knowledge, this represented the largest PV frond biomass reported, demonstrating the unique ability
17 REEs were translocated from the roots to the fronds by the xylem sap and were stored within the xylem
18 rescence staining revealed that regenerating fronds contained peptidergic nociceptive fibers (positiv
19  material along the apical-basal axis of the frond demonstrates that structural colour is confined to
20 en Point, Newfoundland, Canada, rangeomorph "fronds" dominate the earliest (579-565 million years ago
21 niches, leading to generalization within the frond-dominated Community Type.
22 lamentous organic structures preserved among frond-dominated fossil assemblages in Newfoundland (Cana
23 glutaredoxin (Grx) Pv5-6 was isolated from a frond expression cDNA library based on the ability of th
24 a similar profound inhibition of neovascular frond formation in CAI-treated mice in group A.
25                     The gradual unfurling of fronds from tightly coiled tips, termed fiddleheads or c
26            Facile regeneration of transgenic fronds from tissue culture, aided by reduced epigenetic
27                In group B, after neovascular fronds had already formed, CAI administration reduced ne
28 ranching morphology of Ediacaran rangeomorph fronds has no exact counterpart in other complex macroor
29 ds and drag structures generated by uprooted frond holdfasts.
30 petals in flowering plants, the shape of the fronds in ferns, and the branching pattern of the gameto
31 thelial cells of blood vessels and capillary fronds in vivo in both the neural retinal tissue and in
32                                              Frond initials then cleave in two planes to produce a se
33 ovascularization in group A, and neovascular fronds involuted after treatment with CAI in group B.
34 y, this iterative pattern in both shoots and fronds is similar to the developmental process that oper
35  methods and histology, we show that shoots, fronds ('leaves') and pinnae ('leaflets') of the fern Ne
36 ed on uniterminal forms (possessing only one frond), leaving biterminal and multiterminal rangeomorph
37       The branches were probably abscised as frond-like modules.
38 indrical and flexible distal stipes, serrate frond margins and presence of sporophylls) and L. spicat
39 and dormancy that are mobilized to reprogram frond meristems for turion differentiation.
40 ed contributions to productivity within host fronds of Corallina officinalis on upper and lower zones
41  A2aR immunoreactivity was also prominent in fronds of intravitreal neovascularization.
42 ying dysplastic lesions and within papillary fronds of invasive cancers.
43 nce for a preponderance of exocellular As in fronds of Pteris vittata despite numerous reports of a t
44 ow that 43-71% of the As extruded out of the fronds of PV grown in 0.67, 3.3 and 6.7 mM AsV.
45 d and ungerminated soybean axes and also for fronds of several species of Polypodium with varying tol
46  organisms like metazoans (including typical fronds), protists, and algae.
47 esence of Burgess Shale-type preservation of fronds reflects the rarity of fine-grained deposits in t
48 els in the healthy and necrotic parts of the frond shed light on the differential mobility between li
49 tential (Psi), stomatal conductance (gs) and frond stipe hydraulic conductivity (K).
50 acillariophyta), confined to the apex of the frond structure, which were low light acclimated but ret
51 icit, coupled with insect damage, may hamper frond survival.
52 uals of both fucoid species showed increased frond temperature, high desiccation levels and reduced p
53 mparison of turion transcriptomes to that of fronds, the actively growing leaf-like tissue, were carr
54                                      Excised frond tissue infiltrated with arsenate reduced arsenate
55 known to hyperaccumulate arsenic (As) in its fronds to >1% of its dry weight.
56 plasmids from the cDNA library of P. vittata fronds were introduced into Escherichia coli XL-1 Blue a
57  knowledge, of typical Ediacaran rangeomorph fronds with Burgess Shale-type preservation.