ライフサイエンスコーパス: frond

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1 to stromal cells near the regenerating nerve fronds.

2 d that CAI induced regression of neovascular fronds.

3 g the internal tissue of Psaronius tree-fern fronds.

4 structural colouration on the surface of the fronds.

5 soils had approximately 1.5 times more As in fronds (2540, 780, and 920 mg kg(-1)) than those from P-

6 rks, overfolded edges of Dickinsonia, felled fronds and drag structures generated by uprooted frond h

7 roduce a pool of cells from which individual frond apical initials are sequentially specified.

8 sts that the spores produced on Osmunda spp. fronds are probably asexual.

9 of three pinnae to half of the mediolateral frond axis.

10 Its frond biomass in PR-soils (52.2 g plant(-1) year(-1) or

11 In addition, its frond biomass increased by 20% consecutively with each h

12 r knowledge, this represented the largest PV frond biomass reported, demonstrating the unique ability

13 rescence staining revealed that regenerating fronds contained peptidergic nociceptive fibers (positiv

14 material along the apical-basal axis of the frond demonstrates that structural colour is confined to

15 en Point, Newfoundland, Canada, rangeomorph "fronds" dominate the earliest (579-565 million years ago

16 glutaredoxin (Grx) Pv5-6 was isolated from a frond expression cDNA library based on the ability of th

17 a similar profound inhibition of neovascular frond formation in CAI-treated mice in group A.

18 In group B, after neovascular fronds had already formed, CAI administration reduced ne

19 ranching morphology of Ediacaran rangeomorph fronds has no exact counterpart in other complex macroor

20 ds and drag structures generated by uprooted frond holdfasts.

21 thelial cells of blood vessels and capillary fronds in vivo in both the neural retinal tissue and in

22 Frond initials then cleave in two planes to produce a se

23 ovascularization in group A, and neovascular fronds involuted after treatment with CAI in group B.

24 y, this iterative pattern in both shoots and fronds is similar to the developmental process that oper

25 methods and histology, we show that shoots, fronds ('leaves') and pinnae ('leaflets') of the fern Ne

26 The branches were probably abscised as frond-like modules.

27 ed contributions to productivity within host fronds of Corallina officinalis on upper and lower zones

28 A2aR immunoreactivity was also prominent in fronds of intravitreal neovascularization.

29 ying dysplastic lesions and within papillary fronds of invasive cancers.

30 nce for a preponderance of exocellular As in fronds of Pteris vittata despite numerous reports of a t

31 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.

32 d and ungerminated soybean axes and also for fronds of several species of Polypodium with varying tol

33 tential (Psi), stomatal conductance (gs) and frond stipe hydraulic conductivity (K).

34 acillariophyta), confined to the apex of the frond structure, which were low light acclimated but ret

35 icit, coupled with insect damage, may hamper frond survival.

36 uals of both fucoid species showed increased frond temperature, high desiccation levels and reduced p

37 Excised frond tissue infiltrated with arsenate reduced arsenate

38 known to hyperaccumulate arsenic (As) in its fronds to >1% of its dry weight.

39 plasmids from the cDNA library of P. vittata fronds were introduced into Escherichia coli XL-1 Blue a

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