ライフサイエンスコーパス: plant leaf

1 imicking the regeneration functionality of a plant leaf.

2 zed, diverse bacterial community washed from plant leaves.

3 chanism controlling its diurnal breakdown in plant leaves.

4 ion and evaluate the effect of herbicides on plant leaves.

5 thesized and degraded in a diurnal manner in plant leaves.

6 ly the superhydrophobic surfaces inspired by plant leaves.

7 ly related to an increase in SOD activity in plant leaves.

8 r salicylate accumulation in the apoplast of plant leaves.

9 t AvrPto is phosphorylated when expressed in plant leaves.

10 e activity, and attenuated virulence in host plant leaves.

11 ABA) that lead to stomatal closure in higher-plant leaves.

12 yunsaturated fatty acid (PUFA) substrates in plant leaves.

13 onstrating that auxin influx is required for plant leaf and flower development.

14 a global meta-analysis to determine whether plant leaf and litter functional traits, and particularl

15 SM6 efficiently accumulates in plant leaves and assembles correctly into heterooligomer

16 or synthetic sheets, such as rapidly growing plant leaves and crushed foils.

17 ion on natural and artificial surfaces (i.e. plant leaves and glass).

18 usly viewed as a static material property of plant leaves and insect cuticles, we here demonstrate a

19 atrices such as fruits, vegetables, cereals, plant leaves and other green parts were analysed, of whi

20 s(12) is conserved in the ADP-GlcPPases from plant leaves and other tissues except for the monocot en

21 emical functional groups) and environmental (plant leaves and sand) surfaces can be described by clas

22 hat is controlled by stomata, small pores on plant leaves and stems formed by guard cells.

23 icity, such as the self-cleaning surfaces on plant leaves and trapped air on immersed insect surfaces

24 misia tabaci (the TYLCV vector) feeding on R plant leaves, and even more strongly upregulated followi

25 Guard cells are located in the epidermis of plant leaves, and in pairs surround stomatal pores.

26 Results at the whole plant, leaf, and cellular level showed that primary meta

27 Plant leaves are a major potential source of novel food

28 Plant leaves are diverse in their morphology, reflecting

29 In seed plants, leaves are born on radial shoots, but unlike sho

30 re optima were driven by reductions in whole-plant leaf area and increased respiratory carbon losses.

31 Here, by using plant leaves as an example, we show that the causes of d

32 strain UCBPP-PA14 that were identified in a plant leaf assay for less pathogenic mutants also exhibi

33 Inspired by the stomatal closure feature of plant leaves at relatively high temperature, here we rep

34 any time-to-event phenological data, such as plant leafing, bird arrival time, and insect emergence.

35 rains are then co-inoculated into 3-week-old plant leaves by one of three methods: a needleless syrin

36 orescence (DF) from Photosystem II (PSII) of plant leaves can be potentially used to sense herbicide

37 In normal plants, leaf cells divide either transversely or longitu

38 ard cells surround pores in the epidermis of plant leaves, controlling the aperture of the pore to ba

39 Carbon isotope discrimination in plant leaves (Deltaleaf ) is an established indicator of

40 The water status of plant leaves depends on the efficiency of the water supp

41 Plants leaves develop proximodistal, dorsoventral (adaxi

42 The process of nutrient retranslocation from plant leaves during senescence subsequently affects both

43 Electrolyte-release analysis of transgenic plant leaves established a correlation between the level

44 of an ancestral shoot system from which seed plant leaves evolved.

45 Across plants, leaves exhibit profound diversity in shape.

46 te, and nonphotochemical quenching on intact plant leaves exhibiting distinct light responses.

47 from the furrows on our foreheads to crinkly plant leaves, from ripples on plastic-wrapped objects to

48 e fragments that activate defensive genes in plant leaves heretofore have been thought to be generate

49 mental inoculations with fungal pathogens of plant leaves in a tropical rain forest show that most fu

50 cies that can function as a stress signal in plant leaves leading to programmed cell death.

51 xpression of CypA and its mutant in yeast or plant leaves led to inhibition of tombusvirus replicatio

52 soil micro- and macro-fauna that break down plant leaf litter.

53 variant reference signal-embedded within the plant leaf mesophyll.

54 natural and artificial materials, including plant leaves, metal sheets, and construction materials.

55 stabilities occurring in animal epithelia or plant leaves, often emerge from mechanical instabilities

56 ultural practices had significant effects on plant leaf photosynthesis, transpiration, soil respirati

57 of tomato BI-1 by agroinfiltration of intact plant leaves provided protection from damage induced by

58 Antibody yields in transgenic plant leaves reached a maximum of 64 microg/g leaf fresh

59 reased PE levels in yeast surrogate host and plant leaves replicating TBSV.

60 opment of the flattened laminar structure in plant leaves requires highly regulated cell division and

61 The delta(13)C values of plant leaves, roots and soils in non-grazed (NG) and ove

62 neration acts as a negative regulator during plant leaf senescence signaling.

63 take and NO production play pivotal roles in plant leaf senescence.

64 Plant leaves, simple or compound, initiate as peg-like s

65 The stomatal pores of plant leaves, situated in the epidermis and surrounded b

66 terspecific scaling relationships among seed plant leaf, stem, and root biomass.

67 (using 80 per cent aqueous acetone) of whole plant, leaf, stem, washed leaf (WL) and dried water wash

68 Most PAH concentration data from vascular plant leaves suggest that contamination occurs by both d

69 bacterium spp., are persistent colonizers of plant leaf surfaces.

70 anner with the aim of metabolic profiling of plant leaves that have been collected at different time

71 rs from MMRT can serve as thermal traits for plant leaves that represent the collective temperature r

72 age of cAMP elevation in pathogen-inoculated plant leaves to Ca(2+) channels and immune signaling dow

73 Chloroplast absorption from an Elodea plant leaf was used to demonstrate this capability.

74 nor, sodium nitroprusside, on injection into plant leaves, was demonstrated by its abolition with O(3

75 Ultimately, genetic modification of plant leaf waxes or canopy structure could achieve great

76 spheric CO(2) and the stomatal index of land plant leaves, we reconstruct Late Cretaceous-Early Terti

77 Inspired by plant leaves, we used microfluidic devices consisting of

78 duct from photolysis of HNO3/nitrate on most plant leaves, whereas NOx was the major product on most