ライフサイエンスコーパス: plant leaves

1 zed, diverse bacterial community washed from plant leaves.

2 chanism controlling its diurnal breakdown in plant leaves.

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

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

5 ly the superhydrophobic surfaces inspired by plant leaves.

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

7 r salicylate accumulation in the apoplast of plant leaves.

8 t AvrPto is phosphorylated when expressed in plant leaves.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

23 Plant leaves are a major potential source of novel food

24 Plant leaves are diverse in their morphology, reflecting

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

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

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

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

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

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

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

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

33 Plants leaves develop proximodistal, dorsoventral (adaxi

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

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

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

37 Across plants, leaves exhibit profound diversity in shape.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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