ライフサイエンスコーパス: plant leaf

1 imicking the regeneration functionality of a plant leaf.

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

3 ty among the healthy and affected portion of plant leaves.

4 uantify the effects of UVA radiation on live plant leaves.

5 atmosphere and are likely to be deposited on plant leaves.

6 up to half of the soluble protein content in plant leaves.

7 stress-modified flavonoid production in tea plant leaves.

8 f air quality by optimising PM deposition on plant leaves.

9 ing ROS production and leaf damage in tomato plant leaves.

10 , the dynamic ensemble of compounds covering plant leaves.

11 e to those of photocatalytic suspensions and plant leaves.

12 ce of endophytic lactic acid bacteria within plant leaves.

13 the opening and closure of stomatal pores on plant leaves.

14 livery and inducing gene silencing in mature plant leaves.

15 diterpenoids together with lipid droplets in plant leaves.

16 eria to survive the seemingly dry surface of plant leaves.

17 zed, diverse bacterial community washed from plant leaves.

18 ly the superhydrophobic surfaces inspired by plant leaves.

19 chanism controlling its diurnal breakdown in plant leaves.

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

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

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

23 r salicylate accumulation in the apoplast of plant leaves.

24 t AvrPto is phosphorylated when expressed in plant leaves.

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

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

27 A-LFT detected at least 4 ng of PVY per g of plant leaves, 0.04 ng/g for PVS, and 0.04 ng/g for PLRV.

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

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

30 understanding of morphogenetic processes in plant leaves and animal epithelia and perhaps even the f

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

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

33 ther and with MIF in vitro, in yeast, and in plant leaves and formed hetero-oligomeric complexes with

34 applied PULSE to control immune responses in plant leaves and generated Arabidopsis transgenic plants

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

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

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

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

39 and dimethylsulfoniopropionate, in detached plant leaves and rhizomes.

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

41 the coexistence of the two species on melon plant leaves and seeds.

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

43 athogens and pests present on the surface of plant leaves and the grain but also inside the seeds.

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

45 al understanding of the interactions between plant leaves and water.

46 mata control the gas exchange of terrestrial plant leaves, and are therefore essential to plant growt

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

48 d polystyrene (PS) polymers and oligomers in plant leaves, and identify that their levels increase wi

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

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

51 to locate and categorize the numerous tomato plant leaf anomalies.

52 The plant leaf apoplast is a dynamic environment subject to

53 Plant leaves are a major potential source of novel food

54 Plant leaves are diverse in their morphology, reflecting

55 make this complex chemistry more efficient, plant leaves are intricately constructed in 3 dimensions

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

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

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

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

60 In the stomatal lineages on the surfaces of plant leaves, asymmetric and oriented divisions create d

61 d greenhouse experiment, we enriched pitcher-plant leaves at different rates with bovine serum albumi

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

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

64 alent steviol glycoside in Stevia rebaudiana plant leaves, but it has found limited applications in f

65 ght both influence physiological function in plant leaves, but their relative contributions to change

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

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

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

69 es with more plant species imply more varied plant leaf chemistry, more species of crops provide more

70 Plant leaves constitute a huge microbial habitat of glob

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

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

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

74 Plants leaves develop proximodistal, dorsoventral (adaxi

75 ented solution is robust to the detection of plant leaf disease and can replace the manual systems.

76 el thus emerges as an effective solution for plant leaf disease classification, delivering outstandin

77 amely ResNet-34-based Faster-RCNN for tomato plant leaf disease classification.

78 suspected sample has further complicated the plant leaf disease detection process.

79 timized Faster R-CNN (FS-FRNet) for improved plant leaf disease identification and classification.

80 d MobileNet architecture, designed to detect plant leaf diseases across a diverse range of crop types

81 Accurate classification of plant leaf diseases at an early stage is crucial for dia

82 Plant leaf diseases significantly impact crop yield and

83 p learning models that can be used to detect plant leaf diseases.

84 ts efficacy for reliable detection of tomato plant leaf diseases.

85 Plant leaves display considerable variation in shape.

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

87 ed how 41 years of manipulated fire affected plant leaf economics by sampling 89 plant species across

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

89 d plants (e.g., bird feathers, insect wings, plant leaves, etc.) are superhydrophobic with rough surf

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

91 Across plants, leaves exhibit profound diversity in shape.

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

93 Plant leaves feature epidermal stomata that are organize

94 facilitating carbon dioxide influx into the plant leaf for photosynthesis and restricting water effl

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

96 Many plant leaves have two layers of photosynthetic tissue: t

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

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

99 ed with the vast array of shape formation of plant leaves in nature.

100 one hand, a decrease in reflectance of host plant leaves in the near-infrared portion of the radiome

101 The tracheary system of plant leaves is composed of a cellulose skeleton with di

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

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

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

105 Moreover, leachates from plant leaf-litter can serve as an additional source of l

106 as UVA dose increases, the bioimpedance of a plant leaf measured at a frequency of 1 kHz linearly dec

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

108 The CO(2) transfer conductance within plant leaves (mesophyll conductance, g(m) ) is currently

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

110 nt assemblage into the plant-flower-visitor, plant-leaf miner and leaf miner-parasitoid networks usin

111 ption and accumulation of atmospheric MPs by plant leaves occur widely in the environment, and this s

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

113 microbes have the ability to stably colonize plant leaves, overcoming the fluctuating environmental c

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

115 was tested on mammalian, whole plant cells, plant leaf protoplast and fungal cell cultures and obser

116 In terrestrial ecosystems, plant leaves provide the largest biological habitat for

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

118 o, and Ala as the most potent stimulators of plant leaf R(N) Using metabolite combinations, we discov

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

120 f largely non-pathogenic fungi that colonize plant leaves remains an open question.

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

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

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

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

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

126 Plant leaves sense various organic pollutants to generat

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

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

129 In most seed plants, leaf size is isometrically related to stem cross

130 cesses and increase nitrogen contents in the plant leaf, stem and fine root pools.

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

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

133 cted delta(2) H offsets, likely by impacting plant leaf stomatal conductance.

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

135 ication of dsRNA-containing bacterial EVs to plant leaves suppressed B. cinerea infection.

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

137 osite, based on the structure of the natural plant leaf, synergistically improves mechanical strength

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

139 ta are the pores in the epidermal surface of plant leaves that regulate the exchange of water and CO(

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

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

142 THz radiation at multiple frequencies within plant leaves to determine absolute water content in real

143 microbial decomposer communities in pitcher plant leaves to investigate BEF.

144 udies show coordinated relationships between plant leaf traits and their capacity to predict ecosyste

145 Plant leaf traits are key in determining plants' perform

146 Woody plant leaf traits indirectly influenced soil microbes th

147 rmore, the framework can locate the affected plant leaves under the occurrence of blurring, noise, ch

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

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

150 ents with radiocarbon ((14)C) data of higher plant leaf-wax n-alkanoic acids.

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

152 Plant leaf waxes record the delta(2)H of precipitation d

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

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

155 Plant leaves were extracted in methanol (80%), then the

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

157 Plant leaves, whose remarkable ability for morphogenesis