| Reactive oxygen species, oxidative signaling and the regulation of photosynthesis |
77 |
| Plants facing oxidative challenges-A little help from the antioxidant networks |
48 |
| Reactive oxygen species and heavy metal stress in plants: Impact on the cell wall and secondary metabolism |
37 |
| Nitric oxide regulates plant responses to drought, salinity, and heavy metal stress |
37 |
| Can chlorophyll-a fluorescence parameters be used as bio-indicators to distinguish between drought and salinity stress in Tilia cordata Mill? |
34 |
| Endogenous melatonin deficiency aggravates high temperature-induced oxidative stress in Solanum lycopersicum L. |
32 |
| Glutathione S-transferases modulate Cu tolerance in Oryza sativa |
31 |
| Jasmonates in plants under abiotic stresses: Crosstalk with other phytohormones matters |
26 |
| Long-term exogenous application of melatonin improves nutrient uptake fluxes in apple plants under moderate drought stress |
24 |
| Azospirillum lipoferum FK1 confers improved salt tolerance in chickpea (Cicer arietinum L.) by modulating osmolytes, antioxidant machinery and stress-related genes expression |
24 |
| When are foliar anthocyanins useful to plants? Re-evaluation of the photoprotection hypothesis using Arabidopsis thaliana mutants that differ in anthocyanin accumulation |
24 |
| Response of photosynthetic capacity of tomato leaves to different LED light wavelength |
20 |
| Physiological, biochemical, and ultrastructural characterization of selenium toxicity in cowpea plants |
19 |
| Reactive oxygen and nitrogen species as key indicators of plant responses to Cd stress |
19 |
| Combined application of biochar, compost, and bacterial consortia with Italian ryegrass enhanced phytoremediation of petroleum hydrocarbon contaminated soil |
18 |
| Nitric oxide reverses glucose-mediated photosynthetic repression in wheat (Triticum aestivum L.) under salt stress |
18 |
| Identifying differences in carbohydrate dynamics of seedlings and mature trees to improve carbon allocation in models for trees and forests |
18 |
| Assessment of the impacts of climate change on Mediterranean terrestrial ecosystems based on data from field experiments and long-term monitored field gradients in Catalonia |
18 |
| Antioxidant protection and PSII regulation mitigate photo-oxidative stress induced by drought followed by high light in cashew plants |
17 |
| Salicylic acid acts upstream of nitric oxide in elevated carbon dioxide-induced flavonoid biosynthesis in tea plant (Camellia sinensis L.) |
17 |
| Synthesis and future research directions linking tree diversity to growth, survival, and damage in a global network of tree diversity experiments |
17 |
| Effect of green light on nitrate reduction and edible quality of hydroponically grown lettuce (Lactuca sativa L.) under short-term continuous light from red and blue light-emitting diodes |
17 |
| Interactive effects of melatonin and cytokinin on alleviating drought-induced leaf senescence in creeping bentgrass (Agrostis stolonifera) |
16 |
| Efficiency of heavy metals-tolerant plant growth promoting bacteria for alleviating heavy metals toxicity on sorghum |
16 |
| Substituting green or far-red radiation for blue radiation induces shade avoidance and promotes growth in lettuce and kale |
16 |
| Effect of interactions between light intensity and red-to- far-red ratio on the photosynthesis of soybean leaves under shade condition |
16 |
| Blue light associated with low phytochrome activity can promote elongation growth as shade-avoidance response: A comparison with red light in four bedding plant species |
16 |
| Photoinhibition or photoprotection of photosynthesis? Update on the (newly termed) sustained quenching component qH |
15 |
| Selenium reduces cadmium accumulation in seed by increasing cadmium retention in root of oilseed rape (Brassica napus L.) |
15 |
| Plant lipid remodeling in response to abiotic stresses |
15 |
| A methionine-R-sulfoxide reductase, OsMSRB is required for rice defense against copper toxicity |
15 |
| The soybean transcription factor GmNAC085 enhances drought tolerance in Arabidopsis |
14 |
| Characterization of type 3 metallothionein-like gene (OsMT-3a) from rice, revealed its ability to confer tolerance to salinity and heavy metal stresses |
14 |
| Rhizoremediation of petroleum hydrocarbon-contaminated soils: Improvement opportunities and field applications |
14 |
| Individual and combinatorial application of Kocuria rhizophila and citric acid on phytoextraction of multi-metal contaminated soils by Glycine max L |
14 |
| Lipid peroxidation-derived reactive carbonyl species (RCS): Their interaction with ROS and cellular redox during environmental stresses |
14 |
| Chlorophyll fluorescence as a tool to identify drought stress in Acer genotypes |
14 |
| Responses of phenolic acid and flavonoid synthesis to blue and blue-violet light depends on plant species |
14 |
| Influence of selenium on root morphology and photosynthetic characteristics of winter wheat under cadmium stress |
14 |
| Transcriptional and physiological analyses reveal the association of ROS metabolism with cold tolerance in tea plant |
14 |
| Unraveling a crosstalk regulatory network of temporal aroma accumulation in tea plant (Camellia sinensis) leaves by integration of metabolomics and transcriptomics |
13 |
| The Arabidopsis MYB transcription factor, MYB111 modulates salt responses by regulating flavonoid biosynthesis |
13 |
| Root endophytic fungus Piriformospora indica improves drought stress adaptation in barley by metabolic and proteomic reprogramming |
13 |
| Roles of root cell wall components and root plaques in regulating elemental uptake in rice subjected to selenite and different speciation of antimony |
13 |
| Hydrogen sulfide and environmental stresses |
13 |
| Arsenate disrupts ion balance, sulfur and nitric oxide metabolisms in roots and leaves of pea (Pisum sativum L.) plants |
13 |
| Selenium modulates dynamics of antioxidative defence expression, photosynthetic attributes and secondary metabolites to mitigate chromium toxicity in Brassica juncea L. plants |
13 |
| Allocation of the epidermis to stomata relates to stomatal physiological control: Stomatal factors involved in the evolutionary diversification of the angiosperms and development of amphistomaty |
13 |
| Cadmium and arsenic affect root development in Oryza sativa L. negatively interacting with auxin |
13 |
| Interactive role of epibrassinolide and hydrogen peroxide in regulating stomatal physiology, root morphology, photosynthetic and growth traits in Solanum lycopersicum L. under nickel stress |
12 |
