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Abscisic acid collaborates with lignin and flavonoid to improve pre‐silking drought tolerance by tuning stem elongation and ear development in maize (Zea mays L.)

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Trehalose‐Induced Changes in Seed Oil Composition and Antioxidant Potential of Maize Grown Under Drought Stress
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Ethylene increases accumulation of compatible solutes and decreases oxidative stress to improve plant tolerance to water stress in Arabidopsis
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Maize (Zea mays L.) response to a severe soil water-deficit during grain-filling
inferredcites →https://doi.org/10.1016/bs.agron.2017.07.004openalex-snapshot
Harvest Index of Maize ( Zea mays L.): Are There Possibilities for Improvement?
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Gibberellins synthesis is involved in the reduction of cell flux and elemental growth rate in maize leaf under low nitrogen supply
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Grain number and grain weight in wheat lines contrasting for stem water soluble carbohydrate concentration
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Effects of EDAH, a novel plant growth regulator, on mechanical strength, stalk vascular bundles and grain yield of summer maize at high densities
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Lignification: Flexibility, Biosynthesis and Regulation
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inferredcites →https://doi.org/10.1038/nbt.3277openalex-snapshot
Expression of trehalose-6-phosphate phosphatase in maize ears improves yield in well-watered and drought conditions
inferredcites →https://doi.org/10.1038/nclimate2837openalex-snapshot
Accelerated dryland expansion under climate change
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Quantitative analysis of major plant hormones in crude plant extracts by high-performance liquid chromatography–mass spectrometry
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inferredcites →https://doi.org/10.1038/s41467-019-10667-2openalex-snapshot
SLR1 inhibits MOC1 degradation to coordinate tiller number and plant height in rice
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Genotype-specific physiological and transcriptomic responses to drought stress in Setaria italica (an emerging model for Panicoideae grasses)
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Interactive effects of drought and heat stresses on morpho-physiological attributes, yield, nutrient uptake and oxidative status in maize hybrids
inferredcites →https://doi.org/10.1038/s41598-020-69080-1openalex-snapshot
Exogenous abscisic acid induces the lipid and flavonoid metabolism of tea plants under drought stress
inferredcites →https://doi.org/10.1038/s41598-020-72596-1openalex-snapshot
Drought stress triggers proteomic changes involving lignin, flavonoids and fatty acids in tea plants
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Trehalose 6-phosphate signalling and impact on crop yield
inferredcites →https://doi.org/10.1071/fp18099openalex-snapshot
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Plant height and hydraulic vulnerability to drought and cold
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Drought losses in China might double between the 1.5 °C and 2.0 °C warming
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Selectable traits to increase crop photosynthesis and yield of grain crops
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inferredcites →https://doi.org/10.1093/jxb/erx452openalex-snapshot
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inferredcites →https://doi.org/10.1093/jxb/ery013openalex-snapshot
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inferredcites →https://doi.org/10.1093/jxb/erz047openalex-snapshot
Increased biomass accumulation in maize grown in mixed nitrogen supply is mediated by auxin synthesis
inferredcites →https://doi.org/10.1093/plphys/kiab050openalex-snapshot
Transcription-associated metabolomic adjustments in maize occur during combined drought and cold stress
inferredcites →https://doi.org/10.1104/pp.127.1.315openalex-snapshot
Hormonal Changes in the Grains of Rice Subjected to Water Stress during Grain Filling
inferredcites →https://doi.org/10.1104/pp.17.01634openalex-snapshot
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inferredcites →https://doi.org/10.1104/pp.17.01673openalex-snapshot
Trehalose 6-Phosphate Regulates Photosynthesis and Assimilate Partitioning in Reproductive Tissue
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02192.xopenalex-snapshot
ABF2, an ABRE‐binding bZIP factor, is an essential component of glucose signaling and its overexpression affects multiple stress tolerance
inferredcites →https://doi.org/10.1111/j.1399-3054.2012.01711.xopenalex-snapshot
Apoplastic infusion of sucrose into stem internodes during female flowering does not increase grain yield in maize plants grown under nitrogen‐limiting conditions
inferredcites →https://doi.org/10.1111/j.1529-8817.2005.00098.xopenalex-snapshot
TREHALOSE SYNTHESIS IN EUGLENA GRACILIS (EUGLENOPHYCEAE) OCCURS THROUGH AN ENZYME COMPLEX1
inferredcites →https://doi.org/10.1111/j.1574-6941.2008.00599.xopenalex-snapshot
Use of 13C labeling to assess carbon partitioning in transgenic and nontransgenic (parental) rice and their rhizosphere soil microbial communities
inferredcites →https://doi.org/10.1111/j.1742-4658.2007.05658.xopenalex-snapshot
Biochemical characterization of rice trehalose‐6‐phosphate phosphatases supports distinctive functions of these plant enzymes
inferredcites →https://doi.org/10.1111/j.1753-4887.1981.tb06752.xopenalex-snapshot
Proceedings of the National Academy of Sciences of the United States of America
inferredcites →https://doi.org/10.1111/jipb.12925openalex-snapshot
Trehalose‐6‐phosphate phosphatase E modulates ABA‐controlled root growth and stomatal movement in Arabidopsis
inferredcites →https://doi.org/10.1111/jipb.13054openalex-snapshot
Contribution of phenylpropanoid metabolism to plant development and plant–environment interactions
inferredcites →https://doi.org/10.1111/ppl.13247openalex-snapshot
Exogenous abscisic acid and jasmonic acid restrain polyethylene glycol‐induced drought by improving the growth and antioxidative enzyme activities in pearl millet
inferredcites →https://doi.org/10.1111/tpj.12534openalex-snapshot
Abscisic acid inhibits root growth in Arabidopsis through ethylene biosynthesis
inferredcites →https://doi.org/10.1111/tpj.13114openalex-snapshot
Trehalose 6–phosphate coordinates organic and amino acid metabolism with carbon availability
inferredcites →https://doi.org/10.1111/tpj.14477openalex-snapshot
Melatonin enhances cotton immunity to Verticillium wilt via manipulating lignin and gossypol biosynthesis
inferredcites →https://doi.org/10.1111/tpj.14988openalex-snapshot
Gene co‐expression analysis reveals transcriptome divergence between wild and cultivated chickpea under drought stress
inferredcites →https://doi.org/10.1126/science.aaz7614openalex-snapshot
The physiology of plant responses to drought
inferredcites →https://doi.org/10.1177/000271621204000113openalex-snapshot
The United States Department of Agriculture
inferredcites →https://doi.org/10.1186/s12870-017-1018-2openalex-snapshot
The role of Tre6P and SnRK1 in maize early kernel development and events leading to stress-induced kernel abortion
inferredcites →https://doi.org/10.1186/s12870-019-1941-5openalex-snapshot
Effects of maize organ-specific drought stress response on yields from transcriptome analysis
inferredcites →https://doi.org/10.1371/journal.pgen.1004664openalex-snapshot
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inferredcites →https://doi.org/10.2134/agronj1959.00021962005100090002xopenalex-snapshot
A Correlation and Path‐Coefficient Analysis of Components of Crested Wheatgrass Seed Production 1
inferredcites →https://doi.org/10.2135/cropsci1985.0011183x0025000500010xopenalex-snapshot
Carbohydrate Reserves and Reproductive Development at Low Leaf Water Potentials in Maize1
inferredcites →https://doi.org/10.2135/cropsci2007.04.0010ipbsopenalex-snapshot
Physiological Basis of Successful Breeding Strategies for Maize Grain Yield
inferredcites →https://doi.org/10.2135/cropsci2009.09.0521openalex-snapshot
Rapid Analysis of Nonstructural Carbohydrate Components in Grass Forage Using Microplate Enzymatic Assays
inferredcites →https://doi.org/10.3389/fpls.2015.01010openalex-snapshot
Elevated CO2 Reduced Floret Death in Wheat Under Warmer Average Temperatures and Terminal Drought
inferredcites →https://doi.org/10.3389/fpls.2016.01886openalex-snapshot
Transcriptomic and Metabolomic Studies Disclose Key Metabolism Pathways Contributing to Well-maintained Photosynthesis under the Drought and the Consequent Drought-Tolerance in Rice
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Recent Advances for Drought Stress Tolerance in Maize (Zea mays L.): Present Status and Future Prospects

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.2139/ssrn.4659304openalex-extracted
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inferred← citeshttps://doi.org/10.1007/s00271-023-00911-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00299-025-03494-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00425-024-04517-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.eja.2024.127421openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105482openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105900openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fcr.2024.109529openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2025.1693576openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/agronomy15092189openalex-snapshot
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