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Dynamic responses of photosynthesis and the antioxidant system during a drought and rehydration cycle in peanut plants
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jobm.19720120524openalex-snapshot
J. M. Vincent, A Manual for the Practical Study of the Root‐Nodule Bacteria (IBP Handbuch No. 15 des International Biology Program, London). XI u. 164 S., 10 Abb., 17 Tab., 7 Taf. Oxford‐Edinburgh 1970: Blackwell Scientific Publ., 45 s
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A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
inferredcites →https://doi.org/10.1007/978-1-4020-8252-8_105openalex-snapshot
NH4+ Nutrition Affects the Photosynthetic and Respiratory C Sinks in the Dual Symbiosis of a Mycorrhizal Legume
inferredcites →https://doi.org/10.1007/bf02913981openalex-snapshot
Gas exchange and leaf water relations in two peanut cultivars of different drought tolerance
inferredcites →https://doi.org/10.1007/s00122-005-0028-xopenalex-snapshot
A microsatellite-based, gene-rich linkage map for the AA genome of Arachis (Fabaceae)
inferredcites →https://doi.org/10.1007/s00299-007-0406-8openalex-snapshot
Stress-inducible expression of At DREB1A in transgenic peanut (Arachis hypogaea L.) increases transpiration efficiency under water-limiting conditions
inferredcites →https://doi.org/10.1007/s004250000376openalex-snapshot
NADH-stimulated, cyanide-resistant superoxide production in maize coleoptiles analyzed with a tetrazolium-based assay
inferredcites →https://doi.org/10.1007/s10535-012-0296-7openalex-snapshot
Abscisic acid mediates hydrogen peroxide production in peanut induced by water stress
inferredcites →https://doi.org/10.1007/s10725-010-9445-1openalex-snapshot
Drought-induced oxidative damage and antioxidant responses in peanut (Arachis hypogaea L.) seedlings
inferredcites →https://doi.org/10.1007/s11104-008-9613-5openalex-snapshot
Tolerance of common bean to long-term osmotic stress is related to nodule carbon flux and antioxidant defenses: evidence from two cultivars with contrasting tolerance
inferredcites →https://doi.org/10.1016/0005-2795(73)90198-0openalex-snapshot
Isozymes of superoxide dismutase from wheat germ
inferredcites →https://doi.org/10.1016/0306-3623(91)90478-oopenalex-snapshot
Free radicals in biology and medicine
inferredcites →https://doi.org/10.1016/j.copbio.2011.11.003openalex-snapshot
Drought tolerance through biotechnology: improving translation from the laboratory to farmers’ fields
inferredcites →https://doi.org/10.1016/j.jplph.2007.08.005openalex-snapshot
The application of ascorbate or its immediate precursor, galactono-1,4-lactone, does not affect the response of nitrogen-fixing pea nodules to water stress
inferredcites →https://doi.org/10.1016/j.plantsci.2005.05.020openalex-snapshot
Microarray-based screening of differentially expressed genes in peanut in response to Aspergillus parasiticus infection and drought stress
inferredcites →https://doi.org/10.1016/j.plaphy.2006.10.024openalex-snapshot
Differential responses of antioxidative system to chilling and drought in four rice cultivars differing in sensitivity
inferredcites →https://doi.org/10.1016/j.plaphy.2008.10.006openalex-snapshot
Abscisic acid improves drought tolerance of triploid bermudagrass and involves H2O2- and NO-induced antioxidant enzyme activities
inferredcites →https://doi.org/10.1016/j.plaphy.2010.08.016openalex-snapshot
Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants
inferredcites →https://doi.org/10.1016/j.soilbio.2007.11.014openalex-snapshot
The role of arbuscular mycorrhizal colonization in the carbon and nutrient economy of the tripartite symbiosis with nodulated Phaseolus vulgaris
inferredcites →https://doi.org/10.1016/j.soilbio.2009.07.021openalex-snapshot
Arbuscular mycorrhizae affect the N and C economy of nodulated Phaseolus vulgaris (L.) during NH4+ nutrition
inferredcites →https://doi.org/10.1016/s0021-9258(19)42083-8openalex-snapshot
Glutathione S-Transferases
inferredcites →https://doi.org/10.1016/s0076-6879(84)05015-1openalex-snapshot
[12] Assays of glutathione peroxidase
inferredcites →https://doi.org/10.1016/s0076-6879(85)13073-9openalex-snapshot
[70] Determination of glutathione and glutathione disulfide in biological samples
inferredcites →https://doi.org/10.1016/s0378-1127(02)00282-7openalex-snapshot
Effects of understory vegetation on the ecophysiological characteristics of an overstory pine, Pinus densiflora
inferredcites →https://doi.org/10.1016/s0378-4290(01)00137-xopenalex-snapshot
Physiological responses of argentine peanut varieties to water stress.
inferredcites →https://doi.org/10.1016/s1369-5266(00)80054-0openalex-snapshot
Australian journal of plant physiology
inferredcites →https://doi.org/10.1042/bj2100899openalex-snapshot
Glutathione and ascorbic acid in spinach ( Spinacia oleracea ) chloroplasts. The effect of hydrogen peroxide and of Paraquat
inferredcites →https://doi.org/10.1071/pp01061openalex-snapshot
Antioxidant system response of different wheat cultivars under drought: field and in vitro studies
inferredcites →https://doi.org/10.1073/pnas.52.1.119openalex-snapshot
HYDROSTATIC PRESSURE AND OSMOTIC POTENTIAL IN LEAVES OF MANGROVES AND SOME OTHER PLANTS
inferredcites →https://doi.org/10.1073/pnas.83.11.3811openalex-snapshot
Enzymatic reactions of ascorbate and glutathione that prevent peroxide damage in soybean root nodules
inferredcites →https://doi.org/10.1080/07352689409701914openalex-snapshot
Superoxide Dismutase in Plants
inferredcites →https://doi.org/10.1089/ars.2008.2177openalex-snapshot
Redox Regulation in Photosynthetic Organisms: Signaling, Acclimation, and Practical Implications
inferredcites →https://doi.org/10.1093/jxb/erf090openalex-snapshot
Water stress-induced abscisic acid accumulation triggers the increased generation of reactive oxygen species and up-regulates the activities of antioxidant enzymes in maize leaves
inferredcites →https://doi.org/10.1093/jxb/eri039openalex-snapshot
Drought controls on H2O2 accumulation, catalase (CAT) activity and CAT gene expression in wheat
inferredcites →https://doi.org/10.1093/jxb/eri319openalex-snapshot
Nitric oxide is involved in abscisic acid-induced antioxidant activities in Stylosanthes guianensis
inferredcites →https://doi.org/10.1093/jxb/erv089openalex-snapshot
Interplay between reactive oxygen species and hormones in the control of plant development and stress tolerance
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a077268openalex-snapshot
Purification of Ascorbate Peroxidase in Spinach Chloroplasts; Its Inactivation in Ascorbate-Depleted Medium and Reactivation by Monodehydroascorbate Radical
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078621openalex-snapshot
Separate Assays Specific for Ascorbate Peroxidase and Guaiacol Peroxidase and for the Chloroplastic and Cytosolic Isozymes of Ascorbate Peroxidase in Plants
inferredcites →https://doi.org/10.1104/pp.109.2.421openalex-snapshot
Amelioration of Ozone-Induced Oxidative Damage in Wheat Plants Grown under High Carbon Dioxide (Role of Antioxidant Enzymes)
inferredcites →https://doi.org/10.1104/pp.113.233478openalex-snapshot
The Roles of Reactive Oxygen Metabolism in Drought: Not So Cut and Dried
inferredcites →https://doi.org/10.1104/pp.116.1.173openalex-snapshot
Oxidative Damage in Pea Plants Exposed to Water Deficit or Paraquat1
inferredcites →https://doi.org/10.1104/pp.59.5.1011openalex-snapshot
Chloroplast Glutathione Reductase
inferredcites →https://doi.org/10.1105/tpc.114.133090openalex-snapshot
The Roles of ROS and ABA in Systemic Acquired Acclimation
inferredcites →https://doi.org/10.1111/j.1365-313x.1994.00397.xopenalex-snapshot
Regulation of pea cytosolic ascorbate peroxidase and other antioxidant enzymes during the progression of drought stress and following recovery from drought
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02615.xopenalex-snapshot
ABA‐induced NO generation and stomatal closure in Arabidopsis are dependent on H 2 O 2 synthesis
inferredcites →https://doi.org/10.1111/j.1439-0523.2008.01593.xopenalex-snapshot
Over‐expression of a Populus peroxisomal ascorbate peroxidase (PpAPX) gene in tobacco plants enhances stress tolerance
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02071.xopenalex-snapshot
Nitric oxide induced by hydrogen peroxide mediates abscisic acid‐induced activation of the mitogen‐activated protein kinase cascade involved in antioxidant defense in maize leaves
inferredcites →https://doi.org/10.1111/pce.12621openalex-snapshot
Stress‐triggered redox signalling: what's in pROSpect?
inferredcites →https://doi.org/10.1126/science.83.2156.397openalex-snapshot
Glutathione and Ascorbic Acid
inferredcites →https://doi.org/10.1155/2009/848516openalex-snapshot
Heme Oxygenase Contributes to Alleviate Salinity Damage inGlycine maxL. Leaves
inferredcites →https://doi.org/10.1186/s12870-014-0208-4openalex-snapshot
Increased expression of native cytosolic Cu/Zn superoxide dismutase and ascorbate peroxidase improves tolerance to oxidative and chilling stresses in cassava (Manihot esculenta Crantz)
inferredcites →https://doi.org/10.2135/cropsci2005.0346openalex-snapshot
Generation of Expressed Sequence Tags (ESTs) for Gene Discovery and Marker Development in Cultivated Peanut
inferredcites →https://doi.org/10.2135/cropsci2006.06.0407openalex-snapshot
Molecular Characterization of the U.S. Peanut Mini Core Collection Using Microsatellite Markers
inferredcites →https://doi.org/10.3146/i0095-3679-28-2-7openalex-snapshot
History of Arachis Including Evidence of A. hypogaea L. Progenitors
inferredcites →https://doi.org/10.3146/i0095-3679-9-1-11openalex-snapshot
Growth Stages of Peanut (Arachis hypogaea L.)1
inferredcites →https://doi.org/10.4161/psb.3.3.5536openalex-snapshot
Drought stress and reactive oxygen species
inferredcites →https://doi.org/10.4236/ajps.2011.25084openalex-snapshot
Effect of Water Stress and Foliar Boron Application on Seed Protein, Oil, Fatty Acids, and Nitrogen Metabolism in Soybean
inferredcites →https://doi.org/10.5402/2012/318083openalex-snapshot
Physiological and Biochemical Responses to Drought Stress and Subsequent Rehydration in the Symbiotic Association Peanut-Bradyrhizobium sp.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Cultivating Resilience: Use of Water Deficit to Prime Peanut Production and Improve Water Stress Tolerance
inferred← citeshttps://doi.org/10.2139/ssrn.4872007openalex-extracted
Cultivating Resilience: Use of Water Deficit to Prime Peanut Production and Improve Water Stress Tolerance
inferred← citeshttps://doi.org/10.1007/978-3-030-17597-9_17openalex-snapshot
Combined Application of Microbial and Non-Microbial Biostimulants to Improve Growth of Peanut Plants Exposed to Abiotic Stresses
inferred← citeshttps://doi.org/10.1007/978-3-319-66682-2_17openalex-snapshot
Importance of Glutathione in the Legume-Rhizobia Symbiosis
inferred← citeshttps://doi.org/10.1007/s11676-022-01558-2openalex-snapshot
Distinct physiological mechanisms underpin growth and rehydration of Hymenaea courbaril and Hymenaea stigonocarpa upon short-term exposure to drought stress
inferred← citeshttps://doi.org/10.1007/s11676-026-02050-xopenalex-snapshot
Plant midday depression: daily inefficiencies in photosynthesis induced by climate change
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Shade pretreatment enhanced drought resistance of soybean
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e41482openalex-snapshot
Spermidine-induced improvements in water relations and antioxidant defense enhance drought tolerance in yarrow (Achillea millefolium L.)
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2018.10.021openalex-snapshot
Regulation of ROS through proficient modulations of antioxidative defense system maintains the structural and functional integrity of photosynthetic apparatus and confers drought tolerance in the facultative halophyte Salvadora persica L.
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.11.008openalex-snapshot
Increased soybean tolerance to water deficiency through biostimulant based on fulvic acids and Ascophyllum nodosum (L.) seaweed extract
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.107841openalex-snapshot
Responses of Trollius chinensis to drought stress and rehydration: From photosynthetic physiology to gene expression
inferred← citeshttps://doi.org/10.1016/j.sajb.2021.09.025openalex-snapshot
Variability in drought stress-induced physiological, biochemical responses and expression of DREB2A, NAC4 and HSP70 genes in groundnut (Arachis hypogaea L.)
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100637openalex-snapshot
Cultivating resilience: Use of water deficit to prime peanut production and improve water stress tolerance
inferred← citeshttps://doi.org/10.1038/s41598-021-85072-1openalex-snapshot
Physiological changes and transcriptome profiling in Saccharum spontaneum L. leaf under water stress and re-watering conditions
inferred← citeshttps://doi.org/10.1071/fp16263openalex-snapshot
Assessing the suitability of various screening methods as a proxy for drought tolerance in barley
inferred← citeshttps://doi.org/10.1111/pce.15080openalex-snapshot
Rewatering after drought: Unravelling the drought thresholds and function recovery‐limiting factors in maize leaves
inferred← citeshttps://doi.org/10.1111/plb.13740openalex-snapshot
Modulatory responses of physiological and biochemical status are related to drought tolerance levels in peanut cultivars
inferred← citeshttps://doi.org/10.1186/s12870-020-02785-7openalex-snapshot
Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.1371/journal.pone.0304831openalex-snapshot
Mitigation of salinity stress in yarrow (Achillea millefolium L.) plants through spermidine application
inferred← citeshttps://doi.org/10.1590/1519-6984.175284openalex-snapshot
Responses of antioxidant enzymes, photosynthetic pigments and carbohydrates in micropropagated Pitcairnia encholirioides L.B. Sm. (Bromeliaceae) under ex vitro water deficit and after rehydration
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1612341openalex-snapshot
Effects of pathogen infection and Rhizobium inoculation on instantaneous and long-term water use efficiency of peanut with and without drought
inferred← citeshttps://doi.org/10.3389/fpls.2022.823846openalex-snapshot
Rehydration Compensation of Winter Wheat Is Mediated by Hormone Metabolism and De-Peroxidative Activities Under Field Conditions
inferred← citeshttps://doi.org/10.3390/f12121705openalex-snapshot
Transcriptomic Analysis Reveals Regulatory Networks for Osmotic Water Stress and Rewatering Response in the Leaves of Ginkgo biloba
inferred← citeshttps://doi.org/10.3390/plants11020175openalex-snapshot
Antioxidant Defense during Recovery of Resurrection Plant Haberlea rhodopensis from Drought- and Freezing-Induced Desiccation
inferred← citeshttps://doi.org/10.3390/plants13202920openalex-snapshot
The Impact of Short-Term Drought on the Photosynthetic Characteristics and Yield of Peanuts Grown in Saline Alkali Soil
inferred← citeshttps://doi.org/10.3390/plants14111636openalex-snapshot
Physiological and Biochemical Adaptations to Repeated Drought–Rehydration Cycles in Ochroma lagopus Swartz: Implications for Growth and Stress Resilience
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515604openalex-snapshot
Additional file 1 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515607openalex-snapshot
Additional file 2 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515610openalex-snapshot
Additional file 3 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515613openalex-snapshot
Additional file 4 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515616openalex-snapshot
Additional file 5 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515619openalex-snapshot
Additional file 6 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515622openalex-snapshot
Additional file 7 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
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