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Differences in Cowpea Root Growth Triggered by Salinity and Dehydration are Associated with Oxidative Modulation Involving Types I and III Peroxidases and Apoplastic Ascorbate

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

inferredcites →https://doi.org/10.1006/abio.1976.9999openalex-snapshot
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/bf00018060openalex-snapshot
Rapid determination of free proline for water-stress studies
inferredcites →https://doi.org/10.1007/s00425-005-0153-4openalex-snapshot
Two cell wall associated peroxidases from Arabidopsis influence root elongation
inferredcites →https://doi.org/10.1007/s10535-010-0026-yopenalex-snapshot
Antioxidative enzymatic protection in leaves of two contrasting cowpea cultivars under salinity
inferredcites →https://doi.org/10.1007/s10725-006-9000-2openalex-snapshot
A simple colorimetric method for determination of hydrogen peroxide in plant tissues
inferredcites →https://doi.org/10.1016/0031-9422(82)80073-3openalex-snapshot
Quantification of hydrogen peroxide in plant extracts by the chemiluminescence reaction with luminol
inferredcites →https://doi.org/10.1016/b978-0-12-461011-8.50001-9openalex-snapshot
Methods in Plant Biochemistry
inferredcites →https://doi.org/10.1016/b978-0-12-461020-0.50001-9openalex-snapshot
Methods in Plant Biochemistry
inferredcites →https://doi.org/10.1016/j.copbio.2010.03.002openalex-snapshot
More from less: plant growth under limited water
inferredcites →https://doi.org/10.1016/j.envexpbot.2008.12.015openalex-snapshot
Roots and leaves display contrasting osmotic adjustment mechanisms in response to NaCl-salinity in Atriplex nummularia
inferredcites →https://doi.org/10.1016/j.jplph.2006.03.004openalex-snapshot
Roots and leaves display contrasting oxidative response during salt stress and recovery in cowpea
inferredcites →https://doi.org/10.1016/j.jplph.2010.03.005openalex-snapshot
Photosynthetic changes and protective mechanisms against oxidative damage subjected to isolated and combined drought and heat stresses in Jatropha curcas plants
inferredcites →https://doi.org/10.1016/j.jplph.2011.08.001openalex-snapshot
Exogenous ornithine is an effective precursor and the δ-ornithine amino transferase pathway contributes to proline accumulation under high N recycling in salt-stressed cashew leaves
inferredcites →https://doi.org/10.1016/j.plaphy.2010.10.006openalex-snapshot
Differential occurrence of oxidative burst and antioxidative mechanism in compatible and incompatible interactions of Solanum lycopersicum and Ralstonia solanacearum
inferredcites →https://doi.org/10.1016/j.tplants.2004.09.002openalex-snapshot
Performing the paradoxical: how plant peroxidases modify the cell wall
inferredcites →https://doi.org/10.1016/j.tplants.2005.11.002openalex-snapshot
Abiotic stress, the field environment and stress combination
inferredcites →https://doi.org/10.1016/s1360-1385(02)02312-9openalex-snapshot
Oxidative stress, antioxidants and stress tolerance
inferredcites →https://doi.org/10.1017/cbo9780511661587.006openalex-snapshot
Regulation of growth and development of plants growing with a restricted supply of water
inferredcites →https://doi.org/10.1034/j.1399-3054.1992.850216.xopenalex-snapshot
Ascorbate peroxidase - a hydrogen peroxide-scavenging enzyme in plants
inferredcites →https://doi.org/10.1034/j.1399-3054.1997.1010419.xopenalex-snapshot
Changes in ascorbic acid levels in apoplastic fluid during growth of pine hypocotyls. Effect on peroxidase activities associated with cell walls
inferredcites →https://doi.org/10.1038/nature01485openalex-snapshot
Reactive oxygen species produced by NADPH oxidase regulate plant cell growth
inferredcites →https://doi.org/10.1046/j.0016-8025.2001.00808.xopenalex-snapshot
Comparative physiology of salt and water stress
inferredcites →https://doi.org/10.1093/jexbot/51.350.1543openalex-snapshot
Adaptation of roots to low water potentials by changes in cell wall extensibility and cell wall proteins
inferredcites →https://doi.org/10.1093/jexbot/53.372.1305openalex-snapshot
Regulation and function of ascorbate peroxidase isoenzymes
inferredcites →https://doi.org/10.1093/jxb/48.12.2075openalex-snapshot
Can cell wall peroxidase activity explain the leaf growth response ofLolium temulentumL. during drought?
inferredcites →https://doi.org/10.1093/jxb/erh276openalex-snapshot
Root growth maintenance during water deficits: physiology to functional genomics
inferredcites →https://doi.org/10.1093/jxb/ern278openalex-snapshot
The role of xylem class III peroxidases in lignification
inferredcites →https://doi.org/10.1093/jxb/ern318openalex-snapshot
Specific functions of individual class III peroxidase genes
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078591openalex-snapshot
The Association of Ascorbate and Ascorbate Oxidase in the Apoplast with IAA-Enhanced Elongation of Epicotyls from Vigna angularis
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/10.1093/oxfordjournals.pcp.a078634openalex-snapshot
Effects of Ascorbate on the Oxidation of Derivatives of Hydroxycinnamic Acid and the Mechanism of Oxidation of Sinapic Acid by Cell Wall-Bound Peroxidases
inferredcites →https://doi.org/10.1104/pp.103.033431openalex-snapshot
When Defense Pathways Collide. The Response of Arabidopsis to a Combination of Drought and Heat Stress
inferredcites →https://doi.org/10.1104/pp.104.044784openalex-snapshot
Production of Reactive Oxygen Intermediates (O2 ˙ −, H2O2, and ˙ OH) by Maize Roots and Their Role in Wall Loosening and Elongation Growth
inferredcites →https://doi.org/10.1104/pp.107.3.725openalex-snapshot
Effects of Iron Excess on Nicotiana plumbaginifolia Plants (Implications to Oxidative Stress)
inferredcites →https://doi.org/10.1104/pp.43.5.730openalex-snapshot
Pyruvate Kinase Activity of Wheat Plants Grown under Potassium Deficient Conditions
inferredcites →https://doi.org/10.1105/tpc.105.033589openalex-snapshot
Redox Homeostasis and Antioxidant Signaling: A Metabolic Interface between Stress Perception and Physiological Responses
inferredcites →https://doi.org/10.1105/tpc.111.093039openalex-snapshot
The Apoplastic Oxidative Burst Peroxidase in Arabidopsis Is a Major Component of Pattern-Triggered Immunity
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.02041.xopenalex-snapshot
Reactive oxygen species homeostasis and signalling during drought and salinity stresses
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.02064.xopenalex-snapshot
Complexity and coordination of root growth at low water potentials: recent advances from transcriptomic and proteomic analyses
inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02366.xopenalex-snapshot
Role of peroxidases in the compensation of cytosolic ascorbate peroxidase knockdown in rice plants under abiotic stress
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02837.xopenalex-snapshot
Peroxidase‐dependent apoplastic oxidative burst in Arabidopsis required for pathogen resistance
inferredcites →https://doi.org/10.1111/j.1399-3054.1991.tb00121.xopenalex-snapshot
Effect of aluminium on lipid peroxidation, superoxide dismutase, catalase, and peroxidase activities in root tips of soybean (Glycine max)
inferredcites →https://doi.org/10.1111/j.1399-3054.2010.01427.xopenalex-snapshot
The overexpression of AtPrx37, an apoplastic peroxidase, reduces growth in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1439-037x.2010.00432.xopenalex-snapshot
Root Growth Inhibition and Lignification Induced by Salt Stress in Soybean
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01139.xopenalex-snapshot
Superoxide dismutase, catalase and peroxidase activities do not confer protection against oxidative damage in salt‐stressed cowpea leaves
inferredcites →https://doi.org/10.1126/science.148.3668.339openalex-snapshot
Sap Pressure in Vascular Plants
inferredcites →https://doi.org/10.1146/annurev-arplant-042811-105501openalex-snapshot
Control of Arabidopsis Root Development
inferredcites →https://doi.org/10.1146/annurev.arplant.53.091401.143329openalex-snapshot
S ALT AND D ROUGHT S TRESS S IGNAL T RANSDUCTION IN P LANTS
inferredcites →https://doi.org/10.1161/01.atv.0000145574.90840.7dopenalex-snapshot
Reactive Oxygen Species
inferredcites →https://doi.org/10.1590/s0102-33062012000200010openalex-snapshot
Atividade de enzimas antioxidantes e inibição do crescimento radicular de feijão caupi sob diferentes níveis de salinidade
inferredcites →https://doi.org/10.1590/s1677-04202010000200005openalex-snapshot
Salt-induced changes in antioxidative enzyme activities in root tissues do not account for the differential salt tolerance of two cowpea cultivars
inferredcites →https://doi.org/10.2134/agronj1980.00021962007200030007xopenalex-snapshot
Drought Adaptation of Cowpea. IV. Influence of Drought on Water Use, and Relations with Growth and Seed Yield1
inferredcites →https://doi.org/10.2134/agronj1980.00021962007200030008xopenalex-snapshot
Interaction of Planting Date and Fall Fertilization on Winter Barley Performance1
inferredcites →https://doi.org/10.5424/sjar/2003013-36openalex-snapshot
N-compound accumulation and carbohydrate shortage on N2 fixation in drought-stressed and rewatered cowpea plants
inferredcites →https://doi.org/10.5860/choice.31-3785openalex-snapshot
Water deficits: plant responses from cell to community

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/10.1016/b978-0-12-817892-8.00004-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.agron.2017.11.002openalex-snapshot
Rice in Saline Soils: Physiology, Biochemistry, Genetics, and Management
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2016.07.002openalex-snapshot
Salinity and osmotic stress trigger different antioxidant responses related to cytosolic ascorbate peroxidase knockdown in rice roots
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2019.02.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mcu130openalex-snapshot
Salinity stress constrains photosynthesis in Fraxinus ornus more when growing in partial shading than in full sunlight: consequences for the antioxidant defence system
inferred← citeshttps://doi.org/10.1093/plcell/koae055openalex-snapshot
Not so hidden anymore: Advances and challenges in understanding root growth under water deficits
inferred← citeshttps://doi.org/10.1104/pp.19.00921openalex-snapshot
The MicroRNA397b -LACCASE2 Module Regulates Root Lignification under Water and Phosphate Deficiency
inferred← citeshttps://doi.org/10.1111/pbi.13378openalex-snapshot
Root‐specific expression of chickpea cytokinin oxidase/dehydrogenase 6 leads to enhanced root growth, drought tolerance and yield without compromising nodulation
inferred← citeshttps://doi.org/10.1111/plb.12443openalex-snapshot
Root growth restraint can be an acclimatory response to low pH and is associated with reduced cell mortality: a possible role of class III peroxidases and NADPH oxidases
inferred← citeshttps://doi.org/10.1111/plb.13017openalex-snapshot
Salt stress differentially regulates mobilisation of carbon and nitrogen reserves during seedling establishment of Pityrocarpa moniliformis
inferred← citeshttps://doi.org/10.1134/s1021443720020156openalex-snapshot
Ascorbate in the Apoplast: Metabolism and Functions
inferred← citeshttps://doi.org/10.1155/2019/4262013openalex-snapshot
Comparative Water Relations of Two Contrasting Date Palm Genotypes under Salinity
inferred← citeshttps://doi.org/10.12661/pap.2015.001openalex-snapshot
Regulação do acúmulo de Na+ e resistência à salinidade em (Vigna unguiculata (L.) Walp)
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Effect of Salt Stress on Na Accumulation, Antioxidant Enzyme Activities and Activity of Cell Wall Peroxidase of Huckleberry (Solanum scabrum) and Eggplant (Solanum melongena)
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Nutrient Uptake and Agronomic Efficiencies of Leaf Litter Compost as Nitrogen Source in Vegetable Cowpea (Vigna unguiculata subsp. unguiculata)
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Cell wall remodeling under abiotic stress
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Genetic Architecture of Salt Tolerance in Cowpea (Vigna unguiculata (L.) Walp.) at Seedling Stage Using a Whole Genome Resequencing Approach
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