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Nitrogen metabolism in plants under low oxygen stress

https://doi.org/10.1007/s00425-013-2015-9
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What this work says

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

inferredcites →https://doi.org/10.1007/s00360-011-0629-4openalex-snapshot
An enzymatic bridge between carbohydrate and amino acid metabolism: regulation of glutamate dehydrogenase by reversible phosphorylation in a severe hypoxia-tolerant crayfish
inferredcites →https://doi.org/10.1007/s00425-003-1192-3openalex-snapshot
NADH-dependent metabolism of nitric oxide in alfalfa root cultures expressing barley hemoglobin
inferredcites →https://doi.org/10.1007/s00425-007-0496-0openalex-snapshot
Nitrite-driven anaerobic ATP synthesis in barley and rice root mitochondria
inferredcites →https://doi.org/10.1007/s004250050094openalex-snapshot
Nitrate reductase activation state in barley roots in relation to the energy and carbohydrate status
inferredcites →https://doi.org/10.1007/s00726-012-1399-3openalex-snapshot
Effect of oxygen deficiency on nitrogen assimilation and amino acid metabolism of soybean root segments
inferredcites →https://doi.org/10.1007/s11103-004-0650-zopenalex-snapshot
The root-specific glutamate decarboxylase (GAD1) is essential for sustaining GABA levels in Arabidopsis
inferredcites →https://doi.org/10.1007/s11738-010-0503-0openalex-snapshot
Involvement of nitrate reduction in the tolerance of tomato (Solanum lycopersicum L.) plants to prolonged root hypoxia
inferredcites →https://doi.org/10.1016/j.bbabio.2008.06.002openalex-snapshot
Nitrite–nitric oxide control of mitochondrial respiration at the frontier of anoxia
inferredcites →https://doi.org/10.1016/j.jplph.2003.11.003openalex-snapshot
Nitrate uptake and nitrite release by tomato roots in response to anoxia
inferredcites →https://doi.org/10.1016/j.mito.2011.03.005openalex-snapshot
The anoxic plant mitochondrion as a nitrite: NO reductase
inferredcites →https://doi.org/10.1016/j.plaphy.2012.08.005openalex-snapshot
Brassica juncea nitric oxide synthase like activity is stimulated by PKC activators and calcium suggesting modulation by PKC-like kinase
inferredcites →https://doi.org/10.1016/j.plaphy.2013.02.015openalex-snapshot
Nitrogen metabolism and translocation in soybean plants subjected to root oxygen deficiency
inferredcites →https://doi.org/10.1016/j.tplants.2011.12.004openalex-snapshot
Making sense of low oxygen sensing
inferredcites →https://doi.org/10.1016/s1360-1385(99)01393-xopenalex-snapshot
An alternative pathway for nitric oxide production in plants: new features of an old enzyme
inferredcites →https://doi.org/10.1023/a:1024563507275openalex-snapshot
The role of nitrate reduction in the anoxic metabolism of roots I. Characterization of root morphology and normoxic metabolism of wild type tobacco and a transformant lacking root nitrate reductase
inferredcites →https://doi.org/10.1038/nature04027openalex-snapshot
The N-end rule pathway as a nitric oxide sensor controlling the levels of multiple regulators
inferredcites →https://doi.org/10.1038/nature04920openalex-snapshot
Sub1A is an ethylene-response-factor-like gene that confers submergence tolerance to rice
inferredcites →https://doi.org/10.1038/nature06069openalex-snapshot
A central integrator of transcription networks in plant stress and energy signalling
inferredcites →https://doi.org/10.1038/nature08258openalex-snapshot
The ethylene response factors SNORKEL1 and SNORKEL2 allow rice to adapt to deep water
inferredcites →https://doi.org/10.1038/nature10534openalex-snapshot
Homeostatic response to hypoxia is regulated by the N-end rule pathway in plants
inferredcites →https://doi.org/10.1038/nature10536openalex-snapshot
Oxygen sensing in plants is mediated by an N-end rule pathway for protein destabilization
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01846.xopenalex-snapshot
Expression of a stress‐induced hemoglobin affects NO levels produced by alfalfa root cultures under hypoxic stress
inferredcites →https://doi.org/10.1071/fp08029openalex-snapshot
Putrescine enhancement of tolerance to root-zone hypoxia in Cucumis sativus: a role for increased nitrate reduction
inferredcites →https://doi.org/10.1071/pp98096openalex-snapshot
Review: Mechanisms of anoxia tolerance in plants. II. Energy requirements for maintenance and energy distribution to essential processes
inferredcites →https://doi.org/10.1073/pnas.0906131106openalex-snapshot
Profiling translatomes of discrete cell populations resolves altered cellular priorities during hypoxia in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1434381100openalex-snapshot
Nitric oxide regulates K + and Cl - channels in guard cells through a subset of abscisic acid-evoked signaling pathways
inferredcites →https://doi.org/10.1073/pnas.93.10.4718openalex-snapshot
Arabidopsis mutant analysis and gene regulation define a nonredundant role for glutamate dehydrogenase in nitrogen assimilation.
inferredcites →https://doi.org/10.1093/aob/mcf115openalex-snapshot
Plant Haemoglobins, Nitric Oxide and Hypoxic Stress
inferredcites →https://doi.org/10.1093/aob/mcl193openalex-snapshot
Apoplastic pH During Low-oxygen Stress in Barley
inferredcites →https://doi.org/10.1093/aob/mcn100openalex-snapshot
Plant mitochondrial function during anaerobiosis
inferredcites →https://doi.org/10.1093/aob/mcn126openalex-snapshot
Transcript and metabolite profiling of the adaptive response to mild decreases in oxygen concentration in the roots of arabidopsis plants
inferredcites →https://doi.org/10.1093/jexbot/53.366.103openalex-snapshot
Regulation of nitric oxide (NO) production by plant nitrate reductase in vivo and in vitro
inferredcites →https://doi.org/10.1093/jexbot/53.370.875openalex-snapshot
Modulation of nitrate reductase: some new insights, an unusual case and a potentially important side reaction
inferredcites →https://doi.org/10.1093/jxb/erh258openalex-snapshot
Nitrate reductase regulation in tomato roots by exogenous nitrate: a possible role in tolerance to long-term root anoxia
inferredcites →https://doi.org/10.1093/jxb/erh272openalex-snapshot
Nitrate, NO and haemoglobin in plant adaptation to hypoxia: an alternative to classic fermentation pathways
inferredcites →https://doi.org/10.1093/jxb/erl069openalex-snapshot
Characterization of alanine aminotransferase (AlaAT) multigene family and hypoxic response in young seedlings of the model legume Medicago truncatula
inferredcites →https://doi.org/10.1093/jxb/ern102openalex-snapshot
Concerted modulation of alanine and glutamate metabolism in young Medicago truncatula seedlings under hypoxic stress
inferredcites →https://doi.org/10.1093/jxb/ers161openalex-snapshot
Nitric oxide-activated calcium/calmodulin-dependent protein kinase regulates the abscisic acid-induced antioxidant defence in maize
inferredcites →https://doi.org/10.1093/jxb/ers210openalex-snapshot
Haemoglobin modulates NO emission and hyponasty under hypoxia-related stress in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/mp/ssm016openalex-snapshot
Nitric Oxide in Plants: Production and Cross-talk with Ca2+ Signaling
inferredcites →https://doi.org/10.1093/pcp/pcf034openalex-snapshot
Nitric Oxide Production Mediated by Nitrate Reductase in the Green Alga Chlamydomonas reinhardtii: an Alternative NO Production Pathway in Photosynthetic Organisms
inferredcites →https://doi.org/10.1104/pp.102.016907openalex-snapshot
The Pyruvate decarboxylase1 Gene of Arabidopsis Is Required during Anoxia But Not Other Environmental Stresses
inferredcites →https://doi.org/10.1104/pp.103.022244openalex-snapshot
Enhanced Low Oxygen Survival in Arabidopsis through Increased Metabolic Flux in the Fermentative Pathway
inferredcites →https://doi.org/10.1104/pp.104.038968openalex-snapshot
Analysis of Nitric Oxide Signaling Functions in Tobacco Cells Challenged by the Elicitor Cryptogein
inferredcites →https://doi.org/10.1104/pp.104.055475openalex-snapshot
Global Transcription Profiling Reveals Comprehensive Insights into Hypoxic Response in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.057299openalex-snapshot
A Genome-Wide Analysis of the Effects of Sucrose on Gene Expression in Arabidopsis Seedlings under Anoxia
inferredcites →https://doi.org/10.1104/pp.106.088898openalex-snapshot
Nitrite Reduces Cytoplasmic Acidosis under Anoxia
inferredcites →https://doi.org/10.1104/pp.106.093997openalex-snapshot
Transcript Profiling of the Anoxic Rice Coleoptile
inferredcites →https://doi.org/10.1104/pp.106.2.513openalex-snapshot
Ammonium Assimilation and the Role of [gamma]-Aminobutyric Acid in pH Homeostasis in Carrot Cell Suspensions
inferredcites →https://doi.org/10.1104/pp.109.142026openalex-snapshot
Defining Core Metabolic and Transcriptomic Responses to Oxygen Availability in Rice Embryos and Young Seedlings
inferredcites →https://doi.org/10.1104/pp.109.150045openalex-snapshot
Glycolysis and the Tricarboxylic Acid Cycle Are Linked by Alanine Aminotransferase during Hypoxia Induced by Waterlogging of Lotus japonicus
inferredcites →https://doi.org/10.1104/pp.109.151845openalex-snapshot
Cross-Kingdom Comparison of Transcriptomic Adjustments to Low-Oxygen Stress Highlights Conserved and Plant-Specific Responses
inferredcites →https://doi.org/10.1104/pp.110.155077openalex-snapshot
Arabidopsis RAP2.2 : An Ethylene Response Transcription Factor That Is Important for Hypoxia Survival
inferredcites →https://doi.org/10.1104/pp.110.166140openalex-snapshot
Both Plant and Bacterial Nitrate Reductases Contribute to Nitric Oxide Production in Medicago truncatula Nitrogen-Fixing Nodules
inferredcites →https://doi.org/10.1104/pp.111.172486openalex-snapshot
The AP2/ERF Transcription Factor AtERF73/HRE1 Modulates Ethylene Responses during Hypoxia in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.175570openalex-snapshot
Differential Molecular Responses of Rice and Wheat Coleoptiles to Anoxia Reveal Novel Metabolic Adaptations in Amino Acid Metabolism for Tissue Tolerance
inferredcites →https://doi.org/10.1104/pp.125.2.912openalex-snapshot
Origin of the Cytoplasmic pH Changes during Anaerobic Stress in Higher Plant Cells. Carbon-13 and Phosphorous-31 Nuclear Magnetic Resonance Studies
inferredcites →https://doi.org/10.1105/tpc.004747openalex-snapshot
Expression Profile Analysis of the Low-Oxygen Response in Arabidopsis Root Cultures[W]
inferredcites →https://doi.org/10.1105/tpc.111.093880openalex-snapshot
Plant Oxygen Sensing Is Mediated by the N-End Rule Pathway: A Milestone in Plant Anaerobiosis
inferredcites →https://doi.org/10.1111/j.0031-9317.2004.0205.xopenalex-snapshot
Sugar and fructan accumulation during metabolic adjustment between respiration and fermentation under low oxygen conditions in wheat roots
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02335.xopenalex-snapshot
Nitric oxide emission from tobacco leaves and cell suspensions: rate limiting factors and evidence for the involvement of mitochondrial electron transport
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.1365-313x.2010.04149.xopenalex-snapshot
HRE1 and HRE2, two hypoxia-inducible ethylene response factors, affect anaerobic responses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1399-3054.2005.00449.xopenalex-snapshot
Stimulation of alanine amino transferase (AlaAT) gene expression and alanine accumulation in embryo axis of the model legume Medicago truncatula contribute to anoxia stress tolerance
inferredcites →https://doi.org/10.1111/j.1399-3054.2009.01314.xopenalex-snapshot
Anoxic nitric oxide cycling in plants: participating reactions and possible mechanisms
inferredcites →https://doi.org/10.1111/j.1399-3054.2011.01486.xopenalex-snapshot
The hypoxia responsive transcription factor genes ERF71/HRE2 and ERF73/HRE1 of Arabidopsis are differentially regulated by ethylene
inferredcites →https://doi.org/10.1111/j.1438-8677.1999.tb00253.xopenalex-snapshot
Formation of Aerenchyma and the Processes of Plant Ventilation in Relation to Soil Flooding and Submergence
inferredcites →https://doi.org/10.1111/j.1469-8137.1989.tb00677.xopenalex-snapshot
Nitrogen uptake and growth of wheat during O2 deficiency in root media containing NO3− only, or NO3− plus NH4+
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/j.1744-7909.2012.01177.xopenalex-snapshot
Mitochondrial Composition, Function and Stress Response in PlantsF
inferredcites →https://doi.org/10.1111/jipb.12011openalex-snapshot
New Role for an Old Rule: N‐end Rule‐Mediated Degradation of Ethylene Responsive Factor Proteins Governs Low Oxygen Response in PlantsF
inferredcites →https://doi.org/10.1111/ppl.12011openalex-snapshot
Molecular elements of low‐oxygen signaling in plants
inferredcites →https://doi.org/10.1126/scisignal.2000333openalex-snapshot
Coordinated Responses to Oxygen and Sugar Deficiency Allow Rice Seedlings to Tolerate Flooding
inferredcites →https://doi.org/10.1146/annurev.arplant.48.1.223openalex-snapshot
OXYGEN DEFICIENCY AND ROOT METABOLISM: Injury and Acclimation Under Hypoxia and Anoxia
inferredcites →https://doi.org/10.1146/annurev.arplant.56.032604.144224openalex-snapshot
PLANT-SPECIFIC CALMODULIN-BINDING PROTEINS
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092752openalex-snapshot
Flooding Stress: Acclimations and Genetic Diversity
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092830openalex-snapshot
New Insights into Nitric Oxide Signaling in Plants
inferredcites →https://doi.org/10.1146/annurev.pp.36.060185.001045openalex-snapshot
Ethylene and Responses of Plants to Soil Waterlogging and Submergence

What points at this work

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

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Plant response to combined salinity and waterlogging stress: Current research progress and future prospects
inferred← citeshttps://doi.org/10.1002/9781119468677.ch40openalex-snapshot
Compartmentalization of Reactive Oxygen Species and Nitric Oxide Production in Plant Cells
inferred← citeshttps://doi.org/10.1007/978-3-030-78521-5_12openalex-snapshot
Nitric Oxide: A Key Modulator of Plant Responses Under Environmental Stress
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Adaptive Responses of Secale cereale to Temperature Stresses: Role of Cytokinins, Lipoxygenase, and Secondary Metabolites
inferred← citeshttps://doi.org/10.1007/978-3-319-68703-2_10openalex-snapshot
Hypoxic Respiratory Metabolism in Plants: Reorchestration of Nitrogen and Carbon Metabolisms
inferred← citeshttps://doi.org/10.1007/978-981-97-2355-3_6openalex-snapshot
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The role of the NADH-dependent nitrite reductase, Nir, from Escherichia coli in fermentative ammonification
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Fluoride Toxicity Imposes Differential Reprogramming of the Representative Intermediates and Enzymes Belonging to Nitrogen Metabolism in Two indica Rice Varieties, Varying in their Pattern of Fluoride Stress Response
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Distinctive Characteristics of Nitrogen Metabolism in Teosinte Versus Modern Maize for Water-Logging Tolerance
inferred← citeshttps://doi.org/10.1007/s00425-026-05178-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11104-026-08747-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11738-018-2790-9openalex-snapshot
Root flooding-induced changes in the dynamic dissipation of the photosynthetic energy of common bean plants
inferred← citeshttps://doi.org/10.1007/s11738-020-03107-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11756-021-00749-2openalex-snapshot
Genotypic variations in nitrate respiration along with potassium nitrate treatment - accountable for water logging tolerance in maize
inferred← citeshttps://doi.org/10.1007/s40626-020-00186-7openalex-snapshot
Short-term root flooding and recovery conditions—affected photosynthetic process of common bean plants
inferred← citeshttps://doi.org/10.1007/s42729-023-01424-yopenalex-snapshot
Physiological Characteristics, Lint Yield, and Nitrogen Use Efficiency of Cotton Under Different Nitrogen Application Rates and Waterlogging Durations
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Co-contamination of hybrid microplastics and PFOA/GenX alters rhizosphere bacterial–fungal communities and root performance of Eichhornia crassipes
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inferred← citeshttps://doi.org/10.1016/j.plantsci.2017.10.001openalex-snapshot
Expression of phytoglobin affects nitric oxide metabolism and energy state of barley plants exposed to anoxia
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Glutamate dehydrogenase isoenzyme 3 (GDH3) of Arabidopsis thaliana is less thermostable than GDH1 and GDH2 isoenzymes
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inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113469openalex-snapshot
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Carbon allocation to major metabolites in illuminated leaves is not just proportional to photosynthesis when gaseous conditions (CO 2 and O 2 ) vary
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Net photosynthetic CO 2 assimilation: more than just CO 2 and O2 reduction cycles
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Are commercial sweet cherry rootstocks adapted to climate change? Short‐term waterlogging and CO2 effects on sweet cherry cv. ‘Burlat’
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Responses to K deficiency and waterlogging interact via respiratory and nitrogen metabolism
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The Role of Methylation of Glutamate Dehydrogenase Gene Promoters (GDH1 and GDH2) in the Regulation of Their Expression in Corn Leaves under Hypoxia
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The impact of externally supplied protein on root and phytohormone in endangered species cercidiphyllum japonicum cutting seedling
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Oxygen Sensing and Signaling
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Comparative transcriptomic analysis of germinating rice seedlings to individual and combined anaerobic and cold stress
inferred← citeshttps://doi.org/10.1186/s12870-021-03066-7openalex-snapshot
RNA-Seq analysis reveals potential regulators of programmed cell death and leaf remodelling in lace plant (Aponogeton madagascariensis)
inferred← citeshttps://doi.org/10.1371/journal.pone.0147202openalex-snapshot
ALA Pretreatment Improves Waterlogging Tolerance of Fig Plants
inferred← citeshttps://doi.org/10.1371/journal.pone.0181785openalex-snapshot
Nitrogen uptake and assimilation in proliferating embryogenic cultures of Norway spruce—Investigating the specific role of glutamine
inferred← citeshttps://doi.org/10.1371/journal.pone.0213874openalex-snapshot
Effect of nitrogen supply on nitrogen metabolism in the citrus cultivar ‘Huangguogan’
inferred← citeshttps://doi.org/10.1590/1678-992x-2017-0195openalex-snapshot
Nitrogen source influences the antioxidative system of soybean plants under hypoxia and re-oxygenation
inferred← citeshttps://doi.org/10.21203/rs.3.rs-17569/v1openalex-snapshot
Tolerance to Nitrogen ions enrichment in a Gulf of Mexico's freshwater submerged grass
inferred← citeshttps://doi.org/10.2298/gensr2401221sopenalex-snapshot
Biochemical, physiological and molecular aspects of waterlogging tolerance in economically important oilseed crops rapeseed, sesame and soybean
inferred← citeshttps://doi.org/10.2339/politeknik.955013openalex-snapshot
Effects of substrates on the growth of BETA VULGARIS SUBSP. VULGARIS in hydroponic systems
inferred← citeshttps://doi.org/10.24425/jwld.2021.137092openalex-snapshot
Waterlogging tolerance: A review on regulative morpho-physiological homeostasis of crop plants
inferred← citeshttps://doi.org/10.2991/msmee-17.2017.167openalex-snapshot
Effects of externally supplied BSA on ZR, IAA, ABA, GA of plant Cinnamomum camphora cutting seedlings and root
inferred← citeshttps://doi.org/10.3109/07388551.2015.1064856openalex-snapshot
Waterlogging and submergence stress: affects and acclimation
inferred← citeshttps://doi.org/10.31857/s0015330322600425openalex-snapshot
The role of methylation of glutamate dehydrogenase gene promoters (GDH1 and GDH2) in the regulation of their expression in corn leaves under hypoxia
inferred← citeshttps://doi.org/10.3389/fpls.2015.00927openalex-snapshot
Role of ethylene in responses of plants to nitrogen availability
inferred← citeshttps://doi.org/10.3389/fpls.2017.01216openalex-snapshot
Responses of Nitrogen Metabolism, Uptake and Translocation of Maize to Waterlogging at Different Growth Stages
inferred← citeshttps://doi.org/10.3389/fpls.2019.01384openalex-snapshot
Regulation of the Central Carbon Metabolism in Apple Fruit Exposed to Postharvest Low-Oxygen Stress
inferred← citeshttps://doi.org/10.3389/fpls.2020.01313openalex-snapshot
Plant Nitrate Reductases Regulate Nitric Oxide Production and Nitrogen-Fixing Metabolism During the Medicago truncatula–Sinorhizobium meliloti Symbiosis
inferred← citeshttps://doi.org/10.3389/fpls.2020.627331openalex-snapshot
Mechanisms of Waterlogging Tolerance in Plants: Research Progress and Prospects
inferred← citeshttps://doi.org/10.3389/fpls.2022.917652openalex-snapshot
Global proteome analyses of phosphorylation and succinylation of barley root proteins in response to phosphate starvation and recovery
inferred← citeshttps://doi.org/10.3389/fpls.2022.974124openalex-snapshot
Ecological strategy of Phyllostachys heteroclada oliver in the riparian zone based on ecological stoichiometry
inferred← citeshttps://doi.org/10.3390/agronomy11050908openalex-snapshot
Identification of QTL for Tolerance to Flooding Stress at Seedling Stage of Soybean (Glycine max L. Merr.)
inferred← citeshttps://doi.org/10.3390/agronomy14092112openalex-snapshot
N-Acetylcysteine Mitigates Oxidative Stress Induced by Transplanting Lettuce Seedlings into a DFT Hydroponic System
inferred← citeshttps://doi.org/10.3390/agronomy15020482openalex-snapshot
Physiological Mechanism of Welsh Onion (Allium fistulosum L.) in Response to High Temperature and Waterlogging Stress
inferred← citeshttps://doi.org/10.3390/agronomy9080447openalex-snapshot
Physiological Responses of Selected Vegetable Crop Species to Water Stress
inferred← citeshttps://doi.org/10.3390/ijms231911522openalex-snapshot
Nitrate–Nitrite–Nitric Oxide Pathway: A Mechanism of Hypoxia and Anoxia Tolerance in Plants
inferred← citeshttps://doi.org/10.3390/ijms232113057openalex-snapshot
Nitric Oxide Metabolic Pathway in Drought-Stressed Nodules of Faba Bean (Vicia faba L.)
inferred← citeshttps://doi.org/10.3390/molecules29061200openalex-snapshot
Redox Reactivity of Nonsymbiotic Phytoglobins towards Nitrite
inferred← citeshttps://doi.org/10.3390/plants12223824openalex-snapshot
Plant Adaptation to Flooding Stress under Changing Climate Conditions: Ongoing Breakthroughs and Future Challenges
inferred← citeshttps://doi.org/10.3390/plants13020322openalex-snapshot
NPF and NRT2 from Pisum sativum Potentially Involved in Nodule Functioning: Lessons from Medicago truncatula and Lotus japonicus
inferred← citeshttps://doi.org/10.3390/plants5020025openalex-snapshot
Reconfiguration of N Metabolism upon Hypoxia Stress and Recovery: Roles of Alanine Aminotransferase (AlaAT) and Glutamate Dehydrogenase (GDH)
inferred← citeshttps://doi.org/10.3390/plants9020180openalex-snapshot
Nitrous Oxide Emissions from Paddies: Understanding the Role of Rice Plants
inferred← citeshttps://doi.org/10.4018/979-8-2600-0036-6.ch010openalex-snapshot
Surviving Submergence
inferred← citeshttps://doi.org/10.70675/56e9d5ddzdbdaz4034zaab9zc7f9f4263dafopenalex-snapshot
ERF-VII family as key players in hypoxic signaling and adaptation in Medicago truncatula
inferred← citeshttps://doi.org/10.7717/peerj.11834openalex-snapshot
Responses of nitrogen efficiency and antioxidant system of summer maize to waterlogging stress under different tillage
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