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NO signaling is a key component of the root growth response to nitrate inZea maysL.
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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/jpln.200900312openalex-snapshot
Nitric oxide reduces the stress effects of aluminum on the process of germination and early root growth of rice
inferredcites →https://doi.org/10.1007/978-94-009-3627-0_1openalex-snapshot
Nitrogen fertilization in citrus orchards
inferredcites →https://doi.org/10.1007/bf00011100openalex-snapshot
Root distribution in relation to soil nitrogen availability in field-grown tomatoes
inferredcites →https://doi.org/10.1007/bf00195876openalex-snapshot
Postmitotic ‘isodiametric’ cell growth in the maize root apex
inferredcites →https://doi.org/10.1007/s00299-013-1434-1openalex-snapshot
Nitric oxide as a key component in hormone-regulated processes
inferredcites →https://doi.org/10.1007/s00425-003-1172-7openalex-snapshot
Nitric oxide plays a central role in determining lateral root development in tomato
inferredcites →https://doi.org/10.1007/s004250100670openalex-snapshot
Characterisation of the oxygen fluxes in the division, elongation and mature zones of Vitis roots: influence of oxygen availability
inferredcites →https://doi.org/10.1007/s11104-005-6837-5openalex-snapshot
Possible Involvement of Cytokinin in Nitrate-mediated Root Growth in Maize
inferredcites →https://doi.org/10.1007/s11104-009-9929-9openalex-snapshot
Plant root growth, architecture and function
inferredcites →https://doi.org/10.1007/s12217-008-9045-0openalex-snapshot
Distribution of Calcium Ions in Cells of the Root Distal Elongation Zone Under Clinorotation
inferredcites →https://doi.org/10.1016/j.devcel.2010.05.008openalex-snapshot
Nitrate-Regulated Auxin Transport by NRT1.1 Defines a Mechanism for Nutrient Sensing in Plants
inferredcites →https://doi.org/10.1016/j.devcel.2010.05.020openalex-snapshot
Nitrate Contra Auxin: Nutrient Sensing by Roots
inferredcites →https://doi.org/10.1016/j.jplph.2007.02.011openalex-snapshot
Inhibition of maize root growth by high nitrate supply is correlated with reduced IAA levels in roots
inferredcites →https://doi.org/10.1016/j.jplph.2007.07.019openalex-snapshot
Exogenous auxin-induced NO synthesis is nitrate reductase-associated in Arabidopsis thaliana root primordia
inferredcites →https://doi.org/10.1016/j.pbi.2010.09.006openalex-snapshot
Lateral root organogenesis — from cell to organ
inferredcites →https://doi.org/10.1016/j.plantsci.2005.06.007openalex-snapshot
Auxin transport from shoot to root is involved in the response of lateral root growth to localized supply of nitrate in maize
inferredcites →https://doi.org/10.1016/j.plaphy.2011.09.003openalex-snapshot
Exogenous nitrate induces root branching and inhibits primary root growth in Capsicum chinense Jacq.
inferredcites →https://doi.org/10.1016/j.tplants.2007.03.006openalex-snapshot
Molecular and cellular aspects of auxin-transport-mediated development
inferredcites →https://doi.org/10.1016/j.tplants.2007.08.012openalex-snapshot
Root system architecture: opportunities and constraints for genetic improvement of crops
inferredcites →https://doi.org/10.1016/j.tplants.2010.04.007openalex-snapshot
Root apex transition zone: a signalling–response nexus in the root
inferredcites →https://doi.org/10.1016/s0070-2153(10)91003-xopenalex-snapshot
Root Development—Two Meristems for the Price of One?
inferredcites →https://doi.org/10.1016/s1360-1385(01)02156-2openalex-snapshot
Nitric oxide: a non-traditional regulator of plant growth
inferredcites →https://doi.org/10.1016/s1369-5266(03)00035-9openalex-snapshot
The role of nutrient availability in regulating root architecture
inferredcites →https://doi.org/10.1016/s1369-5266(99)00007-2openalex-snapshot
Nitric oxide as a signal in plants
inferredcites →https://doi.org/10.1038/nrm2020openalex-snapshot
Auxin in action: signalling, transport and the control of plant growth and development
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01185.xopenalex-snapshot
ABA plays a central role in mediating the regulatory effects of nitrate on root branching in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01251.xopenalex-snapshot
Nitrate and phosphate availability and distribution have different effects on root system architecture of Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0605275103openalex-snapshot
The Arabidopsis NRT1.1 transporter participates in the signaling pathway triggering root colonization of nitrate-rich patches
inferredcites →https://doi.org/10.1073/pnas.0909571107openalex-snapshot
Nitrate-responsive miR393/ AFB3 regulatory module controls root system architecture in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.1108644108openalex-snapshot
Nitric oxide causes root apical meristem defects and growth inhibition while reducing PIN-FORMED 1 (PIN1)-dependent acropetal auxin transport
inferredcites →https://doi.org/10.1073/pnas.96.11.6529openalex-snapshot
Dual pathways for regulation of root branching by nitrate
inferredcites →https://doi.org/10.1093/aob/mcj605openalex-snapshot
Influence of Inorganic Nitrogen and pH on the Elongation of Maize Seminal Roots
inferredcites →https://doi.org/10.1093/aob/mcm142openalex-snapshot
Nitric Oxide is Involved in Nitrate-induced Inhibition of Root Elongation in Zea mays
inferredcites →https://doi.org/10.1093/aob/mcq202openalex-snapshot
Auxin transport in maize roots in response to localized nitrate supply
inferredcites →https://doi.org/10.1093/aobpla/pls004openalex-snapshot
Non-symbiotic haemoglobins—What's happening beyond nitric oxide scavenging?
inferredcites →https://doi.org/10.1093/aobpla/pls052openalex-snapshot
Nitric oxide in plants: an assessment of the current state of knowledge
inferredcites →https://doi.org/10.1093/jexbot/50.338.1481openalex-snapshot
Acid-induced wall loosening is confined to the accelerating region of the root growing zone
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/jxb/erg060openalex-snapshot
Electrophysiological responses of maize roots to low water potentials: relationship to growth and ABA accumulation
inferredcites →https://doi.org/10.1093/jxb/erl197openalex-snapshot
Aluminium toxicity in plants: internalization of aluminium into cells of the transition zone in Arabidopsis root apices related to changes in plasma membrane potential, endosomal behaviour, and nitric oxide production
inferredcites →https://doi.org/10.1093/jxb/erm293openalex-snapshot
Nitric oxide, stomatal closure, and abiotic stress
inferredcites →https://doi.org/10.1093/jxb/erp033openalex-snapshot
Nitric oxide modulates dynamic actin cytoskeleton and vesicle trafficking in a cell type-specific manner in root apices
inferredcites →https://doi.org/10.1093/jxb/erq410openalex-snapshot
Hormonal control of nitrogen acquisition: roles of auxin, abscisic acid, and cytokinin
inferredcites →https://doi.org/10.1093/jxb/ert155openalex-snapshot
Lateral root initiation is a probabilistic event whose frequency is set by fluctuating levels of auxin response
inferredcites →https://doi.org/10.1093/jxb/ert358openalex-snapshot
NO homeostasis is a key regulator of early nitrate perception and root elongation in maize*
inferredcites →https://doi.org/10.1093/jxb/ert421openalex-snapshot
It’s time to make changes: modulation of root system architecture by nutrient signals
inferredcites →https://doi.org/10.1093/pcp/pcj007openalex-snapshot
Adaptative Response of Vitis Root to Anoxia
inferredcites →https://doi.org/10.1093/pcp/pcp013openalex-snapshot
Different Effects of Aluminum on the Actin Cytoskeleton and Brefeldin A-Sensitive Vesicle Recycling in Root Apex Cells of Two Maize Varieties Differing in Root Elongation Rate and Aluminum Tolerance
inferredcites →https://doi.org/10.1093/pcp/pcq117openalex-snapshot
Nitric Oxide is Involved in Alkamide-Induced Lateral Root Development in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcr061openalex-snapshot
Effect of Hypoxic Acclimation on Anoxia Tolerance in Vitis Roots: Response of Metabolic Activity and K+ Fluxes
inferredcites →https://doi.org/10.1093/pcp/pcs034openalex-snapshot
Local Root Apex Hypoxia Induces NO-Mediated Hypoxic Acclimation of the Entire Root
inferredcites →https://doi.org/10.1104/pp.100.2.762openalex-snapshot
Induction of Curvature in Maize Roots by Calcium or by Thigmostimulation
inferredcites →https://doi.org/10.1104/pp.102.4.1203openalex-snapshot
The Role of the Distal Elongation Zone in the Response of Maize Roots to Auxin and Gravity
inferredcites →https://doi.org/10.1104/pp.104.054494openalex-snapshot
Nitric Oxide Mediates Gravitropic Bending in Soybean Roots
inferredcites →https://doi.org/10.1104/pp.112.1.3openalex-snapshot
Specialized Zones of Development in Roots: View from the Cellular Level
inferredcites →https://doi.org/10.1104/pp.113.218453openalex-snapshot
Plasticity of the Arabidopsis Root System under Nutrient Deficiencies
inferredcites →https://doi.org/10.1104/pp.116.1.155openalex-snapshot
The Distal Part of the Transition Zone Is the Most Aluminum-Sensitive Apical Root Zone of Maize1
inferredcites →https://doi.org/10.1104/pp.119.3.1073openalex-snapshot
Impacts of Aluminum on the Cytoskeleton of the Maize Root Apex. Short-Term Effects on the Distal Part of the Transition Zone1
inferredcites →https://doi.org/10.1104/pp.122.3.945openalex-snapshot
Genotypical Differences in Aluminum Resistance of Maize Are Expressed in the Distal Part of the Transition Zone. Is Reduced Basipetal Auxin Flow Involved in Inhibition of Root Elongation by Aluminum?
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01306.xopenalex-snapshot
Intrinsic and environmental response pathways that regulate root system architecture
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03443.xopenalex-snapshot
Nitrate signalling mediated by the NRT1.1 nitrate transporter antagonises l ‐glutamate‐induced changes in root architecture
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04134.xopenalex-snapshot
A putative transporter is essential for integrating nutrient and hormone signaling with lateral root growth and nodule development in Medicago truncatula
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02820.xopenalex-snapshot
Nitric oxide modulates the influx of extracellular Ca2+ and actin filament organization during cell wall construction in Pinus bungeana pollen tubes
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03822.xopenalex-snapshot
Transcriptome analysis reveals coordinated spatiotemporal regulation of hemoglobin and nitrate reductase in response to nitrate in maize roots
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03996.xopenalex-snapshot
Lateral root initiation: one step at a time
inferredcites →https://doi.org/10.1111/pce.12143openalex-snapshot
Auxin‐mediated nitrate signalling by NRT 1.1 participates in the adaptive response of A rabidopsis root architecture to the spatial heterogeneity of nitrate availability
inferredcites →https://doi.org/10.1126/science.279.5349.407openalex-snapshot
An Arabidopsis MADS Box Gene That Controls Nutrient-Induced Changes in Root Architecture
inferredcites →https://doi.org/10.1146/annurev.arplant.53.100301.135256openalex-snapshot
L OCAL AND L ONG -R ANGE S IGNALING P ATHWAYS R EGULATING P LANT R ESPONSES TO N ITRATE
inferredcites →https://doi.org/10.1146/annurev.arplant.54.031902.134752openalex-snapshot
Nitric Oxide: The Versatility of an Extensive Signal Molecule
inferredcites →https://doi.org/10.1146/annurev.cellbio.21.122303.114753openalex-snapshot
REGULATION OF ROOT APICAL MERISTEM DEVELOPMENT
inferredcites →https://doi.org/10.1242/dev.01153openalex-snapshot
Nitric oxide is involved in growth regulation and re-orientation of pollen tubes
inferredcites →https://doi.org/10.1242/dev.090548openalex-snapshot
To branch or not to branch: the role of pre-patterning in lateral root formation
inferredcites →https://doi.org/10.1242/dev.119.1.57openalex-snapshot
Root development in Arabidopsis : four mutants with dramatically altered root morphogenesis
inferredcites →https://doi.org/10.1371/journal.pgen.1003760openalex-snapshot
Plasticity Regulators Modulate Specific Root Traits in Discrete Nitrogen Environments
inferredcites →https://doi.org/10.3389/fpls.2013.00186openalex-snapshot
Getting to the roots of it: Genetic and hormonal control of root architecture
inferredcites →https://doi.org/10.3389/fpls.2013.00354openalex-snapshot
Root Apex Transition Zone As Oscillatory Zone
inferredcites →https://doi.org/10.3389/fpls.2013.00398openalex-snapshot
Nitric oxide and phytohormone interactions: current status and perspectives
inferredcites →https://doi.org/10.4161/psb.1.1.2398openalex-snapshot
Nitric Oxide Functions as a Positive Regulator of Root Hair Development
inferredcites →https://doi.org/10.4161/psb.1.2.2432openalex-snapshot
Actin Turnover-Mediated Gravity Response in Maize Root Apices
inferredcites →https://doi.org/10.4161/psb.1.6.3511openalex-snapshot
The Root Apex ofArabidopsis thalianaConsists of Four Distinct Zones of Growth Activities
inferredcites →https://doi.org/10.4161/psb.18768openalex-snapshot
NO serves as a signaling intermediate downstream of H2O2to modulate dynamic microtubule cytoskeleton during responses to VD-toxins in Arabidopsis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4828574openalex-extracted
Partial Replacement by Ammonium Nutrition Enhance Brassica Napus Growth by Promoting Root Development, Photosynthesis and Nitrogen Metabolism
inferred← citeshttps://doi.org/10.1002/ange.201906326openalex-snapshot
Genomics‐Driven Discovery of NO‐Donating Diazeniumdiolate Siderophores in Diverse Plant‐Associated Bacteria
inferred← citeshttps://doi.org/10.1002/anie.201906326openalex-snapshot
Genomics‐Driven Discovery of NO‐Donating Diazeniumdiolate Siderophores in Diverse Plant‐Associated Bacteria
inferred← citeshttps://doi.org/10.1007/978-3-030-84985-6_3openalex-snapshot
Molecular Physiology of Nitrate Sensing by Roots
inferred← citeshttps://doi.org/10.1007/978-3-319-75596-0_4openalex-snapshot
Plant Cognition and Behavior: From Environmental Awareness to Synaptic Circuits Navigating Root Apices
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Differential Response of First-Order Lateral Root Elongation to Low Potassium Involves Nitric Oxide in Two Tobacco Cultivars
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Trichoderma-Induced Promotion of Nitrogen Use Efficiency is Mediated by Nitric Oxide Generation Leading to Improved Growth and Yield in Pea (Pisum sativum L.) Plants
inferred← citeshttps://doi.org/10.1007/s00425-018-2892-zopenalex-snapshot
Nitrate inhibits the remobilization of cell wall phosphorus under phosphorus-starvation conditions in rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1007/s11032-021-01273-6openalex-snapshot
Knockdown of OsNRT2.4 modulates root morphology and alters nitrogen metabolism in response to low nitrate availability in rice
inferred← citeshttps://doi.org/10.1016/b978-0-12-821430-5.00004-3openalex-snapshot
Nitrogen metabolism in Chlamydomonas
inferred← citeshttps://doi.org/10.1016/j.bbagen.2025.130837openalex-snapshot
Nitric oxide in plant stress: Rewilding and restoring signaling for enhancing plant growth and development
inferred← citeshttps://doi.org/10.1016/j.jplph.2024.154411openalex-snapshot
Partial replacement by ammonium nutrition enhances Brassica napus growth by promoting root development, photosynthesis, and nitrogen metabolism
inferred← citeshttps://doi.org/10.1016/j.jprot.2020.103781openalex-snapshot
Plant-derived smoke enhances plant growth through ornithine-synthesis pathway and ubiquitin-proteasome pathway in soybean
inferred← citeshttps://doi.org/10.1016/j.niox.2024.10.005openalex-snapshot
Nitric oxide-mediated regulation of macronutrients in plants
inferred← citeshttps://doi.org/10.1016/j.niox.2025.08.003openalex-snapshot
Nitrate-dependent changes in the primary and lateral root growth in wheat seedlings require the coordinated action of auxin, calcium and nitric oxide
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.07.005openalex-snapshot
Nitric oxide regulates water status and associated enzymatic pathways to inhibit nutrients imbalance in maize (Zea mays L.) under drought stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108625openalex-snapshot
Redox regulation in primary nitrate response: Nitric oxide in the spotlight
inferred← citeshttps://doi.org/10.1016/j.scienta.2016.10.008openalex-snapshot
Nitric oxide enhances the nitrate stress tolerance of spinach by scavenging ROS and RNS
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100191openalex-snapshot
Mechanisms of nitric oxide involvement in plant-microbe interaction and its enhancement of stress resistance
inferred← citeshttps://doi.org/10.1016/j.tplants.2016.12.001openalex-snapshot
Nitrate Reductase Regulates Plant Nitric Oxide Homeostasis
inferred← citeshttps://doi.org/10.1038/s41438-021-00500-7openalex-snapshot
Molecular functions of nitric oxide and its potential applications in horticultural crops
inferred← citeshttps://doi.org/10.1038/srep26400openalex-snapshot
Overexpression of spinach non-symbiotic hemoglobin in Arabidopsis resulted in decreased NO content and lowered nitrate and other abiotic stresses tolerance
inferred← citeshttps://doi.org/10.1080/15592324.2016.1274480openalex-snapshot
Multiple roles of nitric oxide in root development and nitrogen uptake
inferred← citeshttps://doi.org/10.1080/15592324.2023.2300228openalex-snapshot
Reciprocal modulation of responses to nitrate starvation and hypoxia in roots and leaves of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/jxb/erv030openalex-snapshot
Nitric oxide generated by nitrate reductase increases nitrogen uptake capacity by inducing lateral root formation and inorganic nitrogen uptake under partial nitrate nutrition in rice
inferred← citeshttps://doi.org/10.1093/jxb/erv165openalex-snapshot
Nitrate sensing by the maize root apex transition zone: a merged transcriptomic and proteomic survey
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How Chlamydomonas handles nitrate and the nitric oxide cycle
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Nitric oxide and plant mineral nutrition: current knowledge
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The Control of Zealactone Biosynthesis and Exudation is Involved in the Response to Nitrogen in Maize Root
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Strigolactones are required for nitric oxide to induce root elongation in response to nitrogen and phosphate deficiencies in rice
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Nitrate affects transcriptional regulation of UPBEAT1 and ROS localisation in roots of Zea mays L.
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A system for the study of roots 3D kinematics in hydroponic culture: a study on the oscillatory features of root tip
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Monitoring Nutrient Uptake of Chard (Beta vulgaris var. cicla L.) Exposed to Exogenously Applied Nitric Oxide under Drought Stress
inferred← citeshttps://doi.org/10.21203/rs.3.rs-669590/v1openalex-snapshot
The Rice NRT2.4 Alters Metabolism and Nitrogen Uptake through Root Modulation
inferred← citeshttps://doi.org/10.3389/fpls.2015.00927openalex-snapshot
Role of ethylene in responses of plants to nitrogen availability
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Plant Survival in a Changing Environment: The Role of Nitric Oxide in Plant Responses to Abiotic Stress
inferred← citeshttps://doi.org/10.3389/fpls.2015.01269openalex-snapshot
Nitric Oxide-Mediated Maize Root Apex Responses to Nitrate are Regulated by Auxin and Strigolactones
inferred← citeshttps://doi.org/10.3389/fpls.2017.00485openalex-snapshot
Nitrate: A Crucial Signal during Lateral Roots Development
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Ectopic Expression of PII Induces Stomatal Closure in Lotus japonicus
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The Interaction between Auxin and Nitric Oxide Regulates Root Growth in Response to Iron Deficiency in Rice
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Trichoderma asperellum T42 Reprograms Tobacco for Enhanced Nitrogen Utilization Efficiency and Plant Growth When Fed with N Nutrients
inferred← citeshttps://doi.org/10.3389/fpls.2018.00659openalex-snapshot
Nitric Oxide Affects Rice Root Growth by Regulating Auxin Transport Under Nitrate Supply
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Nitrate and Ammonium Affect the Overall Maize Response to Nitrogen Availability by Triggering Specific and Common Transcriptional Signatures in Roots
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Nitrate Regulates Maize Root Transcriptome through Nitric Oxide Dependent and Independent Mechanisms
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Humic Acid-Induced Hairy Root Growth in Basil Ismodulated by Nitric Oxide and Reactive Oxygen Species
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Assessment of Tractor Power Variation on Soil Properties under Maize Cultivation in Nkwadi Agricultural Volunteerism Program/Kasai Oriental Province, Democratic Republic of Congo
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