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Loss of AUXIN RESPONSE FACTOR 4 function alters plant growth, stomatal function and improves tomato tolerance to salinity and osmotic stress
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Modeling the Temperature Dependence of C3 Photosynthesis
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Plant Drought Stress: Effects, Mechanisms and Management
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A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species
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Comparison of the Drought Stress Responses of Tolerant and Sensitive Wheat Cultivars During Grain Filling: Changes in Flag Leaf Photosynthetic Activity, ABA Levels, and Grain Yield
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Overexpression of monodehydroascorbate reductase in transgenic tobacco confers enhanced tolerance to ozone, salt and polyethylene glycol stresses
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Expression of cell cycle regulatory genes and morphological alterations in response to salt stress in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s10142-010-0174-3openalex-snapshot
Auxin-related gene families in abiotic stress response in Sorghum bicolor
inferredcites →https://doi.org/10.1007/s11033-011-1100-zopenalex-snapshot
Transcript expression profiling of stress responsive genes in response to short-term salt or PEG stress in sugarcane leaves
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Photosynthesis under stressful environments: An overview
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Overexpression of the Escherichia coli catalase gene, katE, enhances tolerance to salinity stress in the transgenic indica rice cultivar, BR5
inferredcites →https://doi.org/10.1016/j.bbrc.2006.07.026openalex-snapshot
Regulation of ABA level and water-stress tolerance of Arabidopsis by ectopic expression of a peanut 9-cis-epoxycarotenoid dioxygenase gene
inferredcites →https://doi.org/10.1016/j.biotechadv.2014.12.006openalex-snapshot
The CRISPR/Cas9 system for plant genome editing and beyond
inferredcites →https://doi.org/10.1016/j.cell.2009.03.001openalex-snapshot
Auxin: A Trigger for Change in Plant Development
inferredcites →https://doi.org/10.1016/j.jssas.2013.01.001openalex-snapshot
Improving drought and salinity tolerance in barley by application of salicylic acid and potassium nitrate
inferredcites →https://doi.org/10.1016/j.plantsci.2003.12.007openalex-snapshot
Enhanced tolerance to salt stress and water deficit by overexpressing superoxide dismutase in tobacco (Nicotiana tabacum) chloroplasts
inferredcites →https://doi.org/10.1016/j.plantsci.2011.01.013openalex-snapshot
Current advances in the investigation of leaf rolling caused by biotic and abiotic stress factors
inferredcites →https://doi.org/10.1016/j.plaphy.2012.04.012openalex-snapshot
Catalase plays a key role in salt stress acclimation induced by hydrogen peroxide pretreatment in maize
inferredcites →https://doi.org/10.1016/j.plaphy.2014.01.015openalex-snapshot
Hormone profiling and transcription analysis reveal a major role of ABA in tomato salt tolerance
inferredcites →https://doi.org/10.1021/ac60111a017openalex-snapshot
Colorimetric Method for Determination of Sugars and Related Substances
inferredcites →https://doi.org/10.1038/35066500openalex-snapshot
Guard cell abscisic acid signalling and engineering drought hardiness in plants
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Genome editing for horticultural crop improvement
inferredcites →https://doi.org/10.1042/bj1251075openalex-snapshot
Control of leghaemoglobin synthesis in snake beans
inferredcites →https://doi.org/10.1046/j.0016-8025.2003.01121.xopenalex-snapshot
Overexpression of bacterial catalase in tomato leaf chloroplasts enhances photo‐oxidative stress tolerance
inferredcites →https://doi.org/10.1046/j.1365-3040.2000.00602.xopenalex-snapshot
Tolerance of pea (Pisum sativum L.) to long‐term salt stress is associated with induction of antioxidant defences
inferredcites →https://doi.org/10.1046/j.1365-3040.2003.01064.xopenalex-snapshot
Differences in hydraulic architecture account for near‐isohydric and anisohydric behaviour of two field‐grown Vitis vinifera L. cultivars during drought
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00386.xopenalex-snapshot
Characterization of the ABA‐deficient tomato mutant notabilis and its relationship with maize Vp14
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01450.xopenalex-snapshot
Down‐regulation of DR12, an auxin‐response‐factor homolog, in the tomato results in a pleiotropic phenotype including dark green and blotchy ripening fruit
inferredcites →https://doi.org/10.1055/s-2006-923964openalex-snapshot
Stomatal Conductance is a Key Parameter to Assess Limitations to Photosynthesis and Growth Potential in Barley Genotypes
inferredcites →https://doi.org/10.1071/pp98031openalex-snapshot
Interaction of stomatal responses to ABA and CO2 in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/dnares/dst027openalex-snapshot
The Auxin Response Factor Transcription Factor Family in Soybean: Genome-Wide Identification and Expression Analyses During Development and Water Stress
inferredcites →https://doi.org/10.1093/jxb/erj100openalex-snapshot
Approaches to increasing the salt tolerance of wheat and other cereals
inferredcites →https://doi.org/10.1093/jxb/erp094openalex-snapshot
The role of auxin and gibberellin in tomato fruit set
inferredcites →https://doi.org/10.1093/jxb/ers100openalex-snapshot
The interaction of plant biotic and abiotic stresses: from genes to the field
inferredcites →https://doi.org/10.1093/jxb/eru141openalex-snapshot
Down-regulation of AUXIN RESPONSE FACTORS 6 and 8 by microRNA 167 leads to floral development defects and female sterility in tomato
inferredcites →https://doi.org/10.1093/jxb/ery328openalex-snapshot
SlARF10, an auxin response factor, is involved in chlorophyll and sugar accumulation during tomato fruit development
inferredcites →https://doi.org/10.1093/mp/sss078openalex-snapshot
ABA Signaling in Guard Cells Entails a Dynamic Protein–Protein Interaction Relay from the PYL-RCAR Family Receptors to Ion Channels
inferredcites →https://doi.org/10.1093/mp/ssu044openalex-snapshot
CRISPR-P: A Web Tool for Synthetic Single-Guide RNA Design of CRISPR-System in Plants
inferredcites →https://doi.org/10.1093/pcp/pcs101openalex-snapshot
Phenotypes Associated with Down-Regulation of Sl-IAA27 Support Functional Diversity Among Aux/IAA Family Members in Tomato
inferredcites →https://doi.org/10.1093/pcp/pcv082openalex-snapshot
Sucrose Transporter AtSUC9 Mediated by a Low Sucrose Level is Involved in Arabidopsis Abiotic Stress Resistance by Regulating Sucrose Distribution and ABA Accumulation
inferredcites →https://doi.org/10.1093/pcp/pcv136openalex-snapshot
Auxin Response GeneSlARF3Plays Multiple Roles in Tomato Development and is Involved in the Formation of Epidermal Cells and Trichomes
inferredcites →https://doi.org/10.1104/pp.113.213843openalex-snapshot
SlARF4, an Auxin Response Factor Involved in the Control of Sugar Metabolism during Tomato Fruit Development
inferredcites →https://doi.org/10.1104/pp.114.247577openalex-snapshot
Efficient Gene Editing in Tomato in the First Generation Using the Clustered Regularly Interspaced Short Palindromic Repeats/CRISPR-Associated9 System
inferredcites →https://doi.org/10.1104/pp.53.2.258openalex-snapshot
Rapid Estimates of Relative Water Content
inferredcites →https://doi.org/10.1104/pp.82.4.1102openalex-snapshot
Effects of NaCl and CaCl2 on Cell Enlargement and Cell Production in Cotton Roots
inferredcites →https://doi.org/10.1104/pp.95.2.628openalex-snapshot
Effects of Salinity on Stomatal Conductance, Photosynthetic Capacity, and Carbon Isotope Discrimination of Salt-Tolerant ( Gossypium hirsutum L.) and Salt-Sensitive ( Phaseolus vulgaris L.) C 3 Non-Halophytes
inferredcites →https://doi.org/10.1105/tpc.105.033415openalex-snapshot
The Tomato Aux / IAA Transcription Factor IAA9 Is Involved in Fruit Development and Leaf Morphogenesis
inferredcites →https://doi.org/10.1105/tpc.109.072553openalex-snapshot
miR390, Arabidopsis TAS3 tasiRNAs, and Their AUXIN RESPONSE FACTOR Targets Define an Autoregulatory Network Quantitatively Regulating Lateral Root Growth
inferredcites →https://doi.org/10.1105/tpc.9.11.1963openalex-snapshot
Aux/IAA proteins repress expression of reporter genes containing natural and highly active synthetic auxin response elements.
inferredcites →https://doi.org/10.1111/j.1365-3040.2007.001689.xopenalex-snapshot
Major diffusion leaks of clamp‐on leaf cuvettes still unaccounted: how erroneous are the estimates of Farquhar et al. model parameters?
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02683.xopenalex-snapshot
CYP707A3, a major ABA 8′‐hydroxylase involved in dehydration and rehydration response in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1399-3054.2012.01617.xopenalex-snapshot
Auxin: a regulator of cold stress response
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04136.xopenalex-snapshot
Overexpression of MtCAS31 enhances drought tolerance in transgenic Arabidopsis by reducing stomatal density
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.07033.xopenalex-snapshot
Transcript profiling reveals diverse roles of auxin‐responsive genes during reproductive development and abiotic stress in rice
inferredcites →https://doi.org/10.1111/pbi.12601openalex-snapshot
Os ASR 5 enhances drought tolerance through a stomatal closure pathway associated with ABA and H2O2 signalling in rice
inferredcites →https://doi.org/10.1126/science.1126088openalex-snapshot
A Plant miRNA Contributes to Antibacterial Resistance by Repressing Auxin Signaling
inferredcites →https://doi.org/10.1126/science.1151461openalex-snapshot
TOPLESS Mediates Auxin-Dependent Transcriptional Repression During Arabidopsis Embryogenesis
inferredcites →https://doi.org/10.1146/annurev.arplant.51.1.463openalex-snapshot
P LANT C ELLULAR AND M OLECULAR R ESPONSES TO H IGH S ALINITY
inferredcites →https://doi.org/10.1146/annurev.arplant.52.1.627openalex-snapshot
G UARD C ELL S IGNAL T RANSDUCTION
inferredcites →https://doi.org/10.1155/2010/525291openalex-snapshot
Ulvan, a Sulfated Polysaccharide from Green Algae, Activates Plant Immunity through the Jasmonic Acid Signaling Pathway
inferredcites →https://doi.org/10.1186/1471-2164-12-178openalex-snapshot
Genome-wide identification and expression profiling of auxin response factor (ARF) gene family in maize
inferredcites →https://doi.org/10.1186/1746-4811-4-16openalex-snapshot
A rapid and robust method for simultaneously measuring changes in the phytohormones ABA, JA and SA in plants following biotic and abiotic stress
inferredcites →https://doi.org/10.1371/journal.pgen.1005903openalex-snapshot
AUXIN RESPONSE FACTOR 2 Intersects Hormonal Signals in the Regulation of Tomato Fruit Ripening
inferredcites →https://doi.org/10.1371/journal.pone.0084203openalex-snapshot
Characterization of the Tomato ARF Gene Family Uncovers a Multi-Levels Post-Transcriptional Regulation Including Alternative Splicing
inferredcites →https://doi.org/10.1371/journal.pone.0193517openalex-snapshot
Auxin Response Factors (ARFs) are potential mediators of auxin action in tomato response to biotic and abiotic stress (Solanum lycopersicum)
inferredcites →https://doi.org/10.1371/journal.pone.0201024openalex-snapshot
Genome-wide identification and expression profiling of the auxin response factor (ARF) gene family in physic nut
inferredcites →https://doi.org/10.14393/bj-v31n3a2015-23461openalex-snapshot
Physiological and molecular characterization of drought responses and screening of drought tolerant rice varieties
inferredcites →https://doi.org/10.1590/s0100-204x1999000800006openalex-snapshot
Aspects of leaf anatomy of kudzu (Pueraria lobata, Leguminosae-Faboideae) related to water and energy balance
inferredcites →https://doi.org/10.17221/24/2010-pseopenalex-snapshot
Salt resistance of tomato species grown in sand culture
inferredcites →https://doi.org/10.3389/fenvs.2014.00053openalex-snapshot
Reactive oxygen species (ROS) and response of antioxidants as ROS-scavengers during environmental stress in plants
inferredcites →https://doi.org/10.3389/fpls.2013.00442openalex-snapshot
Root traits contributing to plant productivity under drought
inferredcites →https://doi.org/10.3389/fpls.2015.00742openalex-snapshot
The auxin response factor gene family in banana: genome-wide identification and expression analyses during development, ripening, and abiotic stress
inferredcites →https://doi.org/10.3389/fpls.2017.01932openalex-snapshot
Gene Editing and Crop Improvement Using CRISPR-Cas9 System
inferredcites →https://doi.org/10.4161/psb.23681openalex-snapshot
Reactive oxygen species signaling in plants under abiotic stress
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-3-030-84985-6_23openalex-snapshot
Understanding the Regulation of Root Development Towards Environmental Stresses for Crop Improvement
inferred← citeshttps://doi.org/10.1016/j.plgene.2020.100264openalex-snapshot
An overview of recent advancement in phytohormones-mediated stress management and drought tolerance in crop plants
inferred← citeshttps://doi.org/10.1038/s41598-020-69232-3openalex-snapshot
RNA-sequencing analysis revealed genes associated drought stress responses of different durations in hexaploid sweet potato
inferred← citeshttps://doi.org/10.1093/jxb/eraa241openalex-snapshot
Auxin-mediated responses under salt stress: from developmental regulation to biotechnological applications
inferred← citeshttps://doi.org/10.1186/s12870-026-08366-4openalex-snapshot
Transcriptome analysis of safflower (Carthamus tinctorius L.) reveals the roles of osmotic adjustment and regulatory mechanisms in response to drought stress
inferred← citeshttps://doi.org/10.1590/2447-536x.v29i1.2502openalex-snapshot
Analysis of exogenous auxin and cytokinin action in overcoming root restriction in green and variegated Benjamin fig
inferred← citeshttps://doi.org/10.3389/fpls.2024.1400215openalex-snapshot
Date palm transcriptome analysis provides new insights on changes in response to high salt stress of colonized roots with the endophytic fungus Piriformospora indica
inferred← citeshttps://doi.org/10.4236/ajps.2021.122014openalex-snapshot
Drought Tolerance Enhancement with Co-Overexpression of DREB2A and APX in Indica Rice (Oryza sativa L.)
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