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A GH3 family member, OsGH3-2, modulates auxin and abscisic acid levels and differentially affects drought and cold tolerance in rice

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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/j.1460-2075.1996.tb00565.xopenalex-snapshot

A mutation in protein phosphatase 2A regulatory subunit A affects auxin transport in Arabidopsis.

inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

inferredcites →https://doi.org/10.1007/bf00762210openalex-snapshot

Freeze/thaw-induced destabilization of the plasma membrane and the effects of cold acclimation

inferredcites →https://doi.org/10.1007/s10142-005-0142-5openalex-snapshot

The auxin-responsive GH3 gene family in rice (Oryza sativa)

inferredcites →https://doi.org/10.1007/s10295-006-0121-4openalex-snapshot

Structural diversity and functional novelty of new carotenoid biosynthesis genes

inferredcites →https://doi.org/10.1016/j.cub.2011.03.015openalex-snapshot

Evolution of Abscisic Acid Synthesis and Signaling Mechanisms

inferredcites →https://doi.org/10.1016/j.febslet.2005.01.018openalex-snapshot

Auxin‐induced reactive oxygen species production requires the activation of phosphatidylinositol 3‐kinase

inferredcites →https://doi.org/10.1016/j.jplph.2011.12.013openalex-snapshot

Complex phytohormone responses during the cold acclimation of two wheat cultivars differing in cold tolerance, winter Samanta and spring Sandra

inferredcites →https://doi.org/10.1016/j.tplants.2006.07.003openalex-snapshot

A novel role for abscisic acid emerges from underground

inferredcites →https://doi.org/10.1016/s1369-5266(03)00092-xopenalex-snapshot

Regulatory network of gene expression in the drought and cold stress responses

inferredcites →https://doi.org/10.1021/jf0106695openalex-snapshot

Using a Modified Ferrous Oxidation−Xylenol Orange (FOX) Assay for Detection of Lipid Hydroperoxides in Plant Tissue

inferredcites →https://doi.org/10.1038/36285openalex-snapshot

Mutation of the mouse klotho gene leads to a syndrome resembling ageing.

inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01165.xopenalex-snapshot

Maize VP1 complements Arabidopsisabi3 and confers a novel ABA/auxin interaction in roots

inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01707.xopenalex-snapshot

The ABSCISIC ACID INSENSITIVE 3 ( ABI3 ) gene is modulated by farnesylation and is involved in auxin signaling and lateral root development in Arabidopsis

inferredcites →https://doi.org/10.1074/jbc.m110.201707openalex-snapshot

Arabidopsis Monothiol Glutaredoxin, AtGRXS17, Is Critical for Temperature-dependent Postembryonic Growth and Development via Modulating Auxin Response

inferredcites →https://doi.org/10.1093/jxb/erm273openalex-snapshot

A novel bud mutation that confers abnormal patterns of lycopene accumulation in sweet orange fruit (Citrus sinensis L. Osbeck)

inferredcites →https://doi.org/10.1093/jxb/ers115openalex-snapshot

Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus

inferredcites →https://doi.org/10.1093/mp/ssn097openalex-snapshot

Abiotic Stress Tolerance: From Gene Discovery in Model Organisms to Crop Improvement

inferredcites →https://doi.org/10.1093/mp/ssr074openalex-snapshot

A Gain-of-Function Mutation in OsIAA11 Affects Lateral Root Development in Rice

inferredcites →https://doi.org/10.1093/pcp/pcq032openalex-snapshot

Auxin Biosynthesis Inhibitors, Identified by a Genomics-Based Approach, Provide Insights into Auxin Biosynthesis

inferredcites →https://doi.org/10.1094/mpmi-22-2-0201openalex-snapshot

Constitutive Expression of OsGH3.1 Reduces Auxin Content and Enhances Defense Response and Resistance to a Fungal Pathogen in Rice

inferredcites →https://doi.org/10.1101/gad.1035402openalex-snapshot

Trp-dependent auxin biosynthesis in Arabidopsis: involvement of cytochrome P450s CYP79B2 and CYP79B3

inferredcites →https://doi.org/10.1104/pp.104.057927openalex-snapshot

Why Is Golden Rice Golden (Yellow) Instead of Red?

inferredcites →https://doi.org/10.1104/pp.104.2.761openalex-snapshot

Drought Rhizogenesis in Arabidopsis thaliana (Differential Responses of Hormonal Mutants)

inferredcites →https://doi.org/10.1104/pp.109.144220openalex-snapshot

The MYB96 Transcription Factor Mediates Abscisic Acid Signaling during Drought Stress Response in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.109.146803openalex-snapshot

Altered Architecture and Enhanced Drought Tolerance in Rice via the Down-Regulation of Indole-3-Acetic Acid by TLD1/OsGH3.13 Activation

inferredcites →https://doi.org/10.1104/pp.110.163741openalex-snapshot

Characterization of the β-Carotene Hydroxylase Gene DSM2 Conferring Drought and Oxidative Stress Resistance by Increasing Xanthophylls and Abscisic Acid Synthesis in Rice

inferredcites →https://doi.org/10.1104/pp.110.163774openalex-snapshot

Manipulating Broad-Spectrum Disease Resistance by Suppressing Pathogen-Induced Auxin Accumulation in Rice

inferredcites →https://doi.org/10.1104/pp.111.173427openalex-snapshot

Rice ABI5-Like1 Regulates Abscisic Acid and Auxin Responses by Affecting the Expression of ABRE-Containing Genes

inferredcites →https://doi.org/10.1105/tpc.000885openalex-snapshot

Jasmonate Response Locus JAR1 and Several Related Arabidopsis Genes Encode Enzymes of the Firefly Luciferase Superfamily That Show Activity on Jasmonic, Salicylic, and Indole-3-Acetic Acids in an Assay for Adenylation

inferredcites →https://doi.org/10.1105/tpc.003335openalex-snapshot

Disruption of a Guard Cell–Expressed Protein Phosphatase 2A Regulatory Subunit, RCN1 , Confers Abscisic Acid Insensitivity in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.104.026690openalex-snapshot

Characterization of an Arabidopsis Enzyme Family That Conjugates Amino Acids to Indole-3-Acetic Acid

inferredcites →https://doi.org/10.1105/tpc.107.055657openalex-snapshot

Activation of the Indole-3-Acetic Acid–Amido Synthetase GH3-8 Suppresses Expansin Expression and Promotes Salicylate- and Jasmonate-Independent Basal Immunity in Rice

inferredcites →https://doi.org/10.1105/tpc.108.061655openalex-snapshot

The WUSCHEL-Related Homeobox GeneWOX11Is Required to Activate Shoot-Borne Crown Root Development in Rice

inferredcites →https://doi.org/10.1105/tpc.109.069906openalex-snapshot

Auxin Response inArabidopsisunder Cold Stress: Underlying Molecular Mechanisms

inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01451.xopenalex-snapshot

Evidence for altered polar and lateral auxin transport in the gravity persistent signal (gps) mutants of Arabidopsis

inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02426.xopenalex-snapshot

ABA signal transduction at the crossroad of biotic and abiotic stress responses

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02337.xopenalex-snapshot

Genome‐wide profiling of stored mRNA inArabidopsis thalianaseed germination: epigenetic and genetic regulation of transcription in seed

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02593.xopenalex-snapshot

Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stresses that affect plant water status

inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03218.xopenalex-snapshot

Repression of AUXIN RESPONSE FACTOR10 by microRNA160 is critical for seed germination and post‐germination stages

inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03411.xopenalex-snapshot

Mutations of genes in synthesis of the carotenoid precursors of ABA lead to pre‐harvest sprouting and photo‐oxidation in rice

inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04100.xopenalex-snapshot

A dynamic gene expression atlas covering the entire life cycle of rice

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/10.1146/annurev-arplant-042809-112308openalex-snapshot

Auxin Biosynthesis and Its Role in Plant Development

inferredcites →https://doi.org/10.1146/annurev.arplant.56.032604.144046openalex-snapshot

ABSCISIC ACID BIOSYNTHESIS AND CATABOLISM

inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105444openalex-snapshot

TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES

inferredcites →https://doi.org/10.1186/1746-4811-8-2openalex-snapshot

A convenient method for simultaneous quantification of multiple phytohormones and metabolites: application in study of rice-bacterium interaction

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

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Gretchen Hagen 3.6-like promotes anthocyanin accumulation by negatively regulating the expression of basic helix-loop-helix transcription factor 106 in grapevine

inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.114610openalex-snapshot

Dynamic transcriptome profiling revealed key genes and pathways associated with cold stress in castor (Ricinus communis L.)

inferred← citeshttps://doi.org/10.1016/j.jplph.2015.11.012openalex-snapshot

The auxin conjugate indole-3-acetyl-aspartate affects responses to cadmium and salt stress in Pisum sativum L.

inferred← citeshttps://doi.org/10.1016/j.jplph.2016.07.018openalex-snapshot

Abiotic stress and phytohormones affect enzymic activity of 1-O-(indole-3-acetyl)-β-d-glucose: myo-inositol indoleacetyl transferase from rice (Oryza sativa)

inferred← citeshttps://doi.org/10.1016/j.jplph.2018.06.013openalex-snapshot

Phytohormones as targets for improving plant productivity and stress tolerance

inferred← citeshttps://doi.org/10.1016/j.jprot.2016.05.022openalex-snapshot

Transcriptomic and proteomic analyses provide new insights into the regulation mechanism of low-temperature-induced leafy head formation in Chinese cabbage

inferred← citeshttps://doi.org/10.1016/j.mocell.2024.100093openalex-snapshot

OsMYB14, an R2R3-MYB transcription factor, regulates plant height through the control of hormone metabolism in rice

inferred← citeshttps://doi.org/10.1016/j.ncrops.2025.100091openalex-snapshot

Advances in understanding molecular regulatory mechanisms of leaf angle

inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114332openalex-snapshot

Biochemical and proteomic approaches to investigating effects of IAA-aspartate in pea (Pisum sativum L.) seedlings during osmotic shock

inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.03.023openalex-snapshot

The R2R3-type MYB gene OsMYB91 has a function in coordinating plant growth and salt stress tolerance in rice

inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.05.017openalex-snapshot

miRNAs and lncRNAs in reproductive development

inferred← citeshttps://doi.org/10.1016/j.plantsci.2016.07.014openalex-snapshot

A Raf-like MAPKKK gene, GhRaf19, negatively regulates tolerance to drought and salt and positively regulates resistance to cold stress by modulating reactive oxygen species in cotton

inferred← citeshttps://doi.org/10.1016/j.plantsci.2017.04.008openalex-snapshot

SGD1, a key enzyme in tocopherol biosynthesis, is essential for plant development and cold tolerance in rice

inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.02.001openalex-snapshot

Structural and metabolic alterations in root systems under limited water conditions in forage grasses of Lolium-Festuca complex

inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110385openalex-snapshot

Exogenous application of abscisic acid to shoots promotes primary root cell division and elongation

inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110715openalex-snapshot

Genetic basis of vascular bundle variations in rice revealed by genome-wide association study

inferred← citeshttps://doi.org/10.1016/j.plaphy.2014.06.008openalex-snapshot

Modulation of auxin content in Arabidopsis confers improved drought stress resistance

inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.01.005openalex-snapshot

Insight into VvGH3 genes evolutional relationship from monocotyledons and dicotyledons reveals that VvGH3-9 negatively regulates the drought tolerance in transgenic Arabidopsis

inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108129openalex-snapshot

Roles of abscisic acid and auxin in plants during drought: A molecular point of view

inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108363openalex-snapshot

miRNAs and genes as molecular regulators of rice grain morphology and yield

inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109452openalex-snapshot

Molecular insight into auxin signaling and associated network modulating stress responses in rice

inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109455openalex-snapshot

OsNCED5 confers cold stress tolerance through regulating ROS homeostasis in rice

inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109814openalex-snapshot

Uncovering the crucial metabolic pathways in the invasive plant Hydrocotyle verticillata for defence against copper exposure by integrative transcriptome and metabolome analysis

inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109836openalex-snapshot

Multi-omics reveal the molecular mechanisms of Sodium Nitrophenolate in enhancing cold tolerance through hormonal and antioxidant pathways in cucumber

inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111343openalex-snapshot

Effects of low temperature on energy metabolism during germination of foxtail millet (Setaria italica L.) seeds

inferred← citeshttps://doi.org/10.1016/j.plgene.2021.100344openalex-snapshot

Genome-wide exploration of auxin response factors (ARFs) and their expression dynamics in response to abiotic stresses and growth regulators in coconut (Cocos nucifera L.)

inferred← citeshttps://doi.org/10.1016/j.postharvbio.2022.112023openalex-snapshot

RNA-seq based analysis of transcriptomic changes associated with ABA-induced postharvest cold tolerance in zucchini fruit

inferred← citeshttps://doi.org/10.1016/j.postharvbio.2022.112088openalex-snapshot

Hormone profiling and heat-induced tolerance to cold stress in citrus fruit

inferred← citeshttps://doi.org/10.1016/j.postharvbio.2023.112299openalex-snapshot

Indole-3-acetic acid, a hormone potentially involved in chilling-induced seed browning of pepper (Capsicum annuum L.) fruit during cold storage

inferred← citeshttps://doi.org/10.1016/j.postharvbio.2025.113776openalex-snapshot

Indole-3-acetic acid-induced reactive oxygen species production increases chilling sensitivity in pepper (Capsicum annuum L.) fruit

inferred← citeshttps://doi.org/10.1016/j.sajb.2023.10.047openalex-snapshot

Calcium: A master regulator of stress tolerance in plants

inferred← citeshttps://doi.org/10.1016/j.scienta.2017.08.053openalex-snapshot

Adventitious root formation of in vitro peach shoots is regulated by auxin and ethylene

inferred← citeshttps://doi.org/10.1016/j.scienta.2022.110918openalex-snapshot

Physiological response of mango transplants to phytohormones under salinity stress

inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111256openalex-snapshot

Genome-wide identification of CmaGH3 family genes, and expression analysis in response to cold and hormonal stresses in Cucurbita maxima

inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111302openalex-snapshot

Plant hormone-mediated stress regulation responses in fruit crops- a review

inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112265openalex-snapshot

1-methylcyclopropene treatment improves chilling tolerance by regulating IAA biosynthesis, auxin signaling transduction and cell wall degradation in peach fruit

inferred← citeshttps://doi.org/10.1016/j.scienta.2026.114627openalex-snapshot

Integrative identification of regulatory genes for potato root development through GWAS, QTL mapping, and transcriptome analysis

inferred← citeshttps://doi.org/10.1016/j.stress.2023.100152openalex-snapshot

Role of phytohormones in regulating cold stress tolerance: Physiological and molecular approaches for developing cold-smart crop plants

inferred← citeshttps://doi.org/10.1016/j.stress.2024.100621openalex-snapshot

Plant growth promoting signatory volatiles emitted by a drought-tolerant bacterium Bacillus altitudinis FD48 and its role in moisture stress alleviation in rice (Oryza sativa L.)

inferred← citeshttps://doi.org/10.1016/j.stress.2025.100871openalex-snapshot

Transcriptome profiling of Anoectochilus roxburghii L. reveals spermidine-mediated response to drought stress

inferred← citeshttps://doi.org/10.1016/j.stress.2025.101034openalex-snapshot

Auxin metabolism and signaling: Integrating independent mechanisms and crosstalk in plant abiotic stress responses

inferred← citeshttps://doi.org/10.1016/j.stress.2025.101112openalex-snapshot

Morphological, physiological, biochemical, and transcriptome analysis of Phyllostachys edulis seedlings response to low potassium

inferred← citeshttps://doi.org/10.1016/j.stress.2025.101153openalex-snapshot

Plant drought stress: physiological, biochemical and molecular mechanisms

inferred← citeshttps://doi.org/10.1016/j.ygeno.2021.12.015openalex-snapshot

Genome-wide identification of auxin response factor (ARF) gene family and the miR160-ARF18-mediated response to salt stress in peanut (Arachis hypogaea L.)

inferred← citeshttps://doi.org/10.1016/j.ygeno.2023.110688openalex-snapshot

Comparative transcriptome analysis reveals the key genes and pathways involved in drought stress response of two wheat (Triticum aestivum L) varieties

inferred← citeshttps://doi.org/10.1016/s2095-3119(19)62556-6openalex-snapshot

Genome-wide identification and expression analysis of auxin response factor (ARF) gene family in strawberry (Fragaria vesca)

inferred← citeshttps://doi.org/10.1016/s2095-3119(20)63480-3openalex-snapshot

TaIAA15 genes regulate plant architecture in wheat

inferred← citeshttps://doi.org/10.1021/acs.jafc.2c07741openalex-snapshot

Root Hair Development and Adaptation to Abiotic Stress

inferred← citeshttps://doi.org/10.1021/acs.jafc.5c09033openalex-snapshot

Hierarchical Regulation and Adaptive Evolution of Higher Plants Under Abiotic Stress

inferred← citeshttps://doi.org/10.1021/acs.jafc.5c17008openalex-snapshot

Circadian Rhythms Mediate Jinggangmycin’s Suppression of Magnaporthe oryzae Pathogenicity

inferred← citeshttps://doi.org/10.1038/ncomms6087openalex-snapshot

Combining high-throughput phenotyping and genome-wide association studies to reveal natural genetic variation in rice

inferred← citeshttps://doi.org/10.1038/nplants.2017.77openalex-snapshot

MicroRNAs in crop improvement: fine-tuners for complex traits

inferred← citeshttps://doi.org/10.1038/s41467-025-59449-zopenalex-snapshot

Suppressing an auxin efflux transporter enhances rice adaptation to temperate habitats

inferred← citeshttps://doi.org/10.1038/s41598-018-27940-xopenalex-snapshot

Transcriptome analysis of two contrasting rice cultivars during alkaline stress

inferred← citeshttps://doi.org/10.1038/s41598-019-39397-7openalex-snapshot

The interaction between miR160 and miR165/166 in the control of leaf development and drought tolerance in Arabidopsis

inferred← citeshttps://doi.org/10.1038/s41598-021-00370-yopenalex-snapshot

Manganese toxicity disrupts indole acetic acid homeostasis and suppresses the CO2 assimilation reaction in rice leaves

inferred← citeshttps://doi.org/10.1038/s41598-021-90011-1openalex-snapshot

De novo transcriptome assembly and comparative transcriptomic analysis provide molecular insights into low temperature stress response of Canarium album

inferred← citeshttps://doi.org/10.1038/s41598-021-93820-6openalex-snapshot

Physiological and transcriptome analyses for assessing the effects of exogenous uniconazole on drought tolerance in hemp (Cannabis sativa L.)

inferred← citeshttps://doi.org/10.1038/s41598-024-61576-4openalex-snapshot

Integrated multi-omic approach reveals the effect of a Graminaceae-derived biostimulant and its lighter fraction on salt-stressed lettuce plants

inferred← citeshttps://doi.org/10.1038/s41598-025-17383-6openalex-snapshot

Transcriptomic profiling reveals Agave Lechuguilla extract as a multi-target pre-emergent bioherbicide candidate against Chenopodium album

inferred← citeshttps://doi.org/10.1071/fp18012openalex-snapshot

Chitosan and spermine enhance drought resistance in white clover, associated with changes in endogenous phytohormones and polyamines, and antioxidant metabolism

inferred← citeshttps://doi.org/10.1080/13102818.2023.2238847openalex-snapshot

Comparative transcriptome analysis of two varieties of common bean ( Phaseolus vulgaris L. ) to identify candidate drought resistance genes

inferred← citeshttps://doi.org/10.1080/15592324.2022.2065432openalex-snapshot

Functional redundancy of OsPIN1 paralogous genes in regulating plant growth and development in rice

inferred← citeshttps://doi.org/10.1080/17429145.2021.1925759openalex-snapshot

Insight into abscisic acid perception and signaling to increase plant tolerance to abiotic stress

inferred← citeshttps://doi.org/10.1093/aob/mcv053openalex-snapshot

Endogenous hormone concentrations correlate with fructan metabolism throughout the phenological cycle inChrysolaena obovata

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1093/hr/uhac122openalex-snapshot

Engineering drought-tolerant apple by knocking down six GH3 genes and potential application of transgenic apple as a rootstock

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/10.1093/jxb/eraa512openalex-snapshot

A genome-wide association study reveals that the glucosyltransferase OsIAGLU regulates root growth in rice

inferred← citeshttps://doi.org/10.1093/jxb/erab094openalex-snapshot

Potential interaction between autophagy and auxin during maize leaf senescence

inferred← citeshttps://doi.org/10.1093/jxb/erab124openalex-snapshot

Recognizing the hidden half in wheat: root system attributes associated with drought tolerance

inferred← citeshttps://doi.org/10.1093/jxb/erab334openalex-snapshot

Cold response and tolerance in cereal roots

inferred← citeshttps://doi.org/10.1093/jxb/erad071openalex-snapshot

Growth–defence trade-off in rice: fast-growing and acquisitive genotypes have lower expression of genes involved in immunity

inferred← citeshttps://doi.org/10.1093/jxb/eraf445openalex-snapshot

The chloroplast-localized ABC transporter OsABCB24 regulates aleurone cell size and grain nutritional quality in rice by modulating auxin homeostasis

inferred← citeshttps://doi.org/10.1093/jxb/ert139openalex-snapshot

Auxin: simply complicated

inferred← citeshttps://doi.org/10.1093/jxb/erv017openalex-snapshot

Common and specific responses to availability of mineral nutrients and water

inferred← citeshttps://doi.org/10.1093/jxb/erx008openalex-snapshot

Increasing carbon availability stimulates growth and secondary metabolites via modulation of phytohormones in winter wheat

inferred← citeshttps://doi.org/10.1093/jxb/erx228openalex-snapshot

Recent advances in auxin research in rice and their implications for crop improvement

inferred← citeshttps://doi.org/10.1093/jxb/erx309openalex-snapshot

Rice OVATE family protein 6 regulates plant development and confers resistance to drought and cold stresses

inferred← citeshttps://doi.org/10.1093/jxb/erx375openalex-snapshot

Auxin signaling: a big question to be addressed by small molecules

inferred← citeshttps://doi.org/10.1093/mp/ssu013openalex-snapshot

Short-Term and Continuing Stresses Differentially Interplay with Multiple Hormones to Regulate Plant Survival and Growth

inferred← citeshttps://doi.org/10.1093/pcp/pcab053openalex-snapshot

Increased Drought Resistance 1 Mutation Increases Drought Tolerance of Upland Rice by Altering Physiological and Morphological Traits and Limiting ROS Levels

inferred← citeshttps://doi.org/10.1093/pcp/pcab155openalex-snapshot

Auxin-Responsive (Phospho)proteome Analysis Reveals Key Biological Processes and Signaling Associated with Shoot-Borne Crown Root Development in Rice

inferred← citeshttps://doi.org/10.1093/pcp/pcac084openalex-snapshot

Genetic and Hormonal Blueprint of Shoot-Borne Adventitious Root Development in Rice and Maize

inferred← citeshttps://doi.org/10.1093/pcp/pcu212openalex-snapshot

The Characterization of Six Auxin-Induced Tomato GH3 Genes Uncovers a Member, SlGH3.4, Strongly Responsive to Arbuscular Mycorrhizal Symbiosis

inferred← citeshttps://doi.org/10.1093/pcp/pcx157openalex-snapshot

Enhanced Cold Tolerance and Tillering in Switchgrass (Panicum virgatum L.) by Heterologous Expression of Osa-miR393a

inferred← citeshttps://doi.org/10.1093/plcell/koab175openalex-snapshot

AUXIN RESPONSE FACTORS 6 and 17 control the flag leaf angle in rice by regulating secondary cell wall biosynthesis of lamina joints

inferred← citeshttps://doi.org/10.1093/plphys/kiab059openalex-snapshot

OsGRETCHENHAGEN3-2modulates rice seed storability via accumulation of abscisic acid and protective substances

inferred← citeshttps://doi.org/10.1093/plphys/kiad197openalex-snapshot

The trans -zeatin-type side-chain modification of cytokinins controls rice growth

inferred← citeshttps://doi.org/10.1093/plphys/kiae130openalex-snapshot

CALMODULIN-LIKE16 and PIN-LIKES7a cooperatively regulate rice seedling primary root elongation under chilling

inferred← citeshttps://doi.org/10.1093/plphys/kiae159openalex-snapshot

Transcription factor OsWRKY72 controls rice leaf angle by regulating LAZY1-mediated shoot gravitropism

inferred← citeshttps://doi.org/10.1093/plphys/kiaf577openalex-snapshot

The OsDREB1C-OsNAC3-OsGH3.2 module regulates seed germination in rice

inferred← citeshttps://doi.org/10.1093/plphys/kiag024openalex-snapshot

The transcription factor OsPIL13 regulates leaf inclination in rice by modulating brassinosteroid homeostasis

inferred← citeshttps://doi.org/10.1093/plphys/kiag191openalex-snapshot

Drought-responsive TaMIP1 controls root density to confer the tradeoff between grain yield and drought resistance in wheat

inferred← citeshttps://doi.org/10.1101/2020.08.24.264556openalex-snapshot

Mutation of IDR1 enhances drought tolerance by reducing ROS production and activating ROS scavenging in rice

inferred← citeshttps://doi.org/10.1101/2021.09.24.461718openalex-snapshot

Inactivation of the entire Arabidopsis group II GH3s confers tolerance to salinity and drought

inferred← citeshttps://doi.org/10.1101/cshperspect.a039867openalex-snapshot

Auxin Metabolism in Plants

inferred← citeshttps://doi.org/10.1101/cshperspect.a040014openalex-snapshot

Uncovering How Auxin Optimizes Root Systems Architecture in Response to Environmental Stresses

inferred← citeshttps://doi.org/10.1104/pp.15.01863openalex-snapshot

Auxin and Cellular Elongation

inferred← citeshttps://doi.org/10.1104/pp.17.00413openalex-snapshot

Dynamic Cytology and Transcriptional Regulation of Rice Lamina Joint Development

inferred← citeshttps://doi.org/10.1104/pp.19.00248openalex-snapshot

Wheat TaSPL8 Modulates Leaf Angle Through Auxin and Brassinosteroid Signaling

inferred← citeshttps://doi.org/10.1104/pp.19.01364openalex-snapshot

OsNAR2.1 Interaction with OsNIT1 and OsNIT2 Functions in Root-growth Responses to Nitrate and Ammonium

inferred← citeshttps://doi.org/10.1105/tpc.114.124388openalex-snapshot

mRNA and Small RNA Transcriptomes Reveal Insights into Dynamic Homoeolog Regulation of Allopolyploid Heterosis in Nascent Hexaploid Wheat

inferred← citeshttps://doi.org/10.1105/tpc.18.00528openalex-snapshot

Phosphatidic Acid Directly Regulates PINOID-Dependent Phosphorylation and Activation of the PIN-FORMED2 Auxin Efflux Transporter in Response to Salt Stress

inferred← citeshttps://doi.org/10.1111/jipb.12327openalex-snapshot

Genome‐wide identification, expression analysis of auxin‐responsive GH3 family genes in maize ( Zea mays L.) under abiotic stresses

inferred← citeshttps://doi.org/10.1111/jipb.12713openalex-snapshot

Rice miR394 suppresses leaf inclination through targeting an F‐box gene, LEAF INCLINATION 4

inferred← citeshttps://doi.org/10.1111/jipb.12852openalex-snapshot

Coordination of light, circadian clock with temperature: The potential mechanisms regulating chilling tolerance in rice

inferred← citeshttps://doi.org/10.1111/nph.16862openalex-snapshot

Bridging the genotype–phenotype gap for a Mediterranean pine by semi‐automatic crown identification and multispectral imagery

inferred← citeshttps://doi.org/10.1111/nph.18114openalex-snapshot

Inactivation of the entire Arabidopsis group II GH3s confers tolerance to salinity and water deficit

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