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Genome-wide identification, expression analysis of GH3 family genes in Medicago truncatula under stress-related hormones and Sinorhizobium meliloti infection
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Auxin-regulated gene expression in intact soybean hypocotyl and excised hypocotyl sections
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Arabidopsis thaliana GH3.9 influences primary root growth
inferredcites →https://doi.org/10.1007/s00438-011-0602-7openalex-snapshot
Genome-wide analysis of auxin response factor (ARF) gene family from tomato and analysis of their role in flower and fruit development
inferredcites →https://doi.org/10.1007/s00438-011-0672-6openalex-snapshot
Genome-wide investigation and expression analysis suggest diverse roles of auxin-responsive GH3 genes during development and response to different stimuli in tomato (Solanum lycopersicum)
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/s10265-011-0412-3openalex-snapshot
ABA-mediated transcriptional regulation in response to osmotic stress in plants
inferredcites →https://doi.org/10.1007/s11105-010-0266-1openalex-snapshot
Truncation of Medicago truncatula Auxin Conjugate Hydrolases Alters Substrate Specificity
inferredcites →https://doi.org/10.1016/j.bbagrm.2011.09.002openalex-snapshot
The role of WRKY transcription factors in plant abiotic stresses
inferredcites →https://doi.org/10.1016/j.jplph.2012.10.016openalex-snapshot
GH3 expression and IAA-amide synthetase activity in pea (Pisum sativum L.) seedlings are regulated by light, plant hormones and auxinic herbicides
inferredcites →https://doi.org/10.1016/j.pbi.2004.05.006openalex-snapshot
NPR1: the spider in the web of induced resistance signaling pathways
inferredcites →https://doi.org/10.1021/pr4009942openalex-snapshot
Local and Systemic Proteomic Changes in Medicago Truncatula at an Early Phase of Sinorhizobium meliloti Infection
inferredcites →https://doi.org/10.1038/35080508openalex-snapshot
The arms race is ancient history in Arabidopsis, the wildflower
inferredcites →https://doi.org/10.1038/nature01521openalex-snapshot
Unravelling angiosperm genome evolution by phylogenetic analysis of chromosomal duplication events
inferredcites →https://doi.org/10.1038/nature09430openalex-snapshot
Jasmonate perception by inositol-phosphate-potentiated COI1–JAZ co-receptor
inferredcites →https://doi.org/10.1038/ncomms1009openalex-snapshot
The molecular network governing nodule organogenesis and infection in the model legume Lotus japonicus
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00090.xopenalex-snapshot
Auxin transport inhibition precedes root nodule formation in white clover roots and is regulated by flavonoids and derivatives of chitin oligosaccharides
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00957.xopenalex-snapshot
DFL1, an auxin-responsive GH3 gene homologue, negatively regulates shoot cell elongation and lateral root formation, and positively regulates the light response of hypocotyl length
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01973.xopenalex-snapshot
ydk1‐D , an auxin‐responsive GH3 mutant that is involved in hypocotyl and root elongation
inferredcites →https://doi.org/10.1073/pnas.230439797openalex-snapshot
Genetic analysis of calcium spiking responses in nodulation mutants of Medicago truncatula
inferredcites →https://doi.org/10.1073/pnas.95.25.14863openalex-snapshot
Cluster analysis and display of genome-wide expression patterns
inferredcites →https://doi.org/10.1074/jbc.m610524200openalex-snapshot
GH3-mediated Auxin Homeostasis Links Growth Regulation with Stress Adaptation Response in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m806662200openalex-snapshot
Arabidopsis GH3.12 (PBS3) Conjugates Amino Acids to 4-Substituted Benzoates and Is Inhibited by Salicylate
inferredcites →https://doi.org/10.1093/aob/mci083openalex-snapshot
Auxin: Regulation, Action, and Interaction
inferredcites →https://doi.org/10.1093/aob/mct229openalex-snapshot
Auxin and the integration of environmental signals into plant root development
inferredcites →https://doi.org/10.1093/jxb/erq174openalex-snapshot
Sequestration of auxin by the indole-3-acetic acid-amido synthetase GH3-1 in grape berry (Vitis vinifera L.) and the proposed role of auxin conjugation during ripening
inferredcites →https://doi.org/10.1093/jxb/erq412openalex-snapshot
Auxin conjugates: their role for plant development and in the evolution of land plants
inferredcites →https://doi.org/10.1093/jxb/err134openalex-snapshot
Acyl substrate preferences of an IAA-amido synthetase account for variations in grape (Vitis vinifera L.) berry ripening caused by different auxinic compounds indicating the importance of auxin conjugation in plant development
inferredcites →https://doi.org/10.1093/jxb/ers300openalex-snapshot
A GH3 family member, OsGH3-2, modulates auxin and abscisic acid levels and differentially affects drought and cold tolerance in rice
inferredcites →https://doi.org/10.1093/mp/ssm021openalex-snapshot
Comprehensive Transcriptome Analysis of Auxin Responses in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcg130openalex-snapshot
DFL2, a New Member of the Arabidopsis GH3 Gene Family, is Involved in Red Light-Specific Hypocotyl Elongation
inferredcites →https://doi.org/10.1093/pcp/pcq004openalex-snapshot
The Function of LPR1 is Controlled by an Element in the Promoter and is Independent of SUMO E3 Ligase SIZ1 in Response to Low Pi Stress in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pct047openalex-snapshot
ZmLEA3, a Multifunctional Group 3 LEA Protein from Maize (Zea mays L.), is Involved in Biotic and Abiotic Stresses
inferredcites →https://doi.org/10.1093/treephys/20.2.123openalex-snapshot
Dynamics of symbiotic establishment between an IAA-overproducing mutant of the ectomycorrhizal fungus Hebeloma cylindrosporum and Pinus pinaster
inferredcites →https://doi.org/10.1093/treephys/21.8.533openalex-snapshot
Fungal auxin overproduction affects the anatomy of Hebeloma cylindrosporum-Pinus pinaster ectomycorrhizas
inferredcites →https://doi.org/10.1094/mpmi-04-11-0103openalex-snapshot
Pseudonodule Formation by Wild-Type and Symbiotic Mutant Medicago truncatula in Response to Auxin Transport Inhibitors
inferredcites →https://doi.org/10.1094/mpmi-20-6-0619openalex-snapshot
Tryptophan-Dependent Production of Indole-3-Acetic Acid (IAA) Affects Level of Plant Growth Promotion by Bacillus amyloliquefaciens FZB42
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/10.1104/pp.010691openalex-snapshot
Pharmacological Analysis of Nod Factor-Induced Calcium Spiking inMedicago truncatula. Evidence for the Requirement of Type IIA Calcium Pumps and Phosphoinositide Signaling
inferredcites →https://doi.org/10.1104/pp.105.060004openalex-snapshot
Ubiquitin-Mediated Proteolysis. To Be in the Right Place at the Right Moment during Nodule Development
inferredcites →https://doi.org/10.1104/pp.105.075879openalex-snapshot
Defective Long-Distance Auxin Transport Regulation in the Medicago truncatula super numeric nodules Mutant
inferredcites →https://doi.org/10.1104/pp.106.084871openalex-snapshot
Transcriptional Regulation of Gibberellin Metabolism Genes by Auxin Signaling in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.097691openalex-snapshot
The GH3 Acyl Adenylase Family Member PBS3 Regulates Salicylic Acid-Dependent Defense Responses in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.099978openalex-snapshot
Overlap of Proteome Changes inMedicago truncatulain Response to Auxin andSinorhizobium meliloti
inferredcites →https://doi.org/10.1104/pp.107.100404openalex-snapshot
Mutation ofE1-CONJUGATING ENZYME-RELATED1Decreases RELATED TO UBIQUITIN Conjugation and Alters Auxin Response and Development
inferredcites →https://doi.org/10.1104/pp.107.106021openalex-snapshot
Dual Regulation Role of GH3.5 in Salicylic Acid and Auxin Signaling during Arabidopsis-Pseudomonas syringae Interaction
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/10.1105/tpc.000596openalex-snapshot
Cell Signaling during Cold, Drought, and Salt Stress
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.010289openalex-snapshot
AUX/IAA Proteins Are Active Repressors, and Their Stability and Activity Are Modulated by Auxin
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.112.099119openalex-snapshot
Auxin Controls Arabidopsis Adventitious Root Initiation by Regulating Jasmonic Acid Homeostasis
inferredcites →https://doi.org/10.1105/tpc.112.102921openalex-snapshot
Crystal Structure of an Indole-3-Acetic Acid Amido Synthetase from Grapevine Involved in Auxin Homeostasis
inferredcites →https://doi.org/10.1105/tpc.13.12.2809openalex-snapshot
AUX/IAA Proteins Are Active Repressors, and Their Stability and Activity Are Modulated by Auxin
inferredcites →https://doi.org/10.1105/tpc.4.4.485openalex-snapshot
Sequences Flanking the Hexameric G-Box Core CACGTG Affect the Specificity of Protein Binding
inferredcites →https://doi.org/10.1105/tpc.6.5.645openalex-snapshot
Soybean GH3 Promoter Contains Multiple Auxin-Inducible Elements
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01677.xopenalex-snapshot
The auxin‐inducible GH3 homologue Pp‐GH3.16 is downregulated in Pinus pinaster root systems on ectomycorrhizal symbiosis establishment
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02677.xopenalex-snapshot
Moss ( Physcomitrella patens ) GH3 proteins act in auxin homeostasis
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/nph.12550openalex-snapshot
The REL 3‐mediated TAS 3 ta‐si RNA pathway integrates auxin and ethylene signaling to regulate nodulation in L otus japonicus
inferredcites →https://doi.org/10.1111/nph.12613openalex-snapshot
ABA control of plant macroelement membrane transport systems in response to water deficit and high salinity
inferredcites →https://doi.org/10.1111/pce.12397openalex-snapshot
The auxin response factor, OsARF 19, controls rice leaf angles through positively regulating OsGH 3‐5 and OsBRI 1
inferredcites →https://doi.org/10.1126/science.1118642openalex-snapshot
Integration of Plant Responses to Environmentally Activated Phytohormonal Signals
inferredcites →https://doi.org/10.1126/science.1221863openalex-snapshot
Structural Basis for Prereceptor Modulation of Plant Hormones by GH3 Proteins
inferredcites →https://doi.org/10.1126/science.276.5320.1865openalex-snapshot
ARF1, a Transcription Factor That Binds to Auxin Response Elements
inferredcites →https://doi.org/10.1126/science.290.5499.2114openalex-snapshot
The Origins of Genomic Duplications in Arabidopsis
inferredcites →https://doi.org/10.1128/aem.01397-06openalex-snapshot
An Integrated Approach to Functional Genomics: Construction of a Novel Reporter Gene Fusion Library forSinorhizobium meliloti
inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154055openalex-snapshot
Hormonal Modulation of Plant Immunity
inferredcites →https://doi.org/10.1146/annurev.arplant.043008.092007openalex-snapshot
Jasmonate Passes Muster: A Receptor and Targets for the Defense Hormone
inferredcites →https://doi.org/10.1146/annurev.cellbio.23.090506.123214openalex-snapshot
Auxin Receptors and Plant Development: A New Signaling Paradigm
inferredcites →https://doi.org/10.1186/1471-2164-14-297openalex-snapshot
Genome-wide analysis of the GH3 family in apple (Malus × domestica)
inferredcites →https://doi.org/10.1186/s12870-014-0245-zopenalex-snapshot
GmPRP2 promoter drives root-preferential expression in transgenic Arabidopsis and soybean hairy roots
inferredcites →https://doi.org/10.1371/journal.pone.0060355openalex-snapshot
Regulatory Patterns of a Large Family of Defensin-Like Genes Expressed in Nodules of Medicago truncatula
inferredcites →https://doi.org/10.1371/journal.pone.0107495openalex-snapshot
Genome-Wide Identification and Expression Profiling Analysis of the Aux/IAA Gene Family in Medicago truncatula during the Early Phase of Sinorhizobium meliloti Infection
inferredcites →https://doi.org/10.3389/fpls.2012.00096openalex-snapshot
Modeling a Cortical Auxin Maximum for Nodulation: Different Signatures of Potential Strategies
inferredcites →https://doi.org/10.4161/psb.5.12.13941openalex-snapshot
Modulating plant hormones by enzyme action
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The GH3 amidosynthetases family and their role in metabolic crosstalk modulation of plant signaling compounds
inferred← citeshttps://doi.org/10.1002/9781119409144.part10openalex-snapshot
Hormones and the rhizobial and mycorrhizal symbioses: introduction
inferred← citeshttps://doi.org/10.1007/978-3-319-31703-8_9openalex-snapshot
Identification of Gene Families Using Genomics and/or Transcriptomics Data
inferred← citeshttps://doi.org/10.1007/s00438-015-1063-1openalex-snapshot
The ARF, AUX/IAA and GH3 gene families in citrus: genome-wide identification and expression analysis during fruitlet drop from abscission zone A
inferred← citeshttps://doi.org/10.1007/s11033-018-4216-6openalex-snapshot
Prediction of auxin response elements based on data fusion in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11033-020-05477-5openalex-snapshot
Genome-wide identification, characterization analysis and expression profiling of auxin-responsive GH3 family genes in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.1007/s11033-020-05529-wopenalex-snapshot
Identification and expression analysis of auxin-responsive GH3 family genes in Chinese hickory (Carya cathayensis) during grafting
inferred← citeshttps://doi.org/10.1007/s12042-024-09356-2openalex-snapshot
Identification and Expression Profiles of Auxin-Related Gene Families Involved in Fiber Development in Jute (Corchorus capsularis)
inferred← citeshttps://doi.org/10.1007/s13562-018-0477-3openalex-snapshot
Identification and initial characterization of a new subgroup in the GH3 gene family in woody plants
inferred← citeshttps://doi.org/10.1007/s13562-021-00657-1openalex-snapshot
Genome-wide identification, characterization, and expression profiles of auxin responsive GH3 gene family in Salvia miltiorrhiza involved in MeJA treatment
inferred← citeshttps://doi.org/10.1016/j.gene.2022.146982openalex-snapshot
Molecular characterization of the GH3 family in alfalfa under abiotic stress
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.120558openalex-snapshot
Microscopic and transcriptomic comparison of the ovaries between the sexual and apomictic dandelions reveals the developmental process and gene regulation in regard to apomixis
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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.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.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.tplants.2019.05.006openalex-snapshot
Auxin Metabolism Controls Developmental Decisions in Land Plants
inferred← citeshttps://doi.org/10.1038/s41598-018-29627-9openalex-snapshot
Genome-wide Identification of PP2C Genes and Their Expression Profiling in Response to Drought and Cold Stresses in Medicago truncatula
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Common gene expression patterns are observed in rice roots during associations with plant growth-promoting bacteria, Herbaspirillum seropedicae and Azospirillum brasilense
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Involvement of endogenous salicylic acid in iron-deficiency responses in Arabidopsis
inferred← citeshttps://doi.org/10.1094/mpmi-03-19-0069-cropenalex-snapshot
Genius Architect or Clever Thief—How Plasmodiophora brassicae Reprograms Host Development to Establish a Pathogen-Oriented Physiological Sink
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Reduction of indole‐3‐acetic acid methyltransferase activity compensates for high‐temperature male sterility in Arabidopsis
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Induction of Plant Defences and Production of Kaempferol‐7‐O‐Glucoside Against Spodoptera litura in Resistant Wild Mungbean
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STENOFOLIA gene and regulation of somatic embryogenesis in Medicago truncatula
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Evolution of Hormone Signaling Networks in Plant Defense
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Functional characterization of Gh_A08G1120 (GH3.5) gene reveal their significant role in enhancing drought and salt stress tolerance in cotton
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Genome-wide analysis, transcription factor network approach and gene expression profile of GH3 genes over early somatic embryogenesis in Coffea spp
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Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
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Genome-wide analysis of cotton GH3 subfamily II reveals functional divergence in fiber development, hormone response and plant architecture
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Evolution analysis of GH3 gene family in five Rosaceae species and FaGH3.17, FaGH3.18 improve drought tolerance in transgenic Arabidopsis
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Overexpressing GH3.1 and GH3.1L reduces susceptibility to Xanthomonas citri subsp. citri by repressing auxin signaling in citrus (Citrus sinensis Osbeck)
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Evolutionary History of the GH3 Family Based on 48 Sequenced Plants and Identification of Jasmonic Acid-Relate GH3 Genes in Solanum tuberosum
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Production of the Plant Hormone Auxin by Salmonella and Its Role in the Interactions with Plants and Animals
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Identification, Expression and IAA-Amide Synthetase Activity Analysis of Gretchen Hagen 3 in Papaya Fruit (Carica papaya L.) during Postharvest Process
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Mini-Review: Nod Factor Regulation of Phytohormone Signaling and Homeostasis During Rhizobia-Legume Symbiosis
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TMT-Based Quantitative Proteomic Analysis Reveals the Response of Tomato (Solanum lycopersicum L.) Seedlings to Ebb-and-Flow Subirrigation
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Genome-Wide Analysis of the GH3 Gene Family in Nicotiana benthamiana and Its Role in Plant Defense Against Tomato Yellow Leaf Curl Virus
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The Gene Structure and Expression Level Changes of the GH3 Gene Family in Brassica napus Relative to Its Diploid Ancestors
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Nodule-Enriched GRETCHEN HAGEN 3 Enzymes Have Distinct Substrate Specificities and Are Important for Proper Soybean Nodule Development
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Evolutionary History of the Glycoside Hydrolase 3 (GH3) Family Based on the Sequenced Genomes of 48 Plants and Identification of Jasmonic Acid-Related GH3 Proteins in Solanum tuberosum
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Bacterial IAA-Delivery into Medicago Root Nodules Triggers a Balanced Stimulation of C and N Metabolism Leading to a Biomass Increase
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Evolutionary Analysis of GH3 Genes in Six Oryza Species/Subspecies and Their Expression under Salinity Stress in Oryza sativa ssp. japonica
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Additional file 1 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535752openalex-snapshot
Additional file 2 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535758openalex-snapshot
Additional file 3 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535761openalex-snapshot
Additional file 4 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535767openalex-snapshot
Additional file 5 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535773openalex-snapshot
Additional file 7 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535776openalex-snapshot
Additional file 8 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.70675/4d4d8f0bz1ab8z499bz865fz69350644d14copenalex-snapshot
Vers la compréhension de la stimulation du développement racinaire par les signaux symbiotiques chez les légumineuses
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