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Kinetic Basis for the Conjugation of Auxin by a GH3 Family Indole-acetic Acid-Amido Synthetase
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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/bf00410211openalex-snapshot
Auxin-regulated gene expression in intact soybean hypocotyl and excised hypocotyl sections
inferredcites →https://doi.org/10.1007/s00425-006-0462-2openalex-snapshot
Arabidopsis thaliana GH3.9 influences primary root growth
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/s10725-008-9313-4openalex-snapshot
Research progresses on GH3s, one family of primary auxin-responsive genes
inferredcites →https://doi.org/10.1007/s11103-005-6505-4openalex-snapshot
A GH3-like gene, CcGH3, isolated from Capsicum chinense L. fruit is regulated by auxin and ethylene*
inferredcites →https://doi.org/10.1016/0020-711x(94)90021-3openalex-snapshot
Enzyme kinetics; behavior and analysis of rapid equilibrium and steady state enzyme systems
inferredcites →https://doi.org/10.1016/j.ab.2009.04.027openalex-snapshot
A liquid chromatography–tandem mass spectrometry-based assay for indole-3-acetic acid–amido synthetase
inferredcites →https://doi.org/10.1016/j.gene.2005.12.014openalex-snapshot
The GH3 family in plants: Genome wide analysis in rice and evolutionary history based on EST analysis
inferredcites →https://doi.org/10.1016/j.jplph.2003.12.010openalex-snapshot
Loss of GH3 function does not affect phytochrome-mediated development in a moss, Physcomitrella patens
inferredcites →https://doi.org/10.1016/s0014-5793(97)01447-6openalex-snapshot
Isolation by differential display and characterization of a tobacco auxin‐responsive cDNA Nt‐gh3, related to GH3
inferredcites →https://doi.org/10.1016/s0021-9258(18)61815-0openalex-snapshot
Kinetic Studies of the Prolyl Transfer Ribonucleic Acid Synthetase of Escherichia coli
inferredcites →https://doi.org/10.1016/s0021-9258(18)63426-xopenalex-snapshot
The Aminoacyl Transfer Ribonucleic Acid Synthetases
inferredcites →https://doi.org/10.1021/bi011522+openalex-snapshot
Steady-State and Pre-Steady-State Kinetic Analysis of Mycobacterium tuberculosis Pantothenate Synthetase
inferredcites →https://doi.org/10.1021/bi0355701openalex-snapshot
Induced Fit and Kinetic Mechanism of Adenylation Catalyzed by Escherichia coli Threonyl-tRNA Synthetase
inferredcites →https://doi.org/10.1021/bi7011492openalex-snapshot
Steady-State and Pre-steady-State Kinetic Analysis of Mycobacterium smegmatis Cysteine Ligase (MshC)
inferredcites →https://doi.org/10.1023/a:1015207114117openalex-snapshot
Auxin-responsive gene expression: genes, promoters and regulatory factors
inferredcites →https://doi.org/10.1023/a:1015298812300openalex-snapshot
Biosynthesis, conjugation, catabolism and homeostasis of indole-3-acetic acid in Arabidopsis thaliana
inferredcites →https://doi.org/10.1023/a:1016024017872openalex-snapshot
Biosynthesis, conjugation, catabolism and homeostasis of indole-3-acetic acid in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/nature03542openalex-snapshot
The Arabidopsis F-box protein TIR1 is an auxin receptor
inferredcites →https://doi.org/10.1038/nature03543openalex-snapshot
The F-box protein TIR1 is an auxin receptor
inferredcites →https://doi.org/10.1038/nature06006openalex-snapshot
The JAZ family of repressors is the missing link in jasmonate signalling
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/10.1042/bj2970327openalex-snapshot
Steady-state kinetics of malonyl-CoA synthetase from Bradyrhizobium japonicum and evidence for malonyl-AMP formation in the reaction
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/10.1074/jbc.m006413200openalex-snapshot
Affinity Labeling Fatty Acyl-CoA Synthetase with 9-p-Azidophenoxy Nonanoic Acid and the Identification of the Fatty Acid-binding Site
inferredcites →https://doi.org/10.1074/jbc.m111955200openalex-snapshot
Characterization of a Family of IAA-Amino Acid Conjugate Hydrolases from Arabidopsis
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/pcp/pcf033openalex-snapshot
Expression of the AtGH3a Gene, an Arabidopsis Homologue of the Soybean GH3 Gene, is Regulated by Phytochrome B
inferredcites →https://doi.org/10.1093/pcp/pcm086openalex-snapshot
An Arabidopsis GH3 Gene, Encoding an Auxin-Conjugating Enzyme, Mediates Phytochrome B-Regulated Light Signals in Hypocotyl Growth
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/10.1094/mpmi.2004.17.12.1394openalex-snapshot
Induction of Phytohormones and Differential Gene Expression in Citrus Flowers Infected by the Fungus Colletotrichum acutatum
inferredcites →https://doi.org/10.1104/pp.104.039677openalex-snapshot
A Family of Auxin-Conjugate Hydrolases That Contributes to Free Indole-3-Acetic Acid Levels during Arabidopsis Germination
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.107.106021openalex-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.107.115691openalex-snapshot
Regulation and Function of Arabidopsis JASMONATE ZIM -Domain Genes in Response to Wounding and Herbivory
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.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.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.107.050708openalex-snapshot
A Downstream Mediator in the Growth Repression Limb of the Jasmonate Pathway
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/10.1111/j.1365-313x.2007.03130.xopenalex-snapshot
Arabidopsis GH3‐LIKE DEFENSE GENE 1 is required for accumulation of salicylic acid, activation of defense responses and resistance to Pseudomonas syringae
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/10.1128/mcb.5.6.1197openalex-snapshot
Rapid Induction of Selective Transcription by Auxins
inferredcites →https://doi.org/10.4161/psb.2.6.4498openalex-snapshot
Arabidopsis thalianaGH3.9 in Auxin and Jasmonate Cross Talk
inferredcites →https://doi.org/10.4161/psb.3.8.5748openalex-snapshot
Arabidopsis GH3.5 regulates salicylic acid-dependent and both NPR1-dependent and independent defense responses
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.113039zenodo-depositor-declared
The GH3 amidosynthetases family and their role in metabolic crosstalk modulation of plant signaling compounds
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113103zenodo-depositor-declared
Identification of TabZIP family members with possible roles in the response to auxin in wheat roots
inferred← citeshttps://doi.org/10.1002/9781118742921.ch4.1openalex-snapshot
Use of Chemical Biology to Understand Auxin Metabolism, Signaling, and Polar Transport
inferred← citeshttps://doi.org/10.1002/jsfa.70646openalex-snapshot
Honeybee pollination enhances pollen germination, pollen tube growth, phytohormone responses and gene expression in pear pistils
inferred← citeshttps://doi.org/10.1002/ps.71100openalex-snapshot
Amplification of a metabolic shunt for elicitor detoxification: a jasmonate‐exploited insect counter‐defense strategy
inferred← citeshttps://doi.org/10.1007/978-3-319-33705-0_6openalex-snapshot
Epigenetic Advances in Somatic Embryogenesis in Sequenced Genome Crops
inferred← citeshttps://doi.org/10.1007/978-3-319-55520-1_2openalex-snapshot
The Role of MiRNAs in Auxin Signaling and Regulation During Plant Development
inferred← citeshttps://doi.org/10.1007/978-3-319-91352-0_5openalex-snapshot
Structural Biology of Jasmonic Acid Metabolism and Responses in Plants
inferred← citeshttps://doi.org/10.1007/978-94-017-9285-1_6openalex-snapshot
Auxin Signaling System in Plant Innate Immunity
inferred← citeshttps://doi.org/10.1007/s00425-022-04011-0openalex-snapshot
Map-based cloning and transcriptome analysis of the more-tiller and small-grain mutant in rice
inferred← citeshttps://doi.org/10.1007/s00425-026-05083-yopenalex-snapshot
Metabolism meets transport: a new perspective on auxin homeostasis at subcellular level
inferred← citeshttps://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)
inferred← citeshttps://doi.org/10.1007/s00468-019-01904-8openalex-snapshot
A GH3-like gene, LaGH3, isolated from hybrid larch (Larix leptolepis × Larix olgensis) is regulated by auxin and abscisic acid during somatic embryogenesis
inferred← citeshttps://doi.org/10.1007/s10265-022-01387-8openalex-snapshot
Transcriptome revealing the dual regulatory mechanism of ethylene on the rhynchophylline and isorhynchophylline in Uncaria rhynchophylla
inferred← citeshttps://doi.org/10.1007/s10265-024-01602-8openalex-snapshot
Hormone functions in adventitious root formation during cutting propagation of woody plants
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/s11105-011-0306-5openalex-snapshot
Time-Course Analysis of Levels of Indole-3-Acetic Acid and Expression of Auxin-Responsive GH3 Genes in Betula platyphylla
inferred← citeshttps://doi.org/10.1007/s12038-020-00062-1openalex-snapshot
miRNA-mediated regulation of auxin signaling pathway during plant development and stress responses
inferred← citeshttps://doi.org/10.1007/s13562-014-0269-3openalex-snapshot
MicroRNAs as regulators of adventitious root development
inferred← citeshttps://doi.org/10.1016/b978-0-323-90636-4.00011-8openalex-snapshot
Molecular control of adventitious root formation
inferred← citeshttps://doi.org/10.1016/b978-0-443-30244-2.00015-4openalex-snapshot
Auxin receptors: Pivotal regulators of plant development
inferred← citeshttps://doi.org/10.1016/j.algal.2025.104316openalex-snapshot
Hormonal cross-talk in DHA biosynthesis: Regulatory roles of auxin and jasmonic acid in Schizochytrium spp. and Crypthecodinium cohnii
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.11.098openalex-snapshot
Crystal structure of the acyl acid amido synthetase GH3-8 from Oryza sativa
inferred← citeshttps://doi.org/10.1016/j.jbc.2024.107421openalex-snapshot
Fidelity in plant hormone modifications catalyzed by Arabidopsis GH3 acyl acid amido synthetases
inferred← citeshttps://doi.org/10.1016/j.jbc.2025.110634openalex-snapshot
A biosynthetic pathway for ornithine lipid formation dependent on a GH3 (Gretchen Hagen 3)-like enzyme in planctomycetes
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.pbi.2022.102194openalex-snapshot
Connecting primary and specialized metabolism: Amino acid conjugation of phytohormones by GRETCHEN HAGEN 3 (GH3) acyl acid amido synthetases
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.07.001openalex-snapshot
Preference of Arabidopsis thaliana GH3.5 acyl amido synthetase for growth versus defense hormone acyl substrates is dictated by concentration of amino acid substrate aspartate
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111638openalex-snapshot
SlGH3.15, a member of the GH3 gene family, regulates lateral root development and gravitropism response by modulating auxin homeostasis in tomato
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111866openalex-snapshot
The many faces of lysine acylation in proteins: Phytohormones as unexplored substrates
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112904openalex-snapshot
An Integrative morphology–hormone–transcriptome analysis of uniconazole induced internode shortening in Paeonia lactiflora
inferred← citeshttps://doi.org/10.1016/j.plaphy.2016.05.031openalex-snapshot
Cloning and biochemical characterization of indole-3-acetic acid-amino acid synthetase PsGH3 from pea
inferred← citeshttps://doi.org/10.1016/j.scienta.2019.109030openalex-snapshot
Genome-based identification and analysis of the genes involved in auxin biosynthesis and signal transduction during tea plant leaf development
inferred← citeshttps://doi.org/10.1016/j.scienta.2021.110026openalex-snapshot
Cytokinin and auxin modulate cucumber parthenocarpy fruit development
inferred← citeshttps://doi.org/10.1016/j.scienta.2021.110061openalex-snapshot
Sugars enhance parthenocarpic fruit formation in cucumber by promoting auxin and cytokinin signaling
inferred← citeshttps://doi.org/10.1016/j.synbio.2015.12.001openalex-snapshot
Informatic analysis reveals Legionella as a source of novel natural products
inferred← citeshttps://doi.org/10.1016/s2095-3119(15)61076-0openalex-snapshot
Identification and characterization of the GH3 gene family in maize
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c05908openalex-snapshot
Identification of a Novel 2,4- D Metabolic Detoxification Pathway in 2,4- D -Resistant Waterhemp (Amaranthus tuberculatus)
inferred← citeshttps://doi.org/10.1038/nchembio.1591openalex-snapshot
A chemical inhibitor of jasmonate signaling targets JAR1 in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/s41598-024-57506-zopenalex-snapshot
THOUSAND-GRAIN WEIGHT 6, which is an IAA-glucose hydrolase, preferentially recognizes the structure of the indole ring
inferred← citeshttps://doi.org/10.1039/c4mb00608aopenalex-snapshot
Structural and dynamic basis of acid amido synthetase GH3.1: an investigation of substrate selectivity and major active site access channels
inferred← citeshttps://doi.org/10.1073/pnas.1612635113openalex-snapshot
Arabidopsis thaliana GH3.5 acyl acid amido synthetase mediates metabolic crosstalk in auxin and salicylic acid homeostasis
inferred← citeshttps://doi.org/10.1073/pnas.2206869119openalex-snapshot
Chemical inhibition of the auxin inactivation pathway uncovers the roles of metabolic turnover in auxin homeostasis
inferred← citeshttps://doi.org/10.1073/pnas.2209256119openalex-snapshot
Chemical genetic screening identifies nalacin as an inhibitor of GH3 amido synthetase for auxin conjugation
inferred← citeshttps://doi.org/10.1074/jbc.r113.475160openalex-snapshot
Enzyme Action in the Regulation of Plant Hormone Responses
inferred← citeshttps://doi.org/10.1074/jbc.ra118.002006openalex-snapshot
Arabidopsis thaliana GH3.15 acyl acid amido synthetase has a highly specific substrate preference for the auxin precursor indole-3-butyric acid
inferred← citeshttps://doi.org/10.1074/jbc.ra118.004975openalex-snapshot
Modification of auxinic phenoxyalkanoic acid herbicides by the acyl acid amido synthetase GH3.15 from Arabidopsis
inferred← citeshttps://doi.org/10.1074/jbc.ra119.009949openalex-snapshot
Brassicaceae-specific Gretchen Hagen 3 acyl acid amido synthetases conjugate amino acids to chorismate, a precursor of aromatic amino acids and salicylic acid
inferred← citeshttps://doi.org/10.1080/07352689.2015.1090831openalex-snapshot
Physiological and Molecular Regulation of Adventitious Root Formation
inferred← citeshttps://doi.org/10.1080/17429145.2021.2006328openalex-snapshot
RNA-seq reveals that multiple plant hormones are regulated by Bacillus cereus G2 in Glycyrrhiza uralensis subjected to salt stress
inferred← citeshttps://doi.org/10.1093/jxb/erae054openalex-snapshot
Epigenetics and plant hormone dynamics: a functional and methodological perspective
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1093/jxb/ery273openalex-snapshot
Modulation of plant architecture by the miR156f–OsSPL7–OsGH3.8 pathway in rice
inferred← citeshttps://doi.org/10.1093/jxb/erz552openalex-snapshot
Morphological and stage-specific transcriptome analyses reveal distinct regulatory programs underlying yam (Dioscorea alata L.) bulbil growth
inferred← citeshttps://doi.org/10.1093/pcp/pcs035openalex-snapshot
The Interaction and Integration of Auxin Signaling Components
inferred← citeshttps://doi.org/10.1093/pcp/pcy160openalex-snapshot
Members of the GH3 Family of Proteins Conjugate 2,4-D and Dicamba with Aspartate and Glutamate
inferred← citeshttps://doi.org/10.1093/plcell/koae054openalex-snapshot
An auxin research odyssey: 1989–2023
inferred← citeshttps://doi.org/10.1093/plphys/kiaf568openalex-snapshot
The diphenylurea-type GH3 enzyme inhibitor Auxurea A selectively inhibits the auxin inactivation pathway in dicots
inferred← citeshttps://doi.org/10.1093/plphys/kiag412openalex-snapshot
GH3 phylogenetic subgroups define divergent routes of auxin inactivation via aspartate and glutamine conjugation
inferred← citeshttps://doi.org/10.1093/treephys/tpac129openalex-snapshot
Phenotypically abnormal cotyledonaryVitis viniferaembryos differ in anatomy, endogenous hormone levels and transcriptome profiles
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/10.1101/2021.10.12.464031openalex-snapshot
Chemical inhibition of auxin inactivation pathway uncovers the metabolic turnover of auxin homeostasis
inferred← citeshttps://doi.org/10.1105/tpc.112.099119openalex-snapshot
Auxin Controls Arabidopsis Adventitious Root Initiation by Regulating Jasmonic Acid Homeostasis
inferred← citeshttps://doi.org/10.1105/tpc.112.102921openalex-snapshot
Crystal Structure of an Indole-3-Acetic Acid Amido Synthetase from Grapevine Involved in Auxin Homeostasis
inferred← citeshttps://doi.org/10.1107/s0907444913019276openalex-snapshot
Determination of the GH3.12 protein conformation through HPLC-integrated SAXS measurements combined with X-ray crystallography
inferred← citeshttps://doi.org/10.1111/jipb.13764openalex-snapshot
Anchorene, a carotenoid‐derived growth regulator, modulates auxin homeostasis by suppressing GH3‐mediated auxin conjugation
inferred← citeshttps://doi.org/10.1111/nph.18114openalex-snapshot
Inactivation of the entire Arabidopsis group II GH3s confers tolerance to salinity and water deficit
inferred← citeshttps://doi.org/10.1111/pce.13738openalex-snapshot
Sugar enhances waterlogging‐induced adventitious root formation in cucumber by promoting auxin transport and signalling
inferred← citeshttps://doi.org/10.1111/ppl.70270openalex-snapshot
Babaco Mosaic Virus ( BabMV ) Induces Genome‐Wide Transcriptomic Reprogramming in Carica papaya
inferred← citeshttps://doi.org/10.1111/tpj.13460openalex-snapshot
Analysis of plant hormone profiles in response to moderate dehydration stress
inferred← citeshttps://doi.org/10.1126/science.1221863openalex-snapshot
Structural Basis for Prereceptor Modulation of Plant Hormones by GH3 Proteins
inferred← citeshttps://doi.org/10.1126/science.aaw1720openalex-snapshot
Isochorismate-derived biosynthesis of the plant stress hormone salicylic acid
inferred← citeshttps://doi.org/10.1186/s12864-019-6393-7openalex-snapshot
Global scale transcriptome analysis reveals differentially expressed genes involve in early somatic embryogenesis in Dimocarpus longan Lour
inferred← citeshttps://doi.org/10.1186/s12864-020-07345-9openalex-snapshot
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/10.1186/s13007-019-0509-6openalex-snapshot
A bacterial assay for rapid screening of IAA catabolic enzymes
inferred← citeshttps://doi.org/10.1371/journal.pone.0037632openalex-snapshot
A Novel Tool for Studying Auxin-Metabolism: The Inhibition of Grapevine Indole-3-Acetic Acid-Amido Synthetases by a Reaction Intermediate Analogue
inferred← citeshttps://doi.org/10.17352/asb.000011openalex-snapshot
Redox regulation of adventitious root formation through downstream changes in hormonal system in mung bean [Vigna radiata (L.) R. Wilczek]
inferred← citeshttps://doi.org/10.17660/actahortic.2017.1157.1openalex-snapshot
Understanding the control of grape berry ripening and developing opportunities for its manipulation
inferred← citeshttps://doi.org/10.21203/rs.3.rs-114349/v1openalex-snapshot
Transcriptomic and Systematic Analyses Reveal TabZIP Family Members Involved in the Response to Different Concentrations of Auxin in Wheat Root
inferred← citeshttps://doi.org/10.3389/fpls.2011.00074openalex-snapshot
Insights into Auxin Signaling in Plant?Pathogen Interactions
inferred← citeshttps://doi.org/10.3389/fpls.2014.00789openalex-snapshot
Genome-wide analysis and expression profiling suggest diverse roles of GH3 genes during development and abiotic stress responses in legumes
inferred← citeshttps://doi.org/10.3389/fpls.2018.01240openalex-snapshot
Benzyl Cyanide Leads to Auxin-Like Effects Through the Action of Nitrilases in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2021.668548openalex-snapshot
Sedentary Plant-Parasitic Nematodes Alter Auxin Homeostasis via Multiple Strategies
inferred← citeshttps://doi.org/10.3389/fpls.2021.751866openalex-snapshot
Global Transcriptome and Coexpression Network Analyses Reveal New Insights Into Somatic Embryogenesis in Hybrid Sweetgum (Liquidambar styraciflua × Liquidambar formosana)
inferred← citeshttps://doi.org/10.3389/fpls.2022.959053openalex-snapshot
The roles of epigenetic modifications in the regulation of auxin biosynthesis
inferred← citeshttps://doi.org/10.3389/fpls.2023.1176705openalex-snapshot
Allelic variation in the indoleacetic acid-lysine synthase gene of the bacterial pathogen Pseudomonas savastanoi and its role in auxin production
inferred← citeshttps://doi.org/10.3389/fpls.2023.1258410openalex-snapshot
Insight into regulation of adventitious root formation by arbuscular mycorrhizal fungus and exogenous auxin in tea plant (Camellia sinensis L.) cuttings
inferred← citeshttps://doi.org/10.3390/agronomy13030623openalex-snapshot
Integrative Transcriptome and Chlorophyll Fluorescence Test Analysis Shed New Light on the Leaf Senescence Mechanism of Zoysia japonica
inferred← citeshttps://doi.org/10.3390/ijms18122547openalex-snapshot
Nodule-Enriched GRETCHEN HAGEN 3 Enzymes Have Distinct Substrate Specificities and Are Important for Proper Soybean Nodule Development
inferred← citeshttps://doi.org/10.3390/ijms19103115openalex-snapshot
Auxins and Cytokinins—The Role of Subcellular Organization on Homeostasis
inferred← citeshttps://doi.org/10.3390/ijms21010260openalex-snapshot
Rice Senescence-Induced Receptor-Like Kinase (OsSRLK) Is Involved in Phytohormone-Mediated Chlorophyll Degradation
inferred← citeshttps://doi.org/10.3390/ijms22083874openalex-snapshot
Cytokinin-Controlled Gradient Distribution of Auxin in Arabidopsis Root Tip
inferred← citeshttps://doi.org/10.3390/ijms23010510openalex-snapshot
MicroRNAs Are Involved in Regulating Plant Development and Stress Response through Fine-Tuning of TIR1/AFB-Dependent Auxin Signaling
inferred← citeshttps://doi.org/10.3390/plants10102034openalex-snapshot
Genome-Wide Analysis, Modeling, and Identification of Amino Acid Binding Motifs Suggest the Involvement of GH3 Genes during Somatic Embryogenesis of Coffea canephora
inferred← citeshttps://doi.org/10.3390/plants10122607openalex-snapshot
Differences in the Abundance of Auxin Homeostasis Proteins Suggest Their Central Roles for In Vitro Tissue Differentiation in Coffea arabica
inferred← citeshttps://doi.org/10.3390/plants11212995openalex-snapshot
Expression of Genes Involved in ABA and Auxin Metabolism and LEA Gene during Embryogenesis in Hemp
inferred← citeshttps://doi.org/10.3390/plants11233301openalex-snapshot
Transcriptome Dynamics of Rooting Zone and Leaves during In Vitro Adventitious Root Formation in Eucalyptus nitens
inferred← citeshttps://doi.org/10.3390/plants12244111openalex-snapshot
The Roles of GRETCHEN HAGEN3 (GH3)-Dependent Auxin Conjugation in the Regulation of Plant Development and Stress Adaptation
inferred← citeshttps://doi.org/10.3390/plants9111406openalex-snapshot
Expression Analysis of Key Auxin Biosynthesis, Transport, and Metabolism Genes of Betula pendula with Special Emphasis on Figured Wood Formation in Karelian Birch
inferred← citeshttps://doi.org/10.3410/f.717747990.793302858openalex-snapshot
Faculty Opinions recommendation of Auxin controls Arabidopsis adventitious root initiation by regulating jasmonic acid homeostasis.
inferred← citeshttps://doi.org/10.4161/psb.26998openalex-snapshot
Dynamics of the concentration of IAA and some of its conjugates during the induction of somatic embryogenesis inCoffea canephora
inferred← citeshttps://doi.org/10.4161/psb.5.12.13941openalex-snapshot
Modulating plant hormones by enzyme action
inferred← citeshttps://doi.org/10.53846/goediss-9129openalex-snapshot
Physiological, morphological and molecular acclimation of Populus spp. to high salinity
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535746openalex-snapshot
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/10.70675/0b8d0f94z4fcaz4d08zb37eza54139bc572aopenalex-snapshot
Implementing the CRISPR-Cas9 technology in Eucalyptus hairy roots and functional characterization of auxin-dependent transcription factors involved in wood formation
inferred← citeshttps://doi.org/10.70675/293319edze009z40e3z84a6zca9aaaa06a0copenalex-snapshot
Etude fonctionnelle de gènes régulés par le facteur de transcription CROWN ROOT LESS1 impliqués dans l’initiation et le développement des racines coronaires chez le riz
inferred← citeshttps://doi.org/10.70675/d8de36b9zab06z406bzb687z46370517336bopenalex-snapshot
Analyse biologique, génétique et moléculaire de la résistance partielle du riz à Magnaporthe oryzae
inferred← citeshttps://doi.org/10.7717/peerj.5975openalex-snapshot
Transcriptome analysis of oil palm inflorescences revealed candidate genes for an auxin signaling pathway involved in parthenocarpy
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