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Auxin-regulated gene expression in intact soybean hypocotyl and excised hypocotyl sections
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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/bf00392775openalex-snapshot
Auxin-induced changes in the population of translatable messenger RNA in elongating maize coleoptile sections
inferredcites →https://doi.org/10.1016/0003-2697(76)90549-2openalex-snapshot
Specificity of oligo (dT)-cellulose chromatography in the isolation of polyadenylated RNA
inferredcites →https://doi.org/10.1016/0022-2836(77)90052-3openalex-snapshot
Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I
inferredcites →https://doi.org/10.1016/0076-6879(79)68018-7openalex-snapshot
[16] Plasmids of Escherichia coli as cloning vectors
inferredcites →https://doi.org/10.1016/0076-6879(83)01038-1openalex-snapshot
[35] In Vitro transcription: Whole-cell extract
inferredcites →https://doi.org/10.1016/0092-8674(76)90088-xopenalex-snapshot
Dictyostelium 17S, 25S, and 5S rDNAs lie within a 38,000 base pair repeated unit
inferredcites →https://doi.org/10.1016/0092-8674(82)90156-8openalex-snapshot
A transcriptionally active, covalently closed minichromosome of cauliflower mosaic virus DNA isolated from infected turnip leaves
inferredcites →https://doi.org/10.1016/0378-1119(81)90003-2openalex-snapshot
Cloning of α2u globulin cDNA using a high efficiency technique for the cloning of trace messenger RNAs
inferredcites →https://doi.org/10.1016/0968-0004(82)90275-4openalex-snapshot
Levels of genetic control in development
inferredcites →https://doi.org/10.1016/s0021-9258(17)38098-5openalex-snapshot
Synthesis of double-stranded DNA complementary to lysozyme, ovomucoid, and ovalbumin mRNAs. Optimization for full length second strand synthesis by Escherichia coli DNA polymerase I.
inferredcites →https://doi.org/10.1016/s0021-9258(18)43588-0openalex-snapshot
Polyadenylated RNA sequences which are reduced in concentration following auxin treatment of soybean hypocotyls.
inferredcites →https://doi.org/10.1016/s0021-9258(19)86340-8openalex-snapshot
Ribonuclease inhibitor from human placenta: rapid purification and assay.
inferredcites →https://doi.org/10.1021/bi00709a025openalex-snapshot
Ribonucleic acid isolated by cesium chloride centrifugation
inferredcites →https://doi.org/10.1073/pnas.72.10.3961openalex-snapshot
Colony hybridization: a method for the isolation of cloned DNAs that contain a specific gene.
inferredcites →https://doi.org/10.1073/pnas.77.9.5201openalex-snapshot
Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose.
inferredcites →https://doi.org/10.1073/pnas.79.2.418openalex-snapshot
Early auxin-regulated polyadenylylated mRNA sequences in pea stem tissue
inferredcites →https://doi.org/10.1073/pnas.79.23.7185openalex-snapshot
Isolation of cloned cDNAs to auxin-responsive poly(A) + RNAs of elongating soybean hypocotyl
inferredcites →https://doi.org/10.1093/nar/6.11.3559openalex-snapshot
Identification of procollagen mRNAs transferred to diazobenzyloxymethyl paper from formaldehyde agarose gels
inferredcites →https://doi.org/10.1093/nar/7.6.1541openalex-snapshot
Determination of nucleic acid sequence homologies and relative concentrations by a dot hybridization procedure
inferredcites →https://doi.org/10.1093/nar/9.13.2989openalex-snapshot
Rapid and efficient cosmid cloning
inferredcites →https://doi.org/10.1104/pp.69.2.332openalex-snapshot
Auxin-Induced Changes in the Population of Translatable Messenger RNA in Elongating Sections of Soybean Hypocotyl
inferredcites →https://doi.org/10.1104/pp.69.2.338openalex-snapshot
Auxin- and Ethylene-Induced Changes in the Population of Translatable Messenger RNA in Basal Sections and Intact Soybean Hypocotyl
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/10.1002/9780470650561.ch1openalex-snapshot
Molecular and Genetic Approaches to the Study of Plant Hormone Action
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Use of Chemical Biology to Understand Auxin Metabolism, Signaling, and Polar Transport
inferred← citeshttps://doi.org/10.1002/bies.950110204openalex-snapshot
Modulation of gene expression by auxin
inferred← citeshttps://doi.org/10.1002/dvg.1020080506openalex-snapshot
Auxin (2,4‐dichlorophenoxyacetic acid) starvation and treatment with glucan elicitor isolated from Phytophthora megasperma induces similar responses in soybean‐cultured cell suspensions
inferred← citeshttps://doi.org/10.1002/ps.2780170514openalex-snapshot
Biologically active substances from higher plants: Status and future potential
inferred← citeshttps://doi.org/10.1007/7089_038openalex-snapshot
Differential Gene Expression During Somatic Embryogenesis
inferred← citeshttps://doi.org/10.1007/978-1-4020-2686-7_10openalex-snapshot
Auxin and Cell Elongation
inferred← citeshttps://doi.org/10.1007/978-1-4020-6295-7_13openalex-snapshot
Auxin and Cytokinin Signaling Component Genes and Their Potential for Crop Improvement
inferred← citeshttps://doi.org/10.1007/978-1-4613-9365-8_14openalex-snapshot
Gibberellin-Binding Proteins and Hormonal Regulation of Transcription in Cell Nuclei and Chloroplasts of Higher Plants
inferred← citeshttps://doi.org/10.1007/978-1-4684-7047-5_21openalex-snapshot
Regulation of Plant Gene Expression by Auxins
inferred← citeshttps://doi.org/10.1007/978-3-319-33705-0_10openalex-snapshot
The Role of the Auxins During Somatic Embryogenesis
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/10.1007/978-3-540-89228-1_12openalex-snapshot
Signaling in Phototropism
inferred← citeshttps://doi.org/10.1007/978-3-642-74545-4_10openalex-snapshot
Auxin and Gene Expression
inferred← citeshttps://doi.org/10.1007/978-3-642-78852-9_17openalex-snapshot
Auxin-Regulated Gene Expression
inferred← citeshttps://doi.org/10.1007/978-3-7091-6950-6_9openalex-snapshot
Regulation of Gene Expression by Ethylene
inferred← citeshttps://doi.org/10.1007/978-81-322-2683-3_9openalex-snapshot
Role of SERK During Somatic Embryogenesis and Its Interaction with Brassinosteroids
inferred← citeshttps://doi.org/10.1007/978-94-009-0131-5_3openalex-snapshot
Expression of an auxin-inducible promoter of tobacco in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/978-94-009-0131-5_7openalex-snapshot
Regulation of a class of auxin-induced genes in cell-suspension cultures from Nicotiana tabacum
inferred← citeshttps://doi.org/10.1007/978-94-009-3585-3_8openalex-snapshot
Auxin and Cell Elongation
inferred← citeshttps://doi.org/10.1007/978-94-009-3585-3_9openalex-snapshot
The Control of Gene Expression by Auxin
inferred← citeshttps://doi.org/10.1007/978-94-010-0377-3_9openalex-snapshot
Auxin-responsive gene expression: genes, promoters and regulatory factors
inferred← citeshttps://doi.org/10.1007/978-94-011-0239-1_15openalex-snapshot
Molecular genetics of auxin and cytokinin
inferred← citeshttps://doi.org/10.1007/978-94-011-0473-9_11openalex-snapshot
The Control of Gene Expression by Auxin
inferred← citeshttps://doi.org/10.1007/978-94-011-2458-4_13openalex-snapshot
Transcriptional regulation of auxin-responsive genes
inferred← citeshttps://doi.org/10.1007/978-94-011-3052-3_2openalex-snapshot
Hormonal regulation of plant gene expression
inferred← citeshttps://doi.org/10.1007/978-94-011-3176-6_22openalex-snapshot
Molecular aspects of Cytokinin’s stymied action on Auxin mediated new root formation in the hypocotyls of Phaseolus vulgaris L.
inferred← citeshttps://doi.org/10.1007/978-94-015-8927-7_2openalex-snapshot
Endogenous Reactions and Substrate Specificity of Herbicide Metabolizing Enzymes
inferred← citeshttps://doi.org/10.1007/bf00016071openalex-snapshot
Promoters of auxin-induced genes from tobacco can lead to auxin-inducible and root tip-specific expression
inferred← citeshttps://doi.org/10.1007/bf00016152openalex-snapshot
Auxin-induced mRNA species in tobacco cell cultures
inferred← citeshttps://doi.org/10.1007/bf00016487openalex-snapshot
Molecular genetics of auxin and cytokinin
inferred← citeshttps://doi.org/10.1007/bf00019318openalex-snapshot
Expression patterns of three genes in the stem of lucerne (Medicago sativa)
inferred← citeshttps://doi.org/10.1007/bf00020091openalex-snapshot
Phytochrome regulation of phytochrome mRNA abundance
inferred← citeshttps://doi.org/10.1007/bf00020537openalex-snapshot
Characterization of a class of small auxin-inducible soybean polyadenylated RNAs
inferred← citeshttps://doi.org/10.1007/bf00020538openalex-snapshot
An auxin-induced polypeptide in dicotyledonous plants
inferred← citeshttps://doi.org/10.1007/bf00023610openalex-snapshot
Identification of protein-binding DNA sequences in an auxin-regulated gene of soybean
inferred← citeshttps://doi.org/10.1007/bf00027361openalex-snapshot
Expression of the Arabidopsis AtAux2-11 auxin-responsive gene in transgenic plants
inferred← citeshttps://doi.org/10.1007/bf00028482openalex-snapshot
Expression of an auxin-inducible promoter of tobacco in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/bf00036908openalex-snapshot
Analysis of the genes encoding the largest subunit of RNA polymerase II in Arabidopsis and soybean
inferred← citeshttps://doi.org/10.1007/bf00039563openalex-snapshot
Structural organization of str 246C and str 246N, plant defense-related genes from Nicotiana tabacum
inferred← citeshttps://doi.org/10.1007/bf00040658openalex-snapshot
Auxin-induced expression of the soybean GH3 promoter in transgenic tobacco plants
inferred← citeshttps://doi.org/10.1007/bf00040688openalex-snapshot
The ocs element in the soybean GH2/4 promoter is activated by both active and inactive auxin and salicylic acid analogues
inferred← citeshttps://doi.org/10.1007/bf00260628openalex-snapshot
Mutants of Nicotiana plumbaginifolia with specific resistance to auxin
inferred← citeshttps://doi.org/10.1007/bf00268488openalex-snapshot
Patterns of protein synthesis in dividing and auxin-starved soybean cell suspensions. Differential expression of a major group of Mr-17000 peptides
inferred← citeshttps://doi.org/10.1007/bf00391281openalex-snapshot
The action of exogenous abscisic acid on malate-synthase synthesis in germinating castor-bean seeds
inferred← citeshttps://doi.org/10.1007/bf00393868openalex-snapshot
Auxin-induced rapid changes in translatable mRNAs in tobacco cell suspension
inferred← citeshttps://doi.org/10.1007/bf00771014openalex-snapshot
The possible role of redox-associated protons in growth of plant cells
inferred← citeshttps://doi.org/10.1007/bf01968942openalex-snapshot
Transgenic white clover. Studies with the auxin-responsive promoter, GH3, in root gravitropism and lateral root development
inferred← citeshttps://doi.org/10.1007/s00253-014-6311-5openalex-snapshot
Genome-wide identification, expression analysis of GH3 family genes in Medicago truncatula under stress-related hormones and Sinorhizobium meliloti infection
inferred← citeshttps://doi.org/10.1007/s00299-003-0646-1openalex-snapshot
Use of an inducible reporter gene system for the analysis of auxin distribution in the moss Physcomitrella patens
inferred← citeshttps://doi.org/10.1007/s002990000306openalex-snapshot
Auxin-regulated gene expression and embryogenic competence in callus cultures of sweetpotato, Ipomoea batatas (L.) Lam.
inferred← citeshttps://doi.org/10.1007/s00425-022-03908-0openalex-snapshot
Genome-wide characterization and expression analysis of SAUR gene family in Melon (Cucumis melo L.)
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/s10142-003-0093-7openalex-snapshot
The auxin-induced transcriptome for etiolated Arabidopsis seedlings using a structure/function approach
inferred← citeshttps://doi.org/10.1007/s10142-005-0142-5openalex-snapshot
The auxin-responsive GH3 gene family in rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1007/s10265-012-0477-7openalex-snapshot
Visualization of auxin-mediated transcriptional activation using a common auxin-responsive reporter system in the liverwort Marchantia polymorpha
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/s11103-005-6505-4openalex-snapshot
A GH3-like gene, CcGH3, isolated from Capsicum chinense L. fruit is regulated by auxin and ethylene*
inferred← citeshttps://doi.org/10.1007/s11103-011-9776-yopenalex-snapshot
Evolutionary history of the GH3 family of acyl adenylases in rosids
inferred← citeshttps://doi.org/10.1007/s11627-024-10413-4openalex-snapshot
Status and prospects of yam somatic embryogenesis: a pathway for biotechnology applications
inferred← citeshttps://doi.org/10.1016/0014-5793(93)81751-kopenalex-snapshot
Indoleacetic acid pretreatment of tobacco plants in vivo increases the in vitro sensitivity to auxin of the plasma membrane H+‐ATPase from leaves and modifies the polypeptide composition of the membrane
inferred← citeshttps://doi.org/10.1016/0022-2836(85)90280-3openalex-snapshot
Rapid induction of specific mRNAs by auxin in pea epicotyl tissue
inferred← citeshttps://doi.org/10.1016/b978-0-12-185204-7.50013-1openalex-snapshot
Receptors for Plant Auxin Action and Auxin Transport
inferred← citeshttps://doi.org/10.1016/b978-0-12-401350-6.50011-4openalex-snapshot
Reduced Cell Expansion and Changes in Cell Walls of Plant Cells Adapted to NaCl
inferred← citeshttps://doi.org/10.1016/b978-0-12-428781-5.50035-1openalex-snapshot
Transgenic Plants for Studying Responses to the Hormones Auxin and Cytokinin
inferred← citeshttps://doi.org/10.1016/b978-0-12-668610-4.50012-4openalex-snapshot
Growth Regulators: An Account of Hormones and Growth Regulation
inferred← citeshttps://doi.org/10.1016/b978-0-408-00796-2.50009-8openalex-snapshot
DO PLANT HORMONES REGULATE GENE EXPRESSION DURING DEVELOPMENT?
inferred← citeshttps://doi.org/10.1016/b978-0-443-15719-6.00015-5openalex-snapshot
Nucleotidyl cyclase activities of TIR1/AFB auxin receptors: new insights into the mechanism of auxin signaling
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/b978-012660570-9/50157-xopenalex-snapshot
Hormonal Regulation of Cell Division and Cell Growth
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114524openalex-snapshot
Single-cell RNA sequencing reveals dynamics of gene expression for 2D elongation and 3D growth in Physcomitrium patens
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2010.09.003openalex-snapshot
In silico analysis of cis-acting regulatory elements in 5′ regulatory regions of sucrose transporter gene families in rice (Oryza sativa Japonica) and Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.gene.2011.05.033openalex-snapshot
Two GH3 genes from longan are differentially regulated during fruit growth and development
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.jbc.2024.107421openalex-snapshot
Fidelity in plant hormone modifications catalyzed by Arabidopsis GH3 acyl acid amido synthetases
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.jplph.2014.07.026openalex-snapshot
Interplay between GST and nitric oxide in the early response of soybean (Glycine max L.) plants to salinity stress
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.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.plaphy.2013.04.003openalex-snapshot
Knock-down of a member of the isoflavone reductase gene family impairs plant growth and nodulation in Phaseolus vulgaris
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.plgene.2015.12.002openalex-snapshot
A novel EcGH3 gene with a different expression pattern in quinclorac-resistant and susceptible barnyardgrass (Echinochloa crus-galli)
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/s0014-5793(97)01447-6openalex-snapshot
Isolation by differential display and characterization of a tobacco auxin‐responsive cDNA Nt‐gh3, related to GH3
inferred← citeshttps://doi.org/10.1016/s0015-3796(89)80051-4openalex-snapshot
Hormone-induced Alterations in Plant Gene Expression
inferred← citeshttps://doi.org/10.1016/s0021-9258(18)38022-0openalex-snapshot
Sequence and characterization of two auxin-regulated genes from soybean.
inferred← citeshttps://doi.org/10.1016/s0021-9258(18)47573-4openalex-snapshot
Characterization and sequence analysis of a developmentally regulated putative cell wall protein gene isolated from soybean.
inferred← citeshttps://doi.org/10.1016/s0021-9258(18)50071-5openalex-snapshot
Sequence of the fifth largest subunit of RNA polymerase II from plants
inferred← citeshttps://doi.org/10.1016/s0021-9258(18)55475-2openalex-snapshot
Induction and superinduction of auxin-responsive mRNAs with auxin and protein synthesis inhibitors.
inferred← citeshttps://doi.org/10.1016/s0021-9258(18)68806-4openalex-snapshot
Regulation of expression of an auxin-induced soybean sequence by cadmium.
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)62457-2openalex-snapshot
Molecular Analysis of Plant Signaling Elements: Relevance of Eukaryotic Signal Transduction Models
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)62555-3openalex-snapshot
Function and Modulation of Expression of Auxin-Regulated Genes
inferred← citeshttps://doi.org/10.1016/s0167-7306(08)60497-4openalex-snapshot
Molecular approaches to study plant hormone signalling
inferred← citeshttps://doi.org/10.1016/s0167-7306(08)60499-8openalex-snapshot
Auxin-regulated genes and promoters
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c03954openalex-snapshot
AcERF1B and AcERF073 Positively Regulate Indole-3-acetic Acid Degradation by Activating AcGH3.1 Transcription during Postharvest Kiwifruit Ripening
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c10702openalex-snapshot
Genome-wide Identification and Functional Analysis of Gretchen Hagen 3 Genes in Soybean Resistance to Cyst Nematodes
inferred← citeshttps://doi.org/10.1021/jf035134lopenalex-snapshot
Quantitative Expression Analysis of GH3, a Gene Induced by Plant Growth Regulator Herbicides in Soybean
inferred← citeshttps://doi.org/10.1021/jf2024402openalex-snapshot
Effects of Auxins on Sorgoleone Accumulation and Genes for Sorgoleone Biosynthesis in Sorghum Roots
inferred← citeshttps://doi.org/10.1023/a:1015207114117openalex-snapshot
Auxin-responsive gene expression: genes, promoters and regulatory factors
inferred← citeshttps://doi.org/10.1023/a:1019818110761openalex-snapshot
OsARF1, an auxin response factor from rice, is auxin-regulated and classifies as a primary auxin responsive gene
inferred← citeshttps://doi.org/10.1034/j.1399-3054.1997.1000305.xopenalex-snapshot
Expression of auxin-regulated genes
inferred← citeshttps://doi.org/10.1038/331176a0openalex-snapshot
Auxin induces rapid changes in phosphatidylinositol metabolites
inferred← citeshttps://doi.org/10.1038/nplants.2016.25openalex-snapshot
Local auxin metabolism regulates environment-induced hypocotyl elongation
inferred← citeshttps://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
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2002.01488.xopenalex-snapshot
The HAT2 gene, a member of the HD‐Zip gene family, isolated as an auxin inducible gene by DNA microarray screening, affects auxin response in Arabidopsis
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2002.00419.xopenalex-snapshot
The cell biology of phytochrome signalling
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2003.00705.xopenalex-snapshot
Genes and signalling in root development
inferred← citeshttps://doi.org/10.1071/pp98157openalex-snapshot
Auxin induction is a trigger for root gall formation caused by root-knot nematodes in white clover and is associated with the activation of the flavonoid pathway
inferred← citeshttps://doi.org/10.1073/pnas.1609980114openalex-snapshot
Structural basis of jasmonate-amido synthetase FIN219 in complex with glutathione S-transferase FIP1 during the JA signal regulation
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.m110.146431openalex-snapshot
Kinetic Basis for the Conjugation of Auxin by a GH3 Family Indole-acetic Acid-Amido Synthetase
inferred← citeshttps://doi.org/10.1074/jbc.m806662200openalex-snapshot
Arabidopsis GH3.12 (PBS3) Conjugates Amino Acids to 4-Substituted Benzoates and Is Inhibited by Salicylate
inferred← citeshttps://doi.org/10.1080/07352680903436291openalex-snapshot
Regulation of Somatic Embryogenesis in Higher Plants
inferred← citeshttps://doi.org/10.1080/07352688609382226openalex-snapshot
Auxin‐regulated gene expression in higher plants
inferred← citeshttps://doi.org/10.1080/07352689.2015.1090831openalex-snapshot
Physiological and Molecular Regulation of Adventitious Root Formation
inferred← citeshttps://doi.org/10.1080/07352689409701919openalex-snapshot
The Physiology and Molecular Biology of Plant 1,3-β-D-Glucanases and 1,3;1,4-β-D-Glucanases
inferred← citeshttps://doi.org/10.1080/13102818.2015.1031698openalex-snapshot
Is the auxin influx carrierLAX3essential for plant growth and development in the model plantsMedicago truncatula, Lotus japonicusandArabidopsis thaliana?
inferred← citeshttps://doi.org/10.1093/aob/mci083openalex-snapshot
Auxin: Regulation, Action, and Interaction
inferred← citeshttps://doi.org/10.1093/aob/mcy218openalex-snapshot
TaARF4 genes are linked to root growth and plant height in wheat
inferred← citeshttps://doi.org/10.1093/dnares/8.5.193openalex-snapshot
OsIAA1, an Aux/IAA cDNA from Rice, and Changes in Its Expression as Influenced by Auxin and Light
inferred← citeshttps://doi.org/10.1093/jxb/erl182openalex-snapshot
An early auxin-responsive Aux/IAA gene from wheat (Triticum aestivum) is induced by epibrassinolide and differentially regulated by light and calcium
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1093/jxb/ert141openalex-snapshot
The role of auxin in shaping shoot architecture
inferred← citeshttps://doi.org/10.1093/jxb/erx127openalex-snapshot
‘Bending’ models of halotropism: incorporating protein phosphatase 2A, ABCB transporters, and auxin metabolism
inferred← citeshttps://doi.org/10.1093/mp/ssu049openalex-snapshot
Growth–Defense Tradeoffs in Plants: A Balancing Act to Optimize Fitness
inferred← citeshttps://doi.org/10.1093/oxfordjournals.pcp.a029592openalex-snapshot
Expression of the Auxin-Inducible GH3 Promoter/GUS Fusion Gene as a Useful Molecular Marker for Auxin Physiology
inferred← citeshttps://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
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/pcx095openalex-snapshot
The Roles of the Sole Activator-Type Auxin Response Factor in Pattern Formation of Marchantia polymorpha
inferred← citeshttps://doi.org/10.1093/plcell/koac179openalex-snapshot
On the trail of auxin: Reporters and sensors
inferred← citeshttps://doi.org/10.1093/plcell/koae054openalex-snapshot
An auxin research odyssey: 1989–2023
inferred← citeshttps://doi.org/10.1093/plphys/kiab130openalex-snapshot
AUXIN RESPONSE FACTOR 18–HISTONE DEACETYLASE 6 module regulates floral organ identity in rose (Rosa hybrida)
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/10.1094/mpmi-03-19-0089-ropenalex-snapshot
MdWRKY46-Enhanced Apple Resistance to Botryosphaeria dothidea by Activating the Expression of MdPBS3.1 in the Salicylic Acid Signaling Pathway
inferred← citeshttps://doi.org/10.1094/mpmi-21-10-1349openalex-snapshot
2,4-Diacetylphloroglucinol Alters Plant Root Development
inferred← citeshttps://doi.org/10.1094/mpmi.2001.14.10.1235openalex-snapshot
Salicylic Acid and NIM1/NPR1-Independent Gene Induction by Incompatible Peronospora parasitica in Arabidopsis
inferred← citeshttps://doi.org/10.1098/rstb.1986.0063openalex-snapshot
Auxin-regulated gene expression
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/10.1101/gad.14.15.1958openalex-snapshot
FIN219, an auxin-regulated gene, defines a link between phytochrome A and the downstream regulator COP1 in light control of Arabidopsis development
inferred← citeshttps://doi.org/10.1104/pp.015677openalex-snapshot
Dual Genetic Pathways Controlling Nodule Number inMedicago truncatula
inferred← citeshttps://doi.org/10.1104/pp.100.3.1377openalex-snapshot
Effect of Brassinolide on Gene Expression in Elongating Soybean Epicotyls
inferred← citeshttps://doi.org/10.1104/pp.102.2.513openalex-snapshot
Further Characterization of Expression of Auxin-Induced Genes in Tobacco (Nicotiana tabacum) Cell-Suspension Cultures
inferred← citeshttps://doi.org/10.1104/pp.104.041996openalex-snapshot
Overexpression of OsRAA1 Causes Pleiotropic Phenotypes in Transgenic Rice Plants, including Altered Leaf, Flower, and Root Development and Root Response to Gravity
inferred← citeshttps://doi.org/10.1104/pp.104.2.505openalex-snapshot
Investigation of Gene Expression, Growth Kinetics, and Wall Extensibility during Brassinosteroid-Regulated Stem Elongation
inferred← citeshttps://doi.org/10.1104/pp.106.094185openalex-snapshot
GlutathioneS-Transferase Interacting with Far-Red Insensitive 219 Is Involved in Phytochrome A-Mediated Signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.108.3.919openalex-snapshot
The Soybean GH2/4 Gene That Encodes a Glutathione S-Transferase Has a Promoter That Is Activated by a Wide Range of Chemical Agents
inferred← citeshttps://doi.org/10.1104/pp.118.4.1265openalex-snapshot
NPH4, a Conditional Modulator of Auxin-Dependent Differential Growth Responses in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.124.3.1105openalex-snapshot
A Genomics Approach to the Comprehensive Analysis of the Glutathione S-Transferase Gene Family in Soybean and Maize
inferred← citeshttps://doi.org/10.1104/pp.15.01675openalex-snapshot
Type B Heterotrimeric G Protein γ -Subunit Regulates Auxin and ABA Signaling in Tomato
inferred← citeshttps://doi.org/10.1104/pp.80.2.459openalex-snapshot
Hormonal Regulation of α-Amylase Gene Transcription in Wild Oat (Avena fatua L.) Aleurone Protoplasts
inferred← citeshttps://doi.org/10.1104/pp.82.3.713openalex-snapshot
Insensitivity of the Diageotropica Tomato Mutant to Auxin
inferred← citeshttps://doi.org/10.1104/pp.83.1.15openalex-snapshot
Gibberellin-Induced Changes in the Populations of Translatable mRNAs and Accumulated Polypeptides in Dwarfs of Maize and Pea
inferred← citeshttps://doi.org/10.1104/pp.84.2.443openalex-snapshot
Rapid Effects of IAA on Cell Surface Proteins from Intact Carrot Suspension Culture Cells
inferred← citeshttps://doi.org/10.1104/pp.86.2.482openalex-snapshot
Comparative Analysis of Polyadenylated RNA Complexity in Soybean Hypocotyl Tissue and Cultured Suspension Cells
inferred← citeshttps://doi.org/10.1104/pp.95.3.711openalex-snapshot
Induction of Specific mRNAs in Cultured Soybean Cells during Cytokinin or Auxin Starvation
inferred← citeshttps://doi.org/10.1105/tpc.010289openalex-snapshot
AUX/IAA Proteins Are Active Repressors, and Their Stability and Activity Are Modulated by Auxin
inferred← citeshttps://doi.org/10.1105/tpc.1.2.229openalex-snapshot
Transcription, organization, and sequence of an auxin-regulated gene cluster in soybean.
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.113.119727openalex-snapshot
Phototropism: Growing towards an Understanding of Plant Movement
inferred← citeshttps://doi.org/10.1105/tpc.3.4.419openalex-snapshot
Tissue-specific and organ-specific expression of soybean auxin-responsive transcripts GH3 and SAURs.
inferred← citeshttps://doi.org/10.1105/tpc.4.4.451openalex-snapshot
Cytokinins and auxins control the expression of a gene in Nicotiana plumbaginifolia cells by feedback regulation.
inferred← citeshttps://doi.org/10.1105/tpc.6.5.645openalex-snapshot
Soybean GH3 Promoter Contains Multiple Auxin-Inducible Elements
inferred← citeshttps://doi.org/10.1105/tpc.7.10.1611openalex-snapshot
Composite Structure of Auxin Response Elements
inferred← citeshttps://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.
inferred← citeshttps://doi.org/10.1111/1365-3040.ep11603716openalex-snapshot
Rapid cellular responses to auxin and the regulation of growth
inferred← citeshttps://doi.org/10.1111/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
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2004.02220.xopenalex-snapshot
Disruption and overexpression of auxin response factor 8 gene of Arabidopsis affect hypocotyl elongation and root growth habit, indicating its possible involvement in auxin homeostasis in light condition
inferred← citeshttps://doi.org/10.1111/j.1469-185x.1990.tb01234.xopenalex-snapshot
PLANT GROWTH AND DEVELOPMENT IN MOLECULAR PERSPECTIVE
inferred← citeshttps://doi.org/10.1111/j.1469-8137.1995.tb04291.xopenalex-snapshot
Auxin action and auxin‐binding proteins
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2008.02677.xopenalex-snapshot
Moss ( Physcomitrella patens ) GH3 proteins act in auxin homeostasis
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/pce.12121openalex-snapshot
Jasmonate signalling: a copycat of auxin signalling?
inferred← citeshttps://doi.org/10.1111/pce.12201openalex-snapshot
Light induces jasmonate‐isoleucine conjugation via OsJAR1 ‐dependent and ‐independent pathways in rice
inferred← citeshttps://doi.org/10.1111/ppl.70229openalex-snapshot
Transcriptional Tuning: How Auxin Strikes Unique Chords in Gene Regulation
inferred← citeshttps://doi.org/10.1126/science.11540631openalex-snapshot
Rapid Redistribution of Auxin-Rregulated RNAs During Gravitropism
inferred← citeshttps://doi.org/10.1126/science.1221863openalex-snapshot
Structural Basis for Prereceptor Modulation of Plant Hormones by GH3 Proteins
inferred← citeshttps://doi.org/10.1128/mcb.5.6.1197openalex-snapshot
Rapid Induction of Selective Transcription by Auxins
inferred← citeshttps://doi.org/10.1139/gen-2018-0161openalex-snapshot
Genome-wide identification and characterization of Gretchen Hagen3 (GH3) family genes in Brassica napus
inferred← citeshttps://doi.org/10.1146/annurev.pp.38.060187.001253openalex-snapshot
Regulation of Gene Expression in Higher Plants
inferred← citeshttps://doi.org/10.1155/2008/458732openalex-snapshot
Sugarcane Functional Genomics: Gene Discovery for Agronomic Trait Development
inferred← citeshttps://doi.org/10.1186/1471-2164-8-71openalex-snapshot
Signal transduction-related responses to phytohormones and environmental challenges in sugarcane
inferred← citeshttps://doi.org/10.1186/1471-2229-12-110openalex-snapshot
Transcript profiling reveals complex auxin signalling pathway and transcription regulation involved in dedifferentiation and redifferentiation during somatic embryogenesis in cotton
inferred← citeshttps://doi.org/10.1186/1471-2229-8-41openalex-snapshot
The IBR5 phosphatase promotes Arabidopsis auxin responses through a novel mechanism distinct from TIR1-mediated repressor degradation
inferred← citeshttps://doi.org/10.1186/1477-5956-10-3openalex-snapshot
Identification of differentially accumulated proteins associated with embryogenic and non-embryogenic calli in saffron (Crocus sativus L.)
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/s12870-018-1545-5openalex-snapshot
Genome-wide analysis of cotton GH3 subfamily II reveals functional divergence in fiber development, hormone response and plant architecture
inferred← citeshttps://doi.org/10.1186/s12870-025-06689-2openalex-snapshot
Evolution analysis of GH3 gene family in five Rosaceae species and FaGH3.17, FaGH3.18 improve drought tolerance in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1186/s43141-020-00047-5openalex-snapshot
Genes, proteins and other networks regulating somatic embryogenesis in plants
inferred← citeshttps://doi.org/10.1201/b10819-10openalex-snapshot
Auxin Signaling and Response Mechanisms and Roles in Plant Growth and Development
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