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Rational Design of an Auxin Antagonist of the SCF TIR1 Auxin Receptor Complex
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1 of the 31 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1016/j.cub.2011.02.029 (notice 2015-03-16).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/jmbi.1999.3371openalex-snapshot
Knowledge-based scoring function to predict protein-ligand interactions
inferredcites →https://doi.org/10.1007/978-1-59745-477-3_6openalex-snapshot
Pull-Down Assays for Plant Hormone Research
inferredcites →https://doi.org/10.1007/bf01957494openalex-snapshot
A new indolic antiauxin, α-(5,7-dichloroindole-3-)isobutyric acid: its chemical synthesis and biological activity
inferredcites →https://doi.org/10.1007/s10822-007-9114-2openalex-snapshot
Surflex-Dock 2.1: Robust performance from ligand energetic modeling, ring flexibility, and knowledge-based search
inferredcites →https://doi.org/10.1016/j.cub.2010.08.050openalex-snapshot
Physcomitrella patens Auxin-Resistant Mutants Affect Conserved Elements of an Auxin-Signaling Pathway
inferredcites →https://doi.org/10.1016/j.cub.2011.02.029openalex-snapshot
RETRACTED: The AFB4 Auxin Receptor Is a Negative Regulator of Auxin Signaling in Seedlings
inferredcites →https://doi.org/10.1016/j.devcel.2005.05.014openalex-snapshot
Plant Development Is Regulated by a Family of Auxin Receptor F Box Proteins
inferredcites →https://doi.org/10.1016/j.phytochem.2008.12.020openalex-snapshot
Toyocamycin specifically inhibits auxin signaling mediated by SCFTIR1 pathway
inferredcites →https://doi.org/10.1021/cb9001624openalex-snapshot
The Past, Present, and Future of Chemical Biology in Auxin Research
inferredcites →https://doi.org/10.1021/ci049714+openalex-snapshot
ZINC − A Free Database of Commercially Available Compounds for Virtual Screening
inferredcites →https://doi.org/10.1021/jm0203783openalex-snapshot
Comparative Evaluation of 11 Scoring Functions for Molecular Docking
inferredcites →https://doi.org/10.1038/nature03542openalex-snapshot
The Arabidopsis F-box protein TIR1 is an auxin receptor
inferredcites →https://doi.org/10.1038/nature05731openalex-snapshot
Mechanism of auxin perception by the TIR1 ubiquitin ligase
inferredcites →https://doi.org/10.1038/sj.emboj.7600659openalex-snapshot
Developmental specificity of auxin response by pairs of ARF and Aux/IAA transcriptional regulators
inferredcites →https://doi.org/10.1073/pnas.0711146105openalex-snapshot
Small-molecule agonists and antagonists of F-box protein–substrate interactions in auxin perception and signaling
inferredcites →https://doi.org/10.1074/jbc.m300299200openalex-snapshot
Yokonolide B, a Novel Inhibitor of Auxin Action, Blocks Degradation of AUX/IAA Factors
inferredcites →https://doi.org/10.1093/aob/mci083openalex-snapshot
Auxin: Regulation, Action, and Interaction
inferredcites →https://doi.org/10.1104/pp.103.027847openalex-snapshot
p-Chlorophenoxyisobutyric Acid Impairs Auxin Response in Arabidopsis Root
inferredcites →https://doi.org/10.1104/pp.103.031138openalex-snapshot
Chemical Genetic Approaches to Plant Biology
inferredcites →https://doi.org/10.1104/pp.105.068924openalex-snapshot
Characterization of Terfestatin A, a New Specific Inhibitor for Auxin Signaling
inferredcites →https://doi.org/10.1104/pp.106.085969openalex-snapshot
Mutations in an Auxin Receptor Homolog AFB5 and in SGT1b Confer Resistance to Synthetic Picolinate Auxins and Not to 2,4-Dichlorophenoxyacetic Acid or Indole-3-Acetic Acid in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.018630openalex-snapshot
MASSUGU2 Encodes Aux/IAA19, an Auxin-Regulated Protein That Functions Together with the Transcriptional Activator NPH4/ARF7 to Regulate Differential Growth Responses of Hypocotyl and Formation of Lateral Roots in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.10.10.1649openalex-snapshot
age Mutants of Arabidopsis Exhibit Altered Auxin-Regulated Gene Expression
inferredcites →https://doi.org/10.1105/tpc.9.11.1963openalex-snapshot
Aux/IAA proteins repress expression of reporter genes containing natural and highly active synthetic auxin response elements.
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112308openalex-snapshot
Auxin Biosynthesis and Its Role in Plant Development
inferredcites →https://doi.org/10.1146/annurev-genet-102108-134148openalex-snapshot
Mechanism of Auxin-Regulated Gene Expression in Plants
inferredcites →https://doi.org/10.1242/dev.02012openalex-snapshot
AUXIN RESPONSE FACTOR1andAUXIN RESPONSE FACTOR2regulate senescence and floral organ abscission inArabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0010742openalex-snapshot
The Role of Phe82 and Phe351 in Auxin-Induced Substrate Perception by TIR1 Ubiquitin Ligase: A Novel Insight from Molecular Dynamics Simulations
inferredcites →https://doi.org/10.1584/jpestics.23.289openalex-snapshot
Synthesis and Biological Activities of 5, 6-Difluoroindole-3-acetic Acid; a New Fluoroindole Auxin
inferredcites →https://doi.org/10.3390/12010025openalex-snapshot
An Efficient Synthesis and Reactions of Novel Indol-ylpyridazinone Derivatives with Expected Biological Activity
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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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/ajb2.1463openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8_6openalex-snapshot
Auxin Receptors and Perception
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inferred← citeshttps://doi.org/10.1007/s00216-023-04996-xopenalex-snapshot
In situ separation and visualization of isomeric auxin derivatives in Arabidopsis by ion mobility mass spectrometry imaging
inferred← citeshttps://doi.org/10.1007/s00299-015-1791-zopenalex-snapshot
Transcriptional feedback regulation of YUCCA genes in response to auxin levels in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-015-1896-4openalex-snapshot
Enhancement of hypocotyl elongation by LOV KELCH PROTEIN2 production is mediated by auxin and phytochrome-interacting factors in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-019-02395-0openalex-snapshot
Auxins in potato: molecular aspects and emerging roles in tuber formation and stress resistance
inferred← citeshttps://doi.org/10.1007/s00299-020-02643-8openalex-snapshot
ZEITLUPE enhances expression of PIF4 and YUC8 in the upper aerial parts of Arabidopsis seedlings to positively regulate hypocotyl elongation
inferred← citeshttps://doi.org/10.1007/s00344-023-11031-xopenalex-snapshot
New PEO-IAA-Inspired Anti-Auxins: Synthesis, Biological Activity, and Possible Application in Hemp (Cannabis Sativa L.) Micropropagation
inferred← citeshttps://doi.org/10.1007/s00344-025-11807-3openalex-snapshot
Exploring Amino Acid-Derived Thiohydantoins as Promising Plant Growth Regulators
inferred← citeshttps://doi.org/10.1007/s00425-017-2651-6openalex-snapshot
Regulation of seedling growth by ethylene and the ethylene–auxin crosstalk
inferred← citeshttps://doi.org/10.1007/s00425-020-03367-5openalex-snapshot
Endogenous auxin determines the pattern of adventitious shoot formation on internodal segments of ipecac
inferred← citeshttps://doi.org/10.1007/s10725-020-00682-5openalex-snapshot
Design, synthesis and biological activities of novel urea derivatives with superior plant growth-inhibiting activity
inferred← citeshttps://doi.org/10.1007/s10725-023-01083-0openalex-snapshot
New fluorescent auxin derivatives: anti-auxin activity and accumulation patterns in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11030-014-9528-4openalex-snapshot
Antiproliferative activity of the Michael adducts of aroylacrylic acids and cyclic amines
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inferred← citeshttps://doi.org/10.1016/bs.mie.2022.07.038openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cclet.2024.110462openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.celrep.2020.02.087openalex-snapshot
Auxin Signaling-Mediated Apoplastic pH Modification Functions in Petal Conical Cell Shaping
inferred← citeshttps://doi.org/10.1016/j.cub.2021.07.075openalex-snapshot
Auxin requirements for a meristematic state in roots depend on a dual brassinosteroid function
inferred← citeshttps://doi.org/10.1016/j.cub.2023.04.061openalex-snapshot
Photosynthetic sucrose drives the lateral root clock in Arabidopsis seedlings
inferred← citeshttps://doi.org/10.1016/j.devcel.2017.12.021openalex-snapshot
Feedback from Lateral Organs Controls Shoot Apical Meristem Growth by Modulating Auxin Transport
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.09.021openalex-snapshot
Differential growth is an emergent property of mechanochemical feedback mechanisms in curved plant organs
inferred← citeshttps://doi.org/10.1016/j.jplph.2017.07.007openalex-snapshot
Auxin-like effects of the natural coumarin scopoletin on Arabidopsis cell structure and morphology
inferred← citeshttps://doi.org/10.1016/j.molp.2024.04.002openalex-snapshot
FERONIA-mediated TIR1/AFB2 oxidation stimulates auxin signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.nbt.2018.06.003openalex-snapshot
New fluorescently labeled auxins exhibit promising anti-auxin activity
inferred← citeshttps://doi.org/10.1016/j.pbi.2013.08.003openalex-snapshot
From perception to attenuation: auxin signalling and responses
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.05.007openalex-snapshot
Refining the nuclear auxin response pathway through structural biology
inferred← citeshttps://doi.org/10.1016/j.pbi.2017.08.004openalex-snapshot
De novo root regeneration from leaf explants: wounding, auxin, and cell fate transition
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.10.003openalex-snapshot
Auxin signalling in growth: Schrödinger’s cat out of the bag
inferred← citeshttps://doi.org/10.1016/j.pbi.2022.102223openalex-snapshot
Selective chemical probes can untangle the complexity of the plant cell endomembrane system
inferred← citeshttps://doi.org/10.1016/j.plantsci.2016.09.005openalex-snapshot
SlTIR1 is involved in crosstalk of phytohormones, regulates auxin-induced root growth and stimulates stenospermocarpic fruit formation in tomato
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111535openalex-snapshot
Anti-auxin treatment and co-expression networks reveal auxin involvement in the transition to ripening in sweet cherry fruits
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100951openalex-snapshot
Leveraging computer-aided drug design for the discovery of phytohormone analogs: A review
inferred← citeshttps://doi.org/10.1016/j.tetasy.2013.03.008openalex-snapshot
Palladium-catalyzed asymmetric allylic alkylation of indoles by C–N bond axially chiral phosphine ligands
inferred← citeshttps://doi.org/10.1016/j.tips.2014.01.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.xplc.2024.101142openalex-snapshot
UV-B increases active phytochrome B to suppress thermomorphogenesis and enhance UV-B stress tolerance at high temperatures
inferred← citeshttps://doi.org/10.1016/j.ymeth.2019.04.010openalex-snapshot
Generation of conditional auxin-inducible degron (AID) cells and tight control of degron-fused proteins using the degradation inhibitor auxinole
inferred← citeshttps://doi.org/10.1021/acssynbio.4c00186openalex-snapshot
Genetically Encoded, Noise-Tolerant, Auxin Biosensors in Yeast
inferred← citeshttps://doi.org/10.1021/acssynbio.5c00970openalex-snapshot
A Constrained Degron Tag Engineered to Enhance Auxin-Inducible Protein Degradation
inferred← citeshttps://doi.org/10.1021/cb400618mopenalex-snapshot
Defining Binding Efficiency and Specificity of Auxins for SCFTIR1/AFB-Aux/IAA Co-receptor Complex Formation
inferred← citeshttps://doi.org/10.1038/nature13663openalex-snapshot
PLETHORA gradient formation mechanism separates auxin responses
inferred← citeshttps://doi.org/10.1038/nchembio.1524openalex-snapshot
Designed abscisic acid analogs as antagonists of PYL-PP2C receptor interactions
inferred← citeshttps://doi.org/10.1038/nchembio.1575openalex-snapshot
Rational design of a ligand-based antagonist of jasmonate perception
inferred← citeshttps://doi.org/10.1038/nchembio.1671openalex-snapshot
Sculpting the proteome with small molecules
inferred← citeshttps://doi.org/10.1038/s41467-018-03582-5openalex-snapshot
AUX1-mediated root hair auxin influx governs SCFTIR1/AFB-type Ca2+ signaling
inferred← citeshttps://doi.org/10.1038/s41467-025-65792-yopenalex-snapshot
Mutual inhibition between EPFL2 and auxin extends the intervals of periodic leaf morphogenesis
inferred← citeshttps://doi.org/10.1038/s41477-017-0008-6openalex-snapshot
Mechanical regulation of organ asymmetry in leaves
inferred← citeshttps://doi.org/10.1038/s41477-018-0190-1openalex-snapshot
Rapid and reversible root growth inhibition by TIR1 auxin signalling
inferred← citeshttps://doi.org/10.1038/s41586-021-04037-6openalex-snapshot
Cell surface and intracellular auxin signalling for H+ fluxes in root growth
inferred← citeshttps://doi.org/10.1038/s41598-017-14332-wopenalex-snapshot
Yucasin DF, a potent and persistent inhibitor of auxin biosynthesis in plants
inferred← citeshttps://doi.org/10.1038/s41598-018-25963-yopenalex-snapshot
Auxin decreases chromatin accessibility through the TIR1/AFBs auxin signaling pathway in proliferative cells
inferred← citeshttps://doi.org/10.1038/s41598-023-32063-zopenalex-snapshot
Design and synthesis of strong root gravitropism inhibitors with no concomitant growth inhibition
inferred← citeshttps://doi.org/10.1038/s43016-026-01295-3openalex-snapshot
Chemical inhibition of INO1 reduces phytic acid in rice and wheat grains for enhanced micronutrient bioavailability
inferred← citeshttps://doi.org/10.1039/9781839160691-00212openalex-snapshot
Plant E3 Ligases as Versatile Tools for Novel Drug Development and Plant Bioengineering
inferred← citeshttps://doi.org/10.1073/pnas.1407337111openalex-snapshot
Molecular genetic framework for protophloem formation
inferred← citeshttps://doi.org/10.1073/pnas.1413918111openalex-snapshot
Bimodal regulation of ICR1 levels generates self-organizing auxin distribution
inferred← citeshttps://doi.org/10.1073/pnas.1422656112openalex-snapshot
Arabidopsis ribosomal proteins control vacuole trafficking and developmental programs through the regulation of lipid metabolism
inferred← citeshttps://doi.org/10.1073/pnas.1517445113openalex-snapshot
Actin-dependent vacuolar occupancy of the cell determines auxin-induced growth repression
inferred← citeshttps://doi.org/10.1073/pnas.1600739113openalex-snapshot
Auxin-dependent compositional change in Mediator in ARF7- and ARF19-mediated transcription
inferred← citeshttps://doi.org/10.1073/pnas.1719387115openalex-snapshot
E3 ubiquitin ligase SOR1 regulates ethylene response in rice root by modulating stability of Aux/IAA protein
inferred← citeshttps://doi.org/10.1073/pnas.1809037116openalex-snapshot
Selective auxin agonists induce specific AUX/IAA protein degradation to modulate plant development
inferred← citeshttps://doi.org/10.1073/pnas.2121058119openalex-snapshot
RALF1 peptide triggers biphasic root growth inhibition upstream of auxin biosynthesis
inferred← citeshttps://doi.org/10.1073/pnas.2407224122openalex-snapshot
RACK1A positively regulates opening of the apical hook in Arabidopsis thaliana via suppression of its auxin response gradient
inferred← citeshttps://doi.org/10.1073/pnas.2515322122openalex-snapshot
Unveiling FERONIA receptor kinase–mediated cellular mechanisms with a small-molecule inhibitor
inferred← citeshttps://doi.org/10.1080/09168451.2017.1313694openalex-snapshot
Auxin signaling through SCFTIR1/AFBs mediates feedback regulation of IAA biosynthesis
inferred← citeshttps://doi.org/10.1080/09168451.2017.1313696openalex-snapshot
Structural basis for the regulation of phytohormone receptors
inferred← citeshttps://doi.org/10.1080/09168451.2018.1462693openalex-snapshot
Chemical regulators of plant hormones and their applications in basic research and agriculture*
inferred← citeshttps://doi.org/10.1080/15384101.2018.1563395openalex-snapshot
Conditional gene inactivation by combining tetracycline-mediated transcriptional repression and auxin-inducible degron-mediated degradation
inferred← citeshttps://doi.org/10.1080/15592324.2015.1071752openalex-snapshot
Gene expression profile of zeitlupe/lov kelch protein1 T-DNA insertion mutants in Arabidopsis thaliana: Downregulation of auxin-inducible genes in hypocotyls
inferred← citeshttps://doi.org/10.1083/jcb.202006116openalex-snapshot
Chromosome oscillation promotes Aurora A–dependent Hec1 phosphorylation and mitotic fidelity
inferred← citeshttps://doi.org/10.1088/1755-1315/657/1/012024openalex-snapshot
Loss-of-function of vacuolar-type H+ pyrophosphatase gene lead to reduce in stomatal aperture and density
inferred← citeshttps://doi.org/10.1093/genetics/iyag216openalex-snapshot
Conservation and divergence within the Arabidopsis TPL/TPR corepressor family
inferred← citeshttps://doi.org/10.1093/jxb/erae282openalex-snapshot
Arinole, a novel auxin-stimulating benzoxazole, affects root growth and promotes adventitious root formation
inferred← citeshttps://doi.org/10.1093/jxb/ers381openalex-snapshot
Increased levels of IAA are required for system 2 ethylene synthesis causing fruit softening in peach (Prunus persica L. Batsch)
inferred← citeshttps://doi.org/10.1093/jxb/eru470openalex-snapshot
Copper mediates auxin signalling to control cell differentiation in the copper moss Scopelophila cataractae
inferred← citeshttps://doi.org/10.1093/jxb/erv177openalex-snapshot
Auxin-binding pocket of ABP1 is crucial for its gain-of-function cellular and developmental roles
inferred← citeshttps://doi.org/10.1093/jxb/erv265openalex-snapshot
Novel imaging-based phenotyping strategies for dissecting crosstalk in plant development
inferred← citeshttps://doi.org/10.1093/jxb/erx255openalex-snapshot
Auxin-mediated developmental control in the moss Physcomitrella patens
inferred← citeshttps://doi.org/10.1093/jxb/erx258openalex-snapshot
A cheminformatics review of auxins as herbicides
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/jxb/ery034openalex-snapshot
Hydrotropism: how roots search for water
inferred← citeshttps://doi.org/10.1093/molbev/msz202openalex-snapshot
Molecular Evolution of Auxin-Mediated Root Initiation in Plants
inferred← citeshttps://doi.org/10.1093/pcp/pcaa098openalex-snapshot
An Evolutionarily Primitive and Distinct Auxin Metabolism in the Lycophyte Selaginella moellendorffii
inferred← citeshttps://doi.org/10.1093/pcp/pcae071openalex-snapshot
Radicle Growth Regulation of Root Parasitic Plants by Auxin-related Compounds
inferred← citeshttps://doi.org/10.1093/pcp/pcs017openalex-snapshot
A Chemical Biology Approach Reveals an Opposite Action between Thermospermine and Auxin in Xylem Development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/pcp/pcv088openalex-snapshot
Distinct Characteristics of Indole-3-Acetic Acid and Phenylacetic Acid, Two Common Auxins in Plants
inferred← citeshttps://doi.org/10.1093/pcp/pcx007openalex-snapshot
Biochemical and chemical biology study of rice OsTAR1 revealed that tryptophan aminotransferase is involved in auxin biosynthesis; identification of a potent OsTAR1 inhibitor, pyruvamine2031
inferred← citeshttps://doi.org/10.1093/pcp/pcy076openalex-snapshot
Manipulation and Sensing of Auxin Metabolism, Transport and Signaling
inferred← citeshttps://doi.org/10.1093/pcp/pcy182openalex-snapshot
Agrobacterium tumefaciensEnhances Biosynthesis of Two Distinct Auxins in the Formation of Crown Galls
inferred← citeshttps://doi.org/10.1093/plcell/koac250openalex-snapshot
Rice EIL1 interacts with OsIAAs to regulate auxin biosynthesis mediated by the tryptophan aminotransferase MHZ10/OsTAR2 during root ethylene responses
inferred← citeshttps://doi.org/10.1093/plphys/kiab278openalex-snapshot
Fluorescent biosensors illuminating plant hormone research
inferred← citeshttps://doi.org/10.1093/plphys/kiab369openalex-snapshot
A small molecule antagonizes jasmonic acid perception and auxin responses in vascular and nonvascular plants
inferred← citeshttps://doi.org/10.1093/plphys/kiad248openalex-snapshot
WAVE-DAMPENED2-LIKE4 modulates the hyper-elongation of light-grown hypocotyl cells
inferred← citeshttps://doi.org/10.1093/plphys/kiae405openalex-snapshot
Exogenous application of the apocarotenoid retinaldehyde negatively regulates auxin-mediated root growth
inferred← citeshttps://doi.org/10.1093/plphys/kiag586openalex-snapshot
Epigenetic modulators in plants: mechanistic insights, screening approaches, and prospective applications
inferred← citeshttps://doi.org/10.1097/fbp.0000000000000758openalex-snapshot
MA-5 ameliorates autism-like behavior in mice prenatally exposed to valproic acid
inferred← citeshttps://doi.org/10.1101/126466openalex-snapshot
Cell type boundaries organize plant development
inferred← citeshttps://doi.org/10.1101/2022.06.22.497127openalex-snapshot
Auxin-dependent acceleration of cell division rates regulates root growth at elevated temperature
inferred← citeshttps://doi.org/10.1101/2023.03.21.533585openalex-snapshot
Genetically encoded, noise-tolerant, auxin biosensors in yeast facilitate metabolic engineering and directed evolution
inferred← citeshttps://doi.org/10.1101/2024.06.05.597578openalex-snapshot
The Arabidopsis splicing factor PORCUPINE/SmE1 orchestrates temperature-dependent root development via auxin homeostasis maintenance
inferred← citeshttps://doi.org/10.1101/2024.06.17.599171openalex-snapshot
Hierarchical global and local auxin signals coordinate cellular interdigitation in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2024.12.11.628037openalex-snapshot
Effects of an auxin antagonist, PEO-IAA, and an auxin transport inhibitor, NPA, on gametophore development in Physcomitrium patens (Hedw.) Mitt
inferred← citeshttps://doi.org/10.1101/2025.11.04.686542openalex-snapshot
Nuclear auxin signalling induces autophagy for developmental reprogramming
inferred← citeshttps://doi.org/10.1101/716837openalex-snapshot
Rapid degradation of C. elegans proteins at single-cell resolution with a synthetic auxin
inferred← citeshttps://doi.org/10.1101/cshperspect.a039891openalex-snapshot
No Time for Transcription—Rapid Auxin Responses in Plants
inferred← citeshttps://doi.org/10.1101/cshperspect.a039933openalex-snapshot
Auxin in Root Development
inferred← citeshttps://doi.org/10.1101/cshperspect.a040105openalex-snapshot
Chemical Biology in Auxin Research
inferred← citeshttps://doi.org/10.1104/pp.112.196428openalex-snapshot
Auxin Activates the Plasma Membrane H+-ATPase by Phosphorylation during Hypocotyl Elongation in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.113.215582openalex-snapshot
Mutations in the TIR1 Auxin Receptor That Increase Affinity for Auxin/Indole-3-Acetic Acid Proteins Result in Auxin Hypersensitivity
inferred← citeshttps://doi.org/10.1104/pp.114.241844openalex-snapshot
Cotyledon-Generated Auxin Is Required for Shade-Induced Hypocotyl Growth in Brassica rapa
inferred← citeshttps://doi.org/10.1104/pp.15.01540openalex-snapshot
Novel Vein Patterns in Arabidopsis Induced by Small Molecules
inferred← citeshttps://doi.org/10.1104/pp.17.00733openalex-snapshot
Protoplast Swelling and Hypocotyl Growth Depend on Different Auxin Signaling Pathways
inferred← citeshttps://doi.org/10.1104/pp.18.00357openalex-snapshot
Jasmonic Acid Inhibits Auxin-Induced Lateral Rooting Independently of the CORONATINE INSENSITIVE1 Receptor
inferred← citeshttps://doi.org/10.1104/pp.19.00201openalex-snapshot
Pinstatic Acid Promotes Auxin Transport by Inhibiting PIN Internalization
inferred← citeshttps://doi.org/10.1104/pp.20.00090openalex-snapshot
Retrograde Induction of phyB Orchestrates Ethylene-Auxin Hierarchy to Regulate Growth
inferred← citeshttps://doi.org/10.1105/tpc.19.00695openalex-snapshot
Auxin Regulates Sucrose Transport to Repress Petal Abscission in Rose ( Rosa hybrida )
inferred← citeshttps://doi.org/10.1111/jipb.12666openalex-snapshot
Ethylene‐induced microtubule reorientation is essential for fast inhibition of root elongation in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.12880openalex-snapshot
Involvement of YODA and mitogen activated protein kinase 6 in Arabidopsis post‐embryogenic root development through auxin up‐regulation and cell division plane orientation
inferred← citeshttps://doi.org/10.1111/nph.15337openalex-snapshot
Harnessing synthetic chemistry to probe and hijack auxin signaling
inferred← citeshttps://doi.org/10.1111/nph.16068openalex-snapshot
Minimal auxin sensing levels in vegetative moss stem cells revealed by a ratiometric reporter
inferred← citeshttps://doi.org/10.1111/nph.16446openalex-snapshot
Auxin canalization and vascular tissue formation by TIR1/AFB‐mediated auxin signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.16914openalex-snapshot
Studies of moss reproductive development indicate that auxin biosynthesis in apical stem cells may constitute an ancestral function for focal growth control
inferred← citeshttps://doi.org/10.1111/nph.20153openalex-snapshot
The Arabidopsis splicing factor PORCUPINE / S m E 1 orchestrates temperature‐dependent root development via auxin homeostasis maintenance
inferred← citeshttps://doi.org/10.1111/nph.70763openalex-snapshot
A novel mechanism of auxin habituation: upregulation of auxin receptor TRANSPORT INHIBITOR RESPONSE 1 allows cell proliferation independent of external auxin
inferred← citeshttps://doi.org/10.1111/nph.71625openalex-snapshot
OsDRP1C mediates root development by modulating OsPIN1 cycling in rice
inferred← citeshttps://doi.org/10.1111/ppl.12128openalex-snapshot
Auxin biology revealed by small molecules
inferred← citeshttps://doi.org/10.1111/ppl.70023openalex-snapshot
Ectopic expression of LONELY GUY7 in epidermis of internodal segments for de novo shoot regeneration without phytohormone treatment in ipecac
inferred← citeshttps://doi.org/10.1111/tpj.12399openalex-snapshot
Yucasin is a potent inhibitor of YUCCA , a key enzyme in auxin biosynthesis
inferred← citeshttps://doi.org/10.1111/tpj.12824openalex-snapshot
The glucosinolate breakdown product indole‐3‐carbinol acts as an auxin antagonist in roots of A rabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/tpj.13032openalex-snapshot
Small‐molecule auxin inhibitors that target YUCCA are powerful tools for studying auxin function
inferred← citeshttps://doi.org/10.1111/tpj.13197openalex-snapshot
Aminooxy‐naphthylpropionic acid and its derivatives are inhibitors of auxin biosynthesis targeting l ‐tryptophan aminotransferase: structure–activity relationships
inferred← citeshttps://doi.org/10.1111/tpj.14978openalex-snapshot
Rice plants respond to ammonium stress by adopting a helical root growth pattern
inferred← citeshttps://doi.org/10.1111/tpj.15115openalex-snapshot
Ligand–receptor interactions in plant hormone signaling
inferred← citeshttps://doi.org/10.1111/tpj.16430openalex-snapshot
Structure–activity relationship of 2, 4‐D correlates auxinic activity with the induction of somatic embryogenesis in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/tpj.16683openalex-snapshot
Hydrotropism mechanisms and their interplay with gravitropism
inferred← citeshttps://doi.org/10.1126/sciadv.abj1570openalex-snapshot
Biphasic control of cell expansion by auxin coordinates etiolated seedling development
inferred← citeshttps://doi.org/10.1146/annurev-arplant-042916-041107openalex-snapshot
Chemical Genetic Dissection of Membrane Trafficking
inferred← citeshttps://doi.org/10.1146/annurev-arplant-073019-025907openalex-snapshot
Rapid Auxin-Mediated Cell Expansion
inferred← citeshttps://doi.org/10.1186/s12870-018-1477-0openalex-snapshot
Modulation of auxin and cytokinin responses by early steps of the phenylpropanoid pathway
inferred← citeshttps://doi.org/10.1242/dev.149336openalex-snapshot
Self-organizing periodicity in development: organ positioning in plants
inferred← citeshttps://doi.org/10.1242/dev.159707openalex-snapshot
GTL1 and DF1 regulate root hair growth through transcriptional repression of ROOT HAIR DEFECTIVE 6-LIKE 4 in Arabidopsis
inferred← citeshttps://doi.org/10.1242/dev.169839openalex-snapshot
The plant hormone auxin beats the time for oscillating light-regulated lateral root induction
inferred← citeshttps://doi.org/10.1242/dev.201775openalex-snapshot
N6-adenosine methylation of mRNA integrates multilevel auxin response and ground tissue development in Arabidopsis
inferred← citeshttps://doi.org/10.1242/dev.202586openalex-snapshot
HD-Zip II transcription factors control distal stem cell fate in Arabidopsis roots by linking auxin signaling to the FEZ/SOMBRERO pathway
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006360openalex-snapshot
Local Transcriptional Control of YUCCA Regulates Auxin Promoted Root-Growth Inhibition in Response to Aluminium Stress in Arabidopsis
inferred← citeshttps://doi.org/10.1371/journal.pone.0095972openalex-snapshot
miR393 Is Required for Production of Proper Auxin Signalling Outputs
inferred← citeshttps://doi.org/10.1371/journal.pone.0131213openalex-snapshot
Targeting Hormone-Related Pathways to Improve Grain Yield in Rice: A Chemical Approach
inferred← citeshttps://doi.org/10.1371/journal.ppat.1013662openalex-snapshot
Salmonella enterica exploits the auxin signaling pathway to overcome stomatal immunity
inferred← citeshttps://doi.org/10.14945/00008273openalex-snapshot
Studies on Development of ABA Receptor Antagonists
inferred← citeshttps://doi.org/10.15252/embj.2022111926openalex-snapshot
Auxin‐dependent regulation of cell division rates governs root thermomorphogenesis
inferred← citeshttps://doi.org/10.1534/g3.119.400781openalex-snapshot
Rapid Degradation ofCaenorhabditis elegansProteins at Single-Cell Resolution with a Synthetic Auxin
inferred← citeshttps://doi.org/10.1584/jpestics.d16-028openalex-snapshot
Discovery and identification of 2-methoxy-1-naphthaldehyde as a novel strigolactone-signaling inhibitor
inferred← citeshttps://doi.org/10.1584/jpestics.w14-29openalex-snapshot
Small molecule modulators on auxin biosynthesis and signaling
inferred← citeshttps://doi.org/10.1620/tjem.236.225openalex-snapshot
Mitochonic Acid 5 (MA-5), a Derivative of the Plant Hormone Indole-3-Acetic Acid, Improves Survival of Fibroblasts from Patients with Mitochondrial Diseases
inferred← citeshttps://doi.org/10.17660/actahortic.2018.1206.34openalex-snapshot
HPY2gene expression analysis and the role of auxin in early fruit development in tomato
inferred← citeshttps://doi.org/10.18174/511017openalex-snapshot
Proteomics perspective on auxin biology
inferred← citeshttps://doi.org/10.18297/etd/3830openalex-snapshot
Functional role of PPAL and potential for moss in industrial applications.
inferred← citeshttps://doi.org/10.18978/jscrp.47.1_1openalex-snapshot
オーキシンの信号伝達・輸送に関するケミカルバイオロジー(学会賞,受賞業績)
inferred← citeshttps://doi.org/10.2144/btn-2022-0108openalex-snapshot
Auxin-Inducible Degron System: An Efficient Protein Degradation Tool to Study Protein Function
inferred← citeshttps://doi.org/10.2187/bss.25.45openalex-snapshot
New Insights to Auxin Signaling through The Use of Small Molecules
inferred← citeshttps://doi.org/10.3389/fchem.2022.975267openalex-snapshot
Design, synthesis, and herbicidal activity of indole-3-carboxylic acid derivatives as potential transport inhibitor response 1 antagonists
inferred← citeshttps://doi.org/10.3389/fpls.2014.00373openalex-snapshot
Unraveling plant hormone signaling through the use of small molecules
inferred← citeshttps://doi.org/10.3389/fpls.2014.00709openalex-snapshot
Molecular locks and keys: the role of small molecules in phytohormone research
inferred← citeshttps://doi.org/10.3389/fpls.2018.00550openalex-snapshot
Dynamic Modeling of Indole Glucosinolate Hydrolysis and Its Impact on Auxin Signaling
inferred← citeshttps://doi.org/10.3389/fpls.2019.00590openalex-snapshot
The 26S Proteasome Is Required for the Maintenance of Root Apical Meristem by Modulating Auxin and Cytokinin Responses Under High-Boron Stress
inferred← citeshttps://doi.org/10.3389/fpls.2022.1011360openalex-snapshot
Tryptophan synthase ß subunit 1 affects stomatal phenotypes in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2022.1060021openalex-snapshot
Endocytic trafficking induces lateral root founder cell specification in Arabidopsis thaliana in a process distinct from the auxin-induced pathway
inferred← citeshttps://doi.org/10.3389/fpls.2026.1820149openalex-snapshot
Spatiotemporal reprogramming of auxin signaling and resistance outputs across model plants and solanaceae crops under Ralstonia solanacearum infection
inferred← citeshttps://doi.org/10.3390/agronomy12112647openalex-snapshot
Genome-Wide Transcriptome Analysis Reveals That Upregulated Expression of Aux/IAA Genes Is Associated with Defective Leaf Growth of the slf Mutant in Eggplant
inferred← citeshttps://doi.org/10.3390/cells11172652openalex-snapshot
Auxin Regulates Apical Stem Cell Regeneration and Tip Growth in the Marine Red Alga Neopyropia yezoensis
inferred← citeshttps://doi.org/10.3390/computation12050094openalex-snapshot
To Bind or Not to Bind? A Comprehensive Characterization of TIR1 and Auxins Using Consensus In Silico Approaches
inferred← citeshttps://doi.org/10.3390/genes9120638openalex-snapshot
The 5′-3′ Exoribonuclease XRN4 Regulates Auxin Response via the Degradation of Auxin Receptor Transcripts
inferred← citeshttps://doi.org/10.3390/ijms151222155openalex-snapshot
Identification and Evaluation of Reliable Reference Genes for Quantitative Real-Time PCR Analysis in Tea Plant (Camellia sinensis (L.) O. Kuntze)
inferred← citeshttps://doi.org/10.3390/ijms20184428openalex-snapshot
A DAO1-Mediated Circuit Controls Auxin and Jasmonate Crosstalk Robustness during Adventitious Root Initiation in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms21031124openalex-snapshot
Recent Advances in Plant Chemical Biology of Jasmonates
inferred← citeshttps://doi.org/10.3390/ijms22083862openalex-snapshot
Pickle Recruits Retinoblastoma Related 1 to Control Lateral Root Formation in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms222111843openalex-snapshot
Dynamic Hormone Gradients Regulate Wound-Induced de novo Organ Formation in Tomato Hypocotyl Explants
inferred← citeshttps://doi.org/10.3390/ijms23094618openalex-snapshot
The Phytotoxin Myrigalone A Triggers a Phased Detoxification Programme and Inhibits Lepidium sativum Seed Germination via Multiple Mechanisms including Interference with Auxin Homeostasis
inferred← citeshttps://doi.org/10.3390/ijms24108514openalex-snapshot
Precise Regulation of the TAA1/TAR-YUCCA Auxin Biosynthesis Pathway in Plants
inferred← citeshttps://doi.org/10.3390/life12081285openalex-snapshot
New Wine in an Old Bottle: Utilizing Chemical Genetics to Dissect Apical Hook Development
inferred← citeshttps://doi.org/10.3390/microorganisms8040471openalex-snapshot
Pseudomonas PS01 Isolated from Maize Rhizosphere Alters Root System Architecture and Promotes Plant Growth
inferred← citeshttps://doi.org/10.3390/plants15152256openalex-snapshot
Ubiquitination-Mediated Regulation of Brassinosteroid Signaling
inferred← citeshttps://doi.org/10.3390/plants9101270openalex-snapshot
Orange Leafhopper Cicadulina bipunctata Feeding Induces Gall Formation Nitrogen Dependently and Regulates Gibberellin Signaling
inferred← citeshttps://doi.org/10.3390/v8110314openalex-snapshot
Plant Virus Infection and the Ubiquitin Proteasome Machinery: Arms Race along the Endoplasmic Reticulum
inferred← citeshttps://doi.org/10.3987/com-14-12957openalex-snapshot
Sequential Radical Addition and Fischer-Type Indolization Reactions of Conjugated Hydrazones for the Preparation of α-Alkylindole-3-acetic Acids
inferred← citeshttps://doi.org/10.48130/ph-0026-0002openalex-snapshot
Recent advances in the chemical control of plant hormone responses
inferred← citeshttps://doi.org/10.5155/eurjchem.13.2.172-179.2271openalex-snapshot
Describing auxin solid state intermolecular interactions using contact descriptors, shape property and molecular fingerprint: comparison of pure auxin crystal and auxin-TIR1 co-crystal
inferred← citeshttps://doi.org/10.64898/2026.01.02.697414openalex-snapshot
Auxin coordinates cell states during Arabidopsis root development
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