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Local Auxin Biosynthesis Is a Key Regulator of Plant Development
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9781118147634openalex-snapshot
Design and Analysis of Experiments
inferredcites →https://doi.org/10.1007/978-1-4939-1652-8_11openalex-snapshot
A Recombineering-Based Gene Tagging System for Arabidopsis
inferredcites →https://doi.org/10.1007/978-1-4939-6854-1_13openalex-snapshot
The Triple Response Assay and Its Use to Characterize Ethylene Mutants in Arabidopsis
inferredcites →https://doi.org/10.1007/978-1-60761-765-5_12openalex-snapshot
Analysis of Root Meristem Size Development
inferredcites →https://doi.org/10.1007/978-1-62703-580-4_15openalex-snapshot
Arabidopsis Transformation with Large Bacterial Artificial Chromosomes
inferredcites →https://doi.org/10.1007/bf00027120openalex-snapshot
The intron of Arabidopsis thaliana polyubiquitin genes is conserved in location and is a quantitative determinant of chimeric gene expression
inferredcites →https://doi.org/10.1007/bf00262639openalex-snapshot
Comparison of mechanisms controlling uptake and accumulation of 2,4-dichlorophenoxy acetic acid, naphthalene-1-acetic acid, and indole-3-acetic acid in suspension-cultured tobacco cells
inferredcites →https://doi.org/10.1016/j.cell.2008.01.047openalex-snapshot
TAA1-Mediated Auxin Biosynthesis Is Essential for Hormone Crosstalk and Plant Development
inferredcites →https://doi.org/10.1016/j.cell.2008.01.049openalex-snapshot
Rapid Synthesis of Auxin via a New Tryptophan-Dependent Pathway Is Required for Shade Avoidance in Plants
inferredcites →https://doi.org/10.1016/j.cpb.2016.12.001openalex-snapshot
The Bio-Analytic Resource: Data visualization and analytic tools for multiple levels of plant biology
inferredcites →https://doi.org/10.1016/j.cub.2013.09.039openalex-snapshot
Local Auxin Sources Orient the Apical-Basal Axis in Arabidopsis Embryos
inferredcites →https://doi.org/10.1016/j.cub.2015.03.032openalex-snapshot
A Developmental Framework for Graft Formation and Vascular Reconnection in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s0092-8674(00)81536-6openalex-snapshot
WEREWOLF, a MYB-Related Protein in Arabidopsis, Is a Position-Dependent Regulator of Epidermal Cell Patterning
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/10.1038/415806aopenalex-snapshot
Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis
inferredcites →https://doi.org/10.1038/nature01387openalex-snapshot
Auxin promotes Arabidopsis root growth by modulating gibberellin response
inferredcites →https://doi.org/10.1038/nature02085openalex-snapshot
Efflux-dependent auxin gradients establish the apical–basal axis of Arabidopsis
inferredcites →https://doi.org/10.1038/nature03184openalex-snapshot
The PIN auxin efflux facilitator network controls growth and patterning in Arabidopsis roots
inferredcites →https://doi.org/10.1038/nature05703openalex-snapshot
Conserved factors regulate signalling in Arabidopsis thaliana shoot and root stem cell organizers
inferredcites →https://doi.org/10.1038/nature06215openalex-snapshot
Auxin transport is sufficient to generate a maximum and gradient guiding root growth
inferredcites →https://doi.org/10.1038/nature10791openalex-snapshot
A novel sensor to map auxin response and distribution at high spatio-temporal resolution
inferredcites →https://doi.org/10.1038/ncb1754openalex-snapshot
The auxin influx carrier LAX3 promotes lateral root emergence
inferredcites →https://doi.org/10.1038/nmeth.3279openalex-snapshot
Reporters for sensitive and quantitative measurement of auxin response
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/10.1038/s41467-018-03851-3openalex-snapshot
A mechanistic framework for auxin dependent Arabidopsis root hair elongation to low external phosphate
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.6050759.xopenalex-snapshot
Real‐time imaging of phloem unloading in the root tip of Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01419.xopenalex-snapshot
Micrografting techniques for testing long‐distance signalling in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0712307105openalex-snapshot
Auxin acts as a local morphogenetic trigger to specify lateral root founder cells
inferredcites →https://doi.org/10.1073/pnas.1108434108openalex-snapshot
The main auxin biosynthesis pathway in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1400966111openalex-snapshot
Plant roots use a patterning mechanism to position lateral root branches toward available water
inferredcites →https://doi.org/10.1073/pnas.1707566114openalex-snapshot
Predicting gene regulatory networks by combining spatial and temporal gene expression data in Arabidopsis root stem cells
inferredcites →https://doi.org/10.1073/pnas.1717649115openalex-snapshot
The plant hormone ethylene restricts Arabidopsis growth via the epidermis
inferredcites →https://doi.org/10.1093/genetics/139.3.1393openalex-snapshot
Genetic analysis of ethylene signal transduction in Arabidopsis thaliana: five novel mutant loci integrated into a stress response pathway.
inferredcites →https://doi.org/10.1093/pcp/pcu039openalex-snapshot
Auxin Overproduction in Shoots Cannot Rescue Auxin Deficiencies in Arabidopsis Roots
inferredcites →https://doi.org/10.1101/cshperspect.a001537openalex-snapshot
Auxin Control of Root Development
inferredcites →https://doi.org/10.1101/gad.1415106openalex-snapshot
Auxin biosynthesis by the YUCCA flavin monooxygenases controls the formation of floral organs and vascular tissues in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.305504openalex-snapshot
Mosaic analyses using marked activation and deletion clones dissect Arabidopsis SCARECROW action in asymmetric cell division
inferredcites →https://doi.org/10.1104/pp.109.138859openalex-snapshot
The TRANSPORT INHIBITOR RESPONSE2 Gene Is Required for Auxin Synthesis and Diverse Aspects of Plant Development
inferredcites →https://doi.org/10.1104/pp.15.01845openalex-snapshot
Transcriptomic Signature of the SHATTERPROOF2 Expression Domain Reveals the Meristematic Nature of Arabidopsis Gynoecial Medial Domain
inferredcites →https://doi.org/10.1104/pp.94.3.1462openalex-snapshot
The aux1 Mutation of Arabidopsis Confers Both Auxin and Ethylene Resistance
inferredcites →https://doi.org/10.1105/tpc.104.029272openalex-snapshot
Sites and Regulation of Auxin Biosynthesis in Arabidopsis Roots
inferredcites →https://doi.org/10.1105/tpc.105.033365openalex-snapshot
A Link between Ethylene and Auxin Uncovered by the Characterization of Two Root-Specific Ethylene-Insensitive Mutants in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.034637openalex-snapshot
Maintenance of Embryonic Auxin Distribution for Apical-Basal Patterning by PIN-FORMED–Dependent Auxin Transport in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.040782openalex-snapshot
Interactions among PIN-FORMED and P-Glycoprotein Auxin Transporters in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.107.052068openalex-snapshot
Multilevel Interactions between Ethylene and Auxin in Arabidopsis Roots
inferredcites →https://doi.org/10.1105/tpc.107.052100openalex-snapshot
Ethylene Upregulates Auxin Biosynthesis in Arabidopsis Seedlings to Enhance Inhibition of Root Cell Elongation
inferredcites →https://doi.org/10.1105/tpc.107.052126openalex-snapshot
Ethylene Regulates Root Growth through Effects on Auxin Biosynthesis and Transport-Dependent Auxin Distribution
inferredcites →https://doi.org/10.1105/tpc.107.053009openalex-snapshot
Auxin Synthesized by the YUCCA Flavin Monooxygenases Is Essential for Embryogenesis and Leaf Formation in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.088047openalex-snapshot
The Arabidopsis YUCCA1 Flavin Monooxygenase Functions in the Indole-3-Pyruvic Acid Branch of Auxin Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.113.119495openalex-snapshot
Systems Analysis of Auxin Transport in the Arabidopsis Root Apex
inferredcites →https://doi.org/10.1105/tpc.114.134874openalex-snapshot
PIN-Dependent Auxin Transport: Action, Regulation, and Evolution
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/10.1111/j.1365-313x.2005.02519.xopenalex-snapshot
Cellular efflux of auxin catalyzed by the Arabidopsis MDR/PGP transporter AtPGP1
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04509.xopenalex-snapshot
Functional characterization of the CKRC1/TAA1 gene and dissection of hormonal actions in the Arabidopsis root
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05085.xopenalex-snapshot
Tissue‐specific profiling of the Arabidopsis thaliana auxin metabolome
inferredcites →https://doi.org/10.1111/ppl.12098openalex-snapshot
Genetic aspects of auxin biosynthesis and its regulation
inferredcites →https://doi.org/10.1111/tpj.12399openalex-snapshot
Yucasin is a potent inhibitor of YUCCA , a key enzyme in auxin biosynthesis
inferredcites →https://doi.org/10.1111/tpj.13312openalex-snapshot
A high resolution map of the Arabidopsis thaliana developmental transcriptome based on RNA ‐seq profiling
inferredcites →https://doi.org/10.1126/science.1086391openalex-snapshot
Genome-Wide Insertional Mutagenesis of Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1153795openalex-snapshot
Cell Identity Mediates the Response of Arabidopsis Roots to Abiotic Stress
inferredcites →https://doi.org/10.1126/science.291.5502.306openalex-snapshot
A Role for Flavin Monooxygenase-Like Enzymes in Auxin Biosynthesis
inferredcites →https://doi.org/10.1242/dev.127613openalex-snapshot
ClearSee: a rapid optical clearing reagent for whole-plant fluorescence imaging
inferredcites →https://doi.org/10.1263/jbb.104.34openalex-snapshot
Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for plant transformation
inferredcites →https://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
inferredcites →https://doi.org/10.2307/3870557openalex-snapshot
Aux/IAA Proteins Repress Expression of Reporter Genes Containing Natural and Highly Active Synthetic Auxin Response Elements
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Biochar improves root growth and nitrogen metabolism in tobacco through physiological pathways modulation
inferred← citeshttps://doi.org/10.1016/j.rhisph.2025.101160openalex-snapshot
The plant growth-promoting rhizobacteria Azospirillum baldaniorum Sp245 induces root branching through the participation of PLASMODESMATA-LOCATED PROTEIN 5 in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.sajb.2024.02.041openalex-snapshot
Augmenting abiotic stress tolerance and root architecture: The function of phytohormone-producing PGPR and their interaction with nanoparticles
inferred← citeshttps://doi.org/10.1016/j.scienta.2019.109164openalex-snapshot
Untargeted metabolomic analysis using UPLC-MS/MS identifies metabolites involved in shoot growth and development in pruned tea plants (Camellia sinensis (L.) O. Kuntz)
inferred← citeshttps://doi.org/10.1016/j.scienta.2020.109435openalex-snapshot
MicroRNA regulation during the tomato fruit development and ripening: A review
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111536openalex-snapshot
Integrative analysis based on transcriptome revealed the relation of auxin to turnip hypocotyl-tuber formation
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113694openalex-snapshot
Comprehensive identification of PIN and PILS in crape myrtle genomes reveals their putative functions in bud-to-branch development and callus generation
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.162327openalex-snapshot
Heavy metals and arsenic stress in food crops: Elucidating antioxidative defense mechanisms in hyperaccumulators for food security, agricultural sustainability, and human health
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100152openalex-snapshot
Role of phytohormones in regulating cold stress tolerance: Physiological and molecular approaches for developing cold-smart crop plants
inferred← citeshttps://doi.org/10.1016/j.tplants.2019.05.006openalex-snapshot
Auxin Metabolism Controls Developmental Decisions in Land Plants
inferred← citeshttps://doi.org/10.1016/j.tplants.2022.08.002openalex-snapshot
Signaling events for photomorphogenic root development
inferred← citeshttps://doi.org/10.1016/j.tplants.2024.10.015openalex-snapshot
The whole and its parts: cell-specific functions of brassinosteroids
inferred← citeshttps://doi.org/10.1016/j.tplants.2025.02.009openalex-snapshot
Necessity for modeling hormonal crosstalk in arabidopsis root development?
inferred← citeshttps://doi.org/10.1016/j.xplc.2024.100978openalex-snapshot
Single-cell network analysis reveals gene expression programs for Arabidopsis root development and metabolism
inferred← citeshttps://doi.org/10.1017/qpb.2023.13openalex-snapshot
A blast from the past: Understanding stem cell specification in plant roots using laser ablation
inferred← citeshttps://doi.org/10.1021/acs.jced.5c00115openalex-snapshot
Solubility of Indole-3-butyric Acid in 19 Monosolvents: Characterization, Determination, Molecular Simulations, and Model Correlation
inferred← citeshttps://doi.org/10.1038/s41467-021-21802-3openalex-snapshot
Cell kinetics of auxin transport and activity in Arabidopsis root growth and skewing
inferred← citeshttps://doi.org/10.1038/s41467-022-34723-6openalex-snapshot
Specification of female germline by microRNA orchestrated auxin signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41477-020-0648-9openalex-snapshot
The lipid code-dependent phosphoswitch PDK1–D6PK activates PIN-mediated auxin efflux in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41477-020-0737-9openalex-snapshot
Local auxin biosynthesis is required for root regeneration after wounding
inferred← citeshttps://doi.org/10.1038/s41477-024-01810-zopenalex-snapshot
A coherent feed-forward loop in the Arabidopsis root stem cell organizer regulates auxin biosynthesis and columella stem cell maintenance
inferred← citeshttps://doi.org/10.1038/s41580-025-00851-2openalex-snapshot
Mechanisms of auxin action in plant growth and development
inferred← citeshttps://doi.org/10.1038/s41586-020-2778-7openalex-snapshot
A single bacterial genus maintains root growth in a complex microbiome
inferred← citeshttps://doi.org/10.1038/s41586-021-03425-2openalex-snapshot
A biosensor for the direct visualization of auxin
inferred← citeshttps://doi.org/10.1038/s41598-022-12815-zopenalex-snapshot
Belgian endive-derived biostimulants promote shoot and root growth in vitro
inferred← citeshttps://doi.org/10.1038/s41598-026-45070-7openalex-snapshot
Network ontology transcript annotation identifies genetic signals underlying sex determination
inferred← citeshttps://doi.org/10.1038/s42003-024-06747-9openalex-snapshot
Polarly localized Bro1 domain proteins regulate PIN-FORMED abundance and root gravitropic growth in Arabidopsis
inferred← citeshttps://doi.org/10.1071/fp19215openalex-snapshot
Improved reproductive growth of euhalophyte Suaeda salsa under salinity is correlated with altered phytohormone biosynthesis and signal transduction
inferred← citeshttps://doi.org/10.1073/pnas.2013305117openalex-snapshot
The Arabidopsis NRT1/PTR FAMILY protein NPF7.3/NRT1.5 is an indole-3-butyric acid transporter involved in root gravitropism
inferred← citeshttps://doi.org/10.1073/pnas.2023942118openalex-snapshot
Transcriptional control of local auxin distribution by the CsDFB1-CsPHB module regulates floral organogenesis in cucumber
inferred← citeshttps://doi.org/10.1073/pnas.2212881119openalex-snapshot
Mitochondrial GPAT-derived LPA controls auxin-dependent embryonic and postembryonic development
inferred← citeshttps://doi.org/10.1073/pnas.2301054120openalex-snapshot
Plant microbiota controls an alternative root branching regulatory mechanism in plants
inferred← citeshttps://doi.org/10.1073/pnas.2615485123openalex-snapshot
The NAC transcription factor SOMBRERO controls auxin gradients for columella root cap maturation and turnover
inferred← citeshttps://doi.org/10.1080/01904167.2025.2459866openalex-snapshot
Biostimulators in sustainable agriculture: the example of red lettuce
inferred← citeshttps://doi.org/10.1080/07352689.2020.1820203openalex-snapshot
On the Way to Ovules: The Hormonal Regulation of Ovule Development
inferred← citeshttps://doi.org/10.1080/07352689.2023.2211848openalex-snapshot
Functional Versatility of Multi-Protein Mediator Complex in Plant Growth and Development
inferred← citeshttps://doi.org/10.1080/07388551.2023.2240009openalex-snapshot
A crosswalk on the genetic and conventional strategies for enhancing astaxanthin production in Haematococcus pluvialis
inferred← citeshttps://doi.org/10.1080/14620316.2026.2622387openalex-snapshot
Chitosan mediated organogenesis in hybrid Dendrobium (Dendrobium Enopi x Dendrobium Pink Lady) through protocorm-like bodies
inferred← citeshttps://doi.org/10.1080/15592324.2024.2310963openalex-snapshot
Endogenous cAMP elevation in Brassica napus causes changes in phytohormone levels
inferred← citeshttps://doi.org/10.1088/1755-1315/1487/1/012070openalex-snapshot
Micropropagation of Prunus Sp., Factors, Hormones: A Review
inferred← citeshttps://doi.org/10.1088/1755-1315/761/1/012003openalex-snapshot
Microbial Technique for The Production of Growth Regulator Compounds Indole Butyric Acid (IBA) and Its Role on The Rooting and Growth of Bougainvillea Spectabilis L. Stem Cuttings
inferred← citeshttps://doi.org/10.1093/bbb/zbaa033openalex-snapshot
Effect of an auxin biosynthesis inhibitor, p-phenoxyphenyl boronic acid, on auxin biosynthesis and development in rice
inferred← citeshttps://doi.org/10.1093/hr/uhad095openalex-snapshot
Al-induced CsUGT84J2 enhances flavonol and auxin accumulation to promote root growth in tea plants
inferred← citeshttps://doi.org/10.1093/jxb/eraa027openalex-snapshot
Same same, but different: growth responses of primary and lateral roots
inferred← citeshttps://doi.org/10.1093/jxb/eraa033openalex-snapshot
Signaling pathways underlying nitrogen-dependent changes in root system architecture: from model to crop species
inferred← citeshttps://doi.org/10.1093/jxb/eraa242openalex-snapshot
The Arabidopsis NRT1.1 transceptor coordinately controls auxin biosynthesis and transport to regulate root branching in response to nitrate
inferred← citeshttps://doi.org/10.1093/jxb/eraa269openalex-snapshot
Extreme environments: crucibles of potent abiotic stress tolerance
inferred← citeshttps://doi.org/10.1093/jxb/eraa485openalex-snapshot
Endogenous indole-3-acetamide levels contribute to the crosstalk between auxin and abscisic acid, and trigger plant stress responses in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/eraa501openalex-snapshot
Auxin biosynthesis and cellular efflux act together to regulate leaf vein patterning
inferred← citeshttps://doi.org/10.1093/jxb/erab009openalex-snapshot
The production of auxin by dying cells
inferred← citeshttps://doi.org/10.1093/jxb/erab025openalex-snapshot
Coordination between MIDASIN 1 -mediated ribosome biogenesis and auxin modulates plant development
inferred← citeshttps://doi.org/10.1093/jxb/erab272openalex-snapshot
Root stem cell niche networks: it’s complexed! Insights from Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erab274openalex-snapshot
Mechanisms of stress response in the root stem cell niche
inferred← citeshttps://doi.org/10.1093/jxb/erab319openalex-snapshot
The quiescent center and root regeneration
inferred← citeshttps://doi.org/10.1093/jxb/erab360openalex-snapshot
Hormonal orchestration of root apical meristem formation and maintenance in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erab405openalex-snapshot
The quiescent centre and root apical meristem: organization and function
inferred← citeshttps://doi.org/10.1093/jxb/erac280openalex-snapshot
Actin isovariant ACT7 controls root meristem development in Arabidopsis through modulating auxin and ethylene responses
inferred← citeshttps://doi.org/10.1093/jxb/erad244openalex-snapshot
Spatial regulation of plant hormone action
inferred← citeshttps://doi.org/10.1093/jxb/erae201openalex-snapshot
Stem cell quiescence and dormancy in plant meristems
inferred← citeshttps://doi.org/10.1093/jxb/erae305openalex-snapshot
Alternate bearing in ‘Hass’ avocado: fruit load-induced changes in bud auxin homeostasis are associated with flowering repression
inferred← citeshttps://doi.org/10.1093/jxb/eraf225openalex-snapshot
PHLOEM EARLY DOFs (PEARs) are induced within clubroot galls as a consequence of cambial stimulation and vascular reprogramming during Plasmodiophora brassicae infection in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/jxb/erz283openalex-snapshot
Auxin biosynthesis: spatial regulation and adaptation to stress
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/pcaf008openalex-snapshot
Auxin fluctuation and PIN polarization in moss leaf cell reprogramming
inferred← citeshttps://doi.org/10.1093/pcp/pcz156openalex-snapshot
A Positive Feedback Loop Comprising LHW–TMO5 and Local Auxin Biosynthesis Regulates Initial Vascular Development in Arabidopsis Roots
inferred← citeshttps://doi.org/10.1093/plcell/koac177openalex-snapshot
The retrograde signaling regulator ANAC017 recruits the MKK9–MPK3/6, ethylene, and auxin signaling pathways to balance mitochondrial dysfunction with growth
inferred← citeshttps://doi.org/10.1093/plcell/koac179openalex-snapshot
On the trail of auxin: Reporters and sensors
inferred← citeshttps://doi.org/10.1093/plcell/koae071openalex-snapshot
Nonspecific phospholipases C3 and C4 interact with PIN-FORMED2 to regulate growth and tropic responses in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plcell/koaf223openalex-snapshot
AnatomyArray: A high-throughput platform for anatomical phenotyping in plants
inferred← citeshttps://doi.org/10.1093/plcell/koaf242openalex-snapshot
The CYP71A , NIT , AMI , and IAMH gene families are dispensable for indole-3-acetaldoxime-mediated auxin biosynthesis in Arabidopsis
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/kiab132openalex-snapshot
Auxin does not inhibit endocytosis of PIN1 and PIN2 auxin efflux carriers
inferred← citeshttps://doi.org/10.1093/plphys/kiac138openalex-snapshot
MicroRNA858a, its encoded peptide, and phytosulfokine regulate Arabidopsis growth and development
inferred← citeshttps://doi.org/10.1093/plphys/kiad465openalex-snapshot
Changes in cell wall composition due to a pectin biosynthesis enzyme GAUT10 impact root growth
inferred← citeshttps://doi.org/10.1093/plphys/kiaf045openalex-snapshot
Modeling Arabidopsis root growth and development
inferred← citeshttps://doi.org/10.1093/plphys/kiaf667openalex-snapshot
Arabidopsis lines with modified ascorbate concentrations reveal a link between ascorbate and auxin biosynthesis
inferred← citeshttps://doi.org/10.1093/plphys/kiag664openalex-snapshot
Symbiont effectors modulate plant signaling to increase host stress resilience
inferred← citeshttps://doi.org/10.1101/2020.02.03.932574openalex-snapshot
Plastid EF-Tu Regulates Root Development through Both the ATM Pathway and GUN1
inferred← citeshttps://doi.org/10.1101/2020.08.31.275206openalex-snapshot
Perturbations of the AMI1 IAM-amidohydrolase expression trigger plant stress responses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/2020.09.30.320655openalex-snapshot
Momilactone B inhibits Arabidopsis growth and development via disruption of ABA and auxin signaling
inferred← citeshttps://doi.org/10.1101/2021.09.27.461987openalex-snapshot
miPEP858/miR858-MYB3-PSK4 module regulates growth and development in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2022.02.18.481036openalex-snapshot
Progressive maturation of the root apical meristem in Arabidopsis thaliana lateral roots
inferred← citeshttps://doi.org/10.1101/2022.05.11.491551openalex-snapshot
Phosphorylation Status of B Beta Subunit Controls PP2A activity in Ethylene-mediated Root Growth Inhibition
inferred← citeshttps://doi.org/10.1101/2022.06.22.497157openalex-snapshot
Ralstonia solanacearum alters root developmental programs in auxin-dependent and independent manners
inferred← citeshttps://doi.org/10.1101/2022.07.06.499076openalex-snapshot
The mRNA decapping machinery targets LBD3/ASL9 to mediate apical hook and lateral root development in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2022.11.01.514793openalex-snapshot
Molecular Mechanism for Bacterial Degradation of Plant Hormone Auxin
inferred← citeshttps://doi.org/10.1101/2022.12.15.520544openalex-snapshot
Heterologous expression of PtAAS1 reveals the metabolic potential of the common plant metabolite phenylacetaldehyde for auxin synthesis in planta
inferred← citeshttps://doi.org/10.1101/2024.01.23.576781openalex-snapshot
The endophytic fungus Serendipita indica alters auxin distribution in Arabidopsis thaliana roots through alteration of auxin transport and conjugation to promote plant growth
inferred← citeshttps://doi.org/10.1101/2024.06.20.599894openalex-snapshot
Actin isovariant ACT2-mediated cellular auxin homeostasis regulates lateral root organogenesis in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/2025.01.22.634243openalex-snapshot
Root Cap-Specific Transcriptomics Identify the NAC Transcription Factor SOMBRERO as a Versatile Regulator of Auxin Gradients
inferred← citeshttps://doi.org/10.1101/2025.01.29.635412openalex-snapshot
Salicylic acid represses primary root growth through the Glucose-Target of Rapamycin-E2Fa pathway in Arabidopsis
inferred← citeshttps://doi.org/10.1101/645655openalex-snapshot
Root development is maintained by specific bacteria-bacteria interactions within a complex microbiome
inferred← citeshttps://doi.org/10.1101/659276openalex-snapshot
An improved plant toolset for high-throughput recombineering
inferred← citeshttps://doi.org/10.1101/725572openalex-snapshot
Arabidopsis ERF109 regulates auxin transport-related genes in root development
inferred← citeshttps://doi.org/10.1101/783480openalex-snapshot
A dynamic pattern of local auxin sources is required for root regeneration
inferred← citeshttps://doi.org/10.1101/819342openalex-snapshot
Local auxin biosynthesis promotes shoot patterning and stem cell differentiation in Arabidopsis shoot apex
inferred← citeshttps://doi.org/10.1101/847061openalex-snapshot
Phytohormonal cross-talk modulate Bipolaris sorokiniana (Scc.)interaction with Zea mays
inferred← citeshttps://doi.org/10.1101/cshperspect.a039859openalex-snapshot
Fourteen Stations of Auxin
inferred← citeshttps://doi.org/10.1101/cshperspect.a039867openalex-snapshot
Auxin Metabolism in Plants
inferred← citeshttps://doi.org/10.1101/cshperspect.a039966openalex-snapshot
An Essential Function for Auxin in Embryo Development
inferred← citeshttps://doi.org/10.1101/cshperspect.a040006openalex-snapshot
Casting the Net—Connecting Auxin Signaling to the Plant Genome
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.20.00310openalex-snapshot
Structure–Function Analysis of Interallelic Complementation in ROOTY Transheterozygotes
inferred← citeshttps://doi.org/10.1105/tpc.19.00339openalex-snapshot
From Ethylene-Auxin Interactions to Auxin Biosynthesis and Signal Integration
inferred← citeshttps://doi.org/10.1105/tpc.19.00431openalex-snapshot
An Improved Recombineering Toolset for Plants
inferred← citeshttps://doi.org/10.1111/ede.12376openalex-snapshot
A fundamental developmental transition in Physcomitrium patens is regulated by evolutionarily conserved mechanisms
inferred← citeshttps://doi.org/10.1111/jipb.12820openalex-snapshot
Tillering and small grain 1 dominates the tryptophan aminotransferase family required for local auxin biosynthesis in rice
inferred← citeshttps://doi.org/10.1111/jipb.70238openalex-snapshot
Towards an integrated molecular understanding of plant hormones
inferred← citeshttps://doi.org/10.1111/jmi.12909openalex-snapshot
The plant endoplasmic reticulum: an organized chaos of tubules and sheets with multiple functions
inferred← citeshttps://doi.org/10.1111/mpp.70043openalex-snapshot
Ralstonia solanacearum Alters Root Developmental Programmes in Auxin‐Dependent and ‐Independent Manners
inferred← citeshttps://doi.org/10.1111/nph.16629openalex-snapshot
Directional auxin fluxes in plants by intramolecular domain–domain coevolution of PIN auxin transporters
inferred← citeshttps://doi.org/10.1111/nph.16781openalex-snapshot
Auxin is required for the long coleoptile trait in japonica rice under submergence
inferred← citeshttps://doi.org/10.1111/nph.17946openalex-snapshot
How is auxin linked with cellular energy pathways to promote growth?
inferred← citeshttps://doi.org/10.1111/nph.18467openalex-snapshot
Phosphorylation status of Bβ subunit acts as a switch to regulate the function of phosphatase PP2A in ethylene‐mediated root growth inhibition
inferred← citeshttps://doi.org/10.1111/nph.18487openalex-snapshot
Systemic control of plant regeneration and wound repair
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