On the public citation graph
The Interaction and Integration of Auxin Signaling Components
0 signed · 290 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
1 of the 105 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1016/j.cub.2011.02.029 (notice 2015-03-16).
Dataset join, best-effort; this page does not check the publisher record. Retraction Watch data via Crossref Labs, used with credit; OpenCitations Index (CC0) and Meta (CC BY 4.0); dataset doi:10.7910/DVN/WT8VOA (CC BY 4.0).
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1460-2075.1989.tb08380.xopenalex-snapshot
Molecular cloning and structural analysis of a gene from Zea mays (L.) coding for a putative receptor for the plant hormone auxin.
inferredcites →https://doi.org/10.1007/978-94-010-0377-3_10openalex-snapshot
Genetics of Aux/IAA and ARF action in plant growth and development
inferredcites →https://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
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.cell.2010.09.003openalex-snapshot
Cell Surface- and Rho GTPase-Based Auxin Signaling Controls Cellular Interdigitation in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2010.09.027openalex-snapshot
ABP1 Mediates Auxin Inhibition of Clathrin-Dependent Endocytosis in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2006.03.064openalex-snapshot
Specification of Leaf Polarity in Arabidopsis via the trans-Acting siRNA Pathway
inferredcites →https://doi.org/10.1016/j.cub.2006.03.065openalex-snapshot
Regulation of AUXIN RESPONSE FACTOR3 by TAS3 ta-siRNA Affects Developmental Timing and Patterning in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2007.01.052openalex-snapshot
Clathrin-Mediated Constitutive Endocytosis of PIN Auxin Efflux Carriers in Arabidopsis
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.2004.07.002openalex-snapshot
Convergence of Signaling Pathways in the Control of Differential Cell Growth in Arabidopsis
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.ejcb.2009.11.003openalex-snapshot
Subcellular trafficking of PIN auxin efflux carriers in auxin transport
inferredcites →https://doi.org/10.1016/s1360-1385(01)02150-1openalex-snapshot
Auxin binding protein: curiouser and curiouser
inferredcites →https://doi.org/10.1023/a:1005757815212openalex-snapshot
Characterization of two cDNAs encoding auxin-binding proteins in Nicotiana tabacum
inferredcites →https://doi.org/10.1023/a:1005999821066openalex-snapshot
Cloning and expression of two genes encoding auxin-binding proteins from tobacco
inferredcites →https://doi.org/10.1023/a:1015255030047openalex-snapshot
Genetics of Aux/IAA and ARF action in plant growth and development
inferredcites →https://doi.org/10.1038/35096571openalex-snapshot
Auxin transport inhibitors block PIN1 cycling and vesicle trafficking
inferredcites →https://doi.org/10.1038/msb.2011.39openalex-snapshot
The auxin signalling network translates dynamic input into robust patterning at the shoot apex
inferredcites →https://doi.org/10.1038/nature03542openalex-snapshot
The Arabidopsis F-box protein TIR1 is an auxin receptor
inferredcites →https://doi.org/10.1038/nature03543openalex-snapshot
The F-box protein TIR1 is an auxin receptor
inferredcites →https://doi.org/10.1038/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/10.1046/j.1365-313x.1993.04010041.xopenalex-snapshot
Patch‐clamp analysis establishes a role for an auxin binding protein in the auxin stimulation of plasma membrane current in Zea mays protoplasts
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00703.xopenalex-snapshot
Degradation of Aux/IAA proteins is essential for normal auxin signalling
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01103.xopenalex-snapshot
The auxin signal for protoplast swelling is perceived by extracellular ABP1
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01152.xopenalex-snapshot
The role of auxin‐binding protein 1 in the expansion of tobacco leaf cells
inferredcites →https://doi.org/10.1055/s-2006-923952openalex-snapshot
Moss Systems Biology en Route: Phytohormones in Physcomitrella Development
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/10.1073/pnas.0909571107openalex-snapshot
Nitrate-responsive miR393/ AFB3 regulatory module controls root system architecture in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0911967106openalex-snapshot
Complex regulation of the TIR1/AFB family of auxin receptors
inferredcites →https://doi.org/10.1073/pnas.1108434108openalex-snapshot
The main auxin biosynthesis pathway in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1108436108openalex-snapshot
Conversion of tryptophan to indole-3-acetic acid by TRYPTOPHAN AMINOTRANSFERASES OF ARABIDOPSIS and YUCCAs in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.86.3.891openalex-snapshot
Functional evidence for an auxin receptor at the plasmalemma of tobacco mesophyll protoplasts
inferredcites →https://doi.org/10.1073/pnas.90.24.11493openalex-snapshot
Modulation of K+ channels in Vicia stomatal guard cells by peptide homologs to the auxin-binding protein C terminus.
inferredcites →https://doi.org/10.1073/pnas.92.8.3425openalex-snapshot
Auxins induce clustering of the auxin-binding protein at the surface of maize coleoptile protoplasts.
inferredcites →https://doi.org/10.1073/pnas.94.22.11786openalex-snapshot
Protein–protein interactions among the Aux/IAA proteins
inferredcites →https://doi.org/10.1074/jbc.274.40.28314openalex-snapshot
A Novel Immunological Approach Establishes That the Auxin-binding Protein, Nt-abp1, Is an Element Involved in Auxin Signaling at the Plasma Membrane
inferredcites →https://doi.org/10.1074/jbc.275.5.3137openalex-snapshot
Molecular and Biochemical Evidence for the Involvement of Calcium/Calmodulin in Auxin Action
inferredcites →https://doi.org/10.1074/jbc.m110.146431openalex-snapshot
Kinetic Basis for the Conjugation of Auxin by a GH3 Family Indole-acetic Acid-Amido Synthetase
inferredcites →https://doi.org/10.1093/aob/mci083openalex-snapshot
Auxin: Regulation, Action, and Interaction
inferredcites →https://doi.org/10.1093/emboj/17.5.1405openalex-snapshot
The Arabidopsis gene MONOPTEROS encodes a transcription factor mediating embryo axis formation and vascular development
inferredcites →https://doi.org/10.1093/emboj/cdf291openalex-snapshot
Crystal structure of auxin‐binding protein 1 in complex with auxin
inferredcites →https://doi.org/10.1093/emboj/cdg190openalex-snapshot
The RUB/Nedd8 conjugation pathway is required for early development in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erq412openalex-snapshot
Auxin conjugates: their role for plant development and in the evolution of land plants
inferredcites →https://doi.org/10.1093/pcp/pcj080openalex-snapshot
Fluorescence Cross-Correlation Analyses of the Molecular Interaction between an Aux/IAA Protein, MSG2/IAA19, and Protein–Protein Interaction Domains of Auxin Response Factors of Arabidopsis Expressed in HeLa Cells
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.866201openalex-snapshot
ABP1 is required for organized cell elongation and division in Arabidopsis embryogenesis
inferredcites →https://doi.org/10.1104/pp.101.2.595openalex-snapshot
KDEL-Containing Auxin-Binding Protein Is Secreted to the Plasma Membrane and Cell Wall
inferredcites →https://doi.org/10.1104/pp.103.031294openalex-snapshot
Two Distinct Signaling Pathways Participate in Auxin-Induced Swelling of Pea Epidermal Protoplasts
inferredcites →https://doi.org/10.1104/pp.104.039669openalex-snapshot
Contrasting Modes of Diversification in the Aux/IAA and ARF Gene Families
inferredcites →https://doi.org/10.1104/pp.104.044495openalex-snapshot
AtCAND1, A HEAT-Repeat Protein That Participates in Auxin Signaling in Arabidopsis
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/10.1104/pp.107.096628openalex-snapshot
Specificity and Similarity of Functions of the Aux/IAA Genes in Auxin Signaling of Arabidopsis Revealed by Promoter-Exchange Experiments among MSG2/IAA19, AXR2/IAA7, and SLR/IAA14
inferredcites →https://doi.org/10.1104/pp.107.104844openalex-snapshot
Genetic Characterization of Mutants Resistant to the Antiauxinp-Chlorophenoxyisobutyric Acid Reveals ThatAAR3, a Gene Encoding a DCN1-Like Protein, Regulates Responses to the Synthetic Auxin 2,4-Dichlorophenoxyacetic Acid in Arabidopsis Roots
inferredcites →https://doi.org/10.1104/pp.110.168161openalex-snapshot
Unraveling the Evolution of Auxin Signaling
inferredcites →https://doi.org/10.1104/pp.110.171322openalex-snapshot
Identical Amino Acid Substitutions in the Repression Domain of Auxin/Indole-3-Acetic Acid Proteins Have Contrasting Effects on Auxin Signaling
inferredcites →https://doi.org/10.1104/pp.111.180083openalex-snapshot
miR393 and Secondary siRNAs Regulate Expression of the TIR1 / AFB2 Auxin Receptor Clade and Auxin-Related Development of Arabidopsis Leaves
inferredcites →https://doi.org/10.1104/pp.126.2.670openalex-snapshot
The Rop GTPase Switch Controls Multiple Developmental Processes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.006791openalex-snapshot
Arabidopsis E2Fc Functions in Cell Division and Is Degraded by the Ubiquitin-SCF AtSKP2 Pathway in Response to Light
inferredcites →https://doi.org/10.1105/tpc.008417openalex-snapshot
The Roles of Auxin Response Factor Domains in Auxin-Responsive Transcription
inferredcites →https://doi.org/10.1105/tpc.010282openalex-snapshot
AXR1-ECR1–Dependent Conjugation of RUB1 to the Arabidopsis Cullin AtCUL1 Is Required for Auxin Response
inferredcites →https://doi.org/10.1105/tpc.010283openalex-snapshot
Arabidopsis SHY2/IAA3 Inhibits Auxin-Regulated Gene Expression
inferredcites →https://doi.org/10.1105/tpc.010359openalex-snapshot
The Arabidopsis Rop2 GTPase Is a Positive Regulator of Both Root Hair Initiation and Tip Growth
inferredcites →https://doi.org/10.1105/tpc.010884openalex-snapshot
Arabidopsis SGT1b Is Required for SCFTIR1-Mediated Auxin Response
inferredcites →https://doi.org/10.1105/tpc.104.028316openalex-snapshot
Functional Genomic Analysis of the AUXIN RESPONSE FACTOR Gene Family Members in Arabidopsis thaliana : Unique and Overlapping Functions of ARF7 and ARF19
inferredcites →https://doi.org/10.1105/tpc.105.031716openalex-snapshot
MicroRNA-Directed Regulation of Arabidopsis AUXIN RESPONSE FACTOR17 Is Essential for Proper Development and Modulates Expression of Early Auxin Response Genes
inferredcites →https://doi.org/10.1105/tpc.105.039172openalex-snapshot
TheArabidopsisAux/IAA Protein Family Has Diversified in Degradation and Auxin Responsiveness
inferredcites →https://doi.org/10.1105/tpc.108.059048openalex-snapshot
Conditional Repression of AUXIN BINDING PROTEIN1 Reveals That It Coordinates Cell Division and Cell Expansion during Postembryonic Shoot Development in Arabidopsis and Tobacco
inferredcites →https://doi.org/10.1105/tpc.108.064758openalex-snapshot
Phenotypic Plasticity of Adventitious Rooting in Arabidopsis Is Controlled by Complex Regulation of AUXIN RESPONSE FACTOR Transcripts and MicroRNA Abundance
inferredcites →https://doi.org/10.1105/tpc.110.078972openalex-snapshot
The Arabidopsis Cell Cycle F-Box Protein SKP2A Binds to Auxin
inferredcites →https://doi.org/10.1105/tpc.12.5.757openalex-snapshot
The NPH4 Locus Encodes the Auxin Response Factor ARF7, a Conditional Regulator of Differential Growth in Aerial Arabidopsis Tissue
inferredcites →https://doi.org/10.1105/tpc.3.4.419openalex-snapshot
Tissue-specific and organ-specific expression of soybean auxin-responsive transcripts GH3 and SAURs.
inferredcites →https://doi.org/10.1105/tpc.7.10.1611openalex-snapshot
Composite Structure of Auxin Response Elements
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.2006.02832.xopenalex-snapshot
A small acidic protein 1 (SMAP1) mediates responses of the Arabidopsis root to the synthetic auxin 2,4‐dichlorophenoxyacetic acid
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02882.xopenalex-snapshot
PICKLE is required for SOLITARY‐ROOT/IAA14‐mediated repression of ARF7 and ARF19 activity during Arabidopsis lateral root initiation
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03038.xopenalex-snapshot
The auxin‐binding protein 1 is essential for the control of cell cycle
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03218.xopenalex-snapshot
Repression of AUXIN RESPONSE FACTOR10 by microRNA160 is critical for seed germination and post‐germination stages
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03378.xopenalex-snapshot
SKP2A, an F‐box protein that regulates cell division, is degraded via the ubiquitin pathway
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03510.xopenalex-snapshot
The AtGenExpress hormone and chemical treatment data set: experimental design, data evaluation, model data analysis and data access
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04420.xopenalex-snapshot
The heterozygous abp1/ABP1 insertional mutant has defects in functions requiring polar auxin transport and in regulation of early auxin‐regulated genes
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04710.xopenalex-snapshot
A cellular expression map of the Arabidopsis AUXIN RESPONSE FACTOR gene family
inferredcites →https://doi.org/10.1126/science.1126088openalex-snapshot
A Plant miRNA Contributes to Antibacterial Resistance by Repressing Auxin Signaling
inferredcites →https://doi.org/10.1126/science.1151461openalex-snapshot
TOPLESS Mediates Auxin-Dependent Transcriptional Repression During Arabidopsis Embryogenesis
inferredcites →https://doi.org/10.1126/science.276.5320.1865openalex-snapshot
ARF1, a Transcription Factor That Binds to Auxin Response Elements
inferredcites →https://doi.org/10.1126/science.282.5391.1114openalex-snapshot
Auxin-Dependent Cell Expansion Mediated by Overexpressed Auxin-Binding Protein 1
inferredcites →https://doi.org/10.1128/mcb.5.6.1197openalex-snapshot
Rapid Induction of Selective Transcription by Auxins
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/10.1146/annurev.cellbio.23.090506.123214openalex-snapshot
Auxin Receptors and Plant Development: A New Signaling Paradigm
inferredcites →https://doi.org/10.1186/1471-2148-9-126openalex-snapshot
The evolution of nuclear auxin signalling
inferredcites →https://doi.org/10.1242/dev.00659openalex-snapshot
AXR3andSHY2interact to regulate root hair development
inferredcites →https://doi.org/10.1242/dev.01955openalex-snapshot
Auxin response factors ARF6 and ARF8 promote jasmonic acid production and flower maturation
inferredcites →https://doi.org/10.1242/dev.02491openalex-snapshot
Trans-acting siRNA-mediated repression of ETTIN and ARF4 regulates heteroblasty in Arabidopsis
inferredcites →https://doi.org/10.1242/dev.02602openalex-snapshot
Arabidopsis microRNA167controls patterns ofARF6andARF8expression, and regulates both female and male reproduction
inferredcites →https://doi.org/10.1242/dev.030353openalex-snapshot
Auxin transport routes in plant development
inferredcites →https://doi.org/10.1242/dev.121.5.1519openalex-snapshot
Arabidopsis gynoecium structure in the wild type and in ettin mutants
inferredcites →https://doi.org/10.1371/journal.pone.0006648openalex-snapshot
The AUXIN BINDING PROTEIN 1 Is Required for Differential Auxin Responses Mediating Root Growth
inferredcites →https://doi.org/10.1371/journal.pone.0017245openalex-snapshot
Mutant Analysis in Arabidopsis Provides Insight into the Molecular Mode of Action of the Auxinic Herbicide Dicamba
inferredcites →https://doi.org/10.1371/journal.pone.0027364openalex-snapshot
Large-Scale Protein-Protein Interaction Analysis in Arabidopsis Mesophyll Protoplasts by Split Firefly Luciferase Complementation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4688593openalex-extracted
Transgenic Poplar with the Zygophyllum Xanthoxylon Zinc Finger Protein Transcription Factor Zxzf Gene Shows Improved Drought Resistance by Regulating Hormone Signal
inferred← citeshttps://doi.org/10.2139/ssrn.4788804openalex-extracted
Transgenic Poplar with the Zygophyllum Xanthoxylon Zinc Finger Protein Transcription Factor Zxzf Gene Shows Improved Drought Resistance by Regulating Hormone Signal
inferred← citeshttps://doi.org/10.3897/imafungus.16.e142356zenodo-depositor-declared
Suillus bovinus sesquiterpenes stimulate root growth and ramification of host and non-host plants by coordinating plant auxin signaling pathways
inferred← citeshttps://doi.org/10.1002/9781118889022.ch3openalex-snapshot
Integrating the Knowledge of Auxin Homeostasis with Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1002/9781119048800.ch9openalex-snapshot
Role of phytohormones in improving the yield of oilseed crops
inferred← citeshttps://doi.org/10.1002/bem.22086openalex-snapshot
Suppression of Arabidopsis flowering by near‐null magnetic field is mediated by auxin
inferred← citeshttps://doi.org/10.1002/pmic.201200304openalex-snapshot
Interplay between protein carbonylation and nitrosylation in plants
inferred← citeshttps://doi.org/10.1002/yea.2967openalex-snapshot
An expanded tool kit for the auxin‐inducible degron system in budding yeast
inferred← citeshttps://doi.org/10.1007/978-1-4939-9015-3_11openalex-snapshot
New-Generation Chemical Tools for the Manipulation of Auxin Biosynthesis, Action, and Transport
inferred← citeshttps://doi.org/10.1007/978-3-030-18601-2_12openalex-snapshot
The Genomics of Grape Berry Ripening
inferred← citeshttps://doi.org/10.1007/978-3-030-77477-6_4openalex-snapshot
Hormones and Light-Regulated Seedling Development
inferred← citeshttps://doi.org/10.1007/978-3-319-26118-8_2openalex-snapshot
Role of Plant Immune Signals and Signaling Systems in Plant Pathogenesis
inferred← citeshttps://doi.org/10.1007/978-3-642-35299-7_3openalex-snapshot
Signal Integration, Auxin Homeostasis, and Plant Development
inferred← citeshttps://doi.org/10.1007/978-3-662-48535-4_7openalex-snapshot
Tomato Fruit Set and Its Modification Using Molecular Breeding Techniques
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8openalex-snapshot
Auxin and Its Role in Plant Development
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8_13openalex-snapshot
Evolutionary Aspects of Auxin Signalling
inferred← citeshttps://doi.org/10.1007/978-94-017-9285-1_6openalex-snapshot
Auxin Signaling System in Plant Innate Immunity
inferred← citeshttps://doi.org/10.1007/978-981-13-0032-5_10openalex-snapshot
Stimulating Plant Tolerance Against Abiotic Stress Through Seed Priming
inferred← citeshttps://doi.org/10.1007/s00253-019-10045-4openalex-snapshot
Drought tolerance improvement in plants: an endophytic bacterial approach
inferred← citeshttps://doi.org/10.1007/s00299-013-1425-2openalex-snapshot
Micro-regulators of auxin action
inferred← citeshttps://doi.org/10.1007/s00299-016-2060-5openalex-snapshot
Systems biology and genome-wide approaches to unveil the molecular players involved in the pre-germinative metabolism: implications on seed technology traits
inferred← citeshttps://doi.org/10.1007/s00299-021-02712-6openalex-snapshot
ARPI, β-AS, and UGE regulate glycyrrhizin biosynthesis in Glycyrrhiza uralensis hairy roots
inferred← citeshttps://doi.org/10.1007/s00344-015-9518-5openalex-snapshot
Hormone-Induced Gene Expression During Gravicurvature of Brassica Roots
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/s00425-026-05083-yopenalex-snapshot
Metabolism meets transport: a new perspective on auxin homeostasis at subcellular level
inferred← citeshttps://doi.org/10.1007/s00438-012-0718-4openalex-snapshot
Auxin response factor gene family in Brassica rapa: genomic organization, divergence, expression, and evolution
inferred← citeshttps://doi.org/10.1007/s10658-016-0877-yopenalex-snapshot
Putative role of IAA during the early response of Brassica napus L. to Plasmodiophora brassicae
inferred← citeshttps://doi.org/10.1007/s10725-018-0397-1openalex-snapshot
Simplifying the root dynamics: from complex hormone–environment interactions to specific root architectural modulation
inferred← citeshttps://doi.org/10.1007/s11104-024-06773-wopenalex-snapshot
Mechanisms involved in the positive effects of high zinc exposure on growth of Sedum alfredii
inferred← citeshttps://doi.org/10.1007/s11240-015-0731-5openalex-snapshot
Transcriptome analysis reveals the role of BpGH3.5 in root elongation of Betula platyphylla × B. pendula
inferred← citeshttps://doi.org/10.1007/s11240-024-02868-5openalex-snapshot
Elucidating molecular interaction leading to successful grafting of in vitro regenerated shoots of three chickpea (Cicer arietinum L.) cultivars
inferred← citeshttps://doi.org/10.1007/s13593-014-0276-8openalex-snapshot
Agroecological impact of an in vitro biotechnology approach of embryo development and seed filling in legumes
inferred← citeshttps://doi.org/10.1016/b978-0-12-821035-2.00038-3openalex-snapshot
Rinskor active herbicide—A new environment-friendly tool for weed management in rice and aquatic environments
inferred← citeshttps://doi.org/10.1016/b978-0-323-90636-4.00001-5openalex-snapshot
Natural variation in adventitious root formation
inferred← citeshttps://doi.org/10.1016/b978-0-443-13318-3.00018-5openalex-snapshot
Beneficial soil bacteria: a sustainable strategy for enhancing soil fertility
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.09.001openalex-snapshot
Development of 4-methoxy-7-nitroindolinyl (MNI)-caged auxins which are extremely stable in planta
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.126158openalex-snapshot
Transcriptional regulation and expression network responding to cadmium stress in a Cd-tolerant perennial grass Poa Pratensis
inferred← citeshttps://doi.org/10.1016/j.cpb.2022.100255openalex-snapshot
Transcriptome profiling of the chilling response in wheat spikes: I, acclimation response to long-term chilling treatment
inferred← citeshttps://doi.org/10.1016/j.cpb.2022.100264openalex-snapshot
Transcriptome profiling of the chilling response in wheat spikes: II, Response to short-term cold exposure
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2013.11.005openalex-snapshot
Plant hormones and seed germination
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104796openalex-snapshot
Auxin-mediated molecular mechanisms of heavy metal and metalloid stress regulation in plants
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105868openalex-snapshot
Transgenic poplar with the Zygophyllum xanthoxylon zinc finger protein transcription factor ZxZF gene shows improved drought resistance by regulating hormone signal
inferred← citeshttps://doi.org/10.1016/j.isci.2024.109936openalex-snapshot
The first intron of ARF7 is required for expression in root tips
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2020.124250openalex-snapshot
Auxin metabolic network regulates the plant response to metalloids stress
inferred← citeshttps://doi.org/10.1016/j.pbi.2014.06.006openalex-snapshot
Diversity and specificity: auxin perception and signaling through the TIR1/AFB pathway
inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.02.004openalex-snapshot
Ectopic expression of a stress-inducible glycosyltransferase from saffron enhances salt and oxidative stress tolerance in Arabidopsis while alters anchor root formation
inferred← citeshttps://doi.org/10.1016/j.plaphy.2016.06.020openalex-snapshot
Effect of endophytic Bacillus cereus ERBP inoculation into non-native host: Potentials and challenges for airborne formaldehyde removal
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108210openalex-snapshot
Auxin homeostasis in plant responses to heavy metal stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108273openalex-snapshot
The hidden harmony: Exploring ROS-phytohormone nexus for shaping plant root architecture in response to environmental cues
inferred← citeshttps://doi.org/10.1016/j.plgene.2021.100344openalex-snapshot
Genome-wide exploration of auxin response factors (ARFs) and their expression dynamics in response to abiotic stresses and growth regulators in coconut (Cocos nucifera L.)
inferred← citeshttps://doi.org/10.1016/j.pmpp.2018.11.002openalex-snapshot
Transcriptional analysis and histochemistry reveal a dominant role for cell wall signaling in mediating Pythium myriotylum resistance in Zingiber zerumbet
inferred← citeshttps://doi.org/10.1016/j.scienta.2013.07.028openalex-snapshot
SlmiR393 controls the auxin receptor homologous genes expression, and regulates sensitivity to auxin in tomato root growth
inferred← citeshttps://doi.org/10.1016/j.scienta.2016.07.036openalex-snapshot
The effect of IBA on anatomical changes and antioxidant enzyme activity during the in vitro rooting of smoke tree ( Cotinus coggygria Scop.)
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.04.063openalex-snapshot
Modulation of CuO nanoparticles toxicity to green pea (Pisum sativum Fabaceae) by the phytohormone indole-3-acetic acid
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100551openalex-snapshot
Activation of the antioxidant system and transduction of the mediated by exogenous calcium improve drought resistance in tobacco
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100865openalex-snapshot
Time-resolved dual transcriptome profiling of interactions between tea plants (Camellia sinensis (L.) O. Kuntze) and its anthracnose pathogen Colletotrichum gloeosporioides
inferred← citeshttps://doi.org/10.1038/msb.2013.40openalex-snapshot
A map of cell type‐specific auxin responses
inferred← citeshttps://doi.org/10.1038/s41438-021-00535-wopenalex-snapshot
Transcriptomic and epigenomic remodeling occurs during vascular cambium periodicity in Populus tomentosa
inferred← citeshttps://doi.org/10.1038/s41598-020-69729-xopenalex-snapshot
Integrated transcriptomic and metabolomic analyses reveal the effects of callose deposition and multihormone signal transduction pathways on the tea plant-Colletotrichum camelliae interaction
inferred← citeshttps://doi.org/10.1038/s41598-024-60037-2openalex-snapshot
Lactic acid induced defense responses in tobacco against Phytophthora nicotianae
inferred← citeshttps://doi.org/10.1042/bsr20221504openalex-snapshot
Negative regulation of seed germination by maternal AFB1 and AFB5 in Arabidopsis
inferred← citeshttps://doi.org/10.1071/fp13123openalex-snapshot
Overexpression of miR160 affects root growth and nitrogen-fixing nodule number in Medicago truncatula
inferred← citeshttps://doi.org/10.1073/pnas.1214774109openalex-snapshot
Arabidopsis ribosomal proteins control developmental programs through translational regulation of auxin response factors
inferred← citeshttps://doi.org/10.1073/pnas.1408960111openalex-snapshot
Auxin transport sites are visualized in planta using fluorescent auxin analogs
inferred← citeshttps://doi.org/10.1073/pnas.1524390113openalex-snapshot
Tobacco mosaic virus-directed reprogramming of auxin/indole acetic acid protein transcriptional responses enhances virus phloem loading
inferred← citeshttps://doi.org/10.1073/pnas.1817038116openalex-snapshot
Quantification of reaction cycle parameters for an essential molecular switch in an auxin-responsive transcription circuit in rice
inferred← citeshttps://doi.org/10.1073/pnas.2009554117openalex-snapshot
Architecture of DNA elements mediating ARF transcription factor binding and auxin-responsive gene expression in Arabidopsis
inferred← citeshttps://doi.org/10.1080/07352689.2015.1024566openalex-snapshot
Plant F-box Proteins – Judges between Life and Death
inferred← citeshttps://doi.org/10.1080/09168451.2015.1086259openalex-snapshot
Current aspects of auxin biosynthesis in plants
inferred← citeshttps://doi.org/10.1080/14620316.2023.2192213openalex-snapshot
Analysis of the effect of exogenous auxin on the regulatory relationship between miRNAs and their target genes in rose using high-throughput sequencing
inferred← citeshttps://doi.org/10.1080/21655979.2019.1692610openalex-snapshot
Identification and bioinformatic analysis of Aux/IAA family based on transcriptome data of Bletilla striata
inferred← citeshttps://doi.org/10.1088/1755-1315/215/1/012018openalex-snapshot
The analysis of endogenous auxin of shallot and its effect on the germination and the growth of organically cultivated melon (Cucumis Melo)
inferred← citeshttps://doi.org/10.1089/dna.2021.0337openalex-snapshot
Transcriptional Regulation of Different Rhizome Parts Reveal the Candidate Genes That Regulate Rhizome Development in Poa pratensis
inferred← citeshttps://doi.org/10.1093/jxb/ert152openalex-snapshot
Evidence of oxidative attenuation of auxin signalling
inferred← citeshttps://doi.org/10.1093/jxb/eru019openalex-snapshot
Cyclic GMP is involved in auxin signalling during Arabidopsis root growth and development
inferred← citeshttps://doi.org/10.1093/jxb/eru272openalex-snapshot
Homogalacturonan-modifying enzymes: structure, expression, and roles in plants
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/erv397openalex-snapshot
Hormone-mediated growth dynamics of the barley pericarp as revealed by magnetic resonance imaging and transcript profiling
inferred← citeshttps://doi.org/10.1093/pcp/pcs170openalex-snapshot
Auxin Regulation of Embryonic Root Formation
inferred← citeshttps://doi.org/10.1093/pcp/pcs188openalex-snapshot
A Comprehensive Expression Analysis of the Arabidopsis MICRORNA165/6 Gene Family during Embryogenesis Reveals a Conserved Role in Meristem Specification and a Non-Cell-Autonomous Function
inferred← citeshttps://doi.org/10.1093/pcp/pct003openalex-snapshot
UniVIO: A Multiple Omics Database with Hormonome and Transcriptome Data from Rice
inferred← citeshttps://doi.org/10.1093/pcp/pct018openalex-snapshot
GNOM/FEWER ROOTS is Required for the Establishment of an Auxin Response Maximum for Arabidopsis Lateral Root Initiation
inferred← citeshttps://doi.org/10.1093/pcp/pct028openalex-snapshot
Tissue-Specific Expression of SMALL AUXIN UP RNA41 Differentially Regulates Cell Expansion and Root Meristem Patterning in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/pct034openalex-snapshot
Plant Meristems and Organogenesis: The New Era of Plant Developmental Research
inferred← citeshttps://doi.org/10.1093/pcp/pct173openalex-snapshot
UGT74D1 Catalyzes the Glucosylation of 2-Oxindole-3-Acetic Acid in the Auxin Metabolic Pathway in Arabidopsis
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/pcx013openalex-snapshot
Three cis-Regulatory Motifs, AuxRE, MYCRS1 and MYCRS2, are Required for Modulating the Auxin- and Mycorrhiza-Responsive Expression of a Tomato GH3 Gene
inferred← citeshttps://doi.org/10.1093/pcp/pcy018openalex-snapshot
Asymmetric Auxin Distribution is Not Required to Establish Root Phototropism in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/pcy076openalex-snapshot
Manipulation and Sensing of Auxin Metabolism, Transport and Signaling
inferred← citeshttps://doi.org/10.1093/plphys/kiab565openalex-snapshot
The positive feedback regulatory loop of miR160-Auxin Response Factor 17-HYPONASTIC LEAVES 1 mediates drought tolerance in apple trees
inferred← citeshttps://doi.org/10.1093/plphys/kiaf568openalex-snapshot
The diphenylurea-type GH3 enzyme inhibitor Auxurea A selectively inhibits the auxin inactivation pathway in dicots
inferred← citeshttps://doi.org/10.1094/mpmi-08-13-0250-ropenalex-snapshot
Recessive Mutation Identifies Auxin-Repressed Protein ARP1, Which Regulates Growth and Disease Resistance in Tobacco
inferred← citeshttps://doi.org/10.1094/mpmi-08-20-0211-ropenalex-snapshot
Validamycin A Induces Broad-Spectrum Resistance Involving Salicylic Acid and Jasmonic Acid/Ethylene Signaling Pathways
inferred← citeshttps://doi.org/10.1101/2020.06.25.170571openalex-snapshot
Checkpoint phosphorylation sites on budding yeast Rif1 protect nascent DNA from degradation by Sgs1-Dna2
inferred← citeshttps://doi.org/10.1101/781922openalex-snapshot
A fuzzy encounter complex precedes formation of the fully-engaged TIR1-Aux/IAA auxin co-receptor system
inferred← citeshttps://doi.org/10.1101/cshperspect.a040105openalex-snapshot
Chemical Biology in Auxin Research
inferred← citeshttps://doi.org/10.1104/pp.114.246595openalex-snapshot
Auxin Perception Is Required for Arbuscule Development in Arbuscular Mycorrhizal Symbiosis
inferred← citeshttps://doi.org/10.1104/pp.15.00287openalex-snapshot
Comprehensive Tissue-Specific Transcriptome Analysis Reveals Distinct Regulatory Programs during Early Tomato Fruit Development
inferred← citeshttps://doi.org/10.1104/pp.16.00564openalex-snapshot
Gene Regulation by the AGL15 Transcription Factor Reveals Hormone Interactions in Somatic Embryogenesis
inferred← citeshttps://doi.org/10.1104/pp.18.00038openalex-snapshot
SELF-PRUNING Acts Synergistically with DIAGEOTROPICA to Guide Auxin Responses and Proper Growth Form
inferred← citeshttps://doi.org/10.1104/pp.18.00257openalex-snapshot
SMALL AUXIN UP RNA62/75 Are Required for the Translation of Transcripts Essential for Pollen Tube Growth
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.20.00400openalex-snapshot
Cell Wall Invertase Is Essential for Ovule Development through Sugar Signaling Rather Than Provision of Carbon Nutrients
inferred← citeshttps://doi.org/10.1105/tpc.113.111732openalex-snapshot
Genome-Scale Transcriptomic Insights into Early-Stage Fruit Development in Woodland Strawberry Fragaria vesca
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.114.127993openalex-snapshot
TAA1-Regulated Local Auxin Biosynthesis in the Root-Apex Transition Zone Mediates the Aluminum-Induced Inhibition of Root Growth in Arabidopsis
inferred← citeshttps://doi.org/10.1111/j.1399-3054.2012.01719.xopenalex-snapshot
In vitro auxin treatment promotes cell division and delays endoreduplication in developing seeds of the model legume species Medicago truncatula
inferred← citeshttps://doi.org/10.1111/nph.12301openalex-snapshot
The regulation of cambial activity in C hinese fir ( C unninghamia lanceolata) involves extensive transcriptome remodeling
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.16490openalex-snapshot
Osmotic stress inhibits leaf growth of Arabidopsis thaliana by enhancing ARF‐mediated auxin responses
inferred← citeshttps://doi.org/10.1111/pbi.12230openalex-snapshot
A Medicago truncatula rdr6 allele impairs transgene silencing and endogenous phased si RNA production but not development
inferred← citeshttps://doi.org/10.1111/pce.12645openalex-snapshot
miRNA‐mediated auxin signalling repression during Vat‐mediated aphid resistance in Cucumis melo
inferred← citeshttps://doi.org/10.1111/ppl.12709openalex-snapshot
Ectopic expression of the Coffea canephora SERK1 homolog‐induced differential transcription of genes involved in auxin metabolism and in the developmental control of embryogenesis
inferred← citeshttps://doi.org/10.1111/tpj.15424openalex-snapshot
Local regulation of auxin transport in root‐apex transition zone mediates aluminium‐induced Arabidopsis root‐growth inhibition
inferred← citeshttps://doi.org/10.1111/tpj.16132openalex-snapshot
Mdm‐miR160–MdARF17–MdWRKY33 module mediates freezing tolerance in apple
inferred← citeshttps://doi.org/10.1134/s000368382460413xopenalex-snapshot
Enhanced Growth and Development of IAA-mutant dek18 Maize Variety and Alleviation of Abiotic Stresses Through the Synergistic effect of Penicillium roqueforti and Trichoderma reesei
inferred← citeshttps://doi.org/10.11606/t.46.2018.tde-19072018-113726openalex-snapshot
Vias de sinalização por auxinas e sua interação com o relógio biológico de cana-de-açúcar
inferred← citeshttps://doi.org/10.11606/t.9.2017.tde-09022017-142232openalex-snapshot
Ethylene and auxin: new insights into the hormonal regulation of tomato fruit ripening
inferred← citeshttps://doi.org/10.11606/t.9.2020.tde-01072021-173958openalex-snapshot
Avaliação da interação etileno-auxina e de sua influência no metabolismo de compostos voláteis durante o amadurecimento de tomates (>i /i< L.) por análise metabolômica e proteômica comparativa
inferred← citeshttps://doi.org/10.1186/1471-2105-14-321openalex-snapshot
PlantTFcat: an online plant transcription factor and transcriptional regulator categorization and analysis tool
inferred← citeshttps://doi.org/10.1186/s12864-015-2182-0openalex-snapshot
Genome-wide identification and characterization of auxin response factor (ARF) family genes related to flower and fruit development in papaya (Carica papaya L.)
inferred← citeshttps://doi.org/10.1186/s12870-022-03564-2openalex-snapshot
Genome-wide identification and expression of SAUR gene family in peanut (Arachis hypogaea L.) and functional identification of AhSAUR3 in drought tolerance
inferred← citeshttps://doi.org/10.1186/s12870-025-06600-zopenalex-snapshot
Transcriptomic and physiological insights into auxin-mediated root growth and potassium uptake in tobacco under low-potassium stress
inferred← citeshttps://doi.org/10.1242/dev.086363openalex-snapshot
Auxin metabolism and homeostasis during plant development
inferred← citeshttps://doi.org/10.1242/dev.109181openalex-snapshot
Auxin represses stomatal development in dark-grown seedlings via Aux/IAA proteins
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003759openalex-snapshot
The Arabidopsis IDD14, IDD15, and IDD16 Cooperatively Regulate Lateral Organ Morphogenesis and Gravitropism by Promoting Auxin Biosynthesis and Transport
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011044openalex-snapshot
Checkpoint phosphorylation sites on budding yeast Rif1 protect nascent DNA from degradation by Sgs1-Dna2
inferred← citeshttps://doi.org/10.1371/journal.pone.0084203openalex-snapshot
Characterization of the Tomato ARF Gene Family Uncovers a Multi-Levels Post-Transcriptional Regulation Including Alternative Splicing
inferred← citeshttps://doi.org/10.1371/journal.ppat.1004620openalex-snapshot
Regulation of Oncogene Expression in T-DNA-Transformed Host Plant Cells
inferred← citeshttps://doi.org/10.14418/wes01.2.364openalex-snapshot
The Influence of Linker Histone H1 and Histone Variant H2A.Z on Chromosome Condensation in S. cerevisiae
inferred← citeshttps://doi.org/10.1584/jpestics.w14-29openalex-snapshot
Small molecule modulators on auxin biosynthesis and signaling
inferred← citeshttps://doi.org/10.17660/actahortic.2017.1155.74openalex-snapshot
Adventitious root formation inEucalyptus: the role of phytohormones
inferred← citeshttps://doi.org/10.18699/vj21.005openalex-snapshot
The auxin signaling pathway to its PIN transporters: insights based on a meta-analysis of auxin-induced transcriptomes
inferred← citeshttps://doi.org/10.20902/ijctr.2019.120504openalex-snapshot
Study of regulating activity of synthetic low molecular weight heterocyclic compounds, derivatives of pyrimidine on growth of tomato(Solanum lycopersicum L.) seedlings
inferred← citeshttps://doi.org/10.24297/jaa.v10i0.8341openalex-snapshot
Application of Pyrazole Derivatives As New Substitutes of Auxin IAA To Regulate Morphometric and Biochemical Parameters of Wheat (Triticum Aestivum L.) Seedlings
inferred← citeshttps://doi.org/10.26508/lsa.202000725openalex-snapshot
STAG1 vulnerabilities for exploiting cohesin synthetic lethality in STAG2-deficient cancers
inferred← citeshttps://doi.org/10.3233/978-1-60750-972-1-205openalex-snapshot
Signaling and Communication in Plants
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/fgene.2021.791355openalex-snapshot
Transcriptome Analysis Reveals Key Pathways and Candidate Genes Controlling Seed Development and Size in Ricebean (Vigna umbellata)
inferred← citeshttps://doi.org/10.3389/fpls.2014.00052openalex-snapshot
Hormonal networks involved in apical hook development in darkness and their response to light
inferred← citeshttps://doi.org/10.3389/fpls.2015.00073openalex-snapshot
Genome-wide identification and expression analysis of auxin response factor gene family in Medicago truncatula
inferred← citeshttps://doi.org/10.3389/fpls.2015.00295openalex-snapshot
An auxin responsive CLE gene regulates shoot apical meristem development in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2015.00742openalex-snapshot
The auxin response factor gene family in banana: genome-wide identification and expression analyses during development, ripening, and abiotic stress
inferred← citeshttps://doi.org/10.3389/fpls.2016.02038openalex-snapshot
Genome-Wide Transcriptional Profiling to Elucidate Key Candidates Involved in Bud Burst and Rattling Growth in a Subtropical Bamboo (Dendrocalamus hamiltonii)
inferred← citeshttps://doi.org/10.3389/fpls.2021.646736openalex-snapshot
PIP2, An Auxin Induced Plant Peptide Hormone Regulates Root and Hypocotyl Elongation in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2022.1043099openalex-snapshot
Transcriptome mining of hormonal and floral integrators in the leafless flowers of three cymbidium orchids
inferred← citeshttps://doi.org/10.3389/fpls.2022.1120613openalex-snapshot
The role of indole derivative in the growth of plants: A review
inferred← citeshttps://doi.org/10.3389/fpls.2022.861556openalex-snapshot
AGL15 Promotion of Somatic Embryogenesis: Role and Molecular Mechanism
inferred← citeshttps://doi.org/10.3389/fpls.2023.1236315openalex-snapshot
Full-length transcriptome analysis revealed that 2,4-dichlorophenoxyacetic acid promoted in vitro bulblet initiation in lily by affecting carbohydrate metabolism and auxin signaling
inferred← citeshttps://doi.org/10.3389/fpls.2025.1698281openalex-snapshot
Combined transcriptome, metabolome, and miRNA analysis reveals the genetic regulatory network of sweet corn pericarp thickness
inferred← citeshttps://doi.org/10.3389/fpls.2025.1727826openalex-snapshot
Integrated transcriptomic, untargeted and targeted metabolomic analyses reveal seasonal regulatory mechanisms of vascular cambium activity in woody plants: insights from Schima superba
inferred← citeshttps://doi.org/10.3390/biom14101253openalex-snapshot
Investigation of the Roles of Phosphatidylinositol 4-Phosphate 5-Kinases 7,9 and Wall-Associated Kinases 1–3 in Responses to Indole-3-Carbinol and Biotic Stress in Arabidopsis Thaliana
inferred← citeshttps://doi.org/10.3390/f11111211openalex-snapshot
The Prospect of Physiological Events Associated with the Micropropagation of Eucalyptus sp.
inferred← citeshttps://doi.org/10.3390/genes17091008openalex-snapshot
Transcriptomic Characterization of Adventitious Root Formation in Cunninghamia lanceolata (Lamb.) Hook. During Cutting Propagation
inferred← citeshttps://doi.org/10.3390/genes8090202openalex-snapshot
Auxin Response Factor Genes Repertoire in Mulberry: Identification, and Structural, Functional and Evolutionary Analyses
inferred← citeshttps://doi.org/10.3390/ijms232012495openalex-snapshot
Molecular Mechanisms of Diverse Auxin Responses during Plant Growth and Development
inferred← citeshttps://doi.org/10.3390/ijms24043631openalex-snapshot
Insights on Phytohormonal Crosstalk in Plant Response to Nitrogen Stress: A Focus on Plant Root Growth and Development
inferred← citeshttps://doi.org/10.3390/ijms24098293openalex-snapshot
Transcriptome, Ectopic Expression and Genetic Population Analysis Identify Candidate Genes for Fiber Quality Improvement in Cotton
inferred← citeshttps://doi.org/10.3390/ijms25010174openalex-snapshot
Analysis of the Candidate Genes and Underlying Molecular Mechanism of P198, an RNAi-Related Dwarf and Sterile Line
inferred← citeshttps://doi.org/10.3390/ijms25031380openalex-snapshot
Special Issue “Phytohormones: Important Participators in Plant Growth and Development”
inferred← citeshttps://doi.org/10.3390/ijms26083701openalex-snapshot
Bioinformatics Analysis Reveals the Evolutionary Characteristics of the Phoebe bournei ARF Gene Family and Its Expression Patterns in Stress Adaptation
inferred← citeshttps://doi.org/10.3390/ijms26157264openalex-snapshot
Physiological and Transcriptomic Analyses Reveal Regulatory Mechanisms of Adventitious Root Formation in In Vitro Culture of Cinnamomum camphora
inferred← citeshttps://doi.org/10.3390/plants14142194openalex-snapshot
Phosphoinositide Signaling and Actin Polymerization Are Critical for Tip Growth in the Marine Red Alga Pyropia yezoensis
inferred← citeshttps://doi.org/10.3410/f.717963211.793465132openalex-snapshot
Faculty Opinions recommendation of Arabidopsis ribosomal proteins control developmental programs through translational regulation of auxin response factors.
inferred← citeshttps://doi.org/10.3410/f.717963211.793466559openalex-snapshot
Faculty Opinions recommendation of Arabidopsis ribosomal proteins control developmental programs through translational regulation of auxin response factors.
inferred← citeshttps://doi.org/10.35830/cn.vi64.209openalex-snapshot
El transporte de auxinas y su impacto sobre el desarrollo vegetal
inferred← citeshttps://doi.org/10.3897/imafungus.16.142356openalex-snapshot
Suillus bovinus sesquiterpenes stimulate root growth and ramification of host and non-host plants by coordinating plant auxin signaling pathways
inferred← citeshttps://doi.org/10.4161/15592324.2014.973818openalex-snapshot
Calcium signaling and biotic defense responses in plants
inferred← citeshttps://doi.org/10.4161/psb.24526openalex-snapshot
ARF-Aux/IAA interactions through domain III/IV are not strictly required for auxin-responsive gene expression
inferred← citeshttps://doi.org/10.4161/psb.26753openalex-snapshot
miR393 and miR164 influence indeterminate but not determinate nodule development
inferred← citeshttps://doi.org/10.4236/ajps.2015.65067openalex-snapshot
Transcript Profiles of Auxin Efflux Carrier and IAA-Amido Synthetase Genes Suggest the Role of Auxin on Apple (Malus × domestica) Fruit Maturation Patterns
inferred← citeshttps://doi.org/10.4236/ajps.2016.717211openalex-snapshot
Phototropism in the Marine Red Macroalga Pyropia yezoensis
inferred← citeshttps://doi.org/10.48130/frures-2021-0013openalex-snapshot
Ethylene-auxin crosstalk regulates postharvest fruit ripening process in apple
inferred← citeshttps://doi.org/10.4995/thesis/10251/39348openalex-snapshot
The control of auxin homeostasis through the regulation of IAMT1 by DELLA proteins.
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.14.0121aopenalex-snapshot
VP16 fusion efficiently reveals the function of transcriptional repressors in Arabidopsis
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.15.0116aopenalex-snapshot
Altered levels of primary metabolites in response to exogenous indole-3-acetic acid in wild type and auxin signaling mutants of Arabidopsis thaliana: A capillary electrophoresis-mass spectrometry analysis
inferred← citeshttps://doi.org/10.64013/jpbab.v2023i1.6openalex-snapshot
MOLECULAR INSIGHTS INTO PLANT HORMONE SIGNALING UNRAVELING THE GENETIC FOUNDATIONS OF GROWTH, DEVELOPMENT, AND STRESS RESPONSES UNDER CLIMATE CHANGE
inferred← citeshttps://doi.org/10.70675/052c5654z7a9ez4582zb1ffz7c7130c67970openalex-snapshot
The role of auxin in cell differentiation in meristems
inferred← citeshttps://doi.org/10.70675/e862f0a1za0a9z42b9za7ebz51ac8ff7424fopenalex-snapshot
Involvement of auxin in the arbuscular mycorrhizal symbiosis in tomato
inferred← citeshttps://doi.org/10.70675/ec0602d0z747az480dza33cz80ed637b3c45openalex-snapshot
The Role of SlARF8 Transcription Factor in Tomato Fruit Development
inferred← citeshttps://doi.org/10.7717/peerj.19599openalex-snapshot
Predicting and testing a gene network regulating seed germination in Arabidopsis
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.