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Auxin transport is sufficient to generate a maximum and gradient guiding root growth

https://doi.org/10.1038/nature06215
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf01869353openalex-snapshot
Transport of auxin (indoleacetic acid) through lipid bilayer membranes
inferredcites →https://doi.org/10.1016/j.cell.2004.09.018openalex-snapshot
The PLETHORA Genes Mediate Patterning of the Arabidopsis Root Stem Cell Niche
inferredcites →https://doi.org/10.1016/j.cell.2005.06.005openalex-snapshot
Auxin Distribution and Plant Pattern Formation: How Many Angels Can Dance on the Point of PIN?
inferredcites →https://doi.org/10.1016/j.cub.2005.09.052openalex-snapshot
Patterns of Auxin Transport and Gene Expression during Primordium Development Revealed by Live Imaging of the Arabidopsis Inflorescence Meristem
inferredcites →https://doi.org/10.1016/j.jtbi.2005.03.017openalex-snapshot
Self-organization of the vascular system in plant leaves: Inter-dependent dynamics of auxin flux and carrier proteins
inferredcites →https://doi.org/10.1016/j.tplants.2004.10.010openalex-snapshot
PIN and AUX/LAX proteins: their role in auxin accumulation
inferredcites →https://doi.org/10.1016/j.tplants.2006.06.002openalex-snapshot
Auxin transport: a field in flux
inferredcites →https://doi.org/10.1016/j.tplants.2007.03.005openalex-snapshot
Towards the systems biology of auxin-transport-mediated patterning
inferredcites →https://doi.org/10.1016/s0022-5193(69)80016-0openalex-snapshot
Positional information and the spatial pattern of cellular differentiation
inferredcites →https://doi.org/10.1016/s0065-2296(08)60351-1openalex-snapshot
The Control of the Patterned Differentiation of Vascular Tissues
inferredcites →https://doi.org/10.1016/s0092-8674(00)81535-4openalex-snapshot
An Auxin-Dependent Distal Organizer of Pattern and Polarity in the Arabidopsis Root
inferredcites →https://doi.org/10.1016/s0092-8674(02)00656-6openalex-snapshot
AtPIN4 Mediates Sink-Driven Auxin Gradients and Root Patterning in Arabidopsis
inferredcites →https://doi.org/10.1016/s0092-8674(03)00924-3openalex-snapshot
Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation
inferredcites →https://doi.org/10.1016/s0960-9822(03)00533-5openalex-snapshot
Root-Specific CLE19 Overexpression and the sol1/2 Suppressors Implicate a CLV-like Pathway in the Control of Arabidopsis Root Meristem Maintenance
inferredcites →https://doi.org/10.1038/nature02081openalex-snapshot
Regulation of phyllotaxis by polar auxin transport
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/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/nature06206openalex-snapshot
PLETHORA proteins as dose-dependent master regulators of Arabidopsis root development
inferredcites →https://doi.org/10.1073/pnas.0509839103openalex-snapshot
An auxin-driven polarized transport model for phyllotaxis
inferredcites →https://doi.org/10.1073/pnas.0510130103openalex-snapshot
Computer simulations reveal properties of the cell-cell signaling network at the shoot apex in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0510457103openalex-snapshot
A plausible model of phyllotaxis
inferredcites →https://doi.org/10.1073/pnas.78.2.976openalex-snapshot
Mathematical analysis of the chemosmotic polar diffusion of auxin through plant tissues
inferredcites →https://doi.org/10.1093/emboj/18.8.2066openalex-snapshot
AUX1 regulates root gravitropism in Arabidopsis by facilitating auxin uptake within root apical tissues
inferredcites →https://doi.org/10.1093/jexbot/52.suppl_1.403openalex-snapshot
The peri-cell-cycle in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erm060openalex-snapshot
Computer models of auxin transport: a review and commentary
inferredcites →https://doi.org/10.1101/gad.1402406openalex-snapshot
Control of leaf vascular patterning by polar auxin transport
inferredcites →https://doi.org/10.1104/pp.103.022582openalex-snapshot
Transport of the Two Natural Auxins, Indole-3-Butyric Acid and Indole-3-Acetic Acid, in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.4.1335openalex-snapshot
The rhd6 Mutation of Arabidopsis thaliana Alters Root-Hair Initiation through an Auxin- and Ethylene-Associated Process
inferredcites →https://doi.org/10.1104/pp.116.4.1515openalex-snapshot
Analysis of Cell Division and Elongation Underlying the Developmental Acceleration of Root Growth inArabidopsis thaliana1
inferredcites →https://doi.org/10.1104/pp.17.2.236openalex-snapshot
GROWTH, AUXIN, AND TROPISMS IN DECAPITATED AVENA COLEOPTILES
inferredcites →https://doi.org/10.1105/tpc.105.035816openalex-snapshot
PGP4, an ATP Binding Cassette P-Glycoprotein, Catalyzes Auxin Transport in Arabidopsis thaliana Roots
inferredcites →https://doi.org/10.1105/tpc.2.11.1071openalex-snapshot
Growth and Development of the axr1 Mutants of Arabidopsis
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/10.1126/science.1121356openalex-snapshot
Polar PIN Localization Directs Auxin Flow in Plants
inferredcites →https://doi.org/10.1126/science.1121790openalex-snapshot
A Molecular Framework for Plant Regeneration
inferredcites →https://doi.org/10.1126/science.282.5397.2201openalex-snapshot
Auxin Transport: Down and Out and Up Again

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113531zenodo-depositor-declared
Labdane diterpenoids from the heartwood of Leucosceptrum canum that impact on root growth and seed germination of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.2139/ssrn.3910822openalex-extracted
N-Glycosylation is Important for Root Growth Under Alkaline Stress by Involving Auxin Transport and Proton Efflux
inferred← citeshttps://doi.org/10.1002/1873-3468.13987openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470015902.a0002069.pub2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118889022.ch2openalex-snapshot
Mechanism of Auxin Mediated Stress Signaling in Plants
inferred← citeshttps://doi.org/10.1002/9781119053095.ch47openalex-snapshot
Regulation of Nodule Development by Short‐ and Long‐Distance Auxin Transport Control
inferred← citeshttps://doi.org/10.1002/9781119053095.ch66openalex-snapshot
Computational and Experimental Evidence That Auxin Accumulation in Nodule and Lateral Root Primordia Occurs by Different Mechanisms
inferred← citeshttps://doi.org/10.1002/9781119210436.ch10openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119312994.apr0539openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781394302826.ch4openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781444310023.ch1openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527675265.ch37openalex-snapshot
Phosphorus Starvation Response in Plants and Opportunities for Crop Improvement
inferred← citeshttps://doi.org/10.1002/advs.202511837openalex-snapshot
Root Meristem Maintenance Mechanisms are Key to Plant Defense Against Nanoplastics
inferred← citeshttps://doi.org/10.1002/bies.080146openalex-snapshot
Local auxin production: a small contribution to a big field
inferred← citeshttps://doi.org/10.1002/bies.200900185openalex-snapshot
Computer simulation: The imaginary friend of auxin transport biology
inferred← citeshttps://doi.org/10.1002/bies.201900245openalex-snapshot
Competitive and Coordinative Interactions between Body Parts Produce Adaptive Developmental Outcomes
inferred← citeshttps://doi.org/10.1002/dvdy.23878openalex-snapshot
Hormone symphony during root growth and development
inferred← citeshttps://doi.org/10.1002/etc.3833openalex-snapshot
Toxicity of silver nanoparticles to Arabidopsis: Inhibition of root gravitropism by interfering with auxin pathway
inferred← citeshttps://doi.org/10.1002/gch2.202500186openalex-snapshot
Negatively but Not Positively Charged Nanoceria Promoted Lateral Root Growth via Modulating the Distribution of Reactive Oxygen Species Rather than Auxin
inferred← citeshttps://doi.org/10.1002/pld3.273openalex-snapshot
Role of Arabidopsis RAB5 GEF vps9a in maintaining potassium levels under sodium chloride stress
inferred← citeshttps://doi.org/10.1002/pmic.201000598openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/wdev.17openalex-snapshot
Root branching: mechanisms, robustness, and plasticity
inferred← citeshttps://doi.org/10.1002/wdev.49openalex-snapshot
Patterning the primary root in Arabidopsis
inferred← citeshttps://doi.org/10.1007/978-1-0716-1816-5_8openalex-snapshot
The Virtual Root: Mathematical Modeling of Auxin Transport in the Arabidopsis Root Tip Using the Open-Source Software SimuPlant
inferred← citeshttps://doi.org/10.1007/978-1-4020-8843-8_14openalex-snapshot
Qualitative And Quantitative Analyses Of ß-Tubulin Cva (C-Terminal Variable Acidic Amino Acid Region) By Maldi-Tof Mass-Spectrometry
inferred← citeshttps://doi.org/10.1007/978-1-4939-0491-4_10openalex-snapshot
Phytohormonal Crosstalk Under Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-1-4939-6722-3_1openalex-snapshot
Experimental and Theoretical Methods to Approach the Study of Vascular Patterning in the Plant Shoot
inferred← citeshttps://doi.org/10.1007/978-3-030-06128-9_8openalex-snapshot
Plants: Unitary Organisms Emerging From Integration and Self-organization of Modules
inferred← citeshttps://doi.org/10.1007/978-3-030-43939-2_7openalex-snapshot
Stem Cells in Plant Development
inferred← citeshttps://doi.org/10.1007/978-3-030-84985-6_13openalex-snapshot
Interaction of Cytokinin and Ethylene in the Regulation of Primary Root Growth and Development
inferred← citeshttps://doi.org/10.1007/978-3-030-84985-6_15openalex-snapshot
Precise Role of Strigolactones and Its Crosstalk Mechanisms in Root Development
inferred← citeshttps://doi.org/10.1007/978-3-030-84985-6_23openalex-snapshot
Understanding the Regulation of Root Development Towards Environmental Stresses for Crop Improvement
inferred← citeshttps://doi.org/10.1007/978-3-319-47763-3_24openalex-snapshot
Signaling and Genetic Regulation of the Plant Stem Cells
inferred← citeshttps://doi.org/10.1007/978-3-319-73975-5_10openalex-snapshot
Dynamical Features of a Biochemical Interaction in a Plant Root Hair Cell
inferred← citeshttps://doi.org/10.1007/978-3-319-75910-4_1openalex-snapshot
Insights into Pivotal Role of Phytohormonal Cross Talk in Tailoring Underground Plant Root System Architecture
inferred← citeshttps://doi.org/10.1007/978-3-319-79099-2_8openalex-snapshot
Modeling Plant Morphogenesis: An Introduction
inferred← citeshttps://doi.org/10.1007/978-3-319-99070-5_1openalex-snapshot
Physical Models of Plant Morphogenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-99070-5_7openalex-snapshot
Modeling Plant Tissue Growth and Cell Division
inferred← citeshttps://doi.org/10.1007/978-3-540-95885-7_3openalex-snapshot
Multilevel Modeling of Morphogenesis
inferred← citeshttps://doi.org/10.1007/978-3-642-02301-9_1openalex-snapshot
Gene Regulatory Models for Plant Development and Evolution
inferred← citeshttps://doi.org/10.1007/978-3-642-13145-5_2openalex-snapshot
Root Apical Meristem Pattern: Hormone Circuitry and Transcriptional Networks
inferred← citeshttps://doi.org/10.1007/978-3-642-13431-9_17openalex-snapshot
Hormone Transport
inferred← citeshttps://doi.org/10.1007/978-3-642-20164-6_5openalex-snapshot
Integrated Molecular Circuits for Stem Cell Activity in Arabidopsis Roots
inferred← citeshttps://doi.org/10.1007/978-3-642-22746-2_2openalex-snapshot
To Divide and to Rule; Regulating Cell Division in Roots During Post-embryonic Growth
inferred← citeshttps://doi.org/10.1007/978-3-642-30967-0_6openalex-snapshot
Whole-Plant Physiology: Synergistic Emergence Rather Than Modularity
inferred← citeshttps://doi.org/10.1007/978-3-642-35299-7_13openalex-snapshot
From Auxin Transport to Patterning
inferred← citeshttps://doi.org/10.1007/978-3-642-35299-7_2openalex-snapshot
Polar Auxin Transport: Cell Polarity to Patterning
inferred← citeshttps://doi.org/10.1007/978-3-642-35299-7_7openalex-snapshot
Auxin Transport and Signaling in Leaf Vascular Patterning
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8_1openalex-snapshot
The Auxin Question: A Philosophical Overview
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8_15openalex-snapshot
Computational Models of Auxin-Driven Development
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8_7openalex-snapshot
The Interplay Between Auxin and the Cell Cycle During Plant Development
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8_8openalex-snapshot
Auxin on the Road Navigated by Cellular PIN Polarity
inferred← citeshttps://doi.org/10.1007/978-981-19-5121-3_16openalex-snapshot
Cereals and Phytohormones Under Mineral Deficiency Stress
inferred← citeshttps://doi.org/10.1007/978-981-95-7033-1_1openalex-snapshot
Arabidopsis Root Development
inferred← citeshttps://doi.org/10.1007/s00284-021-02375-2openalex-snapshot
Rhizosphere Microbiome Cooperations: Strategies for Sustainable Crop Production
inferred← citeshttps://doi.org/10.1007/s00285-011-0472-yopenalex-snapshot
Multiscale modelling of auxin transport in the plant-root elongation zone
inferred← citeshttps://doi.org/10.1007/s00285-012-0588-8openalex-snapshot
Numerical bifurcation analysis of the pattern formation in a cell based auxin transport model
inferred← citeshttps://doi.org/10.1007/s00299-012-1378-xopenalex-snapshot
DR5 as a reporter system to study auxin response in Populus
inferred← citeshttps://doi.org/10.1007/s00299-014-1728-yopenalex-snapshot
GA3 enhances root responsiveness to exogenous IAA by modulating auxin transport and signalling in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-016-1961-7openalex-snapshot
Topoisomerase II-associated protein PAT1H1 is involved in the root stem cell niche maintenance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-019-02497-9openalex-snapshot
An essential role for Arabidopsis Trs33 in cell growth and organization in plant apical meristems
inferred← citeshttps://doi.org/10.1007/s00299-026-03924-4openalex-snapshot
The bp-miR156c–BpSPL2 module positively regulates drought tolerance by mediating lateral root development and reactive oxygen species scavenging in Betula platyphylla
inferred← citeshttps://doi.org/10.1007/s00344-010-9180-xopenalex-snapshot
The Hormonal Regulation of Flower Development
inferred← citeshttps://doi.org/10.1007/s00344-013-9386-9openalex-snapshot
Overexpression of Arabidopsis Wali7 Domain-Containing Protein ASR Produces Auxin-Mediated Short-Root Phenotype
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/s00344-015-9530-9openalex-snapshot
MeJA Affects Root Growth by Modulation of Transmembrane Auxin Flux in the Transition Zone
inferred← citeshttps://doi.org/10.1007/s00344-017-9688-4openalex-snapshot
Insect Herbivory of Leaves Affects the Auxin Flux Along Root Apices in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00344-021-10527-8openalex-snapshot
Nitrate Application Induces Adventitious Root Growth by Regulating Gene Expression Patterns in Apple Rootstocks
inferred← citeshttps://doi.org/10.1007/s00425-008-0710-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00425-009-0912-8openalex-snapshot
The short-rooted vitamin B6-deficient mutant pdx1 has impaired local auxin biosynthesis
inferred← citeshttps://doi.org/10.1007/s00425-015-2373-6openalex-snapshot
Narciclasine, a potential allelochemical, affects subcellular trafficking of auxin transporter proteins and actin cytoskeleton dynamics in Arabidopsis roots
inferred← citeshttps://doi.org/10.1007/s00425-020-03406-1openalex-snapshot
TDIF peptides regulate root growth by affecting auxin homeostasis and PINs expression in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00425-023-04226-9openalex-snapshot
Regulation of early seedling establishment and root development in Arabidopsis thaliana by light and carbohydrates
inferred← citeshttps://doi.org/10.1007/s00425-023-04283-0openalex-snapshot
BRIP1 and BRIP2 maintain root meristem by affecting auxin-mediated regulation
inferred← citeshttps://doi.org/10.1007/s00425-026-05069-wopenalex-snapshot
High-throughput sequencing reveals that microRNA-based regulation, cell wall remodeling and phytohormone signaling orchestrate wheat seminal root development
inferred← citeshttps://doi.org/10.1007/s00709-010-0211-zopenalex-snapshot
The vascular cambium: molecular control of cellular structure
inferred← citeshttps://doi.org/10.1007/s00709-016-0995-6openalex-snapshot
Exogenous gibberellin enhances secondary xylem development and lignification in carrot taproot
inferred← citeshttps://doi.org/10.1007/s00709-025-02038-0openalex-snapshot
Cerium oxide nanoparticles ameliorate Arabidopsis thaliana root damage under UV-B stress by modulating the cell cycle and auxin pathways
inferred← citeshttps://doi.org/10.1007/s00709-025-02094-6openalex-snapshot
Phosphate deprivation counteracts the cell death caused by loss-of-function of MEDIATOR 18 in Arabidopsis root meristems
inferred← citeshttps://doi.org/10.1007/s10059-013-0097-7openalex-snapshot
Genetic Identification of a Second Site Modifier of ctr1-1 that Controls Ethylene-Responsive and Gravitropic Root Growth in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10725-017-0264-5openalex-snapshot
Effect of exogenous Brassinolide (BR) application on the morphology, hormone status, and gene expression of developing lateral roots in Malus hupehensis
inferred← citeshttps://doi.org/10.1007/s10725-019-00495-1openalex-snapshot
The integration of ACS2-generated ACC with GH3-mediated IAA homeostasis in NaCl-stressed primary root elongation of Arabidopsis seedlings
inferred← citeshttps://doi.org/10.1007/s10725-022-00923-9openalex-snapshot
Use of auxin and cytokinin for somatic embryogenesis in plant: a story from competence towards completion
inferred← citeshttps://doi.org/10.1007/s11101-008-9101-9openalex-snapshot
Root and shoot glucosinolates: a comparison of their diversity, function and interactions in natural and managed ecosystems
inferred← citeshttps://doi.org/10.1007/s11103-008-9396-3openalex-snapshot
Hormone mediated regulation of the shoot apical meristem
inferred← citeshttps://doi.org/10.1007/s11103-009-9546-2openalex-snapshot
Developmental consequences of the tumorous shoot development1 mutation, a novel allele of the cellulose-synthesizing KORRIGAN1 gene
inferred← citeshttps://doi.org/10.1007/s11103-011-9779-8openalex-snapshot
DORNRÖSCHEN-LIKE expression marks Arabidopsis floral organ founder cells and precedes auxin response maxima
inferred← citeshttps://doi.org/10.1007/s11103-012-9954-6openalex-snapshot
A complex systems approach to Arabidopsis root stem-cell niche developmental mechanisms: from molecules, to networks, to morphogenesis
inferred← citeshttps://doi.org/10.1007/s11103-016-0438-yopenalex-snapshot
Hormonal control of sulfate uptake and assimilation
inferred← citeshttps://doi.org/10.1007/s11103-017-0623-7openalex-snapshot
A novel AP2/ERF family transcription factor from Glycine soja, GsERF71, is a DNA binding protein that positively regulates alkaline stress tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11103-020-01006-xopenalex-snapshot
TPST is involved in fructose regulation of primary root growth in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11103-020-01053-4openalex-snapshot
MERISTEM ACTIVITYLESS (MAL) is involved in root development through maintenance of meristem size in rice
inferred← citeshttps://doi.org/10.1007/s11103-022-01289-2openalex-snapshot
The interaction between exogenous IBA with sucrose, light and ventilation alters the expression of ARFs and Aux/IAA genes in Carica papaya plantlets
inferred← citeshttps://doi.org/10.1007/s11240-009-9573-3openalex-snapshot
Acquisition of callogenic capacity in date palm leaf tissues in response to 2,4-D treatment
inferred← citeshttps://doi.org/10.1007/s11240-014-0469-5openalex-snapshot
High efficient transformation of auxin reporter gene into trifoliate orange via Agrobacterium rhizogenes-mediated co-transformation
inferred← citeshttps://doi.org/10.1007/s11240-017-1176-9openalex-snapshot
Wheat ZFP gene TaZFP593;l mediates the N-starvation adaptation of plants through regulating N acquisition and the ROS metabolism
inferred← citeshttps://doi.org/10.1007/s11240-021-02157-5openalex-snapshot
Effect of exogenous abscisic acid (ABA) on the morphology, phytohormones, and related gene expression of developing lateral roots in ‘Qingzhen 1’ apple plants
inferred← citeshttps://doi.org/10.1007/s11274-017-2364-9openalex-snapshot
Mechanisms of action of plant growth promoting bacteria
inferred← citeshttps://doi.org/10.1007/s11538-019-00685-yopenalex-snapshot
Mathematical Modelling of Auxin Transport in Plant Tissues: Flux Meets Signalling and Growth
inferred← citeshttps://doi.org/10.1007/s11538-023-01199-4openalex-snapshot
Multiscale Asymptotic Analysis Reveals How Cell Growth and Subcellular Compartments Affect Tissue-Scale Hormone Transport
inferred← citeshttps://doi.org/10.1007/s11738-019-2878-xopenalex-snapshot
5-Aminolevulinic acid (ALA) promotes primary root elongation through modulation of auxin transport in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11756-022-01031-9openalex-snapshot
Tissue specificity and responses to abiotic stresses and hormones of PIN genes in rice
inferred← citeshttps://doi.org/10.1007/s11816-018-0491-xopenalex-snapshot
Jasmonic acid modulates xylem development by controlling polar auxin transport in vascular tissues
inferred← citeshttps://doi.org/10.1007/s12041-013-0297-0openalex-snapshot
Cloning, characterization and expression of $\emph{OsFMO}_{{\mathbf{(}\emph{t}\mathbf{)}}}$ in rice encoding a flavin monooxygenase
inferred← citeshttps://doi.org/10.1007/s12210-020-00893-yopenalex-snapshot
Root stem cells: how to establish and maintain the eternal youth
inferred← citeshttps://doi.org/10.1007/s12298-015-0323-1openalex-snapshot
Arabidopsis AIR12 influences root development
inferred← citeshttps://doi.org/10.1007/s12374-011-9197-0openalex-snapshot
Calcium Could Be Involved in Auxin-Regulated Maintenance of the Quiescent Center in the Arabidopsis Root
inferred← citeshttps://doi.org/10.1007/s12374-018-0393-zopenalex-snapshot
Rice RHC Encoding a Putative Cellulase is Essential for Normal Root Hair Elongation
inferred← citeshttps://doi.org/10.1007/s12374-018-0394-yopenalex-snapshot
Insights Into the BR2/PGP1-mediated Patterns for Shoot and Root Growth in Maize Early Seedling Development by Comparative Transcriptome Sequencing
inferred← citeshttps://doi.org/10.1007/s12374-019-0230-zopenalex-snapshot
Redox Control on Stem Cell Fate and Maintenance in the Root
inferred← citeshttps://doi.org/10.1007/s13595-016-0613-yopenalex-snapshot
Modelling wood formation and structure: power and limits of a morphogenetic gradient in controlling xylem cell proliferation and growth
inferred← citeshttps://doi.org/10.1007/s40502-016-0259-7openalex-snapshot
Genetic and molecular mechanisms of post-embryonic root radial patterning
inferred← citeshttps://doi.org/10.1007/s42994-020-00020-3openalex-snapshot
Initiation and maintenance of plant stem cells in root and shoot apical meristems
inferred← citeshttps://doi.org/10.1016/b978-0-12-380868-4.00002-8openalex-snapshot
Root System Architecture
inferred← citeshttps://doi.org/10.1016/b978-0-12-381466-1.00024-9openalex-snapshot
Growth control of root architecture
inferred← citeshttps://doi.org/10.1016/b978-0-12-385944-0.00020-4openalex-snapshot
Arabidopsis as a Model for Systems Biology
inferred← citeshttps://doi.org/10.1016/b978-0-12-388403-9.00013-8openalex-snapshot
Multi-Scale Modeling of Tissues Using CompuCell3D
inferred← citeshttps://doi.org/10.1016/b978-0-12-394447-4.40020-9openalex-snapshot
VERTICAL INTEGRATION: APPLICATIONS | Multiscale Analysis of Morphogenesis
inferred← citeshttps://doi.org/10.1016/b978-0-12-811562-6.00012-8openalex-snapshot
Plant hormones and stem cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-811562-6.00013-xopenalex-snapshot
Phytohormonal quantification based on biological principles
inferred← citeshttps://doi.org/10.1016/b978-0-12-819460-7.00132-8openalex-snapshot
Signals | Auxin
inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.40020-9openalex-snapshot
Multiscale Analysis of Morphogenesis
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2019.11.001openalex-snapshot
Small RNAs as plant morphogens
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2019.12.001openalex-snapshot
Just passing through: The auxin gradient of the root meristem
inferred← citeshttps://doi.org/10.1016/j.aac.2025.06.002openalex-snapshot
cAMP: the true second messenger in transcriptional auxin signaling
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2008.09.006openalex-snapshot
Transcriptional networks in root cell fate specification
inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.12.030openalex-snapshot
Inhibition of ribosome biogenesis by actinomycin D affects Arabidopsis root development
inferred← citeshttps://doi.org/10.1016/j.biosystems.2012.03.004openalex-snapshot
Dynamic regulation of growing domains for elongating and branching morphogenesis in plants
inferred← citeshttps://doi.org/10.1016/j.cell.2008.01.040openalex-snapshot
Slicing across Kingdoms: Regeneration in Plants and Animals
inferred← citeshttps://doi.org/10.1016/j.cell.2008.01.047openalex-snapshot
TAA1-Mediated Auxin Biosynthesis Is Essential for Hormone Crosstalk and Plant Development
inferred← citeshttps://doi.org/10.1016/j.cell.2008.02.001openalex-snapshot
Plant Stem Cell Niches: Standing the Test of Time
inferred← citeshttps://doi.org/10.1016/j.cell.2012.02.051openalex-snapshot
RETRACTED: A PLETHORA-Auxin Transcription Module Controls Cell Division Plane Rotation through MAP65 and CLASP
inferred← citeshttps://doi.org/10.1016/j.cell.2012.07.017openalex-snapshot
A Bistable Circuit Involving SCARECROW-RETINOBLASTOMA Integrates Cues to Inform Asymmetric Stem Cell Division
inferred← citeshttps://doi.org/10.1016/j.cell.2017.06.002openalex-snapshot
A Sacrifice-for-Survival Mechanism Protects Root Stem Cell Niche from Chilling Stress
inferred← citeshttps://doi.org/10.1016/j.cell.2020.02.023openalex-snapshot
Form Follows Function: How to Build a Deadly Trap
inferred← citeshttps://doi.org/10.1016/j.cell.2026.06.028openalex-snapshot
Boron-bridged GIPCs stabilize cell wall anchoring and PIN polar domains
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112565openalex-snapshot
ERF1 inhibits lateral root emergence by promoting local auxin accumulation and repressing ARF7 expression
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113617openalex-snapshot
STOP1 attenuates the auxin response to maintain root stem cell niche identity
inferred← citeshttps://doi.org/10.1016/j.coisb.2017.03.005openalex-snapshot
Mechanisms of cell polarization
inferred← citeshttps://doi.org/10.1016/j.coisb.2026.100572openalex-snapshot
Cell sorting models in tissue development
inferred← citeshttps://doi.org/10.1016/j.cpb.2024.100385openalex-snapshot
Auxin signaling, transport, and regulation during adventitious root formation
inferred← citeshttps://doi.org/10.1016/j.cpb.2026.100621openalex-snapshot
Integrated analysis of DNA methylation and transcriptome reveals the mechanism of differences in adventitious root formation ability between juvenile and mature shoots of apricot
inferred← citeshttps://doi.org/10.1016/j.crvi.2010.01.005openalex-snapshot
Recent progress in auxin biology
inferred← citeshttps://doi.org/10.1016/j.cub.2007.11.048openalex-snapshot
Plant Roots: Recycled Auxin Energizes Patterning and Growth
inferred← citeshttps://doi.org/10.1016/j.cub.2011.04.017openalex-snapshot
A Mutually Inhibitory Interaction between Auxin and Cytokinin Specifies Vascular Pattern in Roots
inferred← citeshttps://doi.org/10.1016/j.cub.2011.10.002openalex-snapshot
Positional Information by Differential Endocytosis Splits Auxin Response to Drive Arabidopsis Root Meristem Growth
inferred← citeshttps://doi.org/10.1016/j.cub.2012.04.065openalex-snapshot
A Local Maximum in Gibberellin Levels Regulates Maize Leaf Growth by Spatial Control of Cell Division
inferred← citeshttps://doi.org/10.1016/j.cub.2013.08.008openalex-snapshot
Cytokinin Induces Cell Division in the Quiescent Center of the Arabidopsis Root Apical Meristem
inferred← citeshttps://doi.org/10.1016/j.cub.2013.10.038openalex-snapshot
Modeling Framework for the Establishment of the Apical-Basal Embryonic Axis in Plants
inferred← citeshttps://doi.org/10.1016/j.cub.2014.03.014openalex-snapshot
Physical Forces Regulate Plant Development and Morphogenesis
inferred← citeshttps://doi.org/10.1016/j.cub.2018.05.090openalex-snapshot
A Local Auxin Gradient Regulates Root Cap Self-Renewal and Size Homeostasis
inferred← citeshttps://doi.org/10.1016/j.cub.2021.06.055openalex-snapshot
Periodic root branching is influenced by light through an HY1-HY5-auxin pathway
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.cub.2023.08.030openalex-snapshot
Spatial transcriptomics of a lycophyte root sheds light on root evolution
inferred← citeshttps://doi.org/10.1016/j.cub.2025.06.072openalex-snapshot
Wound repair in plants guided by cell geometry
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.02.004openalex-snapshot
Arabidopsis Regeneration from Multiple Tissues Occurs via a Root Development Pathway
inferred← citeshttps://doi.org/10.1016/j.devcel.2011.06.001openalex-snapshot
Extracellular Movement of Signaling Molecules
inferred← citeshttps://doi.org/10.1016/j.devcel.2014.05.006openalex-snapshot
D6 PROTEIN KINASE Activates Auxin Transport-Dependent Growth and PIN-FORMED Phosphorylation at the Plasma Membrane
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.08.015openalex-snapshot
A Case for Distributed Control of Local Stem Cell Behavior in Plants
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.09.022openalex-snapshot
Local Auxin Biosynthesis Is a Key Regulator of Plant Development
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.11.015openalex-snapshot
Plasma Membrane Domain Patterning and Self-Reinforcing Polarity in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.04.004openalex-snapshot
A Self-Organized PLT/Auxin/ARR-B Network Controls the Dynamics of Root Zonation Development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.07.005openalex-snapshot
A reflux-and-growth mechanism explains oscillatory patterning of lateral root branching sites
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.09.020openalex-snapshot
Transport properties of canonical PIN-FORMED proteins from Arabidopsis and the role of the loop domain in auxin transport
inferred← citeshttps://doi.org/10.1016/j.devcel.2026.06.005openalex-snapshot
Plant stem cell systems: Robust by design
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2021.112168openalex-snapshot
Carbon dots inhibit root growth by disrupting auxin biosynthesis and transport in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2012.05.003openalex-snapshot
Interactions between hormone and redox signalling pathways in the control of growth and cross tolerance to stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104038openalex-snapshot
Mild cadmium stress induces auxin synthesis and accumulation, while severe cadmium stress causes its rapid depletion in barley root tip
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104667openalex-snapshot
Strigolactones affect the root system architecture of cherry rootstock by mediating hormone signaling pathways
inferred← citeshttps://doi.org/10.1016/j.envpol.2019.113516openalex-snapshot
The mechanism of root growth inhibition by the endocrine disruptor bisphenol A (BPA)
inferred← citeshttps://doi.org/10.1016/j.gde.2008.05.001openalex-snapshot
Root layers: complex regulation of developmental patterning
inferred← citeshttps://doi.org/10.1016/j.gde.2008.05.002openalex-snapshot
Vein patterning in growing leaves: axes and polarities
inferred← citeshttps://doi.org/10.1016/j.gde.2010.04.011openalex-snapshot
Built to rebuild: in search of organizing principles in plant regeneration
inferred← citeshttps://doi.org/10.1016/j.hpj.2022.11.001openalex-snapshot
Identification of the HAK gene family reveals their critical response to potassium regulation during adventitious root formation in apple rootstock
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101309openalex-snapshot
Positioning the Root Elongation Zone Is Saltatory and Receives Input from the Shoot
inferred← citeshttps://doi.org/10.1016/j.jplph.2008.07.006openalex-snapshot
Overexpression of IAA1 with domain II mutation impairs cell elongation and cell division in inflorescences and leaves of Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.jplph.2018.08.007openalex-snapshot
The garlic allelochemical DADS influences cucumber root growth involved in regulating hormone levels and modulating cell cycling
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153594openalex-snapshot
Auxin transport in developing protophloem: A case study in canalization
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154651openalex-snapshot
Deficiency of Arabidopsis SMO2 triggers an ANAC082-Dependent pathway to regulate root apical meristem
inferred← citeshttps://doi.org/10.1016/j.jtbi.2009.03.017openalex-snapshot
Dynamic modeling of branching morphogenesis of ureteric bud in early kidney development
inferred← citeshttps://doi.org/10.1016/j.jtbi.2011.05.011openalex-snapshot
The influence of cytokinin–auxin cross-regulation on cell-fate determination in Arabidopsis thaliana root development
inferred← citeshttps://doi.org/10.1016/j.jtbi.2012.08.032openalex-snapshot
The role of auxin and cytokinin signalling in specifying the root architecture of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.jtbi.2014.11.003openalex-snapshot
Modelling of Arabidopsis LAX3 expression suggests auxin homeostasis
inferred← citeshttps://doi.org/10.1016/j.jtbi.2016.04.036openalex-snapshot
A multi-scale model of the interplay between cell signalling and hormone transport in specifying the root meristem of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.jtbi.2023.111415openalex-snapshot
Long-distance hormone transport via the phloem
inferred← citeshttps://doi.org/10.1016/j.mbs.2011.10.005openalex-snapshot
Distinguishing possible mechanisms for auxin-mediated developmental control in Arabidopsis: Models with two Aux/IAA and ARF proteins, and two target gene-sets
inferred← citeshttps://doi.org/10.1016/j.micres.2024.127689openalex-snapshot
Biocompatibility of Brazilian native yeast-derived sophorolipids and Trichoderma harzianum as plant-growth promoting bioformulations
inferred← citeshttps://doi.org/10.1016/j.molp.2015.06.006openalex-snapshot
Abscisic Acid Transport and Homeostasis in the Context of Stomatal Regulation
inferred← citeshttps://doi.org/10.1016/j.molp.2017.11.002openalex-snapshot
Crosstalk Complexities between Auxin, Cytokinin, and Ethylene in Arabidopsis Root Development: From Experiments to Systems Modeling, and Back Again
inferred← citeshttps://doi.org/10.1016/j.molp.2019.04.004openalex-snapshot
A Single-Cell RNA Sequencing Profiles the Developmental Landscape of Arabidopsis Root
inferred← citeshttps://doi.org/10.1016/j.molp.2019.05.003openalex-snapshot
Systems Biology Approach Pinpoints Minimum Requirements for Auxin Distribution during Fruit Opening
inferred← citeshttps://doi.org/10.1016/j.molp.2019.05.006openalex-snapshot
Systems Biology of Plant-Microbiome Interactions
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