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To branch or not to branch: the role of pre-patterning in lateral root formation

https://doi.org/10.1242/dev.090548
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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/bf01276795openalex-snapshot
Lateral root initiation by asymmetrical transverse divisions of pericycle cells in four plant species:Raphanus sativus, Helianthus annuus, Zea mays, andDaucus carota
inferredcites →https://doi.org/10.1007/bf01276979openalex-snapshot
A histological study of lateral root initiation and development inZea mays
inferredcites →https://doi.org/10.1007/s00425-007-0565-4openalex-snapshot
Developmental steps in acquiring competence for shoot development in Arabidopsis tissue culture
inferredcites →https://doi.org/10.1007/s00425-012-1673-3openalex-snapshot
Effects of three auxin-inducible LBD members on lateral root formation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.cub.2010.09.007openalex-snapshot
A Novel Aux/IAA28 Signaling Cascade Activates GATA23-Dependent Specification of Lateral Root Founder Cell Identity
inferredcites →https://doi.org/10.1016/j.devcel.2010.02.004openalex-snapshot
Arabidopsis Regeneration from Multiple Tissues Occurs via a Root Development Pathway
inferredcites →https://doi.org/10.1016/j.pbi.2006.11.011openalex-snapshot
Common regulatory themes in meristem development and whole-plant homeostasis
inferredcites →https://doi.org/10.1016/j.pbi.2007.10.002openalex-snapshot
Conserved and diverse mechanisms in root development
inferredcites →https://doi.org/10.1016/j.pbi.2011.10.003openalex-snapshot
Subterranean space exploration: the development of root system architecture
inferredcites →https://doi.org/10.1016/j.tplants.2011.05.006openalex-snapshot
Root developmental adaptation to phosphate starvation: better safe than sorry
inferredcites →https://doi.org/10.1016/j.tplants.2011.08.005openalex-snapshot
Founder cell specification
inferredcites →https://doi.org/10.1016/j.tplants.2013.04.006openalex-snapshot
Lateral root development in Arabidopsis: fifty shades of auxin
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/10.1038/cr.2012.63openalex-snapshot
LATERAL ORGAN BOUNDARIES DOMAIN transcription factors direct callus formation in Arabidopsis regeneration
inferredcites →https://doi.org/10.1038/emboj.2012.303openalex-snapshot
Auxin reflux between the endodermis and pericycle promotes lateral root initiation
inferredcites →https://doi.org/10.1038/nature02100openalex-snapshot
APL regulates vascular tissue identity in Arabidopsis
inferredcites →https://doi.org/10.1046/j.0960-7412.2001.01201.xopenalex-snapshot
Lateral root formation is blocked by a gain‐of‐function mutation in the SOLITARY‐ROOT/IAA14 gene of Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01652.xopenalex-snapshot
An abscisic acid‐sensitive checkpoint in lateral root development of Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01964.xopenalex-snapshot
Arabidopsis ALF4 encodes a nuclear‐localized protein required for lateral root formation
inferredcites →https://doi.org/10.1055/s-2003-40722openalex-snapshot
Evaluation and Comparison of the GUS, LUC and GFP Reporter System for Gene Expression Studies in Plants
inferredcites →https://doi.org/10.1073/pnas.0308702101openalex-snapshot
Transcript profiling of early lateral root initiation
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.0807814105openalex-snapshot
Mechanical induction of lateral root initiation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0915001107openalex-snapshot
Bimodular auxin response controls organogenesis in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1210807110openalex-snapshot
Lateral root morphogenesis is dependent on the mechanical properties of the overlaying tissues
inferredcites →https://doi.org/10.1073/pnas.85.15.5536openalex-snapshot
Agrobacterium tumefaciens -mediated transformation of Arabidopsis thaliana root explants by using kanamycin selection
inferredcites →https://doi.org/10.1093/aob/mcj604openalex-snapshot
Lateral Root Initiation in Arabidopsis: Developmental Window, Spatial Patterning, Density and Predictability
inferredcites →https://doi.org/10.1093/jxb/erm171openalex-snapshot
Auxin fluxes in the root apex co-regulate gravitropism and lateral root initiation
inferredcites →https://doi.org/10.1093/pcp/pcj082openalex-snapshot
Cytokinin-Mediated Cell Cycling Arrest of Pericycle Founder Cells in Lateral Root Initiation of Arabidopsis
inferredcites →https://doi.org/10.1098/rstb.2011.0239openalex-snapshot
Phloem-associated auxin response maxima determine radial positioning of lateral roots in maize
inferredcites →https://doi.org/10.1101/gad.9.17.2131openalex-snapshot
A pathway for lateral root formation in Arabidopsis thaliana.
inferredcites →https://doi.org/10.1104/pp.107.107870openalex-snapshot
Diarch Symmetry of the Vascular Bundle in Arabidopsis Root Encompasses the Pericycle and Is Reflected in Distich Lateral Root Initiation
inferredcites →https://doi.org/10.1104/pp.109.142448openalex-snapshot
Mechanical Stimuli Modulate Lateral Root Organogenesis
inferredcites →https://doi.org/10.1104/pp.124.4.1648openalex-snapshot
Pericycle Cell Proliferation and Lateral Root Initiation in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.004960openalex-snapshot
Auxin-Mediated Cell Cycle Activation during Early Lateral Root Initiation
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.105.035493openalex-snapshot
Cell Cycle Progression in the Pericycle Is Not Sufficient for SOLITARY ROOT/IAA14-Mediated Lateral Root Initiation inArabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.106.047761openalex-snapshot
ARF7 and ARF19 Regulate Lateral Root Formation via Direct Activation of LBD/ASL Genes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.107.055863openalex-snapshot
Cytokinins Act Directly on Lateral Root Founder Cells to Inhibit Root Initiation
inferredcites →https://doi.org/10.1105/tpc.110.076216openalex-snapshot
Ammonium Triggers Lateral Root Branching in Arabidopsis in an AMMONIUM TRANSPORTER1;3-Dependent Manner
inferredcites →https://doi.org/10.1105/tpc.112.103044openalex-snapshot
Spatiotemporal Regulation of Lateral Root Organogenesis in Arabidopsis by Cytokinin
inferredcites →https://doi.org/10.1111/j.1365-3040.1989.tb01949.xopenalex-snapshot
The pattern of secondary root formation in curving roots of Arabidopsis thaliana (L.) Heynh.
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01306.xopenalex-snapshot
Intrinsic and environmental response pathways that regulate root system architecture
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02425.xopenalex-snapshot
Osmotic regulation of root system architecture
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03715.xopenalex-snapshot
Pluripotency of Arabidopsis xylem pericycle underlies shoot regeneration from root and hypocotyl explants grown in vitro
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02184.xopenalex-snapshot
Waving and skewing: how gravity and the surface of growth media affect root development in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03757.xopenalex-snapshot
Auxin minimum defines a developmental window for lateral root initiation
inferredcites →https://doi.org/10.1111/tpj.12085openalex-snapshot
Incipient stem cell niche conversion in tissue culture: using a systems approach to probe early events in WUSCHEL ‐dependent conversion of lateral root primordia into shoot meristems
inferredcites →https://doi.org/10.1126/science.1146265openalex-snapshot
A High-Resolution Root Spatiotemporal Map Reveals Dominant Expression Patterns
inferredcites →https://doi.org/10.1126/science.1160158openalex-snapshot
Receptor-Like Kinase ACR4 Restricts Formative Cell Divisions in the Arabidopsis Root
inferredcites →https://doi.org/10.1126/science.1191937openalex-snapshot
Oscillating Gene Expression Determines Competence for Periodic Arabidopsis Root Branching
inferredcites →https://doi.org/10.1146/annurev-genet-102108-134148openalex-snapshot
Mechanism of Auxin-Regulated Gene Expression in Plants
inferredcites →https://doi.org/10.1186/1471-2229-12-232openalex-snapshot
Plant growth strategies are remodeled by spaceflight
inferredcites →https://doi.org/10.1242/dev.006296openalex-snapshot
Regulation of theArabidopsisroot vascular initial population byLONESOME HIGHWAY
inferredcites →https://doi.org/10.1242/dev.02753openalex-snapshot
Auxin-dependent regulation of lateral root positioning in the basal meristem of Arabidopsis
inferredcites →https://doi.org/10.1242/dev.071928openalex-snapshot
The establishment of asymmetry in Arabidopsis lateral root founder cells is regulated by LBD16/ASL18 and related LBD/ASL proteins
inferredcites →https://doi.org/10.1242/dev.119.1.71openalex-snapshot
Cellular organisation of the Arabidopsis thaliana root
inferredcites →https://doi.org/10.1242/dev.121.10.3303openalex-snapshot
Formation of lateral root meristems is a two-stage process
inferredcites →https://doi.org/10.1242/dev.124.1.33openalex-snapshot
Organization and cell differentiation in lateral roots of Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pbio.0060307openalex-snapshot
Root System Architecture from Coupling Cell Shape to Auxin Transport
inferredcites →https://doi.org/10.4161/psb.1.6.3511openalex-snapshot
The Root Apex ofArabidopsis thalianaConsists of Four Distinct Zones of Growth Activities

What points at this work

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

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Pericycle
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Lateral Root Formation: Building a Meristemde novo
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Interplay Between Root Structure and Function in Enhancing Efficiency of Nitrogen and Phosphorus Acquisition
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Genetic and Phenotypic Analysis of Lateral Root Development in Arabidopsis thaliana
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The Interplay Between Auxin and the Cell Cycle During Plant Development
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Integration of Ethylene and Auxin Signaling and the Developmental Consequences of Their Crosstalk
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The MEDIATOR genes MED12 and MED13 control Arabidopsis root system configuration influencing sugar and auxin responses
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Lateral Root Initiation
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Brassinosteroids' regulation of plant architecture
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Single-cell omics to dissect molecular features in plant root development
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Root branching plasticity: collective decision-making results from local and global signalling
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The Root Cap Cuticle: A Cell Wall Structure for Seedling Establishment and Lateral Root Formation
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Trichoderma-secreted anthranilic acid promotes lateral root development via auxin signaling and RBOHF-induced endodermal cell wall remodeling
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Root Cap-Derived Auxin Pre-patterns the Longitudinal Axis of the Arabidopsis Root
inferred← citeshttps://doi.org/10.1016/j.cub.2015.04.013openalex-snapshot
Root System Patterning: Auxin Synthesis at the Root Periphery
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Rules and Self-Organizing Properties of Post-embryonic Plant Organ Cell Division Patterns
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Plant Organogenesis: Rules of Order
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Periodic root branching is influenced by light through an HY1-HY5-auxin pathway
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Plant physiology: The to-and-fro of hormone signals to respond to drought
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Arabidopsis LOHN1 peptide modulates lateral root spacing under the control of systemic nitrogen-satiety signaling
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Lateral Inhibition by a Peptide Hormone-Receptor Cascade during Arabidopsis Lateral Root Founder Cell Formation
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Endogenous Hypoxia in Lateral Root Primordia Controls Root Architecture by Antagonizing Auxin Signaling in Arabidopsis
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Receptor-like Kinases in Root Development: Current Progress and Future Directions
inferred← citeshttps://doi.org/10.1016/j.molp.2021.05.028openalex-snapshot
Reconstruction of lateral root formation through single-cell RNA sequencing reveals order of tissue initiation
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Hormonal regulation of cell fate plasticity of xylem-pole-pericycle lineage in Arabidopsis roots
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Talking through walls: mechanisms of lateral root emergence in Arabidopsis thaliana
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Dynamic control of lateral root positioning
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The dynamics of maize leaf development: Patterned to grow while growing a pattern
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Tunable recurrent priming of lateral roots in Arabidopsis: More than just a clock?
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A comparison of lateral root patterning among dicot and monocot plants
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Impact of microplastics from polyethylene and biodegradable mulch films on rice (Oryza sativa L.)
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Beneficial Microbes Affect Endogenous Mechanisms Controlling Root Development
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Genetic Control of Lateral Root Formation in Cereals
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Pseudomonas chlororaphis subsp. aurantiaca Stimulates Lateral Root Development by Integrating Auxin and Reactive Oxygen Species Signaling in Arabidopsis
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Comparison of Growth and Quality between Hydroponically Grown and Soil-Grown Lettuce under the Stress of Microplastics
inferred← citeshttps://doi.org/10.1038/ncomms6833openalex-snapshot
Arabidopsis ERF109 mediates cross-talk between jasmonic acid and auxin biosynthesis during lateral root formation
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A coherent transcriptional feed-forward motif model for mediating auxin-sensitive PIN3 expression during lateral root development
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From microbes to ecosystems: a review of the ecological effects of biodegradable plastics
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Periodic root branching in Arabidopsis requires synthesis of an uncharacterized carotenoid derivative
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Nitrate foraging by Arabidopsis roots is mediated by the transcription factor TCP20 through the systemic signaling pathway
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PLETHORA transcription factors orchestrate de novo organ patterning during Arabidopsis lateral root outgrowth
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CPR5-mediated nucleo-cytoplasmic localization of IAA12 and IAA19 controls lateral root development during abiotic stress
inferred← citeshttps://doi.org/10.1073/pnas.2615485123openalex-snapshot
The NAC transcription factor SOMBRERO controls auxin gradients for columella root cap maturation and turnover
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Omics and modelling approaches for understanding regulation of asymmetric cell divisions in arabidopsis and other angiosperm plants
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Long-term live-cell imaging approaches to study lateral root formation inArabidopsis thaliana
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PHB3 regulates lateral root primordia formation via NO-mediated degradation of AUXIN/INDOLE-3-ACETIC ACID proteins
inferred← citeshttps://doi.org/10.1093/jxb/erad123openalex-snapshot
GOLVEN peptides regulate lateral root spacing as part of a negative feedback loop on the establishment of auxin maxima
inferred← citeshttps://doi.org/10.1093/jxb/erv329openalex-snapshot
The GLV6/RGF8/CLEL2 peptide regulates early pericycle divisions during lateral root initiation
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Priming and positioning of lateral roots in Arabidopsis. An approach for an integrating concept
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Analysis of root growth from a phenotyping data set using a density-based model
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CEP5 and XIP1/CEPR1 regulate lateral root initiation in Arabidopsis
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Lateral root formation and the multiple roles of auxin
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Basic Pentacysteine Proteins Repress Abscisic Acid Insensitive4 Expression via Direct Recruitment of the Polycomb-Repressive Complex 2 in Arabidopsis Root Development
inferred← citeshttps://doi.org/10.1093/pcp/pcx107openalex-snapshot
YUCCA9-Mediated Auxin Biosynthesis and Polar Auxin Transport Synergistically Regulate Regeneration of Root Systems Following Root Cutting
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inferred← citeshttps://doi.org/10.1093/plphys/kiab530openalex-snapshot
Live Plant Cell Tracking: Fiji plugin to analyze cell proliferation dynamics and understand morphogenesis
inferred← citeshttps://doi.org/10.1093/plphys/kiac301openalex-snapshot
SICKLE modulates lateral root development by promoting degradation of lariat intronic RNA
inferred← citeshttps://doi.org/10.1093/plphys/kiac407openalex-snapshot
Abscisic acid inhibits primary root growth by impairing ABI4-mediated cell cycle and auxin biosynthesis
inferred← citeshttps://doi.org/10.1093/plphys/kiad595openalex-snapshot
H2 supplied via ammonia borane stimulates lateral root branching via phytomelatonin signaling
inferred← citeshttps://doi.org/10.1101/2020.03.11.985820openalex-snapshot
Disruption of CYCLOPHILIN 38 function reveals a photosynthesis-dependent systemic signal controlling lateral root emergence
inferred← citeshttps://doi.org/10.1101/2021.11.13.468476openalex-snapshot
Uncovering natural variation in root system architecture and growth dynamics using a robotics-assisted phenomics platform
inferred← citeshttps://doi.org/10.1101/2024.01.30.578043openalex-snapshot
Cell-material interactions in 3D bioprinted plant cells
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/10.1101/2025.11.28.690471openalex-snapshot
Ethylene signal-driven plant-multitrophic synergy boosts crop performance
inferred← citeshttps://doi.org/10.1101/283366openalex-snapshot
Clonal analysis reveals gradual recruitment of lateral root founder cells and a link between root initiation and cambium formation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/cshperspect.a039933openalex-snapshot
Auxin in Root Development
inferred← citeshttps://doi.org/10.1101/cshperspect.a039941openalex-snapshot
Auxin-Regulated Lateral Root Organogenesis
inferred← citeshttps://doi.org/10.1104/pp.114.240507openalex-snapshot
The anthocyanin reduced Tomato Mutant Demonstrates the Role of Flavonols in Tomato Lateral Root and Root Hair Development
inferred← citeshttps://doi.org/10.1104/pp.17.01274openalex-snapshot
SUPPRESSOR OF GAMMA RESPONSE1 Links DNA Damage Response to Organ Regeneration
inferred← citeshttps://doi.org/10.1104/pp.19.00695openalex-snapshot
PI4KIIIβ Activity Regulates Lateral Root Formation Driven by Endocytic Trafficking to the Vacuole
inferred← citeshttps://doi.org/10.1105/tpc.114.132993openalex-snapshot
Inference of the Arabidopsis Lateral Root Gene Regulatory Network Suggests a Bifurcation Mechanism That Defines Primordia Flanking and Central Zones
inferred← citeshttps://doi.org/10.1105/tpc.16.00182openalex-snapshot
Growing Out of Stress: The Role of Cell- and Organ-Scale Growth Control in Plant Water-Stress Responses
inferred← citeshttps://doi.org/10.1105/tpc.16.00638openalex-snapshot
Periodic Lateral Root Priming: What Makes It Tick?
inferred← citeshttps://doi.org/10.1111/ivb.12237openalex-snapshot
How do gastropods grow synchronized shell sculpture? Effect of experimental varix manipulations on shell growth byCeratostoma foliatum(Muricidae: Ocenebrinae)
inferred← citeshttps://doi.org/10.1111/jipb.12347openalex-snapshot
Activated expression of AtEDT1/HDG11 promotes lateral root formation in Arabidopsis mutant edt1 by upregulating jasmonate biosynthesis
inferred← citeshttps://doi.org/10.1111/jipb.13844openalex-snapshot
Cell wall dynamic changes and signaling during plant lateral root development
inferred← citeshttps://doi.org/10.1111/nph.14304openalex-snapshot
Control of Arabidopsis lateral root primordium boundaries by MYB 36
inferred← citeshttps://doi.org/10.1111/nph.14313openalex-snapshot
FUSCA 3 interacting with LEAFY COTYLEDON 2 controls lateral root formation through regulating YUCCA 4 gene expression in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/nph.16599openalex-snapshot
Two receptor‐like protein kinases, MUSTACHES and MUSTACHES‐LIKE, regulate lateral root development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/nph.16915openalex-snapshot
Salicylic acid regulates PIN2 auxin transporter hyperclustering and root gravitropic growth via Remorin‐dependent lipid nanodomain organisation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/nph.17132openalex-snapshot
Network analyses identify a transcriptomic proximodistal prepattern in the maize leaf primordium
inferred← citeshttps://doi.org/10.1111/nph.19284openalex-snapshot
GH3‐mediated auxin inactivation attenuates multiple stages of lateral root development
inferred← citeshttps://doi.org/10.1111/pbi.13378openalex-snapshot
Root‐specific expression of chickpea cytokinin oxidase/dehydrogenase 6 leads to enhanced root growth, drought tolerance and yield without compromising nodulation
inferred← citeshttps://doi.org/10.1111/pce.13635openalex-snapshot
Cadmium stress suppresses lateral root formation by interfering with the root clock
inferred← citeshttps://doi.org/10.1111/pce.14021openalex-snapshot
Volatile compounds from beneficial rhizobacteria Bacillus spp. promote periodic lateral root development in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.14230openalex-snapshot
The volatile cedrene from Trichoderma guizhouense modulates Arabidopsis root development through auxin transport and signalling
inferred← citeshttps://doi.org/10.1111/pce.14270openalex-snapshot
Deconstructing the root system of grasses through an exploration of development, anatomy and function
inferred← citeshttps://doi.org/10.1111/pce.70680openalex-snapshot
Lateral Root Development: Molecular Mechanisms and Adaptive Regulation
inferred← citeshttps://doi.org/10.1111/ppl.14604openalex-snapshot
Deciphering the role of growth regulators in enhancing plant immunity against herbivory
inferred← citeshttps://doi.org/10.1111/ppl.70723openalex-snapshot
L‐Glutamine Modulates Root Architecture and Hormonal Balance in Arabidopsis
inferred← citeshttps://doi.org/10.1111/sum.12868openalex-snapshot
Nanoplastic–plant interaction and implications for soil health
inferred← citeshttps://doi.org/10.1111/tpj.15096openalex-snapshot
Sensors for the quantification, localization and analysis of the dynamics of plant hormones
inferred← citeshttps://doi.org/10.1126/sciadv.abd4722openalex-snapshot
An auxin-regulable oscillatory circuit drives the root clock in Arabidopsis
inferred← citeshttps://doi.org/10.1126/science.aad2776openalex-snapshot
Cyclic programmed cell death stimulates hormone signaling and root development in Arabidopsis
inferred← citeshttps://doi.org/10.1146/annurev-arplant-042916-041107openalex-snapshot
Chemical Genetic Dissection of Membrane Trafficking
inferred← citeshttps://doi.org/10.1146/annurev-arplant-043015-111848openalex-snapshot
Environmental Control of Root System Biology
inferred← citeshttps://doi.org/10.1146/annurev-arplant-050718-100423openalex-snapshot
Molecular and Environmental Regulation of Root Development
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-100617-062949openalex-snapshot
Developmental Responses to Water and Salinity in Root Systems
inferred← citeshttps://doi.org/10.1159/000360658openalex-snapshot
Stem Cells and Regeneration in Plants
inferred← citeshttps://doi.org/10.1186/s12284-019-0364-0openalex-snapshot
OsFPFL4 is Involved in the Root and Flower Development by Affecting Auxin Levels and ROS Accumulation in Rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1186/s12870-019-2002-9openalex-snapshot
Auxin regulates adventitious root formation in tomato cuttings
inferred← citeshttps://doi.org/10.1186/s12915-026-02503-zopenalex-snapshot
Shaping with water: linking moisture perception to development in plant roots
inferred← citeshttps://doi.org/10.1186/s13059-019-1767-3openalex-snapshot
Linker histones are fine-scale chromatin architects modulating developmental decisions in Arabidopsis
inferred← citeshttps://doi.org/10.1186/s13062-024-00535-5openalex-snapshot
Shaping root architecture: towards understanding the mechanisms involved in lateral root development
inferred← citeshttps://doi.org/10.1242/bio.060531openalex-snapshot
An atlas of Brachypodium distachyon lateral root development
inferred← citeshttps://doi.org/10.1242/dev.118364openalex-snapshot
Primary root protophloem differentiation requires balanced phosphatidylinositol-4,5-biphosphate levels and systemically affects root branching
inferred← citeshttps://doi.org/10.1242/dev.169839openalex-snapshot
The plant hormone auxin beats the time for oscillating light-regulated lateral root induction
inferred← citeshttps://doi.org/10.1242/dev.181446openalex-snapshot
The dynamic nature and regulation of the root clock
inferred← citeshttps://doi.org/10.1242/dev.196253openalex-snapshot
Tissue growth constrains root organ outlines into an isometrically scalable shape
inferred← citeshttps://doi.org/10.12703/p7-32openalex-snapshot
Lateral root initiation in Arabidopsis thaliana: a force awakens
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1004450openalex-snapshot
Parsimonious Model of Vascular Patterning Links Transverse Hormone Fluxes to Lateral Root Initiation: Auxin Leads the Way, while Cytokinin Levels Out
inferred← citeshttps://doi.org/10.15389/agrobiology.2017.5.856engopenalex-snapshot
MOLECULAR, GENETIC AND HORMONAL OUTLOOK IN ROOT BRANCHING (review)
inferred← citeshttps://doi.org/10.20868/upm.thesis.69345openalex-snapshot
Modelado computacional de la autoorganización espacial generada por circuitos genéticos multicelulares
inferred← citeshttps://doi.org/10.20868/upm.thesis.72239openalex-snapshot
Unraveling new mechanisms of postembryonic organ formation in Arabidopsis thaliana roots through computational and in vivo approaches
inferred← citeshttps://doi.org/10.3389/fpls.2014.00219openalex-snapshot
Post-embryonic organogenesis and plant regeneration from tissues: two sides of the same coin?
inferred← citeshttps://doi.org/10.3389/fpls.2014.00495openalex-snapshot
Hypocotyl adventitious root organogenesis differs from lateral root development
inferred← citeshttps://doi.org/10.3389/fpls.2019.00021openalex-snapshot
Cell Type-Specific Transcriptomics of Lateral Root Formation and Plasticity
inferred← citeshttps://doi.org/10.3389/fpls.2019.00206openalex-snapshot
Lateral Root Primordium Morphogenesis in Angiosperms
inferred← citeshttps://doi.org/10.3389/fpls.2019.00365openalex-snapshot
Lateral Root Initiation in the Parental Root Meristem of Cucurbits: Old Players in a New Position
inferred← citeshttps://doi.org/10.3389/fpls.2019.00806openalex-snapshot
The Arabidopsis ATP-BINDING CASSETTE Transporter ABCB21 Regulates Auxin Levels in Cotyledons, the Root Pericycle, and Leaves
inferred← citeshttps://doi.org/10.3389/fpls.2020.00317openalex-snapshot
Reprogramming of Cell Fate During Root Regeneration by Transcriptional and Epigenetic Networks
inferred← citeshttps://doi.org/10.3389/fpls.2022.1060021openalex-snapshot
Endocytic trafficking induces lateral root founder cell specification in Arabidopsis thaliana in a process distinct from the auxin-induced pathway
inferred← citeshttps://doi.org/10.3389/fpls.2022.986414openalex-snapshot
Carotenoid-derived bioactive metabolites shape plant root architecture to adapt to the rhizospheric environments
inferred← citeshttps://doi.org/10.3389/fpls.2022.992799openalex-snapshot
Natural variation and domestication selection of ZmSULTR3;4 is associated with maize lateral root length in response to salt stress
inferred← citeshttps://doi.org/10.3389/fpls.2026.1753086openalex-snapshot
Root system architecture and drought adaptation: emerging tools and genetic insights
inferred← citeshttps://doi.org/10.3390/genes17070835openalex-snapshot
Phenotypic Changes and Physiological Genetic Responses of Oryza sativa L. Roots Under Stress of Nanoplastics (NPs) and Cadmium (Cd) in Single and Combination Forms
inferred← citeshttps://doi.org/10.3390/ijms18122587openalex-snapshot
Control of Endogenous Auxin Levels in Plant Root Development
inferred← citeshttps://doi.org/10.3390/ijms19123888openalex-snapshot
Morphological Characterization of Root System Architecture in Diverse Tomato Genotypes during Early Growth
inferred← citeshttps://doi.org/10.3390/ijms20030486openalex-snapshot
Interplay of Auxin and Cytokinin in Lateral Root Development
inferred← citeshttps://doi.org/10.3390/plants9040444openalex-snapshot
Overexpression of MADS-box Gene AGAMOUS-LIKE 12 Activates Root Development in Juglans sp. and Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/toxics9080179openalex-snapshot
Effect of Polystyrene Microplastics on Rice Seed Germination and Antioxidant Enzyme Activity
inferred← citeshttps://doi.org/10.35550/vbio2021.03.098openalex-snapshot
Modern concepts of auxin’s action. 2. Mechanisms of auxin signal transduction and physiological action
inferred← citeshttps://doi.org/10.3791/53481openalex-snapshot
Lateral Root Inducible System in Arabidopsis and Maize
inferred← citeshttps://doi.org/10.4161/15592316.2014.970406openalex-snapshot
AtMYB93is an endodermis-specific transcriptional regulator of lateral root development in arabidopsis
inferred← citeshttps://doi.org/10.4161/psb.28290openalex-snapshot
NO signaling is a key component of the root growth response to nitrate inZea maysL.
inferred← citeshttps://doi.org/10.4161/psb.29808openalex-snapshot
AtMYB93 is an endodermis-specific transcriptional regulator of lateral root development in Arabidopsis
inferred← citeshttps://doi.org/10.48130/sse-2023-0006openalex-snapshot
Promotion of root development by slightly alkaline pH involves an auxin mediated adaption mechanism
inferred← citeshttps://doi.org/10.53846/goediss-8893openalex-snapshot
Impact of mechanically-regulated auxin transport dynamics on plant morphogenesis
inferred← citeshttps://doi.org/10.5772/intechopen.82866openalex-snapshot
Phytohormone-Mediated Homeostasis of Root System Architecture
inferred← citeshttps://doi.org/10.64898/2026.01.02.697414openalex-snapshot
Auxin coordinates cell states during Arabidopsis root development
inferred← citeshttps://doi.org/10.70675/0f4ff90dz54aaz46b9z95fbzca8a03221fb4openalex-snapshot
Gènes et métabolites végétaux marqueurs de l'association riz-bactérie phytobénéfique
inferred← citeshttps://doi.org/10.70675/40f401b4z5e3cz4dfaza070z77c95a145f2eopenalex-snapshot
Glutathione and glutaredoxins, major regulators of root system architecture
inferred← citeshttps://doi.org/10.70675/672118a3zae01z40f4zb4b3z726cc38567d1openalex-snapshot
Gene regulatory network for lateral root formation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.7554/elife.76968openalex-snapshot
Uncovering natural variation in root system architecture and growth dynamics using a robotics-assisted phenomics platform
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