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Lateral Root Priming Synergystically Arises from Root Growth and Auxin Transport Dynamics

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What this work says

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

inferredcites →https://doi.org/10.1016/j.copbio.2014.11.015openalex-snapshot
Regulation of plant root system architecture: implications for crop advancement
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.cub.2014.04.002openalex-snapshot
Cytokinin Controls Polarity of PIN1-Dependent Auxin Transport during Lateral Root Organogenesis
inferredcites →https://doi.org/10.1016/j.cub.2015.03.046openalex-snapshot
Root Cap-Derived Auxin Pre-patterns the Longitudinal Axis of the Arabidopsis Root
inferredcites →https://doi.org/10.1016/j.devcel.2008.09.019openalex-snapshot
The NAC Domain Transcription Factors FEZ and SOMBRERO Control the Orientation of Cell Division Plane in Arabidopsis Root Stem Cells
inferredcites →https://doi.org/10.1016/j.tibtech.2014.09.008openalex-snapshot
Designer crops: optimal root system architecture for nutrient acquisition
inferredcites →https://doi.org/10.1016/j.tplants.2010.08.009openalex-snapshot
The roots of a new green revolution
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/nature06215openalex-snapshot
Auxin transport is sufficient to generate a maximum and gradient guiding root growth
inferredcites →https://doi.org/10.1038/nature13663openalex-snapshot
PLETHORA gradient formation mechanism separates auxin responses
inferredcites →https://doi.org/10.1038/ncb1205-1057openalex-snapshot
Pins for spines
inferredcites →https://doi.org/10.1038/ncb1316openalex-snapshot
Root gravitropism requires lateral root cap and epidermal cells for transport and response to a mobile auxin signal
inferredcites →https://doi.org/10.1038/ncb1754openalex-snapshot
The auxin influx carrier LAX3 promotes lateral root emergence
inferredcites →https://doi.org/10.1046/j.0960-7412.2001.01217.xopenalex-snapshot
Shoot‐derived auxin is essential for early lateral root emergence in Arabidopsis seedlings
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.0906354106openalex-snapshot
The D-type cyclin CYCD4;1 modulates lateral root density in Arabidopsis by affecting the basal meristem region
inferredcites →https://doi.org/10.1073/pnas.0915001107openalex-snapshot
Bimodular auxin response controls organogenesis in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1613499114openalex-snapshot
Auxin steers root cell expansion via apoplastic pH regulation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.1705833114openalex-snapshot
Auxin minimum triggers the developmental switch from cell division to cell differentiation in the Arabidopsis root
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/eru488openalex-snapshot
Length and activity of the root apical meristem revealed in vivo by infrared imaging
inferredcites →https://doi.org/10.1093/jxb/erw448openalex-snapshot
Regulation of vascular cell division
inferredcites →https://doi.org/10.1093/mp/ssr006openalex-snapshot
Transport and Metabolism of the Endogenous Auxin Precursor Indole-3-Butyric Acid
inferredcites →https://doi.org/10.1093/pcp/pcj043openalex-snapshot
Expression Profiling of Auxin-treated Arabidopsis Roots: Toward a Molecular Analysis of Lateral Root Emergence
inferredcites →https://doi.org/10.1093/pcp/pcx091openalex-snapshot
BIG BROTHER Uncouples Cell Proliferation from Elongation in the Arabidopsis Primary Root
inferredcites →https://doi.org/10.1098/rstb.2011.0232openalex-snapshot
Multiple AUX/IAA–ARF modules regulate lateral root formation: the role of Arabidopsis SHY2/IAA3-mediated auxin signalling
inferredcites →https://doi.org/10.1101/gad.210501openalex-snapshot
Localization of the auxin permease AUX1 suggests two functionally distinct hormone transport pathways operate in the Arabidopsis root apex
inferredcites →https://doi.org/10.1101/gad.276964.115openalex-snapshot
Targeted cell elimination reveals an auxin-guided biphasic mode of lateral root initiation
inferredcites →https://doi.org/10.1104/pp.113.218453openalex-snapshot
Plasticity of the Arabidopsis Root System under Nutrient Deficiencies
inferredcites →https://doi.org/10.1104/pp.116.2.455openalex-snapshot
Auxin Transport Is Required for Hypocotyl Elongation in Light-Grown but Not Dark-Grown Arabidopsis1
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/10.1105/tpc.108.058719openalex-snapshot
Phosphate Availability Alters Lateral Root Development inArabidopsisby Modulating Auxin Sensitivity via a Mechanism Involving the TIR1 Auxin Receptor
inferredcites →https://doi.org/10.1105/tpc.112.097766openalex-snapshot
AUX/LAX Genes Encode a Family of Auxin Influx Transporters That Perform Distinct Functions during Arabidopsis Development
inferredcites →https://doi.org/10.1105/tpc.16.00638openalex-snapshot
Periodic Lateral Root Priming: What Makes It Tick?
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02892.xopenalex-snapshot
Time‐lapse analysis of stem‐cell divisions in the Arabidopsis thaliana root meristem
inferredcites →https://doi.org/10.1111/jipb.12471openalex-snapshot
Root architecture
inferredcites →https://doi.org/10.1111/nph.12933openalex-snapshot
The carrier AUXIN RESISTANT (AUX1) dominates auxin flux into Arabidopsis protoplasts
inferredcites →https://doi.org/10.1126/science.1164147openalex-snapshot
A Genetic Framework for the Control of Cell Division and Differentiation in the Root Meristem
inferredcites →https://doi.org/10.1126/science.1191937openalex-snapshot
Oscillating Gene Expression Determines Competence for Periodic Arabidopsis Root Branching
inferredcites →https://doi.org/10.1126/science.273.5277.948openalex-snapshot
Arabidopsis AUX1 Gene: A Permease-Like Regulator of Root Gravitropism
inferredcites →https://doi.org/10.1126/science.aad2776openalex-snapshot
Cyclic programmed cell death stimulates hormone signaling and root development in Arabidopsis
inferredcites →https://doi.org/10.1186/s12870-015-0685-0openalex-snapshot
A detailed expression map of the PIN1 auxin transporter in Arabidopsis thaliana root
inferredcites →https://doi.org/10.1186/s12870-016-0713-8openalex-snapshot
Two members of TaRLK family confer powdery mildew resistance in common wheat
inferredcites →https://doi.org/10.1186/s13007-019-0417-9openalex-snapshot
Week-long imaging of cell divisions in the Arabidopsis root meristem
inferredcites →https://doi.org/10.1201/b14550openalex-snapshot
Plant Roots
inferredcites →https://doi.org/10.1242/dev.02027openalex-snapshot
Functional redundancy of PIN proteins is accompanied by auxin-dependent cross-regulation of PIN expression
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.065102openalex-snapshot
Ethylene inhibits lateral root development, increases IAA transport and expression of PIN3 and PIN7 auxin efflux carriers
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/10.1242/dev.132035openalex-snapshot
Cytokinin acts through the auxin influx carrier AUX1 to regulate cell elongation in the root
inferredcites →https://doi.org/10.1242/dev.135111openalex-snapshot
Modeling halotropism: A key role for root tip architecture and reflux loop remodeling in redistributing auxin
inferredcites →https://doi.org/10.1371/journal.pbio.0060307openalex-snapshot
Root System Architecture from Coupling Cell Shape to Auxin Transport
inferredcites →https://doi.org/10.1371/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
inferredcites →https://doi.org/10.1371/journal.pcbi.1004606openalex-snapshot
A Model of Drosophila Larva Chemotaxis
inferredcites →https://doi.org/10.3389/fpls.2015.00001openalex-snapshot
Control of yellow and purple nutsedge in elevated CO2 environments with glyphosate and halosulfuron
inferredcites →https://doi.org/10.3389/fpls.2015.01187openalex-snapshot
Developmental Nuclear Localization and Quantification of GFP-Tagged EB1c in Arabidopsis Root Using Light-Sheet Microscopy
inferredcites →https://doi.org/10.7554/elife.26792openalex-snapshot
Live tracking of moving samples in confocal microscopy for vertically grown roots

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.molp.2019.03.015openalex-snapshot
The Systems Biology of Lateral Root Formation: Connecting the Dots
inferred← citeshttps://doi.org/10.1016/j.pbi.2020.04.008openalex-snapshot
It’s Morphin’ time: how multiple signals converge on ARF transcription factors to direct development
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111340openalex-snapshot
Integrated comparison of root ion flux dynamics, shoot ionic status, and root anatomy underlies contrasting salinity responses in grasses
inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.10.024openalex-snapshot
Of mice and plants: Comparative developmental systems biology
inferred← citeshttps://doi.org/10.1101/cshperspect.a039941openalex-snapshot
Auxin-Regulated Lateral Root Organogenesis
inferred← citeshttps://doi.org/10.1101/cshperspect.a040089openalex-snapshot
Modeling Auxin Signaling in Roots: Auxin Computations
inferred← citeshttps://doi.org/10.1111/nph.15691openalex-snapshot
Bringing together Europe's young plant scientists
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/10.1242/dev.181446openalex-snapshot
The dynamic nature and regulation of the root clock
inferred← citeshttps://doi.org/10.3390/genes12060884openalex-snapshot
Lateral Root Initiation and the Analysis of Gene Function Using Genome Editing with CRISPR in Arabidopsis
inferred← citeshttps://doi.org/10.53846/goediss-8893openalex-snapshot
Impact of mechanically-regulated auxin transport dynamics on plant morphogenesis
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