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PIN Proteins Perform a Rate-Limiting Function in Cellular Auxin Efflux
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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/bf00262639openalex-snapshot
Comparison of mechanisms controlling uptake and accumulation of 2,4-dichlorophenoxy acetic acid, naphthalene-1-acetic acid, and indole-3-acetic acid in suspension-cultured tobacco cells
inferredcites →https://doi.org/10.1016/j.cub.2005.03.012openalex-snapshot
Plant Development: Auxin in Loops
inferredcites →https://doi.org/10.1016/j.febslet.2005.11.054openalex-snapshot
The ABC of auxin transport: The role of p‐glycoproteins in plant development
inferredcites →https://doi.org/10.1016/j.tplants.2005.02.009openalex-snapshot
The PIN auxin efflux facilitators: evolutionary and functional perspectives
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/s1369526602000031openalex-snapshot
Auxin transport — shaping the plant
inferredcites →https://doi.org/10.1038/415806aopenalex-snapshot
Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis
inferredcites →https://doi.org/10.1038/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/10.1046/j.1365-313x.1997.11030605.xopenalex-snapshot
A glucocorticoid‐mediated transcriptional induction system in transgenic plants
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00868.xopenalex-snapshot
An estrogen receptor‐based transactivator XVE mediates highly inducible gene expression in transgenic plants
inferredcites →https://doi.org/10.1073/pnas.95.25.15112openalex-snapshot
The Arabidopsis thaliana AGRAVITROPIC 1 gene encodes a component of the polar-auxin-transport efflux carrier
inferredcites →https://doi.org/10.1093/aob/mci083openalex-snapshot
Auxin: Regulation, Action, and Interaction
inferredcites →https://doi.org/10.1101/gad.12.14.2175openalex-snapshot
EIR1, a root-specific protein involved in auxin transport, is required for gravitropism inArabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.012740openalex-snapshot
Do Phytotropins Inhibit Auxin Efflux by Impairing Vesicle Traffic?
inferredcites →https://doi.org/10.1105/tpc.010350openalex-snapshot
Multidrug Resistance –like Genes of Arabidopsis Required for Auxin Transport and Auxin-Mediated Development
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.273.5277.948openalex-snapshot
Arabidopsis AUX1 Gene: A Permease-Like Regulator of Root Gravitropism
inferredcites →https://doi.org/10.1242/dev.02027openalex-snapshot
Functional redundancy of PIN proteins is accompanied by auxin-dependent cross-regulation of PIN expression
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1007/978-3-642-35299-7_13openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-35299-7_14openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.ctdb.2018.10.003openalex-snapshot
Patterning at the shoot apical meristem and phyllotaxis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.11.056openalex-snapshot
AUX1 acts upstream of PIN2 in regulating root gravitropism
inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.02.083openalex-snapshot
The Arabidopsis STE20/Hippo kinase SIK1 regulates polarity independently of PIN proteins
inferred← citeshttps://doi.org/10.1016/j.biosystems.2012.05.010openalex-snapshot
A biochemically semi-detailed model of auxin-mediated vein formation in plant leaves
inferred← citeshttps://doi.org/10.1016/j.ceb.2011.09.006openalex-snapshot
Cell polarity in plants: when two do the same, it is not the same....
inferred← citeshttps://doi.org/10.1016/j.cell.2007.07.033openalex-snapshot
Antagonistic Regulation of PIN Phosphorylation by PP2A and PINOID Directs Auxin Flux
inferred← citeshttps://doi.org/10.1016/j.cell.2009.03.001openalex-snapshot
Auxin: A Trigger for Change in Plant Development
inferred← citeshttps://doi.org/10.1016/j.cell.2010.09.003openalex-snapshot
Cell Surface- and Rho GTPase-Based Auxin Signaling Controls Cellular Interdigitation in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cell.2010.09.027openalex-snapshot
ABP1 Mediates Auxin Inhibition of Clathrin-Dependent Endocytosis in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cell.2014.01.039openalex-snapshot
The TPLATE Adaptor Complex Drives Clathrin-Mediated Endocytosis in Plants
inferred← citeshttps://doi.org/10.1016/j.cell.2022.01.026openalex-snapshot
Synthetic mammalian signaling circuits for robust cell population control
inferred← citeshttps://doi.org/10.1016/j.cell.2023.11.038openalex-snapshot
Extracellular pectin-RALF phase separation mediates FERONIA global signaling function
inferred← citeshttps://doi.org/10.1016/j.cell.2025.04.028openalex-snapshot
Structural insights into auxin influx mediated by the Arabidopsis AUX1
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.03.054openalex-snapshot
Meta-regulation of Arabidopsis Auxin Responses Depends on tRNA Maturation
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108463openalex-snapshot
Non-steroidal Anti-inflammatory Drugs Target TWISTED DWARF1-Regulated Actin Dynamics and Auxin Transport-Mediated Plant Development
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114030openalex-snapshot
Trichoderma-secreted anthranilic acid promotes lateral root development via auxin signaling and RBOHF-induced endodermal cell wall remodeling
inferred← citeshttps://doi.org/10.1016/j.chembiol.2007.10.014openalex-snapshot
Arabidopsis P-Glycoprotein19 Participates in the Inhibition of Gravitropism by Gravacin
inferred← citeshttps://doi.org/10.1016/j.chmed.2021.08.001openalex-snapshot
Genome-wide identification and transcriptional profiling analysis of PIN/PILS auxin transporter gene families in Panax ginseng
inferred← citeshttps://doi.org/10.1016/j.crvi.2010.01.004openalex-snapshot
Auxin: A major regulator of organogenesis
inferred← citeshttps://doi.org/10.1016/j.cub.2006.05.014openalex-snapshot
Dynamic Integration of Auxin Transport and Signalling
inferred← citeshttps://doi.org/10.1016/j.cub.2007.01.052openalex-snapshot
Clathrin-Mediated Constitutive Endocytosis of PIN Auxin Efflux Carriers in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cub.2008.03.021openalex-snapshot
ARF GEF-Dependent Transcytosis and Polar Delivery of PIN Auxin Carriers in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cub.2009.01.057openalex-snapshot
Fluorescence Imaging-Based Screen Identifies ARF GEF Component of Early Endosomal Trafficking
inferred← citeshttps://doi.org/10.1016/j.cub.2010.03.059openalex-snapshot
Trafficking to the Outer Polar Domain Defines the Root-Soil Interface
inferred← citeshttps://doi.org/10.1016/j.cub.2011.01.036openalex-snapshot
PIN Polarity Maintenance by the Cell Wall in Arabidopsis
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.2012.05.020openalex-snapshot
ABP1 and ROP6 GTPase Signaling Regulate Clathrin-Mediated Endocytosis in Arabidopsis Roots
inferred← citeshttps://doi.org/10.1016/j.cub.2012.06.050openalex-snapshot
Mechanical Regulation of Auxin-Mediated Growth
inferred← citeshttps://doi.org/10.1016/j.cub.2013.03.064openalex-snapshot
An Auxin Transport Mechanism Restricts Positive Orthogravitropism in Lateral Roots
inferred← citeshttps://doi.org/10.1016/j.cub.2013.08.042openalex-snapshot
Halotropism Is a Response of Plant Roots to Avoid a Saline Environment
inferred← citeshttps://doi.org/10.1016/j.cub.2013.09.039openalex-snapshot
Local Auxin Sources Orient the Apical-Basal Axis in Arabidopsis Embryos
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.2013.11.019openalex-snapshot
Plant Biology: Gatekeepers of the Road to Protein Perdition
inferred← citeshttps://doi.org/10.1016/j.cub.2014.04.002openalex-snapshot
Cytokinin Controls Polarity of PIN1-Dependent Auxin Transport during Lateral Root Organogenesis
inferred← citeshttps://doi.org/10.1016/j.cub.2014.09.056openalex-snapshot
Directional Auxin Transport Mechanisms in Early Diverging Land Plants
inferred← citeshttps://doi.org/10.1016/j.cub.2014.09.080openalex-snapshot
Dynamic Control of Auxin Distribution Imposes a Bilateral-to-Radial Symmetry Switch during Gynoecium Development
inferred← citeshttps://doi.org/10.1016/j.cub.2019.11.058openalex-snapshot
Salicylic Acid Targets Protein Phosphatase 2A to Attenuate Growth in Plants
inferred← citeshttps://doi.org/10.1016/j.cub.2021.02.028openalex-snapshot
AGC kinases and MAB4/MEL proteins maintain PIN polarity by limiting lateral diffusion in plant cells
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.05.008openalex-snapshot
Nitrate-Regulated Auxin Transport by NRT1.1 Defines a Mechanism for Nutrient Sensing in Plants
inferred← citeshttps://doi.org/10.1016/j.devcel.2011.05.013openalex-snapshot
Inositol Trisphosphate-Induced Ca2+ Signaling Modulates Auxin Transport and PIN Polarity
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.09.026openalex-snapshot
Polarized NORTIA accumulation in response to pollen tube arrival at synergids promotes fertilization
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2015.11.038openalex-snapshot
Effects of the ionic liquid 1-hexyl-3-methylimidazolium bromide on root gravitropism in Arabidopsis seedlings
inferred← citeshttps://doi.org/10.1016/j.ejcb.2009.11.003openalex-snapshot
Subcellular trafficking of PIN auxin efflux carriers in auxin transport
inferred← citeshttps://doi.org/10.1016/j.ejcb.2009.11.020openalex-snapshot
Role of the GNOM gene in Arabidopsis apical-basal patterning – From mutant phenotype to cellular mechanism of protein action
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104544openalex-snapshot
NITRIC OXIDE ASSOCIATED PROTEIN1 (AtNOA1) is necessary for copper-induced lateral root elongation in Arabidopsis thaliana
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.febslet.2013.02.041openalex-snapshot
CACTIN is an essential nuclear protein in Arabidopsis and may be associated with the eukaryotic spliceosome
inferred← citeshttps://doi.org/10.1016/j.hpj.2023.10.001openalex-snapshot
Transcriptional regulation of MdPIN7 by MdARF19 during gravity-induced formation of adventitious root GSA in self-rooted apple stock
inferred← citeshttps://doi.org/10.1016/j.hpj.2025.10.011openalex-snapshot
Dioxygenase RhDAO1 regulates floral organ identity by controlling auxin homeostasis in miniature rose (Rosa hybrida)
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.12.230openalex-snapshot
Genome-wide identification and characterization of PIN-FORMED (PIN) and PIN-LIKES (PILS) gene family reveals their role in adventitious root development in tea nodal cutting (Camellia Sinensis)
inferred← citeshttps://doi.org/10.1016/j.indcrop.2020.112978openalex-snapshot
HbARF2 and HbARF16.3 function as negative regulators for the radial trunk growth of rubber tree
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.120558openalex-snapshot
Microscopic and transcriptomic comparison of the ovaries between the sexual and apomictic dandelions reveals the developmental process and gene regulation in regard to apomixis
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.123643openalex-snapshot
Improving pod shattering resistance in rapeseed: insights from related Brassica species
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110363openalex-snapshot
Indole-3-propionic acid regulates lateral root development by targeting auxin signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.jgg.2025.10.008openalex-snapshot
Key divisions and cell specification during embryo pattern formation require SMU1-mediated splicing of CAK genes in Arabidopsis
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.jhazmat.2025.140001openalex-snapshot
Functional evidence for the partial conservation of arsenic tolerance mechanisms in Marchantia polymorpha and Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.jplph.2013.09.026openalex-snapshot
Characterization of transmembrane auxin transport in Arabidopsis suspension-cultured cells
inferred← citeshttps://doi.org/10.1016/j.jplph.2014.04.010openalex-snapshot
Tungsten disrupts root growth in Arabidopsis thaliana by PIN targeting
inferred← citeshttps://doi.org/10.1016/j.jplph.2015.05.006openalex-snapshot
Plant development regulation: Overview and perspectives
inferred← citeshttps://doi.org/10.1016/j.jplph.2017.05.010openalex-snapshot
The dynamics and endocytosis of Flot1 protein in response to flg22 in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154610openalex-snapshot
Diverse functions of FOUR LIPS: Stomatal development and beyond
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154877openalex-snapshot
Concurrent exposure to water deficit and elevated ambient temperature alleviates root growth defects in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.lssr.2018.11.001openalex-snapshot
Polar auxin transport is essential to maintain growth and development of etiolated pea and maize seedlings grown under 1 g conditions: Relevance to the international space station experiment
inferred← citeshttps://doi.org/10.1016/j.lssr.2020.04.005openalex-snapshot
Microarray profile of gene expression in etiolated Pisum sativum seedlings grown under microgravity conditions in space: Relevance to the International Space Station experiment “Auxin Transport”
inferred← citeshttps://doi.org/10.1016/j.mod.2012.02.003openalex-snapshot
Posttranslational modification and trafficking of PIN auxin efflux carriers
inferred← citeshttps://doi.org/10.1016/j.molp.2016.08.010openalex-snapshot
Enquiry into the Topology of Plasma Membrane-Localized PIN Auxin Transport Components
inferred← citeshttps://doi.org/10.1016/j.molp.2021.06.023openalex-snapshot
A novel miR167a-OsARF6-OsAUX3 module regulates grain length and weight in rice
inferred← citeshttps://doi.org/10.1016/j.pbi.2006.07.010openalex-snapshot
A greenprint for growth: signalling the pattern of proliferation
inferred← citeshttps://doi.org/10.1016/j.pbi.2007.07.008openalex-snapshot
Mechanisms of auxin-dependent cell and tissue polarity
inferred← citeshttps://doi.org/10.1016/j.pbi.2007.10.007openalex-snapshot
Talk global, act local—patterning the Arabidopsis embryo
inferred← citeshttps://doi.org/10.1016/j.pbi.2008.06.004openalex-snapshot
Regulation of auxin transport polarity by AGC kinases
inferred← citeshttps://doi.org/10.1016/j.pbi.2009.07.008openalex-snapshot
Back to the future: evolution of computational models in plant morphogenesis
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