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PIN-FORMED and PIN-LIKES auxin transport facilitators
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4939-6469-7_21openalex-snapshot
Use of Xenopus laevis Oocytes to Study Auxin Transport
inferredcites →https://doi.org/10.1016/j.cell.2007.07.033openalex-snapshot
Antagonistic Regulation of PIN Phosphorylation by PP2A and PINOID Directs Auxin Flux
inferredcites →https://doi.org/10.1016/j.celrep.2018.02.074openalex-snapshot
Data-Driven Modeling of Intracellular Auxin Fluxes Indicates a Dominant Role of the ER in Controlling Nuclear Auxin Uptake
inferredcites →https://doi.org/10.1016/j.cub.2013.03.064openalex-snapshot
An Auxin Transport Mechanism Restricts Positive Orthogravitropism in Lateral Roots
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.2014.09.054openalex-snapshot
Plasma Membrane-Targeted PIN Proteins Drive Shoot Development in a Moss
inferredcites →https://doi.org/10.1016/j.cub.2014.09.056openalex-snapshot
Directional Auxin Transport Mechanisms in Early Diverging Land Plants
inferredcites →https://doi.org/10.1016/j.cub.2018.01.069openalex-snapshot
The Road to Auxin-Dependent Growth Repression and Promotion in Apical Hooks
inferredcites →https://doi.org/10.1016/j.molp.2016.08.010openalex-snapshot
Enquiry into the Topology of Plasma Membrane-Localized PIN Auxin Transport Components
inferredcites →https://doi.org/10.1016/j.pbi.2012.10.005openalex-snapshot
Divide Et Impera—cellular auxin compartmentalization
inferredcites →https://doi.org/10.1016/j.pbi.2017.06.012openalex-snapshot
Polar transport in plants mediated by membrane transporters: focus on mechanisms of polar auxin transport
inferredcites →https://doi.org/10.1016/j.pbi.2018.09.009openalex-snapshot
Something ancient and something neofunctionalized—evolution of land plant hormone signaling pathways
inferredcites →https://doi.org/10.1016/j.semcdb.2017.10.005openalex-snapshot
Specificity of plant membrane trafficking – ARFs, regulators and coat proteins
inferredcites →https://doi.org/10.1016/j.tplants.2012.08.009openalex-snapshot
Origin and evolution of PIN auxin transporters in the green lineage
inferredcites →https://doi.org/10.1016/j.tplants.2018.03.009openalex-snapshot
Activation and Polarity Control of PIN-FORMED Auxin Transporters by Phosphorylation
inferredcites →https://doi.org/10.1038/nature03633openalex-snapshot
Auxin inhibits endocytosis and promotes its own efflux from cells
inferredcites →https://doi.org/10.1038/nature08066openalex-snapshot
Subcellular homeostasis of phytohormone auxin is mediated by the ER-localized PIN5 transporter
inferredcites →https://doi.org/10.1038/nature11001openalex-snapshot
A novel putative auxin carrier family regulates intracellular auxin homeostasis in plants
inferredcites →https://doi.org/10.1038/ncb1686openalex-snapshot
Sterol-dependent endocytosis mediates post-cytokinetic acquisition of PIN2 auxin efflux carrier polarity
inferredcites →https://doi.org/10.1038/ncomms10430openalex-snapshot
Pin1At regulates PIN1 polar localization and root gravitropism
inferredcites →https://doi.org/10.1038/ncomms1941openalex-snapshot
ER-localized auxin transporter PIN8 regulates auxin homeostasis and male gametophyte development in Arabidopsis
inferredcites →https://doi.org/10.1038/ncomms4978openalex-snapshot
Klebsormidium flaccidum genome reveals primary factors for plant terrestrial adaptation
inferredcites →https://doi.org/10.1038/ng.2725openalex-snapshot
Control of root system architecture by DEEPER ROOTING 1 increases rice yield under drought conditions
inferredcites →https://doi.org/10.1038/nplants.2016.155openalex-snapshot
Negative gravitropism in plant roots
inferredcites →https://doi.org/10.1038/nplants.2017.105openalex-snapshot
Light triggers PILS-dependent reduction in nuclear auxin signalling for growth transition
inferredcites →https://doi.org/10.1038/s41477-018-0318-3openalex-snapshot
Mechanistic framework for cell-intrinsic re-establishment of PIN2 polarity after cell division
inferredcites →https://doi.org/10.1038/s41477-019-0363-6openalex-snapshot
A SOSEKI-based coordinate system interprets global polarity cues in Arabidopsis
inferredcites →https://doi.org/10.1038/s41586-018-0186-zopenalex-snapshot
A molecular rheostat adjusts auxin flux to promote root protophloem differentiation
inferredcites →https://doi.org/10.1038/s41598-018-28188-1openalex-snapshot
PID/WAG-mediated phosphorylation of the Arabidopsis PIN3 auxin transporter mediates polarity switches during gravitropism
inferredcites →https://doi.org/10.1038/srep24212openalex-snapshot
Hydrolases of the ILR1-like family of Arabidopsis thaliana modulate auxin response by regulating auxin homeostasis in the endoplasmic reticulum
inferredcites →https://doi.org/10.1073/pnas.1408960111openalex-snapshot
Auxin transport sites are visualized in planta using fluorescent auxin analogs
inferredcites →https://doi.org/10.1073/pnas.1614380114openalex-snapshot
Dynamic PIN-FORMED auxin efflux carrier phosphorylation at the plasma membrane controls auxin efflux-dependent growth
inferredcites →https://doi.org/10.1073/pnas.1814015116openalex-snapshot
PILS6 is a temperature-sensitive regulator of nuclear auxin input and organ growth in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/molbev/msu147openalex-snapshot
Paralogous Radiations of PIN Proteins with Multiple Origins of Noncanonical PIN Structure
inferredcites →https://doi.org/10.1093/pcp/pcx104openalex-snapshot
A Critical View on ABC Transporters and Their Interacting Partners in Auxin Transport
inferredcites →https://doi.org/10.1101/646489openalex-snapshot
PIN-LIKES coordinate brassinosteroid signalling with nuclear auxin input in Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.17.00942openalex-snapshot
LAZY Genes Mediate the Effects of Gravity on Auxin Gradients and Plant Architecture
inferredcites →https://doi.org/10.1105/tpc.109.071639openalex-snapshot
PIN Auxin Efflux Carrier Polarity Is Regulated by PINOID Kinase-Mediated Recruitment into GNOM-Independent Trafficking inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.118422openalex-snapshot
Functional Analysis of the Hydrophilic Loop in Intracellular Trafficking of Arabidopsis PIN-FORMED Proteins
inferredcites →https://doi.org/10.1105/tpc.16.00575openalex-snapshot
The Arabidopsis LAZY1 Family Plays a Key Role in Gravity Signaling within Statocytes and in Branch Angle Control of Roots and Shoots
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03856.xopenalex-snapshot
Functional expression and characterization of Arabidopsis ABCB, AUX 1 and PIN auxin transporters in Schizosaccharomyces pombe
inferredcites →https://doi.org/10.1111/jipb.12059openalex-snapshot
Plasma Membrane Protein Ubiquitylation and Degradation as Determinants of Positional Growth in Plants
inferredcites →https://doi.org/10.1111/nph.14019openalex-snapshot
PIN6 auxin transporter at endoplasmic reticulum and plasma membrane mediates auxin homeostasis and organogenesis in Arabidopsis
inferredcites →https://doi.org/10.1111/nph.14923openalex-snapshot
Characterization of auxin transporter PIN 6 plasma membrane targeting reveals a function for PIN 6 in plant bolting
inferredcites →https://doi.org/10.1111/tpj.13470openalex-snapshot
DRO 1 influences root system architecture in Arabidopsis and Prunus species
inferredcites →https://doi.org/10.1126/science.1100618openalex-snapshot
A PINOID-Dependent Binary Switch in Apical-Basal PIN Polar Targeting Directs Auxin Efflux
inferredcites →https://doi.org/10.1126/science.1123542openalex-snapshot
PIN Proteins Perform a Rate-Limiting Function in Cellular Auxin Efflux
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.052456openalex-snapshot
Plasma membrane-bound AGC3 kinases phosphorylate PIN auxin carriers at TPRXS(N/S) motifs to direct apical PIN recycling
inferredcites →https://doi.org/10.3389/fcell.2016.00046openalex-snapshot
Tethering Complexes in the Arabidopsis Endomembrane System
inferredcites →https://doi.org/10.3389/fpls.2012.00227openalex-snapshot
Evolution and structural diversification of PILS putative auxin carriers in plants
inferredcites →https://doi.org/10.3390/ijms19092759openalex-snapshot
The PIN-FORMED Auxin Efflux Carriers in Plants
inferredcites →https://doi.org/10.3390/ijms19113391openalex-snapshot
Advances in Understanding the Mechanism of Action of the Auxin Permease AUX1
inferredcites →https://doi.org/10.7554/elife.02860openalex-snapshot
Auxin efflux by PIN-FORMED proteins is activated by two different protein kinases, D6 PROTEIN KINASE and PINOID
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4480360openalex-extracted
Synergism of Vesicle Trafficking and Cytoskeleton During Regulation of Plant Growth and Development: A Mechanistic Outlook
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/s00344-023-11162-1openalex-snapshot
Comparative Transcriptome Analysis of Hypocotyls During the Developmental Transition of C3 Cotyledons to C4 Leaves in Halimocnemis mollissima Bunge
inferred← citeshttps://doi.org/10.1007/s00425-021-03719-9openalex-snapshot
Functional analysis of indole 3-hexanoic acid as a novel auxin from Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10265-023-01494-0openalex-snapshot
Plasmodesmata callose binding protein 2 contributes to the regulation of cambium/phloem formation and auxin response during the tissue reunion process in incised Arabidopsis stem
inferred← citeshttps://doi.org/10.1007/s10725-023-01052-7openalex-snapshot
Full-length transcriptome and metabolism revealed the difference of callus formation of tea cutting under white, red and blue light
inferred← citeshttps://doi.org/10.1007/s11295-024-01688-0openalex-snapshot
Genome-wide identification of rubber tree PILS auxin transporter gene families and functional characterization of HbPILS6
inferred← citeshttps://doi.org/10.1007/s11738-021-03271-9openalex-snapshot
Identification of the related genes on the asymmetric root growth of Oryza sativa induced by ethylene through transcriptome sequencing, GO and KEGG analysis
inferred← citeshttps://doi.org/10.1016/j.cj.2023.06.001openalex-snapshot
Salt stress responses in foxtail millet: Physiological and molecular regulation
inferred← citeshttps://doi.org/10.1016/j.cj.2026.07.014openalex-snapshot
The peanut PIN-LIKES protein AhPILS regulates growth habit via gravitropism-dependent auxin redistribution
inferred← citeshttps://doi.org/10.1016/j.cub.2020.02.002openalex-snapshot
PIN-LIKES Coordinate Brassinosteroid Signaling with Nuclear Auxin Input in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.cub.2021.03.070openalex-snapshot
Plant cell biology: PIN polarity maintained
inferred← citeshttps://doi.org/10.1016/j.cub.2023.02.024openalex-snapshot
K63-linked ubiquitin chains are a global signal for endocytosis and contribute to selective autophagy in plants
inferred← citeshttps://doi.org/10.1016/j.genrep.2026.102529openalex-snapshot
Genome-wide identification and expression characterization of the PIN gene family in melon (Cucumis melo L.)
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e21976openalex-snapshot
RETRACTED: Synergism of vesicle trafficking and cytoskeleton during regulation of plant growth and development: A mechanistic outlook
inferred← citeshttps://doi.org/10.1016/j.jenvman.2025.127848openalex-snapshot
Molecular mechanisms underlying microplastics-induced inhibition of lateral root development in tomato (Solanum lycopersicum L.)
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153539openalex-snapshot
Arabidopsis antiporter CHX23 and auxin transporter PIN8 coordinately regulate pollen growth
inferred← citeshttps://doi.org/10.1016/j.pbi.2023.102350openalex-snapshot
Flavonols modulate plant development, signaling, and stress responses
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111606openalex-snapshot
pin2 mutant agravitropic root phenotype is conditional and nutrient-sensitive
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112362openalex-snapshot
Integrated transcriptomics and metabolomics analyses provide insights into the mechanisms of capitulum architecture in Argyranthemum frutescens (Asteraceae)
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113694openalex-snapshot
Comprehensive identification of PIN and PILS in crape myrtle genomes reveals their putative functions in bud-to-branch development and callus generation
inferred← citeshttps://doi.org/10.1016/j.tplants.2021.09.008openalex-snapshot
Auxin’s origin: do PILS hold the key?
inferred← citeshttps://doi.org/10.1016/j.xplc.2020.100048openalex-snapshot
All Roads Lead to Auxin: Post-translational Regulation of Auxin Transport by Multiple Hormonal Pathways
inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100669openalex-snapshot
Divergence of trafficking and polarization mechanisms for PIN auxin transporters during land plant evolution
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c02742openalex-snapshot
Novel Plant Growth Regulator Guvermectin Promotes Root Development by Modulating Auxin Signaling
inferred← citeshttps://doi.org/10.1038/s41580-025-00851-2openalex-snapshot
Mechanisms of auxin action in plant growth and development
inferred← citeshttps://doi.org/10.1073/pnas.2212881119openalex-snapshot
Mitochondrial GPAT-derived LPA controls auxin-dependent embryonic and postembryonic development
inferred← citeshttps://doi.org/10.1073/pnas.2218865120openalex-snapshot
Endoplasmic reticulum stress controls PIN-LIKES abundance and thereby growth adaptation
inferred← citeshttps://doi.org/10.1073/pnas.2221313120openalex-snapshot
The nitrate transporter NRT2.1 directly antagonizes PIN7-mediated auxin transport for root growth adaptation
inferred← citeshttps://doi.org/10.1073/pnas.2313216121openalex-snapshot
ZmPILS6 is an auxin efflux carrier required for maize root morphogenesis
inferred← citeshttps://doi.org/10.1080/29932297.2025.2611631openalex-snapshot
How reversible protein phosphorylation regulates polar auxin transport in plant developmental plasticity
inferred← citeshttps://doi.org/10.1093/jxb/eraa169openalex-snapshot
The evolutionary origins of auxin transport: what we know and what we need to know
inferred← citeshttps://doi.org/10.1093/jxb/eraa329openalex-snapshot
The value of asymmetry: how polarity proteins determine plant growth and morphology
inferred← citeshttps://doi.org/10.1093/jxb/erab096openalex-snapshot
Distinct genetic basis for root responses to lipo-chitooligosaccharide signal molecules from different microbial origins
inferred← citeshttps://doi.org/10.1093/jxb/erab357openalex-snapshot
The wheat SHORT ROOT LENGTH 1 gene TaSRL1 controls root length in an auxin-dependent pathway
inferred← citeshttps://doi.org/10.1093/jxb/erac416openalex-snapshot
GhROP6 GTPase modulates auxin accumulation in cotton fibers by regulating cell-specific GhPIN3a localization
inferred← citeshttps://doi.org/10.1093/jxb/erad088openalex-snapshot
LONG HYPOCOTYL IN FAR-RED 1 mediates a trade-off between growth and defence under shade in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erad325openalex-snapshot
Auxin and abiotic stress responses
inferred← citeshttps://doi.org/10.1093/jxb/erad340openalex-snapshot
What a tangled web it weaves: auxin coordination of stem cell maintenance and flower production
inferred← citeshttps://doi.org/10.1093/jxb/erag027openalex-snapshot
Translating Arabidopsis - based insights into gravitropic set-point angle regulation in monocots
inferred← citeshttps://doi.org/10.1093/pcp/pcac163openalex-snapshot
Mapping of the Classical Mutation rosette Highlights a Role for Calcium in Wound-Induced Rooting
inferred← citeshttps://doi.org/10.1093/plcell/koab080openalex-snapshot
The microtubule-associated protein WDL4 modulates auxin distribution to promote apical hook opening in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plcell/koab237openalex-snapshot
Imaging the living plant cell: From probes to quantification
inferred← citeshttps://doi.org/10.1093/plcell/koaf056openalex-snapshot
The protein kinases KIPK and KIPK-LIKE1 suppress overbending during negative hypocotyl gravitropic growth in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiaa082openalex-snapshot
Function of membrane domains in rho-of-plant signaling
inferred← citeshttps://doi.org/10.1093/plphys/kiab242openalex-snapshot
DIOXYGENASE FOR AUXIN OXIDATION 1 catalyzes the oxidation of IAA amino acid conjugates
inferred← citeshttps://doi.org/10.1093/plphys/kiab312openalex-snapshot
Membrane nanodomains and transport functions in plant
inferred← citeshttps://doi.org/10.1093/plphys/kiac288openalex-snapshot
Initiation of aboveground organ primordia depends on combined action of auxin, ERECTA family genes, and PINOID
inferred← citeshttps://doi.org/10.1093/plphys/kiad006openalex-snapshot
Roles of very long-chain fatty acids in compound leaf patterning inMedicago truncatula
inferred← citeshttps://doi.org/10.1093/plphys/kiae130openalex-snapshot
CALMODULIN-LIKE16 and PIN-LIKES7a cooperatively regulate rice seedling primary root elongation under chilling
inferred← citeshttps://doi.org/10.1093/treephys/tpaf009openalex-snapshot
Auxin treatment reduces inflorescences number and delays bud development in the alternate bearing Citrus cultivar Murcott mandarin
inferred← citeshttps://doi.org/10.1094/mpmi-05-21-0118-ropenalex-snapshot
Bradyrhizobium japonicum IRAT FA3 Alters Arabidopsis thaliana Root Architecture via Regulation of Auxin Efflux Transporters PIN2, PIN3, PIN7, and ABCB19
inferred← citeshttps://doi.org/10.1101/2020.10.24.353276openalex-snapshot
A role of DAO1 in oxidation of IAA amino acid conjugates revealed through metabolite, high throughput transcript and protein level analysis
inferred← citeshttps://doi.org/10.1101/2022.05.13.491777openalex-snapshot
Comparative Transcriptome Analysis of Hypocotyls During the Developmental Transition of C 3 cotyledons to C 4 Leaves in Halimocnemis mollissima Bunge
inferred← citeshttps://doi.org/10.1101/2024.05.24.595653openalex-snapshot
KIPK and KIPK-LIKE1 suppress overbending during negative hypocotyl gravitropic growth
inferred← citeshttps://doi.org/10.1101/2024.06.24.599968openalex-snapshot
A Multitrait Genome-Wide Association Study Reveals a Requirement for the Strigolactone Receptor MtDWARF14 in Optimal GOLVEN Signaling
inferred← citeshttps://doi.org/10.1101/2024.10.16.618682openalex-snapshot
The role of IAA and its transport in the complex streptophyte algae Chara braunii
inferred← citeshttps://doi.org/10.1101/808964openalex-snapshot
Xyloglucan remodelling defines differential tissue expansion in plants
inferred← citeshttps://doi.org/10.1101/cshperspect.a039875openalex-snapshot
Auxin Transporters—A Biochemical View
inferred← citeshttps://doi.org/10.1111/ede.12376openalex-snapshot
A fundamental developmental transition in Physcomitrium patens is regulated by evolutionarily conserved mechanisms
inferred← citeshttps://doi.org/10.1111/jipb.70114openalex-snapshot
The auxin–CsHAT14 signaling cascade coordinates somatic embryogenesis in citrus
inferred← citeshttps://doi.org/10.1111/jipb.70277openalex-snapshot
Eukaryotic chaperonin coordinates root meristem activity by regulating SEC31B‐dependent COPII vesicle trafficking of PIN auxin efflux carrier in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.17152openalex-snapshot
Auxin efflux controls orderly nucellar degeneration and expansion of the female gametophyte in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.17867openalex-snapshot
Recent developments in the understanding of PIN polarity
inferred← citeshttps://doi.org/10.1111/nph.18035openalex-snapshot
Plant volatiles as regulators of hormone homeostasis
inferred← citeshttps://doi.org/10.1111/nph.18691openalex-snapshot
A Physcomitrella PIN protein acts in spermatogenesis and sporophyte retention
inferred← citeshttps://doi.org/10.1111/nph.19157openalex-snapshot
The YABBY gene SHATTERING1 controls activation rather than patterning of the abscission zone in Setaria viridis
inferred← citeshttps://doi.org/10.1111/nph.70019openalex-snapshot
The role of indole‐3‐acetic acid and characterization of PIN transporters in complex streptophyte alga Chara braunii
inferred← citeshttps://doi.org/10.1111/nph.71625openalex-snapshot
OsDRP1C mediates root development by modulating OsPIN1 cycling in rice
inferred← citeshttps://doi.org/10.1111/pbi.14503openalex-snapshot
Creeping Stem 1 regulates directional auxin transport for lodging resistance in soybean
inferred← citeshttps://doi.org/10.1111/plb.13303openalex-snapshot
Auxin and its role in plant development: structure, signalling, regulation and response mechanisms
inferred← citeshttps://doi.org/10.1111/ppl.70684openalex-snapshot
Overexpression of AtSUT4 Induces Root Growth Inhibition by Rhizosphere Alkalization and Variation of Auxin Distribution in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/ppl.70957openalex-snapshot
Auxin Transport Gene, ClPILS6 , Promotes Branching in Transgenic Poplar by Altering Auxin Homeostasis
inferred← citeshttps://doi.org/10.1111/tpj.15884openalex-snapshot
OsSPL14 acts upstream of OsPIN1b and PILS6b to modulate axillary bud outgrowth by fine‐tuning auxin transport in rice
inferred← citeshttps://doi.org/10.1111/tpj.17265openalex-snapshot
Molecular chaperon HSP70 ‐9 is required for clathrin‐mediated endocytosis in Arabidopsis
inferred← citeshttps://doi.org/10.1134/s1062359025609759openalex-snapshot
Microbial Phytohormones: Biosynthesis, Function and Regulation
inferred← citeshttps://doi.org/10.1146/annurev-arplant-070722-015329openalex-snapshot
Plant Hormone Transport and Localization: Signaling Molecules on the Move
inferred← citeshttps://doi.org/10.1186/s12870-022-03799-zopenalex-snapshot
TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.1186/s12870-022-03861-wopenalex-snapshot
Functional analysis revealed the involvement of ZmABCB15 in resistance to rice black-streaked dwarf virus infection
inferred← citeshttps://doi.org/10.14397/jals.2025.59.2.13openalex-snapshot
Genome-wide Association Study for Cold Tolerance at Seedling Stage Using a Core Collection of Korean Rice
inferred← citeshttps://doi.org/10.15406/jabb.2023.10.00345openalex-snapshot
Plasmodesmata role on plant development regulation
inferred← citeshttps://doi.org/10.18388/pb.2021_549openalex-snapshot
Biosynteza i metaboliczna inaktywacja auksyn
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1482741/v1openalex-snapshot
Integrative genomic and transcriptomic analyses reveal potential gene regulatory network associated with berry size and early- ripening caused by bud sport in grapes
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1741352/v1openalex-snapshot
TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.29059/cienciauat.v18i2.1833openalex-snapshot
Participación del transporte simplástico de las auxinas durante el desarrollo de las plantas
inferred← citeshttps://doi.org/10.3389/fpls.2020.01027openalex-snapshot
Early Endosomal Trafficking Component BEN2/VPS45 Plays a Crucial Role in Internal Tissues in Regulating Root Growth and Meristem Size in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2020.617162openalex-snapshot
Updates on BES1/BZR1 Regulatory Networks Coordinating Plant Growth and Stress Responses
inferred← citeshttps://doi.org/10.3389/fpls.2020.627969openalex-snapshot
Plant Hormone-Mediated Regulation of Heat Tolerance in Response to Global Climate Change
inferred← citeshttps://doi.org/10.3389/fpls.2021.756968openalex-snapshot
A Retro-Perspective on Auxin Transport
inferred← citeshttps://doi.org/10.3389/fpls.2021.802399openalex-snapshot
Magnesium Limitation Leads to Transcriptional Down-Tuning of Auxin Synthesis, Transport, and Signaling in the Tomato Root
inferred← citeshttps://doi.org/10.3389/fpls.2022.849532openalex-snapshot
MAG2 and MAL Regulate Vesicle Trafficking and Auxin Homeostasis With Functional Redundancy
inferred← citeshttps://doi.org/10.3389/fpls.2022.938476openalex-snapshot
eIF4E1 Regulates Arabidopsis Embryo Development and Root Growth by Interacting With RopGEF7
inferred← citeshttps://doi.org/10.3389/fpls.2022.999990openalex-snapshot
Expression analysis of PIN family genes in Chinese hickory reveals their potential roles during grafting and salt stress
inferred← citeshttps://doi.org/10.3389/fpls.2024.1464053openalex-snapshot
Gallic acid regulates primary root elongation via modulating auxin transport and signal transduction
inferred← citeshttps://doi.org/10.3389/fpls.2025.1635660openalex-snapshot
Distinct gene reprogramming in rosetted and symptomless shoots from the same mature rose plants infected with rose rosette virus
inferred← citeshttps://doi.org/10.3390/agronomy16020226openalex-snapshot
The PIN-LIKES Auxin Transport Genes Involved in Regulating Yield in Soybean
inferred← citeshttps://doi.org/10.3390/antiox11102035openalex-snapshot
Mitochondrial HSC70-1 Regulates Polar Auxin Transport through ROS Homeostasis in Arabidopsis Roots
inferred← citeshttps://doi.org/10.3390/cimb48060580openalex-snapshot
Genome-Wide Identification of the PIN-LIKES (PILS) Gene Family in Alfalfa (Medicago sativa L.) and Its Expression Analysis Under Abiotic Stresses
inferred← citeshttps://doi.org/10.3390/f13040568openalex-snapshot
PIN3 from Liriodendron May Function in Inflorescence Development and Root Elongation
inferred← citeshttps://doi.org/10.3390/genes13050817openalex-snapshot
Novel Role of AaMYBC1 in Regulating Actinidia arguta Vine Architecture by Elongating Internode Based on Multi-Omics Analysis of Transgenic Tobacco
inferred← citeshttps://doi.org/10.3390/horticulturae11020170openalex-snapshot
Transcription Factor RhCUC3 Regulates Petal Numbers in Rose Flowers
inferred← citeshttps://doi.org/10.3390/ijms21186784openalex-snapshot
Improvement of a Genetic Transformation System and Preliminary Study on the Function of LpABCB21 and LpPILS7 Based on Somatic Embryogenesis in Lilium pumilum DC. Fisch
inferred← citeshttps://doi.org/10.3390/ijms22083874openalex-snapshot
Cytokinin-Controlled Gradient Distribution of Auxin in Arabidopsis Root Tip
inferred← citeshttps://doi.org/10.3390/ijms22147396openalex-snapshot
Genome-Wide Identification and Characterization of PIN-FORMED (PIN) Gene Family Reveals Role in Developmental and Various Stress Conditions in Triticum aestivum L.
inferred← citeshttps://doi.org/10.3390/ijms22179222openalex-snapshot
Xyloglucan Remodeling Defines Auxin-Dependent Differential Tissue Expansion in Plants
inferred← citeshttps://doi.org/10.3390/ijms222111357openalex-snapshot
Auxin and Target of Rapamycin Spatiotemporally Regulate Root Organogenesis
inferred← citeshttps://doi.org/10.3390/ijms222111843openalex-snapshot
Dynamic Hormone Gradients Regulate Wound-Induced de novo Organ Formation in Tomato Hypocotyl Explants
inferred← citeshttps://doi.org/10.3390/ijms23158094openalex-snapshot
Evolution of the Membrane Transport Protein Domain
inferred← citeshttps://doi.org/10.3390/plants10010150openalex-snapshot
The TOR–Auxin Connection Upstream of Root Hair Growth
inferred← citeshttps://doi.org/10.3390/plants12010033openalex-snapshot
Genome-Wide Identification of PIN and PILS Gene Families in Areca catechu and the Potential Role of AcPIN6 in Lateral Brace Root Formation
inferred← citeshttps://doi.org/10.3390/plants12030634openalex-snapshot
Terpenoid Transport in Plants: How Far from the Final Picture?
inferred← citeshttps://doi.org/10.3390/plants12040750openalex-snapshot
The ROP2 GTPase Participates in Nitric Oxide (NO)-Induced Root Shortening in Arabidopsis
inferred← citeshttps://doi.org/10.3390/plants12122280openalex-snapshot
Characterization of the PIN Auxin Efflux Carrier Gene Family and Its Expression during Zygotic Embryogenesis in Persea americana
inferred← citeshttps://doi.org/10.3390/plants12152809openalex-snapshot
Overexpression of OsPIN9 Impairs Chilling Tolerance via Disturbing ROS Homeostasis in Rice
inferred← citeshttps://doi.org/10.3390/plants12234058openalex-snapshot
Deficiency of Auxin Efflux Carrier OsPIN1b Impairs Chilling and Drought Tolerance in Rice
inferred← citeshttps://doi.org/10.3390/plants13040556openalex-snapshot
Prefoldin Subunits and Its Associate Partners: Conservations and Specificities in Plants
inferred← citeshttps://doi.org/10.3390/plants9020166openalex-snapshot
Role of the Cytokinin-Activated Type-B Response Regulators in Hormone Crosstalk
inferred← citeshttps://doi.org/10.35550/vbio2020.03.098openalex-snapshot
Modern concepts of auxin’s action. 1. History of discovery, metabolism, transport
inferred← citeshttps://doi.org/10.47749/t/unicamp.2022.1238793openalex-snapshot
Desenvolvimento floral em maracujazeiro
inferred← citeshttps://doi.org/10.48130/ph-0025-0020openalex-snapshot
ABCG transporters in phytohormone dynamics: mechanisms, challenges, and future perspectives
inferred← citeshttps://doi.org/10.64898/2025.12.20.695708openalex-snapshot
Exogenous auxins for proline regulation in heat-stressed plants
inferred← citeshttps://doi.org/10.70675/612d49d7z78ffz428cz9591zf48383026c48openalex-snapshot
Rôles des modifications post-traductionnelles dans l'internalisation du récepteur des brassinostéroides BRI1
inferred← citeshttps://doi.org/10.7554/elife.55832openalex-snapshot
Temporal integration of auxin information for the regulation of patterning
inferred← citeshttps://doi.org/10.7554/elife.72132openalex-snapshot
A coupled mechano-biochemical model for cell polarity guided anisotropic root growth
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