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Auxin transport routes in plant development
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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/bf00260496openalex-snapshot
Mutants of Arabidopsis thaliana with abnormal gravitropic responses
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/10.1007/s00018-007-6566-4openalex-snapshot
Polar transport of the plant hormone auxin – the role of PIN-FORMED (PIN) proteins
inferredcites →https://doi.org/10.1007/s00425-003-1072-xopenalex-snapshot
Gravity-induced modification of auxin transport and distribution for peg formation in cucumber seedlings: possible roles for CS-AUX1 and CS-PIN1
inferredcites →https://doi.org/10.1007/s00425-005-1519-3openalex-snapshot
Studies on the function of TM20, a transmembrane protein present in cereal embryos
inferredcites →https://doi.org/10.1007/s00425-007-0601-4openalex-snapshot
The expression of genes coding for auxin carriers in different tissues and along the organ can explain variations in auxin transport and the growth pattern in etiolated lupin hypocotyls
inferredcites →https://doi.org/10.1007/s004250000300openalex-snapshot
Regulation of auxin transport by aminopeptidases and endogenous flavonoids
inferredcites →https://doi.org/10.1007/s00438-004-1057-xopenalex-snapshot
The PIN and LAX families of auxin transport genes in Medicago truncatula
inferredcites →https://doi.org/10.1016/j.ab.2005.03.054openalex-snapshot
Noninvasive and continuous recordings of auxin fluxes in intact root apex with a carbon nanotube-modified and self-referencing microelectrode
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.chembiol.2007.10.014openalex-snapshot
Arabidopsis P-Glycoprotein19 Participates in the Inhibition of Gravitropism by Gravacin
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.cub.2006.04.029openalex-snapshot
High-Affinity Auxin Transport by the AUX1 Influx Carrier Protein
inferredcites →https://doi.org/10.1016/j.cub.2007.01.052openalex-snapshot
Clathrin-Mediated Constitutive Endocytosis of PIN Auxin Efflux Carriers in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2008.03.021openalex-snapshot
ARF GEF-Dependent Transcytosis and Polar Delivery of PIN Auxin Carriers in Arabidopsis
inferredcites →https://doi.org/10.1016/j.devcel.2005.05.014openalex-snapshot
Plant Development Is Regulated by a Family of Auxin Receptor F Box Proteins
inferredcites →https://doi.org/10.1016/j.febslet.2005.08.061openalex-snapshot
MDR‐like ABC transporter AtPGP4 is involved in auxin‐mediated lateral root and root hair development
inferredcites →https://doi.org/10.1016/j.tplants.2007.03.006openalex-snapshot
Molecular and cellular aspects of auxin-transport-mediated development
inferredcites →https://doi.org/10.1016/j.tplants.2008.02.001openalex-snapshot
Plant ABC proteins – a unified nomenclature and updated inventory
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)80682-0openalex-snapshot
Regulation of Auxin Response by the Protein Kinase PINOID
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)00003-5openalex-snapshot
The Arabidopsis GNOM ARF-GEF Mediates Endosomal Recycling, Auxin Transport, and Auxin-Dependent Plant Growth
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/s0176-1617(00)80053-xopenalex-snapshot
Tissue-specific expression of AUX1 in maize roots
inferredcites →https://doi.org/10.1017/cbo9780511574535openalex-snapshot
Pattern Formation in Plant Tissues
inferredcites →https://doi.org/10.1017/cbo9780511693670openalex-snapshot
The 'Power of movement in plants.'--1880.
inferredcites →https://doi.org/10.1038/35096571openalex-snapshot
Auxin transport inhibitors block PIN1 cycling and vesicle trafficking
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/nature01716openalex-snapshot
Enhanced gravi- and phototropism in plant mdr mutants mislocalizing the auxin efflux protein PIN1
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/nature03633openalex-snapshot
Auxin inhibits endocytosis and promotes its own efflux from cells
inferredcites →https://doi.org/10.1038/nature05046openalex-snapshot
AtSNX1 defines an endosome for auxin-carrier trafficking in Arabidopsis
inferredcites →https://doi.org/10.1038/nature07409openalex-snapshot
Generation of cell polarity in plants links endocytosis, auxin distribution and cell fate decisions
inferredcites →https://doi.org/10.1038/nature07875openalex-snapshot
A regulated auxin minimum is required for seed dispersal in Arabidopsis
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/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/ncb1369openalex-snapshot
Intracellular trafficking and proteolysis of the Arabidopsis auxin-efflux facilitator PIN2 are involved in root gravitropism
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/ncb1754openalex-snapshot
The auxin influx carrier LAX3 promotes lateral root emergence
inferredcites →https://doi.org/10.1038/ncb1815openalex-snapshot
Auxin transport through non-hair cells sustains root-hair development
inferredcites →https://doi.org/10.1038/nprot.2009.1openalex-snapshot
Measurement of auxin transport in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/sj.cr.7290130openalex-snapshot
Isolation and functional analysis of a Brassica juncea gene encoding a component of auxin efflux carrier
inferredcites →https://doi.org/10.1038/sj.cr.7290131openalex-snapshot
A Pin gene families encoding components of auxin efflux carriers in Brassica juncea
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00607.xopenalex-snapshot
The RCN1‐encoded A subunit of protein phosphatase 2A increases phosphatase activity in vivo
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00970.xopenalex-snapshot
Novel auxin transport inhibitors phenocopy the auxin influx carrier mutation aux1
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01173.xopenalex-snapshot
Sites and homeostatic control of auxin biosynthesis in Arabidopsis during vegetative growth
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01705.xopenalex-snapshot
Automated whole mount localisation techniques for plant seedlings
inferredcites →https://doi.org/10.1073/pnas.0510283103openalex-snapshot
Phosphorylation and activation of PINOID by the phospholipid signaling kinase 3-phosphoinositide-dependent protein kinase 1 (PDK1) in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0711414105openalex-snapshot
Auxin transport inhibitors impair vesicle motility and actin cytoskeleton dynamics in diverse eukaryotes
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.0808073105openalex-snapshot
Differential degradation of PIN2 auxin efflux carrier by retromer-dependent vacuolar targeting
inferredcites →https://doi.org/10.1073/pnas.0811539106openalex-snapshot
Cytokinins modulate auxin-induced organogenesis in plants via regulation of the auxin efflux
inferredcites →https://doi.org/10.1073/pnas.0900060106openalex-snapshot
Cytokinin regulates root meristem activity via modulation of the polar auxin transport
inferredcites →https://doi.org/10.1073/pnas.1633693100openalex-snapshot
Polar auxin transport in the wood-forming tissues of hybrid aspen is under simultaneous control of developmental and environmental signals
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/10.1074/jbc.274.39.27734openalex-snapshot
TM20, a Gene Coding for a New Class of Transmembrane Proteins Expressed in the Meristematic Tissues of Maize
inferredcites →https://doi.org/10.1074/jbc.m709655200openalex-snapshot
Modulation of P-glycoproteins by Auxin Transport Inhibitors Is Mediated by Interaction with Immunophilins
inferredcites →https://doi.org/10.1074/jbc.m710122200openalex-snapshot
Flavonoids Redirect PIN-mediated Polar Auxin Fluxes during Root Gravitropic Responses
inferredcites →https://doi.org/10.1091/mbc.e02-10-0698openalex-snapshot
TWISTED DWARF1, a Unique Plasma Membrane-anchored Immunophilin-like Protein, Interacts with Arabidopsis Multidrug Resistance-like Transporters AtPGP1 and AtPGP19
inferredcites →https://doi.org/10.1093/emboj/17.23.6903openalex-snapshot
AtPIN2 defines a locus of Arabidopsis for root gravitropism control
inferredcites →https://doi.org/10.1093/emboj/17.5.1405openalex-snapshot
The Arabidopsis gene MONOPTEROS encodes a transcription factor mediating embryo axis formation and vascular development
inferredcites →https://doi.org/10.1093/genetics/139.3.1393openalex-snapshot
Genetic analysis of ethylene signal transduction in Arabidopsis thaliana: five novel mutant loci integrated into a stress response pathway.
inferredcites →https://doi.org/10.1093/mp/ssm013openalex-snapshot
Disruptions in AUX1-Dependent Auxin Influx Alter Hypocotyl Phototropism in Arabidopsis
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029310openalex-snapshot
AGR,an Agravitropic Locus of Arabidopsis thaliana, Encodes a Novel Membrane-Protein Family Member
inferredcites →https://doi.org/10.1093/pcp/pci183openalex-snapshot
A PIN1 Family Gene, OsPIN1, involved in Auxin-dependent Adventitious Root Emergence and Tillering in Rice
inferredcites →https://doi.org/10.1093/pcp/pcn092openalex-snapshot
The ABC Subfamily B Auxin Transporter AtABCB19 is Involved in the Inhibitory Effects of N-1-Naphthyphthalamic Acid on the Phototropic and Gravitropic Responses of Arabidopsis Hypocotyls
inferredcites →https://doi.org/10.1094/mpmi.2001.14.3.267openalex-snapshot
Expression Studies on AUX1-like Genes in Medicago truncatula Suggest That Auxin Is Required at Two Steps in Early Nodule Development
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/10.1101/gad.1402406openalex-snapshot
Control of leaf vascular patterning by polar auxin transport
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.229402openalex-snapshot
The Arabidopsis BODENLOS gene encodes an auxin response protein inhibiting MONOPTEROS-mediated embryo patterning
inferredcites →https://doi.org/10.1101/gad.390806openalex-snapshot
Canalization of auxin flow by Aux/IAA-ARF-dependent feedback regulation of PIN polarity
inferredcites →https://doi.org/10.1101/gad.462608openalex-snapshot
Auxin influx carriers stabilize phyllotactic patterning
inferredcites →https://doi.org/10.1104/pp.010519openalex-snapshot
Identification, Purification, and Molecular Cloning of N-1-Naphthylphthalmic Acid-Binding Plasma Membrane-Associated Aminopeptidases from Arabidopsis
inferredcites →https://doi.org/10.1104/pp.105.061572openalex-snapshot
Two Homologous ATP-Binding Cassette Transporter Proteins, AtMDR1 and AtPGP1, Regulate Arabidopsis Photomorphogenesis and Root Development by Mediating Polar Auxin Transport
inferredcites →https://doi.org/10.1104/pp.106.080119openalex-snapshot
ZmPIN1aandZmPIN1bEncode Two Novel Putative Candidates for Polar Auxin Transport and Plant Architecture Determination of Maize
inferredcites →https://doi.org/10.1104/pp.107.101337openalex-snapshot
Auxin Influx Activity Is Associated with Frankia Infection during Actinorhizal Nodule Formation in Casuarina glauca
inferredcites →https://doi.org/10.1104/pp.107.109371openalex-snapshot
Functional Characterization of PaLAX1, a Putative Auxin Permease, in Heterologous Plant Systems
inferredcites →https://doi.org/10.1104/pp.125.4.1813openalex-snapshot
ANT1, an Aromatic and Neutral Amino Acid Transporter in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.008433openalex-snapshot
Cell Polarity and PIN Protein Positioning in Arabidopsis Require STEROL METHYLTRANSFERASE1 Function
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/10.1105/tpc.010354openalex-snapshot
AUX1 Promotes Lateral Root Formation by Facilitating Indole-3-Acetic Acid Distribution between Sink and Source Tissues in the Arabidopsis Seedling
inferredcites →https://doi.org/10.1105/tpc.104.029272openalex-snapshot
Sites and Regulation of Auxin Biosynthesis in Arabidopsis Roots
inferredcites →https://doi.org/10.1105/tpc.105.034637openalex-snapshot
Maintenance of Embryonic Auxin Distribution for Apical-Basal Patterning by PIN-FORMED–Dependent Auxin Transport in Arabidopsis
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.106.040782openalex-snapshot
Interactions among PIN-FORMED and P-Glycoprotein Auxin Transporters in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.042770openalex-snapshot
Subcellular Trafficking of the Arabidopsis Auxin Influx Carrier AUX1 Uses a Novel Pathway Distinct from PIN1
inferredcites →https://doi.org/10.1105/tpc.106.048777openalex-snapshot
Mutations inArabidopsis Multidrug Resistance-LikeABC Transporters Separate the Roles of Acropetal and Basipetal Auxin Transport in Lateral Root Development
inferredcites →https://doi.org/10.1105/tpc.107.051599openalex-snapshot
Separating the Roles of Acropetal and Basipetal Auxin Transport on Gravitropism with Mutations in Two Arabidopsis Multidrug Resistance-Like ABC Transporter Genes
inferredcites →https://doi.org/10.1105/tpc.107.052126openalex-snapshot
Ethylene Regulates Root Growth through Effects on Auxin Biosynthesis and Transport-Dependent Auxin Distribution
inferredcites →https://doi.org/10.1105/tpc.107.054288openalex-snapshot
P-Glycoprotein4 Displays Auxin Efflux Transporter–Like Action in Arabidopsis Root Hair Cells and Tobacco Cells
inferredcites →https://doi.org/10.1105/tpc.12.4.507openalex-snapshot
Auxin Regulates the Initiation and Radial Position of Plant Lateral Organs
inferredcites →https://doi.org/10.1105/tpc.3.7.677openalex-snapshot
Requirement of the Auxin Polar Transport System in Early Stages of Arabidopsis Floral Bud Formation.
inferredcites →https://doi.org/10.1105/tpc.9.11.1963openalex-snapshot
Aux/IAA proteins repress expression of reporter genes containing natural and highly active synthetic auxin response elements.
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/10.1111/j.1365-313x.2007.03158.xopenalex-snapshot
MODULATOR OF PIN genes control steady‐state levels of Arabidopsis PIN proteins
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03358.xopenalex-snapshot
Phytochromes and cryptochromes regulate the differential growth of Arabidopsis hypocotyls in both a PGP19‐dependent and a PGP19‐independent manner
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03668.xopenalex-snapshot
ABCB19/PGP19 stabilises PIN1 in membrane microdomains in Arabidopsis
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/j.1399-3054.2005.00466.xopenalex-snapshot
Auxin regulation of cell cycle and its role during lateral root initiation
inferredcites →https://doi.org/10.1111/j.1469-8137.1975.tb02602.xopenalex-snapshot
TRANSPORT OF INDOLEACETIC ACID IN PLANT CELLS IN RELATION TO pH AND ELECTRICAL POTENTIAL GRADIENTS, AND ITS SIGNIFICANCE FOR POLAR IAA TRANSPORT
inferredcites →https://doi.org/10.1126/science.1086072openalex-snapshot
Loss of an MDR Transporter in Compact Stalks of Maize br2 and Sorghum dw3 Mutants
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.1115711openalex-snapshot
Arabidopsis H + -PPase AVP1 Regulates Auxin-Mediated Organ Development
inferredcites →https://doi.org/10.1126/science.1121356openalex-snapshot
Polar PIN Localization Directs Auxin Flow in Plants
inferredcites →https://doi.org/10.1126/science.1122847openalex-snapshot
AXR4 Is Required for Localization of the Auxin Influx Facilitator AUX1
inferredcites →https://doi.org/10.1126/science.1123542openalex-snapshot
PIN Proteins Perform a Rate-Limiting Function in Cellular Auxin Efflux
inferredcites →https://doi.org/10.1126/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.250.4978.274openalex-snapshot
Reversible Root Tip Rotation in Arabidopsis Seedlings Induced by Obstacle-Touching Stimulus
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.282.5397.2226openalex-snapshot
Regulation of Polar Auxin Transport by AtPIN1 in Arabidopsis Vascular Tissue
inferredcites →https://doi.org/10.1146/annurev.pp.25.060174.000245openalex-snapshot
Reflections and Speculations
inferredcites →https://doi.org/10.1146/annurev.pp.28.060177.002255openalex-snapshot
The Polar Transport of Auxin
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.021071openalex-snapshot
Interaction of PIN and PGP transport mechanisms in auxin distribution-dependent development
inferredcites →https://doi.org/10.1242/dev.028365openalex-snapshot
The polarly localized D6 PROTEIN KINASE is required for efficient auxin transport in Arabidopsis thaliana
inferredcites →https://doi.org/10.1242/dev.128.20.4057openalex-snapshot
The PINOID protein kinase regulates organ development inArabidopsisby enhancing polar auxin transport
inferredcites →https://doi.org/10.1371/journal.pone.0001510openalex-snapshot
Light Plays an Essential Role in Intracellular Distribution of Auxin Efflux Carrier PIN2 in Arabidopsis thaliana
inferredcites →https://doi.org/10.2307/3871586openalex-snapshot
Multidrug Resistance-Like Genes of Arabidopsis Required for Auxin Transport and Auxin-Mediated Development
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.3981902openalex-extracted
Uncovering the Genetic Architecture of Replicated Adaptation
inferred← citeshttps://doi.org/10.1002/9780470015902.a0002069.pub2openalex-snapshot
Positional Information in Plant Development
inferred← citeshttps://doi.org/10.1002/9780470015902.a0020116.pub2openalex-snapshot
Polar Auxin Transport
inferred← citeshttps://doi.org/10.1002/9781118297674.ch33openalex-snapshot
Strigolactone Biosynthesis and Biology
inferred← citeshttps://doi.org/10.1002/9781118447093.ch3openalex-snapshot
Genomics of Auxin Action in Roots
inferred← citeshttps://doi.org/10.1002/9781118742921.ch4.1openalex-snapshot
Use of Chemical Biology to Understand Auxin Metabolism, Signaling, and Polar Transport
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0650openalex-snapshot
Lateral Root Formation: Building a Meristemde novo
inferred← citeshttps://doi.org/10.1002/9781119409144.ch92openalex-snapshot
Phytohormone regulation of Medicago truncatula –rhizobia interactions. A review
inferred← citeshttps://doi.org/10.1002/9781394302826.ch4openalex-snapshot
Diverse Roles of Strigolactones in Plant Growth and Development
inferred← citeshttps://doi.org/10.1002/ange.201308972openalex-snapshot
Real‐Time Monitoring of Auxin Vesicular Exocytotic Efflux from Single Plant Protoplasts by Amperometry at Microelectrodes Decorated with Nanowires
inferred← citeshttps://doi.org/10.1002/anie.201308972openalex-snapshot
Real‐Time Monitoring of Auxin Vesicular Exocytotic Efflux from Single Plant Protoplasts by Amperometry at Microelectrodes Decorated with Nanowires
inferred← citeshttps://doi.org/10.1002/bies.201500115openalex-snapshot
Abscisic acid and other plant hormones: Methods to visualize distribution and signaling
inferred← citeshttps://doi.org/10.1002/dvdy.139openalex-snapshot
Regulation of auxin transcriptional responses
inferred← citeshttps://doi.org/10.1002/dvdy.23878openalex-snapshot
Hormone symphony during root growth and development
inferred← citeshttps://doi.org/10.1002/pld3.215openalex-snapshot
A gravitropic stimulus alters the distribution of EHB1, a negative effector of root gravitropism in Arabidopsis
inferred← citeshttps://doi.org/10.1002/pld3.465openalex-snapshot
Opposing effects of trans‐ and cis‐cinnamic acid during rice coleoptile elongation
inferred← citeshttps://doi.org/10.1002/ps.4823openalex-snapshot
Weed resistance to synthetic auxin herbicides
inferred← citeshttps://doi.org/10.1002/rcm.8625openalex-snapshot
Practical optimization of liquid chromatography/mass spectrometry conditions and pretreatment methods toward the sensitive quantification of auxin in plants
inferred← citeshttps://doi.org/10.1002/slct.202101084openalex-snapshot
Conversion of l ‐Tryptophan Derivatives into Biologically Active Amino Acid Ionic Liquids
inferred← citeshttps://doi.org/10.1002/wdev.14openalex-snapshot
Molecular mechanisms of root gravity sensing and signal transduction
inferred← citeshttps://doi.org/10.1002/wdev.49openalex-snapshot
Patterning the primary root in Arabidopsis
inferred← citeshttps://doi.org/10.1007/124_2018_24openalex-snapshot
Stress-Induced Microspore Embryogenesis in Crop Plants: Cell Totipotency Acquisition and Embryo Development
inferred← citeshttps://doi.org/10.1007/978-1-0716-0183-9_9openalex-snapshot
Methods to Visualize Auxin and Cytokinin Signaling Activity in the Shoot Apical Meristem
inferred← citeshttps://doi.org/10.1007/978-1-0716-3299-4_1openalex-snapshot
Flower Development in Arabidopsis
inferred← citeshttps://doi.org/10.1007/978-1-4939-9015-3_13openalex-snapshot
Immunolocalization of IAA Using an Anti-IAA-C-Antibody Raised Against Carboxyl-Linked IAA
inferred← citeshttps://doi.org/10.1007/978-1-62703-592-7_22openalex-snapshot
Determination of Auxin Transport Parameters on the Cellular Level
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/10.1007/978-3-319-06511-3_17openalex-snapshot
IBA Transport by PDR Proteins
inferred← citeshttps://doi.org/10.1007/978-3-319-06511-3_3openalex-snapshot
ABA Transport by ABCG Transporter Proteins
inferred← citeshttps://doi.org/10.1007/978-3-319-19968-9_13openalex-snapshot
Aluminum-Induced Inhibition of Root Growth: Roles of Cell Wall Assembly, Structure, and Function
inferred← citeshttps://doi.org/10.1007/978-3-319-29573-2_17openalex-snapshot
Role of Phytohormones in Stress Tolerance of Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-33705-0_10openalex-snapshot
The Role of the Auxins During Somatic Embryogenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-33705-0_6openalex-snapshot
Epigenetic Advances in Somatic Embryogenesis in Sequenced Genome Crops
inferred← citeshttps://doi.org/10.1007/978-3-319-39126-7_9openalex-snapshot
Apocarotenoids: A New Carotenoid-Derived Pathway
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/10.1007/978-3-319-55520-1_2openalex-snapshot
The Role of MiRNAs in Auxin Signaling and Regulation During Plant Development
inferred← citeshttps://doi.org/10.1007/978-3-319-75103-0_2openalex-snapshot
Azolla: A Model System for Symbiotic Nitrogen Fixation and Evolutionary Developmental Biology
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_6openalex-snapshot
Functional Classification of Plant Plasma Membrane Transporters
inferred← citeshttps://doi.org/10.1007/978-3-642-14369-4_9openalex-snapshot
Auxin Transporters Controlling Plant Development
inferred← citeshttps://doi.org/10.1007/978-3-642-23524-5_4openalex-snapshot
Gravity Sensing, Interpretation, and Response
inferred← citeshttps://doi.org/10.1007/978-3-642-32463-5_8openalex-snapshot
Endocytic Trafficking of PIN Proteins and Auxin Transport
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/10.1007/978-3-642-41787-0_3openalex-snapshot
Auxin Biology: Applications and the Mechanisms Behind
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8openalex-snapshot
Auxin and Its Role in Plant Development
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8_13openalex-snapshot
Evolutionary Aspects of Auxin Signalling
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8_4openalex-snapshot
Intracellular Auxin Transport
inferred← citeshttps://doi.org/10.1007/978-94-017-9285-1_6openalex-snapshot
Auxin Signaling System in Plant Innate Immunity
inferred← citeshttps://doi.org/10.1007/978-94-017-9424-4_3openalex-snapshot
ABA Transmembrane Transport and Transporters
inferred← citeshttps://doi.org/10.1007/978-981-15-4890-1_5openalex-snapshot
Interactive Biology of Auxins and Phenolics in Plant Environment
inferred← citeshttps://doi.org/10.1007/978-981-16-4955-4_12openalex-snapshot
Rice Physiology Under Changing Climate
inferred← citeshttps://doi.org/10.1007/978-981-19-9794-5_11openalex-snapshot
Insight into the Interaction of Strigolactones, Abscisic Acid, and Reactive Oxygen Species Signals
inferred← citeshttps://doi.org/10.1007/978-981-92-1631-4_3openalex-snapshot
Hormone-Responsive Gene Modules in Regeneration
inferred← citeshttps://doi.org/10.1007/s00018-016-2290-2openalex-snapshot
Asymmetric cell division in plants: mechanisms of symmetry breaking and cell fate determination
inferred← citeshttps://doi.org/10.1007/s00122-018-3074-xopenalex-snapshot
Combined fine mapping, genetic diversity, and transcriptome profiling reveals that the auxin transporter gene ns plays an important role in cucumber fruit spine development
inferred← citeshttps://doi.org/10.1007/s00203-021-02413-4openalex-snapshot
Effect of co-application of Trichoderma spp. with organic composts on plant growth enhancement, soil enzymes and fungal community in soil
inferred← citeshttps://doi.org/10.1007/s00253-020-10890-8openalex-snapshot
Auxins of microbial origin and their use in agriculture
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/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/s00299-015-1888-4openalex-snapshot
Mechanisms of thaxtomin A-induced root toxicity revealed by a thaxtomin A sensitive Arabidopsis mutant (ucu2-2/gi-2)
inferred← citeshttps://doi.org/10.1007/s00299-018-2361-yopenalex-snapshot
Transcriptome analysis revealed the interaction among strigolactones, auxin, and cytokinin in controlling the shoot branching of rice
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/s00299-020-02643-8openalex-snapshot
ZEITLUPE enhances expression of PIF4 and YUC8 in the upper aerial parts of Arabidopsis seedlings to positively regulate hypocotyl elongation
inferred← citeshttps://doi.org/10.1007/s00299-023-02990-2openalex-snapshot
An EMS-induced allele of the brachytic2 gene can reduce plant height in maize
inferred← citeshttps://doi.org/10.1007/s00299-026-03862-1openalex-snapshot
From pollen precursor to totipotent embryo: a model system for plant cell developmental plasticity
inferred← citeshttps://doi.org/10.1007/s00344-011-9203-2openalex-snapshot
Expression and Subcellular Localization of Arabidopsis thaliana Auxin-Binding Protein 1 (ABP1)
inferred← citeshttps://doi.org/10.1007/s00344-017-9746-yopenalex-snapshot
The Expression of CpAUX1/LAXs and Most of the Long-distance CpPINs Genes Increases as the Somatic Embryogenesis Process Develops in C. papaya cv. “Red Maradol”
inferred← citeshttps://doi.org/10.1007/s00344-020-10139-8openalex-snapshot
Enhanced Polar Auxin Transport in Tomato Polycotyledon Mutant Seems to be Related to Glutathione Levels
inferred← citeshttps://doi.org/10.1007/s00344-021-10380-9openalex-snapshot
Influence of Endogenous Plant Hormones on Physiological and Growth Attributes of Kinnow Mandarin Grafted on Nine Rootstocks
inferred← citeshttps://doi.org/10.1007/s00344-026-12393-8openalex-snapshot
Heterologous Expression of Liriodendron sino-americanum LhWUS Promotes Branching in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00425-013-1883-3openalex-snapshot
Alteration of flavonoid accumulation patterns in transparent testa mutants disturbs auxin transport, gravity responses, and imparts long-term effects on root and shoot architecture
inferred← citeshttps://doi.org/10.1007/s00425-018-2897-7openalex-snapshot
Tissue accumulation patterns and concentrations of potassium, phosphorus, and carboxyfluorescein translocated from pine seed to the root
inferred← citeshttps://doi.org/10.1007/s00425-018-2905-yopenalex-snapshot
Mitogen-activated protein kinases concentrate in the vicinity of chromosomes and may regulate directly cellular patterning in Vicia faba embryos
inferred← citeshttps://doi.org/10.1007/s00425-018-3068-6openalex-snapshot
Cotyledons contribute to plant growth and hybrid vigor in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00425-020-03367-5openalex-snapshot
Endogenous auxin determines the pattern of adventitious shoot formation on internodal segments of ipecac
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/s00425-021-03709-xopenalex-snapshot
Involvement of the auxin–cytokinin homeostasis in adventitious root formation of rose cuttings as affected by their nodal position in the stock plant
inferred← citeshttps://doi.org/10.1007/s00425-023-04126-yopenalex-snapshot
Novel insights into maize (Zea mays) development and organogenesis for agricultural optimization
inferred← citeshttps://doi.org/10.1007/s00425-023-04136-wopenalex-snapshot
Advances in the study of the function and mechanism of the action of flavonoids in plants under environmental stresses
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/s00425-025-04641-0openalex-snapshot
Genome-wide analysis of ARF gene family and miR160 in avocado (Persea americana Mill.) and their roles in somatic embryogenesis from zygotic embryos
inferred← citeshttps://doi.org/10.1007/s00425-025-04662-9openalex-snapshot
ABCB transporters: functionality extends to more than auxin transportation
inferred← citeshttps://doi.org/10.1007/s00468-019-01940-4openalex-snapshot
The role of plant hormones in tree-ring formation
inferred← citeshttps://doi.org/10.1007/s00497-010-0160-xopenalex-snapshot
The asymmetric division of the Arabidopsis zygote: from cell polarity to an embryo axis
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/s00709-015-0897-zopenalex-snapshot
Inhibitors of plant hormone transport
inferred← citeshttps://doi.org/10.1007/s00709-017-1181-1openalex-snapshot
Localization and transport of indole-3-acetic acid during somatic embryogenesis in Coffea canephora
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/s10142-014-0392-1openalex-snapshot
Linkage of cold acclimation and disease resistance through plant–pathogen interaction pathway in Vitis amurensis grapevine
inferred← citeshttps://doi.org/10.1007/s10142-018-0625-9openalex-snapshot
Structural and functional evolution of an auxin efflux carrier PIN1 and its functional characterization in common wheat
inferred← citeshttps://doi.org/10.1007/s10265-015-0710-2openalex-snapshot
Identification of Arabidopsis thaliana NRT1/PTR FAMILY (NPF) proteins capable of transporting plant hormones
inferred← citeshttps://doi.org/10.1007/s10535-014-0423-8openalex-snapshot
The B subfamily of plant ATP binding cassette transporters and their roles in auxin transport
inferred← citeshttps://doi.org/10.1007/s10681-020-02700-zopenalex-snapshot
Genome wide association mapping and candidate gene mining for root architectural traits in rapeseed/canola (Brassica napus L.) at late growth stage
inferred← citeshttps://doi.org/10.1007/s10725-010-9556-8openalex-snapshot
The brachytic 2 and 3 maize double mutant shows alterations in plant growth and embryo development
inferred← citeshttps://doi.org/10.1007/s10725-013-9880-xopenalex-snapshot
Osmotic stress stimulates shoot organogenesis in callus of rice (Oryza sativa L.) via auxin signaling and carbohydrate metabolism regulation
inferred← citeshttps://doi.org/10.1007/s10725-014-9893-0openalex-snapshot
Coumarin interacts with auxin polar transport to modify root system architecture in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10725-018-0384-6openalex-snapshot
Effects of artemisinin on root gravitropic response and root system development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10725-018-0425-1openalex-snapshot
Temporal root responses in Arabidopsis thaliana L. to chromate reveal structural and regulatory mechanisms involving the SOLITARY ROOT/IAA14 repressor for maintenance of identity meristem genes
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/s10725-024-01228-9openalex-snapshot
The compound NMA regulates root and hypocotyl development in Arabidopsis thaliana via crosstalk between the auxin and ethylene signalling pathways
inferred← citeshttps://doi.org/10.1007/s10886-011-9987-3openalex-snapshot
Effects of a Coumarin Derivative, 4-Methylumbelliferone, on Seed Germination and Seedling Establishment in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11103-011-9769-xopenalex-snapshot
Probing the roles of LRR RLK genes in Arabidopsis thaliana roots using a custom T-DNA insertion set
inferred← citeshttps://doi.org/10.1007/s11103-016-0463-xopenalex-snapshot
Hormones and nitrate: a two-way connection
inferred← citeshttps://doi.org/10.1007/s11103-016-0476-5openalex-snapshot
Auxin response under osmotic stress
inferred← citeshttps://doi.org/10.1007/s11103-017-0647-zopenalex-snapshot
The MEDIATOR genes MED12 and MED13 control Arabidopsis root system configuration influencing sugar and auxin responses
inferred← citeshttps://doi.org/10.1007/s11103-019-00836-8openalex-snapshot
Downregulation of the auxin transporter gene SlPIN8 results in pollen abortion in tomato
inferred← citeshttps://doi.org/10.1007/s11103-022-01255-yopenalex-snapshot
Eucalyptus grandis AUX/INDOLE-3-ACETIC ACID 13 (EgrIAA13) is a novel transcriptional regulator of xylogenesis
inferred← citeshttps://doi.org/10.1007/s11103-025-01631-4openalex-snapshot
To grow or not to grow: the enigma of plant root growth dynamism
inferred← citeshttps://doi.org/10.1007/s11103-025-01671-wopenalex-snapshot
The evolution and developmental expression profile of the PIN-FORMED family in Setaria viridis
inferred← citeshttps://doi.org/10.1007/s11240-011-0016-6openalex-snapshot
In vitro plant regeneration and de novo differentiation of secretory trichomes in Passiflora foetida L. (Passifloraceae)
inferred← citeshttps://doi.org/10.1007/s11240-014-0580-7openalex-snapshot
Species-dependent divergent responses to in vitro somatic embryo induction in Passiflora spp.
inferred← citeshttps://doi.org/10.1007/s11240-014-0663-5openalex-snapshot
Alternative induction of de novo shoot organogenesis or somatic embryogenesis from in vitro cultures of mature zygotic embryos of passion fruit (Passiflora edulis Sims) is modulated by the ratio between auxin and cytokinin in the medium
inferred← citeshttps://doi.org/10.1007/s11240-015-0902-4openalex-snapshot
Somatic plant regeneration from selected common cypress (Cupressus sempervirens L.) clones resistant to the bark canker disease
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/s11295-018-1247-zopenalex-snapshot
Identification of molecular processes that differ among Scots pine somatic embryogenic cell lines leading to the development of normal or abnormal cotyledonary embryos
inferred← citeshttps://doi.org/10.1007/s11738-016-2292-6openalex-snapshot
Response to strigolactone treatment in chrysanthemum axillary buds is influenced by auxin transport inhibition and sucrose availability
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/10.1007/s11756-025-02024-0openalex-snapshot
Genetics and development of pseudanthia in the genus Helianthus: A review
inferred← citeshttps://doi.org/10.1007/s11816-014-0327-2openalex-snapshot
Subcellular localization of endogenous IAA during poplar leaf rhizogenesis revealed by in situ immunocytochemistry
inferred← citeshttps://doi.org/10.1007/s12042-016-9182-3openalex-snapshot
New Insight Into Early Somatic Embryogenesis of Mangosteen (Garcinia mangostana) Through de Novo and Comparative Transcriptome Analyses
inferred← citeshttps://doi.org/10.1007/s12298-022-01239-8openalex-snapshot
Genome-wide identification and expression analysis of PIN gene family under phytohormone and abiotic stresses in Vitis Vinifera L.
inferred← citeshttps://doi.org/10.1007/s12374-020-09270-6openalex-snapshot
Transcriptome Analysis Suggests Cytokinin and Gibberellin Signaling May Account for Differences Between Spring and Winter Canola (Brassica napus L.) Root Development
inferred← citeshttps://doi.org/10.1007/s13199-013-0225-3openalex-snapshot
Review article: The meristem in indeterminate root nodules of Faboideae
inferred← citeshttps://doi.org/10.1007/s13205-017-0689-6openalex-snapshot
Cloning and characterization of auxin efflux carrier genes EcPIN1a and EcPIN1b from finger millet Eleusine coracana L.
inferred← citeshttps://doi.org/10.1007/s13205-023-03709-6openalex-snapshot
Recent advances in auxin biosynthesis and homeostasis
inferred← citeshttps://doi.org/10.1007/s40626-024-00347-yopenalex-snapshot
Drought tolerance: a perspective about leaf venation and the role of auxin
inferred← citeshttps://doi.org/10.1007/s42535-024-01029-5openalex-snapshot
Investigating the function of mangrove mycorrhizal fungi with special emphasis on arbuscular mycorrhizae (AMF) symbiosis in promoting ecosystem health and sustainability
inferred← citeshttps://doi.org/10.1007/s44281-025-00063-wopenalex-snapshot
Dwarfing of fruit trees: from old cognitions to new insights
inferred← citeshttps://doi.org/10.1016/b978-0-12-374881-2.00002-7openalex-snapshot
Phenology and Growth Cycle
inferred← citeshttps://doi.org/10.1016/b978-0-12-387692-8.00006-0openalex-snapshot
The Regulatory Networks of Plant Responses to Abscisic Acid
inferred← citeshttps://doi.org/10.1016/b978-0-12-401667-5.00001-8openalex-snapshot
Control Systems in the Living World
inferred← citeshttps://doi.org/10.1016/b978-0-12-417162-6.00009-2openalex-snapshot
Genetic and Hormonal Regulation of Maize Inflorescence Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-811308-0.00007-7openalex-snapshot
The role of root morphology and architecture in phosphorus acquisition: physiological, genetic, and molecular basis
inferred← citeshttps://doi.org/10.1016/b978-0-12-816365-8.00001-4openalex-snapshot
Taxonomy and anatomy
inferred← citeshttps://doi.org/10.1016/b978-0-12-816365-8.00002-6openalex-snapshot
Phenology and growth cycle
inferred← citeshttps://doi.org/10.1016/b978-0-323-91886-2.00010-0openalex-snapshot
Understanding the role of phytohormones in governing heat, cold, and freezing stress response
inferred← citeshttps://doi.org/10.1016/bs.abr.2019.09.010openalex-snapshot
Hormonal interactions in the regulation of the nitrogen-fixing legume-Rhizobium symbiosis
inferred← citeshttps://doi.org/10.1016/j.actaastro.2020.05.061openalex-snapshot
Enhancing benzene removal by Chlorophytum comosum under simulation microgravity system: Effect of light-dark conditions and indole-3-acetic acid
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.bbrc.2024.149507openalex-snapshot
Arabidopsis plasma membrane H+-ATPase interacts with auxin to regulate Danger-Associated Peptide Pep1-induced root growth inhibition
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.06.090openalex-snapshot
Design and synthesis of photolabile caged cytokinin
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.09.001openalex-snapshot
Development of 4-methoxy-7-nitroindolinyl (MNI)-caged auxins which are extremely stable in planta
inferred← citeshttps://doi.org/10.1016/j.bpj.2024.06.017openalex-snapshot
Auxin-mediated stress relaxation in pericycle and endoderm remodeling drives lateral root initiation
inferred← citeshttps://doi.org/10.1016/j.btre.2026.e00982openalex-snapshot
PIN-FORMED (PIN) gene family in cultivated strawberry (Fragaria x ananassa): Genome-wide characterization and expression profiling under different abiotic stresses and hormonal treatments
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.2016.01.044openalex-snapshot
Information Integration and Communication in Plant Growth Regulation
inferred← citeshttps://doi.org/10.1016/j.cell.2019.06.021openalex-snapshot
Root System Depth in Arabidopsis Is Shaped by EXOCYST70A3 via the Dynamic Modulation of Auxin Transport
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.cellsig.2020.109799openalex-snapshot
Heterotrimeric G-proteins mediated hormonal responses in plants
inferred← citeshttps://doi.org/10.1016/j.cj.2024.06.011openalex-snapshot
Advances in the study of auxin early response genes: Aux/IAA, GH3, and SAUR
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.2011.04.049openalex-snapshot
Phloem-Transported Cytokinin Regulates Polar Auxin Transport and Maintains Vascular Pattern in the Root Meristem
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.2012.06.050openalex-snapshot
Mechanical Regulation of Auxin-Mediated Growth
inferred← citeshttps://doi.org/10.1016/j.cub.2014.03.018openalex-snapshot
Hormone Crosstalk: Directing the Flow
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.2015.01.015openalex-snapshot
Asymmetric Localizations of the ABC Transporter PaPDR1 Trace Paths of Directional Strigolactone Transport
inferred← citeshttps://doi.org/10.1016/j.cub.2015.03.055openalex-snapshot
Plant Grafting: Making the Right Connections
inferred← citeshttps://doi.org/10.1016/j.cub.2022.12.007openalex-snapshot
Plant physiology: The to-and-fro of hormone signals to respond to drought
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.devcel.2017.12.021openalex-snapshot
Feedback from Lateral Organs Controls Shoot Apical Meristem Growth by Modulating Auxin Transport
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.12.001openalex-snapshot
The Arabidopsis Receptor Kinase IRK Is Polarized and Represses Specific Cell Divisions in Roots
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.envexpbot.2017.10.005openalex-snapshot
Cadmium and arsenic affect quiescent centre formation and maintenance in Arabidopsis thaliana post-embryonic roots disrupting auxin biosynthesis and transport
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.10.004openalex-snapshot
Uncovering the physiological and cellular effects of uranium on the root system of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104064openalex-snapshot
Growth and aluminum tolerance of maize roots mediated by auxin- and cytokinin-producing Bacillus toyonensis requires polar auxin transport
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2025.106239openalex-snapshot
Silver nanoparticles inhibit root growth and promote root waving by inhibiting polar auxin transport and local auxin biosynthesis in Arabidopsis root tips
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2025.106279openalex-snapshot
PFOS effects on root stem cell maintenance and regeneration by suppressing the stem cell factor PLT2
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2026.106417openalex-snapshot
Microcystis aeruginosa exudate modulates auxin transport and signaling to reshape plant lateral root development
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.gene.2011.10.040openalex-snapshot
Functional roles of effectors of plant-parasitic nematodes
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.hpj.2022.08.009openalex-snapshot
Root-associated endophytic fungi modulate endogenous auxin and cytokinin levels to improve plant biomass and root morphology of trifoliate orange
inferred← citeshttps://doi.org/10.1016/j.hpj.2023.02.002openalex-snapshot
Insights into flavonoid biosynthesis during cucumber fruit peel coloration based on metabolite profiling and transcriptome analyses
inferred← citeshttps://doi.org/10.1016/j.hpj.2023.04.013openalex-snapshot
Transcriptome profiling of indole-3-butyric acid–induced adventitious root formation in softwood cuttings of walnut
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.146909openalex-snapshot
Functional insights into 4-coumarate-CoA ligase and caffeic acid O-methyltransferase genes involved in lignin biosynthesis in Chinese fir (Cunninghamia lanceolata)
inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.119180openalex-snapshot
Combining high-throughput deep learning phenotyping and GWAS to reveal genetic variants of fruit branch angle in upland cotton
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.121842openalex-snapshot
A multi-stage protocol for indirect somatic embryogenesis and plantlet regeneration from leaf explants of Quercus chungii
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.123222openalex-snapshot
Woody plant medium enhances micropropagation of the medicinal shrub Blumea balsamifera (L.) DC.
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.123891openalex-snapshot
RgTAA1-RgYUCCA6-IAA axis mediates hydrogen gas-induced adventitious root formation in Rehmannia glutinosa root cuttings
inferred← citeshttps://doi.org/10.1016/j.jia.2022.08.011openalex-snapshot
Advances in studies on the physiological and molecular regulation of barley tillering
inferred← citeshttps://doi.org/10.1016/j.jia.2023.05.041openalex-snapshot
The auxin transporter OsAUX1 regulates tillering in rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1016/j.jia.2023.08.007openalex-snapshot
The nitrate-responsive transcription factor MdNLP7 regulates callus formation by modulating auxin response
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.2017.02.012openalex-snapshot
Initiation of leaf somatic embryogenesis involves high pectin esterification, auxin accumulation and DNA demethylation in Quercus alba
inferred← citeshttps://doi.org/10.1016/j.jplph.2018.09.006openalex-snapshot
BIIDXI, a DUF642 cell wall protein, is involved in hypocotyl growth via auxin efflux
inferred← citeshttps://doi.org/10.1016/j.jplph.2020.153333openalex-snapshot
Endogenous auxin accumulation/localization during zygotic and somatic embryogenesis of Capsicum chinense Jacq
inferred← citeshttps://doi.org/10.1016/j.jprot.2021.104126openalex-snapshot
New insight into the rapid growth of the Mikania micrantha stem based on DIA proteomic and RNA-Seq analysis
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.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
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