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Multidrug Resistance-Like Genes of Arabidopsis Required for Auxin Transport and Auxin-Mediated Development

https://doi.org/10.2307/3871586
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inferred← citeshttps://doi.org/10.2139/ssrn.3981902openalex-extracted
Uncovering the Genetic Architecture of Replicated Adaptation
inferred← citeshttps://doi.org/10.1002/9780470015902.a0020090openalex-snapshot
Auxin
inferred← citeshttps://doi.org/10.1002/9780470015902.a0020116.pub2openalex-snapshot
Polar Auxin Transport
inferred← citeshttps://doi.org/10.1002/9780470015902.a0025267openalex-snapshot
Gravitropic Signaling in Plants
inferred← citeshttps://doi.org/10.1002/9780470388297.ch3openalex-snapshot
Auxin Transport and the Integration of Gravitropic Growth
inferred← citeshttps://doi.org/10.1002/9780470531792.ch21openalex-snapshot
Phenylpropanoid Metabolism in Plants: Biochemistry, Functional Biology, and Metabolic Engineering
inferred← citeshttps://doi.org/10.1002/9780470988800.ch9openalex-snapshot
Hormone Distribution and Transport
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/10.1002/9781118889022.ch2openalex-snapshot
Mechanism of Auxin Mediated Stress Signaling in Plants
inferred← citeshttps://doi.org/10.1002/9781118889022.ch3openalex-snapshot
Integrating the Knowledge of Auxin Homeostasis with Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1002/9781119053095.ch47openalex-snapshot
Regulation of Nodule Development by Short‐ and Long‐Distance Auxin Transport Control
inferred← citeshttps://doi.org/10.1002/9781119053095.ch56openalex-snapshot
The Role of Hormones in Rhizobial Infection
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0111openalex-snapshot
Mechanisms of Cell Polarity Establishment and Polar Auxin Transport
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0152openalex-snapshot
Membrane Transport and Soil Bioremediation
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0153openalex-snapshot
Auxin as an Intercellular Signal
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0250openalex-snapshot
Hormone Distribution and Transport
inferred← citeshttps://doi.org/10.1002/9781119357254.ch5openalex-snapshot
Auxin
inferred← citeshttps://doi.org/10.1002/bies.080146openalex-snapshot
Local auxin production: a small contribution to a big field
inferred← citeshttps://doi.org/10.1002/bies.20322openalex-snapshot
Regulating the regulator: the control of auxin transport
inferred← citeshttps://doi.org/10.1002/dvdy.23878openalex-snapshot
Hormone symphony during root growth and development
inferred← citeshttps://doi.org/10.1002/pld3.361openalex-snapshot
Electrophysiological study of Arabidopsis ABCB4 and PIN2 auxin transporters: Evidence of auxin activation and interaction enhancing auxin selectivity
inferred← citeshttps://doi.org/10.1002/wdev.193openalex-snapshot
Auxin and cytokinin act during gynoecial patterning and the development of ovules from the meristematic medial domain
inferred← citeshttps://doi.org/10.1016/j.crvi.2010.01.005openalex-snapshot
Recent progress in auxin biology
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.febslet.2005.11.054openalex-snapshot
The ABC of auxin transport: The role of p‐glycoproteins in plant development
inferred← citeshttps://doi.org/10.1016/j.febslet.2005.12.009openalex-snapshot
ABC transporters involved in the transport of plant secondary metabolites
inferred← citeshttps://doi.org/10.1016/j.febslet.2006.01.002openalex-snapshot
Genomics of plant ABC transporters: The alphabet of photosynthetic life forms or just holes in membranes?
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2002.01321.xopenalex-snapshot
The ABC transporter SpTUR2 confers resistance to the antifungal diterpene sclareol
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2003.01792.xopenalex-snapshot
Identification of regulatory sequence elements within the transcription promoter region of NpABC1, a gene encoding a plant ABC transporter induced by diterpenes
inferred← citeshttps://doi.org/10.1055/s-2004-830475openalex-snapshot
Specificity Patterns Indicate that Auxin Exporters and Receptors are the Same Proteins
inferred← citeshttps://doi.org/10.1073/pnas.1005878107openalex-snapshot
Arabidopsis PIS1 encodes the ABCG37 transporter of auxinic compounds including the auxin precursor indole-3-butyric acid
inferred← citeshttps://doi.org/10.1073/pnas.1309057110openalex-snapshot
ECHIDNA-mediated post-Golgi trafficking of auxin carriers for differential cell elongation
inferred← citeshttps://doi.org/10.1073/pnas.2007400117openalex-snapshot
Fluctuating auxin response gradients determine pavement cell-shape acquisition
inferred← citeshttps://doi.org/10.1073/pnas.2020857118openalex-snapshot
Naphthylphthalamic acid associates with and inhibits PIN auxin transporters
inferred← citeshttps://doi.org/10.1104/pp.102.014720openalex-snapshot
The ATP-Binding Cassette Transporters: Structure, Function, and Gene Family Comparison between Rice and Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.112.195776openalex-snapshot
Hypocotyl Directional Growth in Arabidopsis: A Complex Trait
inferred← citeshttps://doi.org/10.1105/tpc.016121openalex-snapshot
The VTI Family of SNARE Proteins Is Necessary for Plant Viability and Mediates Different Protein Transport Pathways[W]
inferred← citeshttps://doi.org/10.1105/tpc.020313openalex-snapshot
The transparent testa4 Mutation Prevents Flavonoid Synthesis and Alters Auxin Transport and the Response of Arabidopsis Roots to Gravity and Light[W]
inferred← citeshttps://doi.org/10.1105/tpc.021501openalex-snapshot
Variation in Expression and Protein Localization of the PIN Family of Auxin Efflux Facilitator Proteins in Flavonoid Mutants with Altered Auxin Transport in Arabidopsis thaliana [W]
inferred← citeshttps://doi.org/10.1105/tpc.15.00726openalex-snapshot
TWISTED DWARF1 Mediates the Action of Auxin Transport Inhibitors on Actin Cytoskeleton Dynamics
inferred← citeshttps://doi.org/10.1111/j.0960-7412.2004.02064.xopenalex-snapshot
Expression of rolB in tobacco flowers affects the coordinated processes of anther dehiscence and style elongation
inferred← citeshttps://doi.org/10.1111/j.1364-3703.2008.00486.xopenalex-snapshot
Transcriptional analysis of the sweet orange interaction with the citrus canker pathogens Xanthomonas axonopodis pv. citri and Xanthomonas axonopodis pv. aurantifolii
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2005.01489.xopenalex-snapshot
Diurnal regulation of plant growth*
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2004.02230.xopenalex-snapshot
Potassium carrier TRH1 is required for auxin transport in Arabidopsis roots
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2005.02519.xopenalex-snapshot
Cellular efflux of auxin catalyzed by the Arabidopsis MDR/PGP transporter AtPGP1
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2006.02939.xopenalex-snapshot
Role of plant CBP/p300‐like genes in the regulation of flowering time
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2006.02977.xopenalex-snapshot
Dynamics of MONOPTEROS and PIN‐FORMED1 expression during leaf vein pattern formation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2007.03044.xopenalex-snapshot
The ABC transporter AtPDR8 is a cadmium extrusion pump conferring heavy metal resistance
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2008.03495.xopenalex-snapshot
Ethylene regulates lateral root formation and auxin transport in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2008.03668.xopenalex-snapshot
ABCB19/PGP19 stabilises PIN1 in membrane microdomains in Arabidopsis
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2011.04818.xopenalex-snapshot
The Arabidopsis concentration‐dependent influx/efflux transporter ABCB4 regulates cellular auxin levels in the root epidermis
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2012.05024.xopenalex-snapshot
Arabidopsis SMALL AUXIN UP RNA63 promotes hypocotyl and stamen filament elongation
inferred← citeshttps://doi.org/10.1111/j.1399-3054.2009.01271.xopenalex-snapshot
Changes in growth kinetics of stamen filaments cause inefficient pollination in massugu2, an auxin insensitive, dominant mutant of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/j.1399-3054.2010.01439.xopenalex-snapshot
Root cap angle and gravitropic response rate are uncoupled in the Arabidopsis pgm‐1 mutant
inferred← citeshttps://doi.org/10.1111/j.1438-8677.2010.00388.xopenalex-snapshot
Modelling polar auxin transport in developmental patterning
inferred← citeshttps://doi.org/10.1111/j.1440-169x.2006.00893.xopenalex-snapshot
Increase in multidrug transport activity is associated with oocyte maturation in sea stars*
inferred← citeshttps://doi.org/10.1111/j.1467-7652.2011.00637.xopenalex-snapshot
Over‐expression of OsPIN2 leads to increased tiller numbers, angle and shorter plant height through suppression of OsLAZY1
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2007.02324.xopenalex-snapshot
Genes for control of plant stature and form
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2011.03757.xopenalex-snapshot
Auxin minimum defines a developmental window for lateral root initiation
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2008.00225.xopenalex-snapshot
Convergent evolution of shoots in land plants: lack of auxin polar transport in moss shoots
inferred← citeshttps://doi.org/10.1111/j.1742-4658.2010.07706.xopenalex-snapshot
Expression profile of PIN, AUX/LAX and PGP auxin transporter gene families in Sorghum bicolor under phytohormone and abiotic stress
inferred← citeshttps://doi.org/10.1111/j.1744-7909.2007.00440.xopenalex-snapshot
Effects of P‐Glycoprotein Inhibitor and Elicitor on the Salt Tolerance of Rice Seedlings
inferred← citeshttps://doi.org/10.1111/jipb.12332openalex-snapshot
ABCB1 and ABCB19 auxin transporters have synergistic effects on early and late Arabidopsis anther development
inferred← citeshttps://doi.org/10.1111/jipb.12747openalex-snapshot
Translating auxin responses into ovules, seeds and yield: Insight from Arabidopsis and the cereals
inferred← citeshttps://doi.org/10.1111/jipb.13441openalex-snapshot
To curve for survival: Apical hook development
inferred← citeshttps://doi.org/10.1111/nph.12558openalex-snapshot
Kaempferol 3‐O‐rhamnoside‐7‐O‐rhamnoside is an endogenous flavonol inhibitor of polar auxin transport in Arabidopsis shoots
inferred← citeshttps://doi.org/10.1111/nph.12831openalex-snapshot
PIN ‐driven polar auxin transport in plant developmental plasticity: a key target for environmental and endogenous signals
inferred← citeshttps://doi.org/10.1111/nph.13161openalex-snapshot
Repression of flowering under a noninductive photoperiod by the HDA 9‐ AGL 19‐ FT module in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.13725openalex-snapshot
The volatile 6‐pentyl‐2H‐pyran‐2‐one from Trichoderma atroviride regulates Arabidopsis thaliana root morphogenesis via auxin signaling and ETHYLENE INSENSITIVE 2 functioning
inferred← citeshttps://doi.org/10.1111/nph.14207openalex-snapshot
An auxin maximum in the middle layer controls stamen development and pollen maturation in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.14333openalex-snapshot
Auxin transport in the evolution of branching forms
inferred← citeshttps://doi.org/10.1111/nph.17955openalex-snapshot
Developmental regulation of leaf venation patterns: monocot versus eudicots and the role of auxin
inferred← citeshttps://doi.org/10.1111/nph.18196openalex-snapshot
A novel chemical inhibitor of polar auxin transport promotes shoot regeneration by local enhancement of HD‐ZIP III transcription
inferred← citeshttps://doi.org/10.1111/pce.12093openalex-snapshot
Auxin and its transport play a role in plant tolerance to arsenite‐induced oxidative stress in A rabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/pce.13478openalex-snapshot
The auxin influx carrier, OsAUX3, regulates rice root development and responses to aluminium stress
inferred← citeshttps://doi.org/10.1111/pce.14290openalex-snapshot
Jasmonic acid coordinates with light, glucose and auxin signalling in regulating branching angle of Arabidopsis lateral roots
inferred← citeshttps://doi.org/10.1111/plb.12030openalex-snapshot
Auxin transport during root gravitropism: transporters and techniques
inferred← citeshttps://doi.org/10.1111/plb.12101openalex-snapshot
Close relationships between polar auxin transport and graviresponse in plants
inferred← citeshttps://doi.org/10.1111/ppl.12182openalex-snapshot
Measure for measure: determining, inferring and guessing auxin gradients at the root tip
inferred← citeshttps://doi.org/10.1111/ppl.13908openalex-snapshot
Auxin participates in regulating the leaf curl development of Wucai (Brassica campestris L.)
inferred← citeshttps://doi.org/10.1111/tpj.12103openalex-snapshot
Sterols and sphingolipids differentially function in trafficking of the A rabidopsis ABCB 19 auxin transporter
inferred← citeshttps://doi.org/10.1111/tpj.12118openalex-snapshot
A t LAZY 1 is a signaling component required for gravitropism of the A rabidopsis thaliana inflorescence
inferred← citeshttps://doi.org/10.1111/tpj.12544openalex-snapshot
Os ABCB 14 functions in auxin transport and iron homeostasis in rice ( Oryza sativa L.)
inferred← citeshttps://doi.org/10.1111/tpj.12595openalex-snapshot
Leaf phenomics: a systematic reverse genetic screen for Arabidopsis leaf mutants
inferred← citeshttps://doi.org/10.1111/tpj.12929openalex-snapshot
The auxin transporter, Os AUX 1, is involved in primary root and root hair elongation and in Cd stress responses in rice ( Oryza sativa L.)
inferred← citeshttps://doi.org/10.1111/tpj.13095openalex-snapshot
ABCB 19‐mediated polar auxin transport modulates Arabidopsis hypocotyl elongation and the endoreplication variant of the cell cycle
inferred← citeshttps://doi.org/10.1111/tpj.13208openalex-snapshot
Gene coexpression network analysis of oil biosynthesis in an interspecific backcross of oil palm
inferred← citeshttps://doi.org/10.1111/tpj.15086openalex-snapshot
The AGCVIII kinase Dw2 modulates cell proliferation, endomembrane trafficking, and MLG/xylan cell wall localization in elongating stem internodes of Sorghum bicolor
inferred← citeshttps://doi.org/10.11606/d.11.2020.tde-27112020-161945openalex-snapshot
The role of microRNA156-regulated >i /i< in the control of shoot branching in tomato
inferred← citeshttps://doi.org/10.1186/s12864-020-06947-7openalex-snapshot
Fine mapping of the BnUC2 locus related to leaf up-curling and plant semi-dwarfing in Brassica napus
inferred← citeshttps://doi.org/10.1186/s12864-020-07121-9openalex-snapshot
Genome-wide identification of ATP binding cassette (ABC) transporter and heavy metal associated (HMA) gene families in flax (Linum usitatissimum L.)
inferred← citeshttps://doi.org/10.1186/s12864-020-6614-0openalex-snapshot
Transcriptome profiling provides insights into molecular mechanism in Peanut semi-dwarf mutant
inferred← citeshttps://doi.org/10.1186/s12864-024-10227-zopenalex-snapshot
A transcriptome-wide identification of ATP-binding cassette (ABC) transporters revealed participation of ABCB subfamily in abiotic stress management of Glycyrrhiza glabra L
inferred← citeshttps://doi.org/10.1186/s12870-019-2002-9openalex-snapshot
Auxin regulates adventitious root formation in tomato cuttings
inferred← citeshttps://doi.org/10.1186/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/10.1186/s12870-025-06201-wopenalex-snapshot
A global overview of transcriptome dynamics during the late stage of flower bud development in Camellia oleifera
inferred← citeshttps://doi.org/10.1242/dev.00926openalex-snapshot
Partial loss-of-function alleles reveal a role forGNOMin auxin transport-related, post-embryonic development ofArabidopsis
inferred← citeshttps://doi.org/10.1242/dev.009654openalex-snapshot
The geneMACCHI-BOU 4/ENHANCER OF PINOIDencodes a NPH3-like protein and reveals similarities between organogenesis and phototropism at the molecular level
inferred← citeshttps://doi.org/10.1242/dev.01952openalex-snapshot
Surge and destroy: the role of auxin in plant embryogenesis
inferred← citeshttps://doi.org/10.1242/dev.021071openalex-snapshot
Interaction of PIN and PGP transport mechanisms in auxin distribution-dependent development
inferred← citeshttps://doi.org/10.1242/dev.030353openalex-snapshot
Auxin transport routes in plant development
inferred← citeshttps://doi.org/10.1360/csb2010-55-13-1240openalex-snapshot
一个水稻卷叶突变体rl11(t)的遗传分析和基因定位
inferred← citeshttps://doi.org/10.1371/journal.pbio.1002446openalex-snapshot
Connective Auxin Transport in the Shoot Facilitates Communication between Shoot Apices
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007695openalex-snapshot
INDUCER OF CBF EXPRESSION 1 is a male fertility regulator impacting anther dehydration in Arabidopsis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008023openalex-snapshot
Connective auxin transport contributes to strigolactone-mediated shoot branching control independent of the transcription factor BRC1
inferred← citeshttps://doi.org/10.1371/journal.pone.0001510openalex-snapshot
Light Plays an Essential Role in Intracellular Distribution of Auxin Efflux Carrier PIN2 in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1371/journal.pone.0060809openalex-snapshot
The ATP-Binding Cassette Transporter ABCB19 Regulates Postembryonic Organ Separation in Arabidopsis
inferred← citeshttps://doi.org/10.1371/journal.pone.0157168openalex-snapshot
The Protein Kinase CK2 Mediates Cross-Talk between Auxin- and Salicylic Acid-Signaling Pathways in the Regulation of PINOID Transcription
inferred← citeshttps://doi.org/10.1371/journal.pone.0215901openalex-snapshot
Genome-wide identification and gene expression pattern of ABC transporter gene family in Capsicum spp.
inferred← citeshttps://doi.org/10.1371/journal.pone.0238144openalex-snapshot
Investigation of physiological and molecular mechanisms conferring diurnal variation in auxinic herbicide efficacy
inferred← citeshttps://doi.org/10.15252/embj.2020104416openalex-snapshot
Flavonol‐mediated stabilization of PIN efflux complexes regulates polar auxin transport
inferred← citeshttps://doi.org/10.15252/embj.2022113018openalex-snapshot
The birth of a giant: evolutionary insights into the origin of auxin responses in plants
inferred← citeshttps://doi.org/10.18174/511001openalex-snapshot
Evolutionary analysis of a billion years of auxin biology
inferred← citeshttps://doi.org/10.21203/rs.2.17556/v1openalex-snapshot
The constitutive expression of the chrysanthemum gene CmERF110 in Arabidopsis thaliana affects lateral branching
inferred← citeshttps://doi.org/10.2135/cropsci2005.07-0189openalex-snapshot
Effect of Cyclanilide, Ethephon, Auxin Transport Inhibitors, and Temperature on Whole Plant Defoliation
inferred← citeshttps://doi.org/10.3389/fpls.2011.00108openalex-snapshot
Plant Lessons: Exploring ABCB Functionality Through Structural Modeling
inferred← citeshttps://doi.org/10.3389/fpls.2012.00017openalex-snapshot
Diversification and Expression of the PIN, AUX/LAX, and ABCB Families of Putative Auxin Transporters in Populus
inferred← citeshttps://doi.org/10.3389/fpls.2012.00096openalex-snapshot
Modeling a Cortical Auxin Maximum for Nodulation: Different Signatures of Potential Strategies
inferred← citeshttps://doi.org/10.3389/fpls.2012.00274openalex-snapshot
Multiple roles for membrane-associated protein trafficking and signaling in gravitropism
inferred← citeshttps://doi.org/10.3389/fpls.2013.00441openalex-snapshot
Differential growth at the apical hook: all roads lead to auxin
inferred← citeshttps://doi.org/10.3732/ajb.1200299openalex-snapshot
Phototropism: Translating light into directional growth
inferred← citeshttps://doi.org/10.3732/ajb.1200318openalex-snapshot
Gravity Sensing and Signal Transduction in Vascular Plant Primary Roots
inferred← citeshttps://doi.org/10.3732/ajb.1400285openalex-snapshot
Auxin activity: Past, present, and future
inferred← citeshttps://doi.org/10.53846/goediss-491openalex-snapshot
Einfluss von Gibberellin auf den Gravitropismus der Wurzel durch Regulation der PIN-Stabilität
inferred← citeshttps://doi.org/10.7124/bc.0006ebopenalex-snapshot
Genetic and epigenetic control of plant growth and development. Molecular-genetic control of transmission and realization of auxin signals
inferred← citeshttps://doi.org/10.7150/ijbs.14577openalex-snapshot
RNA-Seq and iTRAQ Reveal the Dwarfing Mechanism of Dwarf Polish Wheat (Triticum polonicum L.)
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