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ABA homeostasis and long-distance translocation are redundantly regulated by ABCG ABA importers
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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/s10265-008-0201-9openalex-snapshot
Activation of abscisic acid biosynthesis in the leaves of Arabidopsis thaliana in response to water deficit
inferredcites →https://doi.org/10.1007/s10265-011-0411-4openalex-snapshot
Transport of ABA from the site of biosynthesis to the site of action
inferredcites →https://doi.org/10.1007/s11103-019-00953-4openalex-snapshot
The Arabidopsis UDP-glycosyltransferase75B1, conjugates abscisic acid and affects plant response to abiotic stresses
inferredcites →https://doi.org/10.1016/bs.mie.2016.04.001openalex-snapshot
Functional Expression and Characterization of Plant ABC Transporters in Xenopus laevis Oocytes for Transport Engineering Purposes
inferredcites →https://doi.org/10.1016/j.cell.2006.09.001openalex-snapshot
A Quick Release Mechanism for Abscisic Acid
inferredcites →https://doi.org/10.1016/j.cell.2016.08.029openalex-snapshot
Abiotic Stress Signaling and Responses in Plants
inferredcites →https://doi.org/10.1016/j.cub.2011.04.045openalex-snapshot
Chemical Genetics Reveals Negative Regulation of Abscisic Acid Signaling by a Plant Immune Response Pathway
inferredcites →https://doi.org/10.1016/j.cub.2012.11.022openalex-snapshot
The Stomatal Response to Reduced Relative Humidity Requires Guard Cell-Autonomous ABA Synthesis
inferredcites →https://doi.org/10.1016/j.envexpbot.2017.05.004openalex-snapshot
Leaf dehydration is needed to induce abscisic acid accumulation in roots of citrus plants
inferredcites →https://doi.org/10.1016/j.molp.2015.06.006openalex-snapshot
Abscisic Acid Transport and Homeostasis in the Context of Stomatal Regulation
inferredcites →https://doi.org/10.1016/j.pbi.2016.06.007openalex-snapshot
Long-distance transport of phytohormones through the plant vascular system
inferredcites →https://doi.org/10.1016/j.pbi.2017.08.003openalex-snapshot
Functions of ABC transporters in plant growth and development
inferredcites →https://doi.org/10.1016/j.tplants.2013.01.007openalex-snapshot
ABA transport and transporters
inferredcites →https://doi.org/10.1016/j.tplants.2018.04.001openalex-snapshot
ABA Transport and Plant Water Stress Responses
inferredcites →https://doi.org/10.1038/emboj.2012.120openalex-snapshot
Regulation of ABCB1/PGP1‐catalysed auxin transport by linker phosphorylation
inferredcites →https://doi.org/10.1038/ncomms11486openalex-snapshot
The Arabidopsis NPF3 protein is a GA transporter
inferredcites →https://doi.org/10.1038/ncomms9113openalex-snapshot
Abscisic acid transporters cooperate to control seed germination
inferredcites →https://doi.org/10.1038/s41467-018-06410-yopenalex-snapshot
A transportome-scale amiRNA-based screen identifies redundant roles of Arabidopsis ABCB6 and ABCB20 in auxin transport
inferredcites →https://doi.org/10.1038/s41598-019-47916-9openalex-snapshot
ABCG1 contributes to suberin formation in Arabidopsis thaliana roots
inferredcites →https://doi.org/10.1038/s41598-019-51258-xopenalex-snapshot
Genomic Prediction of 16 Complex Disease Risks Including Heart Attack, Diabetes, Breast and Prostate Cancer
inferredcites →https://doi.org/10.1046/j.0016-8025.2001.00824.xopenalex-snapshot
ABA‐based chemical signalling: the co‐ordination of responses to stress in plants
inferredcites →https://doi.org/10.1046/j.1365-3040.2000.00579.xopenalex-snapshot
Protection against the photo‐induced inactivation of the photosystem II complex by abscisic acid
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01652.xopenalex-snapshot
An abscisic acid‐sensitive checkpoint in lateral root development of Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01786.xopenalex-snapshot
Molecular characterization of the Arabidopsis 9 ‐cis epoxycarotenoid dioxygenase gene family
inferredcites →https://doi.org/10.1073/pnas.0909222107openalex-snapshot
PDR-type ABC transporter mediates cellular uptake of the phytohormone abscisic acid
inferredcites →https://doi.org/10.1073/pnas.0912516107openalex-snapshot
ABC transporter AtABCG25 is involved in abscisic acid transport and responses
inferredcites →https://doi.org/10.1073/pnas.1012896107openalex-snapshot
A seed coat bedding assay shows that RGL2-dependent release of abscisic acid by the endosperm controls embryo growth in Arabidopsis dormant seeds
inferredcites →https://doi.org/10.1073/pnas.1203567109openalex-snapshot
Identification of an abscisic acid transporter by functional screening using the receptor complex as a sensor
inferredcites →https://doi.org/10.1073/pnas.1300436110openalex-snapshot
Gibberellins accumulate in the elongating endodermal cells of Arabidopsis root
inferredcites →https://doi.org/10.1073/pnas.1305919110openalex-snapshot
Activation of dimeric ABA receptors elicits guard cell closure, ABA-regulated gene expression, and drought tolerance
inferredcites →https://doi.org/10.1093/jexbot/51.346.937openalex-snapshot
Extracellular β‐glucosidase activity in barley involved in the hydrolysis of ABA glucose conjugate in leaves
inferredcites →https://doi.org/10.1093/jexbot/52.363.1991openalex-snapshot
The long‐distance abscisic acid signal in the droughted plant: the fate of the hormone on its way from root to shoot
inferredcites →https://doi.org/10.1093/jexbot/53.373.1503openalex-snapshot
Stomatal control in tomato with ABA-deficient roots: response of grafted plants to soil drying
inferredcites →https://doi.org/10.1093/jxb/28.6.1342openalex-snapshot
Abscisic Acid Translocation and Influence of Water Stress on Grain Abscisic Acid Content
inferredcites →https://doi.org/10.1093/jxb/46.8.881openalex-snapshot
REVIEW ARTICLE: Compartmental redistribution and long-distance transport of abscisic acid (ABA) in plants as influenced by environmental changes in the rhizosphere —a biomathematical model
inferredcites →https://doi.org/10.1093/jxb/erg122openalex-snapshot
Do increases in xylem sap pH and/or ABA concentration mediate stomatal closure following nitrate deprivation?
inferredcites →https://doi.org/10.1093/jxb/erm127openalex-snapshot
Long-distance signalling of abscisic acid (ABA): the factors regulating the intensity of the ABA signal
inferredcites →https://doi.org/10.1093/jxb/ert208openalex-snapshot
Chlorophyll fluorescence analysis: a guide to good practice and understanding some new applications
inferredcites →https://doi.org/10.1093/jxb/erx159openalex-snapshot
The Solanum tuberosum KST1 partial promoter as a tool for guard cell expression in multiple plant species
inferredcites →https://doi.org/10.1093/mp/ssu063openalex-snapshot
A DTX/MATE-Type Transporter Facilitates Abscisic Acid Efflux and Modulates ABA Sensitivity and Drought Tolerance in Arabidopsis
inferredcites →https://doi.org/10.1093/nar/gkl635openalex-snapshot
Advancing uracil-excision based cloning towards an ideal technique for cloning PCR fragments
inferredcites →https://doi.org/10.1093/pcp/pcv161openalex-snapshot
Root ABA Accumulation in Long-Term Water-Stressed Plants is Sustained by Hormone Transport from Aerial Organs
inferredcites →https://doi.org/10.1093/plphys/kiaa032openalex-snapshot
Characterization ofCYCLOPHILLIN38shows that a photosynthesis-derived systemic signal controls lateral root emergence
inferredcites →https://doi.org/10.1104/pp.103.036970openalex-snapshot
Tissue-Specific Localization of an Abscisic Acid Biosynthetic Enzyme, AAO3, in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.053082openalex-snapshot
Generation of Active Pools of Abscisic Acid Revealed by In Vivo Imaging of Water-Stressed Arabidopsis
inferredcites →https://doi.org/10.1104/pp.113.2.559openalex-snapshot
Xylem Sap pH Increase: A Drought Signal Received at the Apoplastic Face of the Guard Cell That Involves the Suppression of Saturable Abscisic Acid Uptake by the Epidermal Symplast
inferredcites →https://doi.org/10.1104/pp.113.222547openalex-snapshot
Vacuolar Transport of Abscisic Acid Glucosyl Ester Is Mediated by ATP-Binding Cassette and Proton-Antiport Mechanisms in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.114.235556openalex-snapshot
Intertissue Signal Transfer of Abscisic Acid from Vascular Cells to Guard Cells
inferredcites →https://doi.org/10.1104/pp.114.244871openalex-snapshot
Beyond the Barrier: Communication in the Root through the Endodermis
inferredcites →https://doi.org/10.1104/pp.15.00053openalex-snapshot
UDP-Glucosyltransferase71C5, a Major Glucosyltransferase, Mediates Abscisic Acid Homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.17.00912openalex-snapshot
Stomatal VPD Response: There Is More to the Story Than ABA
inferredcites →https://doi.org/10.1104/pp.20.00485openalex-snapshot
The Tomato DELLA Protein PROCERA Promotes Abscisic Acid Responses in Guard Cells by Upregulating an Abscisic Acid Transporter
inferredcites →https://doi.org/10.1104/pp.65.6.1111openalex-snapshot
Effect of Obstructed Translocation on Leaf Abscisic Acid, and Associated Stomatal Closure and Photosynthesis Decline
inferredcites →https://doi.org/10.1104/pp.67.4.774openalex-snapshot
Abscisic Acid Translocation and Metabolism in Soybeans following Depodding and Petiole Girdling Treatments
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.112.107227openalex-snapshot
Endodermal ABA Signaling Promotes Lateral Root Quiescence during Salt Stress in Arabidopsis Seedlings
inferredcites →https://doi.org/10.1105/tpc.113.112805openalex-snapshot
A Genomic-Scale Artificial MicroRNA Library as a Tool to Investigate the Functionally Redundant Gene Space inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.112896openalex-snapshot
A Spatio-Temporal Understanding of Growth Regulation during the Salt Stress Response in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.129049openalex-snapshot
ABCG Transporters Are Required for Suberin and Pollen Wall Extracellular Barriers inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.12.11.2075openalex-snapshot
Oriented Asymmetric Divisions That Generate the Stomatal Spacing Pattern in Arabidopsis Are Disrupted by the too many mouths Mutation
inferredcites →https://doi.org/10.1105/tpc.16.00490openalex-snapshot
MYB107 and MYB9 Homologs Regulate Suberin Deposition in Angiosperms
inferredcites →https://doi.org/10.1111/j.1365-2818.2004.01269.xopenalex-snapshot
An easy and versatile embedding method for transverse sections
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02881.xopenalex-snapshot
Regulation of hormone metabolism in Arabidopsis seeds: phytochrome regulation of abscisic acid metabolism and abscisic acid regulation of gibberellin metabolism
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03234.xopenalex-snapshot
A hydraulic signal in root‐to‐shoot signalling of water shortage
inferredcites →https://doi.org/10.1111/nph.12713openalex-snapshot
Putting the brakes on: abscisic acid as a central environmental regulator of stomatal development
inferredcites →https://doi.org/10.1111/pce.12669openalex-snapshot
Shoot‐derived abscisic acid promotes root growth
inferredcites →https://doi.org/10.1111/tpj.14234openalex-snapshot
Mt ABCG 20 is an ABA exporter influencing root morphology and seed germination of Medicago truncatula
inferredcites →https://doi.org/10.1111/tpj.14690openalex-snapshot
ATP binding cassette transporters ABCG1 and ABCG16 affect reproductive development via auxin signalling in Arabidopsis
inferredcites →https://doi.org/10.1126/sciadv.abc8873openalex-snapshot
Leaf-derived ABA regulates rice seed development via a transporter-mediated and temperature-sensitive mechanism
inferredcites →https://doi.org/10.1126/science.aaf7254openalex-snapshot
Plant development regulated by cytokinin sinks
inferredcites →https://doi.org/10.1126/scisignal.2005051openalex-snapshot
The ABA Receptor PYL8 Promotes Lateral Root Growth by Enhancing MYB77-Dependent Transcription of Auxin-Responsive Genes
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112122openalex-snapshot
Abscisic Acid: Emergence of a Core Signaling Network
inferredcites →https://doi.org/10.1146/annurev.arplant.39.1.439openalex-snapshot
Metabolism And Physiology Of Abscisic Acid
inferredcites →https://doi.org/10.1146/annurev.arplant.53.091401.143329openalex-snapshot
S ALT AND D ROUGHT S TRESS S IGNAL T RANSDUCTION IN P LANTS
inferredcites →https://doi.org/10.1146/annurev.arplant.56.032604.144046openalex-snapshot
ABSCISIC ACID BIOSYNTHESIS AND CATABOLISM
inferredcites →https://doi.org/10.1146/annurev.pp.20.060169.001001openalex-snapshot
Vascular Transport and its Significance in Plant Growth
inferredcites →https://doi.org/10.1186/1746-4811-5-16openalex-snapshot
Tape-Arabidopsis Sandwich - a simpler Arabidopsis protoplast isolation method
inferredcites →https://doi.org/10.1186/1746-4811-9-1openalex-snapshot
Novel scanning procedure enabling the vectorization of entire rhizotron-grown root systems
inferredcites →https://doi.org/10.1186/1746-4811-9-14openalex-snapshot
An efficient flat-surface collar-free grafting method for Arabidopsis thaliana seedlings
inferredcites →https://doi.org/10.1186/s12915-017-0443-xopenalex-snapshot
Plant hormone transporters: what we know and what we would like to know
inferredcites →https://doi.org/10.1242/dev.177097openalex-snapshot
Abiotic stress modulates root patterning via ABA-regulated microRNA expression in the endodermis initials
inferredcites →https://doi.org/10.3389/fpls.2014.00687openalex-snapshot
Membrane transporters and drought resistance – a complex issue
inferredcites →https://doi.org/10.3390/ijms19113643openalex-snapshot
Molecular Mechanism for the Regulation of ABA Homeostasis During Plant Development and Stress Responses
inferredcites →https://doi.org/10.3791/51381openalex-snapshot
Histochemical Staining of Arabidopsis thaliana Secondary Cell Wall Elements
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Metabolomics of Mung Bean (Vigna Radiata) Reveals L-Glutamate and Biotin as Key Metabolites in Physiology and Nodulation Regulation Under Differential Light Intensity and Water Conditions
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GABA as a Signaling Molecule in Plants
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Parallels between drought and flooding: An integrated framework for plant eco‐physiological responses to water stress
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Evolutionarily conserved bacterial effectors hijack abscisic acid signaling to induce an aqueous environment in the apoplast
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Comprehensive analysis of NAC transcription factors in Scutellaria baicalensis and their response to exogenous ABA and GA3
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Long-distance hormone transport via the phloem
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Endomembrane-biased dimerization of ABCG16 and ABCG25 transporters determines their substrate selectivity in ABA-regulated plant growth and stress responses
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Transport mechanisms of plant hormones
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BAM1/2-mediated phosphorylation of ABCG16 reduces its stability and ABA export activity to suppress root growth in Arabidopsis
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Gibberellin and abscisic acid transporters facilitate endodermal suberin formation in Arabidopsis
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Abscisic acid root-to-shoot translocation by transporter AtABCG25 mediates stomatal movements in Arabidopsis
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Arabidopsis ABCG21 is an ABA efflux transporter involved in seed germination under salt stress
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ATP-Binding Cassette G Transporters and Their Multiple Roles Especially for Male Fertility in Arabidopsis, Rice and Maize
inferred← citeshttps://doi.org/10.3390/ijms24043090openalex-snapshot
Do Opposites Attract? Auxin-Abscisic Acid Crosstalk: New Perspectives
inferred← citeshttps://doi.org/10.3390/ijms251910724openalex-snapshot
ABCG Transporters in the Adaptation of Rice to Salt Stresses
inferred← citeshttps://doi.org/10.3390/plants12020227openalex-snapshot
Transcriptomic Insights into Functions of LkABCG36 and LkABCG40 in Nicotiana tabacum
inferred← citeshttps://doi.org/10.3390/plants12030634openalex-snapshot
Terpenoid Transport in Plants: How Far from the Final Picture?
inferred← citeshttps://doi.org/10.48130/ph-0025-0014openalex-snapshot
Abscisic acid mediated salinity stress tolerance in crops
inferred← citeshttps://doi.org/10.48130/ph-0025-0020openalex-snapshot
ABCG transporters in phytohormone dynamics: mechanisms, challenges, and future perspectives
inferred← citeshttps://doi.org/10.48130/vr-2023-0013openalex-snapshot
Comparative transcriptome-based identification and expression analysis of ATP-binding cassette (ABC) transporters reveals a likely role in the transport of β-caryophyllene and response to abiotic stress in Brassica campestris
inferred← citeshttps://doi.org/10.64013/bbasrjlifess.v2022i1.2openalex-snapshot
THE ROLE OF ABSCISIC ACID IN INDUCING COLD TOLERANCE IN PLANTS
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