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The ABA receptor PYL9 together with PYL8 plays an important role in regulating lateral root growth

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/j.molcel.2011.05.011openalex-snapshot
The Molecular Basis of ABA-Independent Inhibition of PP2Cs by a Subclass of PYL Proteins
inferredcites →https://doi.org/10.1016/j.tplants.2006.07.003openalex-snapshot
A novel role for abscisic acid emerges from underground
inferredcites →https://doi.org/10.1016/j.tplants.2010.06.005openalex-snapshot
MYB transcription factors in Arabidopsis
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(03)00924-3openalex-snapshot
Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation
inferredcites →https://doi.org/10.1016/s1360-1385(03)00011-6openalex-snapshot
Sugar and hormone connections
inferredcites →https://doi.org/10.1023/a:1006104205959openalex-snapshot
Isolation and characterization of cDNA clones corresponding with mRNAs that accumulate during auxin-induced lateral root formation
inferredcites →https://doi.org/10.1038/cr.2013.143openalex-snapshot
Molecular basis for the selective and ABA-independent inhibition of PP2CA by PYL13
inferredcites →https://doi.org/10.1038/cr.2013.149openalex-snapshot
The unique mode of action of a divergent member of the ABA-receptor protein family in ABA and stress signaling
inferredcites →https://doi.org/10.1038/nature08599openalex-snapshot
In vitro reconstitution of an abscisic acid signalling pathway
inferredcites →https://doi.org/10.1038/ncb2573openalex-snapshot
Auxin regulates aquaporin function to facilitate lateral root emergence
inferredcites →https://doi.org/10.1038/nmeth0305-213openalex-snapshot
Profiling histone modification patterns in plants using genomic tiling microarrays
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00454.xopenalex-snapshot
The sax1 dwarf mutant of Arabidopsis thaliana shows altered sensitivity of growth responses to abscisic acid, auxin, gibberellins and ethylene and is partially rescued by exogenous brassinosteroid
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01165.xopenalex-snapshot
Maize VP1 complements Arabidopsisabi3 and confers a novel ABA/auxin interaction in roots
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.2003.01707.xopenalex-snapshot
The ABSCISIC ACID INSENSITIVE 3 ( ABI3 ) gene is modulated by farnesylation and is involved in auxin signaling and lateral root development in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1304651110openalex-snapshot
Auxin controls seed dormancy through stimulation of abscisic acid signaling by inducing ARF-mediated ABI3 activation in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1522840113openalex-snapshot
ABA receptor PYL9 promotes drought resistance and leaf senescence
inferredcites →https://doi.org/10.1093/jxb/erh276openalex-snapshot
Root growth maintenance during water deficits: physiology to functional genomics
inferredcites →https://doi.org/10.1093/jxb/eru202openalex-snapshot
HDG11 upregulates cell-wall-loosening protein genes to promote root elongation in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcj043openalex-snapshot
Expression Profiling of Auxin-treated Arabidopsis Roots: Toward a Molecular Analysis of Lateral Root Emergence
inferredcites →https://doi.org/10.1104/pp.107.110981openalex-snapshot
Overexpression of AtMYB44 Enhances Stomatal Closure to Confer Abiotic Stress Tolerance in Transgenic Arabidopsis
inferredcites →https://doi.org/10.1104/pp.112.208678openalex-snapshot
PYRABACTIN RESISTANCE1-LIKE8 Plays an Important Role for the Regulation of Abscisic Acid Signaling in Root
inferredcites →https://doi.org/10.1104/pp.123.2.563openalex-snapshot
AXR2 Encodes a Member of the Aux/IAA Protein Family
inferredcites →https://doi.org/10.1105/tpc.004960openalex-snapshot
Auxin-Mediated Cell Cycle Activation during Early Lateral Root Initiation
inferredcites →https://doi.org/10.1105/tpc.006494openalex-snapshot
A Unique Short-Chain Dehydrogenase/Reductase in Arabidopsis Glucose Signaling and Abscisic Acid Biosynthesis and Functions
inferredcites →https://doi.org/10.1105/tpc.106.048538openalex-snapshot
Identification of Two Protein Kinases Required for Abscisic Acid Regulation of Seed Germination, Root Growth, and Gene Expression in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.107.050963openalex-snapshot
The Arabidopsis Transcription Factor MYB77 Modulates Auxin Signal Transduction
inferredcites →https://doi.org/10.1105/tpc.109.067702openalex-snapshot
Abscisic Acid Represses Growth of theArabidopsisEmbryonic Axis after Germination by Enhancing Auxin Signaling
inferredcites →https://doi.org/10.1105/tpc.110.074641openalex-snapshot
ABI4 Mediates Abscisic Acid and Cytokinin Inhibition of Lateral Root Formation by Reducing Polar Auxin Transport in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.098574openalex-snapshot
Arabidopsis PYR/PYL/RCAR Receptors Play a Major Role in Quantitative Regulation of Stomatal Aperture and Transcriptional Response to Abscisic Acid
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.6.2.251openalex-snapshot
A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low-temperature, or high-salt stress.
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02192.xopenalex-snapshot
ABF2, an ABRE‐binding bZIP factor, is an essential component of glucose signaling and its overexpression affects multiple stress tolerance
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02425.xopenalex-snapshot
Osmotic regulation of root system architecture
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04367.xopenalex-snapshot
ABA promotes quiescence of the quiescent centre and suppresses stem cell differentiation in the Arabidopsis primary root meristem
inferredcites →https://doi.org/10.1111/j.1744-7909.2012.01101.xopenalex-snapshot
ROP11 GTPase Negatively Regulates ABA Signaling by Protecting ABI1 Phosphatase Activity from Inhibition by the ABA Receptor RCAR1/PYL9 in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.12013openalex-snapshot
LBD18 acts as a transcriptional activator that directly binds to the EXPANSIN14 promoter in promoting lateral root emergence of Arabidopsis
inferredcites →https://doi.org/10.1126/science.1172408openalex-snapshot
Regulators of PP2C Phosphatase Activity Function as Abscisic Acid Sensors
inferredcites →https://doi.org/10.1126/science.1173041openalex-snapshot
Abscisic Acid Inhibits Type 2C Protein Phosphatases via the PYR/PYL Family of START Proteins
inferredcites →https://doi.org/10.1126/science.1215106openalex-snapshot
Molecular Mimicry Regulates ABA Signaling by SnRK2 Kinases and PP2C Phosphatases
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.57.032905.105444openalex-snapshot
TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES
inferredcites →https://doi.org/10.1186/1471-2229-13-192openalex-snapshot
Multiple roles of the transcription factor AtMYBR1/AtMYB44 in ABA signaling, stress responses, and leaf senescence
inferredcites →https://doi.org/10.1242/dev.121.10.3303openalex-snapshot
Formation of lateral root meristems is a two-stage process
inferredcites →https://doi.org/10.1371/journal.pgen.1002172openalex-snapshot
Auxin Response Factor2 (ARF2) and Its Regulated Homeodomain Gene HB33 Mediate Abscisic Acid Response in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0057547openalex-snapshot
Tight Interconnection and Multi-Level Control of Arabidopsis MYB44 in MAPK Cascade Signalling
inferredcites →https://doi.org/10.1371/journal.pone.0095246openalex-snapshot
Identification and Characterization of ABA Receptors in Oryza sativa
inferredcites →https://doi.org/10.3390/ijms15058473openalex-snapshot
Arabidopsis ABA Receptor RCAR1/PYL9 Interacts with an R2R3-Type MYB Transcription Factor, AtMYB44
inferredcites →https://doi.org/10.4141/p99-056openalex-snapshot
Improvement of soybean somatic embryo development and maturation by abscisic acid treatment

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.4829059openalex-extracted
Integrated Transcriptomic and Proteomic Analyses Reveals the Impact of Drought and Heat Stress Combination on Morus Alba
inferred← citeshttps://doi.org/10.1002/pld3.70169openalex-snapshot
Exogenous Hormone Treatments Reveal Species‐Specific Regulation of Individual Components of Root Architecture and Salt Ion Accumulation in Cultivated and Wild Tomatoes
inferred← citeshttps://doi.org/10.1007/978-981-95-7844-3_3openalex-snapshot
Hormonal and Molecular Regulation of Root Traits in Arabidopsis in Response to Abiotic Stress: A Way Forward to Climate-Smart Crop Improvement Program
inferred← citeshttps://doi.org/10.1007/s00299-022-02953-zopenalex-snapshot
AtTLP2, a Tubby-like protein, plays intricate roles in abiotic stress signalling
inferred← citeshttps://doi.org/10.1007/s00299-025-03495-wopenalex-snapshot
Unveiling the molecular mechanism underlying PSKR-mediated amplification of the ABA signaling in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-026-03924-4openalex-snapshot
The bp-miR156c–BpSPL2 module positively regulates drought tolerance by mediating lateral root development and reactive oxygen species scavenging in Betula platyphylla
inferred← citeshttps://doi.org/10.1007/s00344-024-11443-3openalex-snapshot
Foliar Application of Abscisic Acid Alleviates Cadmium Stress by Modulating Differential Physiological and Transcriptome Response in Leaves, Stems, and Roots of Mung Bean Seedlings
inferred← citeshttps://doi.org/10.1007/s00425-021-03672-7openalex-snapshot
Transcriptomics and targeted metabolomics reveal the regulatory network of Lilium davidii var. unicolor during bulb dormancy release
inferred← citeshttps://doi.org/10.1007/s10142-017-0546-zopenalex-snapshot
Abscisic acid, sucrose, and auxin coordinately regulate berry ripening process of the Fujiminori grape
inferred← citeshttps://doi.org/10.1007/s10265-019-01089-8openalex-snapshot
Water transport, perception, and response in plants
inferred← citeshttps://doi.org/10.1007/s11103-017-0692-7openalex-snapshot
Interaction network of core ABA signaling components in maize
inferred← citeshttps://doi.org/10.1007/s11103-026-01753-3openalex-snapshot
Exogenous ABA regulates stress tolerance of Leymus chinensis via modulation of PYL‑mediated signaling and antioxidant enzymes
inferred← citeshttps://doi.org/10.1007/s11104-021-05271-7openalex-snapshot
Transcriptomic analyses reveal the effect of nitric oxide on the lateral root development and growth of mangrove plant Kandelia obovata
inferred← citeshttps://doi.org/10.1007/s11240-021-02157-5openalex-snapshot
Effect of exogenous abscisic acid (ABA) on the morphology, phytohormones, and related gene expression of developing lateral roots in ‘Qingzhen 1’ apple plants
inferred← citeshttps://doi.org/10.1007/s11240-021-02178-0openalex-snapshot
Increased abscisic acid sensitivity and drought tolerance of Arabidopsis by overexpression of poplar abscisic acid receptors
inferred← citeshttps://doi.org/10.1007/s12033-018-0076-5openalex-snapshot
Ectopic Expression of Rice PYL3 Enhances Cold and Drought Tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s12298-021-01015-0openalex-snapshot
Identification of tomato root growth regulatory genes and transcription factors through comparative transcriptomic profiling of different tissues
inferred← citeshttps://doi.org/10.1007/s13765-017-0297-5openalex-snapshot
Intergenic transformation of AtMYB44 confers drought stress tolerance in rice seedlings
inferred← citeshttps://doi.org/10.1016/bs.mie.2022.03.062openalex-snapshot
Synthesis and characterization of abscisic acid receptor modulators
inferred← citeshttps://doi.org/10.1016/j.apsoil.2017.06.007openalex-snapshot
Hypothetical framework integrating the main mechanisms involved in the promoting action of rhizospheric humic substances on plant root- and shoot- growth
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.11.057openalex-snapshot
AtMYB44 interacts with TOPLESS-RELATED corepressors to suppress protein phosphatase 2C gene transcription
inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.12.046openalex-snapshot
Studies on the interactions of AFPs and bZIP transcription factor ABI5
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112809openalex-snapshot
The ABI3-ERF1 module mediates ABA-auxin crosstalk to regulate lateral root emergence
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.07.001openalex-snapshot
Nitric oxide is involved in abscisic acid-induced photosynthesis and antioxidant system of tall fescue seedlings response to low-light stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105706openalex-snapshot
Overexpression of ABA receptor gene VsPYL5 from common vetch enhances salt and cold tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105988openalex-snapshot
Integrated transcriptomic and proteomic analyses reveal the impact of drought and heat stress combination on Morus alba
inferred← citeshttps://doi.org/10.1016/j.gde.2017.03.010openalex-snapshot
Spatiotemporal mechanisms of root branching
inferred← citeshttps://doi.org/10.1016/j.gep.2020.119117openalex-snapshot
Overexpression of a sour jujube gene ZjPYR1, encoding a putative abscisic acid receptor, increases sensitivity of the stomata and roots to ABA in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.hpj.2021.06.005openalex-snapshot
Virus-induced gene silencing of SlPYL4 decreases the drought tolerance of tomato
inferred← citeshttps://doi.org/10.1016/j.hpj.2025.06.006openalex-snapshot
The role of PYL genes as core components of abscisic acid signaling in plant abiotic stress response
inferred← citeshttps://doi.org/10.1016/j.jia.2024.11.003openalex-snapshot
Comparative transcriptome analysis reveals the key factors regulating nitrogen use efficiency in Chrysanthemum
inferred← citeshttps://doi.org/10.1016/j.jplph.2023.154042openalex-snapshot
Ethylene enhanced waterlogging tolerance by changing root architecture and inducing aerenchyma formation in maize seedlings
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154692openalex-snapshot
ABA receptors: function and post-translational modifications in plants
inferred← citeshttps://doi.org/10.1016/j.molp.2020.02.001openalex-snapshot
PHYTOCHROME-INTERACTING FACTORS Interact with the ABA Receptors PYL8 and PYL9 to Orchestrate ABA Signaling in Darkness
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111222openalex-snapshot
Orphan gene PpARDT positively involved in drought tolerance potentially by enhancing ABA response in Physcomitrium (Physcomitrella) patens
inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.05.033openalex-snapshot
Overexpression of AtPYL5 under the control of guard cell specific promoter improves drought stress tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.02.008openalex-snapshot
Grapevine ABA receptor VvPYL1 regulates root hair development in Transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.12.018openalex-snapshot
Regulation of growth in peach roots by exogenous hydrogen sulfide based on RNA-Seq
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.02.023openalex-snapshot
Comparative transcriptome and genome analysis unravels the response of Tatary buckwheat root to nitrogen deficiency
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108072openalex-snapshot
Genome-wide identification and expression analysis of PYL family genes and functional characterization of GhPYL8D2 under drought stress in Gossypium hirsutum
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110118openalex-snapshot
Genome-wide identification of the PYL gene family and functional validation of SiPYL3 in foxtail millet (Setaria italica)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110339openalex-snapshot
PYRABACTIN RESISTANCE 1 – LIKE 8 and AKT1 INTERACTING PROTEIN PHOSPHATASE 1 are involved in ammonium transport regulation
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111200openalex-snapshot
Genome-wide identification, characterization and expression analysis of the ABA receptor PYL gene family in response to ABA, photoperiod, and chilling in vegetative buds of Liriodendron chinense
inferred← citeshttps://doi.org/10.1016/j.scienta.2025.113981openalex-snapshot
Comparison of the effect of organic versus non-organic biostimulants application on plant growth and transcriptome analysis of cucumber plants
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100428openalex-snapshot
Nutrient flow environment as a eustress that promotes root growth by regulating phytohormone synthesis and signal transduction in hydroponics
inferred← citeshttps://doi.org/10.1016/j.stress.2025.101069openalex-snapshot
Tissue-specific phosphorus stress adaptation in Brassica rapa: WGCNA reveals root hormonal triad and leaf lipid remodeling as key tolerance mechanisms
inferred← citeshttps://doi.org/10.1016/j.tplants.2019.04.008openalex-snapshot
Revisiting the Basal Role of ABA – Roles Outside of Stress
inferred← citeshttps://doi.org/10.1016/j.tplants.2020.06.008openalex-snapshot
How Plant Hormones Mediate Salt Stress Responses
inferred← citeshttps://doi.org/10.1016/j.xplc.2022.100306openalex-snapshot
Transcriptional landscapes of de novo root regeneration from detached Arabidopsis leaves revealed by time-lapse and single-cell RNA sequencing analyses
inferred← citeshttps://doi.org/10.1021/acschembio.1c00451openalex-snapshot
New Abscisic Acid Derivatives Revealed Adequate Regulation of Stomatal, Transcriptional, and Developmental Responses to Conquer Drought
inferred← citeshttps://doi.org/10.1021/acschembio.9b00453openalex-snapshot
Abscisic Acid Derivatives with Different Alkyl Chain Lengths Activate Distinct Abscisic Acid Receptor Subfamilies
inferred← citeshttps://doi.org/10.1038/s41598-017-17140-4openalex-snapshot
Transcriptome analysis of watermelon (Citrullus lanatus) fruits in response to Cucumber green mottle mosaic virus (CGMMV) infection
inferred← citeshttps://doi.org/10.1038/s41598-024-77962-xopenalex-snapshot
Genome-wide analysis of the PYL gene family and identification of PYL genes that respond to cold stress in Triticum monococcum L. Subsp. Aegilopoides
inferred← citeshttps://doi.org/10.1038/s41598-025-29074-3openalex-snapshot
Tuber mustard BjuFIP gene negatively regulates plant sensitivity to abscisic acid
inferred← citeshttps://doi.org/10.1073/pnas.1804774115openalex-snapshot
Mutations in a subfamily of abscisic acid receptor genes promote rice growth and productivity
inferred← citeshttps://doi.org/10.1073/pnas.2102544118openalex-snapshot
TMK1-based auxin signaling regulates abscisic acid responses via phosphorylating ABI1/2 in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.2512997122openalex-snapshot
Abscisic acid regulates iron accumulation in plant seeds via the PYLs–bHLH IVc–YSLs module
inferred← citeshttps://doi.org/10.1080/09168451.2017.1313696openalex-snapshot
Structural basis for the regulation of phytohormone receptors
inferred← citeshttps://doi.org/10.1080/14620316.2017.1379364openalex-snapshot
Effects of abscisic acid agonist or antagonist applications on aroma volatiles and anthocyanin biosynthesis in grape berries
inferred← citeshttps://doi.org/10.1080/15592324.2016.1214793openalex-snapshot
The spatio-temporal specificity of PYR1/PYL/RCAR ABA receptors in response to developmental and environmental cues
inferred← citeshttps://doi.org/10.1080/15592324.2021.1891756openalex-snapshot
Synthesis and regulation of auxin and abscisic acid in maize
inferred← citeshttps://doi.org/10.1093/jxb/eraa512openalex-snapshot
A genome-wide association study reveals that the glucosyltransferase OsIAGLU regulates root growth in rice
inferred← citeshttps://doi.org/10.1093/jxb/erad131openalex-snapshot
The dynamics of H2A.Z on SMALL AUXIN UP RNAs regulate abscisic acid–auxin signaling crosstalk in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erae192openalex-snapshot
Interplay of light and abscisic acid signaling to modulate plant development
inferred← citeshttps://doi.org/10.1093/jxb/erz511openalex-snapshot
Genome-wide phylogenetic and structural analysis reveals the molecular evolution of the ABA receptor gene family
inferred← citeshttps://doi.org/10.1093/nar/gkaa264openalex-snapshot
Prediction of condition-specific regulatory genes using machine learning
inferred← citeshttps://doi.org/10.1093/plphys/kiab145openalex-snapshot
Lateral root formation and nutrients: nitrogen in the spotlight
inferred← citeshttps://doi.org/10.1093/plphys/kiac407openalex-snapshot
Abscisic acid inhibits primary root growth by impairing ABI4-mediated cell cycle and auxin biosynthesis
inferred← citeshttps://doi.org/10.1093/plphys/kiag394openalex-snapshot
Arabidopsis MYC2–ARF16–ABI5 complex functions as a transcriptional switch to regulate jasmonate, auxin, and abscisic acid signaling synergy
inferred← citeshttps://doi.org/10.1093/treephys/tpx137openalex-snapshot
Transcriptome analysis of Pinus halepensis under drought stress and during recovery
inferred← citeshttps://doi.org/10.1094/mpmi-03-16-0063-ropenalex-snapshot
AtMYB44 Positively Regulates the Enhanced Elongation of Primary Roots Induced by N-3-Oxo-Hexanoyl-Homoserine Lactone in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/2021.04.25.441358openalex-snapshot
Abscisic acid modulates auxin-responsive hypocotyl elongation
inferred← citeshttps://doi.org/10.1101/cshperspect.a039990openalex-snapshot
Auxin Interactions with Other Hormones in Plant Development
inferred← citeshttps://doi.org/10.1111/jipb.12899openalex-snapshot
Abscisic acid dynamics, signaling, and functions in plants
inferred← citeshttps://doi.org/10.1111/nph.18149openalex-snapshot
Monomerization of abscisic acid receptors through CARKs‐mediated phosphorylation
inferred← citeshttps://doi.org/10.1111/pce.14137openalex-snapshot
ABA regulation of root growth during soil drying and recovery can involve auxin response
inferred← citeshttps://doi.org/10.1111/pce.15163openalex-snapshot
PeFUS3 Drives Lateral Root Growth Via Auxin and ABA Signalling Under Drought Stress in Populus
inferred← citeshttps://doi.org/10.1111/pce.70680openalex-snapshot
Lateral Root Development: Molecular Mechanisms and Adaptive Regulation
inferred← citeshttps://doi.org/10.1111/ppl.13651openalex-snapshot
Shaping the root system architecture in plants for adaptation to drought stress
inferred← citeshttps://doi.org/10.1111/ppl.13781openalex-snapshot
Tartary buckwheat FtMYB30 transcription factor improves the salt/drought tolerance of transgenic Arabidopsis in an ABA ‐dependent manner
inferred← citeshttps://doi.org/10.1111/ppl.13878openalex-snapshot
Insights into the environmental factors shaping lateral root development
inferred← citeshttps://doi.org/10.1186/s12864-019-5839-2openalex-snapshot
Genome-wide identification and characterization of ABA receptor PYL/RCAR gene family reveals evolution and roles in drought stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.1186/s12864-020-07083-yopenalex-snapshot
Genome-wide identification and characterization of ABA receptor PYL gene family in rice
inferred← citeshttps://doi.org/10.1186/s12864-024-10158-9openalex-snapshot
Structural and functional characterization of genes PYL-PP2C-SnRK2s in the ABA signalling pathway of Cucurbita pepo
inferred← citeshttps://doi.org/10.1186/s12864-024-10665-9openalex-snapshot
Genome-wide analysis of the PYL-PP2C-SnRK2s family in the ABA signaling pathway of pitaya reveals its expression profiles under canker disease stress
inferred← citeshttps://doi.org/10.1186/s12870-018-1499-7openalex-snapshot
Proteomic and ecophysiological responses of soybean (Glycine max L.) root nodules to Pb and hg stress
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/s12870-021-02839-4openalex-snapshot
Heterologous expression of Arabidopsis thaliana rty gene in strawberry (Fragaria × ananassa Duch.) improves drought tolerance
inferred← citeshttps://doi.org/10.1186/s12870-022-03704-8openalex-snapshot
Overexpression VaPYL9 improves cold tolerance in tomato by regulating key genes in hormone signaling and antioxidant enzyme
inferred← citeshttps://doi.org/10.1186/s12870-023-04330-8openalex-snapshot
GhPYL9-5D and GhPYR1-3 A positively regulate Arabidopsis and cotton responses to ABA, drought, high salinity and osmotic stress
inferred← citeshttps://doi.org/10.1186/s12870-024-05447-0openalex-snapshot
Genome-wide identification, abiotic stress, and expression analysis of PYL family in Tartary buckwheat (Fagopyrum tataricum (L.) Gaertn.) during grain development
inferred← citeshttps://doi.org/10.1186/s12870-024-05879-8openalex-snapshot
Biochemical and yield response of spring wheat to drought stress through gibberellic and abscisic acids
inferred← citeshttps://doi.org/10.1186/s12870-025-06505-xopenalex-snapshot
Integrated metabolome and transcriptome analysis of maize roots response to different degrees of drought stress
inferred← citeshttps://doi.org/10.1186/s12870-025-07156-8openalex-snapshot
Characterization of the ABA receptor PYL gene family and identification of DoPYL1-interacting proteins in Dendrobium officinale
inferred← citeshttps://doi.org/10.1186/s43897-025-00155-1openalex-snapshot
The triggering mechanism for predominant hormonal signal production in fleshy fruit ripening
inferred← citeshttps://doi.org/10.1242/dev.177097openalex-snapshot
Abiotic stress modulates root patterning via ABA-regulated microRNA expression in the endodermis initials
inferred← citeshttps://doi.org/10.1242/dev.202106openalex-snapshot
Abscisic acid biosynthesis is necessary for full auxin effects on hypocotyl elongation
inferred← citeshttps://doi.org/10.12688/f1000research.140649.1openalex-snapshot
Tapping into the plasticity of plant architecture for increased stress resilience
inferred← citeshttps://doi.org/10.1371/journal.pone.0304503openalex-snapshot
Integrated physiological, transcriptomics and metabolomics analysis revealed the molecular mechanism of Bupleurum chinense seedlings to drought stress
inferred← citeshttps://doi.org/10.15252/embr.202152457openalex-snapshot
MPK3/6-induced degradation of ARR1/10/12 promotes salt tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.21203/rs.2.19941/v1openalex-snapshot
Transcriptome profiling provides new insights into florets number difference of inflorescence in lavandula angustifolia
inferred← citeshttps://doi.org/10.21203/rs.3.rs-126184/v1openalex-snapshot
WITHDRAWN: Transcriptome and targeted metabolome reveal the regulation network of Lilium davidii var. unicolor during dormancy release
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2237961/v1openalex-snapshot
Comparative transcriptome analysis unravels key factors regulating nitrogen use efficiency in chrysanthemum
inferred← citeshttps://doi.org/10.21203/rs.3.rs-670691/v1openalex-snapshot
Effect of Exogenous Abscisic acid (ABA) on the Morphology, Phytohormones, and Related Gene Expression of Developing Lateral Roots in ‘Qingzhen 1’
inferred← citeshttps://doi.org/10.21203/rs.3.rs-703845/v1openalex-snapshot
Increased Abscisic Acid Sensitivity And Drought Stress By Overexpression of Abscisic Acid Receptors In Arabidopsis Thaliana
inferred← citeshttps://doi.org/10.24326/asp.hc.2023.5154openalex-snapshot
Functional characterization of ZjPYL8 from sour jujube: enhancing the sensitivity of stomata and roots to ABA in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2017.01453openalex-snapshot
Activation of ABA Receptors Gene GhPYL9-11A Is Positively Correlated with Cotton Drought Tolerance in Transgenic Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2019.00716openalex-snapshot
Abscisic Acid Regulates Auxin Distribution to Mediate Maize Lateral Root Development Under Salt Stress
inferred← citeshttps://doi.org/10.3389/fpls.2020.00437openalex-snapshot
Arabidopsis Lectin EULS3 Is Involved in ABA Signaling in Roots
inferred← citeshttps://doi.org/10.3389/fpls.2020.587620openalex-snapshot
ABA-Dependent and ABA-Independent Functions of RCAR5/PYL11 in Response to Cold Stress
inferred← citeshttps://doi.org/10.3389/fpls.2022.1041649openalex-snapshot
Proteomics approach to investigating osmotic stress effects on pistachio
inferred← citeshttps://doi.org/10.3389/fpls.2022.1050840openalex-snapshot
Combined full-length transcriptomic and metabolomic analysis reveals the regulatory mechanisms of adaptation to salt stress in asparagus
inferred← citeshttps://doi.org/10.3389/fpls.2022.928386openalex-snapshot
The Indole-3-Acetamide-Induced Arabidopsis Transcription Factor MYB74 Decreases Plant Growth and Contributes to the Control of Osmotic Stress Responses
inferred← citeshttps://doi.org/10.3389/fpls.2023.1204828openalex-snapshot
Resistant cumin cultivar, GC-4 counters Fusarium oxysporum f. sp. cumini infection through up-regulation of steroid biosynthesis, limonene and pinene degradation and butanoate metabolism pathways
inferred← citeshttps://doi.org/10.3390/agronomy10091323openalex-snapshot
Implications of Abscisic Acid in the Drought Stress Tolerance of Plants
inferred← citeshttps://doi.org/10.3390/agronomy12061318openalex-snapshot
The Potassium-Dependent Transcriptome Analysis of Maize Provides Novel Insights into the Rescue Role of Auxin in Responses to Potassium Deficiency
inferred← citeshttps://doi.org/10.3390/antiox11101962openalex-snapshot
Charged Gold Nanoparticles Promote In Vitro Proliferation in Nardostachys jatamansi by Differentially Regulating Chlorophyll Content, Hormone Concentration, and Antioxidant Activity
inferred← citeshttps://doi.org/10.3390/biom10020281openalex-snapshot
Auxin-Abscisic Acid Interactions in Plant Growth and Development
inferred← citeshttps://doi.org/10.3390/biom11060788openalex-snapshot
Improving Performance of Salt-Grown Crops by Exogenous Application of Plant Growth Regulators
inferred← citeshttps://doi.org/10.3390/genes12081141openalex-snapshot
Arabidopsis Hypocotyl Adventitious Root Formation Is Suppressed by ABA Signaling
inferred← citeshttps://doi.org/10.3390/genes9030156openalex-snapshot
Genome-Wide Analysis of the PYL Gene Family and Identification of PYL Genes That Respond to Abiotic Stress in Brassica napus
inferred← citeshttps://doi.org/10.3390/ijms18091841openalex-snapshot
Arabidopsis E3 Ubiquitin Ligases PUB22 and PUB23 Negatively Regulate Drought Tolerance by Targeting ABA Receptor PYL9 for Degradation
inferred← citeshttps://doi.org/10.3390/ijms19092728openalex-snapshot
Regulatory Mechanism of ABA and ABI3 on Vegetative Development in the Moss Physcomitrella patens
inferred← citeshttps://doi.org/10.3390/ijms20061422openalex-snapshot
MicroRNA Sequencing Revealed Citrus Adaptation to Long-Term Boron Toxicity through Modulation of Root Development by miR319 and miR171
inferred← citeshttps://doi.org/10.3390/ijms20092076openalex-snapshot
Comparative Transcriptomic Analysis of Biological Process and Key Pathway in Three Cotton (Gossypium spp.) Species Under Drought Stress
inferred← citeshttps://doi.org/10.3390/ijms252010940openalex-snapshot
Understanding of Plant Salt Tolerance Mechanisms and Application to Molecular Breeding
inferred← citeshttps://doi.org/10.3390/ijms252212101openalex-snapshot
Mining of Candidate Genes Associated with Leaf Shape Traits in Grapes
inferred← citeshttps://doi.org/10.3390/ijms252413728openalex-snapshot
Genome-Wide Analysis of the PYL Gene Family in Betula platyphylla and Its Responses to Abiotic Stresses
inferred← citeshttps://doi.org/10.3390/ijms26073422openalex-snapshot
Identification of R2R3-MYB Gene Family and Functional Analysis of Responses of S22 Subfamily to Abiotic Stresses in Dandelion (Taraxacum mongolicum Hand.-Mazz.)
inferred← citeshttps://doi.org/10.3390/ijms26146986openalex-snapshot
The Identification of Transcriptomic and Phytohormonal Biomarkers for Monitoring Drought and Evaluating the Potential of Acibenzolar-S-Methyl Root Application to Prime Two Apple Rootstock Genotypes for Drought Resistance
inferred← citeshttps://doi.org/10.3390/metabo15010056openalex-snapshot
Role of Carrot (Daucus carota L.) Storage Roots in Drought Stress Adaptation: Hormonal Regulation and Metabolite Accumulation
inferred← citeshttps://doi.org/10.3390/plants10091804openalex-snapshot
Plant CDKs—Driving the Cell Cycle through Climate Change
inferred← citeshttps://doi.org/10.3390/plants11233205openalex-snapshot
Metabolites from Bacillus subtilis J-15 Affect Seedling Growth of Arabidopsis thaliana and Cotton Plants
inferred← citeshttps://doi.org/10.3390/plants13071005openalex-snapshot
Functional Analysis of the GhIQD1 Gene in Cotton Resistance to Verticillium Wilt
inferred← citeshttps://doi.org/10.3390/plants13223126openalex-snapshot
Overexpression of the Kiwifruit Transcription Factor AaMYB44 Decreases the Cold Tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/plants14172731openalex-snapshot
Genome-Wide Identification of the StPYL Gene Family and Analysis of the Functional Role of StPYL9a-like in Salt Tolerance in Potato (Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.3390/plants9081028openalex-snapshot
Genome-Wide Identification of the ABA Receptors Genes and Their Response to Abiotic Stress in Apple
inferred← citeshttps://doi.org/10.3390/plants9091059openalex-snapshot
Gaining Insight into Exclusive and Common Transcriptomic Features Linked to Drought and Salinity Responses across Fruit Tree Crops
inferred← citeshttps://doi.org/10.3390/plants9091106openalex-snapshot
A Synthetic Cytokinin Improves Photosynthesis in Rice under Drought Stress by Modulating the Abundance of Proteins Related to Stomatal Conductance, Chlorophyll Contents, and Rubisco Activity
inferred← citeshttps://doi.org/10.48130/forres-0025-0012openalex-snapshot
Identification of Malus sieversii ABA receptor PYL8 interacting proteome using Y2H-seq
inferred← citeshttps://doi.org/10.5204/thesis.eprints.115120openalex-snapshot
Characterisation of Root Architectural Responses of Mungbean to Water Deficit
inferred← citeshttps://doi.org/10.53846/goediss-8610openalex-snapshot
Down-Stream molecular Responses to Volatile Signaling in Roots
inferred← citeshttps://doi.org/10.6084/m9.figshare.13031227openalex-snapshot
Additional file 12 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13031230openalex-snapshot
Additional file 13 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13031233openalex-snapshot
Additional file 1 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13031236openalex-snapshot
Additional file 2 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13031239openalex-snapshot
Additional file 3 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13031242openalex-snapshot
Additional file 4 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13031245openalex-snapshot
Additional file 5 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13627483openalex-snapshot
Additional file 1 of Heterologous expression of Arabidopsis thaliana rty gene in strawberry (Fragaria × ananassa Duch.) improves drought tolerance
inferred← citeshttps://doi.org/10.6084/m9.figshare.13627486openalex-snapshot
Additional file 2 of Heterologous expression of Arabidopsis thaliana rty gene in strawberry (Fragaria × ananassa Duch.) improves drought tolerance
inferred← citeshttps://doi.org/10.6084/m9.figshare.13627489openalex-snapshot
Additional file 3 of Heterologous expression of Arabidopsis thaliana rty gene in strawberry (Fragaria × ananassa Duch.) improves drought tolerance
inferred← citeshttps://doi.org/10.6084/m9.figshare.13627492openalex-snapshot
Additional file 4 of Heterologous expression of Arabidopsis thaliana rty gene in strawberry (Fragaria × ananassa Duch.) improves drought tolerance
inferred← citeshttps://doi.org/10.6084/m9.figshare.13627495openalex-snapshot
Additional file 5 of Heterologous expression of Arabidopsis thaliana rty gene in strawberry (Fragaria × ananassa Duch.) improves drought tolerance
inferred← citeshttps://doi.org/10.6084/m9.figshare.13627498openalex-snapshot
Additional file 6 of Heterologous expression of Arabidopsis thaliana rty gene in strawberry (Fragaria × ananassa Duch.) improves drought tolerance
inferred← citeshttps://doi.org/10.6084/m9.figshare.13627501openalex-snapshot
Additional file 7 of Heterologous expression of Arabidopsis thaliana rty gene in strawberry (Fragaria × ananassa Duch.) improves drought tolerance
inferred← citeshttps://doi.org/10.6084/m9.figshare.20327392openalex-snapshot
Additional file 10 of Overexpression VaPYL9 improves cold tolerance in tomato by regulating key genes in hormone signaling and antioxidant enzyme
inferred← citeshttps://doi.org/10.6084/m9.figshare.20327395openalex-snapshot
Additional file 1 of Overexpression VaPYL9 improves cold tolerance in tomato by regulating key genes in hormone signaling and antioxidant enzyme
inferred← citeshttps://doi.org/10.6084/m9.figshare.20327398openalex-snapshot
Additional file 2 of Overexpression VaPYL9 improves cold tolerance in tomato by regulating key genes in hormone signaling and antioxidant enzyme
inferred← citeshttps://doi.org/10.6084/m9.figshare.20327401openalex-snapshot
Additional file 3 of Overexpression VaPYL9 improves cold tolerance in tomato by regulating key genes in hormone signaling and antioxidant enzyme
inferred← citeshttps://doi.org/10.6084/m9.figshare.20327404openalex-snapshot
Additional file 4 of Overexpression VaPYL9 improves cold tolerance in tomato by regulating key genes in hormone signaling and antioxidant enzyme
inferred← citeshttps://doi.org/10.6084/m9.figshare.20327407openalex-snapshot
Additional file 5 of Overexpression VaPYL9 improves cold tolerance in tomato by regulating key genes in hormone signaling and antioxidant enzyme
inferred← citeshttps://doi.org/10.6084/m9.figshare.20327410openalex-snapshot
Additional file 6 of Overexpression VaPYL9 improves cold tolerance in tomato by regulating key genes in hormone signaling and antioxidant enzyme
inferred← citeshttps://doi.org/10.6084/m9.figshare.20327413openalex-snapshot
Additional file 7 of Overexpression VaPYL9 improves cold tolerance in tomato by regulating key genes in hormone signaling and antioxidant enzyme
inferred← citeshttps://doi.org/10.6084/m9.figshare.20327416openalex-snapshot
Additional file 8 of Overexpression VaPYL9 improves cold tolerance in tomato by regulating key genes in hormone signaling and antioxidant enzyme
inferred← citeshttps://doi.org/10.6084/m9.figshare.20327419openalex-snapshot
Additional file 9 of Overexpression VaPYL9 improves cold tolerance in tomato by regulating key genes in hormone signaling and antioxidant enzyme
inferred← citeshttps://doi.org/10.6084/m9.figshare.25389514openalex-snapshot
Additional file 1 of Structural and functional characterization of genes PYL-PP2C-SnRK2s in the ABA signalling pathway of Cucurbita pepo
inferred← citeshttps://doi.org/10.6084/m9.figshare.25389932openalex-snapshot
Additional file 2 of Structural and functional characterization of genes PYL-PP2C-SnRK2s in the ABA signalling pathway of Cucurbita pepo
inferred← citeshttps://doi.org/10.6084/m9.figshare.26596214openalex-snapshot
Additional file 1 of GhPYL9-5D and GhPYR1-3 A positively regulate Arabidopsis and cotton responses to ABA, drought, high salinity and osmotic stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.26596217openalex-snapshot
Additional file 2 of GhPYL9-5D and GhPYR1-3 A positively regulate Arabidopsis and cotton responses to ABA, drought, high salinity and osmotic stress
inferred← citeshttps://doi.org/10.7287/peerj.4126v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Genome-wide identification of ABA receptor PYL family and expression analysis of PYLs in response to ABA and osmotic stress in Gossypium (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.4126v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Genome-wide identification of ABA receptor PYL family and expression analysis of PYLs in response to ABA and osmotic stress in Gossypium (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.4126v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Genome-wide identification of ABA receptor PYL family and expression analysis of PYLs in response to ABA and osmotic stress in Gossypium (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.4126openalex-snapshot
Genome-wide identification of ABA receptor PYL family and expression analysis of PYLs in response to ABA and osmotic stress in Gossypium
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.