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Abscisic acid perception and signaling: structural mechanisms and applications
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/jmbi.1998.2369openalex-snapshot
Structure of the protein tyrosine kinase domain of C-terminal Src kinase (CSK) in complex with staurosporine 1 1Edited by I. A. Wilson
inferredcites →https://doi.org/10.1006/jmbi.1999.2640openalex-snapshot
Mechanisms of cyclin-dependent kinase regulation: structures of cdks, their cyclin activators, and cip and INK4 inhibitors
inferredcites →https://doi.org/10.1016/0040-4020(95)00340-eopenalex-snapshot
Synthesis, biological activity and metabolism of (S)-(+)-3′-Fluoroabscisic acid
inferredcites →https://doi.org/10.1016/j.bbrc.2011.12.145openalex-snapshot
Crystal structures of the Arabidopsis thaliana abscisic acid receptor PYL10 and its complex with abscisic acid
inferredcites →https://doi.org/10.1016/j.bmc.2003.10.048openalex-snapshot
Metabolism of 5′α,8′-cycloabscisic acid, a highly potent and long-lasting abscisic acid analogue, in radish seedlings
inferredcites →https://doi.org/10.1016/j.cell.2006.05.013openalex-snapshot
An Allosteric Mechanism for Activation of the Kinase Domain of Epidermal Growth Factor Receptor
inferredcites →https://doi.org/10.1016/j.cell.2006.07.034openalex-snapshot
Activation of Glucosidase via Stress-Induced Polymerization Rapidly Increases Active Pools of Abscisic Acid
inferredcites →https://doi.org/10.1016/j.cell.2008.12.026openalex-snapshot
Two Novel GPCR-Type G Proteins Are Abscisic Acid Receptors in Arabidopsis
inferredcites →https://doi.org/10.1016/j.febslet.2006.07.047openalex-snapshot
A hypermorphic mutation in the protein phosphatase 2C HAB1 strongly affects ABA signaling inArabidopsis
inferredcites →https://doi.org/10.1016/j.jmb.2011.09.041openalex-snapshot
The Structure of Arabidopsis thaliana OST1 Provides Insights into the Kinase Regulation Mechanism in Response to Osmotic Stress
inferredcites →https://doi.org/10.1016/j.molcel.2004.08.024openalex-snapshot
Regulation of Protein Kinases
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.pbi.2008.06.014openalex-snapshot
The ABA receptors – we report you decide
inferredcites →https://doi.org/10.1016/j.pbi.2010.09.007openalex-snapshot
Structural and functional insights into core ABA signaling
inferredcites →https://doi.org/10.1016/j.str.2012.02.019openalex-snapshot
Complex Structures of the Abscisic Acid Receptor PYL3/RCAR13 Reveal a Unique Regulatory Mechanism
inferredcites →https://doi.org/10.1016/j.tplants.2004.03.007openalex-snapshot
Plant PP2C phosphatases: emerging functions in stress signaling
inferredcites →https://doi.org/10.1016/j.tplants.2006.11.005openalex-snapshot
SNF1/AMPK/SnRK1 kinases, global regulators at the heart of energy control?
inferredcites →https://doi.org/10.1016/j.tplants.2010.06.005openalex-snapshot
MYB transcription factors in Arabidopsis
inferredcites →https://doi.org/10.1016/j.tplants.2013.01.007openalex-snapshot
ABA transport and transporters
inferredcites →https://doi.org/10.1016/s0014-5793(97)01558-5openalex-snapshot
ABI2, a second protein phosphatase 2C involved in abscisic acid signal transduction in Arabidopsis
inferredcites →https://doi.org/10.1016/s0968-0004(00)89118-5openalex-snapshot
The G-box: a ubiquitous regulatory DNA element in plants bound by the GBF family of bZIP proteins
inferredcites →https://doi.org/10.1016/s1097-2765(03)00392-7openalex-snapshot
Structural Basis of Aurora-A Activation by TPX2 at the Mitotic Spindle
inferredcites →https://doi.org/10.1016/s1360-1385(01)02223-3openalex-snapshot
bZIP transcription factors in Arabidopsis
inferredcites →https://doi.org/10.1016/s1360-1385(99)01497-1openalex-snapshot
Formation and breakdown of ABA
inferredcites →https://doi.org/10.1016/s1369-5266(03)00092-xopenalex-snapshot
Regulatory network of gene expression in the drought and cold stress responses
inferredcites →https://doi.org/10.1016/s1572-5995(02)80040-0openalex-snapshot
Abscisic acid analogs for probing the mechanism of abscisic acid reception and inactivation
inferredcites →https://doi.org/10.1021/bi0014453openalex-snapshot
Inhibitors of Abscisic Acid 8‘-Hydroxylase
inferredcites →https://doi.org/10.1023/a:1006012218704openalex-snapshot
Molecular cloning in Arabidopsis thaliana of a new protein phosphatase 2C (PP2C) with homology to ABI1 and ABI2
inferredcites →https://doi.org/10.1023/a:1006058700720openalex-snapshot
Regulation of abscisic acid-induced transcription
inferredcites →https://doi.org/10.1038/376313a0openalex-snapshot
Mechanism of CDK activation revealed by the structure of a cyclinA-CDK2 complex
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/cr.2013.95openalex-snapshot
An ABA-mimicking ligand that reduces water loss and promotes drought resistance in plants
inferredcites →https://doi.org/10.1038/emboj.2011.294openalex-snapshot
A thermodynamic switch modulates abscisic acid receptor sensitivity
inferredcites →https://doi.org/10.1038/nature04373openalex-snapshot
The RNA-binding protein FCA is an abscisic acid receptor
inferredcites →https://doi.org/10.1038/nature05176openalex-snapshot
The Mg-chelatase H subunit is an abscisic acid receptor
inferredcites →https://doi.org/10.1038/nature06608openalex-snapshot
SLAC1 is required for plant guard cell S-type anion channel function in stomatal signalling
inferredcites →https://doi.org/10.1038/nature06720openalex-snapshot
CO2 regulator SLAC1 and its homologues are essential for anion homeostasis in plant cells
inferredcites →https://doi.org/10.1038/nature08075openalex-snapshot
Structural insight into the autoinhibition mechanism of AMP-activated protein kinase
inferredcites →https://doi.org/10.1038/nature08583openalex-snapshot
Structural basis of abscisic acid signalling
inferredcites →https://doi.org/10.1038/nature08591openalex-snapshot
The abscisic acid receptor PYR1 in complex with abscisic acid
inferredcites →https://doi.org/10.1038/nature08599openalex-snapshot
In vitro reconstitution of an abscisic acid signalling pathway
inferredcites →https://doi.org/10.1038/nature08613openalex-snapshot
A gate–latch–lock mechanism for hormone signalling by abscisic acid receptors
inferredcites →https://doi.org/10.1038/nsmb.1730openalex-snapshot
Structural insights into the mechanism of abscisic acid signaling by PYL proteins
inferredcites →https://doi.org/10.1038/nsmb.1887openalex-snapshot
Identification and mechanism of ABA receptor antagonism
inferredcites →https://doi.org/10.1038/nsmb.1898openalex-snapshot
Structural basis for selective activation of ABA receptors
inferredcites →https://doi.org/10.1038/sj.emboj.7600121openalex-snapshot
The Arabidopsis cytochrome P450 CYP707A encodes ABA 8′‐hydroxylases: key enzymes in ABA catabolism
inferredcites →https://doi.org/10.1042/bj20091221openalex-snapshot
Threonine at position 306 of the KAT1 potassium channel is essential for channel activity and is a target site for ABA-activated SnRK2/OST1/SnRK2.6 protein kinase
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.5060765.xopenalex-snapshot
Mutations at two new Arabidopsis ABA response loci are similar to the abi3 mutations
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00965.xopenalex-snapshot
The ABI1 and ABI2 protein phosphatases 2C act in a negative feedback regulatory loop of the abscisic acid signalling pathway
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01782.xopenalex-snapshot
Visualization of abscisic acid‐perception sites on the plasma membrane of stomatal guard cells
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01966.xopenalex-snapshot
Gain‐of‐function and loss‐of‐function phenotypes of the protein phosphatase 2C HAB1 reveal its role as a negative regulator of abscisic acid signalling
inferredcites →https://doi.org/10.1073/pnas.0505667103openalex-snapshot
Abscisic acid-dependent multisite phosphorylation regulates the activity of a transcription activator AREB1
inferredcites →https://doi.org/10.1073/pnas.0607656103openalex-snapshot
Surface comparison of active and inactive protein kinases identifies a conserved activation mechanism
inferredcites →https://doi.org/10.1073/pnas.0610251104openalex-snapshot
The hallmark of AGC kinase functional divergence is its C-terminal tail, a cis-acting regulatory module
inferredcites →https://doi.org/10.1073/pnas.081594298openalex-snapshot
A postgermination developmental arrest checkpoint is mediated by abscisic acid and requires the ABI5 transcription factor in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0903144106openalex-snapshot
Arabidopsis mutant deficient in 3 abscisic acid-activated protein kinases reveals critical roles in growth, reproduction, and stress
inferredcites →https://doi.org/10.1073/pnas.0907095106openalex-snapshot
Type 2C protein phosphatases directly regulate abscisic acid-activated protein kinases in Arabidopsis
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.0910601106openalex-snapshot
A protein kinase-phosphatase pair interacts with an ion channel to regulate ABA signaling in plant guard cells
inferredcites →https://doi.org/10.1073/pnas.0912021106openalex-snapshot
Activity of guard cell anion channel SLAC1 is controlled by drought-stress signaling kinase-phosphatase pair
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.1018367108openalex-snapshot
Arabidopsis decuple mutant reveals the importance of SnRK2 kinases in osmotic stress responses in vivo
inferredcites →https://doi.org/10.1073/pnas.1112838108openalex-snapshot
Potent and selective activation of abscisic acid receptors in vivo by mutational stabilization of their agonist-bound conformation
inferredcites →https://doi.org/10.1073/pnas.1118651109openalex-snapshot
Structural basis for basal activity and autoactivation of abscisic acid (ABA) signaling SnRK2 kinases
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.1305919110openalex-snapshot
Activation of dimeric ABA receptors elicits guard cell closure, ABA-regulated gene expression, and drought tolerance
inferredcites →https://doi.org/10.1073/pnas.190309197openalex-snapshot
Arabidopsis basic leucine zipper transcription factors involved in an abscisic acid-dependent signal transduction pathway under drought and high-salinity conditions
inferredcites →https://doi.org/10.1073/pnas.95.3.975openalex-snapshot
Mutational analysis of protein phosphatase 2C involved in abscisic acid signal transduction in higher plants
inferredcites →https://doi.org/10.1074/jbc.275.3.1723openalex-snapshot
ABFs, a Family of ABA-responsive Element Binding Factors
inferredcites →https://doi.org/10.1074/jbc.m110.149005openalex-snapshot
Functional Mechanism of the Abscisic Acid Agonist Pyrabactin
inferredcites →https://doi.org/10.1074/jbc.m110.160192openalex-snapshot
Single Amino Acid Alteration between Valine and Isoleucine Determines the Distinct Pyrabactin Selectivity by PYL1 and PYL2
inferredcites →https://doi.org/10.1074/jbc.m111.313106openalex-snapshot
Molecular Mechanism for Inhibition of a Critical Component in the Arabidopsis thaliana Abscisic Acid Signal Transduction Pathways, SnRK2.6, by Protein Phosphatase ABI1
inferredcites →https://doi.org/10.1074/jbc.m405259200openalex-snapshot
Identification of Nine Sucrose Nonfermenting 1-related Protein Kinases 2 Activated by Hyperosmotic and Saline Stresses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/jbc.m509820200openalex-snapshot
The Regulatory Domain of SRK2E/OST1/SnRK2.6 Interacts with ABI1 and Integrates Abscisic Acid (ABA) and Osmotic Stress Signals Controlling Stomatal Closure in Arabidopsis
inferredcites →https://doi.org/10.1093/bioinformatics/bti490openalex-snapshot
Cis-regulatory element based targeted gene finding: genome-wide identification of abscisic acid- and abiotic stress-responsive genes in Arabidopsis thaliana
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/jxb/47.8.1085openalex-snapshot
Metabolism of xylem-delivered ABA in relation to ABA flux and concentration in leaves of maize andCommelina communis
inferredcites →https://doi.org/10.1093/jxb/eri050openalex-snapshot
Characterization of three homologous basic leucine zipper transcription factors (bZIP) of the ABI5 family during Arabidopsis thaliana embryo maturation
inferredcites →https://doi.org/10.1093/jxb/eri290openalex-snapshot
Abscisic acid regulation of heterophylly in Marsilea quadrifolia L.: effects of R-(−) and S-(+) isomers
inferredcites →https://doi.org/10.1093/jxb/erq331openalex-snapshot
The sucrose non-fermenting-1-related (SnRK) family of protein kinases: potential for manipulation to improve stress tolerance and increase yield
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029375openalex-snapshot
Biological Activities of an Abscisic Acid Analog in Barley, Cress, and Rice
inferredcites →https://doi.org/10.1093/pcp/pcf188openalex-snapshot
ABA-Activated SnRK2 Protein Kinase is Required for Dehydration Stress Signaling in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pch171openalex-snapshot
Isolation and Characterization of Novel Mutants Affecting the Abscisic Acid Sensitivity of Arabidopsis Germination and Seedling Growth
inferredcites →https://doi.org/10.1093/pcp/pcp083openalex-snapshot
Three Arabidopsis SnRK2 Protein Kinases, SRK2D/SnRK2.2, SRK2E/SnRK2.6/OST1 and SRK2I/SnRK2.3, Involved in ABA Signaling are Essential for the Control of Seed Development and Dormancy
inferredcites →https://doi.org/10.1093/pcp/pcp147openalex-snapshot
Three SnRK2 Protein Kinases are the Main Positive Regulators of Abscisic Acid Signaling in Response to Water Stress in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcq156openalex-snapshot
Molecular Basis of the Core Regulatory Network in ABA Responses: Sensing, Signaling and Transport
inferredcites →https://doi.org/10.1096/fj.09-148064openalex-snapshot
Structure and function of polarity‐inducing kinase family MARK/Par‐1 within the branch of AMPK/Snf1‐related kinases
inferredcites →https://doi.org/10.1104/pp.003566openalex-snapshot
Arabidopsis ABI5 Subfamily Members Have Distinct DNA-Binding and Transcriptional Activities
inferredcites →https://doi.org/10.1104/pp.101.2.469openalex-snapshot
Competitive Inhibition of Abscisic Acid-Regulated Gene Expression by Stereoisomeric Acetylenic Analogs of Abscisic Acid
inferredcites →https://doi.org/10.1104/pp.102.011999openalex-snapshot
The Arabidopsis CDPK-SnRK Superfamily of Protein Kinases
inferredcites →https://doi.org/10.1104/pp.103.037614openalex-snapshot
Arabidopsis CYP707A s Encode (+)-Abscisic Acid 8′-Hydroxylase, a Key Enzyme in the Oxidative Catabolism of Abscisic Acid
inferredcites →https://doi.org/10.1104/pp.106.079327openalex-snapshot
Identification of Features Regulating OST1 Kinase Activity and OST1 Function in Guard Cells
inferredcites →https://doi.org/10.1104/pp.106.081018openalex-snapshot
Enhancement of Abscisic Acid Sensitivity and Reduction of Water Consumption in Arabidopsis by Combined Inactivation of the Protein Phosphatases Type 2C ABI1 and HAB1
inferredcites →https://doi.org/10.1104/pp.106.4.1279openalex-snapshot
The 7[prime]-Methyl Group of Abscisic Acid Is Critical for Biological Activity in Wheat Embryo Germination
inferredcites →https://doi.org/10.1104/pp.108.129791openalex-snapshot
Transcriptional Regulatory Networks in Response to Abiotic Stresses in Arabidopsis and Grasses
inferredcites →https://doi.org/10.1104/pp.108.130823openalex-snapshot
High Humidity Induces Abscisic Acid 8′-Hydroxylase in Stomata and Vasculature to Regulate Local and Systemic Abscisic Acid Responses in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.2.563openalex-snapshot
Induction of Lipid and Oleosin Biosynthesis by (+)-Abscisic Acid and Its Metabolites in Microspore-Derived Embryos of Brassica napus L.cv Reston (Biological Responses in the Presence of 8[prime]-Hydroxyabscisic Acid)
inferredcites →https://doi.org/10.1104/pp.109.137174openalex-snapshot
Triple Loss of Function of Protein Phosphatases Type 2C Leads to Partial Constitutive Response to Endogenous Abscisic Acid
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.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.113.224162openalex-snapshot
The PYL4 A194T Mutant Uncovers a Key Role of PYR1-LIKE4/PROTEIN PHOSPHATASE 2CA Interaction for Abscisic Acid Signaling and Plant Drought Resistance
inferredcites →https://doi.org/10.1105/tpc.000596openalex-snapshot
Cell Signaling during Cold, Drought, and Salt Stress
inferredcites →https://doi.org/10.1105/tpc.000869openalex-snapshot
The Homologous ABI5 and EEL Transcription Factors Function Antagonistically to Fine-Tune Gene Expression during Late Embryogenesis
inferredcites →https://doi.org/10.1105/tpc.007906openalex-snapshot
Arabidopsis OST1 Protein Kinase Mediates the Regulation of Stomatal Aperture by Abscisic Acid and Acts Upstream of Reactive Oxygen Species Production
inferredcites →https://doi.org/10.1105/tpc.010101openalex-snapshot
The Arabidopsis LOS5/ABA3 Locus Encodes a Molybdenum Cofactor Sulfurase and Modulates Cold Stress– and Osmotic Stress–Responsive Gene Expression
inferredcites →https://doi.org/10.1105/tpc.010362openalex-snapshot
Arabidopsis Basic Leucine Zipper Proteins That Mediate Stress-Responsive Abscisic Acid Signaling
inferredcites →https://doi.org/10.1105/tpc.10.6.1043openalex-snapshot
The Arabidopsis Abscisic Acid Response Locus ABI4 Encodes an APETALA2 Domain Protein
inferredcites →https://doi.org/10.1105/tpc.105.035659openalex-snapshot
AREB1 Is a Transcription Activator of Novel ABRE-Dependent ABA Signaling That Enhances Drought Stress Tolerance in Arabidopsis
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.11.10.1897openalex-snapshot
ABI1 Protein Phosphatase 2C Is a Negative Regulator of Abscisic Acid Signaling
inferredcites →https://doi.org/10.1105/tpc.112.095935openalex-snapshot
A Vacuolar β-Glucosidase Homolog That Possesses Glucose-Conjugated Abscisic Acid Hydrolyzing Activity Plays an Important Role in Osmotic Stress Responses 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.12.4.599openalex-snapshot
The Arabidopsis Abscisic Acid Response Gene ABI5 Encodes a Basic Leucine Zipper Transcription Factor
inferredcites →https://doi.org/10.1105/tpc.6.11.1567openalex-snapshot
Regulation of gene expression programs during Arabidopsis seed development: roles of the ABI3 locus and of endogenous abscisic acid.
inferredcites →https://doi.org/10.1105/tpc.9.5.759openalex-snapshot
The Arabidopsis ABSCISIC ACID-INSENSITIVE2 (ABI2) and ABI1 genes encode homologous protein phosphatases 2C involved in abscisic acid signal transduction.
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.2006.02683.xopenalex-snapshot
CYP707A3, a major ABA 8′‐hydroxylase involved in dehydration and rehydration response in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03056.xopenalex-snapshot
Structural analogs of ABA reveal novel features of ABA perception and signaling in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03454.xopenalex-snapshot
Nuclear localization of the mutant protein phosphatase abi1 is required for insensitivity towards ABA responses in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03981.xopenalex-snapshot
EXPRESSION OF CONCERN: Modulation of drought resistance by the abscisic acid receptor PYL5 through inhibition of clade A PP2Cs
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04054.xopenalex-snapshot
PYR/PYL/RCAR family members are major in‐vivo ABI1 protein phosphatase 2C‐interacting proteins in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04092.xopenalex-snapshot
AREB1, AREB2, and ABF3 are master transcription factors that cooperatively regulate ABRE-dependent ABA signaling involved in drought stress tolerance and require ABA for full activation
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04281.xopenalex-snapshot
Phospho-site mapping, genetic and in planta activation studies reveal key aspects of the different phosphorylation mechanisms involved in activation of SnRK2s
inferredcites →https://doi.org/10.1111/j.1399-3054.1984.tb06343.xopenalex-snapshot
The isolation and characterization of abscisic acid‐insensitive mutants of Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1399-3054.2005.00601.xopenalex-snapshot
The role of ABF family bZIP class transcription factors in stress response
inferredcites →https://doi.org/10.1126/science.1135882openalex-snapshot
A G Protein-Coupled Receptor Is a Plasma Membrane Receptor for the Plant Hormone Abscisic Acid
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.1181829openalex-snapshot
Structural Mechanism of Abscisic Acid Binding and Signaling by Dimeric PYR1
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/science.298.5602.2296openalex-snapshot
Small RNAs Make Big Splash
inferredcites →https://doi.org/10.1126/science.7910981openalex-snapshot
Arabidopsis ABA Response Gene ABI1 : Features of a Calcium-Modulated Protein Phosphatase
inferredcites →https://doi.org/10.1126/science.8197457openalex-snapshot
A Protein Phosphatase 2C Involved in ABA Signal Transduction in Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/scisignal.3103eg1openalex-snapshot
2009: Signaling Breakthroughs of the Year
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-042809-112226openalex-snapshot
Guard Cell Signal Transduction Network: Advances in Understanding Abscisic Acid, CO2, and Ca2+Signaling
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.25.060174.001355openalex-snapshot
The Chemistry and Physiology of Abscisic Acid
inferredcites →https://doi.org/10.1186/1471-2164-8-260openalex-snapshot
Genome-wide analysis of ABA-responsive elements ABRE and CE3 reveals divergent patterns in Arabidopsis and rice
inferredcites →https://doi.org/10.1371/journal.pone.0067477openalex-snapshot
Structural Insights into the Abscisic Acid Stereospecificity by the ABA Receptors PYR/PYL/RCAR
inferredcites →https://doi.org/10.21273/horttech.16.1.0071openalex-snapshot
Evaluation of Abscisic Acid Analogs as Holding Agents for Bedding Plant Seedlings
inferredcites →https://doi.org/10.2307/3871428openalex-snapshot
The Arabidopsis LOS5/ABA3 Locus Encodes a Molybdenum Cofactor Sulfurase and Modulates Cold Stress- and Osmotic Stress-Responsive Gene Expression
inferredcites →https://doi.org/10.4161/psb.19694openalex-snapshot
Catalytic mechanism and kinase interactions of ABA-signaling PP2C phosphatases
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1007/s00425-026-05082-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11816-023-00852-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-90594-7.00007-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-91225-9.00014-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-91722-3.00018-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-95375-7.00001-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-18927-2.00009-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-30244-2.00027-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-44994-9.00009-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.abr.2022.03.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.abr.2022.03.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.aac.2023.09.003openalex-snapshot
Development of abscisic acid receptor agonists/antagonists and their application prospect in agriculture: An overview
inferred← citeshttps://doi.org/10.1016/j.agwat.2020.106528openalex-snapshot
Yield improvement by antitranspirant application in droughted wheat is associated with reduced endogenous abscisic acid concentration
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.10.028openalex-snapshot
Mutations in the Arabidopsis Lst8 and Raptor genes encoding partners of the TOR complex, or inhibition of TOR activity decrease abscisic acid (ABA) synthesis
inferred← citeshttps://doi.org/10.1016/j.biocel.2016.03.006openalex-snapshot
Abscisic acid influx into human nucleated cells occurs through the anion exchanger AE2
inferred← citeshttps://doi.org/10.1016/j.cj.2021.06.011openalex-snapshot
RNAi-mediated suppression of the abscisic acid catabolism gene OsABA8ox1 increases abscisic acid content and tolerance to saline–alkaline stress in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/j.cpb.2025.100532openalex-snapshot
The carotenoid biosynthesis pathway revealed to respond to Na2SiO3 stress on cotton growth
inferred← citeshttps://doi.org/10.1016/j.cpb.2025.100544openalex-snapshot
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Amino acid motifs for the identification of novel protein interactants
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104404openalex-snapshot
NCED expression is related to increased ABA biosynthesis and stomatal closure under aluminum stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2025.106240openalex-snapshot
From signal perception to adaptive responses: A comprehensive review of plant mechanisms under cadmium, lead, and aluminum stress
inferred← citeshttps://doi.org/10.1016/j.fcr.2016.12.024openalex-snapshot
Priming of rice ( Oryza sativa L.) seedlings with abscisic acid enhances seedling survival, plant growth, and grain yield in saline-alkaline paddy fields
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.ijbiomac.2024.134950openalex-snapshot
ArNAC148 induces Acer rubrum leaf senescence by activating the transcription of the ABA receptor gene ArPYR13
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144004openalex-snapshot
Methyl jasmonate-loaded chitosan nanoparticles improve tea drought resistance on drought-sensitive cultivar ‘Zhongcha 108’
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.149871openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.119087openalex-snapshot
Identification of SnRK2 family and functional study of PeSnRK2.2A and PeSnRK2.2B for drought resistance in Phyllostachys edulis
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133462openalex-snapshot
Overexpression of NtDOGL4 improves cadmium tolerance through abscisic acid signaling pathway in tobacco
inferred← citeshttps://doi.org/10.1016/j.jksus.2024.103412openalex-snapshot
An overview of the molecular and biochemical components of seed dormancy and germination in Brassica napus
inferred← citeshttps://doi.org/10.1016/j.jplph.2023.154060openalex-snapshot
A novel ABA-induced transcript factor from Millettia pinnata, MpAITR1, enhances salt and drought tolerance through ABA signaling in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.jplph.2024.154413openalex-snapshot
Overexpression of the constitutively-active AtCPK1 mutant in tobacco plants confers cold and heat tolerance, possibly through modulating abscisic acid and salicylic acid signalling
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154710openalex-snapshot
The transcription factor OsERF74 positively regulates drought resistance by modulating abscisic acid catabolism in rice
inferred← citeshttps://doi.org/10.1016/j.microb.2025.100561openalex-snapshot
Trehalose–abscisic acid pathway feedback loops in wheat – Piriformospora indica symbiosis: Mechanisms and drought resilience
inferred← citeshttps://doi.org/10.1016/j.phytochem.2014.11.008openalex-snapshot
Interplays between the cell wall and phytohormones in interaction between plants and necrotrophic pathogens
inferred← citeshttps://doi.org/10.1016/j.plana.2026.100256openalex-snapshot
Unravelling the nanoparticle-mediated regulation of phytohormone biosynthesis and signalling
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110188openalex-snapshot
OsNCED5, a 9-cis-epoxycarotenoid dioxygenase gene, regulates salt and water stress tolerance and leaf senescence in rice
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.110983openalex-snapshot
AtMYB32 regulates the ABA response by targeting ABI3, ABI4 and ABI5 and the drought response by targeting CBF4 in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111432openalex-snapshot
Genetic variation of seed dormancy in wheat (Triticum aestivum L.) is mediated by transcriptional regulation of abscisic acid metabolism and signaling
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111608openalex-snapshot
GhMYB102 promotes drought resistance by regulating drought-responsive genes and ABA biosynthesis in cotton (Gossypium hirsutum L.)
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112541openalex-snapshot
ABA and defoliation improve phenolic composition of wine grapes while ABA reduces must free amino acid content and modifies its profile
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112690openalex-snapshot
PYL2 regulates drought and blast (Magnaporthe oryzae) resistance in rice
inferred← citeshttps://doi.org/10.1016/j.plaphy.2017.12.016openalex-snapshot
Abscisic acid mediated differential growth responses of root and shoot of Vigna radiata (L.) Wilczek seedlings under water stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108259openalex-snapshot
The molecular paradigm of reactive oxygen species (ROS) and reactive nitrogen species (RNS) with different phytohormone signaling pathways during drought stress in plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108409openalex-snapshot
Melatonin-mediated regulation of autophagy is independent of ABA under drought stress in sensitive variety of Gossypium hirsutum L.
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111732openalex-snapshot
Beyond stomata: a novel role of EPFL9-2 in regulating root system architecture and hydraulics in grapevine
inferred← citeshttps://doi.org/10.1016/j.plgene.2017.04.008openalex-snapshot
Abscisic acid — An enigma in the abiotic stress tolerance of crop plants
inferred← citeshttps://doi.org/10.1016/j.plgene.2017.07.003openalex-snapshot
Abscisic acid: A key regulator of abiotic stress tolerance in plants
inferred← citeshttps://doi.org/10.1016/j.scib.2026.03.023openalex-snapshot
Molecular mechanisms and genic resources responsive to salinity stress and their applications in maize and other crop breeding
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111302openalex-snapshot
Plant hormone-mediated stress regulation responses in fruit crops- a review
inferred← citeshttps://doi.org/10.1016/j.scienta.2025.114119openalex-snapshot
Genome-wide analysis of potato xyloglucan endotransglucosylase/hydrolase (XTH) gene family revealed StXTH9 involved in drought stress responses
inferred← citeshttps://doi.org/10.1016/j.scienta.2026.114888openalex-snapshot
Combined foliar application of CLE25 and EGCG enhances drought resilience and recovery in tea plants
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100359openalex-snapshot
Unlocking nature's stress buster: Abscisic acid's crucial role in defending plants against abiotic stress
inferred← citeshttps://doi.org/10.1016/j.tibs.2020.11.004openalex-snapshot
A Tour of TOR Complex Signaling in Plants
inferred← citeshttps://doi.org/10.1016/j.ygeno.2025.111088openalex-snapshot
DNA methylation, metabolome, and transcriptome analysis reveal epigenomic differences between diploid Chinese cabbage seeds and tetraploid Chinese cabbage seeds
inferred← citeshttps://doi.org/10.1021/acs.biomac.4c01095openalex-snapshot
Recombinant Fusion Proteins with Embedded Sensing Functions as Versatile Tools for Protocell Development
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c09429openalex-snapshot
Synthesis, Plant Growth Regulatory Activity, and Transcriptome Analysis of Novel Opabactin Analogs
inferred← citeshttps://doi.org/10.1038/s41467-025-59329-6openalex-snapshot
Unveiling the regulatory role of GRP7 in ABA signal-mediated mRNA translation efficiency regulation
inferred← citeshttps://doi.org/10.1038/s41467-025-59332-xopenalex-snapshot
A SnRK2-HAK regulatory module confers natural variation of salt tolerance in maize
inferred← citeshttps://doi.org/10.1038/s41477-023-01510-0openalex-snapshot
Structural basis for abscisic acid efflux mediated by ABCG25 in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/s41597-024-04324-7openalex-snapshot
Transcriptome and translatome profiling of Col-0 and grp7grp8 under ABA treatment in Arabidopsis
inferred← citeshttps://doi.org/10.1038/srep26658openalex-snapshot
G-protein coupling and nuclear translocation of the human abscisic acid receptor LANCL2
inferred← citeshttps://doi.org/10.1071/cp19392openalex-snapshot
Genome-wide identification and expression analysis of SnRK2 gene family in mungbean (Vigna radiata) in response to drought stress
inferred← citeshttps://doi.org/10.1071/cp25043openalex-snapshot
The role of wheat long intergenic non-coding RNAs in drought stress
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/10.1080/17429145.2021.1925759openalex-snapshot
Insight into abscisic acid perception and signaling to increase plant tolerance to abiotic stress
inferred← citeshttps://doi.org/10.1093/jxb/eraa291openalex-snapshot
Integration of silicon and secondary metabolites in plants: a significant association in stress tolerance
inferred← citeshttps://doi.org/10.1093/jxb/erad087openalex-snapshot
Laminarin-triggered defence responses are geographically dependent in natural populations of Solanum chilense
inferred← citeshttps://doi.org/10.1093/jxb/erae482openalex-snapshot
Toward understanding grapevine responses to climate change: a multi-stress and holistic approach
inferred← citeshttps://doi.org/10.1093/jxb/eraf418openalex-snapshot
The confluence of TOR signalling and plant growth regulators in development and stress responses
inferred← citeshttps://doi.org/10.1093/jxb/erz531openalex-snapshot
ABA perception is modulated by membrane receptor-like kinases
inferred← citeshttps://doi.org/10.1093/pcp/pcx074openalex-snapshot
Dormancy-Associated MADS-Box (DAM) and the Abscisic Acid Pathway Regulate Pear Endodormancy Through a Feedback Mechanism
inferred← citeshttps://doi.org/10.1093/pcp/pcx096openalex-snapshot
An Apple Protein Kinase MdSnRK1.1 Interacts with MdCAIP1 to Regulate ABA Sensitivity
inferred← citeshttps://doi.org/10.1093/plphys/kiac280openalex-snapshot
Analysis of the Arabidopsiscoilinmutant reveals a positive role of AtCOILIN in plant immunity
inferred← citeshttps://doi.org/10.1093/plphys/kiad051openalex-snapshot
Mutations in RZF1, a zinc-finger protein, reduce magnesium uptake in roots and translocation to shoots in rice
inferred← citeshttps://doi.org/10.1093/plphys/kiae215openalex-snapshot
Spider mite herbivory induces an ABA-driven stomatal defense
inferred← citeshttps://doi.org/10.1093/plphys/kiae674openalex-snapshot
Phase separation of MYB73 regulates seed oil biosynthesis in Arabidopsis
inferred← citeshttps://doi.org/10.1093/treephys/tpac130openalex-snapshot
High abscisic acid and low root hydraulic conductivity may explain low leaf hydration in ‘Mandarin’ lime exposed to aluminum
inferred← citeshttps://doi.org/10.1101/2021.04.25.441358openalex-snapshot
Abscisic acid modulates auxin-responsive hypocotyl elongation
inferred← citeshttps://doi.org/10.1101/2022.06.21.497044openalex-snapshot
MicroProteins miP1b/BBX30 and miP1a/BBX31 form a positive feedback loop with ABI5 to retard seedling establishment
inferred← citeshttps://doi.org/10.1101/2023.05.16.540971openalex-snapshot
Sense and Screen-ability: Development of tuneable, biosensor-based screening platforms for abscisic acid
inferred← citeshttps://doi.org/10.1101/2023.09.29.555308openalex-snapshot
Stomata, a vulnerability in the plant defence against phytophagous mites that ABA can overcome
inferred← citeshttps://doi.org/10.1101/2025.01.03.631192openalex-snapshot
Spatiotemporal transcriptional networks control the plasticity of chickpea root exodermis
inferred← citeshttps://doi.org/10.1101/2025.01.24.634672openalex-snapshot
High-resolution spatial transcriptomics of stem and storage root vascular cambia highlights key regulatory processes for xylem parenchyma differentiation in cassava
inferred← citeshttps://doi.org/10.1101/519199openalex-snapshot
Rice annexin OsANN4 interacting with OsCDPK24, reduces root aerenchyma formation by modulating H 2 O 2 under ABA treatment
inferred← citeshttps://doi.org/10.1101/813717openalex-snapshot
Biochemical, Biophysical, and Functional Analyses of Two Isoforms of the SnRK2 inhibitor AtSCS
inferred← citeshttps://doi.org/10.1104/pp.19.00900openalex-snapshot
Two SnRK2-Interacting Calcium Sensor Isoforms Negatively Regulate SnRK2 Activity by Different Mechanisms
inferred← citeshttps://doi.org/10.1111/jipb.13225openalex-snapshot
Auxin signaling: Research advances over the past 30 years
inferred← citeshttps://doi.org/10.1111/jipb.70238openalex-snapshot
Towards an integrated molecular understanding of plant hormones
inferred← citeshttps://doi.org/10.1111/nph.71203openalex-snapshot
Pseudomonas volatiles shape the root transcriptome and microbiome to promote plant growth under drought
inferred← citeshttps://doi.org/10.1111/nph.71537openalex-snapshot
The CmABI5 ‐ CmKN1 module regulates seasonal growth and flowering in response to chilling in chrysanthemum
inferred← citeshttps://doi.org/10.1111/pbi.70597openalex-snapshot
The BAHD Acyltransferase Gene Family: Evolutionary Dynamics, Biochemical Mechanisms, and Roles in Plant Stress Adaptation
inferred← citeshttps://doi.org/10.1111/ppl.14271openalex-snapshot
Ascorbic acid releases dormancy and promotes germination by an integrated regulation of abscisic acid and gibberellin in Pyrus betulifolia seeds
inferred← citeshttps://doi.org/10.1111/ppl.70000openalex-snapshot
Diverse functional interactions between ABA and ethylene in plant development and responses to stress
inferred← citeshttps://doi.org/10.1111/ppl.70159openalex-snapshot
Role of pepper bZIP transcription factor CaADBZ1 in abscisic acid signalling and drought stress response
inferred← citeshttps://doi.org/10.1111/ppl.70522openalex-snapshot
Functional Analysis of the Pepper RING ‐Type E3 Ligase CaANKR1 Involved in Drought Stress Tolerance via Modulation of Abscisic Acid Signaling
inferred← citeshttps://doi.org/10.1126/sciadv.adt2842openalex-snapshot
Abscisic acid enhances DNA damage response through the nuclear shuttling of clathrin light chain 2 in plant cells
inferred← citeshttps://doi.org/10.1128/mmbr.00261-25openalex-snapshot
Phytohormones in fungi: inter-kingdom modulators or fungal self-controlling elements?
inferred← citeshttps://doi.org/10.1146/annurev-arplant-060625-095356openalex-snapshot
Structural Insights into Plant Hormone-Sensing Mechanisms
inferred← citeshttps://doi.org/10.1186/s12864-024-11089-1openalex-snapshot
Identifying candidate genes for sugar accumulation in sugarcane: an integrative approach
inferred← citeshttps://doi.org/10.1186/s12864-025-12076-wopenalex-snapshot
High-resolution transcriptomics of stem and storage root vascular cambia highlight regulatory processes for xylem parenchyma differentiation in cassava
inferred← citeshttps://doi.org/10.1186/s12870-018-1250-4openalex-snapshot
Comparative analysis of alfalfa (Medicago sativa L.) leaf transcriptomes reveals genotype-specific salt tolerance mechanisms
inferred← citeshttps://doi.org/10.1186/s12870-019-1665-6openalex-snapshot
Transcriptome and metabolome analyses of two contrasting sesame genotypes reveal the crucial biological pathways involved in rapid adaptive response to salt stress
inferred← citeshttps://doi.org/10.1186/s12870-019-1970-0openalex-snapshot
Integrative omics analysis on phytohormones involved in oil palm seed germination
inferred← citeshttps://doi.org/10.1186/s12870-024-06010-7openalex-snapshot
The StbHLH47 transcription factor negatively regulates drought tolerance in potato (Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.1186/s12870-025-06654-zopenalex-snapshot
Mapping the molecular signature of ABA-regulated gene expression in germinating barley embryos
inferred← citeshttps://doi.org/10.1186/s12870-025-07938-0openalex-snapshot
An evolutionary conserved CBL1–CIPK6 complex of oil persimmon involved in responses to ABA, salt and drought stress
inferred← citeshttps://doi.org/10.1186/s12870-026-08477-yopenalex-snapshot
Molecular mechanisms of ABA-mediated cold stress response in Dendrobium officinale
inferred← citeshttps://doi.org/10.1242/jcs.210492openalex-snapshot
Abscisic acid – an anti-angiogenic phytohormone that modulates the phenotypical plasticity of endothelial cells and macrophages
inferred← citeshttps://doi.org/10.13080/z-a.2022.109.003openalex-snapshot
Effect of pre-sowing priming of seeds with exogenous abscisic acid on endogenous hormonal balance of spelt wheat under heat stress
inferred← citeshttps://doi.org/10.1371/journal.pone.0113643openalex-snapshot
H2O2 Inhibits ABA-Signaling Protein Phosphatase HAB1
inferred← citeshttps://doi.org/10.1371/journal.pone.0213963openalex-snapshot
An abscisic acid (ABA) homeostasis regulated by its production, catabolism and transport in peanut leaves in response to drought stress
inferred← citeshttps://doi.org/10.1371/journal.pone.0234317openalex-snapshot
Comparative physiological and proteomic analysis indicates lower shock response to drought stress conditions in a self-pollinating perennial ryegrass
inferred← citeshttps://doi.org/10.1371/journal.pone.0253555openalex-snapshot
Environmental responsiveness of flowering time in cassava genotypes and associated transcriptome changes
inferred← citeshttps://doi.org/10.14719/pst.2021.8.3.1208openalex-snapshot
In silico promoter and expression analyses of rice Auxin Binding Protein 57 (ABP57)
inferred← citeshttps://doi.org/10.15666/aeer/1604_50055023openalex-snapshot
ENHANCEMENT IN PLANT WATER RELATIONS AND FATTY ACID PROFILE IN SUNFLOWER (HELIANTHUS ANNUUS L.) THROUGH APPLICATION OF ABSCISIC ACID UNDER VARIED WATER LEVELS
inferred← citeshttps://doi.org/10.15666/aeer/1906_46994720openalex-snapshot
A GIBBERELLIN, ABSCISIC ACID, AND DELAY OF GERMINATION 1 INTERACTION NETWORK REGULATES CRITICAL DEVELOPMENTAL TRANSITIONS IN MODEL PLANT ARABIDOPSIS THALIANA – A REVIEW
inferred← citeshttps://doi.org/10.17660/ejhs.2023/019openalex-snapshot
Retardation of ABA 8′-hydroxylase affects endogenous ABA, sugar metabolism, and aroma volatiles in grape berries
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3344350/v1openalex-snapshot
Physiological characteristics and transcriptomic analysis of response patterns of Gynura divaricata under NaCl stress
inferred← citeshttps://doi.org/10.26420/annagriccropsci.2021.1070openalex-snapshot
Role of ABA in Overcoming Environmental Stress: Sensing, Signaling and Crosstalk
inferred← citeshttps://doi.org/10.31390/gradschool_dissertations.5692openalex-snapshot
Insights into Abscisic Acid and Phosphatidic Acid Signal Transduction Dynamics in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.32604/phyton.2024.058012openalex-snapshot
Interplay between Plants and Microbial Communities: Insights from Holobionts and Environmental Interactions
inferred← citeshttps://doi.org/10.32717/0131-0062-2020-68-63-75openalex-snapshot
ЕФЕКТИВНІСТЬ РЕГУЛЯТОРІВ РОСТУ В ОВОЧІВНИЦТВІ
inferred← citeshttps://doi.org/10.3389/fagro.2023.1293555openalex-snapshot
Insights into mode of action mediated responses following pharmaceutical uptake and accumulation in plants
inferred← citeshttps://doi.org/10.3389/feart.2022.848924openalex-snapshot
Characteristics of Plastic Greenhouse High-Temperature and High-Humidity Events and Their Impacts on Facility Tomatoes Growth
inferred← citeshttps://doi.org/10.3389/fpls.2016.00571openalex-snapshot
Abscisic Acid and Abiotic Stress Tolerance in Crop Plants
inferred← citeshttps://doi.org/10.3389/fpls.2016.00612openalex-snapshot
Heterologous Overexpression of Poplar SnRK2 Genes Enhanced Salt Stress Tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2016.01099openalex-snapshot
Molecular Characterization of the 14-3-3 Gene Family in Brachypodium distachyon L. Reveals High Evolutionary Conservation and Diverse Responses to Abiotic Stresses
inferred← citeshttps://doi.org/10.3389/fpls.2016.01489openalex-snapshot
Abscisic Acid-Induced H2O2 Accumulation Enhances Antioxidant Capacity in Pumpkin-Grafted Cucumber Leaves under Ca(NO3)2 Stress
inferred← citeshttps://doi.org/10.3389/fpls.2017.01362openalex-snapshot
Ascophyllum nodosum Seaweed Extract Alleviates Drought Stress in Arabidopsis by Affecting Photosynthetic Performance and Related Gene Expression
inferred← citeshttps://doi.org/10.3389/fpls.2018.00162openalex-snapshot
9-cis-Epoxycarotenoid Dioxygenase 3 Regulates Plant Growth and Enhances Multi-Abiotic Stress Tolerance in Rice
inferred← citeshttps://doi.org/10.3389/fpls.2018.00668openalex-snapshot
Molecular Mechanisms Underlying Abscisic Acid/Gibberellin Balance in the Control of Seed Dormancy and Germination in Cereals
inferred← citeshttps://doi.org/10.3389/fpls.2018.00838openalex-snapshot
Regulation of Seed Germination and Abiotic Stresses by Gibberellins and Abscisic Acid
inferred← citeshttps://doi.org/10.3389/fpls.2018.01771openalex-snapshot
Abiotic Stresses: General Defenses of Land Plants and Chances for Engineering Multistress Tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2019.00267openalex-snapshot
Somatic Embryogenesis in the Medicago truncatula Model: Cellular and Molecular Mechanisms
inferred← citeshttps://doi.org/10.3389/fpls.2019.01722openalex-snapshot
Photosynthetic Regulation Under Salt Stress and Salt-Tolerance Mechanism of Sweet Sorghum
inferred← citeshttps://doi.org/10.3389/fpls.2020.00785openalex-snapshot
SiMYB56 Confers Drought Stress Tolerance in Transgenic Rice by Regulating Lignin Biosynthesis and ABA Signaling Pathway
inferred← citeshttps://doi.org/10.3389/fpls.2020.582353openalex-snapshot
Ribosomal Protein RPL10A Contributes to Early Plant Development and Abscisic Acid-Dependent Responses in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2020.583767openalex-snapshot
Promoted ABA Hydroxylation by Capsicum annuum CYP707As Overexpression Suppresses Pollen Maturation in Nicotiana tabacum
inferred← citeshttps://doi.org/10.3389/fpls.2021.644823openalex-snapshot
Signal Integration in Plant Abiotic Stress Responses via Multistep Phosphorelay Signaling
inferred← citeshttps://doi.org/10.3389/fpls.2021.743832openalex-snapshot
The Loss of Function of the NODULE INCEPTION-Like PROTEIN 7 Enhances Salt Stress Tolerance in Arabidopsis Seedlings
inferred← citeshttps://doi.org/10.3389/fpls.2022.1028392openalex-snapshot
Role of pepper MYB transcription factor CaDIM1 in regulation of the drought response
inferred← citeshttps://doi.org/10.3389/fpls.2022.882596openalex-snapshot
RNA-Binding Proteins: The Key Modulator in Stress Granule Formation and Abiotic Stress Response
inferred← citeshttps://doi.org/10.3389/fpls.2022.972856openalex-snapshot
Abscisic acid: Metabolism, transport, crosstalk with other plant growth regulators, and its role in heavy metal stress mitigation
inferred← citeshttps://doi.org/10.3389/fpls.2023.1121809openalex-snapshot
SiNCED1, a 9-cis-epoxycarotenoid dioxygenase gene in Setaria italica, is involved in drought tolerance and seed germination in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2023.1154571openalex-snapshot
Detoxifying the heavy metals: a multipronged study of tolerance strategies against heavy metals toxicity in plants
inferred← citeshttps://doi.org/10.3389/fpls.2023.1192652openalex-snapshot
Dry side of the core: a meta-analysis addressing the original nature of the ABA signalosome at the onset of seed imbibition
inferred← citeshttps://doi.org/10.3389/fpls.2023.1227507openalex-snapshot
Analysis of the response mechanisms of Pinellia ternata to terahertz wave stresses using transcriptome and metabolic data
inferred← citeshttps://doi.org/10.3389/fpls.2024.1437184openalex-snapshot
Unveiling the crucial roles of abscisic acid in plant physiology: implications for enhancing stress tolerance and productivity
inferred← citeshttps://doi.org/10.3389/fpls.2026.1809056openalex-snapshot
Abscisic acid binds to an Arabidopsis thaliana phosphodiesterase and tunes its activity
inferred← citeshttps://doi.org/10.3390/agronomy13041088openalex-snapshot
Outcome of Microalgae Biomass Application on Seed Germination and Hormonal Activity in Winter Wheat Leaves
inferred← citeshttps://doi.org/10.3390/agronomy13122957openalex-snapshot
A Review of the Diverse Genes and Molecules Involved in Sucrose Metabolism and Innovative Approaches to Improve Sucrose Content in Sugarcane
inferred← citeshttps://doi.org/10.3390/agronomy14081736openalex-snapshot
Transcriptome Analysis Reveals the Effects of Exogenous Gibberellin on the Germination of Solanum torvum Seeds
inferred← citeshttps://doi.org/10.3390/biology12081143openalex-snapshot
Plant Hormone Modularity and the Survival-Reproduction Trade-Off
inferred← citeshttps://doi.org/10.3390/biom10020281openalex-snapshot
Auxin-Abscisic Acid Interactions in Plant Growth and Development
inferred← citeshttps://doi.org/10.3390/biom13101554openalex-snapshot
Effect of ABA Pre-Treatment on Rice Plant Transcriptome Response to Multiple Abiotic Stress
inferred← citeshttps://doi.org/10.3390/books978-3-0365-5023-7openalex-snapshot
Advances in the Molecular Mechanisms of Abscisic Acid and Gibberellins Functions in Plants 2.0
inferred← citeshttps://doi.org/10.3390/cells10092180openalex-snapshot
The Multifaceted Regulation of SnRK2 Kinases
inferred← citeshttps://doi.org/10.3390/cells11081352openalex-snapshot
PYR/PYL/RCAR Receptors Play a Vital Role in the Abscisic-Acid-Dependent Responses of Plants to External or Internal Stimuli
inferred← citeshttps://doi.org/10.3390/ijms21249517openalex-snapshot
Transcriptional Regulation of Protein Phosphatase 2C Genes to Modulate Abscisic Acid Signaling
inferred← citeshttps://doi.org/10.3390/ijms22062914openalex-snapshot
Jasmonic Acid Signaling and Molecular Crosstalk with Other Phytohormones
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