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Group A PP2Cs evolved in land plants as key regulators of intrinsic desiccation tolerance
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00201503openalex-snapshot
Abscisic-acid-induced drought tolerance in Funaria hygrometrica Hedw.
inferredcites →https://doi.org/10.1007/s00425-004-1361-zopenalex-snapshot
Cold acclimation in bryophytes: low-temperature-induced freezing tolerance in Physcomitrella patens is associated with increases in expression levels of stress-related genes but not with increase in level of endogenous abscisic acid
inferredcites →https://doi.org/10.1007/s10265-011-0410-5openalex-snapshot
ABA in bryophytes: how a universal growth regulator in life became a plant hormone?
inferredcites →https://doi.org/10.1007/s10725-010-9490-9openalex-snapshot
Desiccation sensitivity and tolerance in the moss Physcomitrella patens: assessing limits and damage
inferredcites →https://doi.org/10.1007/s11103-006-9079-xopenalex-snapshot
A rice dehydration-inducible SNF1-related protein kinase 2 phosphorylates an abscisic acid responsive element-binding factor and associates with ABA signaling
inferredcites →https://doi.org/10.1007/s11103-006-9103-1openalex-snapshot
Different phosphorylation mechanisms are involved in the activation of sucrose non-fermenting 1 related protein kinases 2 by osmotic stresses and abscisic acid
inferredcites →https://doi.org/10.1007/s11103-009-9476-zopenalex-snapshot
Functional analyses of the ABI1-related protein phosphatase type 2C reveal evolutionarily conserved regulation of abscisic acid signaling between Arabidopsis and the moss Physcomitrella patens
inferredcites →https://doi.org/10.1016/j.cub.2011.04.032openalex-snapshot
Regulatory Mechanism Controlling Stomatal Behavior Conserved across 400 Million Years of Land Plant Evolution
inferredcites →https://doi.org/10.1016/j.cub.2011.04.044openalex-snapshot
Land Plants Acquired Active Stomatal Control Early in Their Evolutionary History
inferredcites →https://doi.org/10.1016/j.jplph.2011.08.004openalex-snapshot
Cold acclimation in the moss Physcomitrella patens involves abscisic acid-dependent signaling
inferredcites →https://doi.org/10.1016/j.phytochem.2006.01.031openalex-snapshot
Accumulation of theanderose in association with development of freezing tolerance in the moss Physcomitrella patens
inferredcites →https://doi.org/10.1016/s0065-2296(08)00404-7openalex-snapshot
Late Embryogenesis Abundant Proteins
inferredcites →https://doi.org/10.1023/a:1026550808557openalex-snapshot
The evolution of vegetative desiccation tolerance in land plants
inferredcites →https://doi.org/10.1038/nature08583openalex-snapshot
Structural basis of abscisic acid signalling
inferredcites →https://doi.org/10.1038/nature08613openalex-snapshot
A gate–latch–lock mechanism for hormone signalling by abscisic acid receptors
inferredcites →https://doi.org/10.1042/bj0570508openalex-snapshot
The estimation of carbohydrates in plant extracts by anthrone
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.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.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.1118651109openalex-snapshot
Structural basis for basal activity and autoactivation of abscisic acid (ABA) signaling SnRK2 kinases
inferredcites →https://doi.org/10.1073/pnas.2034853100openalex-snapshot
A novel domain in the protein kinase SOS2 mediates interaction with the protein phosphatase 2C ABI2
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/emboj/cdf316openalex-snapshot
Homeodomain protein ATHB6 is a target of the protein phosphatase ABI1 and regulates hormone responses in Arabidopsis
inferredcites →https://doi.org/10.1093/icb/45.5.788openalex-snapshot
Desiccation Tolerance in Bryophytes: A Reflection of the Primitive Strategy for Plant Survival in Dehydrating Habitats?
inferredcites →https://doi.org/10.1093/jexbot/52.354.181openalex-snapshot
The AKT3 potassium channel protein interacts with the AtPP2CA protein phosphatase 2C
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/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/10.1104/pp.106.079327openalex-snapshot
Identification of Features Regulating OST1 Kinase Activity and OST1 Function in Guard Cells
inferredcites →https://doi.org/10.1104/pp.108.120725openalex-snapshot
The Enigmatic LEA Proteins and Other Hydrophilins
inferredcites →https://doi.org/10.1104/pp.110.153387openalex-snapshot
Evolutionarily Conserved Regulatory Mechanisms of Abscisic Acid Signaling in Land Plants: Characterization of ABSCISIC ACID INSENSITIVE1 -Like Type 2C Protein Phosphatase in the Liverwort Marchantia polymorpha
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.010441openalex-snapshot
Abscisic Acid Signaling in Seeds and Seedlings
inferredcites →https://doi.org/10.1105/tpc.107.056705openalex-snapshot
HAB1–SWI3B Interaction Reveals a Link between Abscisic Acid Signaling and Putative SWI/SNF Chromatin-Remodeling Complexes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.096404openalex-snapshot
Fern and Lycophyte Guard Cells Do Not Respond to Endogenous Abscisic Acid
inferredcites →https://doi.org/10.1105/tpc.7.5.499openalex-snapshot
Molecular Responses to Abscisic Acid and Stress Are Conserved between Moss and Cereals.
inferredcites →https://doi.org/10.1105/tpc.8.12.2359openalex-snapshot
An Abscisic Acid-Activated and Calcium-Independent Protein Kinase from Guard Cells of Fava Bean
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.2005.02583.xopenalex-snapshot
Abscisic acid‐activated SNRK2 protein kinases function in the gene‐regulation pathway of ABA signal transduction by phosphorylating ABA response element‐binding factors
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03107.xopenalex-snapshot
ABA‐Hypersensitive Germination1 encodes a protein phosphatase 2C, an essential component of abscisic acid signaling in Arabidopsis seed
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.1438-8677.1993.tb00344.xopenalex-snapshot
Abscisic Acid and Desiccation Tolerance in Mosses
inferredcites →https://doi.org/10.1126/science.1150646openalex-snapshot
The Physcomitrella Genome Reveals Evolutionary Insights into the Conquest of Land by Plants
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.1183672openalex-snapshot
Role of ABA and ABI3 in Desiccation Tolerance
inferredcites →https://doi.org/10.1126/science.1197985openalex-snapshot
Passive Origins of Stomatal Control in Vascular Plants
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.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/10.1139/b93-183openalex-snapshot
Redifferentiation of moss protonemata: an experimental and immunofluorescence study of brood cell formation
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.56.032604.144046openalex-snapshot
ABSCISIC ACID BIOSYNTHESIS AND CATABOLISM
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092740openalex-snapshot
Molecular Aspects of Seed Dormancy
inferredcites →https://doi.org/10.2307/2656880openalex-snapshot
ABA prevents the second cytokinin‐mediated event during the induction of shoot buds in the moss Funaria hygrometrica
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2015.05.009zenodo-depositor-declared
Abscisic acid induces biosynthesis of bisbibenzyls and tolerance to UV-C in the liverwort Marchantia polymorpha
inferred← citeshttps://doi.org/10.1002/9781118889022.ch8openalex-snapshot
Mechanism of ABA Signaling in Response to Abiotic Stress in Plants
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0744openalex-snapshot
Abscisic Acid Regulates Fleshy Fruit Ripening and Stress Resistance
inferred← citeshttps://doi.org/10.1007/978-3-319-93594-2_4openalex-snapshot
Leaf Water Transport: A Core System in the Evolution and Physiology of Photosynthesis
inferred← citeshttps://doi.org/10.1007/978-94-017-9424-4_22openalex-snapshot
Improvement of Stress Tolerance in Crops by Genetic Manipulation of ABA Metabolism, Signaling, and Regulation
inferred← citeshttps://doi.org/10.1007/978-981-13-1244-1_10openalex-snapshot
Mechanisms Underlying Freezing and Desiccation Tolerance in Bryophytes
inferred← citeshttps://doi.org/10.1007/s00299-019-02500-3openalex-snapshot
Cytokinin oxidase PpCKX1 plays regulatory roles in development and enhances dehydration and salt tolerance in Physcomitrella patens
inferred← citeshttps://doi.org/10.1007/s00299-020-02520-4openalex-snapshot
Wheat PP2C-a10 regulates seed germination and drought tolerance in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00425-014-2240-xopenalex-snapshot
Acquisition and loss of desiccation tolerance in seeds: from experimental model to biological relevance
inferred← citeshttps://doi.org/10.1007/s00709-016-0981-zopenalex-snapshot
SmLEA2, a gene for late embryogenesis abundant protein isolated from Salvia miltiorrhiza, confers tolerance to drought and salt stress in Escherichia coli and S. miltiorrhiza
inferred← citeshttps://doi.org/10.1007/s10265-025-01627-7openalex-snapshot
Abscisic acid enhances non-photochemical quenching through SnRK2 and ABI3 in Physcomitrium patens
inferred← citeshttps://doi.org/10.1007/s11032-017-0750-5openalex-snapshot
EhEm1, a novel Em-like protein from Eutrema halophilum, confers tolerance to salt and drought stresses in rice
inferred← citeshttps://doi.org/10.1007/s11103-021-01167-3openalex-snapshot
Pseudocrossidium replicatum (Taylor) R.H. Zander is a fully desiccation-tolerant moss that expresses an inducible molecular mechanism in response to severe abiotic stress
inferred← citeshttps://doi.org/10.1007/s11103-021-01172-6openalex-snapshot
Phytohormone biosynthesis and signaling pathways of mosses
inferred← citeshttps://doi.org/10.1007/s12298-018-0607-3openalex-snapshot
Enriched networks ‘nucleoside/nucleotide and ribonucleoside/ribonucleotide metabolic processes’ and ‘response to stimulus’ potentially conferred to drought adaptation of the epiphytic orchid Dendrobium wangliangii
inferred← citeshttps://doi.org/10.1007/s12298-020-00910-2openalex-snapshot
Isolation and characterization of maize ZmPP2C26 gene promoter in drought-response
inferred← citeshttps://doi.org/10.1007/s13595-015-0468-7openalex-snapshot
Can mosses serve as model organisms for forest research?
inferred← citeshttps://doi.org/10.1016/b978-0-12-816451-8.00021-6openalex-snapshot
Abscisic Acid, a Principal Regulator of Plant Abiotic Stress Responses
inferred← citeshttps://doi.org/10.1016/bs.abr.2019.06.003openalex-snapshot
Evolution of ABA signaling pathways
inferred← citeshttps://doi.org/10.1016/j.algal.2025.104385openalex-snapshot
A PP2C-SnRK2-MnSOD module modulates ROS homeostasis in Ulva prolifera response to salt stress
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.11.035openalex-snapshot
Negative regulation of abscisic acid signaling by the Brassica oleracea ABI1 ortholog
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.03.043openalex-snapshot
Expression of the moss PpLEA4-20 gene in rice enhances membrane protection and client proteins stability
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.02.024openalex-snapshot
Large-scale proteome analysis of abscisic acid and ABSCISIC ACID INSENSITIVE3-dependent proteins related to desiccation tolerance in Physcomitrella patens
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.150981openalex-snapshot
Remodeling of membrane lipids associated with ABA-induced desiccation tolerance in Physcomitrium patens
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.127157openalex-snapshot
Response of hormone in rice seedlings to irrigation contaminated with cyanobacterial extract containing microcystins
inferred← citeshttps://doi.org/10.1016/j.cub.2015.01.032openalex-snapshot
Stomatal Closure: The Old Guard Takes Up the SLAC
inferred← citeshttps://doi.org/10.1016/j.cub.2018.10.018openalex-snapshot
An Evolutionarily Conserved Abscisic Acid Signaling Pathway Regulates Dormancy in the Liverwort Marchantia polymorpha
inferred← citeshttps://doi.org/10.1016/j.cub.2020.09.016openalex-snapshot
BONZAI Proteins Control Global Osmotic Stress Responses in Plants
inferred← citeshttps://doi.org/10.1016/j.devcel.2022.09.012openalex-snapshot
Root twisting drives halotropism via stress-induced microtubule reorientation
inferred← citeshttps://doi.org/10.1016/j.isci.2022.103754openalex-snapshot
Stress-associated developmental reprogramming in moss protonemata by synthetic activation of the common symbiosis pathway
inferred← citeshttps://doi.org/10.1016/j.jia.2026.03.035openalex-snapshot
Integrated physiological, transcriptomic and metabolomic analyses reveal that ABA-linked carbohydrate metabolic imbalance causes low temperature-induced pollen sterility in peanut
inferred← citeshttps://doi.org/10.1016/j.jplph.2017.02.006openalex-snapshot
Spatio-temporal dynamics in global rice gene expression (Oryza sativa L.) in response to high ammonium stress
inferred← citeshttps://doi.org/10.1016/j.molp.2016.10.003openalex-snapshot
Deletion of an Endoplasmic Reticulum Stress Response Element in a ZmPP2C-A Gene Facilitates Drought Tolerance of Maize Seedlings
inferred← citeshttps://doi.org/10.1016/j.pbi.2018.09.009openalex-snapshot
Something ancient and something neofunctionalized—evolution of land plant hormone signaling pathways
inferred← citeshttps://doi.org/10.1016/j.plantsci.2016.05.007openalex-snapshot
The evolution of the role of ABA in the regulation of water-use efficiency: From biochemical mechanisms to stomatal conductance
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.12.010openalex-snapshot
Review: ABA, flavonols, and the evolvability of land plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113386openalex-snapshot
MiPP2C44 promotes early flowering in Arabidopsis and enhances abiotic stress tolerance in mango hairy roots
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108456openalex-snapshot
Drought responses and population differentiation of Calohypnum plumiforme inferred from comparative transcriptome analysis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110201openalex-snapshot
A novel ABA insensitive mutant reveals the role of clade H CpPP2C-H1A of Cucurbita pepo in seed germination, stomata closure and water stress tolerance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110279openalex-snapshot
Transcriptome analysis of OsNCED3 transgenic rice reveals the response mechanism to alkaline stress
inferred← citeshttps://doi.org/10.1016/j.semcdb.2020.06.006openalex-snapshot
The evolving role of abscisic acid in cell function and plant development over geological time
inferred← citeshttps://doi.org/10.1016/j.semcdb.2020.07.007openalex-snapshot
On the biosynthesis and evolution of apocarotenoid plant growth regulators
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101252openalex-snapshot
Hormones, particularly ABA-based signal transduction, play a pivotal role in alleviating photosynthetic inhibition in rice induced by NaHCO3 stress
inferred← citeshttps://doi.org/10.1016/j.tplants.2016.09.005openalex-snapshot
Molecular Evolution of Grass Stomata
inferred← citeshttps://doi.org/10.1016/j.tplants.2019.01.002openalex-snapshot
Acquiring Control: The Evolution of Stomatal Signalling Pathways
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101892openalex-snapshot
Evolutionary shifts in plant adaptation mediated by phytohormones
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c00385openalex-snapshot
Rapeseed PP2C37 Interacts with PYR/PYL Abscisic Acid Receptors and Negatively Regulates Drought Tolerance
inferred← citeshttps://doi.org/10.1038/nchembio.1529openalex-snapshot
Abscisic acid receptor hole-in-one
inferred← citeshttps://doi.org/10.1038/s41467-020-19977-2openalex-snapshot
Role of Raf-like kinases in SnRK2 activation and osmotic stress response in plants
inferred← citeshttps://doi.org/10.1038/s41598-017-12249-yopenalex-snapshot
Integrating transcriptome and microRNA analysis identifies genes and microRNAs for AHO-induced systemic acquired resistance in N. tabacum
inferred← citeshttps://doi.org/10.1038/s41598-018-29627-9openalex-snapshot
Genome-wide Identification of PP2C Genes and Their Expression Profiling in Response to Drought and Cold Stresses in Medicago truncatula
inferred← citeshttps://doi.org/10.1038/s42003-019-0281-1openalex-snapshot
SnRK2 protein kinases represent an ancient system in plants for adaptation to a terrestrial environment
inferred← citeshttps://doi.org/10.1038/s44318-024-00277-0openalex-snapshot
Osmotic signaling releases PP2C-mediated inhibition of Arabidopsis SnRK2s via the receptor-like cytoplasmic kinase BIK1
inferred← citeshttps://doi.org/10.1038/srep40625openalex-snapshot
P-HYDROXYPHENYLPYRUVATE DIOXYGENASE from Medicago sativa is involved in vitamin E biosynthesis and abscisic acid-mediated seed germination
inferred← citeshttps://doi.org/10.1071/fp15278openalex-snapshot
Physiological factors determine the accumulation of D-glycero-D-ido-octulose (D-g-D-i-oct) in the desiccation tolerant resurrection plant Craterostigma plantagineum
inferred← citeshttps://doi.org/10.1073/pnas.1511238112openalex-snapshot
Plant Raf-like kinase integrates abscisic acid and hyperosmotic stress signaling upstream of SNF1-related protein kinase2
inferred← citeshttps://doi.org/10.1080/15592324.2017.1365210openalex-snapshot
Abscisic acid (ABA) and key proteins in its perception and signaling pathways are ancient, but their roles have changed through time
inferred← citeshttps://doi.org/10.1093/aob/mcag137openalex-snapshot
Intraspecific communication through volatile organic compounds in the mosses Didymodon vinealis and Syntrichia caninervis from an arid temperate desert
inferred← citeshttps://doi.org/10.1093/jxb/eraa336openalex-snapshot
Abiotic stress signalling in extremophile land plants
inferred← citeshttps://doi.org/10.1093/jxb/ery157openalex-snapshot
Molecular mechanisms controlling plant growth during abiotic stress
inferred← citeshttps://doi.org/10.1093/pcp/pcaa021openalex-snapshot
Quantitative Imaging Reveals Distinct Contributions of SnRK2 and ABI3 in Plasmodesmatal Permeability in Physcomitrella patens
inferred← citeshttps://doi.org/10.1093/pcp/pcaa129openalex-snapshot
Hormonal Diterpenoids Distinct to Gibberellins Regulate Protonema Differentiation in the Moss Physcomitrium patens
inferred← citeshttps://doi.org/10.1093/pcp/pcy249openalex-snapshot
Abscisic Acid Acts as a Regulator of Molecular Trafficking through Plasmodesmata in the MossPhyscomitrella patens
inferred← citeshttps://doi.org/10.1093/plphys/kiaa046openalex-snapshot
Activation of SnRK2 by Raf-like kinase ARK represents a primary mechanism of ABA and abiotic stress responses
inferred← citeshttps://doi.org/10.1101/2020.04.03.024448openalex-snapshot
Activation of SnRK2 by the Raf-like kinase ARK represents a common mechanism of ABA response in embryophytes
inferred← citeshttps://doi.org/10.1101/2023.09.18.558310openalex-snapshot
Role of C2-domain protein CAR1 in the plasma membrane ABA signaling response
inferred← citeshttps://doi.org/10.1101/2024.04.28.591503openalex-snapshot
The alternative splicing of ZmHsf23 regulates heat stress tolerance in maize
inferred← citeshttps://doi.org/10.1101/2025.04.28.650909openalex-snapshot
Control of leaflet movement pattern by a novel PP2C phosphatase DLM1 in Medicago truncatula
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.15.00233openalex-snapshot
An Ancestral Role for CONSTITUTIVE TRIPLE RESPONSE1 Proteins in Both Ethylene and Abscisic Acid Signaling
inferred← citeshttps://doi.org/10.1104/pp.16.00469openalex-snapshot
Feedback Regulation of ABA Signaling and Biosynthesis by a bZIP Transcription Factor Targets Drought-Resistance-Related Genes
inferred← citeshttps://doi.org/10.1104/pp.16.01088openalex-snapshot
Sporophyte formation and life cycle completion in moss requires heterotrimeric G-proteins
inferred← citeshttps://doi.org/10.1104/pp.18.00761openalex-snapshot
Archetypal Roles of an Abscisic Acid Receptor in Drought and Sugar Responses in Liverworts
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/10.1105/tpc.15.00774openalex-snapshot
An Innate Immunity Pathway in the Moss Physcomitrella patens
inferred← citeshttps://doi.org/10.1105/tpc.16.00091openalex-snapshot
Genetic analysis of Physcomitrella patens identifies ABSCISIC ACID NON-RESPONSIVE (ANR), a regulator of ABA responses unique to basal land plants and required for desiccation tolerance
inferred← citeshttps://doi.org/10.1111/jipb.12523openalex-snapshot
What are the evolutionary origins of stomatal responses to abscisic acid in land plants?
inferred← citeshttps://doi.org/10.1111/jipb.12899openalex-snapshot
Abscisic acid dynamics, signaling, and functions in plants
inferred← citeshttps://doi.org/10.1111/nph.13231openalex-snapshot
Epoxycarotenoid‐mediated synthesis of abscisic acid in Physcomitrella patens implicating conserved mechanisms for acclimation to hyperosmosis in embryophytes
inferred← citeshttps://doi.org/10.1111/nph.13938openalex-snapshot
An ancient and conserved function for Armadillo‐related proteins in the control of spore and seed germination by abscisic acid
inferred← citeshttps://doi.org/10.1111/nph.14018openalex-snapshot
The decision to germinate is regulated by divergent molecular networks in spores and seeds
inferred← citeshttps://doi.org/10.1111/nph.18706openalex-snapshot
Pepper SnRK2 .6‐activated MEKK protein CaMEKK23 is directly and indirectly modulated by clade A PP2Cs in response to drought stress
inferred← citeshttps://doi.org/10.1111/nph.20172openalex-snapshot
Gaining or cutting SLAC : the evolution of plant guard cell signalling pathways
inferred← citeshttps://doi.org/10.1111/nph.20195openalex-snapshot
Antioxidants by nature: an ancient feature at the heart of flavonoids' multifunctionality
inferred← citeshttps://doi.org/10.1111/nph.70703openalex-snapshot
Surviving dehydration: shutdown–restart dynamics in Physcomitrium patens avoids the metabolic collapse seen in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.71438openalex-snapshot
A RAF ‐ SnRK2 ‐ PP2C functional module regulates cell survival in the chlorophyte Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1111/pce.13096openalex-snapshot
Desiccation tolerance in Physcomitrella patens : Rate of dehydration and the involvement of endogenous abscisic acid (ABA)
inferred← citeshttps://doi.org/10.1111/pce.13869openalex-snapshot
Decoding ABA and osmostress signalling in plants from an evolutionary point of view
inferred← citeshttps://doi.org/10.1111/tpj.13891openalex-snapshot
Phosphoproteomic profiling reveals ABA ‐responsive phosphosignaling pathways in Physcomitrella patens
inferred← citeshttps://doi.org/10.1111/tpj.14561openalex-snapshot
From reproduction to production, stomata are the master regulators
inferred← citeshttps://doi.org/10.1111/tpj.14596openalex-snapshot
Vegetative desiccation tolerance in the resurrection plant Xerophyta humilis has not evolved through reactivation of the seed canonical LAFL regulatory network
inferred← citeshttps://doi.org/10.1111/tpj.15067openalex-snapshot
Signaling mechanisms in abscisic acid‐mediated stomatal closure
inferred← citeshttps://doi.org/10.1111/tpj.16757openalex-snapshot
Recruitment of HAB1 and SnRK2 .2 by C2 ‐domain protein CAR1 in plasma membrane ABA signaling
inferred← citeshttps://doi.org/10.1111/tpj.70291openalex-snapshot
Algal origins of core land plant stress response subnetworks
inferred← citeshttps://doi.org/10.1126/sciadv.adr8298openalex-snapshot
Abscisic acid signaling regulates primary plasmodesmata density for plant cell-to-cell communication
inferred← citeshttps://doi.org/10.1155/2019/2965035openalex-snapshot
Genome-Wide Identification, Evolution, and Transcriptional Profiling ofPP2CGene Family inBrassica rapa
inferred← citeshttps://doi.org/10.1186/1471-2164-15-773openalex-snapshot
Maize protein phosphatase gene family: identification and molecular characterization
inferred← citeshttps://doi.org/10.1186/s12864-015-2071-6openalex-snapshot
MicroRNA and mRNA expression profiling analysis revealed the regulation of plant height in Gossypium hirsutum
inferred← citeshttps://doi.org/10.1186/s12870-016-0764-xopenalex-snapshot
Contrasting transcriptional responses of PYR1/PYL/RCAR ABA receptors to ABA or dehydration stress between maize seedling leaves and roots
inferred← citeshttps://doi.org/10.1186/s12870-017-1013-7openalex-snapshot
Sporobolus stapfianus: Insights into desiccation tolerance in the resurrection grasses from linking transcriptomics to metabolomics
inferred← citeshttps://doi.org/10.1186/s12870-020-02358-8openalex-snapshot
Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.1186/s12870-023-04611-2openalex-snapshot
Transcriptomics reveals a core transcriptional network of K-type cytoplasmic male sterility microspore abortion in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.1371/journal.pone.0147306openalex-snapshot
Transcriptomic Analysis of Tea Plant Responding to Drought Stress and Recovery
inferred← citeshttps://doi.org/10.14719/pst.2018.5.2.388openalex-snapshot
An insight into drought stress and signal transduction of abscisic acid
inferred← citeshttps://doi.org/10.14945/00008273openalex-snapshot
Studies on Development of ABA Receptor Antagonists
inferred← citeshttps://doi.org/10.18297/etd/3973openalex-snapshot
Determination of the functional role of Rab-GGT in Physcomitrium patens.
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2408018/v1openalex-snapshot
Genome-wide identification, evolutionary, and expression analyses of the PP2C gene family in Castanea mollissima Blume.
inferred← citeshttps://doi.org/10.3109/07388551.2015.1083941openalex-snapshot
Plant protein phosphatases 2C: from genomic diversity to functional multiplicity and importance in stress management
inferred← citeshttps://doi.org/10.3389/fgene.2019.00956openalex-snapshot
Molecular Evolution and Interaction of Membrane Transport and Photoreception in Plants
inferred← citeshttps://doi.org/10.3389/fgene.2021.770014openalex-snapshot
Genome-wide Identification and Evolution of the PP2C Gene Family in Eight Rosaceae Species and Expression Analysis Under Stress in Pyrus bretschneideri
inferred← citeshttps://doi.org/10.3389/fpls.2014.00170openalex-snapshot
The transcriptional regulatory network in the drought response and its crosstalk in abiotic stress responses including drought, cold, and heat
inferred← citeshttps://doi.org/10.3389/fpls.2015.00642openalex-snapshot
Identification and expression profile analysis of NUCLEAR FACTOR-Y families in Physcomitrella patens
inferred← citeshttps://doi.org/10.3389/fpls.2016.01029openalex-snapshot
Transcription Factors and Plants Response to Drought Stress: Current Understanding and Future Directions
inferred← citeshttps://doi.org/10.3389/fpls.2017.01599openalex-snapshot
ABSCISIC ACID INSENSITIVE3 Is Involved in Cold Response and Freezing Tolerance Regulation in Physcomitrella patens
inferred← citeshttps://doi.org/10.3389/fpls.2019.00315openalex-snapshot
ABA-Induced Vegetative Diaspore Formation in Physcomitrella patens
inferred← citeshttps://doi.org/10.3389/fpls.2020.00574openalex-snapshot
Decoding Gene Networks Modules That Explain the Recovery of Hymenoglossum cruentum Cav. After Extreme Desiccation
inferred← citeshttps://doi.org/10.3389/fpls.2020.00845openalex-snapshot
A Chloroplast COR413 Protein From Physcomitrella patens Is Required for Growth Regulation Under High Light and ABA Responses
inferred← citeshttps://doi.org/10.3389/fpls.2020.00909openalex-snapshot
Evolution of Abscisic Acid Signaling for Stress Responses to Toxic Metals and Metalloids
inferred← citeshttps://doi.org/10.3389/fpls.2020.00934openalex-snapshot
Evolution of Abscisic Acid Signaling Module and Its Perception
inferred← citeshttps://doi.org/10.3389/fpls.2020.564665openalex-snapshot
Overexpression of Maize ZmMYB59 Gene Plays a Negative Regulatory Role in Seed Germination in Nicotiana tabacum and Oryza sativa
inferred← citeshttps://doi.org/10.3389/fpls.2020.576941openalex-snapshot
Maize Response to Low Temperatures at the Gene Expression Level: A Critical Survey of Transcriptomic Studies
inferred← citeshttps://doi.org/10.3389/fpls.2021.646707openalex-snapshot
Mitogen-Activated Protein Kinase CaDIMK1 Functions as a Positive Regulator of Drought Stress Response and Abscisic Acid Signaling in Capsicum annuum
inferred← citeshttps://doi.org/10.3389/fpls.2022.851531openalex-snapshot
ZmPP2C26 Alternative Splicing Variants Negatively Regulate Drought Tolerance in Maize
inferred← citeshttps://doi.org/10.3389/fpls.2022.952820openalex-snapshot
Differential regulations of abscisic acid-induced desiccation tolerance and vegetative dormancy by group B3 Raf kinases in liverworts
inferred← citeshttps://doi.org/10.3389/fpls.2023.1303195openalex-snapshot
ABA signaling converts stem cell fate by substantiating a tradeoff between cell polarity, growth and cell cycle progression and abiotic stress responses in the moss Physcomitrium patens
inferred← citeshttps://doi.org/10.3389/fpls.2025.1547526openalex-snapshot
Genome-wide identification, phylogenetic investigation and abiotic stress responses analysis of the PP2C gene family in litchi (Litchi chinensis Sonn.)
inferred← citeshttps://doi.org/10.3389/fpls.2026.1917865openalex-snapshot
PpLEA genes in embryophytes,instead of LEAs being angiosperm-unique
inferred← citeshttps://doi.org/10.3390/genes13040604openalex-snapshot
Genome-Wide Analysis of the Protein Phosphatase 2C Genes in Tomato
inferred← citeshttps://doi.org/10.3390/genes13050834openalex-snapshot
Genome-Wide Identification and Transcriptional Expression Profiles of PP2C in the Barley (Hordeum vulgare L.) Pan-Genome
inferred← citeshttps://doi.org/10.3390/genes15010041openalex-snapshot
Genome-Wide Identification, Expression and Interaction Analyses of PP2C Family Genes in Chenopodium quinoa
inferred← citeshttps://doi.org/10.3390/genes15121644openalex-snapshot
Drought Stress Inhibits the Accumulation of Rotenoids and the Biosynthesis of Drought-Responsive Phytohormones in Mirabilis himalaica (Edgew.) Heim Calli
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/ijms23095284openalex-snapshot
Beyond Photoprotection: The Multifarious Roles of Flavonoids in Plant Terrestrialization
inferred← citeshttps://doi.org/10.3390/ijms24043210openalex-snapshot
Overexpression of Water-Responsive Genes Promoted by Elevated CO2 Reduces ROS and Enhances Drought Tolerance in Coffea Species
inferred← citeshttps://doi.org/10.3390/plants10122769openalex-snapshot
Molecular and Physiological Perspectives of Abscisic Acid Mediated Drought Adjustment Strategies
inferred← citeshttps://doi.org/10.3390/plants14060865openalex-snapshot
Multi-Omics Approaches Against Abiotic and Biotic Stress—A Review
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.22.0107aopenalex-snapshot
Abscisic acid switches cell division modes of asymmetric cell division and symmetric cell division in stem cells of protonemal filaments in the moss Physcomitrium patens
inferred← citeshttps://doi.org/10.6084/m9.figshare.12135384openalex-snapshot
Additional file 10 of Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.6084/m9.figshare.12135387openalex-snapshot
Additional file 11 of Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.6084/m9.figshare.12135390openalex-snapshot
Additional file 12 of Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.6084/m9.figshare.12135393openalex-snapshot
Additional file 1 of Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.6084/m9.figshare.12135396openalex-snapshot
Additional file 2 of Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.6084/m9.figshare.12135399openalex-snapshot
Additional file 3 of Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.6084/m9.figshare.12135402openalex-snapshot
Additional file 4 of Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.6084/m9.figshare.12135405openalex-snapshot
Additional file 5 of Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.6084/m9.figshare.12135408openalex-snapshot
Additional file 6 of Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.6084/m9.figshare.12135411openalex-snapshot
Additional file 7 of Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.6084/m9.figshare.12135414openalex-snapshot
Additional file 8 of Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.6084/m9.figshare.12135417openalex-snapshot
Additional file 9 of Coordinated mechanisms of leaves and roots in response to drought stress underlying full-length transcriptome profiling in Vicia sativa L
inferred← citeshttps://doi.org/10.70675/bfab313ez7d9az411czbb63z16057ed985adopenalex-snapshot
Strigolactones perception and signal transduction in the moss Physcomitrium patens
inferred← citeshttps://doi.org/10.7554/elife.23361openalex-snapshot
A chloroplast retrograde signal, 3’-phosphoadenosine 5’-phosphate, acts as a secondary messenger in abscisic acid signaling in stomatal closure and germination
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