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Guard cell abscisic acid signalling and engineering drought hardiness in plants
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0968-0004(89)90272-7openalex-snapshot
Involvement of ion channels and active transport in osmoregulation and signaling of higher plant cells
inferredcites →https://doi.org/10.1016/s0014-5793(99)01109-6openalex-snapshot
Calcium‐induced calcium release mediated by a voltage‐activated cation channel in vacuolar vesicles from red beet
inferredcites →https://doi.org/10.1016/s0014-5793(99)01396-4openalex-snapshot
Unitary exocytotic and endocytotic events in guard‐cell protoplasts during osmotically driven volume changes
inferredcites →https://doi.org/10.1016/s0378-1119(00)00150-5openalex-snapshot
Cloning of regulatory sequences mediating guard-cell-specific gene expression
inferredcites →https://doi.org/10.1038/343186a0openalex-snapshot
Abscisic acid-induced elevation of guard cell cytosolic Ca2+ precedes stomatal closure
inferredcites →https://doi.org/10.1038/35021067openalex-snapshot
Calcium channels activated by hydrogen peroxide mediate abscisic acid signalling in guard cells
inferredcites →https://doi.org/10.1046/j.1365-313x.1997.12061387.xopenalex-snapshot
Slowly activating vacuolar channels can not mediate Ca2+‐induced Ca2+ release
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00574.xopenalex-snapshot
Cameleon calcium indicator reports cytoplasmic calcium dynamics in Arabidopsis guard cells
inferredcites →https://doi.org/10.1073/pnas.080068897openalex-snapshot
Ca 2+ channels at the plasma membrane of stomatal guard cells are activated by hyperpolarization and abscisic acid
inferredcites →https://doi.org/10.1073/pnas.140217497openalex-snapshot
Inositol hexakisphosphate is a physiological signal regulating the K + -inward rectifying conductance in guard cells
inferredcites →https://doi.org/10.1073/pnas.220417197openalex-snapshot
ABA activates multiple Ca 2+ fluxes in stomatal guard cells, triggering vacuolar K + (Rb + ) release
inferredcites →https://doi.org/10.1073/pnas.92.21.9520openalex-snapshot
Sensitivity to abscisic acid of guard-cell K+ channels is suppressed by abi1-1, a mutant Arabidopsis gene encoding a putative protein phosphatase.
inferredcites →https://doi.org/10.1073/pnas.92.21.9535openalex-snapshot
Strong regulation of slow anion channels and abscisic acid signaling in guard cells by phosphorylation and dephosphorylation events.
inferredcites →https://doi.org/10.1073/pnas.94.25.14156openalex-snapshot
Evidence for the existence of a sulfonylurea-receptor-like protein in plants: Modulation of stomatal movements and guard cell potassium channels by sulfonylureas and potassium channel openers
inferredcites →https://doi.org/10.1073/pnas.95.26.15837openalex-snapshot
Abscisic acid-induced stomatal closure mediated by cyclic ADP-ribose
inferredcites →https://doi.org/10.1073/pnas.95.8.4778openalex-snapshot
Membrane voltage initiates Ca 2+ waves and potentiates Ca 2+ increases with abscisic acid in stomatal guard cells
inferredcites →https://doi.org/10.1073/pnas.96.21.12192openalex-snapshot
Abscisic acid signal transduction in guard cells is mediated by phospholipase D activity
inferredcites →https://doi.org/10.1073/pnas.96.23.13577openalex-snapshot
Ozone inhibits guard cell K + channels implicated in stomatal opening
inferredcites →https://doi.org/10.1073/pnas.96.4.1779openalex-snapshot
Abscisic acid induces oscillations in guard-cell cytosolic free calcium that involve phosphoinositide-specific phospholipase C
inferredcites →https://doi.org/10.1093/emboj/18.20.5548openalex-snapshot
Blue light activates the plasma membrane H+‐ATPase by phosphorylation of the C‐terminus in stomatal guard cells
inferredcites →https://doi.org/10.1093/jexbot/49.suppl_1.351openalex-snapshot
Co-ordination of signalling elements in guard cell ion channel control
inferredcites →https://doi.org/10.1098/rstb.1998.0299openalex-snapshot
Signalling of abscisic acid to regulate plant growth
inferredcites →https://doi.org/10.1098/rstb.1998.0303openalex-snapshot
Signal transduction and ion channels in guard cells
inferredcites →https://doi.org/10.1104/pp.113.3.833openalex-snapshot
Abscisic Acid Activates a 48-Kilodalton Protein Kinase in Guard Cell Protoplasts
inferredcites →https://doi.org/10.1104/pp.119.3.809openalex-snapshot
The Multisensory Guard Cell. Stomatal Responses to Blue Light and Abscisic Acid1
inferredcites →https://doi.org/10.1104/pp.121.1.147openalex-snapshot
Oligogalacturonic Acid and Chitosan Reduce Stomatal Aperture by Inducing the Evolution of Reactive Oxygen Species from Guard Cells of Tomato and Commelina communis
inferredcites →https://doi.org/10.1104/pp.124.1.223openalex-snapshot
Distinct Abscisic Acid Signaling Pathways for Modulation of Guard Cell versus Mesophyll Cell Potassium Channels Revealed by Expression Studies in Xenopus laevisOocytes
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.11.6.1141openalex-snapshot
ATP Binding Cassette Modulators Control Abscisic Acid–Regulated Slow Anion Channels in Guard Cells
inferredcites →https://doi.org/10.1105/tpc.11.9.1785openalex-snapshot
Arabidopsis abi1-1 and abi2-1 Phosphatase Mutations Reduce Abscisic Acid–Induced Cytoplasmic Calcium Rises in Guard Cells
inferredcites →https://doi.org/10.1105/tpc.3.4.333openalex-snapshot
Role of Calcium in Signal Transduction of Commelina Guard Cells
inferredcites →https://doi.org/10.1105/tpc.7.7.833openalex-snapshot
Roles of Ion Channels in Initiation of Signal Transduction in Higher Plants.
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.8.6.1061openalex-snapshot
Abscisic Acid Induces Mitogen-Activated Protein Kinase Activation in Barley Aleurone Protoplasts.
inferredcites →https://doi.org/10.1105/tpc.9.3.409openalex-snapshot
Differential abscisic acid regulation of guard cell slow anion channels in Arabidopsis wild-type and abi1 and abi2 mutants.
inferredcites →https://doi.org/10.1111/j.1399-3054.1997.tb03451.xopenalex-snapshot
Calcium ions as second messengers in guard cell signal transduction
inferredcites →https://doi.org/10.1126/science.271.5250.785openalex-snapshot
Human Appropriation of Renewable Fresh Water
inferredcites →https://doi.org/10.1126/science.273.5279.1239openalex-snapshot
A Protein Farnesyl Transferase Involved in Abscisic Acid Signal Transduction in Arabidopsis
inferredcites →https://doi.org/10.1126/science.274.5294.1900openalex-snapshot
Ca 2+ -Dependent Protein Kinases and Stress Signal Transduction in Plants
inferredcites →https://doi.org/10.1126/science.278.5346.2075openalex-snapshot
Signaling Through Scaffold, Anchoring, and Adaptor Proteins
inferredcites →https://doi.org/10.1126/science.278.5346.2126openalex-snapshot
Abscisic Acid Signaling Through Cyclic ADP-Ribose in Plants
inferredcites →https://doi.org/10.1126/science.282.5387.287openalex-snapshot
Role of Farnesyltransferase in ABA Regulation of Guard Cell Anion Channels and Plant Water Loss
inferredcites →https://doi.org/10.1126/science.283.5401.537openalex-snapshot
A Tobacco Syntaxin with a Role in Hormonal Control of Guard Cell Ion Channels
inferredcites →https://doi.org/10.1126/science.287.5451.300openalex-snapshot
Regulation of Abscisic Acid-Induced Stomatal Closure and Anion Channels by Guard Cell AAPK Kinase
inferredcites →https://doi.org/10.1126/science.289.5488.2338openalex-snapshot
Alteration of Stimulus-Specific Guard Cell Calcium Oscillations and Stomatal Closing in Arabidopsis det3 Mutant
inferredcites →https://doi.org/10.1146/annurev.arplant.47.1.49openalex-snapshot
14-3-3 PROTEINS AND SIGNAL TRANSDUCTION
inferredcites →https://doi.org/10.1146/annurev.arplant.49.1.199openalex-snapshot
ABSCISIC ACID SIGNAL TRANSDUCTION
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Morphological and physiological plasticity of Catalpa bungei roots under partial root-zone drought as affected by nitrogen forms
inferred← citeshttps://doi.org/10.1007/s11103-005-7294-5openalex-snapshot
Arabidopsis ERF4 is a transcriptional repressor capable of modulating ethylene and abscisic acid responses
inferred← citeshttps://doi.org/10.1007/s11103-007-9219-yopenalex-snapshot
Isolation and characterization of shs1, a sugar-hypersensitive and ABA-insensitive mutant with multiple stress responses
inferred← citeshttps://doi.org/10.1007/s11103-008-9427-0openalex-snapshot
Hormone interactions in stomatal function
inferred← citeshttps://doi.org/10.1007/s11103-009-9503-0openalex-snapshot
AtMKK1 and AtMPK6 are involved in abscisic acid and sugar signaling in Arabidopsis seed germination
inferred← citeshttps://doi.org/10.1007/s11103-011-9738-4openalex-snapshot
The soybean GmbZIP1 transcription factor enhances multiple abiotic stress tolerances in transgenic plants
inferred← citeshttps://doi.org/10.1007/s11103-011-9796-7openalex-snapshot
A dual role for MYB60 in stomatal regulation and root growth of Arabidopsis thaliana under drought stress
inferred← citeshttps://doi.org/10.1007/s11103-013-0038-zopenalex-snapshot
Strategies to ameliorate abiotic stress-induced plant senescence
inferred← citeshttps://doi.org/10.1007/s11103-014-0217-6openalex-snapshot
Expression of a gene encoding a rice RING zinc-finger protein, OsRZFP34, enhances stomata opening
inferred← citeshttps://doi.org/10.1007/s11103-014-0232-7openalex-snapshot
Expression and characterization of plasma membrane aquaporins in stomatal complexes of Zea mays
inferred← citeshttps://doi.org/10.1007/s11103-016-0441-3openalex-snapshot
WRKY1 regulates stomatal movement in drought-stressed Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11103-016-0451-1openalex-snapshot
Identification and functional characterization of the pepper CaDRT1 gene involved in the ABA-mediated drought stress response
inferred← citeshttps://doi.org/10.1007/s11103-016-0476-5openalex-snapshot
Auxin response under osmotic stress
inferred← citeshttps://doi.org/10.1007/s11103-016-0500-9openalex-snapshot
SUMO proteases ULP1c and ULP1d are required for development and osmotic stress responses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11103-016-0544-xopenalex-snapshot
Overexpression of OsDT11, which encodes a novel cysteine-rich peptide, enhances drought tolerance and increases ABA concentration in rice
inferred← citeshttps://doi.org/10.1007/s11105-010-0275-0openalex-snapshot
Overexpression of a Wheat CCaMK Gene Reduces ABA Sensitivity of Arabidopsis thaliana During Seed Germination and Seedling Growth
inferred← citeshttps://doi.org/10.1007/s11105-013-0687-8openalex-snapshot
Overexpression of Transcription Factor OsWR2 Regulates Wax and Cutin Biosynthesis in Rice and Enhances its Tolerance to Water Deficit
inferred← citeshttps://doi.org/10.1007/s11105-021-01297-4openalex-snapshot
The Soybean Transcriptogram Allows a Wide Genome-to-Single-Gene Analysis That Evinces Time-Dependent Drought Response
inferred← citeshttps://doi.org/10.1007/s11120-013-9844-zopenalex-snapshot
Diffusional conductances to CO2 as a target for increasing photosynthesis and photosynthetic water-use efficiency
inferred← citeshttps://doi.org/10.1007/s11240-013-0374-3openalex-snapshot
Overexpression of Os2H16 enhances resistance to phytopathogens and tolerance to drought stress in rice
inferred← citeshttps://doi.org/10.1007/s11240-021-02146-8openalex-snapshot
Characterization on the P-associated and agronomic traits as well as associated molecular processes in wheat under Pi deprivation condition
inferred← citeshttps://doi.org/10.1007/s11295-017-1175-3openalex-snapshot
Identification of the SRO gene family in apples (Malus×domestica) with a functional characterization of MdRCD1
inferred← citeshttps://doi.org/10.1007/s11356-020-10407-wopenalex-snapshot
Effects of regulated deficit irrigation applied at different growth stages of greenhouse grown tomato on substrate moisture, yield, fruit quality, and physiological traits
inferred← citeshttps://doi.org/10.1007/s11356-023-31597-zopenalex-snapshot
Physio-anatomical modifications and element allocation pattern in Alternanthera tenella Colla. associated with phytoextraction of chromium
inferred← citeshttps://doi.org/10.1007/s11368-015-1128-0openalex-snapshot
Acid-tolerant plant species screened for rehabilitating acid mine drainage sites
inferred← citeshttps://doi.org/10.1007/s11426-009-0251-4openalex-snapshot
Effects of La3+ and Eu3+ on outward potassium channels in Vicia guard cells
inferred← citeshttps://doi.org/10.1007/s11434-006-2173-2openalex-snapshot
Identification and primary genetic analysis of Arabidopsis stomatal mutants in response to multiple stresses
inferred← citeshttps://doi.org/10.1007/s11434-013-0031-6openalex-snapshot
Generation of the genetic mutant population for the screening and characterization of the mutants in response to drought in maize
inferred← citeshttps://doi.org/10.1007/s11557-015-1108-1openalex-snapshot
Contributions of an arbuscular mycorrhizal fungus to growth and physiology of loquat (Eriobotrya japonica) plants subjected to drought stress
inferred← citeshttps://doi.org/10.1007/s11676-015-0075-3openalex-snapshot
Use of infrared thermal imaging to diagnose health of Ammopiptanthus mongolicus in northwestern China
inferred← citeshttps://doi.org/10.1007/s11703-011-1148-5openalex-snapshot
Molecular characterization and roles of AP2 transcription factors on drought tolerance in plants
inferred← citeshttps://doi.org/10.1007/s11738-009-0298-zopenalex-snapshot
Differences in abscisic acid concentration in roots and leaves of two young Olive (Olea europaea L.) cultivars in response to water deficit
inferred← citeshttps://doi.org/10.1007/s11738-014-1538-4openalex-snapshot
Control of plant growth and water loss by a lack of light-harvesting complexes in photosystem II in Arabidopsis thaliana ch1-1 mutant
inferred← citeshttps://doi.org/10.1007/s11738-014-1596-7openalex-snapshot
Glycine betaine application in grain filling wheat plants alleviates heat and high light-induced photoinhibition by enhancing the psbA transcription and stomatal conductance
inferred← citeshttps://doi.org/10.1007/s11738-022-03390-xopenalex-snapshot
Role of sucrose and phloem–xylem interaction in recovery of water status and hydraulic dehydration impacts in tobacco plants (Nicotiana tabacum)
inferred← citeshttps://doi.org/10.1007/s12038-011-9002-8openalex-snapshot
Overexpression of the mitogen-activated protein kinase gene OsMAPK33 enhances sensitivity to salt stress in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s12298-020-00918-8openalex-snapshot
The application of exogenous PopW increases the tolerance of Solanum lycopersicum L. to drought stress through multiple mechanisms
inferred← citeshttps://doi.org/10.1007/s12374-017-0277-7openalex-snapshot
The Arabidopsis Mediator Complex Subunit MED19a is Involved in ABI5-mediated ABA Responses
inferred← citeshttps://doi.org/10.1007/s13199-009-0009-yopenalex-snapshot
Piriformospora indica, a cultivable root endophyte with multiple biotechnological applications
inferred← citeshttps://doi.org/10.1007/s13205-019-2023-yopenalex-snapshot
A putative tomato inositol polyphosphate 5-phosphatase, Le5PT1, is involved in plant growth and abiotic stress responses
inferred← citeshttps://doi.org/10.1007/s13258-012-0081-1openalex-snapshot
ABA signal transduction from ABA receptors to ion channels
inferred← citeshttps://doi.org/10.1007/s13562-012-0150-1openalex-snapshot
Protein phosphatases: a genomic outlook to understand their function in plants
inferred← citeshttps://doi.org/10.1007/s13593-015-0338-6openalex-snapshot
Regulated deficit irrigation for crop production under drought stress. A review
inferred← citeshttps://doi.org/10.1007/s40003-018-0308-8openalex-snapshot
Effect of No-Till and Raised-Bed Planting on Soil Moisture Conservation and Productivity of Summer Maize (Zea mays) in Eastern Himalayas
inferred← citeshttps://doi.org/10.1007/s40415-021-00745-5openalex-snapshot
2,4-Epibrassinolide mechanisms regulating water use efficiency and fruit production in tomato plants
inferred← citeshttps://doi.org/10.1007/s40502-016-0218-3openalex-snapshot
Tolerance to water deficit in cowpea populations resulting from breeding program: detection by gas exchange and chlorophyll fluorescence
inferred← citeshttps://doi.org/10.1007/s40626-016-0077-3openalex-snapshot
Grapevine RD22a constitutive expression in tobacco enhances stomatal adjustment and confers drought tolerance
inferred← citeshttps://doi.org/10.1007/s42729-022-00984-9openalex-snapshot
Staphylococcus Sciuri SAT-17 Facilitated in Vitro Regenerated Sugarcane Plantlets Cultivation in Saline Soil by Harmonizing Oxidative Signaling, Photosynthetic Efficiency and Nutrients Uptake Patterns
inferred← citeshttps://doi.org/10.1016/b978-0-12-381466-1.00018-3openalex-snapshot
Integrating genomics and genetics to accelerate development of drought and salinity tolerant crops
inferred← citeshttps://doi.org/10.1016/b978-0-12-387692-8.00007-2openalex-snapshot
Molecular Mechanisms of Abscisic Acid Action in Plants and Its Potential Applications to Human Health
inferred← citeshttps://doi.org/10.1016/b978-0-12-387692-8.00012-6openalex-snapshot
Engineering Salinity and Water-Stress Tolerance in Crop Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-394382-8.00003-4openalex-snapshot
Climate Change and Defense against Pathogens in Plants
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/b978-0-12-817112-7.00011-0openalex-snapshot
Small RNAs and cold stress tolerance
inferred← citeshttps://doi.org/10.1016/b978-0-12-818204-8.00026-6openalex-snapshot
Plant single-cell biology and abiotic stress tolerance
inferred← citeshttps://doi.org/10.1016/b978-0-12-821394-0.00006-8openalex-snapshot
The role of fungi in abiotic stress tolerance of plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-821792-4.00002-3openalex-snapshot
Calcium channels and transporters in plants under salinity stress
inferred← citeshttps://doi.org/10.1016/b978-0-323-85665-2.00010-8openalex-snapshot
Role of plant hormones in combating biotic stress in plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-90617-3.00009-xopenalex-snapshot
Role of engineered nanomaterials in augmenting plant response to abiotic stresses
inferred← citeshttps://doi.org/10.1016/b978-0-443-30244-2.00027-0openalex-snapshot
Structure and function of diverse abscisic acid receptors and coreceptors in modulating developmental and stress responses
inferred← citeshttps://doi.org/10.1016/b978-0-444-59576-8.00038-2openalex-snapshot
Trichoderma Species as Abiotic Stress Relievers in Plants
inferred← citeshttps://doi.org/10.1016/bs.abr.2022.02.008openalex-snapshot
Stomatal regulation and adaptation to salinity in glycophytes and halophytes
inferred← citeshttps://doi.org/10.1016/j.aac.2023.08.006openalex-snapshot
A novel ABA structural analogues enhanced plant resistance by inducing the plant immunity and inactivating ABA signaling pathway
inferred← citeshttps://doi.org/10.1016/j.abb.2004.06.017openalex-snapshot
Modulation of plant ion channels by oxidizing and reducing agents
inferred← citeshttps://doi.org/10.1016/j.agwat.2024.108949openalex-snapshot
Achieving sustainable rice production through nitrogen-potassium harmony for enhanced economic and environmental gains
inferred← citeshttps://doi.org/10.1016/j.agwat.2024.108960openalex-snapshot
Comprehensive analysis on investigating water-saving potentials of irrigated cotton in semi-arid area in China
inferred← citeshttps://doi.org/10.1016/j.algal.2017.09.020openalex-snapshot
Effect of phytohormones on growth and accumulation of pigments and fatty acids in the microalgae Scenedesmus quadricauda
inferred← citeshttps://doi.org/10.1016/j.algal.2018.08.009openalex-snapshot
The combined influence of 24‑epibrassinolide and 3‑indoleacetic acid on growth and accumulation of pigments and fatty acids in the microalgae Scenedesmus quadricauda (CPCC-158)
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2011.08.005openalex-snapshot
Targeting metabolic pathways for genetic engineering abiotic stress-tolerance in crops
inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.11.041openalex-snapshot
A protective role for the polyamine spermine against drought stress in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.11.102openalex-snapshot
Expression analysis of histone acetyltransferases in rice under drought stress
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2013.09.006openalex-snapshot
The role of ABA and MAPK signaling pathways in plant abiotic stress responses
inferred← citeshttps://doi.org/10.1016/j.cej.2021.132920openalex-snapshot
Promoting efficacy and environmental safety of photosensitive agrochemical stabilizer via lignin/surfactant coacervates
inferred← citeshttps://doi.org/10.1016/j.cj.2020.08.012openalex-snapshot
Exogenous abscisic acid coordinating leaf senescence and transport of assimilates into wheat grains under drought stress by regulating hormones homeostasis
inferred← citeshttps://doi.org/10.1016/j.cj.2026.04.002openalex-snapshot
Achieving high seed protein content in soybean by combining gene mining, genomic selection models, and genetic crosses
inferred← citeshttps://doi.org/10.1016/j.copbio.2006.02.002openalex-snapshot
Engineering drought tolerance in plants: discovering and tailoring genes to unlock the future
inferred← citeshttps://doi.org/10.1016/j.cub.2005.05.048openalex-snapshot
A Guard-Cell-Specific MYB Transcription Factor Regulates Stomatal Movements and Plant Drought Tolerance
inferred← citeshttps://doi.org/10.1016/j.cub.2005.06.041openalex-snapshot
AtMYB61, an R2R3-MYB Transcription Factor Controlling Stomatal Aperture in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.ecolmodel.2008.12.020openalex-snapshot
Mechanisms of moisture stress in a mid-latitude temperate forest: Implications for feedforward and feedback controls from an irrigation experiment
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2008.07.002openalex-snapshot
Over-expression of the stress-induced OsWRKY45 enhances disease resistance and drought tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2010.09.008openalex-snapshot
Time course analysis of ABA and non-ionic osmotic stress-induced changes in water status, chlorophyll fluorescence and osmotic adjustment in Arabidopsis thaliana wild-type (Columbia) and ABA-deficient mutant (aba2)
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2019.103965openalex-snapshot
Calcium-dependent changes in physicochemical properties and the proteome dynamics influence dehydration responses in rice
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104468openalex-snapshot
In situ determination of guard cell ion flux underpins the mechanism of ABA-mediated stomatal closure in barley plants exposed to PEG-induced drought stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104523openalex-snapshot
MdCIB1, an apple bHLH transcription factor, plays a positive regulator in response to drought stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105037openalex-snapshot
Mycorrhizal symbiosis and water condition affect ozone sensitivity of Medicago sativa L. by mediating stomatal conductance
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105346openalex-snapshot
Independent and combined influence of drought stress and nitrogen deficiency on physiological and proteomic changes of barley leaves
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2025.106142openalex-snapshot
Functional lack of SLAC1 modifies guard cell metabolism without impacting photosynthesis under elevated [CO2] and moderated water restriction
inferred← citeshttps://doi.org/10.1016/j.fcr.2005.08.018openalex-snapshot
Role of ABA in integrating plant responses to drought and salt stresses
inferred← citeshttps://doi.org/10.1016/j.fcr.2020.107861openalex-snapshot
Morpho-physiological and molecular evaluation of drought tolerance in cassava (Manihot esculenta Crantz)
inferred← citeshttps://doi.org/10.1016/j.fcr.2023.109154openalex-snapshot
Diagnosing crop water status based on canopy temperature as a function of film mulching and deficit irrigation
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