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Mechanisms of cytosolic calcium elevation in plants: the role of ion channels, calcium extrusion systems and NADPH oxidase-mediated ‘ROS-Ca2+ Hub’
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Voltage‐dependent calcium‐permeable channels in the plasma membrane of a higher plant cell.
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Calcium Buffering Capacity of Neuronal Cell Cytosol Measured by Flash Photolysis of Calcium Buffer NP-EGTA
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The Plasma Membrane Ca2+ ATPase: Purification by Calmodulin Affinity Chromatography, and Reconstitution of the Purified Protein
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Hyperpolarization-activated Ca 2+ -permeable Channels in the Plasma Membrane of Tomato Cells
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Glutamate activates cation currents in the plasma membrane of Arabidopsis root cells
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The Arabidopsis cax3 mutants display altered salt tolerance, pH sensitivity and reduced plasma membrane H+-ATPase activity
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OsACA6, a P-type 2B Ca2+ ATPase functions in cadmium stress tolerance in tobacco by reducing the oxidative stress load
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Salicylic acid in plant salinity stress signalling and tolerance
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The origin and function of calmodulin regulated Ca2+ pumps in plants
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NaCl-induced expression of glutathione reductase in roots of rice (Oryza sativa L.) seedlings is mediated through hydrogen peroxide but not abscisic acid
inferredcites →https://doi.org/10.1007/s11183-005-0038-1openalex-snapshot
Calcium signaling system in plants
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Activation of plasma membrane voltage‐dependent calcium‐permeable channels by disruption of microtubules in carrot cells
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Two MscS Homologs Provide Mechanosensitive Channel Activities in the Arabidopsis Root
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The Cyclic Nucleotide-Gated Channel CNGC14 Regulates Root Gravitropism in Arabidopsis thaliana
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Mechanisms of oxidative stress in plants: From classical chemistry to cell biology
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Salt and osmotic stress cause rapid increases in Arabidopsis thaliana cGMP levels
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Vacuolar ion channels: Roles in plant nutrition and signalling
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Characterisation of 13 glutamate receptor-like genes encoded in the tomato genome by structure, phylogeny and expression profiles
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Direct Regulation of the NADPH Oxidase RBOHD by the PRR-Associated Kinase BIK1 during Plant Immunity
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Transport Across Chloroplast Membranes: Optimizing Photosynthesis for Adverse Environmental Conditions
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Functions of the respiratory burst oxidase in biotic interactions, abiotic stress and development
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Arabidopsis NADPH oxidases, AtrbohD and AtrbohF, are essential for jasmonic acid-induced expression of genes regulated by MYC2 transcription factor
inferredcites →https://doi.org/10.1016/j.plantsci.2015.10.003openalex-snapshot
Salt stress sensing and early signalling events in plant roots: Current knowledge and hypothesis
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Genome-wide analysis of plant-type II Ca2+ATPases gene family from rice and Arabidopsis: Potential role in abiotic stresses
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An ethylene and ROS-dependent pathway is involved in low ammonium-induced root hair elongation in Arabidopsis seedlings
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Cation channels are involved in brassinosteroid signalling in higher plants
inferredcites →https://doi.org/10.1016/j.str.2008.01.011openalex-snapshot
Crystal Structure of the CaV2 IQ Domain in Complex with Ca2+/Calmodulin: High-Resolution Mechanistic Implications for Channel Regulation by Ca2+
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Molecular aspects of higher plant P-type Ca2+-ATPases
inferredcites →https://doi.org/10.1016/s0005-2736(02)00509-6openalex-snapshot
Genes for calcium-permeable channels in the plasma membrane of plant root cells
inferredcites →https://doi.org/10.1016/s0021-9258(18)92938-8openalex-snapshot
Calcium binding to calmodulin and its globular domains
inferredcites →https://doi.org/10.1016/s0896-6273(03)00560-9openalex-snapshot
Unified Mechanisms of Ca2+ Regulation across the Ca2+ Channel Family
inferredcites →https://doi.org/10.1016/s0960-9822(02)00510-9openalex-snapshot
Calcium-mediated apoptosis in a plant hypersensitive disease resistance response
inferredcites →https://doi.org/10.1021/bi901846yopenalex-snapshot
Identification of the Binding Site for the Regulatory Calcium-Binding Domain in the Catalytic Domain of NOX5
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Is the infiltration‐centrifugation technique appropriate for the isolation of apoplastic fluid? A critical evaluation with different plant species
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Calcium channels activated by hydrogen peroxide mediate abscisic acid signalling in guard cells
inferredcites →https://doi.org/10.1038/nature01485openalex-snapshot
Reactive oxygen species produced by NADPH oxidase regulate plant cell growth
inferredcites →https://doi.org/10.1038/nature11539openalex-snapshot
A bimodular mechanism of calcium control in eukaryotes
inferredcites →https://doi.org/10.1038/nature12233openalex-snapshot
Structural basis for alternating access of a eukaryotic calcium/proton exchanger
inferredcites →https://doi.org/10.1038/nature13593openalex-snapshot
OSCA1 mediates osmotic-stress-evoked Ca2+ increases vital for osmosensing in Arabidopsis
inferredcites →https://doi.org/10.1038/nature16446openalex-snapshot
Structure of the voltage-gated two-pore channel TPC1 from Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/nature17194openalex-snapshot
Structure, inhibition and regulation of two-pore channel TPC1 from Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/srep17117openalex-snapshot
A rice tonoplastic calcium exchanger, OsCCX2 mediates Ca2+/cation transport in yeast
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Plasma membrane depolarization‐activated calcium channels, stimulated by microtubule‐depolymerizing drugs in wild‐type Arabidopsis thaliana protoplasts, display constitutively large activities and a longer half‐life in ton 2 mutant cells affected in the organization of cortical microtubules
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Characterisation of a novel gene family of putative cyclic nucleotide‐ and calmodulin‐regulated ion channels in Arabidopsis thaliana
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Protein phosphorylation activates the guard cell Ca2+ channel and is a prerequisite for gating by abscisic acid
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01467.xopenalex-snapshot
Arabidopsis thaliana root non‐selective cation channels mediate calcium uptake and are involved in growth
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01849.xopenalex-snapshot
A role for glycine in the gating of plant NMDA‐like receptors
inferredcites →https://doi.org/10.1071/fp15109openalex-snapshot
Signalling via glutamate and GLRs in Arabidopsis thaliana
inferredcites →https://doi.org/10.1071/fp15252openalex-snapshot
Root-to-shoot signalling: integration of diverse molecules, pathways and functions
inferredcites →https://doi.org/10.1073/pnas.012452499openalex-snapshot
Arabidopsis gp91 phox homologues AtrbohD and AtrbohF are required for accumulation of reactive oxygen intermediates in the plant defense response
inferredcites →https://doi.org/10.1073/pnas.0333408100openalex-snapshot
Blue light activates calcium-permeable channels in Arabidopsis mesophyll cells via the phototropin signaling pathway
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.1221294110openalex-snapshot
Calcium-dependent protein kinase/NADPH oxidase activation circuit is required for rapid defense signal propagation
inferredcites →https://doi.org/10.1073/pnas.1302515110openalex-snapshot
Crystal structure of Ca 2+ /H + antiporter protein YfkE reveals the mechanisms of Ca 2+ efflux and its pH regulation
inferredcites →https://doi.org/10.1073/pnas.1524629113openalex-snapshot
Cyclic nucleotide-gated channel 18 is an essential Ca 2+ channel in pollen tube tips for pollen tube guidance to ovules in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.160250397openalex-snapshot
Hyperpolarization-activated calcium channels at the tip of Arabidopsis root hairs
inferredcites →https://doi.org/10.1074/jbc.m112.351643openalex-snapshot
A Na+/Ca2+ Exchanger-like Protein (AtNCL) Involved in Salt Stress in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m115.692574openalex-snapshot
Transmembrane Topologies of Ca2+-permeable Mechanosensitive Channels MCA1 and MCA2 in Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/jbc.m310268200openalex-snapshot
Mechanism of Ca2+ Activation of the NADPH Oxidase 5 (NOX5)
inferredcites →https://doi.org/10.1074/jbc.m608966200openalex-snapshot
Novel Mechanism of Activation of NADPH Oxidase 5
inferredcites →https://doi.org/10.1074/jbc.o114.555565openalex-snapshot
The Plasma Membrane Calcium Pump: New Ways to Look at an Old Enzyme
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Why Calcium? How Calcium Became the Best Communicator
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Proteomic Study of Microsomal Proteins Reveals a Key Role for Arabidopsis Annexin 1 in Mediating Heat Stress-Induced Increase in Intracellular Calcium Levels
inferredcites →https://doi.org/10.1080/09168451.2016.1179094openalex-snapshot
Indole-3-acetic acid-induced oxidative burst and an increase in cytosolic calcium ion concentration in rice suspension culture
inferredcites →https://doi.org/10.1089/ars.2006.8.1103openalex-snapshot
A Computational Model for Free Radicals Transport in the Microcirculation
inferredcites →https://doi.org/10.1093/jxb/erj064openalex-snapshot
Arabidopsis thaliana Cyclic Nucleotide Gated Channel 3 forms a non-selective ion transporter involved in germination and cation transport
inferredcites →https://doi.org/10.1093/jxb/erq424openalex-snapshot
Heterotrimeric G-protein regulation of ROS signalling and calcium currents in Arabidopsis guard cells
inferredcites →https://doi.org/10.1093/jxb/ert152openalex-snapshot
Evidence of oxidative attenuation of auxin signalling
inferredcites →https://doi.org/10.1093/jxb/ert375openalex-snapshot
ROS as key players in plant stress signalling
inferredcites →https://doi.org/10.1093/jxb/ert423openalex-snapshot
Cross-talk between reactive oxygen species and polyamines in regulation of ion transport across the plasma membrane: implications for plant adaptive responses
inferredcites →https://doi.org/10.1093/jxb/ert430openalex-snapshot
ROS homeostasis in halophytes in the context of salinity stress tolerance
inferredcites →https://doi.org/10.1093/jxb/erv099openalex-snapshot
ROS and RNS in plant physiology: an overview
inferredcites →https://doi.org/10.1093/jxb/erv294openalex-snapshot
A calcium-binding protein, rice annexin OsANN1, enhances heat stress tolerance by modulating the production of H2O2
inferredcites →https://doi.org/10.1093/jxb/erv465openalex-snapshot
On a quest for stress tolerance genes: membrane transporters in sensing and adapting to hostile soils
inferredcites →https://doi.org/10.1093/jxb/erv500openalex-snapshot
AtCNGC2 is involved in jasmonic acid-induced calcium mobilization
inferredcites →https://doi.org/10.1093/jxb/erv576openalex-snapshot
The Arabidopsis glutamate receptor-like geneGLR3.6controls root development by repressing the Kip-related protein geneKRP4
inferredcites →https://doi.org/10.1093/jxb/erw034openalex-snapshot
Tissue-specific root ion profiling reveals essential roles of the CAX and ACA calcium transport systems in response to hypoxia in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erw378openalex-snapshot
Revealing the roles of GORK channels and NADPH oxidase in acclimation to hypoxia in Arabidopsis
inferredcites →https://doi.org/10.1093/mp/ssr018openalex-snapshot
The Role of Cyclic Nucleotide-Gated Ion Channels in Plant Immunity
inferredcites →https://doi.org/10.1093/mp/sst125openalex-snapshot
A Calcium-Dependent Protein Kinase Interacts with and Activates A Calcium Channel to Regulate Pollen Tube Growth
inferredcites →https://doi.org/10.1093/mp/sst174openalex-snapshot
Arabidopsis CNGC18 Is a Ca2+-Permeable Channel
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026167openalex-snapshot
Molecular evolution of glutamate receptors: a primitive signaling mechanism that existed before plants and animals diverged
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029426openalex-snapshot
Salicylic Acid Induces Extracellular Superoxide Generation Followed by an Increase in Cytosolic Calcium Ion in Tobacco Suspension Culture: The Earliest Events in Salicylic Acid Signal Transduction
inferredcites →https://doi.org/10.1093/pcp/pci063openalex-snapshot
Ca2+ Influx into Lily Pollen Grains Through a Hyperpolarization-activated Ca2+-permeable Channel Which Can be Regulated by Extracellular CaM
inferredcites →https://doi.org/10.1093/pcp/pct021openalex-snapshot
An IQ Domain Mediates the Interaction with Calmodulin in a Plant Cyclic Nucleotide-Gated Channel
inferredcites →https://doi.org/10.1093/pcp/pcv063openalex-snapshot
Regulation of the NADPH Oxidase RBOHD During Plant Immunity
inferredcites →https://doi.org/10.1094/mpmi.2001.14.10.1261openalex-snapshot
Ectopic Expression of an Arabidopsis Calmodulin-Like Domain Protein Kinase-Enhanced NADPH Oxidase Activity and Oxidative Burst in Tomato Protoplasts
inferredcites →https://doi.org/10.1101/cshperspect.a003947openalex-snapshot
Voltage-Gated Calcium Channels
inferredcites →https://doi.org/10.1101/cshperspect_biol/openalex-snapshot
Cold Spring Harbor Perspectives in Biology
inferredcites →https://doi.org/10.1104/pp.005769openalex-snapshot
The Voltage-Independent Cation Channel in the Plasma Membrane of Wheat Roots Is Permeable to Divalent Cations and May Be Involved in Cytosolic Ca2+ Homeostasis
inferredcites →https://doi.org/10.1104/pp.010524openalex-snapshot
Sodium Fluxes through Nonselective Cation Channels in the Plasma Membrane of Protoplasts from Arabidopsis Roots
inferredcites →https://doi.org/10.1104/pp.104.042069openalex-snapshot
Reactive Oxygen Species Activation of Plant Ca2+ Channels. A Signaling Mechanism in Polar Growth, Hormone Transduction, Stress Signaling, and Hypothetically Mechanotransduction
inferredcites →https://doi.org/10.1104/pp.104.042754openalex-snapshot
Ca2+-Permeable Channels in the Plasma Membrane of Arabidopsis Pollen Are Regulated by Actin Microfilaments
inferredcites →https://doi.org/10.1104/pp.105.062257openalex-snapshot
Heat Stress Phenotypes of Arabidopsis Mutants Implicate Multiple Signaling Pathways in the Acquisition of Thermotolerance
inferredcites →https://doi.org/10.1104/pp.106.077073openalex-snapshot
Reactive Species and Antioxidants. Redox Biology Is a Fundamental Theme of Aerobic Life
inferredcites →https://doi.org/10.1104/pp.106.082388openalex-snapshot
Extracellular Ca2+ Ameliorates NaCl-Induced K+ Loss from Arabidopsis Root and Leaf Cells by Controlling Plasma Membrane K+-Permeable Channels
inferredcites →https://doi.org/10.1104/pp.106.088989openalex-snapshot
Calcium Entry Mediated by GLR3.3, an Arabidopsis Glutamate Receptor with a Broad Agonist Profile
inferredcites →https://doi.org/10.1104/pp.109.135228openalex-snapshot
The Role of Annexin 1 in Drought Stress in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.174722openalex-snapshot
Receptor-Like Activity Evoked by Extracellular ADP in Arabidopsis Root Epidermal Plasma Membrane
inferredcites →https://doi.org/10.1104/pp.112.197509openalex-snapshot
Ca2+ Conduction by an Amino Acid-Gated Ion Channel Related to Glutamate Receptors
inferredcites →https://doi.org/10.1104/pp.113.217810openalex-snapshot
Salinity-Induced Calcium Signaling and Root Adaptation in Arabidopsis Require the Calcium Regulatory Protein Annexin1
inferredcites →https://doi.org/10.1104/pp.113.220855openalex-snapshot
Plant Calcium-Permeable Channels
inferredcites →https://doi.org/10.1104/pp.113.225045openalex-snapshot
Identification of Cyclic GMP-Activated Nonselective Ca2+-Permeable Cation Channels and Associated CNGC5 and CNGC6 Genes in Arabidopsis Guard Cells
inferredcites →https://doi.org/10.1104/pp.124.4.1511openalex-snapshot
Glutamate-Gated Calcium Fluxes in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.16.00938openalex-snapshot
Recent Progress in Understanding the Role of Reactive Oxygen Species in Plant Cell Signaling
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An NADPH-Oxidase/Polyamine Oxidase Feedback Loop Controls Oxidative Burst Under Salinity
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A Plant Homolog of the Neutrophil NADPH Oxidase gp91phox Subunit Gene Encodes a Plasma Membrane Protein with Ca2+ Binding Motifs
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Death Don't Have No Mercy and Neither Does Calcium: Arabidopsis CYCLIC NUCLEOTIDE GATED CHANNEL2 and Innate Immunity
inferredcites →https://doi.org/10.1105/tpc.106.048884openalex-snapshot
Calcium-Dependent Protein Kinases Regulate the Production of Reactive Oxygen Species by Potato NADPH Oxidase
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Zea mays Annexins Modulate Cytosolic Free Ca2+ and Generate a Ca2+-Permeable Conductance
inferredcites →https://doi.org/10.1105/tpc.11.11.2113openalex-snapshot
Expression of Arabidopsis CAX1 in Tobacco: Altered Calcium Homeostasis and Increased Stress Sensitivity
inferredcites →https://doi.org/10.1105/tpc.113.120642openalex-snapshot
Ca2+-Activated Reactive Oxygen Species Production by Arabidopsis RbohH and RbohJ Is Essential for Proper Pollen Tube Tip Growth
inferredcites →https://doi.org/10.1105/tpc.15.00870openalex-snapshot
Multiple Calmodulin-binding Sites Positively and Negatively Regulate Arabidopsis CYCLIC NUCLEOTIDE-GATED CHANNEL12
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Elevation of cytosolic calcium precedes anoxic gene expression in maize suspension-cultured cells.
inferredcites →https://doi.org/10.1105/tpc.6.9.1301openalex-snapshot
Oxidative Signals in Tobacco Increase Cytosolic Calcium.
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Investigating glutamate receptor‐like gene co‐expression inArabidopsis thaliana
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NaCl‐induced changes in cytosolic free Ca2+ in Arabidopsis thaliana are heterogeneous and modified by external ionic composition
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Spatial variation in H 2 O 2 response of Arabidopsis thaliana root epidermal Ca 2+ flux and plasma membrane Ca 2+ channels
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Plant extracellular ATP signalling by plasma membrane NADPH oxidase and Ca2+channels
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.04969.xopenalex-snapshot
A heat‐activated calcium‐permeable channel – Arabidopsis cyclic nucleotide‐gated ion channel 6 – is involved in heat shock responses
inferredcites →https://doi.org/10.1111/j.1399-3054.2008.01157.xopenalex-snapshot
The cyclic nucleotide‐gated channel, AtCNGC10, influences salt tolerance in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1399-3054.2010.01366.xopenalex-snapshot
The cyclic nucleotide-gated channel AtCNGC10 transports Ca2+and Mg2+inArabidopsis
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Further Studies of the Phloem Loading Process in Leaves of Barley and Spinach. The Comparison of Metabolite Concentrations in the Apoplastic Compartment with those in the Cytosolic Compartment and in the Sieve Tubes1
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The plant Ca 2+ ‐ATPase repertoire: biochemical features and physiological functions
inferredcites →https://doi.org/10.1111/j.1438-8677.2011.00466.xopenalex-snapshot
Plant cation/H+ exchangers (CAXs): biological functions and genetic manipulations
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01408.xopenalex-snapshot
Mutations in CAX1 produce phenotypes characteristic of plants tolerant to serpentine soils
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02042.xopenalex-snapshot
Reactive oxygen species produced by NADPH oxidase are involved in pollen tube growth
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02069.xopenalex-snapshot
Identification of hyperpolarization‐activated calcium channels in apical pollen tubes of Pyrus pyrifolia
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02128.xopenalex-snapshot
Physiological roles of nonselective cation channels in plants: from salt stress to signalling and development
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02465.xopenalex-snapshot
Two voltage‐dependent calcium channels co‐exist in the apical plasma membrane of Arabidopsis thaliana root hairs
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02831.xopenalex-snapshot
Root development under metal stress in Arabidopsis thaliana requires the H + /cation antiporter CAX4
inferredcites →https://doi.org/10.1111/j.1742-4658.2008.06488.xopenalex-snapshot
Structure, regulation and evolution of Nox‐family NADPH oxidases that produce reactive oxygen species
inferredcites →https://doi.org/10.1111/j.1742-4658.2011.08369.xopenalex-snapshot
Calcium‐permeable channels in plant cells
inferredcites →https://doi.org/10.1111/nph.12380openalex-snapshot
Nitro‐oxidative stress vs oxidative or nitrosative stress in higher plants
inferredcites →https://doi.org/10.1111/pce.12280openalex-snapshot
Cadmium induces two waves of reactive oxygen species in G lycine max ( L .) roots
inferredcites →https://doi.org/10.1111/pce.12620openalex-snapshot
Ca2+‐regulated and diurnal rhythm‐regulated Na+/Ca2+ exchanger AtNCL affects flowering time and auxin signalling in Arabidopsis
inferredcites →https://doi.org/10.1111/pce.12621openalex-snapshot
Stress‐triggered redox signalling: what's in pROSpect?
inferredcites →https://doi.org/10.1111/plb.12460openalex-snapshot
CAX ‐ing a wide net: Cation/H+ transporters in metal remediation and abiotic stress signalling
inferredcites →https://doi.org/10.1111/tpj.12311openalex-snapshot
Involvement of the glutamate receptor A t GLR 3.3 in plant defense signaling and resistance to H yaloperonospora arabidopsidis
inferredcites →https://doi.org/10.1111/tpj.12352openalex-snapshot
Os ACA 6 , a P‐type IIB Ca 2+ ATP ase promotes salinity and drought stress tolerance in tobacco by ROS scavenging and enhancing the expression of stress‐responsive genes
inferredcites →https://doi.org/10.1111/tpj.13105openalex-snapshot
Engineered silver nanoparticles are sensed at the plasma membrane and dramatically modify the physiology ofArabidopsis thalianaplants
inferredcites →https://doi.org/10.1111/tpj.13120openalex-snapshot
Orchestration of hydrogen peroxide and nitric oxide in brassinosteroid‐mediated systemic virus resistance in Nicotiana benthamiana
inferredcites →https://doi.org/10.1124/pr.110.002980openalex-snapshot
NADPH Oxidase-Mediated Redox Signaling: Roles in Cellular Stress Response, Stress Tolerance, and Tissue Repair
inferredcites →https://doi.org/10.1126/science.1071505openalex-snapshot
RopGAP4-Dependent Rop GTPase Rheostat Control of Arabidopsis Oxygen Deprivation Tolerance
inferredcites →https://doi.org/10.1126/science.1201101openalex-snapshot
Glutamate Receptor–Like Genes Form Ca 2+ Channels in Pollen Tubes and Are Regulated by Pistil d -Serine
inferredcites →https://doi.org/10.1126/science.1239002openalex-snapshot
Structural Basis for the Counter-Transport Mechanism of a H + /Ca 2+ Exchanger
inferredcites →https://doi.org/10.1146/annurev-arplant-043014-114700openalex-snapshot
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inferredcites →https://doi.org/10.1146/annurev-arplant-043015-112130openalex-snapshot
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inferredcites →https://doi.org/10.1146/annurev-arplant-050312-120150openalex-snapshot
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inferredcites →https://doi.org/10.1146/annurev-arplant-070109-104628openalex-snapshot
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inferredcites →https://doi.org/10.1146/annurev.arplant.53.091901.161540openalex-snapshot
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inferredcites →https://doi.org/10.1186/1471-2148-7-109openalex-snapshot
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inferredcites →https://doi.org/10.1186/s12284-016-0081-xopenalex-snapshot
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inferredcites →https://doi.org/10.1186/s12864-016-2750-yopenalex-snapshot
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inferredcites →https://doi.org/10.1242/jcs.00201openalex-snapshot
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inferredcites →https://doi.org/10.1371/journal.pone.0012348openalex-snapshot
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inferredcites →https://doi.org/10.3389/fpls.2011.00085openalex-snapshot
Calcium Efflux Systems in Stress Signaling and Adaptation in Plants
inferredcites →https://doi.org/10.3389/fpls.2012.00001openalex-snapshot
Protein Phylogenetic Analysis of Ca2+/cation Antiporters and Insights into their Evolution in Plants
inferredcites →https://doi.org/10.3389/fpls.2014.00467openalex-snapshot
Regulation of Na+ fluxes in plants
inferredcites →https://doi.org/10.3389/fpls.2015.00427openalex-snapshot
Plant signaling networks involving Ca2+ and Rboh/Nox-mediated ROS production under salinity stress
inferredcites →https://doi.org/10.3389/fpls.2015.00809openalex-snapshot
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inferredcites →https://doi.org/10.3389/fpls.2016.00187openalex-snapshot
Global Plant Stress Signaling: Reactive Oxygen Species at the Cross-Road
inferredcites →https://doi.org/10.3389/fpls.2016.00327openalex-snapshot
Calcium Sensors as Key Hubs in Plant Responses to Biotic and Abiotic Stresses
inferredcites →https://doi.org/10.3389/fpls.2016.01296openalex-snapshot
Calcium-Mediated Abiotic Stress Signaling in Roots
inferredcites →https://doi.org/10.3390/ijms14022652openalex-snapshot
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inferredcites →https://doi.org/10.3390/plants2040541openalex-snapshot
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Expression of Arabidopsis MCA1 enhanced mechanosensitive channel activity in theXenopus laevisoocyte plasma membrane
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The Role of Reactive Oxygen Species and Calcium Ions in the Implementation of the Stress-Protective Effect of Brassinosteroids on Plant Cells
What points at this work
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inferred← citeshttps://doi.org/10.32607/actanaturae.27477openalex-snapshot
Reactive Byproducts of Plant Redox Metabolism and Protein Functions
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inferred← citeshttps://doi.org/10.3389/fpls.2019.01407openalex-snapshot
Illumination/Darkness-Induced Changes in Leaf Surface Potential Linked With Kinetics of Ion Fluxes
inferred← citeshttps://doi.org/10.3389/fpls.2020.598327openalex-snapshot
Ca2+/Calmodulin Complex Triggers CAMTA Transcriptional Machinery Under Stress in Plants: Signaling Cascade and Molecular Regulation
inferred← citeshttps://doi.org/10.3389/fpls.2020.613936openalex-snapshot
Sodium Influx and Potassium Efflux Currents in Sunflower Root Cells Under High Salinity
inferred← citeshttps://doi.org/10.3389/fpls.2022.1098146openalex-snapshot
Phosphate-deprivation and damage signalling by extracellular ATP
inferred← citeshttps://doi.org/10.3389/fpls.2022.864215openalex-snapshot
Function of Protein Kinases in Leaf Senescence of Plants
inferred← citeshttps://doi.org/10.3389/fpls.2022.964059openalex-snapshot
Calcium channels and transporters: Roles in response to biotic and abiotic stresses
inferred← citeshttps://doi.org/10.3389/fpls.2023.1282465openalex-snapshot
Editorial: Plant signaling in response to environmental stresses
inferred← citeshttps://doi.org/10.3389/fpls.2024.1376427openalex-snapshot
Increasing Ca2+ accumulation in salt glands under salt stress increases stronger selective secretion of Na+ in Plumbago auriculata tetraploids
inferred← citeshttps://doi.org/10.3389/fpls.2025.1553057openalex-snapshot
Functional analysis and interaction networks of Rboh in poplar under abiotic stress
inferred← citeshttps://doi.org/10.3389/fpls.2026.1765513openalex-snapshot
Hormonal priming with indole-3-acetic acid modulates antioxidant defense, gene expression, and physiological responses under salinity in Limonium spp.
inferred← citeshttps://doi.org/10.3390/antiox8090384openalex-snapshot
Regulation of Ascorbate-Glutathione Pathway in Mitigating Oxidative Damage in Plants under Abiotic Stress
inferred← citeshttps://doi.org/10.3390/antiox9050435openalex-snapshot
A Novel and Potentially Multifaceted Dehydroascorbate Reductase Increasing the Antioxidant Systems is Induced by Beauvericin in Tomato
inferred← citeshttps://doi.org/10.3390/app11156668openalex-snapshot
The Genetic Regulation of Secondary Metabolic Pathways in Response to Salinity and Drought as Abiotic Stresses
inferred← citeshttps://doi.org/10.3390/biom11060788openalex-snapshot
Improving Performance of Salt-Grown Crops by Exogenous Application of Plant Growth Regulators
inferred← citeshttps://doi.org/10.3390/cells11121896openalex-snapshot
Reactive Oxygen Species Distribution Involved in Stipe Gradient Elongation in the Mushroom Flammulina filiformis
inferred← citeshttps://doi.org/10.3390/ijms19030702openalex-snapshot
Hydrogen Peroxide-Induced Root Ca2+ and K+ Fluxes Correlate with Salt Tolerance in Cereals: Towards the Cell-Based Phenotyping
inferred← citeshttps://doi.org/10.3390/ijms19030897openalex-snapshot
An Anion Conductance, the Essential Component of the Hydroxyl-Radical-Induced Ion Current in Plant Roots
inferred← citeshttps://doi.org/10.3390/ijms19041263openalex-snapshot
ROS-Activated Ion Channels in Plants: Biophysical Characteristics, Physiological Functions and Molecular Nature
inferred← citeshttps://doi.org/10.3390/ijms19092812openalex-snapshot
Hydrogen Peroxide: Its Role in Plant Biology and Crosstalk with Signalling Networks
inferred← citeshttps://doi.org/10.3390/ijms19113456openalex-snapshot
Plant Calcium Signaling in Response to Potassium Deficiency
inferred← citeshttps://doi.org/10.3390/ijms20030699openalex-snapshot
Identification of QTL Related to ROS Formation under Hypoxia and Their Association with Waterlogging and Salt Tolerance in Barley
inferred← citeshttps://doi.org/10.3390/ijms21144882openalex-snapshot
Changes in Expression Level of OsHKT1;5 Alters Activity of Membrane Transporters Involved in K+ and Ca2+ Acquisition and Homeostasis in Salinized Rice Roots
inferred← citeshttps://doi.org/10.3390/ijms221910715openalex-snapshot
Electrical Signaling of Plants under Abiotic Stressors: Transmission of Stimulus-Specific Information
inferred← citeshttps://doi.org/10.3390/ijpb15010016openalex-snapshot
Calcium-Mediated Modulation of GC Switch Regulates Peroxisomal H2O2 Levels in Response to Wounding in Plants
inferred← citeshttps://doi.org/10.3390/plants10030436openalex-snapshot
Antioxidant Enzymatic Activity and Osmotic Adjustment as Components of the Drought Tolerance Mechanism in Carex duriuscula
inferred← citeshttps://doi.org/10.3390/plants10081513openalex-snapshot
Revealing the Role of the Calcineurin B-Like Protein-Interacting Protein Kinase 9 (CIPK9) in Rice Adaptive Responses to Salinity, Osmotic Stress, and K+ Deficiency
inferred← citeshttps://doi.org/10.3390/plants10102178openalex-snapshot
Emerging Roles of γ Aminobutyric Acid (GABA) Gated Channels in Plant Stress Tolerance
inferred← citeshttps://doi.org/10.3390/plants10112433openalex-snapshot
Differential Physiological Responses to Salt Stress between Salt-Sensitive and Salt-Tolerant japonica Rice Cultivars at the Post-Germination and Seedling Stages
inferred← citeshttps://doi.org/10.3390/plants11081084openalex-snapshot
Differential Impact of Nitric Oxide and Abscisic Acid on the Cellular and Physiological Functioning of sub1A QTL Bearing Rice Genotype under Salt Stress
inferred← citeshttps://doi.org/10.3390/plants11101351openalex-snapshot
Crosstalk between Ca2+ and Other Regulators Assists Plants in Responding to Abiotic Stress
inferred← citeshttps://doi.org/10.3390/plants13010046openalex-snapshot
Ion Changes and Signaling under Salt Stress in Wheat and Other Important Crops
inferred← citeshttps://doi.org/10.3390/plants14213383openalex-snapshot
Functional Trait Variability of Salicornia europaea L. Across Inland Saline Habitats: Integrating Shoot and Root Morphometrics with Soil Salinity and Trophic Status
inferred← citeshttps://doi.org/10.3390/plants15142212openalex-snapshot
Reactive Oxygen Species in Crop Plants: Production, Detoxification, Signaling, and Molecular Cross-Talk
inferred← citeshttps://doi.org/10.3390/plants9091108openalex-snapshot
Keep Calm and Survive: Adaptation Strategies to Energy Crisis in Fruit Trees under Root Hypoxia
inferred← citeshttps://doi.org/10.3390/plants9091216openalex-snapshot
Potassium Efflux and Cytosol Acidification as Primary Anoxia-Induced Events in Wheat and Rice Seedlings
inferred← citeshttps://doi.org/10.3390/plants9121781openalex-snapshot
Decoding Heavy Metal Stress Signalling in Plants: Towards Improved Food Security and Safety
inferred← citeshttps://doi.org/10.35550/vbio2020.02.070openalex-snapshot
Functional state of plasmalemma and apoplast in barley mesophyll under conditions of hyperthermia and Bipolaris sorokiniana infection
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787524openalex-snapshot
Additional file 10 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787530openalex-snapshot
Additional file 11 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787533openalex-snapshot
Additional file 12 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787539openalex-snapshot
Additional file 13 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787542openalex-snapshot
Additional file 14 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787548openalex-snapshot
Additional file 15 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787551openalex-snapshot
Additional file 16 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787557openalex-snapshot
Additional file 17 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787560openalex-snapshot
Additional file 18 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787563openalex-snapshot
Additional file 1 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787566openalex-snapshot
Additional file 2 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787572openalex-snapshot
Additional file 3 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787575openalex-snapshot
Additional file 4 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787578openalex-snapshot
Additional file 5 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787581openalex-snapshot
Additional file 6 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787584openalex-snapshot
Additional file 7 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787590openalex-snapshot
Additional file 8 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.6084/m9.figshare.13787593openalex-snapshot
Additional file 9 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters
inferred← citeshttps://doi.org/10.70675/bcbfe84azc088z4e0fzb940za4ba8f1bd287openalex-snapshot
Rôle de la protéine de la signalisation du calcium CML8 dans la réponse d'Arabidopsis thaliana à de multiples stress : implication dans l'immunité contre plusieurs pathogènes et importance de l'auxine
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