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Structure, Function, and Regulation of the Plasma Membrane Na+/H+ Antiporter Salt Overly Sensitive 1 in Plants
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00299-013-1528-9openalex-snapshot
A constitutively active form of a durum wheat Na+/H+ antiporter SOS1 confers high salt tolerance to transgenic Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-004-1333-3openalex-snapshot
Integration and channeling of calcium signaling through the CBL calcium sensor/CIPK protein kinase network
inferredcites →https://doi.org/10.1007/s00438-006-0184-yopenalex-snapshot
Arabidopsis–rice–wheat gene orthologues for Na+ transport and transcript analysis in wheat–L. elongatum aneuploids under salt stress
inferredcites →https://doi.org/10.1007/s00709-013-0540-9openalex-snapshot
Co-expression of the Arabidopsis SOS genes enhances salt tolerance in transgenic tall fescue (Festuca arundinacea Schreb.)
inferredcites →https://doi.org/10.1007/s11032-006-9005-6openalex-snapshot
Co-expression of the Suaeda salsa SsNHX1 and Arabidopsis AVP1 confer greater salt tolerance to transgenic rice than the single SsNHX1
inferredcites →https://doi.org/10.1007/s11103-010-9680-xopenalex-snapshot
The woody plant poplar has a functionally conserved salt overly sensitive pathway in response to salinity stress
inferredcites →https://doi.org/10.1007/s11103-016-0520-5openalex-snapshot
Stability and localization of 14-3-3 proteins are involved in salt tolerance in Arabidopsis
inferredcites →https://doi.org/10.1007/s12374-010-9135-6openalex-snapshot
Overexpression of OsVP1 and OsNHX1 Increases Tolerance to Drought and Salinity in Rice
inferredcites →https://doi.org/10.1016/0092-8674(95)90405-0openalex-snapshot
Protein kinases and phosphatases: The Yin and Yang of protein phosphorylation and signaling
inferredcites →https://doi.org/10.1016/j.abb.2008.02.018openalex-snapshot
Functional characterization of a wheat plasma membrane Na+/H+ antiporter in yeast
inferredcites →https://doi.org/10.1016/j.biochi.2011.05.019openalex-snapshot
Calcium decoding mechanisms in plants
inferredcites →https://doi.org/10.1016/j.cell.2006.06.011openalex-snapshot
A Protein Kinase, Interacting with Two Calcineurin B-like Proteins, Regulates K+ Transporter AKT1 in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2009.07.004openalex-snapshot
CHL1 Functions as a Nitrate Sensor in Plants
inferredcites →https://doi.org/10.1016/j.cell.2016.08.029openalex-snapshot
Abiotic Stress Signaling and Responses in Plants
inferredcites →https://doi.org/10.1016/j.copbio.2013.12.004openalex-snapshot
Salt resistant crop plants
inferredcites →https://doi.org/10.1016/j.devcel.2019.02.010openalex-snapshot
The SOS2-SCaBP8 Complex Generates and Fine-Tunes an AtANN4-Dependent Calcium Signature under Salt Stress
inferredcites →https://doi.org/10.1016/j.ecoenv.2004.06.010openalex-snapshot
Salt tolerance and salinity effects on plants: a review
inferredcites →https://doi.org/10.1016/j.envexpbot.2021.104752openalex-snapshot
The calcium sensor CBL10 negatively regulates plasma membrane H+-ATPase activity and alkaline stress response in Arabidopsis
inferredcites →https://doi.org/10.1016/j.jmb.2008.12.042openalex-snapshot
Conformations of NhaA, the Na/H Exchanger from Escherichia coli, in the pH-Activated and Ion-Translocating States
inferredcites →https://doi.org/10.1016/j.jmb.2012.09.015openalex-snapshot
Structural Insights on the Plant Salt-Overly-Sensitive 1 (SOS1) Na+/H+ Antiporter
inferredcites →https://doi.org/10.1016/j.plantsci.2013.09.009openalex-snapshot
A gateway with a guard: How the endodermis regulates growth through hormone signaling
inferredcites →https://doi.org/10.1016/j.plantsci.2016.09.016openalex-snapshot
Hyperactive mutant of a wheat plasma membrane Na+/H+ antiporter improves the growth and salt tolerance of transgenic tobacco
inferredcites →https://doi.org/10.1016/j.tplants.2006.06.001openalex-snapshot
Nomenclature for HKT transporters, key determinants of plant salinity tolerance
inferredcites →https://doi.org/10.1016/j.tplants.2009.08.009openalex-snapshot
HKT transporter-mediated salinity resistance mechanisms in Arabidopsis and monocot crop plants
inferredcites →https://doi.org/10.1016/j.tplants.2014.02.001openalex-snapshot
Plant salt-tolerance mechanisms
inferredcites →https://doi.org/10.1016/j.tplants.2020.01.009openalex-snapshot
The CBL–CIPK Calcium Signaling Network: Unified Paradigm from 20 Years of Discoveries
inferredcites →https://doi.org/10.1016/j.xinn.2020.100017openalex-snapshot
Mechanisms of Plant Responses and Adaptation to Soil Salinity
inferredcites →https://doi.org/10.1016/s0005-2736(00)00135-8openalex-snapshot
Sodium transport in plant cells
inferredcites →https://doi.org/10.1016/s0014-5793(00)02016-0openalex-snapshot
CEO1, a new protein from Arabidopsis thaliana, protects yeast against oxidative damage1
inferredcites →https://doi.org/10.1016/s0076-6879(07)28024-3openalex-snapshot
Mechanisms of High Salinity Tolerance in Plants
inferredcites →https://doi.org/10.1016/s0092-8674(03)00429-xopenalex-snapshot
Inducers of Plant Systemic Acquired Resistance Regulate NPR1 Function through Redox Changes
inferredcites →https://doi.org/10.1016/s0968-0004(00)01720-5openalex-snapshot
Macromolecular electron microscopy in the era of structural genomics
inferredcites →https://doi.org/10.1016/s0968-0004(99)01383-3openalex-snapshot
The Ca2+–calmodulin-dependent protein kinase cascade
inferredcites →https://doi.org/10.1016/s1360-1385(00)01577-6openalex-snapshot
CDPKs – a kinase for every Ca2+ signal?
inferredcites →https://doi.org/10.1016/s1360-1385(99)01428-4openalex-snapshot
Molecular pieces to the puzzle of the interaction between potassium and sodium uptake in plants
inferredcites →https://doi.org/10.1038/cr.2011.50openalex-snapshot
Calcium-dependent modulation and plasma membrane targeting of the AKT2 potassium channel by the CBL4/CIPK6 calcium sensor/protein kinase complex
inferredcites →https://doi.org/10.1038/emboj.2010.321openalex-snapshot
Structure of the archaeal Na+/H+ antiporter NhaP1 and functional role of transmembrane helix 1
inferredcites →https://doi.org/10.1038/nature03692openalex-snapshot
Structure of a Na+/H+ antiporter and insights into mechanism of action and regulation by pH
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/nbt766openalex-snapshot
Overexpression of a plasma membrane Na+/H+ antiporter gene improves salt tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/ncomms2357openalex-snapshot
Release of SOS2 kinase from sequestration with GIGANTEA determines salt tolerance in Arabidopsis
inferredcites →https://doi.org/10.1038/ng1643openalex-snapshot
A rice quantitative trait locus for salt tolerance encodes a sodium transporter
inferredcites →https://doi.org/10.1038/s41586-019-1449-zopenalex-snapshot
Plant cell-surface GIPC sphingolipids sense salt to trigger Ca2+ influx
inferredcites →https://doi.org/10.1038/srep44637openalex-snapshot
EIN3 and SOS2 synergistically modulate plant salt tolerance
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01309.xopenalex-snapshot
Differential expression and function of Arabidopsis thaliana NHX Na+/H+ antiporters in the salt stress response
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01871.xopenalex-snapshot
Vacuolar cation/H + exchange, ion homeostasis, and leaf development are altered in a T‐DNA insertional mutant of AtNHX1 , the Arabidopsis vacuolar Na + /H + antiporter
inferredcites →https://doi.org/10.1073/pnas.0604421103openalex-snapshot
Suppression of Arabidopsis vesicle-SNARE expression inhibited fusion of H 2 O 2 -containing vesicles with tonoplast and increased salt tolerance
inferredcites →https://doi.org/10.1073/pnas.0604711103openalex-snapshot
The plasma membrane Na + /H + antiporter SOS1 interacts with RCD1 and functions in oxidative stress tolerance in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0707912104openalex-snapshot
A protein phosphorylation/dephosphorylation network regulates a plant potassium channel
inferredcites →https://doi.org/10.1073/pnas.1018921108openalex-snapshot
Activation of the plasma membrane Na/H antiporter Salt-Overly-Sensitive 1 (SOS1) by phosphorylation of an auto-inhibitory C-terminal domain
inferredcites →https://doi.org/10.1073/pnas.1103741108openalex-snapshot
CIRCADIAN CLOCK-ASSOCIATED 1 and LATE ELONGATED HYPOCOTYL regulate expression of the C-REPEAT BINDING FACTOR (CBF) pathway in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.120170197openalex-snapshot
The Arabidopsis thaliana salt tolerance gene SOS1 encodes a putative Na + /H + antiporter
inferredcites →https://doi.org/10.1073/pnas.122224699openalex-snapshot
Regulation of SOS1, a plasma membrane Na + /H + exchanger in Arabidopsis thaliana , by SOS2 and SOS3
inferredcites →https://doi.org/10.1073/pnas.132092099openalex-snapshot
Reconstitution in yeast of the Arabidopsis SOS signaling pathway for Na + homeostasis
inferredcites →https://doi.org/10.1073/pnas.1407610111openalex-snapshot
Structural basis of the regulatory mechanism of the plant CIPK family of protein kinases controlling ion homeostasis and abiotic stress
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/10.1073/pnas.241501798openalex-snapshot
AtHKT1 is a salt tolerance determinant that controls Na + entry into plant roots
inferredcites →https://doi.org/10.1073/pnas.97.7.3730openalex-snapshot
The Arabidopsis thaliana SOS2 gene encodes a protein kinase that is required for salt tolerance
inferredcites →https://doi.org/10.1073/pnas.97.7.3735openalex-snapshot
The Arabidopsis SOS2 protein kinase physically interacts with and is activated by the calcium-binding protein SOS3
inferredcites →https://doi.org/10.1074/jbc.m307982200openalex-snapshot
Regulation of Vacuolar Na+/H+ Exchange in Arabidopsis thaliana by the Salt-Overly-Sensitive (SOS) Pathway
inferredcites →https://doi.org/10.1093/aob/mcg058openalex-snapshot
Na+ Tolerance and Na+ Transport in Higher Plants
inferredcites →https://doi.org/10.1093/aob/mcu219openalex-snapshot
Rapid regulation of the plasma membrane H+-ATPase activity is essential to salinity tolerance in two halophyte species, Atriplex lentiformis and Chenopodium quinoa
inferredcites →https://doi.org/10.1093/jxb/erj114openalex-snapshot
Alkali cation exchangers: roles in cellular homeostasis and stress tolerance
inferredcites →https://doi.org/10.1093/jxb/erp391openalex-snapshot
Intracellular consequences of SOS1 deficiency during salt stress
inferredcites →https://doi.org/10.1093/jxb/erx156openalex-snapshot
A bioassay-guided fractionation system to identify endogenous small molecules that activate plasma membrane H+-ATPase activity in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erz549openalex-snapshot
The protein kinase complex CBL10–CIPK8–SOS1 functions in Arabidopsis to regulate salt tolerance
inferredcites →https://doi.org/10.1093/molbev/msu152openalex-snapshot
Distinct Roles for SOS1 in the Convergent Evolution of Salt Tolerance in Eutrema salsugineum and Schrenkiella parvula
inferredcites →https://doi.org/10.1093/mp/sst017openalex-snapshot
The Salt Overly Sensitive (SOS) Pathway: Established and Emerging Roles
inferredcites →https://doi.org/10.1093/mp/sst072openalex-snapshot
Inositol Polyphosphate Phosphatidylinositol 5-Phosphatase9 (At5PTase9) Controls Plant Salt Tolerance by Regulating Endocytosis
inferredcites →https://doi.org/10.1093/nar/gkn238openalex-snapshot
The Jpred 3 secondary structure prediction server
inferredcites →https://doi.org/10.1093/pcp/pcp143openalex-snapshot
Dynamic Aspects of Ion Accumulation by Vesicle Traffic Under Salt Stress in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.004507openalex-snapshot
Biochemical Characterization of the Arabidopsis Protein Kinase SOS2 That Functions in Salt Tolerance
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.103.025379openalex-snapshot
Induction of Salt and Osmotic Stress Tolerance by Overexpression of an Intracellular Vesicle Trafficking Protein AtRab7 (AtRabG3e)
inferredcites →https://doi.org/10.1104/pp.104.042234openalex-snapshot
AtHKT1 Facilitates Na+ Homeostasis and K+ Nutrition in Planta
inferredcites →https://doi.org/10.1104/pp.106.091025openalex-snapshot
Functional Analysis of SPINDLY in Gibberellin Signaling in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.092635openalex-snapshot
Conservation of the Salt Overly Sensitive Pathway in Rice
inferredcites →https://doi.org/10.1104/pp.109.137802openalex-snapshot
Loss of Halophytism by Interference with SOS1 Expression
inferredcites →https://doi.org/10.1104/pp.109.3.735openalex-snapshot
Ion Homeostasis in NaCl Stress Environments
inferredcites →https://doi.org/10.1104/pp.111.173377openalex-snapshot
Phosphorylation of SOS3-Like Calcium-Binding Proteins by Their Interacting SOS2-Like Protein Kinases Is a Common Regulatory Mechanism in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.16.00334openalex-snapshot
Arabidopsis CALCINEURIN B-LIKE10 Functions Independently of the SOS Pathway during Reproductive Development in Saline Conditions
inferredcites →https://doi.org/10.1105/tpc.000596openalex-snapshot
Cell Signaling during Cold, Drought, and Salt Stress
inferredcites →https://doi.org/10.1105/tpc.010021openalex-snapshot
Molecular Characterization of Functional Domains in the Protein Kinase SOS2 That Is Required for Plant Salt Tolerance
inferredcites →https://doi.org/10.1105/tpc.010371openalex-snapshot
The Putative Plasma Membrane Na + /H + Antiporter SOS1 Controls Long-Distance Na + Transport in Plants
inferredcites →https://doi.org/10.1105/tpc.10.7.1181openalex-snapshot
Genetic Analysis of Salt Tolerance in Arabidopsis: Evidence for a Critical Role of Potassium Nutrition
inferredcites →https://doi.org/10.1105/tpc.105.033589openalex-snapshot
Redox Homeostasis and Antioxidant Signaling: A Metabolic Interface between Stress Perception and Physiological Responses
inferredcites →https://doi.org/10.1105/tpc.105.035626openalex-snapshot
Arabidopsis Protein Kinase PKS5 Inhibits the Plasma Membrane H + -ATPase by Preventing Interaction with 14-3-3 Protein
inferredcites →https://doi.org/10.1105/tpc.106.042291openalex-snapshot
SCABP8/CBL10, a Putative Calcium Sensor, Interacts with the Protein Kinase SOS2 to Protect Arabidopsis Shoots from Salt Stress
inferredcites →https://doi.org/10.1105/tpc.108.064568openalex-snapshot
Shoot Na+ Exclusion and Increased Salinity Tolerance Engineered by Cell Type–Specific Alteration of Na+ Transport in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.066217openalex-snapshot
Phosphorylation of SOS3-LIKE CALCIUM BINDING PROTEIN8 by SOS2 Protein Kinase Stabilizes Their Protein Complex and Regulates Salt Tolerance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.069609openalex-snapshot
The Arabidopsis Chaperone J3 Regulates the Plasma Membrane H+-ATPase through Interaction with the PKS5 Kinase
inferredcites →https://doi.org/10.1105/tpc.111.089581openalex-snapshot
The Arabidopsis Na+/H+ Antiporters NHX1 and NHX2 Control Vacuolar pH and K+ Homeostasis to Regulate Growth, Flower Development, and Reproduction
inferredcites →https://doi.org/10.1105/tpc.111.095273openalex-snapshot
Ion Exchangers NHX1 and NHX2 Mediate Active Potassium Uptake into Vacuoles to Regulate Cell Turgor and Stomatal Function in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.104182openalex-snapshot
Phosphatidic Acid Regulates Microtubule Organization by Interacting with MAP65-1 in Response to Salt Stress in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.106393openalex-snapshot
UBIQUITIN-SPECIFIC PROTEASE16 Modulates Salt Tolerance in Arabidopsis by Regulating Na+/H+ Antiport Activity and Serine Hydroxymethyltransferase Stability
inferredcites →https://doi.org/10.1105/tpc.113.115659openalex-snapshot
An Arabidopsis Soil-Salinity–Tolerance Mutation Confers Ethylene-Mediated Enhancement of Sodium/Potassium Homeostasis
inferredcites →https://doi.org/10.1105/tpc.113.117069openalex-snapshot
Inhibition of the Arabidopsis Salt Overly Sensitive Pathway by 14-3-3 Proteins
inferredcites →https://doi.org/10.1105/tpc.114.135095openalex-snapshot
A Chaperone Function of NO CATALASE ACTIVITY1 Is Required to Maintain Catalase Activity and for Multiple Stress Responses in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.12.9.1667openalex-snapshot
SOS3 Function in Plant Salt Tolerance Requires N-Myristoylation and Calcium Binding
inferredcites →https://doi.org/10.1105/tpc.13.6.1383openalex-snapshot
Molecular Characterization of Functional Domains in the Protein Kinase SOS2 That Is Required for Plant Salt Tolerance
inferredcites →https://doi.org/10.1105/tpc.18.00568openalex-snapshot
The Ca 2+ Sensor SCaBP3/CBL7 Modulates Plasma Membrane H + -ATPase Activity and Promotes Alkali Tolerance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.8.4.617openalex-snapshot
SOS1, a Genetic Locus Essential for Salt Tolerance and Potassium Acquisition
inferredcites →https://doi.org/10.1111/j.1365-3040.2007.01637.xopenalex-snapshot
The Na + transporter AtHKT1;1 controls retrieval of Na + from the xylem in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.01971.xopenalex-snapshot
The plasma membrane Na+/H+ antiporter SOS1 is essential for salt tolerance in tomato and affects the partitioning of Na+ between plant organs
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.02056.xopenalex-snapshot
A conserved primary salt tolerance mechanism mediated by HKT transporters: a mechanism for sodium exclusion and maintenance of high K + /Na + ratio in leaves during salinity stress
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02595.xopenalex-snapshot
Enhanced salt tolerance mediated by AtHKT1 transporter‐induced Na + unloading from xylem vessels to xylem parenchyma cells
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02990.xopenalex-snapshot
AtNHX8, a member of the monovalent cation:proton antiporter‐1 family in Arabidopsis thaliana, encodes a putative Li+/H+ antiporter
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03236.xopenalex-snapshot
Two calcineurin B‐like calcium sensors, interacting with protein kinase CIPK23, regulate leaf transpiration and root potassium uptake in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1438-8677.2011.00560.xopenalex-snapshot
Isolation and characterisation of Chrysanthemum crassum SOS1, encoding a putative plasma membrane Na+/H+ antiporter
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.1469-8137.2010.03405.xopenalex-snapshot
The SOS1 transporter of Physcomitrella patens mediates sodium efflux in planta
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03422.xopenalex-snapshot
Phosphatidic acid mediates salt stress response by regulation of MPK6 in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/nph.12997openalex-snapshot
New insights into plant salt acclimation: the roles of vesicle trafficking and reactive oxygen species signalling in mitochondria and the endomembrane system
inferredcites →https://doi.org/10.1111/nph.13519openalex-snapshot
Salinity tolerance of crops – what is the cost?
inferredcites →https://doi.org/10.1111/nph.14679openalex-snapshot
MYB30 transcription factor regulates oxidative and heat stress responses through ANNEXIN‐mediated cytosolic calcium signaling in Arabidopsis
inferredcites →https://doi.org/10.1111/pce.12274openalex-snapshot
A step towards understanding plant responses to multiple environmental stresses: a genome‐wide study
inferredcites →https://doi.org/10.1111/ppl.13125openalex-snapshot
Isolation and characterization of Salt Overly Sensitive family genes in spinach
inferredcites →https://doi.org/10.1111/ppl.13245openalex-snapshot
Characterization of the Salt Overly Sensitive pathway genes in sugarcane under salinity stress
inferredcites →https://doi.org/10.1111/tpj.12123openalex-snapshot
Calcineurin B‐like protein CBL 10 directly interacts with AKT 1 and modulates K + homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1126/science.280.5371.1943openalex-snapshot
A Calcium Sensor Homolog Required for Plant Salt Tolerance
inferredcites →https://doi.org/10.1126/science.285.5431.1256openalex-snapshot
Salt Tolerance Conferred by Overexpression of a Vacuolar Na + /H + Antiport in Arabidopsis
inferredcites →https://doi.org/10.1128/mcb.00429-07openalex-snapshot
Interaction of SOS2 with Nucleoside Diphosphate Kinase 2 and Catalases Reveals a Point of Connection between Salt Stress and H 2 O 2 Signaling in Arabidopsis thaliana
inferredcites →https://doi.org/10.1128/mcb.01989-06openalex-snapshot
An Enhancer Mutant of Arabidopsis salt overly sensitive 3 Mediates both Ion Homeostasis and the Oxidative Stress Response
inferredcites →https://doi.org/10.1146/annurev-arplant-042916-040936openalex-snapshot
Genomics, Physiology, and Molecular Breeding Approaches for Improving Salt Tolerance
inferredcites →https://doi.org/10.1146/annurev-arplant-050718-100005openalex-snapshot
Salt Tolerance Mechanisms of Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.51.1.463openalex-snapshot
P LANT C ELLULAR AND M OLECULAR R ESPONSES TO H IGH S ALINITY
inferredcites →https://doi.org/10.1146/annurev.arplant.53.091401.143329openalex-snapshot
S ALT AND D ROUGHT S TRESS S IGNAL T RANSDUCTION IN P LANTS
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092911openalex-snapshot
Mechanisms of Salinity Tolerance
inferredcites →https://doi.org/10.1152/ajpcell.00360.2004openalex-snapshot
Evolutionary origins of eukaryotic sodium/proton exchangers
inferredcites →https://doi.org/10.1159/000356667openalex-snapshot
Calcium's Role in Mechanotransduction during Muscle Development
inferredcites →https://doi.org/10.1186/s12870-019-1680-7openalex-snapshot
Co-expression of SpSOS1 and SpAHA1 in transgenic Arabidopsis plants improves salinity tolerance
inferredcites →https://doi.org/10.1371/journal.pone.0137447openalex-snapshot
SpAHA1 and SpSOS1 Coordinate in Transgenic Yeast to Improve Salt Tolerance
inferredcites →https://doi.org/10.1371/journal.pone.0224672openalex-snapshot
Genome-wide identification and gene expression analysis of SOS family genes in tuber mustard (Brassica juncea var. tumida)
inferredcites →https://doi.org/10.1371/journal.pone.0254189openalex-snapshot
Transcriptome analysis of bread wheat leaves in response to salt stress
inferredcites →https://doi.org/10.2174/1389202918666170228133621openalex-snapshot
A Salt Overly Sensitive Pathway Member from Brassica juncea BjSOS3 Can Functionally Complement ΔAtsos3 in Arabidopsis
inferredcites →https://doi.org/10.3389/fpls.2014.00151openalex-snapshot
Tolerance to drought and salt stress in plants: Unraveling the signaling networks
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.2015.00581openalex-snapshot
Co-expression of xerophyte Zygophyllum xanthoxylum ZxNHX and ZxVP1-1 confers enhanced salinity tolerance in chimeric sugar beet (Beta vulgaris L.)
inferredcites →https://doi.org/10.3389/fpls.2021.670369openalex-snapshot
Crucial Cell Signaling Compounds Crosstalk and Integrative Multi-Omics Techniques for Salinity Stress Tolerance in Plants
inferredcites →https://doi.org/10.3390/ijms21165668openalex-snapshot
The CBL–CIPK Pathway in Plant Response to Stress Signals
inferredcites →https://doi.org/10.3390/ijms22094609openalex-snapshot
Regulation of Plant Responses to Salt Stress
inferredcites →https://doi.org/10.3390/metabo11110724openalex-snapshot
Soil Salinity, a Serious Environmental Issue and Plant Responses: A Metabolomics Perspective
inferredcites →https://doi.org/10.4161/psb.22455openalex-snapshot
Reactive oxygen species generation and signaling in plants
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4663385openalex-extracted
Plant response to combined salinity and waterlogging stress: Current research progress and future prospects
inferred← citeshttps://doi.org/10.1002/fes3.70151openalex-snapshot
Adaptive Remodeling of the Proteome in Pistachio Roots Under Salt Stress: Implications for Food and Energy Security in Arid Regions
inferred← citeshttps://doi.org/10.1007/978-3-031-48542-8_3openalex-snapshot
Protective Mechanisms of Salinity Stress: How Do Plants Resilient Salinity Conditions?
inferred← citeshttps://doi.org/10.1007/978-981-95-7354-7_4openalex-snapshot
Plant Growth and Development in the Changing Environment
inferred← citeshttps://doi.org/10.1007/s00299-024-03407-4openalex-snapshot
Characterization of the wall-associated kinase (WAK) gene family in Gossypium barbadense reveals the positive role of GbWAK5 in salt tolerance
inferred← citeshttps://doi.org/10.1007/s00344-026-12378-7openalex-snapshot
Threshold-like Responses of White Mulberry (Morus alba L.) Seedlings to Salt Stress: Growth, Physio-biochemical, Ionic, and Structural Changes
inferred← citeshttps://doi.org/10.1007/s00709-025-02035-3openalex-snapshot
Typical tetra-mediated signaling and plant architectural changes regulate salt-stress tolerance in indica rice genotypes
inferred← citeshttps://doi.org/10.1007/s10142-025-01795-8openalex-snapshot
Molecular networks and signaling pathways governing abiotic stress tolerance in cotton: advances and perspectives
inferred← citeshttps://doi.org/10.1007/s11274-025-04342-6openalex-snapshot
Transformative strategies for saline soil restoration: Harnessing halotolerant microorganisms and advanced technologies
inferred← citeshttps://doi.org/10.1007/s11368-026-04231-xopenalex-snapshot
Differential responses of sunflower to neutral versus alkaline salt stress: growth–biochemical thresholds and implications for saline–alkali land utilization
inferred← citeshttps://doi.org/10.1007/s11816-025-01027-2openalex-snapshot
Integrative physiological and transcriptomic analyses reveal distinct shoot and root adaptations to salinity in indica rice cultivars
inferred← citeshttps://doi.org/10.1007/s12355-024-01518-6openalex-snapshot
Genome-Wide Analysis of Ca2+-ATPases and their Salt Stress Responses in Sugar Beet
inferred← citeshttps://doi.org/10.1007/s13580-024-00673-9openalex-snapshot
Comparative salt stress responses in two turnip cultivars: insights into ion homeostasis, osmotic regulation, and antioxidant capacity
inferred← citeshttps://doi.org/10.1007/s40502-026-00943-xopenalex-snapshot
Responses of rice to saline water flooding: interaction between salinity and hypoxia specific effects
inferred← citeshttps://doi.org/10.1007/s42976-025-00741-5openalex-snapshot
Melatonin mitigates Na⁺/K⁺ imbalance caused by abscisic acid deficiency in rice under salt stress through regulation of energy supply
inferred← citeshttps://doi.org/10.1016/b978-0-443-18500-7.00002-8openalex-snapshot
Molecular mechanism of abiotic stress regulation in crop plants
inferred← citeshttps://doi.org/10.1016/b978-0-443-27424-4.00005-7openalex-snapshot
Modulation of ion transport and uptake dynamics in plants under multiple abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.bcab.2023.102892openalex-snapshot
Nano priming for boosting growth and resilience in crops under abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e34486openalex-snapshot
Mechanistic insights of salicylic acid-mediated salt stress tolerance in Zea mays L. seedlings
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115375openalex-snapshot
The Dendrobium catenatum DcCIPK24 increases drought and salt tolerance of transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.119775openalex-snapshot
The role of biochar nanoparticles in reducing salt stress in tomato (Solanum lycopersicum) plants grown in fields
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110482openalex-snapshot
Manipulation of ion/electron carrier genes in the model diatom Phaeodactylum tricornutum enables its growth under lethal acidic stress
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110804openalex-snapshot
Bridging gaps and seeding futures: A synthesis of soil salinization and the role of plant-soil interactions under climate change
inferred← citeshttps://doi.org/10.1016/j.jgeb.2024.100432openalex-snapshot
Mapping proteomic response to salinity stress tolerance in oil crops: Towards enhanced plant resilience
inferred← citeshttps://doi.org/10.1016/j.jplph.2024.154295openalex-snapshot
Exploring lipid signaling in plant physiology: From cellular membranes to environmental adaptation
inferred← citeshttps://doi.org/10.1016/j.jplph.2024.154318openalex-snapshot
NHX5/NHX6/SPY22 complex regulates BRI1 and brassinosteroid signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112324openalex-snapshot
Sodium and chloride accumulation and repartition differed between the cultivated tomato (Solanum lycopersicum) and its wild halophyte relative Solanum chilense under salt stress
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100137openalex-snapshot
Plant response to combined salinity and waterlogging stress: Current research progress and future prospects
inferred← citeshttps://doi.org/10.1021/acsagscitech.5c00443openalex-snapshot
Microbiome-Mediated Physiological Mechanisms for Improving Soil Health and Crop Salt Tolerance
inferred← citeshttps://doi.org/10.1038/s41477-023-01551-5openalex-snapshot
Structure and activation mechanism of the rice Salt Overly Sensitive 1 (SOS1) Na+/H+ antiporter
inferred← citeshttps://doi.org/10.1051/bioconf/202520203013openalex-snapshot
Local maize responses to salinity stress through morphological and molecular alterations of r40C1-like and SOS1 gene
inferred← citeshttps://doi.org/10.1073/pnas.2505598122openalex-snapshot
Secreting salt glands constrain cuticle fracture to enhance desalination efficiency
inferred← citeshttps://doi.org/10.1080/15592324.2026.2687962openalex-snapshot
Role of primary protectors of plant cells in salinity tolerance: molecular mechanisms and adaptive strategies
inferred← citeshttps://doi.org/10.1093/jxb/erag107openalex-snapshot
Sphingolipids in plant abiotic stress responses
inferred← citeshttps://doi.org/10.1101/2024.12.07.627310openalex-snapshot
Element partitioning, element localisation and transcriptome responses of date palms exposed to NaCl
inferred← citeshttps://doi.org/10.1111/pce.14820openalex-snapshot
The signalling pathways, calcineurin B‐like protein 5 (CBL5)‐CBL‐interacting protein kinase 8 (CIPK8)/CIPK24‐salt overly sensitive 1 (SOS1), transduce salt signals in seed germination in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.15544openalex-snapshot
Molecular Insights Into Salt Stress Adaptation in Plants
inferred← citeshttps://doi.org/10.1111/pce.15621openalex-snapshot
Inoculation With Salt‐Tolerant Rhizobia and AMF Regulates K + /Na + Homeostasis in Robinia pseudoacacia L. Alleviating Salinity
inferred← citeshttps://doi.org/10.1111/plb.70162openalex-snapshot
Genome‐wide analysis, expression profiling and molecular docking of tomato ( Solanum lycopersicum ) calmodulin ( SlCaM ) proteins in cadmium stress adaptation
inferred← citeshttps://doi.org/10.1186/s12284-022-00599-9openalex-snapshot
Variety-Specific Transcriptional and Alternative Splicing Regulations Modulate Salt Tolerance in Rice from Early Stage of Stress
inferred← citeshttps://doi.org/10.18805/ag.r-2628openalex-snapshot
Insights into the Detrimental Impacts and Coping Mechanisms under Salinity Stress in Mungbean (Vigna radiata L.)
inferred← citeshttps://doi.org/10.2139/ssrn.5246732openalex-snapshot
Root Proteomics Revealed a Shift in Pathways in Response to Varying Nacl Levels, as an Adaptability to Salt Stress in Pistachio Rootstock Ucb1
inferred← citeshttps://doi.org/10.2306/scienceasia1513-1874.2024.068openalex-snapshot
Salinity tolerance in Oryza sativa L. and its wild relatives
inferred← citeshttps://doi.org/10.3389/fpls.2022.1041764openalex-snapshot
Regulation of Na+/H+ exchangers, Na+/K+ transporters, and lignin biosynthesis genes, along with lignin accumulation, sodium extrusion, and antioxidant defense, confers salt tolerance in alfalfa
inferred← citeshttps://doi.org/10.3389/fpls.2023.1135552openalex-snapshot
Ectopic expression of DnaJ type-I protein homolog of Vigna aconitifolia (VaDJI) confers ABA insensitivity and multiple stress tolerance in transgenic tobacco plants
inferred← citeshttps://doi.org/10.3389/fpls.2023.1201730openalex-snapshot
Genome-wide characterization of SOS1 gene family in potato (Solanum tuberosum) and expression analyses under salt and hormone stress
inferred← citeshttps://doi.org/10.3389/fpls.2024.1378738openalex-snapshot
Genome-wide identification of Shaker K+ channel family in Nicotiana tabacum and functional analysis of NtSKOR1B in response to salt stress
inferred← citeshttps://doi.org/10.3389/fpls.2025.1648092openalex-snapshot
Salt gradient-driven adaptation in okra: uncovering mechanisms of tolerance and growth regulation
inferred← citeshttps://doi.org/10.3389/fpls.2026.1734646openalex-snapshot
Evolutionary analysis of MOCA1 gene in Arabidopsis thaliana and functional comparison with PGSIP7 and PGSIP8 genes
inferred← citeshttps://doi.org/10.3389/fpls.2026.1780410openalex-snapshot
Novel insights into SOS1 in managing vacuolar sodium toxicity
inferred← citeshttps://doi.org/10.3389/fpls.2026.1824871openalex-snapshot
Bacterial cell-free supernatants as metabolite-based biostimulants for alleviating salinity stress in plants
inferred← citeshttps://doi.org/10.3389/fpls.2026.1892395openalex-snapshot
Symbiotic interactions of plant microbiota in alleviating stress: a review
inferred← citeshttps://doi.org/10.3389/fpls.2026.1971866openalex-snapshot
Deciphering plant stress resilience in different millet crops: from multi-omics discoveries to predictive breeding for climate-resilient crop enhancement
inferred← citeshttps://doi.org/10.3390/agriculture15070721openalex-snapshot
Advancing Stress-Resilient Rice: Mechanisms, Genes, and Breeding Strategies
inferred← citeshttps://doi.org/10.3390/agronomy16060606openalex-snapshot
Morphophysiological and Nutritional Responses of West Indian Gherkin Cultivars Under Salt Stress and Exogenous Carnitine Application
inferred← citeshttps://doi.org/10.3390/cimb48030317openalex-snapshot
Time-Series-Based Co-Expression Network Analysis Reveals Key Regulatory Modules and Hub Genes in Salt-Tolerant Wheat Under Salt Stress
inferred← citeshttps://doi.org/10.3390/f14010007openalex-snapshot
Molecular Traits for Adaptation to Drought and Salt Stress in Birch, Oak and Poplar Species
inferred← citeshttps://doi.org/10.3390/genes14122213openalex-snapshot
The Euphrates Poplar Responses to Abiotic Stress and Its Unique Traits in Dry Regions of China (Xinjiang and Inner Mongolia): What Should We Know?
inferred← citeshttps://doi.org/10.3390/horticulturae10080780openalex-snapshot
Improving the Salt Tolerance of “Old Limachino Tomato” by Using a New Salt-Tolerant Rootstock
inferred← citeshttps://doi.org/10.3390/horticulturae11030280openalex-snapshot
Feasibility of Nano-Urea and PGPR on Salt Stress Amelioration in Reshmi Amaranth (Amaranthus tricolor): Stress Markers and Enzymatic Response
inferred← citeshttps://doi.org/10.3390/horticulturae11070855openalex-snapshot
Characterization of the Salt Overly Sensitive 1 (SOS1) Pathway Genes in Tea Plant (Cameliia sinensis) Under Environmental Stress
inferred← citeshttps://doi.org/10.3390/ijms24043549openalex-snapshot
Salinity-Induced Cytosolic Alkaline Shifts in Arabidopsis Roots Require the SOS Pathway
inferred← citeshttps://doi.org/10.3390/ijms25115950openalex-snapshot
Identification and Functional Analysis of KH Family Genes Associated with Salt Stress in Rice
inferred← citeshttps://doi.org/10.3390/plants11243532openalex-snapshot
Cell-Type-Specific Length and Cytosolic pH Response of Superficial Cells of Arabidopsis Root to Chronic Salinity
inferred← citeshttps://doi.org/10.3390/plants12223831openalex-snapshot
Comparison of the Efficiency of Hyperspectral and Pulse Amplitude Modulation Imaging Methods in Pre-Symptomatic Virus Detection in Tobacco Plants
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/plants14131916openalex-snapshot
Structure-Based Function of Humic Acid in Abiotic Stress Alleviation in Plants: A Review
inferred← citeshttps://doi.org/10.3390/plants15111593openalex-snapshot
Initial Physiological and Molecular Adjustments Underpin Salinity Tolerance During Wheat Germination and Early Seedling Development
inferred← citeshttps://doi.org/10.3390/plants15152356openalex-snapshot
Fungal Endophytes Are Associated with Improved Salinity Responses Across Quinoa Ecotypes
inferred← citeshttps://doi.org/10.3390/plants15182745openalex-snapshot
REM Gene Family in Sugar Beet and Functional BvREM12 in Salt Stress Tolerance
inferred← citeshttps://doi.org/10.66835/psh.2026.e0007openalex-snapshot
The Role of Calcium in Salinity Stress Alleviation: Mechanisms and Implications
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