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Salt-stress signaling
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/yea.1357openalex-snapshot
Yeast systems biology to unravel the network of life
inferredcites →https://doi.org/10.1007/bf03030421openalex-snapshot
Influence of NaCl salinity on the behavior of hydrolases and phosphatases in mulberry genotypes: Relationship to salt tolerance
inferredcites →https://doi.org/10.1007/bf03030429openalex-snapshot
NaCl stress causes changes in photosynthetic pigments, proteins, and other metabolic components in the leaves of a true mangrove,Bruguiera parviflora, in hydroponic cultures
inferredcites →https://doi.org/10.1007/bf03030488openalex-snapshot
Alteration of starch- sucrose transition in germinating wheat seed under sodium chloride salinity
inferredcites →https://doi.org/10.1007/s00425-005-0074-2openalex-snapshot
Salinity-induced ion flux patterns from the excised roots of Arabidopsis sos mutants
inferredcites →https://doi.org/10.1016/j.bbrc.2004.08.127openalex-snapshot
Athb-12, a homeobox-leucine zipper domain protein from Arabidopsis thaliana, increases salt tolerance in yeast by regulating sodium exclusion
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/s0021-9258(17)37038-2openalex-snapshot
The protein phosphatase calcineurin is essential for NaCl tolerance of Saccharomyces cerevisiae.
inferredcites →https://doi.org/10.1016/s0168-9525(02)02723-3openalex-snapshot
Yeast go the whole HOG for the hyperosmotic response
inferredcites →https://doi.org/10.1016/s1369-5266(03)00085-2openalex-snapshot
Regulation of ion homeostasis under salt stress
inferredcites →https://doi.org/10.1016/s1369-5266(03)00090-6openalex-snapshot
Relay and control of abscisic acid signaling
inferredcites →https://doi.org/10.1016/s1534-5807(01)00087-9openalex-snapshot
Modulation of Abscisic Acid Signal Transduction and Biosynthesis by an Sm-like Protein in Arabidopsis
inferredcites →https://doi.org/10.1023/a:1019859319617openalex-snapshot
Regulation of expression of the vacuolar Na+/H+ antiporter gene AtNHX1 by salt stress and abscisic acid
inferredcites →https://doi.org/10.1038/369242a0openalex-snapshot
A two-component system that regulates an osmosensing MAP kinase cascade in yeast
inferredcites →https://doi.org/10.1038/nrg927openalex-snapshot
A fortunate choice: the history of Arabidopsis as a model plant
inferredcites →https://doi.org/10.1046/j.1365-313x.1997.12010133.xopenalex-snapshot
Transformation of Arabidopsis thaliana with the codA gene for choline oxidase; accumulation of glycinebetaine and enhanced tolerance to salt and cold stress
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/10.1073/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.241501798openalex-snapshot
AtHKT1 is a salt tolerance determinant that controls Na + entry into plant roots
inferredcites →https://doi.org/10.1073/pnas.89.9.3736openalex-snapshot
Functional expression of a probable Arabidopsis thaliana potassium channel in Saccharomyces cerevisiae.
inferredcites →https://doi.org/10.1073/pnas.94.26.14960openalex-snapshot
An Arabidopsis mutant that requires increased calcium for potassium nutrition and salt tolerance
inferredcites →https://doi.org/10.1093/genetics/154.1.421openalex-snapshot
Genetic Analysis of Salt-Tolerant Mutants in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jb/mvh135openalex-snapshot
Regulation of the Osmoregulatory HOG MAPK Cascade in Yeast
inferredcites →https://doi.org/10.1093/jexbot/50.suppl_1.1073openalex-snapshot
Identification and characterization of plant transporters using heterologous expression systems
inferredcites →https://doi.org/10.1093/jexbot/52.363.1969openalex-snapshot
Significance of the V‐type ATPase for the adaptation to stressful growth conditions and its regulation on the molecular and biochemical level
inferredcites →https://doi.org/10.1093/jexbot/52.365.2355openalex-snapshot
Effects of salt treatment and osmotic stress on V‐ATPase and V‐PPase in leaves of the halophyte Suaeda salsa
inferredcites →https://doi.org/10.1093/jxb/50.special_issue.1073openalex-snapshot
Identification and characterization of plant transporters
inferredcites →https://doi.org/10.1093/pcp/pce008openalex-snapshot
Overexpression of the AtGluR2 Gene Encoding anArabidopsis Homolog of Mammalian Glutamate Receptors Impairs CalciumUtilization and Sensitivity to Ionic Stress in TransgenicPlants
inferredcites →https://doi.org/10.1104/pp.010752openalex-snapshot
Learning from the Arabidopsis Experience. The Next Gene Search Paradigm
inferredcites →https://doi.org/10.1104/pp.101.3.839openalex-snapshot
Mutants of Arabidopsis thaliana Capable of Germination under Saline Conditions
inferredcites →https://doi.org/10.1104/pp.103.025395openalex-snapshot
Regulation of Abscisic Acid Biosynthesis
inferredcites →https://doi.org/10.1104/pp.104.041723openalex-snapshot
Salt Cress. A Halophyte and Cryophyte Arabidopsis Relative Model System and Its Applicability to Molecular Genetic Analyses of Growth and Development of Extremophiles
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.104.046490openalex-snapshot
The Calcium Conundrum. Both Versatile Nutrient and Specific Signal
inferredcites →https://doi.org/10.1104/pp.104.049213openalex-snapshot
Protection of Plasma Membrane K+ Transport by the Salt Overly Sensitive1 Na+-H+ Antiporter during Salinity Stress
inferredcites →https://doi.org/10.1104/pp.105.067850openalex-snapshot
Salt Stress in Thellungiella halophila Activates Na+ Transport Mechanisms Required for Salinity Tolerance
inferredcites →https://doi.org/10.1104/pp.109.3.735openalex-snapshot
Ion Homeostasis in NaCl Stress Environments
inferredcites →https://doi.org/10.1104/pp.118.3.1021openalex-snapshot
Expression Studies of the Zeaxanthin Epoxidase Gene in Nicotiana plumbaginifolia
inferredcites →https://doi.org/10.1104/pp.124.3.941openalex-snapshot
Genetic Analysis of Plant Salt Tolerance Using Arabidopsis
inferredcites →https://doi.org/10.1104/pp.124.4.1814openalex-snapshot
The ACA4 Gene of Arabidopsis Encodes a Vacuolar Membrane Calcium Pump That Improves Salt Tolerance in Yeast
inferredcites →https://doi.org/10.1104/pp.78.1.163openalex-snapshot
Na+/H+ Antiport in Isolated Tonoplast Vesicles from Storage Tissue of Beta vulgaris
inferredcites →https://doi.org/10.1104/pp.83.3.510openalex-snapshot
Influx of Na+, K+, and Ca2+ into Roots of Salt-Stressed Cotton Seedlings
inferredcites →https://doi.org/10.1105/tpc.11.4.677openalex-snapshot
Energization of Plant Cell Membranes by H + -Pumping ATPases: Regulation and Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.11.7.1195openalex-snapshot
A Recessive Arabidopsis Mutant That Grows Photoautotrophically under Salt Stress Shows Enhanced Active Oxygen Detoxification
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.9.11.1935openalex-snapshot
Genetic analysis of osmotic and cold stress signal transduction in Arabidopsis: interactions and convergence of abscisic acid-dependent and abscisic acid-independent pathways.
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01487.xopenalex-snapshot
Genes and salt tolerance: bringing them together
inferredcites →https://doi.org/10.1126/science.280.5365.918openalex-snapshot
A Role for the AKT1 Potassium Channel in Plant Nutrition
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/10.1126/science.7624781openalex-snapshot
Activation of Yeast PBS2 MAPKK by MAPKKKs or by Binding of an SH3-Containing Osmosensor
inferredcites →https://doi.org/10.1126/stke.2002.140.pl10openalex-snapshot
Screening for Gene Regulation Mutants by Bioluminescence Imaging
inferredcites →https://doi.org/10.1128/jb.181.1.91-99.1999openalex-snapshot
Characterization of Biosynthetic Enzymes for Ectoine as a Compatible Solute in a Moderately Halophilic Eubacterium, Halomonas elongata
inferredcites →https://doi.org/10.1128/mcb.16.5.2226openalex-snapshot
Calcineurin Inhibits VCX 1-Dependent H + /Ca 2 + Exchange and Induces Ca 2 + ATPases in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1146/annurev.arplant.49.1.199openalex-snapshot
ABSCISIC ACID SIGNAL TRANSDUCTION
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.pp.28.060177.000513openalex-snapshot
The Mechanism of Salt Tolerance in Halophytes
inferredcites →https://doi.org/10.2135/cropsci2005.0437openalex-snapshot
Understanding and Improving Salt Tolerance in Plants
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/herpetozoa.37.e130028zenodo-depositor-declared
Water bodies created by peatland restoration are potential habitats for amphibians and reptiles
inferred← citeshttps://doi.org/10.1002/9781394186457.ch12openalex-snapshot
Metabolites and Their Regulation During Salinity Stress in Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-75671-4_14openalex-snapshot
Single-Gene Versus Multigene Transfer Approaches for Crop Salt Tolerance
inferred← citeshttps://doi.org/10.1007/978-981-10-9044-8_19openalex-snapshot
Salinity Stress Alleviation by Organic and Inorganic Fertilization
inferred← citeshttps://doi.org/10.1007/bf03036129openalex-snapshot
Mitogen-activated protein kinase is involved in the symbiotic interaction betweenBradyrhizobium japonicum USDA110 and soybean
inferred← citeshttps://doi.org/10.1007/s00299-012-1360-7openalex-snapshot
Identification of wild soybean (Glycine soja) TIFY family genes and their expression profiling analysis under bicarbonate stress
inferred← citeshttps://doi.org/10.1007/s00344-025-11656-0openalex-snapshot
Aeromonas hydrophila by Quorum Sensing Auto-Inducers on Growth Amelioration, Enhance Salt Tolerance and Mechanism of Encoding Genes in Rapeseed
inferred← citeshttps://doi.org/10.1007/s00709-015-0914-2openalex-snapshot
Ectopic expression of PgRab7 in rice plants (Oryza sativa L.) results in differential tolerance at the vegetative and seed setting stage during salinity and drought stress
inferred← citeshttps://doi.org/10.1007/s11103-008-9403-8openalex-snapshot
Cloning and functional analysis of wheat V-H+-ATPase subunit genes
inferred← citeshttps://doi.org/10.1007/s11104-011-1109-zopenalex-snapshot
Molybdenum improves antioxidant and osmotic-adjustment ability against salt stress in Chinese cabbage (Brassica campestris L. ssp. Pekinensis)
inferred← citeshttps://doi.org/10.1007/s11105-017-1059-6openalex-snapshot
Comparative Transcriptional Profiling of Soybean Orthologs of Arabidopsis Trichome Developmental Genes under Salt Stress
inferred← citeshttps://doi.org/10.1007/s11240-008-9461-2openalex-snapshot
In vitro selection and identification of sweetpotato (Ipomoea batatas (L.) Lam.) plants tolerant to NaCl
inferred← citeshttps://doi.org/10.1007/s12042-020-09265-0openalex-snapshot
Mechanisms and Signaling Pathways of Salt Tolerance in Crops: Understanding from the Transgenic Plants
inferred← citeshttps://doi.org/10.1007/s12374-008-9004-8openalex-snapshot
Expression of Yeast YAP1 in Transgenic Arabidopsis Results in Increased Salt Tolerance
inferred← citeshttps://doi.org/10.1007/s12374-009-9036-8openalex-snapshot
In Planta Measurements of Na+ Using Fluorescent Dye CoroNa Green
inferred← citeshttps://doi.org/10.1007/s43393-026-00461-9openalex-snapshot
RNA helicase gene CgDBP7 improves the high salt tolerance of Candida glycerinogenes by regulating CgMAK5
inferred← citeshttps://doi.org/10.1016/b978-0-12-816451-8.00001-0openalex-snapshot
Signaling Molecules in Ecophysiological Response Mechanisms of Salt-Stressed Plants
inferred← citeshttps://doi.org/10.1016/j.bbrc.2008.07.128openalex-snapshot
Overexpression of Arabidopsis ZEP enhances tolerance to osmotic stress
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2011.12.011openalex-snapshot
Identification of genes associated with adaptation to NaCl toxicity in perennial ryegrass (Lolium perenne L.)
inferred← citeshttps://doi.org/10.1016/j.ecoleng.2016.11.060openalex-snapshot
Effect of silica ions and nano silica on rice plants under salinity stress
inferred← citeshttps://doi.org/10.1016/j.molp.2015.01.011openalex-snapshot
SKIP Confers Osmotic Tolerance during Salt Stress by Controlling Alternative Gene Splicing in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.niox.2017.09.008openalex-snapshot
NO, hydrogen sulfide does not come first during tomato response to high salinity
inferred← citeshttps://doi.org/10.1016/j.plantsci.2010.07.017openalex-snapshot
Isolation and expression analysis of salt induced genes from contrasting grapevine (Vitis vinifera L.) cultivars
inferred← citeshttps://doi.org/10.1016/j.sajb.2023.06.029openalex-snapshot
Advanced study of functional proteins involved in salt stress regulatory pathways in plants
inferred← citeshttps://doi.org/10.1016/j.tplants.2023.04.003openalex-snapshot
Revisiting plant salt tolerance: novel components of the SOS pathway
inferred← citeshttps://doi.org/10.1038/s41598-024-61576-4openalex-snapshot
Integrated multi-omic approach reveals the effect of a Graminaceae-derived biostimulant and its lighter fraction on salt-stressed lettuce plants
inferred← citeshttps://doi.org/10.1063/5.0015860openalex-snapshot
The effect of rice husk ash on growth of rice (Oryza sativa L. ‘Sembada Merah’) on salinity stress
inferred← citeshttps://doi.org/10.1071/bt17089openalex-snapshot
Aeluropus littoralis maintains adequate gas exchange, pigment composition and phenolic contents under combined effects of salinity and phosphorus deficiency
inferred← citeshttps://doi.org/10.1080/00380768.2015.1051928openalex-snapshot
Genotypic differences in the antioxidant and carbon–nitrogen metabolism of acid-tolerant and acid-sensitive rice ( Oryzasativa L .) cultivars under acid stress
inferred← citeshttps://doi.org/10.1080/01904167.2018.1554078openalex-snapshot
Effect of potassium on uptake and translocation of sodium and potassium in Chinese cabbage under NaCl stress
inferred← citeshttps://doi.org/10.1088/1755-1315/423/1/012041openalex-snapshot
The potential of silicate fertilizer for salinity stress alleviation on red rice (Oryza sativa L. ‘Sembada Merah’)
inferred← citeshttps://doi.org/10.1111/j.1601-5223.2010.02133.xopenalex-snapshot
Genotypic differences in root and shoot growth of barley (Hordeum vulgare L.) grown under different salinity levels
inferred← citeshttps://doi.org/10.1111/j.1744-7909.2008.00760.xopenalex-snapshot
Salt Tolerance in Soybean
inferred← citeshttps://doi.org/10.1111/pbr.12140openalex-snapshot
Expression profiles of Pr5 CS 1 and Pr5 CS 2 genes and proline accumulation under salinity stress in perennial ryegrass (Lolium perenne L.)
inferred← citeshttps://doi.org/10.1111/ppl.13112openalex-snapshot
Reassessing the role of ion homeostasis for improving salinity tolerance in crop plants
inferred← citeshttps://doi.org/10.1111/tpj.12159openalex-snapshot
A rabidopsis transcription factor WRKY 8 functions antagonistically with its interacting partner VQ 9 to modulate salinity stress tolerance
inferred← citeshttps://doi.org/10.1146/annurev.arplant.59.032607.092911openalex-snapshot
Mechanisms of Salinity Tolerance
inferred← citeshttps://doi.org/10.1186/s42269-021-00576-0openalex-snapshot
Identification of salt-tolerant barley genotypes using multiple-traits index and yield performance at the early growth and maturity stages
inferred← citeshttps://doi.org/10.1266/ggs.15-00052openalex-snapshot
Identification of gamma ray irradiation-induced mutations in membrane transport genes in a rice population by TILLING
inferred← citeshttps://doi.org/10.14348/molcells.2016.0083openalex-snapshot
A New Insight of Salt Stress Signalingin Plant
inferred← citeshttps://doi.org/10.1515/johr-2016-0014openalex-snapshot
Growth of Ornamental Grasses Under Salinity Stress
inferred← citeshttps://doi.org/10.15835/nbha4119031openalex-snapshot
Effects of Salinity on the Development of Hydroponically Grown Borage (Borago officinalis L.) Male Gametophyte
inferred← citeshttps://doi.org/10.1670/09-211.1openalex-snapshot
Increased Conductivity Affects Corticosterone Levels and Prey Consumption in Larval Amphibians
inferred← citeshttps://doi.org/10.21203/rs.3.rs-304576/v1openalex-snapshot
MGIDI and WAASB indices: The useful approaches for selection of salt-tolerant barley genotype at the early growth and maturity stages
inferred← citeshttps://doi.org/10.29133/yyutbd.802653openalex-snapshot
Determination of the Stress Responses and Mineral Compositions of Some Common Wheats (Triticum aestivum L.) under Salt Treatment
inferred← citeshttps://doi.org/10.3389/fpls.2014.00211openalex-snapshot
When supply does not meet demand-ER stress and plant programmed cell death
inferred← citeshttps://doi.org/10.3390/ijms20051059openalex-snapshot
Role and Functional Differences of HKT1-Type Transporters in Plants under Salt Stress
inferred← citeshttps://doi.org/10.3390/ijms22168398openalex-snapshot
Rootstocks Overexpressing StNPR1 and StDREB1 Improve Osmotic Stress Tolerance of Wild-Type Scion in Transgrafted Tobacco Plants
inferred← citeshttps://doi.org/10.3390/ijms222212238openalex-snapshot
Genome-Wide Characterization of Salt-Responsive miRNAs, circRNAs and Associated ceRNA Networks in Tomatoes
inferred← citeshttps://doi.org/10.3390/molecules26040782openalex-snapshot
Transcriptome Changes Reveal the Molecular Mechanisms of Humic Acid-Induced Salt Stress Tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.5010/jpb.2016.43.3.281openalex-snapshot
Biological function of nonxpressor of pathogenesis-related genes 1 (NPR1) in response to biotic and abiotic stresses
inferred← citeshttps://doi.org/10.5352/jls.2010.20.8.1173openalex-snapshot
Responses of Photosynthetic Efficiency and Ascorbate Peroxidase Induced by Salt Stress in Rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.5352/jls.2018.28.7.772openalex-snapshot
Analysis of Antioxidant Enzyme Activity During Seedling Growth of Leymus chinensis Trin Under Salt and Dehydration Stresses
inferred← citeshttps://doi.org/10.7235/hort.20220003openalex-snapshot
Salinity Stress Relief of Lettuce through Microbubbles Generated in Hydroponic Cultivation
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