On the public citation graph

Root vacuolar Na + sequestration but not exclusion from uptake correlates with barley salt tolerance

https://doi.org/10.1111/tpj.14424
0 signed · 191 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/abio.2001.5564openalex-snapshot
Elimination of Primer–Dimer Artifacts and Genomic Coamplification Using a Two-Step SYBR Green I Real-Time RT-PCR
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/bf01871102openalex-snapshot
Amiloride and its analogs as tools in the study of ion transport
inferredcites →https://doi.org/10.1007/s00425-015-2317-1openalex-snapshot
Developing and validating a high-throughput assay for salinity tissue tolerance in wheat and barley
inferredcites →https://doi.org/10.1007/s10725-015-0063-9openalex-snapshot
Expressing AtNHX1 in barley (Hordium vulgare L.) does not improve plant performance under saline conditions
inferredcites →https://doi.org/10.1007/s11032-006-9048-8openalex-snapshot
Over-expression of a vacuolar Na+/H+ antiporter gene improves salt tolerance in an upland rice
inferredcites →https://doi.org/10.1007/s11032-011-9559-9openalex-snapshot
Quantitative trait loci for salinity tolerance in barley (Hordeum vulgare L.)
inferredcites →https://doi.org/10.1007/s11103-011-9787-8openalex-snapshot
Regulation of durum wheat Na+/H+ exchanger TdSOS1 by phosphorylation
inferredcites →https://doi.org/10.1007/s11103-012-9901-6openalex-snapshot
Expression of wheat Na+/H+ antiporter TNHXS1 and H+- pyrophosphatase TVP1 genes in tobacco from a bicistronic transcriptional unit improves salt tolerance
inferredcites →https://doi.org/10.1007/s11442-014-1130-2openalex-snapshot
Soil salinization research in China: Advances and prospects
inferredcites →https://doi.org/10.1016/0014-5793(89)81067-1openalex-snapshot
Ion channels in vacuoles from halophytes and glycophytes
inferredcites →https://doi.org/10.1016/j.cj.2018.01.003openalex-snapshot
Plant salt tolerance and Na+ sensing and transport
inferredcites →https://doi.org/10.1016/j.jplph.2004.03.010openalex-snapshot
Molecular characterization of Na+/H+ antiporters (ZmNHX) of maize (Zea mays L.) and their expression under salt stress
inferredcites →https://doi.org/10.1016/j.jplph.2010.12.006openalex-snapshot
Improved measurements of Na+ fluxes in plants using calixarene-based microelectrodes
inferredcites →https://doi.org/10.1016/j.jplph.2011.10.007openalex-snapshot
SOS1 gene overexpression increased salt tolerance in transgenic tobacco by maintaining a higher K+/Na+ ratio
inferredcites →https://doi.org/10.1016/j.plantsci.2004.05.034openalex-snapshot
Enhanced salt tolerance of transgenic wheat (Tritivum aestivum L.) expressing a vacuolar Na+/H+ antiporter gene with improved grain yields in saline soils in the field and a reduced level of leaf Na+
inferredcites →https://doi.org/10.1016/j.tplants.2007.01.004openalex-snapshot
Stress-induced morphogenic responses: growing out of trouble?
inferredcites →https://doi.org/10.1016/j.tplants.2010.04.007openalex-snapshot
Root apex transition zone: a signalling–response nexus in the root
inferredcites →https://doi.org/10.1034/j.1399-3054.1997.990216.xopenalex-snapshot
Sodium-calcium interactions in two wheat species differing in salinity tolerance
inferredcites →https://doi.org/10.1034/j.1399-3054.1998.1020105.xopenalex-snapshot
Early changes of Cl− efflux and H+ extrusion induced by osmotic stress in Arabidopsis thaliana cells
inferredcites →https://doi.org/10.1038/nbt.2120openalex-snapshot
Wheat grain yield on saline soils is improved by an ancestral Na+ transporter gene
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/10.1039/c8en00323hopenalex-snapshot
Hydroxyl radical scavenging by cerium oxide nanoparticles improves Arabidopsis salinity tolerance by enhancing leaf mesophyll potassium retention
inferredcites →https://doi.org/10.1046/j.1365-3040.2001.00661.xopenalex-snapshot
Ion transport in roots: measurement of fluxes using ion‐selective microelectrodes to characterize transporter function
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.2003.01764.xopenalex-snapshot
Sodium transport and HKT transporters: the rice model
inferredcites →https://doi.org/10.1071/fp06237openalex-snapshot
Potassium and sodium relations in salinised barley tissues as a basis of differential salt tolerance
inferredcites →https://doi.org/10.1071/fp09051openalex-snapshot
Ionic relations and osmotic adjustment in durum and bread wheat under saline conditions
inferredcites →https://doi.org/10.1071/fp09229openalex-snapshot
Wheat cultivars can be screened for NaCl salinity tolerance by measuring leaf chlorophyll content and shoot sap potassium
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.86.24.9856openalex-snapshot
In vivo 23Na and 31P NMR measurement of a tonoplast Na+/H+ exchange process and its characteristics in two barley cultivars.
inferredcites →https://doi.org/10.1080/07352689.2010.524517openalex-snapshot
Halophyte Improvement for a Salinized World
inferredcites →https://doi.org/10.1093/aob/mcg058openalex-snapshot
Na+ Tolerance and Na+ Transport in Higher Plants
inferredcites →https://doi.org/10.1093/aob/mct205openalex-snapshot
Learning from halophytes: physiological basis and strategies to improve abiotic stress tolerance in crops
inferredcites →https://doi.org/10.1093/jexbot/52.355.361openalex-snapshot
Brief exposure to low‐pH stress causes irreversible damage to the growing root in Arabidopsis thaliana : pectin–Ca interaction may play an important role in proton rhizotoxicity
inferredcites →https://doi.org/10.1093/jxb/erh070openalex-snapshot
Effect of salt and osmotic stresses on the expression of genes for the vacuolar H+-pyrophosphatase, H+-ATPase subunit A, and Na+/H+ antiporter from barley
inferredcites →https://doi.org/10.1093/jxb/eri229openalex-snapshot
Salt tolerance in wild Hordeum species is associated with restricted entry of Na+ and Cl− into the shoots
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/erl251openalex-snapshot
Overexpression of wheat Na+/H+ antiporter TNHX1 and H+-pyrophosphatase TVP1 improve salt- and drought-stress tolerance in Arabidopsis thaliana plants
inferredcites →https://doi.org/10.1093/jxb/erq346openalex-snapshot
A SOS3 homologue maps to HvNax4, a barley locus controlling an environmentally sensitive Na+ exclusion trait
inferredcites →https://doi.org/10.1093/jxb/ery194openalex-snapshot
Na+ extrusion from the cytosol and tissue-specific Na+ sequestration in roots confer differential salt stress tolerance between durum and bread wheat
inferredcites →https://doi.org/10.1093/mp/ssn058openalex-snapshot
Overexpression of SOS (Salt Overly Sensitive) Genes Increases Salt Tolerance in Transgenic Arabidopsis
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029357openalex-snapshot
Na+/H+ Antiporter in Tonoplast Vesicles from Rice Roots
inferredcites →https://doi.org/10.1093/pcp/pch060openalex-snapshot
Aluminum Targets Elongating Cells by Reducing Cell Wall Extensibility in Wheat Roots
inferredcites →https://doi.org/10.1093/pcp/pcu105openalex-snapshot
Durum and Bread Wheat Differ in Their Ability to Retain Potassium in Leaf Mesophyll: Implications for Salinity Stress Tolerance
inferredcites →https://doi.org/10.1104/pp.102.010421openalex-snapshot
Na+/H+ Exchange Activity in the Plasma Membrane of Arabidopsis
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.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.106.088864openalex-snapshot
A Sodium Transporter (HKT7) Is a Candidate for Nax1 , a Gene for Salt Tolerance in Durum Wheat
inferredcites →https://doi.org/10.1104/pp.106.093476openalex-snapshot
HKT1;5-Like Cation Transporters Linked to Na + Exclusion Loci in Wheat, Nax2 and Kna1
inferredcites →https://doi.org/10.1104/pp.107.110262openalex-snapshot
Root Plasma Membrane Transporters Controlling K+/Na+ Homeostasis in Salt-Stressed Barley
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.113.216572openalex-snapshot
Reduced Tonoplast Fast-Activating and Slow-Activating Channel Activity Is Essential for Conferring Salinity Tolerance in a Facultative Halophyte, Quinoa
inferredcites →https://doi.org/10.1104/pp.16.01347openalex-snapshot
Cell-Type-Specific H + -ATPase Activity in Root Tissues Enables K + Retention and Mediates Acclimation of Barley ( Hordeum vulgare ) to Salinity Stress
inferredcites →https://doi.org/10.1104/pp.85.1.30openalex-snapshot
Inhibition of Na+/H+ Antiport Activity in Sugar Beet Tonoplast by Analogs of Amiloride
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.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/10.1111/1477-8947.12054openalex-snapshot
Economics of salt‐induced land degradation and restoration
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01364.xopenalex-snapshot
Screening plants for salt tolerance by measuring K+ flux: a case study for barley
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01502.xopenalex-snapshot
Evidence that differential gene expression between the halophyte, Thellungiella halophila, and Arabidopsis thaliana is responsible for higher levels of the compatible osmolyte proline and tight control of Na+ uptake in T. halophila
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01592.xopenalex-snapshot
Photosynthetic capacity is related to the cellular and subcellular partitioning of Na+, K+ and Cl‐ in salt‐affected barley and durum wheat
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.1365-3040.2011.02296.xopenalex-snapshot
Assessing the role of root plasma membrane and tonoplast Na + /H + exchangers in salinity tolerance in wheat: in planta quantification methods
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02971.xopenalex-snapshot
Spatial variation in H 2 O 2 response of Arabidopsis thaliana root epidermal Ca 2+ flux and plasma membrane Ca 2+ channels
inferredcites →https://doi.org/10.1111/j.1399-3054.1991.tb01298.xopenalex-snapshot
Characterization of Na+ exclusion mechanisms of salt‐tolerant reed plants in comparison with salt‐sensitive rice plants
inferredcites →https://doi.org/10.1111/jipb.12238openalex-snapshot
K+ retention in leaf mesophyll, an overlooked component of salinity tolerance mechanism: A case study for barley
inferredcites →https://doi.org/10.1111/nph.13519openalex-snapshot
Salinity tolerance of crops – what is the cost?
inferredcites →https://doi.org/10.1111/nph.15555openalex-snapshot
Energy costs of salinity tolerance in crop plants
inferredcites →https://doi.org/10.1111/nph.15758openalex-snapshot
The energy cost of the tonoplast futile sodium leak
inferredcites →https://doi.org/10.1111/nph.15864openalex-snapshot
Energy costs of salt tolerance in crop plants
inferredcites →https://doi.org/10.1111/tpj.12651openalex-snapshot
The Na+ transporter, Ta HKT 1;5‐D, limits shoot Na+ accumulation in bread wheat
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/10.1146/annurev.arplant.59.032607.092911openalex-snapshot
Mechanisms of Salinity Tolerance
inferredcites →https://doi.org/10.1146/annurev.pharmtox.42.092001.143801openalex-snapshot
The Changing Face of the Na+/H+ Exchanger, NHE1: Structure, Regulation, and Cellular Actions
inferredcites →https://doi.org/10.1186/1471-2229-10-261openalex-snapshot
Comparative genomic analysis of 1047 completely sequenced cDNAs from an Arabidopsis-related model halophyte, Thellungiella halophila
inferredcites →https://doi.org/10.3389/fpls.2014.00154openalex-snapshot
Polyamines control of cation transport across plant membranes: implications for ion homeostasis and abiotic stress signaling
inferredcites →https://doi.org/10.3389/fpls.2014.00467openalex-snapshot
Regulation of Na+ fluxes in plants
inferredcites →https://doi.org/10.3389/fpls.2015.00071openalex-snapshot
Linking salinity stress tolerance with tissue-specific Na+ sequestration in wheat roots
inferredcites →https://doi.org/10.3390/ijms14059267openalex-snapshot
Differential Activity of Plasma and Vacuolar Membrane Transporters Contributes to Genotypic Differences in Salinity Tolerance in a Halophyte Species, Chenopodium quinoa
inferredcites →https://doi.org/10.4161/psb.1.6.3511openalex-snapshot
The Root Apex ofArabidopsis thalianaConsists of Four Distinct Zones of Growth Activities
inferredcites →https://doi.org/10.4161/psb.4.8.9236openalex-snapshot
Regulation by salt of vacuolar H + -ATPase and H + -pyrophosphatase activities and Na + /H + exchange

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.4673992openalex-extracted
inferred← citeshttps://doi.org/10.1002/advs.202103414openalex-snapshot
Recent Advances in Plant Nanoscience
inferred← citeshttps://doi.org/10.1002/ajb2.1506openalex-snapshot
Phenotypic and physiological responses to salt exposure in Sorghum reveal diversity among domesticated landraces
inferred← citeshttps://doi.org/10.1002/jsfa.70495openalex-snapshot
Improvement of salt stress tolerance in Salvia officinalis L. by co‐culture with halophytic plants: comparative study with Aptenia cordifolia and Spergularia salina
inferred← citeshttps://doi.org/10.1002/pld3.315openalex-snapshot
Root vacuolar sequestration and suberization are prominent responses of Pistacia spp. rootstocks during salinity stress
inferred← citeshttps://doi.org/10.1007/978-981-16-3832-9_11openalex-snapshot
Mechanisms of Salinity Tolerance in Quinoa
inferred← citeshttps://doi.org/10.1007/978-981-19-5841-0_10openalex-snapshot
Mangroves: An Underutilized Gene Pool to Combat Salinity
inferred← citeshttps://doi.org/10.1007/s00299-025-03506-wopenalex-snapshot
Dynamic transcriptomics and physiological insights reveal multi-tissue salt adaptation mechanisms in Amaranthus hypochondriacus across stress gradients
inferred← citeshttps://doi.org/10.1007/s00344-022-10655-9openalex-snapshot
Role of Vacuolar Membrane Transport Systems in Plant Salinity Tolerance
inferred← citeshttps://doi.org/10.1007/s00344-022-10664-8openalex-snapshot
Regulation Effects of Na+/H+ Antiporter (NHX1) on Nicotiana tabacum Stressed with Metals of Different Valences
inferred← citeshttps://doi.org/10.1007/s00425-020-03395-1openalex-snapshot
Understanding the role of root-related traits in salinity tolerance of quinoa accessions with contrasting epidermal bladder cell patterning
inferred← citeshttps://doi.org/10.1007/s10343-023-00933-1openalex-snapshot
Determination of Salinity Tolerance in Pigmented Rice Genotypes at Seedling Stage
inferred← citeshttps://doi.org/10.1007/s10653-024-01921-8openalex-snapshot
Zinc oxide nanoparticles influence on plant tolerance to salinity stress: insights into physiological, biochemical, and molecular responses
inferred← citeshttps://doi.org/10.1007/s10725-020-00619-yopenalex-snapshot
Leaf mesophyll K+ and Cl− fluxes and reactive oxygen species production predict rice salt tolerance at reproductive stage in greenhouse and field conditions
inferred← citeshttps://doi.org/10.1007/s11104-024-06714-7openalex-snapshot
Dealing with elemental toxicities in crops: hot topics and likely solutions
inferred← citeshttps://doi.org/10.1007/s11270-023-06286-9openalex-snapshot
Characteristics of Cd Uptake by the Roots of Bidens tripartita L. Under Salinity and pH Variations Assessed by Applying Non-invasive Micro-test Technology
inferred← citeshttps://doi.org/10.1007/s11676-022-01486-1openalex-snapshot
Adaptive strategy of Nitraria sibirica to transient salt, alkali and osmotic stresses via the alteration of Na+/K+ fluxes around root tips
inferred← citeshttps://doi.org/10.1007/s43621-025-00855-0openalex-snapshot
Biogenic nanoparticles for managing salinity stress-related crop and environmental risks: realistic applications and challenges
inferred← citeshttps://doi.org/10.1007/s44154-022-00065-yopenalex-snapshot
Improvement of leaf K+ retention is a shared mechanism behind CeO2 and Mn3O4 nanoparticles improved rapeseed salt tolerance
inferred← citeshttps://doi.org/10.1016/bs.abr.2022.02.012openalex-snapshot
Stomata under salt stress—What can mechanistic modeling tell us?
inferred← citeshttps://doi.org/10.1016/j.crope.2023.03.002openalex-snapshot
Mechanisms of nanomaterials for improving plant salt tolerance
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2019.109894openalex-snapshot
Thymol confers tolerance to salt stress by activating anti-oxidative defense and modulating Na+ homeostasis in rice root
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.113706openalex-snapshot
Application of Non-invasive Micro-test Technology (NMT) in environmental fields: A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105455openalex-snapshot
Na+ and K+ homeostasis in different organs of contrasting Zoysia japonica accessions under salt stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105585openalex-snapshot
One size does not fit all: Different strategies employed by triticale and barley plants to deal with soil salinity
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105690openalex-snapshot
Understanding the mechanistic basis of ameliorative effects of boron on salinity in barley (Hordeum vulgare)
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.123758openalex-snapshot
Hydroponic electrochemical phenotyping of root surfaces for rapid screening of salt-tolerant rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153418openalex-snapshot
Plant electrical signals: A multidisciplinary challenge
inferred← citeshttps://doi.org/10.1016/j.jplph.2022.153708openalex-snapshot
Evaluation of salt tolerance of oat cultivars and the mechanism of adaptation to salinity
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154784openalex-snapshot
Genome-wide association mapping reveals pleiotropic loci coupling antioxidant defense with redox homeostasis in barley under combined drought and salinity
inferred← citeshttps://doi.org/10.1016/j.jprot.2022.104502openalex-snapshot
Distinct salinity-induced changes in wheat metabolic machinery in different root tissue types
inferred← citeshttps://doi.org/10.1016/j.measurement.2023.112972openalex-snapshot
An improved extracellular ion fluxes measurement system based on Nernst-Planck equation
inferred← citeshttps://doi.org/10.1016/j.plana.2025.100196openalex-snapshot
Nano-improved plant salinity tolerance: The importance of K+/Na+ homeostasis and crosstalk between Ca2+ and hormones
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112804openalex-snapshot
Nitric oxide-induced Na+/H+ exchange activity confers salt tolerance in pea (Pisum sativum L.) mesophyll cells
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.04.022openalex-snapshot
Comparative transcriptome analysis of NaCl and KCl stress response in Malus hupehensis Rehd. Provide insight into the regulation involved in Na+ and K+ homeostasis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.11.032openalex-snapshot
Foxtail millet MYB-like transcription factor SiMYB16 confers salt tolerance in transgenic rice by regulating phenylpropane pathway
inferred← citeshttps://doi.org/10.1016/j.rhisph.2023.100841openalex-snapshot
Four Ethiopian barley (H. Vulgare) varieties with a range of tolerance to salinity and water stress
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111622openalex-snapshot
Transcriptome responses to salt stress in roots and leaves of Lilium pumilum
inferred← citeshttps://doi.org/10.1016/j.stress.2021.100024openalex-snapshot
QTL mapping in an interspecific sorghum population uncovers candidate regulators of salinity tolerance
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101243openalex-snapshot
Halophyte Halogeton glomeratus HKT1;2 confers salt tolerance in transgenic Arabidopsis by modulating ion homeostasis
inferred← citeshttps://doi.org/10.1016/j.tplants.2020.04.008openalex-snapshot
Crop Halophytism: An Environmentally Sustainable Solution for Global Food Security
inferred← citeshttps://doi.org/10.1038/s41396-022-01238-3openalex-snapshot
Synthetic bacterial community derived from a desert rhizosphere confers salt stress resilience to tomato in the presence of a soil microbiome
inferred← citeshttps://doi.org/10.1038/s41438-020-00358-1openalex-snapshot
Overexpression of phosphatidylserine synthase IbPSS1 affords cellular Na+ homeostasis and salt tolerance by activating plasma membrane Na+/H+ antiport activity in sweet potato roots
inferred← citeshttps://doi.org/10.1038/s41598-023-40337-9openalex-snapshot
Irrigated barley–grass pea crop mixtures can revive soil microbial activities and alleviate salinity in desertic conditions of southern Morocco
inferred← citeshttps://doi.org/10.1071/fp21336openalex-snapshot
Unravelling the physiological basis of salinity stress tolerance in cultivated and wild rice species
inferred← citeshttps://doi.org/10.1080/15548627.2024.2394302openalex-snapshot
Myotubularin 2 interacts with SEC23A and negatively regulates autophagy at ER exit sites in Arabidopsis
inferred← citeshttps://doi.org/10.1093/aob/mcac022openalex-snapshot
Plant responses to heterogeneous salinity: agronomic relevance and research priorities
inferred← citeshttps://doi.org/10.1093/g3journal/jkaf149openalex-snapshot
The genetic basis of chloride exclusion in grapevines
inferred← citeshttps://doi.org/10.1093/jxb/eraa175openalex-snapshot
Microsensors in plant biology: in vivo visualization of inorganic analytes with high spatial and/or temporal resolution
inferred← citeshttps://doi.org/10.1093/jxb/erab215openalex-snapshot
Multiomics reveal pivotal roles of sodium translocation and compartmentation in regulating salinity resistance in allotetraploid rapeseed
inferred← citeshttps://doi.org/10.1093/plphys/kiad304openalex-snapshot
A Tunisian wild grape leads to metabolic fingerprints of salt tolerance
inferred← citeshttps://doi.org/10.1093/treephys/tpaa174openalex-snapshot
Tissue tolerance mechanisms conferring salinity tolerance in a halophytic perennial species Nitraria sibirica Pall.
inferred← citeshttps://doi.org/10.1101/2020.08.05.238972openalex-snapshot
QTL mapping in an interspecific sorghum population uncovers candidate regulators of salinity tolerance
inferred← citeshttps://doi.org/10.1101/2022.04.29.489905openalex-snapshot
Isotope-based visualization of element distribution in phloem provides functional evidence for the operation of SOS1 Na + /H + exchangers in mature zones of Arabidopsis root
inferred← citeshttps://doi.org/10.1104/pp.20.00196openalex-snapshot
Calmodulin HvCaM1 Negatively Regulates Salt Tolerance via Modulation of HvHKT1s and HvCAMTA4
inferred← citeshttps://doi.org/10.1111/jac.70214openalex-snapshot
Assessing Suitability of Various Morphological and Ionic Traits as Proxies for Barley Tolerance to Combined Salinity and Waterlogging Stress
inferred← citeshttps://doi.org/10.1111/jipb.13839openalex-snapshot
The SlWRKY42–SlMYC2 module synergistically enhances tomato saline–alkali tolerance by activating the jasmonic acid signaling and spermidine biosynthesis pathway
inferred← citeshttps://doi.org/10.1111/nph.18501openalex-snapshot
Tobacco leaf tissue rapidly detoxifies direct salt loads without activation of calcium and SOS signaling
inferred← citeshttps://doi.org/10.1111/nph.71397openalex-snapshot
Cell‐based crop phenotyping for future climates
inferred← citeshttps://doi.org/10.1111/pce.70317openalex-snapshot
SALT OVERLY SENSITIVE 1 Na + /H + Exchanger Operates in Mature Root Zone and Is a Major Contributor to Root Na + Exclusion During Shoot‐to‐Root Na + Recirculation
inferred← citeshttps://doi.org/10.1111/pce.70427openalex-snapshot
Ethylene Inhibited Plasma Membrane H + ‐ATPase to Decrease Root Na + Efflux in Maize to Break Na + /H + Homeostasis Under Salt Stress
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/10.1186/s12870-020-02718-4openalex-snapshot
Tissue-specific expression analysis of Na+ and Cl− transporter genes associated with salt removal ability in rice leaf sheath
inferred← citeshttps://doi.org/10.1186/s12870-020-02734-4openalex-snapshot
Comprehensive dissection into morpho-physiologic responses, ionomic homeostasis, and transcriptomic profiling reveals the systematic resistance of allotetraploid rapeseed to salinity
inferred← citeshttps://doi.org/10.1186/s12870-024-06033-0openalex-snapshot
Ion homeostasis and coordinated salt tolerance mechanisms in a barley (Hordeum vulgare L.)doubled haploid line
inferred← citeshttps://doi.org/10.1186/s12870-026-08861-8openalex-snapshot
Glycine betaine alleviates salt stress in tomato by enhancing the chlorophyll synthesis pathway, photosynthesis, and regulating m6A methyltransferase related genes
inferred← citeshttps://doi.org/10.1186/s12870-026-08936-6openalex-snapshot
Comparative analysis of salt tolerance and associated physiological traits in wild and cultivated barley at the seedling stage
inferred← citeshttps://doi.org/10.1186/s12951-021-00892-7openalex-snapshot
Cerium oxide nanoparticles improve cotton salt tolerance by enabling better ability to maintain cytosolic K+/Na+ ratio
inferred← citeshttps://doi.org/10.1270/jsbbs.20123openalex-snapshot
Functions and structure of roots and their contributions to salinity tolerance in plants
inferred← citeshttps://doi.org/10.15252/embj.2019103256openalex-snapshot
Loss of salt tolerance during tomato domestication conferred by variation in a Na+/K+ transporter
inferred← citeshttps://doi.org/10.1590/s1678-3921.pab2023.v58.03131openalex-snapshot
Na+ exclusion and proline accumulation in Urochloa spp. cultivars
inferred← citeshttps://doi.org/10.1631/jzus.b1900400openalex-snapshot
Salinity tolerance in barley during germination—homologs and potential genes
inferred← citeshttps://doi.org/10.32604/biocell.2021.014336openalex-snapshot
Overexpression of rice F-box phloem protein gene OsPP12-A13 confers salinity tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2019.01290openalex-snapshot
Grafting Cucumber Onto Pumpkin Induced Early Stomatal Closure by Increasing ABA Sensitivity Under Salinity Conditions
inferred← citeshttps://doi.org/10.3389/fpls.2019.01361openalex-snapshot
Tissue-Specific Regulation of Na+ and K+ Transporters Explains Genotypic Differences in Salinity Stress Tolerance in Rice
inferred← citeshttps://doi.org/10.3389/fpls.2020.595055openalex-snapshot
Investigation of Salt Tolerance Mechanisms Across a Root Developmental Gradient in Almond Rootstocks
inferred← citeshttps://doi.org/10.3389/fpls.2022.1008172openalex-snapshot
Gain time to adapt: How sorghum acquires tolerance to salinity
inferred← citeshttps://doi.org/10.3389/fpls.2022.1040142openalex-snapshot
Na+/K+-ATPase regulates the K+/Na+ homeostasis in the intertidal macroalgae, Neoporphyra haitanensis, in response to salt stress
inferred← citeshttps://doi.org/10.3389/fpls.2022.772948openalex-snapshot
Trehalose Alleviated Salt Stress in Tomato by Regulating ROS Metabolism, Photosynthesis, Osmolyte Synthesis, and Trehalose Metabolic Pathways
inferred← citeshttps://doi.org/10.3389/fpls.2022.843994openalex-snapshot
Plant Salinity Stress Response and Nano-Enabled Plant Salt Tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2022.955199openalex-snapshot
Genome-wide analysis of the homeodomain-leucine zipper family in Lotus japonicus and the overexpression of LjHDZ7 in Arabidopsis for salt tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2023.1284480openalex-snapshot
Eugenol improves salt tolerance via enhancing antioxidant capacity and regulating ionic balance in tobacco seedlings
inferred← citeshttps://doi.org/10.3389/fpls.2024.1310328openalex-snapshot
Research progress of the detection and analysis methods of heavy metals in plants
inferred← citeshttps://doi.org/10.3389/fsci.2024.1416023openalex-snapshot
Adapting crops for climate change: regaining lost abiotic stress tolerance in crops
inferred← citeshttps://doi.org/10.3390/agronomy11081481openalex-snapshot
Short-Term Responses to Salinity of Soybean and Chenopodium album Grown in Single and Mixed-Species Hydroponic Systems
inferred← citeshttps://doi.org/10.3390/agronomy14061259openalex-snapshot
Effect of Salt-Induced Stress on the Calorific Value of Two Miscanthus sacchariflorus (Amur Silvergrass) Varieties
inferred← citeshttps://doi.org/10.3390/bioengineering9090410openalex-snapshot
Transcriptome-Wide Analysis Revealed the Potential of the High-Affinity Potassium Transporter (HKT) Gene Family in Rice Salinity Tolerance via Ion Homeostasis
inferred← citeshttps://doi.org/10.3390/horticulturae10050510openalex-snapshot
Physiological Studies and Transcriptomic Analysis Reveal the Mechanism of Saline-Alkali Stress Resistance of Malus sieversii f. niedzwetzkyan
inferred← citeshttps://doi.org/10.3390/ijms23179900openalex-snapshot
Comparing Essentiality of SOS1-Mediated Na+ Exclusion in Salinity Tolerance between Cultivated and Wild Rice Species
inferred← citeshttps://doi.org/10.3390/ijms262311369openalex-snapshot
Special Issue “Molecular Regulation of Drought and Salinity Tolerance in Plants”
inferred← citeshttps://doi.org/10.3390/mi12030273openalex-snapshot
An Improved Transwell Design for Microelectrode Ion-Flux Measurements
inferred← citeshttps://doi.org/10.3390/plants10071393openalex-snapshot
Genetic Diversity and Synergistic Modulation of Salinity Tolerance Genes in Aegilops tauschii Coss
inferred← citeshttps://doi.org/10.3390/plants11050656openalex-snapshot
Comparative Analysis of Root Na+ Relation under Salinity between Oryza sativa and Oryza coarctata
inferred← citeshttps://doi.org/10.3390/plants12010044openalex-snapshot
Selenium Regulates Antioxidant, Photosynthesis, and Cell Permeability in Plants under Various Abiotic Stresses: A Review
inferred← citeshttps://doi.org/10.3390/plants13071036openalex-snapshot
Screening of Rice (Oryza sativa L.) Genotypes for Salinity Tolerance and Dissecting Determinants of Tolerance Mechanism
inferred← citeshttps://doi.org/10.3390/plants13192673openalex-snapshot
Agro-Physiological and DNA Methylation Responses to Salinity Stress in Wheat (Triticum aestivum L.), Aegilops cylindrica Host, and Their Introgressed Lines
inferred← citeshttps://doi.org/10.3390/plants8110472openalex-snapshot
Identification of Superior Alleles for Seedling Stage Salt Tolerance in the USDA Rice Mini-Core Collection
inferred← citeshttps://doi.org/10.4081/ija.2021.1830openalex-snapshot
Salinity tolerance evaluation of barley germplasm for marginal soil utilization
inferred← citeshttps://doi.org/10.6084/m9.figshare.13186029openalex-snapshot
Additional file 1 of Tissue-specific expression analysis of Na+ and Cl− transporter genes associated with salt removal ability in rice leaf sheath
inferred← citeshttps://doi.org/10.6084/m9.figshare.13186032openalex-snapshot
Additional file 2 of Tissue-specific expression analysis of Na+ and Cl− transporter genes associated with salt removal ability in rice leaf sheath
inferred← citeshttps://doi.org/10.6084/m9.figshare.13186035openalex-snapshot
Additional file 3 of Tissue-specific expression analysis of Na+ and Cl− transporter genes associated with salt removal ability in rice leaf sheath
inferred← citeshttps://doi.org/10.6084/m9.figshare.13186041openalex-snapshot
Additional file 4 of Tissue-specific expression analysis of Na+ and Cl− transporter genes associated with salt removal ability in rice leaf sheath
inferred← citeshttps://doi.org/10.6084/m9.figshare.13186044openalex-snapshot
Additional file 5 of Tissue-specific expression analysis of Na+ and Cl− transporter genes associated with salt removal ability in rice leaf sheath
inferred← citeshttps://doi.org/10.6084/m9.figshare.13186047openalex-snapshot
Additional file 6 of Tissue-specific expression analysis of Na+ and Cl− transporter genes associated with salt removal ability in rice leaf sheath
inferred← citeshttps://doi.org/10.6084/m9.figshare.13186050openalex-snapshot
Additional file 7 of Tissue-specific expression analysis of Na+ and Cl− transporter genes associated with salt removal ability in rice leaf sheath
inferred← citeshttps://doi.org/10.6084/m9.figshare.13186053openalex-snapshot
Additional file 8 of Tissue-specific expression analysis of Na+ and Cl− transporter genes associated with salt removal ability in rice leaf sheath
inferred← citeshttps://doi.org/10.6084/m9.figshare.13186056openalex-snapshot
Additional file 9 of Tissue-specific expression analysis of Na+ and Cl− transporter genes associated with salt removal ability in rice leaf sheath
inferred← citeshttps://doi.org/10.6084/m9.figshare.13279848openalex-snapshot
Additional file 1 of Comprehensive dissection into morpho-physiologic responses, ionomic homeostasis, and transcriptomic profiling reveals the systematic resistance of allotetraploid rapeseed to salinity
inferred← citeshttps://doi.org/10.6084/m9.figshare.13279851openalex-snapshot
Additional file 2 of Comprehensive dissection into morpho-physiologic responses, ionomic homeostasis, and transcriptomic profiling reveals the systematic resistance of allotetraploid rapeseed to salinity
inferred← citeshttps://doi.org/10.6084/m9.figshare.14676610openalex-snapshot
Additional file 1 of Cerium oxide nanoparticles improve cotton salt tolerance by enabling better ability to maintain cytosolic K+/Na+ ratio
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.