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A rice really interesting new gene H 2‐type E 3 ligase, OsSIRH2‐14 , enhances salinity tolerance via ubiquitin/26 S proteasome‐mediated degradation of salt‐related proteins
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0471140864.ps1917s52openalex-snapshot
Membrane‐Based Yeast Two‐Hybrid System to Detect Protein Interactions
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/s00425-011-1386-zopenalex-snapshot
A novel rice calmodulin-like gene, OsMSR2, enhances drought and salt tolerance and increases ABA sensitivity in Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-017-2834-1openalex-snapshot
The microtubule-associated RING finger protein 1 (OsMAR1) acts as a negative regulator for salt-stress response through the regulation of OCPI2 (O. sativa chymotrypsin protease inhibitor 2)
inferredcites →https://doi.org/10.1007/s00425-017-2838-xopenalex-snapshot
Oryza sativa salt-induced RING E3 ligase 2 (OsSIRP2) acts as a positive regulator of transketolase in plant response to salinity and osmotic stress
inferredcites →https://doi.org/10.1007/s10265-015-0764-1openalex-snapshot
OsHKT2;2/1-mediated Na+ influx over K+ uptake in roots potentially increases toxic Na+ accumulation in a salt-tolerant landrace of rice Nona Bokra upon salinity stress
inferredcites →https://doi.org/10.1007/s11103-008-9309-5openalex-snapshot
Characterization of transcription factor gene SNAC2 conferring cold and salt tolerance in rice
inferredcites →https://doi.org/10.1007/s11103-009-9524-8openalex-snapshot
Identification and expression profiling analysis of TIFY family genes involved in stress and phytohormone responses in rice
inferredcites →https://doi.org/10.1007/s11103-009-9576-9openalex-snapshot
A gene family encoding RING finger proteins in rice: their expansion, expression diversity, and co-expressed genes
inferredcites →https://doi.org/10.1007/s11103-015-0375-1openalex-snapshot
Molecular dissection of a rice microtubule-associated RING finger protein and its potential role in salt tolerance in Arabidopsis
inferredcites →https://doi.org/10.1007/s11104-018-3770-yopenalex-snapshot
It is not all about sodium: revealing tissue specificity and signalling roles of potassium in plant responses to salt stress
inferredcites →https://doi.org/10.1007/s11105-012-0548-xopenalex-snapshot
Overexpression of TaSRK2C1, a Wheat SNF1-Related Protein Kinase 2 Gene, Increases Tolerance to Dehydration, Salt, and Low Temperature in Transgenic Tobacco
inferredcites →https://doi.org/10.1007/s12551-009-0010-yopenalex-snapshot
Structure and functions of profilins
inferredcites →https://doi.org/10.1016/j.jneumeth.2006.01.009openalex-snapshot
Properties of the new fluorescent Na+ indicator CoroNa Green: Comparison with SBFI and confocal Na+ imaging
inferredcites →https://doi.org/10.1016/j.jplph.2014.08.002openalex-snapshot
Molecular dissection of the response of a rice leucine-rich repeat receptor-like kinase (LRR-RLK) gene to abiotic stresses
inferredcites →https://doi.org/10.1016/j.jplph.2015.11.008openalex-snapshot
PDH45 transgenic rice maintain cell viability through lower accumulation of Na+, ROS and calcium homeostasis in roots under salinity stress
inferredcites →https://doi.org/10.1016/j.plantsci.2011.07.008openalex-snapshot
Overexpression of the mitochondrial PPR40 gene improves salt tolerance in Arabidopsis
inferredcites →https://doi.org/10.1016/j.rsci.2016.09.004openalex-snapshot
Salt Tolerance in Rice: Focus on Mechanisms and Approaches
inferredcites →https://doi.org/10.1016/j.sjbs.2014.12.001openalex-snapshot
Soil salinity: A serious environmental issue and plant growth promoting bacteria as one of the tools for its alleviation
inferredcites →https://doi.org/10.1016/j.tplants.2004.08.009openalex-snapshot
Reactive oxygen gene network of plants
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/s0168-9452(03)00014-1openalex-snapshot
Accumulation of SALT protein in rice plants as a response to environmental stresses
inferredcites →https://doi.org/10.1016/s1672-6308(08)60091-8openalex-snapshot
Comparative Effects of Salt Stress and Extreme pH Stress Combined on Glycinebetaine Accumulation, Photosynthetic Abilities and Growth Characters of Two Rice Genotypes
inferredcites →https://doi.org/10.1038/370655a0openalex-snapshot
Structure and transport mechanism of a high-affinity potassium uptake transporter from higher plants
inferredcites →https://doi.org/10.1038/nature07523openalex-snapshot
Altered circadian rhythms regulate growth vigour in hybrids and allopolyploids
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/sj.emboj.7601732openalex-snapshot
Rice OsHKT2;1 transporter mediates large Na+ influx component into K+‐starved roots for growth
inferredcites →https://doi.org/10.1042/bcj20160719openalex-snapshot
Systematic approaches to identify E3 ligase substrates
inferredcites →https://doi.org/10.1046/j.1365-313x.1996.10050869.xopenalex-snapshot
Alkali cation selectivity of the wheat root high‐affinity potassium transporter HKT1
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01077.xopenalex-snapshot
Two types of HKT transporters with different properties of Na+ and K+ transport in Oryza sativa
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01410.xopenalex-snapshot
A role for HKT1 in sodium uptake by wheat roots
inferredcites →https://doi.org/10.1073/pnas.0405902101openalex-snapshot
Insertional assembly of actin filament barbed ends in association with formins produces piconewton forces
inferredcites →https://doi.org/10.1073/pnas.082123799openalex-snapshot
Glycine residues in potassium channel-like selectivity filters determine potassium selectivity in four-loop-per-subunit HKT transporters from plants
inferredcites →https://doi.org/10.1073/pnas.1000698107openalex-snapshot
A rice high-affinity potassium transporter (HKT) conceals a calcium-permeable cation channel
inferredcites →https://doi.org/10.1073/pnas.231476498openalex-snapshot
Engineering salt-tolerant Brassica plants: Characterization of yield and seed oil quality in transgenic plants with increased vacuolar sodium accumulation
inferredcites →https://doi.org/10.1073/pnas.94.20.11079openalex-snapshot
Molecular and functional characterization of a novel low-affinity cation transporter (LCT1) in higher plants
inferredcites →https://doi.org/10.1080/07352689.2011.605739openalex-snapshot
Gene Expression Profiling of Plants under Salt Stress
inferredcites →https://doi.org/10.1093/aobpla/ply028openalex-snapshot
Degradation of chlorophyll and synthesis of flavonols during autumn senescence—the story told by individual leaves
inferredcites →https://doi.org/10.1093/dnares/dst011openalex-snapshot
Comprehensive Analysis of the Rice RING E3 Ligase Family Reveals Their Functional Diversity in Response to Abiotic stress
inferredcites →https://doi.org/10.1093/jxb/erj064openalex-snapshot
Arabidopsis thaliana Cyclic Nucleotide Gated Channel 3 forms a non-selective ion transporter involved in germination and cation transport
inferredcites →https://doi.org/10.1093/jxb/erl199openalex-snapshot
Expressions of OsHKT1, OsHKT2, and OsVHA are differentially regulated under NaCl stress in salt-sensitive and salt-tolerant rice (Oryza sativa L.) cultivars
inferredcites →https://doi.org/10.1093/jxb/erp184openalex-snapshot
Cloning of a high-affinity K+ transporter gene PutHKT2;1 from Puccinellia tenuiflora and its functional comparison with OsHKT2;1 from rice in yeast and Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/ert085openalex-snapshot
Salicylic acid improves salinity tolerance in Arabidopsis by restoring membrane potential and preventing salt-induced K+ loss via a GORK channel
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/pcp/pch014openalex-snapshot
Function, Intracellular Localization and the Importance in Salt Tolerance of a Vacuolar Na+/H+ Antiporter from Rice
inferredcites →https://doi.org/10.1093/pcp/pcy009openalex-snapshot
A Negative Regulator in Response to Salinity in Rice: Oryza sativa Salt-, ABA- and Drought-Induced RING Finger Protein 1 (OsSADR1)
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.103.026062openalex-snapshot
Overexpression of SOD2 Increases Salt Tolerance of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.052423openalex-snapshot
Functional Analysis of the RING-Type Ubiquitin Ligase Family of Arabidopsi s
inferredcites →https://doi.org/10.1104/pp.109.138008openalex-snapshot
Diversity in Expression Patterns and Functional Properties in the Rice HKT Transporter Family
inferredcites →https://doi.org/10.1104/pp.109.145722openalex-snapshot
Differential Sodium and Potassium Transport Selectivities of the Rice OsHKT2;1 and OsHKT2;2 Transporters in Plant Cells
inferredcites →https://doi.org/10.1104/pp.110.168047openalex-snapshot
K+ Transport by the OsHKT2;4 Transporter from Rice with Atypical Na+ Transport Properties and Competition in Permeation of K+ over Mg2+ and Ca2+ Ions
inferredcites →https://doi.org/10.1104/pp.112.194936openalex-snapshot
The Rice Monovalent Cation Transporter OsHKT2;4: Revisited Ionic Selectivity
inferredcites →https://doi.org/10.1104/pp.115.1.159openalex-snapshot
Effects of Osmoprotectants upon NaCl Stress in Rice
inferredcites →https://doi.org/10.1104/pp.122.4.1249openalex-snapshot
TheArabidopsis HKT1Gene Homolog Mediates Inward Na+ Currents inXenopus laevisOocytes and Na+ Uptake inSaccharomyces cerevisiae
inferredcites →https://doi.org/10.1104/pp.17.00532openalex-snapshot
A Magnesium Transporter OsMGT1 Plays a Critical Role in Salt Tolerance in Rice
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.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.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.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.9.12.2243openalex-snapshot
Antagonistic effects of abscisic acid and jasmonates on salt stress-inducible transcripts in rice roots.
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.1365-3040.2009.02056.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.1365-3040.2009.02105.xopenalex-snapshot
Variation in salinity tolerance and shoot sodium accumulation in Arabidopsis ecotypes linked to differences in the natural expression levels of transporters involved in sodium transport
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02836.xopenalex-snapshot
Early infection of scutellum tissue with Agrobacterium allows high‐speed transformation of rice
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03318.xopenalex-snapshot
Duplicated P5CS genes of Arabidopsis play distinct roles in stress regulation and developmental control of proline biosynthesis
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03612.xopenalex-snapshot
Multicolor bimolecular fluorescence complementation reveals simultaneous formation of alternative CBL/CIPK complexes in planta
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04701.xopenalex-snapshot
Over‐expression of an Na + ‐ and K + ‐permeable HKT transporter in barley improves salt tolerance
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05031.xopenalex-snapshot
HKT2;2/1, a K+‐permeable transporter identified in a salt‐tolerant rice cultivar through surveys of natural genetic polymorphism
inferredcites →https://doi.org/10.1111/j.1399-3054.2010.01366.xopenalex-snapshot
The cyclic nucleotide-gated channel AtCNGC10 transports Ca2+and Mg2+inArabidopsis
inferredcites →https://doi.org/10.1111/j.1467-7652.2008.00393.xopenalex-snapshot
Identification of a rice Actin2 gene regulatory region for high‐level expression of transgenes in monocots‡
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01487.xopenalex-snapshot
Genes and salt tolerance: bringing them together
inferredcites →https://doi.org/10.1111/jipb.12376openalex-snapshot
OsSIDP366 , a DUF1644 gene, positively regulates responses to drought and salt stresses in rice
inferredcites →https://doi.org/10.1111/nph.15605openalex-snapshot
A domestication‐associated reduction in K+‐preferring HKT transporter activity underlies maize shoot K+ accumulation and salt tolerance
inferredcites →https://doi.org/10.1111/ppl.12356openalex-snapshot
Comprehensive phenotypic analysis of rice (Oryza sativa) response to salinity stress
inferredcites →https://doi.org/10.1126/science.270.5242.1660openalex-snapshot
Sodium-Driven Potassium Uptake by the Plant Potassium Transporter HKT1 and Mutations Conferring Salt Tolerance
inferredcites →https://doi.org/10.1134/s1021443708040158openalex-snapshot
OsLEA3, a late embryogenesis abundant protein gene from rice, confers tolerance to water deficit and salt stress to transgenic rice
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092911openalex-snapshot
Mechanisms of Salinity Tolerance
inferredcites →https://doi.org/10.1146/annurev.biochem.78.101807.093809openalex-snapshot
RING Domain E3 Ubiquitin Ligases
inferredcites →https://doi.org/10.1186/s12575-014-0013-3openalex-snapshot
Model of Cation Transportation Mediated by High-Affinity Potassium Transporters (HKTs) in Higher Plants
inferredcites →https://doi.org/10.1186/s12870-016-0761-0openalex-snapshot
PtrA/NINV, an alkaline/neutral invertase gene of Poncirus trifoliata, confers enhanced tolerance to multiple abiotic stresses by modulating ROS levels and maintaining photosynthetic efficiency
inferredcites →https://doi.org/10.1186/s12870-017-1089-0openalex-snapshot
Comparative studies on tolerance of rice genotypes differing in their tolerance to moderate salt stress
inferredcites →https://doi.org/10.17221/413/2011-pseopenalex-snapshot
Effect of salt stress on physiological response and leaf polyamine content in NERICA rice seedlings
inferredcites →https://doi.org/10.21769/bioprotoc.263openalex-snapshot
Detection of Hydrogen Peroxide by DAB Staining in Arabidopsis Leaves
inferredcites →https://doi.org/10.22058/jpmb.2015.15369openalex-snapshot
The effect of salinity stress on Na+, K+ concentration, Na+/K+ ratio, electrolyte leakage and HKT expression profile in roots of Aeluropus littoralis
inferredcites →https://doi.org/10.2307/3870582openalex-snapshot
Antagonistic Effects of Abscisic Acid and Jasmonates on Salt Stress-Inducible Transcripts in Rice Roots
inferredcites →https://doi.org/10.3389/fpls.2013.00410openalex-snapshot
Sodium transport system in plant cells
inferredcites →https://doi.org/10.3389/fpls.2015.00175openalex-snapshot
Development of salinity tolerance in rice by constitutive-overexpression of genes involved in the regulation of programmed cell death
inferredcites →https://doi.org/10.3389/fpls.2015.01092openalex-snapshot
ROS Regulation During Abiotic Stress Responses in Crop Plants
inferredcites →https://doi.org/10.3389/fpls.2017.00576openalex-snapshot
SOS1, HKT1;5, and NHX1 Synergistically Modulate Na+ Homeostasis in the Halophytic Grass Puccinellia tenuiflora
inferredcites →https://doi.org/10.3389/fpls.2017.01823openalex-snapshot
The Rice High-Affinity K+ Transporter OsHKT2;4 Mediates Mg2+ Homeostasis under High-Mg2+ Conditions in Transgenic Arabidopsis
inferredcites →https://doi.org/10.3390/ijms14047660openalex-snapshot
Plant High-Affinity Potassium (HKT) Transporters Involved in Salinity Tolerance: Structural Insights to Probe Differences in Ion Selectivity
inferredcites →https://doi.org/10.4161/psb.3.6.5429openalex-snapshot
Na+- K+transport in roots under salt stress
inferredcites →https://doi.org/10.4161/psb.6.1.14202openalex-snapshot
Cytoskeleton and plant salt stress tolerance
inferredcites →https://doi.org/10.5402/2012/927436openalex-snapshot
Ion Transporters and Abiotic Stress Tolerance in Plants
inferredcites →https://doi.org/10.5511/plantbiotechnology.25.233openalex-snapshot
Functions of HKT transporters in sodium transport in roots and in protecting leaves from salinity stress
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.4846940openalex-extracted
Ring E3 Ubiquitin Ligase Bvrnf170 Postively Regulates Salt Tolerance in Transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-023-03093-8openalex-snapshot
Identification of hub genes that variate the qCSS12-mediated cold tolerance between indica and japonica rice using WGCNA
inferred← citeshttps://doi.org/10.1007/s00425-020-03431-0openalex-snapshot
Molecular dissection of two homoeologous wheat genes encoding RING H2-type E3 ligases: TaSIRFP-3A and TaSIRFP-3B
inferred← citeshttps://doi.org/10.1007/s00425-023-04243-8openalex-snapshot
Evolution of the Tóxicos en Levadura 63 (TL63) gene family in plants and functional characterization of Arabidopsis thaliana TL63 under oxidative stress
inferred← citeshttps://doi.org/10.1007/s10681-020-02685-9openalex-snapshot
Quantitative analysis of allelic differences in the grain proteome between the Wxg2 and Wxg3 alleles in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s11033-021-06595-4openalex-snapshot
SSR marker-based genetic diversity analysis and SNP haplotyping of genes associating abiotic and biotic stress tolerance, rice growth and development and yield across 93 rice landraces
inferred← citeshttps://doi.org/10.1007/s11103-021-01232-xopenalex-snapshot
How salt stress-responsive proteins regulate plant adaptation to saline conditions
inferred← citeshttps://doi.org/10.1007/s11356-024-34933-zopenalex-snapshot
Chitosan nanoparticles (CSNPs) conferred salinity tolerance in maize by upregulating E3 ubiquitin-protein ligase, P5CS1, HKT1, NHX1, and PMP3 genes
inferred← citeshttps://doi.org/10.1007/s12374-023-09382-9openalex-snapshot
Overexpression of Rice C3HC4-Type RING Finger Protein Gene, OsSIRHC-2, Improves Salinity Tolerance Through Low Na+ Accumulation
inferred← citeshttps://doi.org/10.1007/s12374-024-09433-9openalex-snapshot
Rice H2-Type RING E3 Ligase Gene, OsSIRH2-3, Positively Regulates Salt Tolerance by Maintaining Na+/K+ Homeostasis
inferred← citeshttps://doi.org/10.1016/j.cropd.2024.100077openalex-snapshot
Decoding post-translational modification for understanding stress tolerance in plant
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104715openalex-snapshot
OsSIRH2-23, a rice salt-induced RING finger protein H2-23, contributes to insensitivity to salinity stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105224openalex-snapshot
Overexpression of a C3HC4-type RING E3 ligase gene, OsRFPHC-13, improves salinity resistance in rice, Oryza sativa, by altering the expression of Na+/K+ transporter genes
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2021.03.185openalex-snapshot
Role of ubiquitination enzymes in abiotic environmental interactions with plants
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.125162openalex-snapshot
Genome-wide analysis and identification of TaRING-H2 gene family and TaSDIR1 positively regulates salt stress tolerance in wheat
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.111057openalex-snapshot
Genic male sterility increases rice drought tolerance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108260openalex-snapshot
The B3 gene family in Medicago truncatula: Genome-wide identification and the response to salt stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111585openalex-snapshot
Multifunctional roles of the rice mannose-binding lectin OsMBL1 in biotic and abiotic stress responses
inferred← citeshttps://doi.org/10.1016/j.rsci.2025.06.005openalex-snapshot
Functions of Rice E3 Ubiquitin Ligases in Response to Environmental Stress and in Regulating Grain Size
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100451openalex-snapshot
Overexpression of E3 ligase RING finger protein BrRING509 enhances salt stress tolerance in transgenic Arabidopsis plants
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c08042openalex-snapshot
Wheat TaPUB1 Regulates Cd Uptake and Tolerance by Promoting the Degradation of TaIRT1 and TaIAA17
inferred← citeshttps://doi.org/10.1079/9781800623033.0007openalex-snapshot
Updates on Protein Post-Translational Modifications for Modulating Response to Salinity
inferred← citeshttps://doi.org/10.1080/07352689.2026.2732811openalex-snapshot
The dual role of ethylene in plant salt tolerance: mechanisms and species specificity
inferred← citeshttps://doi.org/10.1080/15592324.2020.1732103openalex-snapshot
AtPPRT1 negatively regulates salt stress response in Arabidopsis seedlings
inferred← citeshttps://doi.org/10.1093/jxb/erad333openalex-snapshot
Modulation of potassium transport to increase abiotic stress tolerance in plants
inferred← citeshttps://doi.org/10.1093/plphys/kiag591openalex-snapshot
MdXERICO negatively regulates salt tolerance in apple through ubiquitination and degradation of MdJAZ10
inferred← citeshttps://doi.org/10.1111/jipb.13599openalex-snapshot
Designing salt stress‐resilient crops: Current progress and future challenges
inferred← citeshttps://doi.org/10.1111/jipb.13641openalex-snapshot
The RING zinc finger protein LbRZF1 promotes salt gland development and salt tolerance in Limonium bicolor
inferred← citeshttps://doi.org/10.1111/pbi.13857openalex-snapshot
Ubiquitin ligase OsRINGzf1 regulates drought resistance by controlling the turnover of OsPIP2 ;1
inferred← citeshttps://doi.org/10.1111/pbi.70312openalex-snapshot
Rice RING E3 Ligase OsRMT1 Negatively Regulates Salt Tolerance by Degrading the Canonical Salt‐Responsive Protein OsMBL1
inferred← citeshttps://doi.org/10.1111/pce.14835openalex-snapshot
The rice LATE ELONGATED HYPOCOTYL enhances salt tolerance by regulating Na+/K+ homeostasis and ABA signalling
inferred← citeshttps://doi.org/10.1111/pce.15544openalex-snapshot
Molecular Insights Into Salt Stress Adaptation in Plants
inferred← citeshttps://doi.org/10.1111/ppl.13481openalex-snapshot
Oryza sativa , C4HC3 ‐type really interesting new gene (RING), OsRFPv6 , is a positive regulator in response to salt stress by regulating Na+absorption
inferred← citeshttps://doi.org/10.1111/ppl.14075openalex-snapshot
Overexpression of a C3HC4 ‐type E3 ‐ubiquitin ligase contributes to salinity tolerance by modulating Na+ homeostasis in rice
inferred← citeshttps://doi.org/10.1111/ppl.70327openalex-snapshot
Rice RING E3 Ligase OsRFP45 Negatively Regulates Salt Tolerance by Modulating Na+/K+ Transporter Genes
inferred← citeshttps://doi.org/10.1111/tpj.70595openalex-snapshot
Bax inhibitor‐1 like ( CmoBI1L ) functions in pumpkin salt tolerance by stabilizing Na + transporters and modulating the transcription of peroxidases
inferred← citeshttps://doi.org/10.1111/tpj.70598openalex-snapshot
The RING ‐finger E3 ubiquitin ligase SlMIEL1 interacts with SlNAC35 to regulate JA biosynthesis and mediate saline‐alkali stress responses in tomato
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/s12870-023-04659-0openalex-snapshot
Genome-wide analysis of long noncoding RNAs in response to salt stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.1186/s12870-024-05156-8openalex-snapshot
GhVIM28, a negative regulator identified from VIM family genes, positively responds to salt stress in cotton
inferred← citeshttps://doi.org/10.1186/s12870-025-06343-xopenalex-snapshot
Genome-wide analysis of CHYR gene family and BnA03.CHYR.1 functional verification under salt stress in Brassica napus L.
inferred← citeshttps://doi.org/10.15252/embj.2020105086openalex-snapshot
Clock component OsPRR73 positively regulates rice salt tolerance by modulating OsHKT2;1‐mediated sodium homeostasis
inferred← citeshttps://doi.org/10.21203/rs.3.rs-11124777/v1openalex-snapshot
The RING-type E3 ubiquitin ligase BnaC02.RZFP confers salt tolerance via a 26S proteasome-dependent pathway in Brassica napus
inferred← citeshttps://doi.org/10.3389/fpls.2021.640193openalex-snapshot
Modulation of Abiotic Stress Responses in Rice by E3-Ubiquitin Ligases: A Promising Way to Develop Stress-Tolerant Crops
inferred← citeshttps://doi.org/10.3389/fpls.2021.797940openalex-snapshot
The Rice Abscisic Acid-Responsive RING Finger E3 Ligase OsRF1 Targets OsPP2C09 for Degradation and Confers Drought and Salinity Tolerance in Rice
inferred← citeshttps://doi.org/10.3389/fpls.2022.1083960openalex-snapshot
The intertwining of Zn-finger motifs and abiotic stress tolerance in plants: Current status and future prospects
inferred← citeshttps://doi.org/10.3389/fpls.2022.877011openalex-snapshot
RING Zinc Finger Proteins in Plant Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2022.912637openalex-snapshot
Combining GWAS, Genome-Wide Domestication and a Transcriptomic Analysis Reveals the Loci and Natural Alleles of Salt Tolerance in Rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.3389/fpls.2023.1226297openalex-snapshot
A meta-QTL analysis highlights genomic hotspots associated with phosphorus use efficiency in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.3390/biom11081145openalex-snapshot
Evolutionary and Characteristic Analysis of RING-DUF1117 E3 Ubiquitin Ligase Genes in Gossypium Discerning the Role of GhRDUF4D in Verticillium dahliae Resistance
inferred← citeshttps://doi.org/10.3390/cells11050890openalex-snapshot
Plant E3 Ligases and Their Role in Abiotic Stress Response
inferred← citeshttps://doi.org/10.3390/genes10120973openalex-snapshot
Research Progress on Plant RING-Finger Proteins
inferred← citeshttps://doi.org/10.3390/genes14091771openalex-snapshot
Using High-Throughput Phenotyping Analysis to Decipher the Phenotypic Components and Genetic Architecture of Maize Seedling Salt Tolerance
inferred← citeshttps://doi.org/10.3390/ijms242115737openalex-snapshot
A High-K+ Affinity Transporter (HKT) from Actinidia valvata Is Involved in Salt Tolerance in Kiwifruit
inferred← citeshttps://doi.org/10.3390/microorganisms10010015openalex-snapshot
Transcriptome Analysis of Arbuscular Mycorrhizal Casuarina glauca in Damage Mitigation of Roots on NaCl Stress
inferred← citeshttps://doi.org/10.3390/plants13111468openalex-snapshot
The Role of Plant Ubiquitin-like Modifiers in the Formation of Salt Stress Tolerance
inferred← citeshttps://doi.org/10.3390/plants13152047openalex-snapshot
The RING-Type E3 Ubiquitin Ligase Gene GhDIRP1 Negatively Regulates Verticillium dahliae Resistance in Cotton (Gossypium hirsutum)
inferred← citeshttps://doi.org/10.3390/plants14152404openalex-snapshot
Genome-Wide Identification, Characterization, and Comparison of C3HC4 Family Genes in Salt Tolerance Between Barley and Rice
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.24819618openalex-snapshot
Additional file 1 of Genome-wide analysis of long noncoding RNAs in response to salt stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.6084/m9.figshare.24820091openalex-snapshot
Additional file 2 of Genome-wide analysis of long noncoding RNAs in response to salt stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.6084/m9.figshare.25876169openalex-snapshot
Additional file 1 of GhVIM28, a negative regulator identified from VIM family genes, positively responds to salt stress in cotton
inferred← citeshttps://doi.org/10.6084/m9.figshare.25876282openalex-snapshot
Additional file 2 of GhVIM28, a negative regulator identified from VIM family genes, positively responds to salt stress in cotton
inferred← citeshttps://doi.org/10.6084/m9.figshare.26654395openalex-snapshot
Additional file 3 of Genome-wide analysis of long noncoding RNAs in response to salt stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26654398openalex-snapshot
Additional file 4 of Genome-wide analysis of long noncoding RNAs in response to salt stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26654401openalex-snapshot
Additional file 5 of Genome-wide analysis of long noncoding RNAs in response to salt stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26654404openalex-snapshot
Additional file 6 of Genome-wide analysis of long noncoding RNAs in response to salt stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26654407openalex-snapshot
Additional file 7 of Genome-wide analysis of long noncoding RNAs in response to salt stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26654410openalex-snapshot
Additional file 8 of Genome-wide analysis of long noncoding RNAs in response to salt stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26654413openalex-snapshot
Additional file 9 of Genome-wide analysis of long noncoding RNAs in response to salt stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26654416openalex-snapshot
Additional file 10 of Genome-wide analysis of long noncoding RNAs in response to salt stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26654419openalex-snapshot
Additional file 11 of Genome-wide analysis of long noncoding RNAs in response to salt stress in Nicotiana tabacum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26723166openalex-snapshot
Additional file 3 of GhVIM28, a negative regulator identified from VIM family genes, positively responds to salt stress in cotton
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