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Oryza sativa , C4HC3 ‐type really interesting new gene (RING), OsRFPv6 , is a positive regulator in response to salt stress by regulating Na+absorption
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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/abio.2000.4696openalex-snapshot
A Critical Evaluation of the Effect of Sorbitol on the Ferric–Xylenol Orange Hydroperoxide Assay
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/10.1007/12892.2005-8276openalex-snapshot
Journal of Crop Science and Biotechnology
inferredcites →https://doi.org/10.1007/978-3-540-72954-9_9openalex-snapshot
Oxidative Stress and Salt Tolerance in Plants
inferredcites →https://doi.org/10.1007/bf03325836openalex-snapshot
Effect of salinity on chlorophyll concentration, leaf area, yield and yield components of rice genotypes grown under saline environment
inferredcites →https://doi.org/10.1007/s00425-004-1437-9openalex-snapshot
Rice K+ uptake channel OsAKT1 is sensitive to salt stress
inferredcites →https://doi.org/10.1007/s00425-011-1403-2openalex-snapshot
Physiological mechanisms underlying OsNAC5-dependent tolerance of rice plants to abiotic stress
inferredcites →https://doi.org/10.1007/s11103-019-00835-9openalex-snapshot
Oryza sativa heat-induced RING finger protein 1 (OsHIRP1) positively regulates plant response to heat stress
inferredcites →https://doi.org/10.1007/s11103-020-01084-xopenalex-snapshot
E3 ligase, the Oryza sativa salt-induced RING finger protein 4 (OsSIRP4), negatively regulates salt stress responses via degradation of the OsPEX11-1 protein
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/s12892-017-0104-0openalex-snapshot
Functional diversity of RING E3 ligases of major cereal crops in response to abiotic stresses
inferredcites →https://doi.org/10.1016/j.bbrc.2006.04.140openalex-snapshot
Validation of housekeeping genes as internal control for studying gene expression in rice by quantitative real-time PCR
inferredcites →https://doi.org/10.1023/a:1020763218045openalex-snapshot
Salinity stress-tolerant and -sensitive rice (Oryza sativa L.) regulate AKT1-type potassium channel transcripts differently
inferredcites →https://doi.org/10.1038/186124d0openalex-snapshot
Biochemical and Biophysical Research Communications
inferredcites →https://doi.org/10.1038/nature07523openalex-snapshot
Altered circadian rhythms regulate growth vigour in hybrids and allopolyploids
inferredcites →https://doi.org/10.1038/s41598-017-09708-xopenalex-snapshot
2,4-D attenuates salinity-induced toxicity by mediating anatomical changes, antioxidant capacity and cation transporters in the roots of rice cultivars
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/10.1073/pnas.1116437108openalex-snapshot
Global food demand and the sustainable intensification of agriculture
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/pcp/pch014openalex-snapshot
Function, Intracellular Localization and the Importance in Salt Tolerance of a Vacuolar Na+/H+ Antiporter from Rice
inferredcites →https://doi.org/10.1104/pp.106.092635openalex-snapshot
Conservation of the Salt Overly Sensitive Pathway in Rice
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.127.4.1773openalex-snapshot
Role of Root Hairs and Lateral Roots in Silicon Uptake by Rice
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/10.1111/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.1469-8137.2005.01487.xopenalex-snapshot
Genes and salt tolerance: bringing them together
inferredcites →https://doi.org/10.1111/pce.12586openalex-snapshot
The potassium transporter O s HAK 21 functions in the maintenance of ion homeostasis and tolerance to salt stress in rice
inferredcites →https://doi.org/10.1111/pce.13619openalex-snapshot
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
inferredcites →https://doi.org/10.1111/tpj.13595openalex-snapshot
OsHKT1;5 mediates Na + exclusion in the vasculature to protect leaf blades and reproductive tissues from salt toxicity in rice
inferredcites →https://doi.org/10.1126/science.42.1074.161openalex-snapshot
The Proceedings of the National Academy of Sciences
inferredcites →https://doi.org/10.1146/annurev.biochem.78.101807.093809openalex-snapshot
RING Domain E3 Ubiquitin Ligases
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/s12870-018-1586-9openalex-snapshot
Na+/K+ Balance and Transport Regulatory Mechanisms in Weedy and Cultivated Rice (Oryza sativa L.) Under Salt Stress
inferredcites →https://doi.org/10.1271/bbb.70216openalex-snapshot
Improved Gateway Binary Vectors: High-Performance Vectors for Creation of Fusion Constructs in Transgenic Analysis of Plants
inferredcites →https://doi.org/10.1371/journal.pone.0031101openalex-snapshot
Isolation and Characterization of Maize PMP3 Genes Involved in Salt Stress Tolerance
inferredcites →https://doi.org/10.17221/71/2010-pseopenalex-snapshot
The effect of salinity stress on ions and soluble sugars distribution in leaves, leaf sheaths and roots of rice (Oryza sativa L.) seedlings
inferredcites →https://doi.org/10.17582/journal.pjar/2019/32.1.140.151openalex-snapshot
Exogenous Application of Proline Improved Salt Tolerance in Rice through Modulation of Antioxidant Activities
inferredcites →https://doi.org/10.2135/cropsci2005.0437openalex-snapshot
Understanding and Improving Salt Tolerance in Plants
inferredcites →https://doi.org/10.21769/bioprotoc.263openalex-snapshot
Detection of Hydrogen Peroxide by DAB Staining in Arabidopsis Leaves
inferredcites →https://doi.org/10.3389/fphys.2017.00509openalex-snapshot
The Role of Na+ and K+ Transporters in Salt Stress Adaptation in Glycophytes
inferredcites →https://doi.org/10.3389/fpls.2018.01135openalex-snapshot
High Performance of Photosynthesis and Osmotic Adjustment Are Associated With Salt Tolerance Ability in Rice Carrying Drought Tolerance QTL: Physiological and Co-expression Network Analysis
inferredcites →https://doi.org/10.3390/ijmsopenalex-snapshot
International Journal of Molecular Sciences
inferredcites →https://doi.org/10.3390/ijms20051059openalex-snapshot
Role and Functional Differences of HKT1-Type Transporters in Plants under Salt Stress
inferredcites →https://doi.org/10.3390/ijms21020454openalex-snapshot
Overexpression of Rice Expansin7 (Osexpa7) Confers Enhanced Tolerance to Salt Stress in Rice
inferredcites →https://doi.org/10.4161/psb.21949openalex-snapshot
Role of proline under changing environments
inferredcites →https://doi.org/10.5511/plantbiotechnology.25.241openalex-snapshot
Expression of OsHAK genes encoding potassium ion transporters in rice
inferredcites →https://doi.org/10.5772/63007openalex-snapshot
Advances in International Rice Research
inferredcites →https://doi.org/10.5772/67098openalex-snapshot
Salt Stress Tolerance in Rice: Emerging Role of Exogenous Phytoprotectants
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/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/10.1016/j.algal.2024.103677openalex-snapshot
Scenedesmus acuminatus as a potential phycoremediator: Enrichment and detoxification of cadmium/lead
inferred← citeshttps://doi.org/10.1016/j.cj.2025.01.013openalex-snapshot
ZmZFP2 encoding a C4HC3-type RING zinc finger protein regulates kernel size and weight in maize
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.envexpbot.2023.105273openalex-snapshot
Molecular dissection of a rice plant with mutation of the leucine carboxyl methyl transferase gene
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.jia.2025.04.031openalex-snapshot
Dissecting the genetic architecture of microelement accumulation in wheat grains through genome-wide association study
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112808openalex-snapshot
Identification of transcriptional regulators interacting with PEPC genes and characterization of bHLH49 in Suaeda aralocaspica
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.12.004openalex-snapshot
RING E3 ubiquitin ligase TaSADR1 negatively regulates drought resistance in transgenic Arabidopsis
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.2024.108928openalex-snapshot
Rab7 GTPase-Mediated stress signaling enhances salinity tolerance in AlRabring7 tobacco transgenics by modulating physio-biochemical parameters
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.scienta.2023.111868openalex-snapshot
Overexpression of mango MiRZFP34 confers early flowering and stress tolerance in transgenic Arabidopsis
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/10.1111/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.14407openalex-snapshot
Deciphering the mechanism of E3 ubiquitin ligases in plant responses to abiotic and biotic stresses and perspectives on PROTACs for crop resistance
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.14565openalex-snapshot
Mutation of a RING E3 ligase, OsDIRH2, enhances drought tolerance in rice with low stomata density
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.70491openalex-snapshot
Rice E3 ligase OsRFPH2 ‐16 acts as a negative regulator to mediate the degradation of OsPIP1 ;1 under salt stress
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.2022.877011openalex-snapshot
RING Zinc Finger Proteins in Plant Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2023.1144486openalex-snapshot
Identification and validation of two major QTLs for spikelet number per spike in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.3390/j7010006openalex-snapshot
Self-Defense Mechanism in Rice to Salinity: Proline
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