On the public citation graph
Molecular dissection of Oryza sativa salt‐induced RING Finger Protein 1 ( OsSIRP1 ): possible involvement in the sensitivity response to salinity stress
0 signed · 83 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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/10.1007/978-4-431-55251-2_14openalex-snapshot
RNA-Seq Data Analysis for Studying Abiotic Stress in Horticultural Plants
inferredcites →https://doi.org/10.1007/s00425-015-2242-3openalex-snapshot
Rice RING E3 ligase may negatively regulate gamma-ray response to mediate the degradation of photosynthesis-related proteins
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/s11103-014-0190-0openalex-snapshot
Positive regulation of rice RING E3 ligase OsHIR1 in arsenic and cadmium uptakes
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/10.1016/0092-8674(91)90229-ropenalex-snapshot
A novel gysteine-rich sequence motif
inferredcites →https://doi.org/10.1016/j.ecoenv.2004.06.010openalex-snapshot
Salt tolerance and salinity effects on plants: a review
inferredcites →https://doi.org/10.1016/j.envint.2009.02.006openalex-snapshot
The toxicology of climate change: Environmental contaminants in a warming world
inferredcites →https://doi.org/10.1016/j.febslet.2013.06.038openalex-snapshot
Suppression of Arabidopsis RING E3 ubiquitin ligase AtATL78 increases tolerance to cold stress and decreases tolerance to drought stress
inferredcites →https://doi.org/10.1016/j.gene.2014.09.018openalex-snapshot
Overexpression of the OsChI1 gene, encoding a putative laccase precursor, increases tolerance to drought and salinity stress in transgenic Arabidopsis
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.plantsci.2009.01.016openalex-snapshot
Genome-wide survey and expression profiling of heat shock proteins and heat shock factors revealed overlapped and stress specific response under abiotic stresses in rice
inferredcites →https://doi.org/10.1016/s0076-6879(07)28024-3openalex-snapshot
Mechanisms of High Salinity Tolerance in Plants
inferredcites →https://doi.org/10.1038/nrm2688openalex-snapshot
The ubiquitin–26S proteasome system at the nexus of plant biology
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00626.xopenalex-snapshot
Arabidopsis thaliana AtHAL3: a flavoprotein related to salt and osmotic tolerance and plant growth
inferredcites →https://doi.org/10.1073/pnas.0602874103openalex-snapshot
The negative regulator of plant cold responses, HOS1, is a RING E3 ligase that mediates the ubiquitination and degradation of ICE1
inferredcites →https://doi.org/10.1093/bioinformatics/btm404openalex-snapshot
Clustal W and Clustal X version 2.0
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/dnares/dst042openalex-snapshot
Deep Transcriptome Sequencing of Wild Halophyte Rice, Porteresia coarctata, Provides Novel Insights into the Salinity and Submergence Tolerance Factors
inferredcites →https://doi.org/10.1093/jxb/err310openalex-snapshot
Abiotic stress tolerance mediated by protein ubiquitination
inferredcites →https://doi.org/10.1093/jxb/ert143openalex-snapshot
The rice RING finger E3 ligase, OsHCI1, drives nuclear export of multiple substrate proteins and its heterogeneous overexpression enhances acquired thermotolerance
inferredcites →https://doi.org/10.1093/pcp/pcr107openalex-snapshot
Membrane Transport, Sensing and Signaling in Plant Adaptation to Environmental Stress
inferredcites →https://doi.org/10.1104/pp.103.020800openalex-snapshot
AtCHIP, a U-Box-Containing E3 Ubiquitin Ligase, Plays a Critical Role in Temperature Stress Tolerance in 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.104.900188openalex-snapshot
Abiotic Stress in Rice. An “Omic” Approach
inferredcites →https://doi.org/10.1104/pp.105.067983openalex-snapshot
Genome Analysis and Functional Characterization of the E2 and RING-Type E3 Ligase Ubiquitination Enzymes of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.110.154773openalex-snapshot
Root-Specific Expression of OsNAC10 Improves Drought Tolerance and Grain Yield in Rice under Field Drought Conditions
inferredcites →https://doi.org/10.1105/tpc.106.048488openalex-snapshot
SDIR1 Is a RING Finger E3 Ligase That Positively Regulates Stress-Responsive Abscisic Acid Signaling inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.121913openalex-snapshot
Machine Learning–Based Differential Network Analysis: A Study of Stress-Responsive Transcriptomes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.134163openalex-snapshot
The RING Finger Ubiquitin E3 Ligase SDIR1 Targets SDIR1-INTERACTING PROTEIN1 for Degradation to Modulate the Salt Stress Response and ABA Signaling in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02730.xopenalex-snapshot
AtCHIP functions as an E3 ubiquitin ligase of protein phosphatase 2A subunits and alters plant response to abscisic acid treatment
inferredcites →https://doi.org/10.1111/j.1399-3054.1992.tb04710.xopenalex-snapshot
Supplemental manganese improves the relative growth, net assimilation and photosynthetic rates of salt‐stressed barley
inferredcites →https://doi.org/10.1111/pbi.12270openalex-snapshot
Overexpression of a NF ‐ YC transcription factor from bermudagrass confers tolerance to drought and salinity in transgenic rice
inferredcites →https://doi.org/10.1146/annurev.arplant.51.1.463openalex-snapshot
P LANT C ELLULAR AND M OLECULAR R ESPONSES TO H IGH S ALINITY
inferredcites →https://doi.org/10.1146/annurev.arplant.53.091401.143329openalex-snapshot
S ALT AND D ROUGHT S TRESS S IGNAL T RANSDUCTION IN P LANTS
inferredcites →https://doi.org/10.1146/annurev.arplant.55.031903.141801openalex-snapshot
THE UBIQUITIN 26S PROTEASOME PROTEOLYTIC PATHWAY
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/10.1385/1-59259-827-7:091openalex-snapshot
Floral Dip: Agrobacterium-Mediated Germ Line Transformation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s00344-023-11000-4openalex-snapshot
A Comprehensive Meta-analysis to Identify the Responsive Genes in Sorghum Under Salinity and Drought Stresses (Sorghum bicolor)
inferred← citeshttps://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)
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/s10142-024-01347-6openalex-snapshot
CRISPR/Cas9 targeted mutations of OsDSG1 gene enhanced salt tolerance in rice
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/s11103-020-00989-xopenalex-snapshot
Oryza sativa drought-, heat-, and salt-induced RING finger protein 1 (OsDHSRP1) negatively regulates abiotic stress-responsive gene expression
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/s12298-026-01790-8openalex-snapshot
Negative regulators that mitigate abiotic stress sensitivity of rice: insights and future perspectives
inferred← citeshttps://doi.org/10.1007/s12892-017-0104-0openalex-snapshot
Functional diversity of RING E3 ligases of major cereal crops in response to abiotic stresses
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2018.05.012openalex-snapshot
Role of the Ubiquitin Proteasome System in Plant Response to Abiotic Stress
inferred← citeshttps://doi.org/10.1016/j.cj.2024.11.011openalex-snapshot
WRKY10 and ABF1/2 bind to VQ8 to form an accelerator-brake module for the regulation of dark- and ABA-induced leaf senescence in rice
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.06.017openalex-snapshot
Role of salt-induced RING finger protein 3 (OsSIRP3), a negative regulator of salinity stress response by modulating the level of its target proteins
inferred← citeshttps://doi.org/10.1016/j.plaphy.2017.11.017openalex-snapshot
Overexpression of the maize E3 ubiquitin ligase gene ZmAIRP4 enhances drought stress tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.11.042openalex-snapshot
A potato RING-finger protein gene StRFP2 is involved in drought tolerance
inferred← citeshttps://doi.org/10.1016/j.rsci.2019.12.011openalex-snapshot
Effects of Space Flight on Expression of Key Proteins in Rice Leaves
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/10.1079/9781800623033.0007openalex-snapshot
Updates on Protein Post-Translational Modifications for Modulating Response to Salinity
inferred← citeshttps://doi.org/10.1093/jhered/esx067openalex-snapshot
Genetic Dissection of Seedling Stage Salinity Tolerance in Rice Using Introgression Lines of a Salt Tolerant Landrace Nona Bokra
inferred← citeshttps://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)
inferred← citeshttps://doi.org/10.1093/pcp/pcz133openalex-snapshot
Molecular Functions of Rice Cytosol-Localized RING Finger Protein 1 in Response to Salt and Drought and Comparative Analysis of Its Grass Orthologs
inferred← citeshttps://doi.org/10.1093/plphys/kiad530openalex-snapshot
Long noncoding RNA TRABA suppresses β-glucosidase-encoding BGLU24 to promote salt tolerance in cotton
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.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/pce.13633openalex-snapshot
The ubiquitin‐proteasome system in plant responses to environments
inferred← citeshttps://doi.org/10.1111/pce.14818openalex-snapshot
A pepper RING‐finger E3 ligase, CaFIRF1, negatively regulates the high‐salt stress response by modulating the stability of CaFAF1
inferred← citeshttps://doi.org/10.1111/ppl.12620openalex-snapshot
Phospholipases AtPLDζ1 and AtPLDζ2 function differently in hypoxia
inferred← citeshttps://doi.org/10.1111/ppl.12719openalex-snapshot
Genome‐wide analysis of Glycine soja ubiquitin (UBQ) genes and functional analysis ofGsUBQ10in response to alkaline stress
inferred← citeshttps://doi.org/10.1111/tpj.70746openalex-snapshot
The E3 ligase TaGW2L mediates the ubiquitination and degradation of TaHMT1 to negatively regulate salt tolerance in wheat
inferred← citeshttps://doi.org/10.1186/s12284-025-00763-xopenalex-snapshot
E3 Ubiquitin Ligase OsRFI2 Regulates Salinity Tolerance by Targeting Ascorbate Peroxidase OsAPX8 for its Degradation in Rice
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/10.1371/journal.pgen.1006332openalex-snapshot
PARAQUAT TOLERANCE3 Is an E3 Ligase That Switches off Activated Oxidative Response by Targeting Histone-Modifying PROTEIN METHYLTRANSFERASE4b
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/10.3390/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/genes9120594openalex-snapshot
Two-State Co-Expression Network Analysis to Identify Genes Related to Salt Tolerance in Thai Rice
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/10.5483/bmbrep.2017.50.8.128openalex-snapshot
RING E3 ligases: key regulatory elements are involved in abiotic stress responses in plants
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.