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Effect of salt stress on genes encoding translation-associated proteins inArabidopsis thaliana

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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/pmic.200401282openalex-snapshot
Identification of Arabidopsis salt and osmotic stress responsive proteins using two‐dimensional difference gel electrophoresis and mass spectrometry
inferredcites →https://doi.org/10.1007/0-387-29362-0_23openalex-snapshot
limma: Linear Models for Microarray Data
inferredcites →https://doi.org/10.1007/s11738-011-0809-6openalex-snapshot
Transcript profiling during salt stress of young cotton (Gossypium hirsutum) seedlings via Solexa sequencing
inferredcites →https://doi.org/10.1016/0377-0427(87)90125-7openalex-snapshot
Silhouettes: A graphical aid to the interpretation and validation of cluster analysis
inferredcites →https://doi.org/10.1016/j.bbamcr.2009.10.009openalex-snapshot
Driving ribosome assembly
inferredcites →https://doi.org/10.1016/j.bbrc.2004.05.192openalex-snapshot
A pea chloroplast translation elongation factor that is regulated by abiotic factors
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.gene.2004.01.008openalex-snapshot
An improved prediction of chloroplast proteins reveals diversities and commonalities in the chloroplast proteomes of Arabidopsis and rice
inferredcites →https://doi.org/10.1016/j.jmva.2006.11.013openalex-snapshot
Comparing clusterings—an information based distance
inferredcites →https://doi.org/10.1016/j.jphotobiol.2011.02.016openalex-snapshot
Analysis of salt stress induced changes in Photosystem II heterogeneity by prompt fluorescence and delayed fluorescence in wheat (Triticum aestivum) leaves
inferredcites →https://doi.org/10.1016/j.jprot.2011.02.006openalex-snapshot
Plant proteome changes under abiotic stress — Contribution of proteomics studies to understanding plant stress response
inferredcites →https://doi.org/10.1016/j.pbi.2006.05.014openalex-snapshot
Crosstalk between abiotic and biotic stress responses: a current view from the points of convergence in the stress signaling networks
inferredcites →https://doi.org/10.1016/j.plantsci.2004.03.004openalex-snapshot
The biochemical reaction of maize (Zea mays L.) to salt stress is characterized by a mitigation of symptoms and not by a specific adaptation
inferredcites →https://doi.org/10.1016/s0378-1119(03)00629-2openalex-snapshot
Ribosome assembly in eukaryotes
inferredcites →https://doi.org/10.1016/s0968-0004(99)01460-7openalex-snapshot
The economics of ribosome biosynthesis in yeast
inferredcites →https://doi.org/10.1021/pr100034fopenalex-snapshot
Comparative Proteomics of Salt Tolerance in Arabidopsis thaliana and Thellungiella halophila
inferredcites →https://doi.org/10.1038/nrm1333openalex-snapshot
Protein import into chloroplasts
inferredcites →https://doi.org/10.1038/sj.emboj.7601472openalex-snapshot
ATAB2 is a novel factor in the signalling pathway of light‐controlled synthesis of photosystem proteins
inferredcites →https://doi.org/10.1042/bj20071641openalex-snapshot
Insights into the substrate specificity of plant peptide deformylase, an essential enzyme with potential for the development of novel biotechnology applications in agriculture
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01076.xopenalex-snapshot
Knock‐out of the plastid ribosomal protein L11 in Arabidopsis: effects on mRNA translation and photosynthesis
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01173.xopenalex-snapshot
Sites and homeostatic control of auxin biosynthesis in Arabidopsis during vegetative growth
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01719.xopenalex-snapshot
The translation initiation factor eIF1A is an important determinant in the tolerance to NaCl stress in yeast and plants
inferredcites →https://doi.org/10.1073/pnas.0504682102openalex-snapshot
Dual targeting is the rule for organellar aminoacyl-tRNA synthetases in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/aob/mcn125openalex-snapshot
Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell
inferredcites →https://doi.org/10.1093/bioinformatics/btp578openalex-snapshot
HTqPCR: high-throughput analysis and visualization of quantitative real-time PCR data in R
inferredcites →https://doi.org/10.1093/emboj/cdg007openalex-snapshot
Control of protein life‐span by N‐terminal methionine excision
inferredcites →https://doi.org/10.1093/jxb/erl164openalex-snapshot
Gene networks involved in drought stress response and tolerance
inferredcites →https://doi.org/10.1093/pcp/pcn121openalex-snapshot
Rice Peptide Deformylase PDF1B is Crucial for Development of Chloroplasts
inferredcites →https://doi.org/10.1104/pp.104.039909openalex-snapshot
Comparative Genomics in Salt Tolerance between Arabidopsis and Arabidopsis-Related Halophyte Salt Cress Using Arabidopsis Microarray
inferredcites →https://doi.org/10.1104/pp.110.164152openalex-snapshot
Linking the Salt Transcriptome with Physiological Responses of a Salt-Resistant Populus Species as a Strategy to Identify Genes Important for Stress Acclimation
inferredcites →https://doi.org/10.1104/pp.127.1.97openalex-snapshot
Eukaryotic Peptide Deformylases. Nuclear-Encoded and Chloroplast-Targeted Enzymes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.060392openalex-snapshot
Rpl33, a Nonessential Plastid-Encoded Ribosomal Protein in Tobacco, Is Required under Cold Stress Conditions
inferredcites →https://doi.org/10.1105/tpc.13.4.889openalex-snapshot
Gene Expression Profiles during the Initial Phase of Salt Stress in Rice
inferredcites →https://doi.org/10.1109/tassp.1975.1162641openalex-snapshot
Minimum prediction residual principle applied to speech recognition
inferredcites →https://doi.org/10.1109/tassp.1978.1163055openalex-snapshot
Dynamic programming algorithm optimization for spoken word recognition
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02575.xopenalex-snapshot
AtNAC2, a transcription factor downstream of ethylene and auxin signaling pathways, is involved in salt stress response and lateral root development
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02580.xopenalex-snapshot
Requirement of aminoacyl‐tRNA synthetases for gametogenesis and embryo development in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03602.xopenalex-snapshot
Functional gene‐mining for salt‐tolerance genes with the power of Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04393.xopenalex-snapshot
APUM23, a nucleolar Puf domain protein, is involved in pre-ribosomal RNA processing and normal growth patterning in Arabidopsis
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092911openalex-snapshot
Mechanisms of Salinity Tolerance
inferredcites →https://doi.org/10.1186/1471-2105-12-292openalex-snapshot
Unraveling gene regulatory networks from time-resolved gene expression data -- a measures comparison study
inferredcites →https://doi.org/10.1186/gb-2002-3-7-research0034openalex-snapshot
Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes
inferredcites →https://doi.org/10.1242/dev.016469openalex-snapshot
ThreePIGGYBACKgenes that specifically influence leaf patterning encode ribosomal proteins
inferredcites →https://doi.org/10.1371/journal.pone.0028058openalex-snapshot
Transcriptional Downregulation of Rice rpL32 Gene under Abiotic Stress Is Associated with Removal of Transcription Factors within the Promoter Region
inferredcites →https://doi.org/10.18637/jss.v031.i07openalex-snapshot
Computing and Visualizing Dynamic Time Warping Alignments inR: ThedtwPackage

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.4812893openalex-extracted
Transcriptional Profiling and Proteomic Validation Revealed Higher Boron Tolerance in Arabidopsis Thaliana Exposed to Salt Pre-Treatment
inferred← citeshttps://doi.org/10.1007/978-3-032-24001-9_12openalex-snapshot
Salinity Stress Affecting Organelles Responses & Modified Gene Expression in Plants: An Assessment
inferred← citeshttps://doi.org/10.1007/s00299-016-1986-yopenalex-snapshot
Transcriptome analysis reveals translational regulation in barley microspore-derived embryogenic callus under salt stress
inferred← citeshttps://doi.org/10.1007/s00299-024-03237-4openalex-snapshot
Comparative proteomic and metabolomic analyses reveal stress responses of hemp to salinity
inferred← citeshttps://doi.org/10.1007/s00343-022-2130-1openalex-snapshot
Identification of novel salt stress-responsive microRNAs through sequencing and bioinformatic analysis in a unique halophilic Dunaliella salina strain
inferred← citeshttps://doi.org/10.1007/s00425-025-04665-6openalex-snapshot
Implication of ribosomal protein in abiotic and biotic stress
inferred← citeshttps://doi.org/10.1007/s10142-016-0507-yopenalex-snapshot
Comparative transcriptomics of rice plants under cold, iron, and salt stresses
inferred← citeshttps://doi.org/10.1007/s10811-018-1410-9openalex-snapshot
Alleviation of NaCl toxicity in the cyanobacterium Synechococcus sp. PCC 7942 by exogenous calcium supplementation
inferred← citeshttps://doi.org/10.1007/s11103-021-01167-3openalex-snapshot
Pseudocrossidium replicatum (Taylor) R.H. Zander is a fully desiccation-tolerant moss that expresses an inducible molecular mechanism in response to severe abiotic stress
inferred← citeshttps://doi.org/10.1007/s11103-025-01643-0openalex-snapshot
Single-cell transcriptional profiling in Arabidopsis root exposed to boron toxicity at seedling stages
inferred← citeshttps://doi.org/10.1007/s42976-026-00815-yopenalex-snapshot
Radiometric analysis and the effects of NaCl–MgO nanoparticle interactions and gamma irradiation on stress-responsive genes in Triticale (Triticale x Secale) callus
inferred← citeshttps://doi.org/10.1016/j.aquatox.2021.105970openalex-snapshot
RNA-seq analyses of Marine Medaka (Oryzias melastigma) reveals salinity responsive transcriptomes in the gills and livers
inferred← citeshttps://doi.org/10.1016/j.bbapap.2015.11.002openalex-snapshot
The intriguing realm of protein biogenesis: Facing the green co-translational protein maturation networks
inferred← citeshttps://doi.org/10.1016/j.cbd.2019.100612openalex-snapshot
Transcriptome profiling of the low-salinity stress responses in the gills of the juvenile Pseudopleuronectes yokohamae
inferred← citeshttps://doi.org/10.1016/j.gene.2021.145670openalex-snapshot
Constitutive expression of Ribosomal Protein L6 modulates salt tolerance in rice transgenic plants
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2016.11.088openalex-snapshot
Artemin protects cells and proteins against oxidative and salt stress
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.147778openalex-snapshot
Whole genome sequencing reveals the role of the ribosome protein complex in salt stress in Bacillus subtilis.
inferred← citeshttps://doi.org/10.1016/j.jprot.2018.11.015openalex-snapshot
A resistant cowpea (Vigna unguiculata [L.] Walp.) genotype became susceptible to cowpea severe mosaic virus (CPSMV) after exposure to salt stress
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113108openalex-snapshot
VviAHA10, a tonoplast P3A-type ATPase from Vitis vinifera, reveals a functional link between vacuolar flavonoid accumulation and abiotic stress responses
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.07.029openalex-snapshot
Unveiling the functions of plastid ribosomal proteins in plant development and abiotic stress tolerance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109453openalex-snapshot
How abscisic acid collaborates in Brassica napus responses to salt and drought stress: An in silico approach
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2015.10.008openalex-snapshot
Metabolite and transcriptomic analysis reveals metabolic and regulatory features associated with Powell orange pulp deterioration during room temperature and cold storage
inferred← citeshttps://doi.org/10.1016/j.sajb.2025.03.011openalex-snapshot
Transcriptional profiling and proteomic validation revealed higher boron tolerance in Arabidopsis thaliana exposed to salt pre-treatment
inferred← citeshttps://doi.org/10.1016/j.sjbs.2021.03.035openalex-snapshot
Molecular characterization and expression analysis of ribosomal L18/L5e gene in Pennisetum glaucum (L.) R. Br
inferred← citeshttps://doi.org/10.1016/j.tplants.2015.11.004openalex-snapshot
Redox Regulation of Cytosolic Translation in Plants
inferred← citeshttps://doi.org/10.1038/s41598-020-78118-3openalex-snapshot
De-novo transcriptome analysis unveils differentially expressed genes regulating drought and salt stress response in Panicum sumatrense
inferred← citeshttps://doi.org/10.1071/fp23002openalex-snapshot
Meta-analysis of transcriptomic profiles in Dunaliella tertiolecta reveals molecular pathway responses to different abiotic stresses
inferred← citeshttps://doi.org/10.1074/jbc.m117.799866openalex-snapshot
Transient alkalinization of the leaf apoplast stiffens the cell wall during onset of chloride salinity in corn leaves
inferred← citeshttps://doi.org/10.1080/07391102.2021.1894980openalex-snapshot
Evolution and identification of DREB transcription factors in the wheat genome: modeling, docking and simulation of DREB proteins associated with salt stress
inferred← citeshttps://doi.org/10.1093/bioinformatics/btab829openalex-snapshot
EnGRaiN: a supervised ensemble learning method for recovery of large-scale gene regulatory networks
inferred← citeshttps://doi.org/10.1101/2020.05.31.126102openalex-snapshot
Ribosomal Protein Large subunit RPL6 modulates salt tolerance in rice
inferred← citeshttps://doi.org/10.1101/2020.06.07.139238openalex-snapshot
Temporal transcriptome profiling of Microchloropsis gaditana CCMP526 under hyper-saline conditions
inferred← citeshttps://doi.org/10.1101/2022.04.11.487921openalex-snapshot
Trascriptome meta-analysis of microalga Dunaliella tertiolecta under stress condition
inferred← citeshttps://doi.org/10.1104/pp.15.00605openalex-snapshot
The Arabidopsis transcription factor MYB112 promotes anthocyanin formation during salinity and under high light stress
inferred← citeshttps://doi.org/10.1111/jipb.12151openalex-snapshot
A step‐by‐step protocol for formaldehyde‐assisted isolation of regulatory elements from Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/nph.13761openalex-snapshot
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