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Overexpression of a Malus baccata WRKY transcription factor gene (MbWRKY5) increases drought and salt tolerance in transgenic tobacco
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
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Rapid systemic accumulation of transcripts encoding a tobacco WRKY transcription factor upon wounding
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Role of DREB transcription factors in abiotic and biotic stress tolerance in plants
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A WRKY transcription factor participates in dehydration tolerance in Boea hygrometrica by binding to the W-box elements of the galactinol synthase (BhGolS1) promoter
inferredcites →https://doi.org/10.1007/s10725-017-0274-3openalex-snapshot
Isolation and functional analysis of MxCS3: a gene encoding a citrate synthase in Malus xiaojinensis, with functions in tolerance to iron stress and abnormal flower in transgenic Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s11103-004-2142-6openalex-snapshot
Targets of the WRKY53 transcription factor and its role during leaf senescence in Arabidopsis
inferredcites →https://doi.org/10.1007/s11103-012-9941-yopenalex-snapshot
OsWRKY30 is activated by MAP kinases to confer drought tolerance in rice
inferredcites →https://doi.org/10.1007/s11105-013-0639-3openalex-snapshot
Functional Analysis of a Novel Chrysanthemum WRKY Transcription Factor Gene Involved in Salt Tolerance
inferredcites →https://doi.org/10.1007/s11105-014-0735-zopenalex-snapshot
Isolation and Preliminary Functional Analysis of MxCS2: a Gene Encoding a Citrate Synthase in Malus xiaojinensis
inferredcites →https://doi.org/10.1007/s11240-012-0267-xopenalex-snapshot
Genetic transformation and genes for resistance to abiotic and biotic stresses in Citrus and its related genera
inferredcites →https://doi.org/10.1007/s12374-016-0577-3openalex-snapshot
Identification and expression analysis of WRKY transcription factor genes in response to fungal pathogen and hormone treatments in apple (Malus domestica)
inferredcites →https://doi.org/10.1007/s40415-015-0218-yopenalex-snapshot
Effect of salinity stress on chlorophyll, carotenoid content, and proline in Salicornia prostrata Pall. and Suaeda prostrata Pall. subsp. prostrata (Amaranthaceae)
inferredcites →https://doi.org/10.1016/0003-2697(71)90370-8openalex-snapshot
Superoxide dismutase: Improved assays and an assay applicable to acrylamide gels
inferredcites →https://doi.org/10.1016/0003-9861(83)90405-8openalex-snapshot
The effect of sucrose on the rate of de novo sucrose biosynthesis in leaf protoplasts from spinach wheat and barley
inferredcites →https://doi.org/10.1016/j.bbagrm.2011.09.002openalex-snapshot
The role of WRKY transcription factors in plant abiotic stresses
inferredcites →https://doi.org/10.1016/j.plaphy.2016.02.006openalex-snapshot
Genome-wide identification and characterization of WRKY transcriptional factor family in apple and analysis of their responses to waterlogging and drought stress
inferredcites →https://doi.org/10.1016/j.tplants.2010.02.006openalex-snapshot
WRKY transcription factors
inferredcites →https://doi.org/10.1016/s0168-9452(00)00352-6openalex-snapshot
Redox state and peroxidase system in sunflower plants exposed to ozone
inferredcites →https://doi.org/10.1016/s1360-1385(02)02312-9openalex-snapshot
Oxidative stress, antioxidants and stress tolerance
inferredcites →https://doi.org/10.1023/a:1014062714786openalex-snapshot
Cloning and characterization of a thermal hysteresis (antifreeze) protein with DNA-binding activity from winter bittersweet nightshade, Solanum dulcamara
inferredcites →https://doi.org/10.1023/a:1020780022549openalex-snapshot
Expression profiles of the Arabidopsis WRKY gene superfamily during plant defense response
inferredcites →https://doi.org/10.1038/415977aopenalex-snapshot
MAP kinase signalling cascade in Arabidopsis innate immunity
inferredcites →https://doi.org/10.1046/j.1365-3040.2001.00778.xopenalex-snapshot
The effect of drought and ultraviolet radiation on growth and stress markers in pea and wheat
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01364.xopenalex-snapshot
Molecular and biochemical mechanisms associated with dormancy and drought tolerance in the desert legume Retama raetam
inferredcites →https://doi.org/10.1074/jbc.m313350200openalex-snapshot
The Zinc Finger Protein Zat12 Is Required for Cytosolic Ascorbate Peroxidase 1 Expression during Oxidative Stress in Arabidopsis
inferredcites →https://doi.org/10.1080/17429145.2018.1447698openalex-snapshot
Isolation and characterization of MbWRKY2 gene involved in enhanced drought tolerance in transgenic tobacco
inferredcites →https://doi.org/10.1080/17429145.2018.1478994openalex-snapshot
Molecular cloning and functional analysis of MbWRKY3 involved in improved drought tolerance in transformed tobacco
inferredcites →https://doi.org/10.1093/aob/mcn178openalex-snapshot
The Iron-regulated Transporter, MbNRAMP1, Isolated from Malus baccata is Involved in Fe, Mn and Cd Trafficking
inferredcites →https://doi.org/10.1093/jxb/erh005openalex-snapshot
Molecular genetic perspectives on cross-talk and specificity in abiotic stress signalling in plants
inferredcites →https://doi.org/10.1093/mutage/gew034openalex-snapshot
Role of the antioxidant defence system and telomerase in arsenic-induced genomic instability
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078386openalex-snapshot
Enhanced Tolerance to Photooxidative Stress of Transgenic Nicotiana tabacum with High Chloroplastic Glutathione Reductase Activity
inferredcites →https://doi.org/10.1104/pp.103.034967openalex-snapshot
A Rice WRKY Gene Encodes a Transcriptional Repressor of the Gibberellin Signaling Pathway in Aleurone Cells
inferredcites →https://doi.org/10.1104/pp.109.152371openalex-snapshot
Mutations in the Hyperosmotic Stress-Responsive Mitochondrial BASIC AMINO ACID CARRIER2 Enhance Proline Accumulation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.114.247866openalex-snapshot
Mitochondrial Alternative Oxidase Maintains Respiration and Preserves Photosynthetic Capacity during Moderate Drought in Nicotiana tabacum
inferredcites →https://doi.org/10.1104/pp.81.1.301openalex-snapshot
Transformation of Tobacco, Tomato, Potato, and Arabidopsis thaliana Using a Binary Ti Vector System
inferredcites →https://doi.org/10.1105/tpc.001404openalex-snapshot
TRANSPARENT TESTA GLABRA2 , a Trichome and Seed Coat Development Gene of Arabidopsis, Encodes a WRKY Transcription Factor
inferredcites →https://doi.org/10.1111/j.1365-3040.2012.02480.xopenalex-snapshot
Wheat WRKY genes TaWRKY2 and TaWRKY19 regulate abiotic stress tolerance in transgenic Arabidopsis plants
inferredcites →https://doi.org/10.1111/j.1399-3054.1992.tb08764.xopenalex-snapshot
Water stress induced changes in concentrations of proline and total soluble sugars in nodulated alfalfa ( Medicago sativa ) plants
inferredcites →https://doi.org/10.1111/j.1469-8137.1996.tb01856.xopenalex-snapshot
Antioxidant responses to drought in sunflower and sorghum seedlings
inferredcites →https://doi.org/10.1111/j.1742-4658.2011.08056.xopenalex-snapshot
Cotton GhMPK2 is involved in multiple signaling pathways and mediates defense responses to pathogen infection and oxidative stress
inferredcites →https://doi.org/10.1111/tpj.12352openalex-snapshot
Os ACA 6 , a P‐type IIB Ca 2+ ATP ase promotes salinity and drought stress tolerance in tobacco by ROS scavenging and enhancing the expression of stress‐responsive genes
inferredcites →https://doi.org/10.5897/ajmr11.964openalex-snapshot
The effect of drought stress on leaf chlorophyll content and stress resistance in maize cultivars (Zea mays)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-3-032-01059-9_1openalex-snapshot
Decoding the Dynamic Epigenetic Interplay in Plant Transcriptional Regulation Under Salinity Stress
inferred← citeshttps://doi.org/10.1007/978-981-15-0690-1_2openalex-snapshot
Promising Transcription Factors for Salt and Drought Tolerance in Plants
inferred← citeshttps://doi.org/10.1007/s10142-022-00886-0openalex-snapshot
The roles of WRKY transcription factors in Malus spp. and Pyrus spp.
inferred← citeshttps://doi.org/10.1007/s10658-022-02497-8openalex-snapshot
Identification of genes responsible for stress resistance in fusarium oxysporum- inoculated flax seedlings using weighted gene co-expression network analysis
inferred← citeshttps://doi.org/10.1007/s11105-020-01216-zopenalex-snapshot
Picea wilsonii NAC Transcription Factor PwNAC30 Negatively Regulates Abiotic Stress Tolerance in Transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11105-020-01229-8openalex-snapshot
Regulation of Anthocyanin Accumulation by a Transcription Factor LcTT8 From Lonicera caerulea L.
inferred← citeshttps://doi.org/10.1007/s11627-020-10129-1openalex-snapshot
Overexpression of a Malus xiaojinensis WRKY transcription factor gene (MxWRKY55) increased iron and high salinity stress tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11627-021-10241-wopenalex-snapshot
Overexpression of MxWRKY53 increased iron and high salinity stress tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s13580-020-00239-5openalex-snapshot
Expression of SOD2 enhances tolerance to drought stress in roses
inferred← citeshttps://doi.org/10.1016/j.gene.2024.149176openalex-snapshot
The physiological and molecular mechanisms of WRKY transcription factors regulating drought tolerance: A review
inferred← citeshttps://doi.org/10.1016/j.indcrop.2021.114497openalex-snapshot
Overexpressing hemp salt stress induced transcription factor genes enhances tobacco salt tolerance
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153592openalex-snapshot
Dioscorea composita WRKY3 positively regulates salt-stress tolerance in transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111035openalex-snapshot
The transcription factor GsWRKY23 gene from wild soybean confers enhanced salt tolerance by regulating GsPER3 expression via ROS homeostasis
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2025.113673openalex-snapshot
Comparative transcriptomics unveils nitric oxide delaying leaf senescence in Chinese flowering cabbage by enhancing BrGATA21-mediated ROS scavenging
inferred← citeshttps://doi.org/10.1016/j.scienta.2019.109140openalex-snapshot
Physiological change and screening of differentially expressed genes of wild Chinese Vitis yeshanensis and American Vitis riparia in response to drought stress
inferred← citeshttps://doi.org/10.1071/fp22158openalex-snapshot
Tolerance and adaptation mechanism of Solanaceous crops under salinity stress
inferred← citeshttps://doi.org/10.1093/hr/uhad144openalex-snapshot
Insights into the molecular mechanisms underlying responses of apple trees to abiotic stresses
inferred← citeshttps://doi.org/10.1111/ppl.13268openalex-snapshot
Transcription factors as key molecular target to strengthen the drought stress tolerance in plants
inferred← citeshttps://doi.org/10.1186/s12866-021-02132-2openalex-snapshot
Interactional mechanisms of Paenibacillus polymyxa SC2 and pepper (Capsicum annuum L.) suggested by transcriptomics
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3675629/v1openalex-snapshot
Genome-wide identification of WRKY in cotton and the positive role of GhWRKY31 in response to salt and drought stress
inferred← citeshttps://doi.org/10.3389/fgene.2023.1274288openalex-snapshot
The role of WRKY transcription factors in exogenous potassium (K+) response to NaCl stress in Tamarix ramosissima
inferred← citeshttps://doi.org/10.3389/fpls.2022.1039329openalex-snapshot
WRKY transcription factors (TFs): Molecular switches to regulate drought, temperature, and salinity stresses in plants
inferred← citeshttps://doi.org/10.3389/fpls.2023.1238507openalex-snapshot
Plant salinity stress, sensing, and its mitigation through WRKY
inferred← citeshttps://doi.org/10.3390/agronomy10111634openalex-snapshot
Genome-Wide Identification and Analysis of the WRKY Gene Family in the Xerophytic Evergreen Ammopiptanthus nanus
inferred← citeshttps://doi.org/10.3390/agronomy13041051openalex-snapshot
FvMYB44, a Strawberry R2R3-MYB Transcription Factor, Improved Salt and Cold Stress Tolerance in Transgenic Arabidopsis
inferred← citeshttps://doi.org/10.3390/biology13090673openalex-snapshot
Regulatory Dynamics of Plant Hormones and Transcription Factors under Salt Stress
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/horticulturae12050602openalex-snapshot
Effects of Hot Water Treatment on Plant Performance, Bud Break, and Yield in Strawberry and Raspberry
inferred← citeshttps://doi.org/10.3390/ijms23148007openalex-snapshot
Overexpression of MxbHLH18 Increased Iron and High Salinity Stress Tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/ijms23179827openalex-snapshot
Isolation and Functional Analysis of MbCBF2, a Malus baccata (L.) Borkh CBF Transcription Factor Gene, with Functions in Tolerance to Cold and Salt Stress in Transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/ijms231810947openalex-snapshot
Molecular Pathways of WRKY Genes in Regulating Plant Salinity Tolerance
inferred← citeshttps://doi.org/10.3390/ijms232113418openalex-snapshot
Isolation and Functional Analysis of VvWRKY28, a Vitis vinifera WRKY Transcription Factor Gene, with Functions in Tolerance to Cold and Salt Stress in Transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/ijms24065261openalex-snapshot
Overexpression of a Fragaria vesca 1R-MYB Transcription Factor Gene (FvMYB114) Increases Salt and Cold Tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/ijms27073215openalex-snapshot
Special Issue “Regulatory Mechanism and Network of Abiotic Stress Response in Plants 2.0”
inferred← citeshttps://doi.org/10.3390/ijms27094085openalex-snapshot
Phytohormone-Mediated Regulation of Plant Cold Stress Tolerance: Signaling, Hormonal Crosstalk, and Translational Perspectives
inferred← citeshttps://doi.org/10.3390/plants13131814openalex-snapshot
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inferred← citeshttps://doi.org/10.5376/mpb.2024.15.0006openalex-snapshot
Research Progress of WRKY Transcription Factor Family in Plant Stress Resistance
inferred← citeshttps://doi.org/10.6084/m9.figshare.14168551openalex-snapshot
Additional file 1 of Interactional mechanisms of Paenibacillus polymyxa SC2 and pepper (Capsicum annuum L.) suggested by transcriptomics
inferred← citeshttps://doi.org/10.6084/m9.figshare.14168554openalex-snapshot
Additional file 2 of Interactional mechanisms of Paenibacillus polymyxa SC2 and pepper (Capsicum annuum L.) suggested by transcriptomics
inferred← citeshttps://doi.org/10.6084/m9.figshare.14168560openalex-snapshot
Additional file 3 of Interactional mechanisms of Paenibacillus polymyxa SC2 and pepper (Capsicum annuum L.) suggested by transcriptomics
inferred← citeshttps://doi.org/10.6084/m9.figshare.14168563openalex-snapshot
Additional file 4 of Interactional mechanisms of Paenibacillus polymyxa SC2 and pepper (Capsicum annuum L.) suggested by transcriptomics
inferred← citeshttps://doi.org/10.6084/m9.figshare.14168569openalex-snapshot
Additional file 5 of Interactional mechanisms of Paenibacillus polymyxa SC2 and pepper (Capsicum annuum L.) suggested by transcriptomics
inferred← citeshttps://doi.org/10.6084/m9.figshare.14168575openalex-snapshot
Additional file 6 of Interactional mechanisms of Paenibacillus polymyxa SC2 and pepper (Capsicum annuum L.) suggested by transcriptomics
inferred← citeshttps://doi.org/10.6084/m9.figshare.14168581openalex-snapshot
Additional file 7 of Interactional mechanisms of Paenibacillus polymyxa SC2 and pepper (Capsicum annuum L.) suggested by transcriptomics
inferred← citeshttps://doi.org/10.7287/peerj.14845v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Cloning and comparative modeling identifies a highly stress tolerant Cu/Zn cytosolic super oxide dismutase 2 from a drought tolerant maize inbred line (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.14845v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Cloning and comparative modeling identifies a highly stress tolerant Cu/Zn cytosolic super oxide dismutase 2 from a drought tolerant maize inbred line (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.14845v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Cloning and comparative modeling identifies a highly stress tolerant Cu/Zn cytosolic super oxide dismutase 2 from a drought tolerant maize inbred line (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.14845v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Cloning and comparative modeling identifies a highly stress tolerant Cu/Zn cytosolic super oxide dismutase 2 from a drought tolerant maize inbred line (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.14845v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Cloning and comparative modeling identifies a highly stress tolerant Cu/Zn cytosolic super oxide dismutase 2 from a drought tolerant maize inbred line (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.14845v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Cloning and comparative modeling identifies a highly stress tolerant Cu/Zn cytosolic super oxide dismutase 2 from a drought tolerant maize inbred line (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.14845openalex-snapshot
Cloning and comparative modeling identifies a highly stress tolerant Cu/Zn cytosolic super oxide dismutase 2 from a drought tolerant maize inbred line
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