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Over-expression of the stress-induced OsWRKY45 enhances disease resistance and drought tolerance in Arabidopsis

https://doi.org/10.1016/j.envexpbot.2008.07.002
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf00017731openalex-snapshot
Cloning and characterization of a cold-and ABA-inducible Arabidopsis gene
inferredcites →https://doi.org/10.1007/bf00018452openalex-snapshot
cDNA sequence analysis and expression of two cold-regulated genes ofArabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf00026794openalex-snapshot
Structure and expression of kin2, one of two cold- and ABA-induced genes of Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf00029852openalex-snapshot
The 5?-region of Arabidopsis thaliana cor15a has cis-acting elements that confer cold-, drought- and ABA-regulated gene expression
inferredcites →https://doi.org/10.1007/bf00040716openalex-snapshot
Phytohormone-regulated ?-amylase gene expression in rice
inferredcites →https://doi.org/10.1007/bf00279525openalex-snapshot
The plant hormone abscisic acid mediates the drought-induced expression but not the seed-specific expression of rd22, a gene responsive to dehydration stress in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf00392281openalex-snapshot
Tobacco-mosaic-virus-induced increase in abscisic-acid concentration in tobacco leaves:
inferredcites →https://doi.org/10.1007/bf03185783openalex-snapshot
Cloning and analysis of expression profile of 13 WRKY genes in rice
inferredcites →https://doi.org/10.1007/pl00008673openalex-snapshot
Rapid systemic accumulation of transcripts encoding a tobacco WRKY transcription factor upon wounding
inferredcites →https://doi.org/10.1007/s00299-006-0138-1openalex-snapshot
A comprehensive expression analysis of the WRKY gene superfamily in rice plants during defense response
inferredcites →https://doi.org/10.1007/s00425-003-1086-4openalex-snapshot
A survey of genes differentially expressed during long-term heat-induced chilling tolerance in citrus fruit
inferredcites →https://doi.org/10.1007/s00425-006-0474-yopenalex-snapshot
The WRKY70 transcription factor of Arabidopsis influences both the plant senescence and defense signaling pathways
inferredcites →https://doi.org/10.1007/s004250000512openalex-snapshot
Identification of a transcription factor specifically expressed at the onset of leaf senescence
inferredcites →https://doi.org/10.1007/s004250050212openalex-snapshot
The induction of kin genes in cold-acclimating Arabidopsis thaliana. Evidence of a role for calcium
inferredcites →https://doi.org/10.1007/s00438-002-0651-zopenalex-snapshot
Identification of early-responsive genes associated with the hypersensitive response to tobacco mosaic virus and characterization of a WRKY-type transcription factor in tobacco plants
inferredcites →https://doi.org/10.1007/s11103-004-0906-7openalex-snapshot
Hv-WRKY38: a new transcription factor involved in cold- and drought-response in barley
inferredcites →https://doi.org/10.1016/0003-2697(87)90086-8openalex-snapshot
Improved method for the isolation of RNA from plant tissues
inferredcites →https://doi.org/10.1016/j.cell.2006.06.054openalex-snapshot
Plant Stomata Function in Innate Immunity against Bacterial Invasion
inferredcites →https://doi.org/10.1016/j.cell.2006.08.020openalex-snapshot
Plant Pathogens Trick Guard Cells into Opening the Gates
inferredcites →https://doi.org/10.1016/j.febslet.2006.04.062openalex-snapshot
Constitutive expression of abiotic stress‐inducible hot pepper CaXTH3 , which encodes a xyloglucan endotransglucosylase/hydrolase homolog, improves drought and salt tolerance in transgenic Arabidopsis plants
inferredcites →https://doi.org/10.1016/j.jplph.2006.07.006openalex-snapshot
OsWRKY71, a rice transcription factor, is involved in rice defense response
inferredcites →https://doi.org/10.1016/j.pbi.2005.05.015openalex-snapshot
The role of abscisic acid in plant–pathogen interactions
inferredcites →https://doi.org/10.1016/j.tplants.2004.12.012openalex-snapshot
Organization of cis-acting regulatory elements in osmotic- and cold-stress-responsive promoters
inferredcites →https://doi.org/10.1016/s0167-4781(02)00298-1openalex-snapshot
Leucine zipper-containing WRKY proteins widen the spectrum of immediate early elicitor-induced WRKY transcription factors in parsley
inferredcites →https://doi.org/10.1016/s1369-5266(00)00195-3openalex-snapshot
From milliseconds to millions of years: guard cells and environmental responses
inferredcites →https://doi.org/10.1016/s1369-5266(00)80068-0openalex-snapshot
Molecular responses to dehydration and low temperature: differences and cross-talk between two stress signaling pathways
inferredcites →https://doi.org/10.1016/s1369-5266(01)00219-9openalex-snapshot
Seed dormancy and germination
inferredcites →https://doi.org/10.1023/a:1006399311615openalex-snapshot
Isolation and characterization of two pathogen- and salicylic acid-induced genes encoding WRKY DNA-binding proteins from tobacco
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/10.1038/35066500openalex-snapshot
Guard cell abscisic acid signalling and engineering drought hardiness in plants
inferredcites →https://doi.org/10.1038/415977aopenalex-snapshot
MAP kinase signalling cascade in Arabidopsis innate immunity
inferredcites →https://doi.org/10.1038/82521openalex-snapshot
The transcriptome of Arabidopsis thaliana during systemic acquired resistance
inferredcites →https://doi.org/10.1042/bst0200102openalex-snapshot
Growth substances in context: a decade of sensitivity
inferredcites →https://doi.org/10.1046/j.1365-3040.2002.00782.xopenalex-snapshot
Molecular and genetic aspects of plant responses to osmotic stress
inferredcites →https://doi.org/10.1046/j.1365-313x.1996.10040655.xopenalex-snapshot
Isolation and characterization of abscisic acid‐deficient Arabidopsis mutants at two new loci
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00437.xopenalex-snapshot
A pathogen‐ and salicylic acid‐induced WRKY DNA‐binding activity recognizes the elicitor response element of the tobacco class I chitinase gene promoter
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00923.xopenalex-snapshot
Identification of genes encoding receptor-like protein kinases as possible targets of pathogen- and salicylic acid-induced WRKY DNA-binding proteins in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01070.xopenalex-snapshot
Evidence for a disease‐resistance pathway in rice similar to the NPR1‐mediated signaling pathway in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01131.xopenalex-snapshot
A new member of the Arabidopsis WRKY transcription factor family, At WRKY6, is associated with both senescence‐ and defence‐related processes
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.2641043.xopenalex-snapshot
Impaired sucrose‐induction mutants reveal the modulation of sugar‐induced starch biosynthetic gene expression by abscisic acid signalling
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/10.1046/j.1469-8137.2000.00769.xopenalex-snapshot
Tansley Review No. 120
inferredcites →https://doi.org/10.1071/fp02231openalex-snapshot
Abscisic acid influences the susceptibility of Arabidopsis thaliana to Pseudomonas syringae pv. tomato and Peronospora parasitica
inferredcites →https://doi.org/10.1073/pnas.081594298openalex-snapshot
A postgermination developmental arrest checkpoint is mediated by abscisic acid and requires the ABI5 transcription factor in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m408536200openalex-snapshot
A WRKY Gene from Creosote Bush Encodes an Activator of the Abscisic Acid Signaling Pathway
inferredcites →https://doi.org/10.1093/emboj/18.17.4689openalex-snapshot
Early nuclear events in plant defence signalling: rapid gene activation by WRKY transcription factors
inferredcites →https://doi.org/10.1093/genetics/154.1.421openalex-snapshot
Genetic Analysis of Salt-Tolerant Mutants in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jexbot/51.350.1575openalex-snapshot
Endogenous ABA maintains shoot growth in tomato independently of effects on plant water balance: evidence for an interaction with ethylene
inferredcites →https://doi.org/10.1093/jxb/erm062openalex-snapshot
Isolation and characterization of a Vitis vinifera transcription factor, VvWRKY1, and its effect on responses to fungal pathogens in transgenic tobacco plants
inferredcites →https://doi.org/10.1093/nar/24.23.4624openalex-snapshot
Characterization of a zinc-dependent transcriptional activator from Arabidopsis
inferredcites →https://doi.org/10.1094/mpmi-18-0511openalex-snapshot
Overexpression of a Rice NPR1 Homolog Leads to Constitutive Activation of Defense Response and Hypersensitivity to Light
inferredcites →https://doi.org/10.1094/mpmi.2000.13.10.1092openalex-snapshot
A Potato Gene Encoding a WRKY-like Transcription Factor Is Induced in Interactions with Erwinia carotovora subsp. atroseptica and Phytophthora infestans and Is Coregulated with Class I Endochitinase Expression
inferredcites →https://doi.org/10.1094/mpmi.2003.16.4.295openalex-snapshot
Members of the Arabidopsis WRKY Group III Transcription Factors Are Part of Different Plant Defense Signaling Pathways
inferredcites →https://doi.org/10.1094/phyto-86-1156openalex-snapshot
Identifying and Mapping a New Gene for Bacterial Blight Resistance in Rice Based on RFLP Markers
inferredcites →https://doi.org/10.1101/gad.222702openalex-snapshot
Targets of AtWRKY6 regulation during plant senescence and pathogen defense
inferredcites →https://doi.org/10.1104/pp.001057openalex-snapshot
Potentiation of Developmentally Regulated Plant Defense Response by AtWRKY18, a Pathogen-Induced Arabidopsis Transcription Factor
inferredcites →https://doi.org/10.1104/pp.006858openalex-snapshot
The Combined Effect of Drought Stress and Heat Shock on Gene Expression in Tobacco
inferredcites →https://doi.org/10.1104/pp.103.025395openalex-snapshot
Regulation of Abscisic Acid Biosynthesis
inferredcites →https://doi.org/10.1104/pp.103.025569openalex-snapshot
Negative Regulation of Abscisic Acid Signaling by theFagus sylvaticaFsPP2C1 Plays A Role in Seed Dormancy Regulation and Promotion of Seed Germination
inferredcites →https://doi.org/10.1104/pp.103.034199openalex-snapshot
Stress Tolerance and Glucose Insensitive Phenotypes in Arabidopsis Overexpressing theCpMYB10Transcription Factor Gene
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.103.4.1035openalex-snapshot
Molecular Responses to Water Deficit
inferredcites →https://doi.org/10.1104/pp.104.052084openalex-snapshot
The Arabidopsis Trehalose-6-P SynthaseAtTPS1Gene Is a Regulator of Glucose, Abscisic Acid, and Stress Signaling
inferredcites →https://doi.org/10.1104/pp.104.054312openalex-snapshot
Annotations and Functional Analyses of the Rice WRKY Gene Superfamily Reveal Positive and Negative Regulators of Abscisic Acid Signaling in Aleurone Cells
inferredcites →https://doi.org/10.1104/pp.105.065458openalex-snapshot
A Lily ASR Protein Involves Abscisic Acid Signaling and Confers Drought and Salt Resistance in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.105.065698openalex-snapshot
Enhancing Arabidopsis Salt and Drought Stress Tolerance by Chemical Priming for Its Abscisic Acid Responses
inferredcites →https://doi.org/10.1104/pp.105.066324openalex-snapshot
ABR1, an APETALA2-Domain Transcription Factor That Functions as a Repressor of ABA Response in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.084103openalex-snapshot
Ectopic Expression of ABSCISIC ACID 2/GLUCOSE INSENSITIVE 1 in Arabidopsis Promotes Seed Dormancy and Stress Tolerance
inferredcites →https://doi.org/10.1104/pp.106.084681openalex-snapshot
Overexpression of a Protein Phosphatase 2C from Beech Seeds in Arabidopsis Shows Phenotypes Related to Abscisic Acid Responses and Gibberellin Biosynthesis
inferredcites →https://doi.org/10.1104/pp.106.086223openalex-snapshot
EARLY RESPONSIVE TO DEHYDRATION 15, a Negative Regulator of Abscisic Acid Responses in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.094532openalex-snapshot
Overexpression of an R1R2R3 MYB Gene, OsMYB3R - 2 , Increases Tolerance to Freezing, Drought, and Salt Stress in Transgenic Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.2.363openalex-snapshot
The Interaction of Light and Abscisic Acid in the Regulation of Plant Gene Expression
inferredcites →https://doi.org/10.1104/pp.116.3.1037openalex-snapshot
Differential Expression of a Novel Gene in Response to Coronatine, Methyl Jasmonate, and Wounding in the Coi1Mutant of Arabidopsis1
inferredcites →https://doi.org/10.1104/pp.122.2.415openalex-snapshot
Gibberellin Requirement for Arabidopsis Seed Germination Is Determined Both by Testa Characteristics and Embryonic Abscisic Acid
inferredcites →https://doi.org/10.1104/pp.124.3.941openalex-snapshot
Genetic Analysis of Plant Salt Tolerance Using Arabidopsis
inferredcites →https://doi.org/10.1104/pp.99.2.519openalex-snapshot
DNA Sequence Analysis of a Complementary DNA for Cold-Regulated Arabidopsis Gene cor15 and Characterization of the COR 15 Polypeptide
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/10.1105/tpc.002477openalex-snapshot
The Short-Chain Alcohol Dehydrogenase ABA2 Catalyzes the Conversion of Xanthoxin to Abscisic Aldehyde[W]
inferredcites →https://doi.org/10.1105/tpc.006494openalex-snapshot
A Unique Short-Chain Dehydrogenase/Reductase in Arabidopsis Glucose Signaling and Abscisic Acid Biosynthesis and Functions
inferredcites →https://doi.org/10.1105/tpc.010101openalex-snapshot
The Arabidopsis LOS5/ABA3 Locus Encodes a Molybdenum Cofactor Sulfurase and Modulates Cold Stress– and Osmotic Stress–Responsive Gene Expression
inferredcites →https://doi.org/10.1105/tpc.010115openalex-snapshot
Evidence for an Important Role of WRKY DNA Binding Proteins in the Regulation of NPR1 Gene Expression
inferredcites →https://doi.org/10.1105/tpc.010362openalex-snapshot
Arabidopsis Basic Leucine Zipper Proteins That Mediate Stress-Responsive Abscisic Acid Signaling
inferredcites →https://doi.org/10.1105/tpc.010441openalex-snapshot
Abscisic Acid Signaling in Seeds and Seedlings
inferredcites →https://doi.org/10.1105/tpc.012393openalex-snapshot
CBL1, a Calcium Sensor That Differentially Regulates Salt, Drought, and Cold Responses in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.016980openalex-snapshot
The WRKY70 Transcription Factor: A Node of Convergence for Jasmonate-Mediated and Salicylate-Mediated Signals in Plant Defense[W]
inferredcites →https://doi.org/10.1105/tpc.104.024810openalex-snapshot
Stimulus-Dependent, Promoter-Specific Binding of Transcription Factor WRKY1 to Its Native Promoter and the Defense-Related GenePcPR1-1in Parsley[W]
inferredcites →https://doi.org/10.1105/tpc.104.025833openalex-snapshot
Antagonistic Interaction between Abscisic Acid and Jasmonate-Ethylene Signaling Pathways Modulates Defense Gene Expression and Disease Resistance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.037523openalex-snapshot
Physical and Functional Interactions between Pathogen-Induced Arabidopsis WRKY18, WRKY40, and WRKY60 Transcription Factors
inferredcites →https://doi.org/10.1105/tpc.106.044149openalex-snapshot
The Transcription Factors WRKY11 and WRKY17 Act as Negative Regulators of Basal Resistance inArabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.106.046250openalex-snapshot
Rice WRKY45 Plays a Crucial Role in Benzothiadiazole-Inducible Blast Resistance
inferredcites →https://doi.org/10.1105/tpc.12.4.599openalex-snapshot
The Arabidopsis Abscisic Acid Response Gene ABI5 Encodes a Basic Leucine Zipper Transcription Factor
inferredcites →https://doi.org/10.1105/tpc.12.7.1117openalex-snapshot
Regulation of Abscisic Acid Signaling by the Ethylene Response Pathway in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.2.6.503openalex-snapshot
Gene Expression in Response to Abscisic Acid and Osmotic Stress
inferredcites →https://doi.org/10.1105/tpc.3.1.49openalex-snapshot
Identification of Pseudomonas syringae pathogens of Arabidopsis and a bacterial locus determining avirulence on both Arabidopsis and soybean.
inferredcites →https://doi.org/10.1105/tpc.6.2.251openalex-snapshot
A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low-temperature, or high-salt stress.
inferredcites →https://doi.org/10.1105/tpc.8.10.1809openalex-snapshot
Systemic Acquired Resistance.
inferredcites →https://doi.org/10.1105/tpc.9.1.5openalex-snapshot
Hexokinase as a Sugar Sensor in Higher Plants
inferredcites →https://doi.org/10.1105/tpc.9.7.1055openalex-snapshot
Seed Germination and Dormancy.
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02086.xopenalex-snapshot
Drought tolerance established by enhanced expression of the CC–NBS–LRR gene, ADR1, requires salicylic acid, EDS1 and ABI1
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02267.xopenalex-snapshot
Endogenous salicylic acid protects rice plants from oxidative damage caused by aging as well as biotic and abiotic stress
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02678.xopenalex-snapshot
Identification of AtHD2C as a novel regulator of abscisic acid responses in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02694.xopenalex-snapshot
Interactions of two abscisic‐acid induced WRKY genes in repressing gibberellin signaling in aleurone cells
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02782.xopenalex-snapshot
Upregulation of an Arabidopsis RING‐H2 gene, XERICO , confers drought tolerance through increased abscisic acid biosynthesis
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03034.xopenalex-snapshot
Regulation and functional analysis of ZmDREB2A in response to drought and heat stresses in Zea mays L
inferredcites →https://doi.org/10.1111/j.1399-3011.2004.00126.xopenalex-snapshot
The coactivator LXXLL nuclear receptor recognition motif
inferredcites →https://doi.org/10.1111/j.1399-3054.1995.tb05114.xopenalex-snapshot
Arabidopsis mutants with reduced response to NaCl and osmotic stress
inferredcites →https://doi.org/10.1126/science.1059046openalex-snapshot
G Protein Regulation of Ion Channels and Abscisic Acid Signaling in Arabidopsis Guard Cells
inferredcites →https://doi.org/10.1126/science.1081288openalex-snapshot
Collection, Mapping, and Annotation of Over 28,000 cDNA Clones from japonica Rice
inferredcites →https://doi.org/10.1126/science.282.5387.287openalex-snapshot
Role of Farnesyltransferase in ABA Regulation of Guard Cell Anion Channels and Plant Water Loss
inferredcites →https://doi.org/10.1146/annurev.arplant.45.1.113openalex-snapshot
Gene Expression Regulated by Abscisic Acid and its Relation to Stress Tolerance
inferredcites →https://doi.org/10.1146/annurev.arplant.47.1.377openalex-snapshot
THE MOLECULAR BASIS OF DEHYDRATION TOLERANCE IN PLANTS
inferredcites →https://doi.org/10.1146/annurev.arplant.49.1.199openalex-snapshot
ABSCISIC ACID SIGNAL TRANSDUCTION
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.571openalex-snapshot
PLANT COLD ACCLIMATION: Freezing Tolerance Genes and Regulatory Mechanisms
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.57.032905.105444openalex-snapshot
TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Isolation and Functional Analysis of Malus Baccata (L.) Borkh. Wrky Transcription Factors Mbwrky50
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Toward integration of a systems‐based approach for understanding drought stress in plants
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MicroRNAs and their role in drought stress response in plants
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Host Defense Inducers
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Transcription Factors: Modulating Plant Adaption in the Scenario of Changing Climate
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Role of Transcription Factors in Abiotic Stress Tolerance in Crop Plants
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Host Defense Inducers
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Identification microRNAs and target genes in Tibetan hulless barley to BLS infection
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Transcription factors as tools to engineer enhanced drought stress tolerance in plants
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Network‐based feature selection reveals substructures of gene modules responding to salt stress in rice
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Genetic Engineering of Miscanthus
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Crop Improvement Through Plant Tissue Culture
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Transcription Factors in Abiotic Stress Responses: Their Potentials in Crop Improvement
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Towards Understanding the Transcriptional Control of Abiotic Stress Tolerance Mechanisms in Food Legumes
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Expression and Regulation of Stress-Responsive Genes in Plants Under Harsh Environmental Conditions
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The Role of Transcription Factors in Response to Biotic Stresses in Tomato
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Exploring the Critical Function and Molecular Mechanism of WRKY Transcription Factor Family in Regulating Plant Response Under Abiotic Stress Conditions
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Decoding the Dynamic Epigenetic Interplay in Plant Transcriptional Regulation Under Salinity Stress
inferred← citeshttps://doi.org/10.1007/978-3-319-07899-1_10openalex-snapshot
Impact of Concurrent Drought Stress and Pathogen Infection on Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-22518-0_10openalex-snapshot
Transgenic Approaches for Abiotic Stress Tolerance in Crop Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-28899-4_3openalex-snapshot
Mechanisms of Hormone Regulation for Drought Tolerance in Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-32423-4_12openalex-snapshot
Transcription Factors Involved in Plant Drought Tolerance Regulation
inferred← citeshttps://doi.org/10.1007/978-3-319-75671-4_7openalex-snapshot
Transcription Factor-Based Genetic Engineering for Salinity Tolerance in Crops
inferred← citeshttps://doi.org/10.1007/978-3-319-90650-8_7openalex-snapshot
Transgenic Plants for Improved Salinity and Drought Tolerance
inferred← citeshttps://doi.org/10.1007/978-3-319-97217-6_7openalex-snapshot
Genes/Quantitative Trait Loci and Associated Molecular Mechanisms Identified in Capsicum Genome for Tolerance to Abiotic and Biotic Stresses
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Integrating Transcriptome and Chromatin Landscapes for Deciphering the Epigenetic Regulation of Drought Response in Maize
inferred← citeshttps://doi.org/10.1007/978-81-322-3706-8_10openalex-snapshot
Simultaneous Expression of Abiotic Stress-Responsive Genes: An Approach to Improve Multiple Stress Tolerance in Crops
inferred← citeshttps://doi.org/10.1007/978-81-322-3706-8_9openalex-snapshot
Plant Responses to Combined Drought and Pathogen Infection: Current Understanding on the Role of Phytohormones
inferred← citeshttps://doi.org/10.1007/978-981-10-5254-5_6openalex-snapshot
ROS-Induced Transcription Factors During Oxidative Stress in Plants: A Tabulated Review
inferred← citeshttps://doi.org/10.1007/978-981-15-2172-0_9openalex-snapshot
Biochemical and Molecular Mechanisms of Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.1007/978-981-15-6345-4_3openalex-snapshot
Arabidopsis thaliana: Model Plant for the Study of Abiotic Stress Responses
inferred← citeshttps://doi.org/10.1007/978-981-15-9380-2_11openalex-snapshot
Role of WRKY Transcription Factor Superfamily in Plant Disease Management
inferred← citeshttps://doi.org/10.1007/978-981-19-2119-3_4openalex-snapshot
Transgenics and Crop Improvement
inferred← citeshttps://doi.org/10.1007/978-981-97-0672-3_13openalex-snapshot
Transcriptional Regulation of Gene Expression in Plant Abiotic Stress Response
inferred← citeshttps://doi.org/10.1007/978-981-99-4669-3_13openalex-snapshot
Transcriptional Regulatory Network Involved in Drought and Salt Stress Response in Rice
inferred← citeshttps://doi.org/10.1007/978-981-99-5890-0_8openalex-snapshot
Omics-Based Approaches in Improving Drought Stress Tolerance in Pearl Millet
inferred← citeshttps://doi.org/10.1007/s00299-015-1787-8openalex-snapshot
Activated expression of AtWRKY53 negatively regulates drought tolerance by mediating stomatal movement
inferred← citeshttps://doi.org/10.1007/s00299-015-1910-xopenalex-snapshot
Overexpression of VaPAT1, a GRAS transcription factor from Vitis amurensis, confers abiotic stress tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-017-2190-4openalex-snapshot
Genome-wide characterization of the WRKY gene family in radish (Raphanus sativus L.) reveals its critical functions under different abiotic stresses
inferred← citeshttps://doi.org/10.1007/s00299-018-2302-9openalex-snapshot
Overexpression of VaWRKY14 increases drought tolerance in Arabidopsis by modulating the expression of stress-related genes
inferred← citeshttps://doi.org/10.1007/s00299-021-02683-8openalex-snapshot
Phytohormone signaling and crosstalk in regulating drought stress response in plants
inferred← citeshttps://doi.org/10.1007/s00299-021-02691-8openalex-snapshot
WRKY transcription factors and plant defense responses: latest discoveries and future prospects
inferred← citeshttps://doi.org/10.1007/s00344-014-9444-yopenalex-snapshot
Arabidopsis Plants Overexpressing the MsDREB2C Exhibit Increased Susceptibility to Alternaria mali Infection
inferred← citeshttps://doi.org/10.1007/s00344-021-10344-zopenalex-snapshot
Expression of an A20/AN1 Stress-Associated Protein from Aeluropus littoralis in Rice Deregulates Stress-Related Genes
inferred← citeshttps://doi.org/10.1007/s00344-021-10429-9openalex-snapshot
De Novo Transcriptome Assembly and Identification of Brassinosteroid Biosynthetic Pathway in Safflower
inferred← citeshttps://doi.org/10.1007/s00344-022-10639-9openalex-snapshot
Enhancement of Drought Tolerance in Transgenic Arabidopsis thaliana Plants Overexpressing Chickpea Ca14-3-3 Gene
inferred← citeshttps://doi.org/10.1007/s00425-010-1258-yopenalex-snapshot
Expression and functional analysis of two genes encoding transcription factors, VpWRKY1 and VpWRKY2, isolated from Chinese wild Vitis pseudoreticulata
inferred← citeshttps://doi.org/10.1007/s00425-011-1375-2openalex-snapshot
Arabidopsis thaliana WRKY25, WRKY26, and WRKY33 coordinate induction of plant thermotolerance
inferred← citeshttps://doi.org/10.1007/s00425-013-1985-yopenalex-snapshot
A systems biology perspective on the role of WRKY transcription factors in drought responses in plants
inferred← citeshttps://doi.org/10.1007/s00425-022-03871-wopenalex-snapshot
Functions of OsWRKY24, OsWRKY70 and OsWRKY53 in regulating grain size in rice
inferred← citeshttps://doi.org/10.1007/s00425-026-04973-5openalex-snapshot
Molecular orchestration and health implications of fruit pigmentation: from metabolic pathways to nutritional quality
inferred← citeshttps://doi.org/10.1007/s00709-015-0769-6openalex-snapshot
Isolation of a WRKY30 gene from Muscadinia rotundifolia (Michx) and validation of its function under biotic and abiotic stresses
inferred← citeshttps://doi.org/10.1007/s00894-015-2798-7openalex-snapshot
Protein modeling and molecular dynamics simulation of SlWRKY4 protein cloned from drought tolerant tomato (Solanum habrochaites) line EC520061
inferred← citeshttps://doi.org/10.1007/s10059-011-0047-1openalex-snapshot
WRKY22 Transcription Factor Mediates Dark-Induced Leaf Senescence in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s10142-014-0399-7openalex-snapshot
The CarERF genes in chickpea (Cicer arietinum L.) and the identification of CarERF116 as abiotic stress responsive transcription factor
inferred← citeshttps://doi.org/10.1007/s10142-022-00847-7openalex-snapshot
Dissection of valine-glutamine genes and their responses to drought stress in Arachis hypogaea cv. Tifrunner
inferred← citeshttps://doi.org/10.1007/s10343-025-01275-wopenalex-snapshot
Seed Priming for Drought Tolerance: Mechanisms, Innovations, and Implications for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/s10535-011-0091-xopenalex-snapshot
Beyond osmolytes and transcription factors: drought tolerance in plants via protective proteins and aquaporins
inferred← citeshttps://doi.org/10.1007/s10535-011-0104-9openalex-snapshot
Beyond osmolytes and transcription factors: drought tolerance in plants via protective proteins and aquaporins
inferred← citeshttps://doi.org/10.1007/s10535-016-0584-8openalex-snapshot
Photosynthesis and antioxidative defense mechanisms in deciphering drought stress tolerance of crop plants
inferred← citeshttps://doi.org/10.1007/s10658-017-1399-yopenalex-snapshot
Identification of Magnaporthe oryzae-elicited rice novel miRNAs and their targets by miRNA and degradome sequencing
inferred← citeshttps://doi.org/10.1007/s10709-025-00227-6openalex-snapshot
Comparative analysis of the WRKY gene family between Chimonanthus praecox and C. salicifolius
inferred← citeshttps://doi.org/10.1007/s10725-009-9366-zopenalex-snapshot
Heterologous expression of OsWRKY23 gene enhances pathogen defense and dark-induced leaf senescence in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s10725-013-9792-9openalex-snapshot
ZmWRKY33, a WRKY maize transcription factor conferring enhanced salt stress tolerances in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s10725-021-00766-wopenalex-snapshot
MdWRKY74 is involved in resistance response to apple replant disease
inferred← citeshttps://doi.org/10.1007/s11033-010-0504-5openalex-snapshot
WRKY: its structure, evolutionary relationship, DNA-binding selectivity, role in stress tolerance and development of plants
inferred← citeshttps://doi.org/10.1007/s11103-016-0539-7openalex-snapshot
Multidimensional patterns of metabolic response in abiotic stress-induced growth of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11105-019-01187-wopenalex-snapshot
First Expressed TFome of Physic Nut (Jatropha curcas L.) After Salt Stimulus
inferred← citeshttps://doi.org/10.1007/s11240-014-0463-yopenalex-snapshot
Overexpression of Glycine soja WRKY20 enhances both drought and salt tolerance in transgenic alfalfa (Medicago sativa L.)
inferred← citeshttps://doi.org/10.1007/s11240-015-0815-2openalex-snapshot
SpWRKY1 mediates resistance to Phytophthora infestans and tolerance to salt and drought stress by modulating reactive oxygen species homeostasis and expression of defense-related genes in tomato
inferred← citeshttps://doi.org/10.1007/s11240-017-1335-zopenalex-snapshot
Over-expression of a grape WRKY transcription factor gene, VlWRKY48, in Arabidopsis thaliana increases disease resistance and drought stress tolerance
inferred← citeshttps://doi.org/10.1007/s11240-021-02115-1openalex-snapshot
VuWRKY, a group I WRKY gene from Vaccinium uliginosum, confers tolerance to cold and salt stresses in plant
inferred← citeshttps://doi.org/10.1007/s11295-015-0929-zopenalex-snapshot
Gene regulatory network in almond (Prunus dulcis Mill.) in response to frost stress
inferred← citeshttps://doi.org/10.1007/s11430-013-4766-3openalex-snapshot
Variations in leaf characteristics of three species of angiosperms with changing of altitude in Qilian Mountains and their inland high-altitude pattern
inferred← citeshttps://doi.org/10.1007/s11434-009-0710-5openalex-snapshot
Overexpression of the stress-induced OsWRKY08 improves osmotic stress tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11627-024-10458-5openalex-snapshot
Overexpression of a Malus baccata (L.) Borkh WRKY transcription factor gene MbWRKY65 increased the tolerance to cold and drought in transgenic tomato
inferred← citeshttps://doi.org/10.1007/s11676-020-01134-6openalex-snapshot
Identification of yellowhorn (Xanthoceras sorbifolium) WRKY transcription factor family and analysis of abiotic stress response model
inferred← citeshttps://doi.org/10.1007/s11738-011-0896-4openalex-snapshot
Gene expression profiles in maize (Zea mays L.) leaves inoculation with southern corn rust (Puccinia polysora Underw.)
inferred← citeshttps://doi.org/10.1007/s11738-013-1434-3openalex-snapshot
A WRKY transcription factor from Malus domestica negatively regulates dehydration stress in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11738-017-2423-8openalex-snapshot
Overexpression of NbWRKY79 enhances salt stress tolerance in Nicotiana benthamiana
inferred← citeshttps://doi.org/10.1007/s12038-010-0051-1openalex-snapshot
Overexpression of OsWRKY72 gene interferes in the abscisic acid signal and auxin transport pathway of Arabidopsis
inferred← citeshttps://doi.org/10.1007/s12298-020-00835-wopenalex-snapshot
Tomato contrasting genotypes responses under combined salinity and viral stresses
inferred← citeshttps://doi.org/10.1007/s12355-014-0343-0openalex-snapshot
Effects of Exogenous Abscisic Acid on Cell Membrane and Endogenous Hormone Contents in Leaves of Sugarcane Seedlings under Cold Stress
inferred← citeshttps://doi.org/10.1007/s12374-010-9129-4openalex-snapshot
Analysis of the Cold-Responsive Transcriptome in the Mature Pollen of Arabidopsis
inferred← citeshttps://doi.org/10.1007/s12374-013-0511-xopenalex-snapshot
Ectopic expression of CaWRKY1, a pepper transcription factor, enhances drought tolerance in transgenic potato plants
inferred← citeshttps://doi.org/10.1007/s13205-016-0416-8openalex-snapshot
Investigating the effect of drought stress on expression of WRKY1 and EREBP1 genes and antioxidant enzyme activities in lemon balm (Melissa Officinalis L.)
inferred← citeshttps://doi.org/10.1007/s13237-026-00666-2openalex-snapshot
Genome-wide insights of finger millet reveal EcWRKY99 as candidate gene for drought and salinity stress tolerance
inferred← citeshttps://doi.org/10.1007/s13258-013-0065-9openalex-snapshot
Molecular cloning and characterization of SoNCED, a novel gene encoding 9-cis-epoxycarotenoid dioxygenase from sugarcane (Saccharum officinarum L.)
inferred← citeshttps://doi.org/10.1007/s13258-018-00780-9openalex-snapshot
Genome-wide identification and expression analyses of WRKY transcription factor family members from chickpea (Cicer arietinum L.) reveal their role in abiotic stress-responses
inferred← citeshttps://doi.org/10.1007/s13562-018-0440-3openalex-snapshot
Genome-wide identification of major transcription factor superfamilies in rice identifies key candidates involved in abiotic stress dynamism
inferred← citeshttps://doi.org/10.1007/s40415-019-00566-7openalex-snapshot
Transcriptional and post-transcriptional responses of diploid and autotetraploid Paulownia tomentosa × Paulownia fortunei under water-deficit condition
inferred← citeshttps://doi.org/10.1016/b978-0-12-803158-2.00004-7openalex-snapshot
Resistance of Plants to Cu Stress
inferred← citeshttps://doi.org/10.1016/b978-0-12-817892-8.00017-9openalex-snapshot
Abiotic and biotic stress interactions in plants: A cross-tolerance perspective
inferred← citeshttps://doi.org/10.1016/b978-0-12-819334-1.00007-1openalex-snapshot
Major transcription factor families involved in salinity stress tolerance in plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-819334-1.00011-3openalex-snapshot
Transcription factors and their roles in phosphorus stress tolerance in crop plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-819334-1.00013-7openalex-snapshot
Engineering transcription factors: An emerging strategy for developing abiotic stress-tolerant crops
inferred← citeshttps://doi.org/10.1016/b978-0-12-819527-7.00007-8openalex-snapshot
Salt responsive transcription factors in wheat
inferred← citeshttps://doi.org/10.1016/b978-0-12-819527-7.00011-xopenalex-snapshot
Role of transcription factors in drought mediating pathways in wheat
inferred← citeshttps://doi.org/10.1016/b978-0-323-85665-2.00003-0openalex-snapshot
Physiological, biochemical, and molecular adaptation mechanisms of photosynthesis and respiration under challenging environments
inferred← citeshttps://doi.org/10.1016/b978-0-323-90613-5.00006-6openalex-snapshot
Plant transcription factors: important factors controlling oxidative stress in plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-90613-5.00009-1openalex-snapshot
Transcription factors: master regulators of disease resistance in crop plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-90943-3.00018-3openalex-snapshot
Transcription factors involved in plant responses to stress adaptation
inferred← citeshttps://doi.org/10.1016/b978-0-323-91883-1.00010-3openalex-snapshot
Genetic engineering strategies for regulation of phytohormones in plants exposed to biotic and abiotic stresses
inferred← citeshttps://doi.org/10.1016/b978-0-443-13490-6.00025-4openalex-snapshot
Plant gene networks involved in drought stress response and tolerance
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2011.09.002openalex-snapshot
The role of WRKY transcription factors in plant abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.bbrc.2012.09.120openalex-snapshot
The tomato SlWRKY gene plays an important role in the regulation of defense responses in tobacco
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.10.088openalex-snapshot
Constitutive expression of a salinity-induced wheat WRKY transcription factor enhances salinity and ionic stress tolerance in transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.06.128openalex-snapshot
A wheat salinity-induced WRKY transcription factor TaWRKY93 confers multiple abiotic stress tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2017.05.011openalex-snapshot
Plant growth-promoting abilities and biocontrol efficacy of Streptomyces sp. UPMRS4 against Pyricularia oryzae
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2023.105286openalex-snapshot
Induction of systemic resistance in rice plants against Burkholderia glumae infection by bioformulation of Streptomyces spp. under greenhouse conditions
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2011.09.006openalex-snapshot
Role of transgenic plants in agriculture and biopharming
inferred← citeshttps://doi.org/10.1016/j.cpb.2024.100380openalex-snapshot
Deciphering the role of SlWRKY36 and SlWRKY51 in salt stress tolerance via modulating ion homeostasis and proline biosynthesis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104117openalex-snapshot
PtrWRKY75 overexpression reduces stomatal aperture and improves drought tolerance by salicylic acid-induced reactive oxygen species accumulation in poplar
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104373openalex-snapshot
MsWRKY11, activated by MsWRKY22, functions in drought tolerance and modulates lignin biosynthesis in alfalfa (Medicago sativa L.)
inferred← citeshttps://doi.org/10.1016/j.gene.2013.04.047openalex-snapshot
Genome-wide analysis of the WRKY gene family in physic nut (Jatropha curcas L.)
inferred← citeshttps://doi.org/10.1016/j.gene.2015.04.002openalex-snapshot
Phylogenetic and stress-responsive expression analysis of 20 WRKY genes in Populus simonii×Populus nigra
inferred← citeshttps://doi.org/10.1016/j.gene.2020.144480openalex-snapshot
Identification of key genes related to seedlessness by genome-wide detection of structural variation and transcriptome analysis in ‘Shijiwuhe’ pear
inferred← citeshttps://doi.org/10.1016/j.gene.2021.145561openalex-snapshot
Identification and expression analysis of the WRKY gene family in Isatis indigotica
inferred← citeshttps://doi.org/10.1016/j.gene.2022.146377openalex-snapshot
The WRKY transcription factor family in cowpea: Genomic characterization and transcriptomic profiling under root dehydration
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.hpj.2023.05.005openalex-snapshot
Overexpression of the transcription factor MdWRKY115 improves drought and osmotic stress tolerance by directly binding to the MdRD22 promoter in apple
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.128769openalex-snapshot
Review: Structural-functional relationship of WRKY transcription factors: Unfolding the role of WRKY in plants
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.117996openalex-snapshot
Combined analysis of GC-MS, RNA-seq and ATAC-seq elucidates the essential oils variation and terpenes biosynthesis in Citrus grandis ‘Tomentosa’
inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.118158openalex-snapshot
Genome-wide analysis of WRKY gene family in high-CBD hemp (Cannabis sativa L.) and identification of the WRKY genes involved in abiotic stress responses and regulation cannabinoid accumulation
inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.119224openalex-snapshot
A WRKY-regulated TLP gene mediates the response to cold, drought, and wound stress in jojoba
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2016.11.017openalex-snapshot
The sunflower transcription factor HaHB11 confers tolerance to water deficit and salinity to transgenic Arabidopsis and alfalfa plants
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2020.12.020openalex-snapshot
Transcriptome analysis of salt stress responsiveness in the seedlings of wild and cultivated Ricinus communis L
inferred← citeshttps://doi.org/10.1016/j.jplph.2022.153741openalex-snapshot
Overexpressing VvWRKY18 from grapevine reduces the drought tolerance in Arabidopsis by increasing leaf stomatal density
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154526openalex-snapshot
MbWRKY50 confers cold and drought tolerance through upregulating antioxidant capacity associated with ROS scavenging
inferred← citeshttps://doi.org/10.1016/j.micpath.2019.103610openalex-snapshot
Molecular regulation of pepper innate immunity and stress tolerance: An overview of WRKY TFs
inferred← citeshttps://doi.org/10.1016/j.plantsci.2013.08.002openalex-snapshot
Transcriptomics of induced defense responses to greenbug aphid feeding in near isogenic wheat lines
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.03.036openalex-snapshot
Comparative analysis of root transcriptome profiles between drought-tolerant and susceptible wheat genotypes in response to water stress
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.07.010openalex-snapshot
Ectopic expression of FvWRKY42 , a WRKY transcription factor from the diploid woodland strawberry ( Fragaria vesca ), enhances resistance to powdery mildew, improves osmotic stress resistance, and increases abscisic acid sensitivity in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110285openalex-snapshot
DkWRKY interacts with pyruvate kinase gene DkPK1 and promotes natural deastringency in C-PCNA persimmon
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111282openalex-snapshot
Interaction between MdWRKY55 and MdNAC17-L enhances salt tolerance in apple by activating MdNHX1 expression
inferred← citeshttps://doi.org/10.1016/j.plaphy.2016.06.018openalex-snapshot
The differential expression of soybean [ Glycine max (L.) Merrill] WRKY genes in response to water deficit
inferred← citeshttps://doi.org/10.1016/j.plaphy.2017.07.016openalex-snapshot
Wheat and rye genome confer specific phytohormone profile features and interplay under water stress in two phenotypes of triticale
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.10.006openalex-snapshot
A novel SAPK10-WRKY87-ABF1 biological pathway synergistically enhance abiotic stress tolerance in transgenic rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.01.002openalex-snapshot
Tomato (Solanum lycopersicum) WRKY23 enhances salt and osmotic stress tolerance by modulating the ethylene and auxin pathways in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111123openalex-snapshot
Distinct transcriptional programs control polyethylene glycol (PEG)-induced drought stress responses in oat (Avena sativa L.) shoot and roots
inferred← citeshttps://doi.org/10.1016/j.plgene.2017.11.002openalex-snapshot
Genome wide expression analysis of WRKY genes in tomato (Solanum lycopersicum) under drought stress
inferred← citeshttps://doi.org/10.1016/j.plgene.2021.100294openalex-snapshot
Plant miRNAs: Biogenesis and its functional validation to combat drought stress with special focus on maize
inferred← citeshttps://doi.org/10.1016/j.sajb.2023.08.028openalex-snapshot
Molecular regulation of antioxidants and secondary metabolites act in conjunction to defend plants against pathogenic infection
inferred← citeshttps://doi.org/10.1016/j.scib.2017.12.002openalex-snapshot
SRWD1 , a novel target gene of DELLA and WRKY proteins, participates in the development and immune response of rice ( Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/j.scienta.2015.06.037openalex-snapshot
Stress responses in citrus peel: Comparative analysis of host responses to Huanglongbing disease and puffing disorder
inferred← citeshttps://doi.org/10.1016/j.scienta.2021.110848openalex-snapshot
Overexpression of watermelon ClWRKY20 in transgenic Arabidopsis improves salt and low-temperature tolerance
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111716openalex-snapshot
Blue light exposure intensifies leaf red pigmentation and enhances oxidative stress tolerance in the ornamental bromeliad Neoregelia ‘Fireball’
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.111827openalex-snapshot
Strigolactone and salicylic acid regulate the expression of multiple stress-related genes and enhance the drought resistance of cherry rootstocks
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100814openalex-snapshot
Pearl millet WRKY transcription factor PgWRKY52 positively regulates salt stress tolerance through ABA-MeJA mediated transcriptional regulation
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100956openalex-snapshot
Systematic identification and characterization of Group Ⅳ WRKYs in Osmanthus fragrans and induction of salt-sensitivity by OfWRKY157
inferred← citeshttps://doi.org/10.1016/j.tplants.2010.02.006openalex-snapshot
WRKY transcription factors
inferred← citeshttps://doi.org/10.1016/s1006-8104(13)60016-1openalex-snapshot
Regulatory Network of Transcription Factors in Response to Drought in Arabidopsis and Crops
inferred← citeshttps://doi.org/10.1016/s1671-2927(11)60074-6openalex-snapshot
Isolation and Expression Patterns of Rice WRKY82 Transcription Factor Gene Responsive to Both Biotic and Abiotic Stresses
inferred← citeshttps://doi.org/10.1016/s1672-6308(08)60105-5openalex-snapshot
Research Progress on Functional Analysis of Rice WRKY Genes
inferred← citeshttps://doi.org/10.1017/s0021859616000873openalex-snapshot
Foxtail milletWRKYgenes and drought stress
inferred← citeshttps://doi.org/10.1017/s0021859616000885openalex-snapshot
Identification and characterization of two faba bean (Vicia faba L.) WRKY transcription factors and their expression analysis during salt and drought stress
inferred← citeshttps://doi.org/10.1038/s41438-020-00355-4openalex-snapshot
Woodland strawberry WRKY71 acts as a promoter of flowering via a transcriptional regulatory cascade
inferred← citeshttps://doi.org/10.1038/s41598-017-06518-zopenalex-snapshot
Physiological and transcriptome analysis of He-Ne laser pretreated wheat seedlings in response to drought stress
inferred← citeshttps://doi.org/10.1038/s41598-018-34920-8openalex-snapshot
Comparative genome-wide analysis of WRKY transcription factors in two Asian legume crops: Adzuki bean and Mung bean
inferred← citeshttps://doi.org/10.1038/s41598-022-04903-xopenalex-snapshot
Essential oil from Lavandula angustifolia elicits expression of three SbWRKY transcription factors and defense-related genes against sorghum damping-off
inferred← citeshttps://doi.org/10.1038/s44383-026-00043-7openalex-snapshot
Functional genomics in the WRKY transcription factor family: from model systems to crop species and beyond
inferred← citeshttps://doi.org/10.1038/srep37025openalex-snapshot
Analysis of carotenogenic genes promoters and WRKY transcription factors in response to salt stress in Dunaliella bardawil
inferred← citeshttps://doi.org/10.1071/fp23077openalex-snapshot
Identification of WRKY transcription factors in Rosa chinensis and analysis of their expression response to alkali stress response
inferred← citeshttps://doi.org/10.1071/fp24023openalex-snapshot
Investigating the combined effects of β-sitosterol and biochar on nutritional value and drought tolerance in Phaseolus vulgaris under drought stress
inferred← citeshttps://doi.org/10.1073/pnas.1319388111openalex-snapshot
Linking toxicity and adaptive responses across the transcriptome, proteome, and phenotype of Chlamydomonas reinhardtii exposed to silver
inferred← citeshttps://doi.org/10.1080/01140671.2025.2455050openalex-snapshot
SpWRKY71 is required for drought tolerance in tomato
inferred← citeshttps://doi.org/10.1080/03235408.2019.1606490openalex-snapshot
Regulation ofWRKYgenes in plant defence with beneficial fungusTrichoderma: current perspectives and future prospects
inferred← citeshttps://doi.org/10.1080/07352689.2014.870417openalex-snapshot
Functional Genomics of Drought Tolerance in Bioenergy Crops
inferred← citeshttps://doi.org/10.1080/07352689.2016.1265357openalex-snapshot
Sub-Functionalization in Rice Gene Families with Regulatory Roles in Abiotic Stress Responses
inferred← citeshttps://doi.org/10.1080/07388551.2019.1710459openalex-snapshot
Phytohormones regulate convergent and divergent responses between individual and combined drought and pathogen infection
inferred← citeshttps://doi.org/10.1080/15592324.2020.1844508openalex-snapshot
Transcriptome-wide identification of WRKY family genes and their expression profiling toward salicylic acid in Camellia japonica
inferred← citeshttps://doi.org/10.1080/17429145.2023.2299865openalex-snapshot
WRKY proteins regulate the development of plants in response to abiotic stresses
inferred← citeshttps://doi.org/10.1089/dna.2019.4895openalex-snapshot
Functional Validation of JcWRKY2 , a Group III Transcription Factor Toward Mitigating Salinity Stress in Transgenic Tobacco
inferred← citeshttps://doi.org/10.1089/omi.2011.0095openalex-snapshot
Transcription Regulation of Abiotic Stress Responses in Rice: A Combined Action of Transcription Factors and Epigenetic Mechanisms
inferred← citeshttps://doi.org/10.1089/omi.2013.0177openalex-snapshot
The Potential of Transcription Factor-Based Genetic Engineering in Improving Crop Tolerance to Drought
inferred← citeshttps://doi.org/10.1093/aobpla/plaf038openalex-snapshot
Drought tolerance of cowpea is associated with rapid abscisic acid biosynthesis via VuWRKY57 in root
inferred← citeshttps://doi.org/10.1093/hr/uhad172openalex-snapshot
VvWRKY5 enhances white rot resistance in grape by promoting the jasmonic acid pathway
inferred← citeshttps://doi.org/10.1093/jambio/lxae266openalex-snapshot
A rice rhizosphere plant growth-promoting Streptomyces corchorusii isolate antagonizes Magnaporthe oryzae and elicits defense responses in rice
inferred← citeshttps://doi.org/10.1093/jxb/eraa135openalex-snapshot
WRKY10 transcriptional regulatory cascades in rice are involved in basal defense and Xa1-mediated resistance
inferred← citeshttps://doi.org/10.1093/jxb/erq204openalex-snapshot
Male gametophyte-specific WRKY34 transcription factor mediates cold sensitivity of mature pollen in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/ers100openalex-snapshot
The interaction of plant biotic and abiotic stresses: from genes to the field
inferred← citeshttps://doi.org/10.1093/jxb/erv287openalex-snapshot
Expression of Brassica napus TTG2 , a regulator of trichome development, increases plant sensitivity to salt stress by suppressing the expression of auxin biosynthesis genes
inferred← citeshttps://doi.org/10.1093/mp/sss080openalex-snapshot
Activated Expression of WRKY57 Confers Drought Tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1093/mp/sss147openalex-snapshot
Recent Advances in Dissecting Stress-Regulatory Crosstalk in Rice
inferred← citeshttps://doi.org/10.1093/pcp/pcu133openalex-snapshot
The Cotton WRKY Transcription Factor GhWRKY17 Functions in Drought and Salt Stress in Transgenic Nicotiana benthamiana Through ABA Signaling and the Modulation of Reactive Oxygen Species Production
inferred← citeshttps://doi.org/10.1093/pcp/pcv174openalex-snapshot
Genome-Wide Transcriptome Analysis During Anthesis Reveals New Insights into the Molecular Basis of Heat Stress Responses in Tolerant and Sensitive Rice Varieties
inferred← citeshttps://doi.org/10.1093/plphys/kiaf257openalex-snapshot
The transcription factor TaWRKY27 confers enhanced stripe rust susceptibility by facilitating auxin accumulation in wheat
inferred← citeshttps://doi.org/10.1093/treephys/tpx020openalex-snapshot
Populus simonii × Populus nigra WRKY70 is involved in salt stress and leaf blight disease responses
inferred← citeshttps://doi.org/10.1094/mpmi-23-5-0558openalex-snapshot
Wounding-Induced WRKY8 Is Involved in Basal Defense in Arabidopsis
inferred← citeshttps://doi.org/10.1094/mpmi-23-6-0791openalex-snapshot
Abscisic Acid Interacts Antagonistically with Salicylic Acid Signaling Pathway in Rice–Magnaporthe griseaInteraction
inferred← citeshttps://doi.org/10.1094/pbiomes-01-22-0006-fiopenalex-snapshot
Fungal Symbionts Generate Water-Saver and Water-Spender Plant Drought Strategies via Diverse Effects on Host Gene Expression
inferred← citeshttps://doi.org/10.1101/2023.08.20.551368openalex-snapshot
Comparative Analysis of Salinity Response Transcriptomes in Salt-Tolerant Pokkali and Susceptible IR29 Rice
inferred← citeshttps://doi.org/10.1101/2023.12.10.571021openalex-snapshot
HGNNPIP: A Hybrid Graph Neural Network framework for Protein-protein Interaction Prediction
inferred← citeshttps://doi.org/10.1104/pp.109.138990openalex-snapshot
The Role of WRKY Transcription Factors in Plant Immunity
inferred← citeshttps://doi.org/10.1104/pp.109.145623openalex-snapshot
A Pair of Allelic WRKY Genes Play Opposite Roles in Rice-Bacteria Interactions
inferred← citeshttps://doi.org/10.1104/pp.112.207720openalex-snapshot
RhNAC2 and RhEXPA4 Are Involved in the Regulation of Dehydration Tolerance during the Expansion of Rose Petals
inferred← citeshttps://doi.org/10.1111/j.1364-3703.2012.00795.xopenalex-snapshot
OsWRKY22 , a monocot WRKY gene, plays a role in the resistance response to blast
inferred← citeshttps://doi.org/10.1111/j.1467-7652.2011.00634.xopenalex-snapshot
WRKY transcription factors: key components in abscisic acid signalling
inferred← citeshttps://doi.org/10.1111/jipb.12513openalex-snapshot
WRKY transcription factors in plant responses to stresses
inferred← citeshttps://doi.org/10.1111/mpp.13010openalex-snapshot
The Arabidopsis small G‐protein AtRAN1 is a positive regulator in chitin‐induced stomatal closure and disease resistance
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