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Role of Plant Transcription Factors in Abiotic Stress Tolerance
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/btpr.514openalex-snapshot
Transcription factors as tools to engineer enhanced drought stress tolerance in plants
inferredcites →https://doi.org/10.1002/j.1460-2075.1987.tb02684.xopenalex-snapshot
The regulatory c1 locus of Zea mays encodes a protein with homology to myb proto‐oncogene products and with structural similarities to transcriptional activators.
inferredcites →https://doi.org/10.1007/978-3-540-39402-0_11openalex-snapshot
Transcriptome analysis in abiotic stress conditions in higher plants
inferredcites →https://doi.org/10.1007/978-90-481-2666-8_12openalex-snapshot
Plant Drought Stress: Effects, Mechanisms and Management
inferredcites →https://doi.org/10.1007/bf00016490openalex-snapshot
Current advances in abscisic acid action and signalling
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/pl00006285openalex-snapshot
Molecular Evolution of the Myb Family of Transcription Factors: Evidence for Polyphyletic Origin
inferredcites →https://doi.org/10.1007/s00122-002-1131-xopenalex-snapshot
An EREBP/AP2-type protein in Triticum aestivum was a DRE-binding transcription factor induced by cold, dehydration and ABA stress
inferredcites →https://doi.org/10.1007/s00122-003-1226-zopenalex-snapshot
Characterization of a DRE-binding transcription factor from a halophyte Atriplex hortensis
inferredcites →https://doi.org/10.1007/s00122-004-1867-6openalex-snapshot
Soybean DRE-binding transcription factors that are responsive to abiotic stresses
inferredcites →https://doi.org/10.1007/s00299-006-0204-8openalex-snapshot
Role of DREB transcription factors in abiotic and biotic stress tolerance in plants
inferredcites →https://doi.org/10.1007/s00299-008-0587-9openalex-snapshot
Osmyb4 expression improves adaptive responses to drought and cold stress in transgenic apples
inferredcites →https://doi.org/10.1007/s00299-010-0896-7openalex-snapshot
SbDREB2A, an A-2 type DREB transcription factor from extreme halophyte Salicornia brachiata confers abiotic stress tolerance in Escherichia coli
inferredcites →https://doi.org/10.1007/s00425-004-1412-5openalex-snapshot
Isolation and functional characterization of the Ca-DREBLP1 gene encoding a dehydration-responsive element binding-factor-like protein�1 in hot pepper (Capsicum annuum L. cv. Pukang)
inferredcites →https://doi.org/10.1007/s00425-005-0030-1openalex-snapshot
Expression of a novel NAC domain-containing transcription factor (CaNAC1) is preferentially associated with incompatible interactions between chili pepper and pathogens
inferredcites →https://doi.org/10.1007/s00425-008-0731-3openalex-snapshot
Soybean GmbZIP44, GmbZIP62 and GmbZIP78 genes function as negative regulator of ABA signaling and confer salt and freezing tolerance in transgenic Arabidopsis
inferredcites →https://doi.org/10.1007/s00438-006-0183-zopenalex-snapshot
Stress-inducible DREB2A transcription factor from Pennisetum glaucum is a phosphoprotein and its phosphorylation negatively regulates its DNA-binding activity
inferredcites →https://doi.org/10.1007/s00438-009-0506-yopenalex-snapshot
Comprehensive analysis of rice DREB2-type genes that encode transcription factors involved in the expression of abiotic stress-responsive genes
inferredcites →https://doi.org/10.1007/s10265-007-0140-xopenalex-snapshot
Molecular cloning, expression profiling and trans-activation property studies of a DREB2-like gene from chrysanthemum (Dendranthema vestitum)
inferredcites →https://doi.org/10.1007/s10265-008-0195-3openalex-snapshot
Isolation and functional characterization of HvDREB1—a gene encoding a dehydration-responsive element binding protein in Hordeum vulgare
inferredcites →https://doi.org/10.1007/s10529-008-9811-5openalex-snapshot
Over-expression of OsDREB genes lead to enhanced drought tolerance in rice
inferredcites →https://doi.org/10.1007/s10535-010-0038-7openalex-snapshot
Transcription factors in plants and ABA dependent and independent abiotic stress signalling
inferredcites →https://doi.org/10.1007/s11032-007-9116-8openalex-snapshot
Identification of genes involved in the response of leaves of Phaseolus vulgaris to drought stress
inferredcites →https://doi.org/10.1007/s11033-007-9153-8openalex-snapshot
Identification and characterization of two chrysanthemum (Dendronthema × moriforlium) DREB genes, belonging to the AP2/EREBP family
inferredcites →https://doi.org/10.1007/s11033-009-9885-8openalex-snapshot
Overexpression of PgDREB2A transcription factor enhances abiotic stress tolerance and activates downstream stress-responsive genes
inferredcites →https://doi.org/10.1007/s11033-010-0023-4openalex-snapshot
Characterization of a novel wheat NAC transcription factor gene involved in defense response against stripe rust pathogen infection and abiotic stresses
inferredcites →https://doi.org/10.1007/s11103-005-2910-yopenalex-snapshot
The MYB Transcription Factor Superfamily of Arabidopsis: Expression Analysis and Phylogenetic Comparison with the Rice MYB Family
inferredcites →https://doi.org/10.1007/s11103-005-6503-6openalex-snapshot
Transcription Factors in Rice: A Genome-wide Comparative Analysis between Monocots and Eudicots
inferredcites →https://doi.org/10.1007/s11103-006-9089-8openalex-snapshot
A novel drought-inducible gene, ATAF1, encodes a NAC family protein that negatively regulates the expression of stress-responsive genes in Arabidopsis
inferredcites →https://doi.org/10.1007/s11103-007-9244-xopenalex-snapshot
Overexpression of rice WRKY89 enhances ultraviolet B tolerance and disease resistance in rice plants
inferredcites →https://doi.org/10.1007/s11103-008-9298-4openalex-snapshot
A bZIP transcription factor, OsABI5, is involved in rice fertility and stress tolerance
inferredcites →https://doi.org/10.1007/s11103-008-9309-5openalex-snapshot
Characterization of transcription factor gene SNAC2 conferring cold and salt tolerance in rice
inferredcites →https://doi.org/10.1007/s11103-008-9340-6openalex-snapshot
Overexpression of a rice OsDREB1F gene increases salt, drought, and low temperature tolerance in both Arabidopsis and rice
inferredcites →https://doi.org/10.1007/s12033-011-9385-7openalex-snapshot
Molecular Cloning and Characterization of a Membrane Associated NAC Family Gene, SiNAC from Foxtail Millet [Setaria italica (L.) P. Beauv.]
inferredcites →https://doi.org/10.1016/0092-8674(82)90138-6openalex-snapshot
Nucleotide sequence of the retroviral leukemia gene v-myb and its cellular progenitor c-myb: The architecture of a transduced oncogene
inferredcites →https://doi.org/10.1016/b978-012406360-0/50004-6openalex-snapshot
Isolation and identification
inferredcites →https://doi.org/10.1016/j.bbrc.2006.12.027openalex-snapshot
GmDREB2, a soybean DRE-binding transcription factor, conferred drought and high-salt tolerance in transgenic plants
inferredcites →https://doi.org/10.1016/j.bbrc.2007.08.007openalex-snapshot
Over-expression of the Arabidopsis DRE/CRT-binding transcription factor DREB2C enhances thermotolerance
inferredcites →https://doi.org/10.1016/j.bbrc.2007.09.124openalex-snapshot
Identification of stress-tolerance-related transcription-factor genes via mini-scale Full-length cDNA Over-eXpressor (FOX) gene hunting system
inferredcites →https://doi.org/10.1016/j.bbrc.2008.11.071openalex-snapshot
Expression profiling and functional characterization of a DREB2-type gene from Populus euphratica
inferredcites →https://doi.org/10.1016/j.bbrc.2008.12.163openalex-snapshot
Overexpression of a NAC transcription factor enhances rice drought and salt tolerance
inferredcites →https://doi.org/10.1016/j.copbio.2006.02.002openalex-snapshot
Engineering drought tolerance in plants: discovering and tailoring genes to unlock the future
inferredcites →https://doi.org/10.1016/j.cub.2005.05.048openalex-snapshot
A Guard-Cell-Specific MYB Transcription Factor Regulates Stomatal Movements and Plant Drought Tolerance
inferredcites →https://doi.org/10.1016/j.cub.2005.06.041openalex-snapshot
AtMYB61, an R2R3-MYB Transcription Factor Controlling Stomatal Aperture in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.envexpbot.2008.07.002openalex-snapshot
Over-expression of the stress-induced OsWRKY45 enhances disease resistance and drought tolerance in Arabidopsis
inferredcites →https://doi.org/10.1016/j.gene.2009.05.012openalex-snapshot
Complete inventory of soybean NAC transcription factors: Sequence conservation and expression analysis uncover their distinct roles in stress response
inferredcites →https://doi.org/10.1016/j.plantsci.2007.05.007openalex-snapshot
Evaluation of transgenic tomato plants ectopically expressing the rice Osmyb4 gene
inferredcites →https://doi.org/10.1016/j.plaphy.2009.09.002openalex-snapshot
Characterization of a chickpea (Cicer arietinum L.) NAC family gene, CarNAC5, which is both developmentally- and stress-regulated
inferredcites →https://doi.org/10.1016/j.tplants.2010.06.005openalex-snapshot
MYB transcription factors in Arabidopsis
inferredcites →https://doi.org/10.1016/s0092-8674(00)80902-2openalex-snapshot
A Homolog of NO APICAL MERISTEM Is an Immediate Target of the Floral Homeotic Genes APETALA3/PISTILLATA
inferredcites →https://doi.org/10.1016/s0092-8674(00)81093-4openalex-snapshot
The No Apical Meristem Gene of Petunia Is Required for Pattern Formation in Embryos and Flowers and Is Expressed at Meristem and Primordia Boundaries
inferredcites →https://doi.org/10.1016/s0960-9822(09)00431-xopenalex-snapshot
Proceedings of the National Academy of Sciences, USA
inferredcites →https://doi.org/10.1016/s1360-1385(01)02223-3openalex-snapshot
bZIP transcription factors in Arabidopsis
inferredcites →https://doi.org/10.1016/s1369-5266(00)00199-0openalex-snapshot
The R2R3-MYB gene family in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s1673-8527(09)60003-5openalex-snapshot
Transgenic expression of MYB15 confers enhanced sensitivity to abscisic acid and improved drought tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1017/cbo9780511790515.006openalex-snapshot
Transcriptional Regulatory Networks
inferredcites →https://doi.org/10.1017/s0021859610000742openalex-snapshot
Transgenic expression of sorghum DREB2 in rice improves tolerance and yield under water limitation
inferredcites →https://doi.org/10.1023/a:1006011002499openalex-snapshot
Two novel MYB homologues with changed expression in late embryogenesis-defective Arabidopsis mutants
inferredcites →https://doi.org/10.1023/a:1006058700720openalex-snapshot
Regulation of abscisic acid-induced transcription
inferredcites →https://doi.org/10.1023/a:1006319732410openalex-snapshot
Multifunctionality and diversity within the plant MYB-gene family
inferredcites →https://doi.org/10.1023/a:1006321900483openalex-snapshot
Organization and expression of two Arabidopsis DREB2 genes encoding DRE-binding proteins involved in dehydration- and high-salinity-responsive gene expression
inferredcites →https://doi.org/10.1023/a:1010639225091openalex-snapshot
Differential induction of two potato genes, Stprx2 and StNAC, in response to infection by Phytophthora infestans and to wounding
inferredcites →https://doi.org/10.1023/b:plan.0000006944.61384.11openalex-snapshot
Molecular characterization of Brassica napus NAC domain transcriptional activators induced in response to biotic and abiotic stress
inferredcites →https://doi.org/10.1038/186124d0openalex-snapshot
Biochemical and Biophysical Research Communications
inferredcites →https://doi.org/10.1038/7036openalex-snapshot
Improving plant drought, salt, and freezing tolerance by gene transfer of a single stress-inducible transcription factor
inferredcites →https://doi.org/10.1038/cr.2008.280openalex-snapshot
Soybean GmMYB76, GmMYB92, and GmMYB177 genes confer stress tolerance in transgenic Arabidopsis plants
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00310.xopenalex-snapshot
Low temperature regulation of theArabidopsisCBF family of AP2 transcriptional activators as an early step in cold‐inducedCORgene expression
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00947.xopenalex-snapshot
A novel cold‐inducible zinc finger protein from soybean, SCOF‐1, enhances cold tolerance in transgenic plants
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01325.xopenalex-snapshot
Maize DRE‐binding proteins DBF1 and DBF2 are involved in rab17 regulation through the drought‐responsive element in an ABA‐dependent pathway
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01359.xopenalex-snapshot
Monitoring the expression profiles of 7000 Arabidopsis genes under drought, cold and high‐salinity stresses using a full‐length cDNA microarray
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01661.xopenalex-snapshot
OsDREB genes in rice, Oryza sativa L., encode transcription activators that function in drought‐, high‐salt‐ and cold‐responsive gene expression
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01791.xopenalex-snapshot
AtMYB103 regulates tapetum and trichome development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01924.xopenalex-snapshot
Stress‐responsive zinc finger gene ZPT2‐3 plays a role in drought tolerance in petunia
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01938.xopenalex-snapshot
Overexpression of the rice Osmyb4 gene increases chilling and freezing tolerance of Arabidopsis thaliana plants
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01953.xopenalex-snapshot
Involvement of the R2R3‐MYB, At MYB61, in the ectopic lignification and dark‐photomorphogenic components of the det3 mutant phenotype
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01963.xopenalex-snapshot
HvDRF1 is involved in abscisic acid‐mediated gene regulation in barley and produces two forms of AP2 transcriptional activators, interacting preferably with a CT‐rich element
inferredcites →https://doi.org/10.1051/agro:2008021openalex-snapshot
Plant drought stress: effects, mechanisms and management
inferredcites →https://doi.org/10.1073/pnas.0401572101openalex-snapshot
Overexpression of a zinc-finger protein gene from rice confers tolerance to cold, dehydration, and salt stress in transgenic tobacco
inferredcites →https://doi.org/10.1073/pnas.0403166101openalex-snapshot
An Arabidopsis homeodomain transcription factor gene, HOS9 , mediates cold tolerance through a CBF-independent pathway
inferredcites →https://doi.org/10.1073/pnas.0407758101openalex-snapshot
SRK2C, a SNF1-related protein kinase 2, improves drought tolerance by controlling stress-responsive gene expression in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0503960102openalex-snapshot
RETRACTED: HOS10 encodes an R2R3-type MYB transcription factor essential for cold acclimation in plants
inferredcites →https://doi.org/10.1073/pnas.0505667103openalex-snapshot
Abscisic acid-dependent multisite phosphorylation regulates the activity of a transcription activator AREB1
inferredcites →https://doi.org/10.1073/pnas.0604882103openalex-snapshot
Overexpressing a NAM, ATAF, and CUC (NAC) transcription factor enhances drought resistance and salt tolerance in rice
inferredcites →https://doi.org/10.1073/pnas.0605639103openalex-snapshot
Dual function of an Arabidopsis transcription factor DREB2A in water-stress-responsive and heat-stress-responsive gene expression
inferredcites →https://doi.org/10.1073/pnas.0707294104openalex-snapshot
Improvement of water use efficiency in rice by expression of HARDY , an Arabidopsis drought and salt tolerance gene
inferredcites →https://doi.org/10.1073/pnas.190309197openalex-snapshot
Arabidopsis basic leucine zipper transcription factors involved in an abscisic acid-dependent signal transduction pathway under drought and high-salinity conditions
inferredcites →https://doi.org/10.1073/pnas.94.3.1035openalex-snapshot
Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/DRE, a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit
inferredcites →https://doi.org/10.1073/pnas.96.26.15348openalex-snapshot
A bZIP factor, TRAB1, interacts with VP1 and mediates abscisic acid-induced transcription
inferredcites →https://doi.org/10.1074/jbc.275.3.1723openalex-snapshot
ABFs, a Family of ABA-responsive Element Binding Factors
inferredcites →https://doi.org/10.1074/jbc.m403171200openalex-snapshot
Mitotic Cyclins Stimulate the Activity of c-Myb-like Factors for Transactivation of G2/M Phase-specific Genes in Tobacco
inferredcites →https://doi.org/10.1074/jbc.m605895200openalex-snapshot
A R2R3 Type MYB Transcription Factor Is Involved in the Cold Regulation of CBF Genes and in Acquired Freezing Tolerance
inferredcites →https://doi.org/10.1074/jbc.m611093200openalex-snapshot
The EAR-motif of the Cys2/His2-type Zinc Finger Protein Zat7 Plays a Key Role in the Defense Response of Arabidopsis to Salinity Stress
inferredcites →https://doi.org/10.1079/9781789247350.0021openalex-snapshot
Responses to Abiotic Stresses
inferredcites →https://doi.org/10.1080/07352680590910410openalex-snapshot
Drought and Salt Tolerance in Plants
inferredcites →https://doi.org/10.1093/aob/mcn227openalex-snapshot
Transcription factors and regulation of photosynthetic and related metabolism under environmental stresses
inferredcites →https://doi.org/10.1093/aob/mcr053openalex-snapshot
Abiotic Stress Adaptation in Plants. Physiological, Molecular and Genomic Foundation
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/jxb/ern014openalex-snapshot
Development of abiotic stress tolerance via bZIP-type transcription factor LIP19 in common wheat
inferredcites →https://doi.org/10.1093/jxb/erp214openalex-snapshot
Overexpression of the soybean GmERF3 gene, an AP2/ERF type transcription factor for increased tolerances to salt, drought, and diseases in transgenic tobacco
inferredcites →https://doi.org/10.1093/jxb/err016openalex-snapshot
Association of an SNP in a novel DREB2-like gene SiDREB2 with stress tolerance in foxtail millet [Setaria italica (L.)]
inferredcites →https://doi.org/10.1093/pcp/pcf188openalex-snapshot
ABA-Activated SnRK2 Protein Kinase is Required for Dehydration Stress Signaling in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pch037openalex-snapshot
A Combination of the Arabidopsis DREB1A Gene and Stress-Inducible rd29A Promoter Improved Drought- and Low-Temperature Stress Tolerance in Tobacco by Gene Transfer
inferredcites →https://doi.org/10.1093/pcp/pci165openalex-snapshot
The Effect of Overexpression of Two Brassica CBF/DREB1-like Transcription Factors on Photosynthetic Capacity and Freezing Tolerance in Brassica napus
inferredcites →https://doi.org/10.1093/pcp/pci230openalex-snapshot
Functional Analysis of Rice DREB1/CBF-type Transcription Factors Involved in Cold-responsive Gene Expression in Transgenic Rice
inferredcites →https://doi.org/10.1093/pcp/pcn025openalex-snapshot
SodERF3, a Novel Sugarcane Ethylene Responsive Factor (ERF), Enhances Salt and Drought Tolerance when Overexpressed in Tobacco Plants
inferredcites →https://doi.org/10.1093/pcp/pcp159openalex-snapshot
Arabidopsis NAC Transcription Factor, ANAC078, Regulates Flavonoid Biosynthesis under High-light
inferredcites →https://doi.org/10.1101/gad.852200openalex-snapshot
Arabidopsis NAC1 transduces auxin signal downstream of TIR1 to promote lateral root development
inferredcites →https://doi.org/10.1104/pp.002857openalex-snapshot
Transcriptional Profiling Reveals Novel Interactions between Wounding, Pathogen, Abiotic Stress, and Hormonal Responses in Arabidopsis,
inferredcites →https://doi.org/10.1104/pp.003442openalex-snapshot
Heterology Expression of the Arabidopsis C-Repeat/Dehydration Response Element Binding Factor 1 Gene Confers Elevated Tolerance to Chilling and Oxidative Stresses in Transgenic Tomato
inferredcites →https://doi.org/10.1104/pp.006478openalex-snapshot
Transcription Factor CBF4 Is a Regulator of Drought Adaptation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.102.019273openalex-snapshot
Integration of Wounding and Osmotic Stress Signals Determines the Expression of the AtMYB102 Transcription Factor Gene
inferredcites →https://doi.org/10.1104/pp.104.040295openalex-snapshot
From Laboratory to Field. Using Information from Arabidopsis to Engineer Salt, Cold, and Drought Tolerance in Crops
inferredcites →https://doi.org/10.1104/pp.104.042176openalex-snapshot
Genome-Wide ORFeome Cloning and Analysis of Arabidopsis Transcription Factor Genes
inferredcites →https://doi.org/10.1104/pp.104.054783openalex-snapshot
Organ-Specific Expression of Arabidopsis Genome during Development
inferredcites →https://doi.org/10.1104/pp.104.059147openalex-snapshot
Arabidopsis CBF3/DREB1A and ABF3 in Transgenic Rice Increased Tolerance to Abiotic Stress without Stunting Growth
inferredcites →https://doi.org/10.1104/pp.105.068254openalex-snapshot
The Zinc-Finger Protein Zat12 Plays a Central Role in Reactive Oxygen and Abiotic Stress Signaling in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.105.073783openalex-snapshot
Genome-Wide Analysis of the ERF Gene Family in Arabidopsis and Rice
inferredcites →https://doi.org/10.1104/pp.106.081752openalex-snapshot
Expression of CAP2, an APETALA2-Family Transcription Factor from Chickpea, Enhances Growth and Tolerance to Dehydration and Salt Stress in Transgenic Tobacco
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.107.098061openalex-snapshot
Legume Transcription Factors: Global Regulators of Plant Development and Response to the Environment
inferredcites →https://doi.org/10.1104/pp.107.110981openalex-snapshot
Overexpression of AtMYB44 Enhances Stomatal Closure to Confer Abiotic Stress Tolerance in Transgenic Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.128199openalex-snapshot
Characterization of OsbZIP23 as a Key Player of the Basic Leucine Zipper Transcription Factor Family for Conferring Abscisic Acid Sensitivity and Salinity and Drought Tolerance in Rice
inferredcites →https://doi.org/10.1104/pp.108.129791openalex-snapshot
Transcriptional Regulatory Networks in Response to Abiotic Stresses in Arabidopsis and Grasses
inferredcites →https://doi.org/10.1104/pp.108.134874openalex-snapshot
AtMyb41 Regulates Transcriptional and Metabolic Responses to Osmotic Stress in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.110.154617openalex-snapshot
DREB2C Interacts with ABF2, a bZIP Protein Regulating Abscisic Acid-Responsive Gene Expression, and Its Overexpression Affects Abscisic Acid Sensitivity
inferredcites →https://doi.org/10.1104/pp.110.163634openalex-snapshot
Expression of StMYB1R - 1 , a Novel Potato Single MYB-Like Domain Transcription Factor, Increases Drought Tolerance
inferredcites →https://doi.org/10.1104/pp.119.2.463openalex-snapshot
The Arabidopsis CBF Gene Family Is Composed of Three Genes Encoding AP2 Domain-Containing Proteins Whose Expression Is Regulated by Low Temperature but Not by Abscisic Acid or Dehydration1
inferredcites →https://doi.org/10.1104/pp.120.2.473openalex-snapshot
Transgenic Overexpression of the Transcription FactorAlfin1Enhances Expression of the Endogenous MsPRP2Gene in Alfalfa and Improves Salinity Tolerance of the Plants1
inferredcites →https://doi.org/10.1104/pp.124.4.1854openalex-snapshot
Overexpression of the ArabidopsisCBF3Transcriptional Activator Mimics Multiple Biochemical Changes Associated with Cold Acclimation
inferredcites →https://doi.org/10.1105/tpc.000869openalex-snapshot
The Homologous ABI5 and EEL Transcription Factors Function Antagonistically to Fine-Tune Gene Expression during Late Embryogenesis
inferredcites →https://doi.org/10.1105/tpc.003483openalex-snapshot
Arabidopsis Transcriptome Profiling Indicates That Multiple Regulatory Pathways Are Activated during Cold Acclimation in Addition to the CBF Cold Response Pathway[W]
inferredcites →https://doi.org/10.1105/tpc.006130openalex-snapshot
Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) Function as Transcriptional Activators in Abscisic Acid Signaling
inferredcites →https://doi.org/10.1105/tpc.007096openalex-snapshot
The Transcription Factors HvABI5 and HvVP1 Are Required for the Abscisic Acid Induction of Gene Expression in Barley Aleurone Cells
inferredcites →https://doi.org/10.1105/tpc.007906openalex-snapshot
Arabidopsis OST1 Protein Kinase Mediates the Regulation of Stomatal Aperture by Abscisic Acid and Acts Upstream of Reactive Oxygen Species Production
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.10.8.1391openalex-snapshot
Two Transcription Factors, DREB1 and DREB2, with an EREBP/AP2 DNA Binding Domain Separate Two Cellular Signal Transduction Pathways in Drought- and Low-Temperature-Responsive Gene Expression, Respectively, in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.104.022699openalex-snapshot
Isolation and Functional Analysis of Arabidopsis Stress-Inducible NAC Transcription Factors That Bind to a Drought-Responsivecis-Element in theearly responsive to dehydration stress 1Promoter[W]
inferredcites →https://doi.org/10.1105/tpc.104.023135openalex-snapshot
From Endonucleases to Transcription Factors: Evolution of the AP2 DNA Binding Domain in Plants[W]
inferredcites →https://doi.org/10.1105/tpc.105.035659openalex-snapshot
AREB1 Is a Transcription Activator of Novel ABRE-Dependent ABA Signaling That Enhances Drought Stress Tolerance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.058263openalex-snapshot
Activated Expression of an Arabidopsis HD-START Protein Confers Drought Tolerance with Improved Root System and Reduced Stomatal Density
inferredcites →https://doi.org/10.1105/tpc.12.12.2383openalex-snapshot
Activation Tagging Identifies a Conserved MYB Regulator of Phenylpropanoid Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.5.11.1529openalex-snapshot
An Arabidopsis myb homolog is induced by dehydration stress and its gene product binds to the conserved MYB recognition sequence.
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.8.7.1107openalex-snapshot
Modular nature of abscisic acid (ABA) response complexes: composite promoter units that are necessary and sufficient for ABA induction of gene expression in barley.
inferredcites →https://doi.org/10.1105/tpc.9.10.1859openalex-snapshot
Role of arabidopsis MYC and MYB homologs in drought- and abscisic acid-regulated gene expression.
inferredcites →https://doi.org/10.1105/tpc.9.6.841openalex-snapshot
Genes involved in organ separation in Arabidopsis: an analysis of the cup-shaped cotyledon mutant.
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01363.xopenalex-snapshot
Analysis of gene expression profiles in Arabidopsis salt overly sensitive mutants sos2−1 and sos3 −1
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02192.xopenalex-snapshot
ABF2, an ABRE‐binding bZIP factor, is an essential component of glucose signaling and its overexpression affects multiple stress tolerance
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.2006.02655.xopenalex-snapshot
Metabolic engineering of proanthocyanidins through co‐expression of anthocyanidin reductase and the PAP1 MYB transcription factor
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02723.xopenalex-snapshot
AtNAP, a NAC family transcription factor, has an important role in leaf senescence
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02932.xopenalex-snapshot
Co‐expression of the stress‐inducible zinc finger homeodomain ZFHD1 and NAC transcription factors enhances expression of the ERD1 gene in Arabidopsis
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.1365-313x.2007.03133.xopenalex-snapshot
The R2R3‐MYB transcription factor HAG1/MYB28 is a regulator of methionine‐derived glucosinolate biosynthesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03168.xopenalex-snapshot
Functional analysis of a NAC‐type transcription factor OsNAC6 involved in abiotic and biotic stress‐responsive gene expression in rice
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03310.xopenalex-snapshot
Over‐expression of the Arabidopsis AtMYB41 gene alters cell expansion and leaf surface permeability
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03350.xopenalex-snapshot
XND1, a member of the NAC domain family in Arabidopsis thaliana , negatively regulates lignocellulose synthesis and programmed cell death in xylem
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03493.xopenalex-snapshot
A membrane‐bound NAC transcription factor NTL8 regulates gibberellic acid‐mediated salt signaling in Arabidopsis seed germination
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04092.xopenalex-snapshot
AREB1, AREB2, and ABF3 are master transcription factors that cooperatively regulate ABRE-dependent ABA signaling involved in drought stress tolerance and require ABA for full activation
inferredcites →https://doi.org/10.1111/j.1399-3054.2005.00551.xopenalex-snapshot
Overexpression of Osmyb4 enhances compatible solute accumulation and increases stress tolerance of Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1399-3054.2005.00592.xopenalex-snapshot
Regulons involved in osmotic stress‐responsive and cold stress‐responsive gene expression in plants
inferredcites →https://doi.org/10.1111/j.1467-7652.2008.00336.xopenalex-snapshot
Soybean WRKY‐type transcription factor genes, GmWRKY13, GmWRKY21 , and GmWRKY54 , confer differential tolerance to abiotic stresses in transgenic Arabidopsis plants
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02160.xopenalex-snapshot
Cotton GhDREB1 increases plant tolerance to low temperature and is negatively regulated by gibberellic acid
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.07219.xopenalex-snapshot
CAP2 enhances germination of transgenic tobacco seeds at high temperature and promotes heat stress tolerance in yeast
inferredcites →https://doi.org/10.1111/j.1744-7909.2007.00593.xopenalex-snapshot
Role of Soybean GmbZIP132 under Abscisic Acid and Salt Stresses
inferredcites →https://doi.org/10.1126/science.280.5360.104openalex-snapshot
Arabidopsis CBF1 Overexpression Induces COR Genes and Enhances Freezing Tolerance
inferredcites →https://doi.org/10.1126/science.290.5499.2105openalex-snapshot
Arabidopsis Transcription Factors: Genome-Wide Comparative Analysis Among Eukaryotes
inferredcites →https://doi.org/10.1139/g03-140openalex-snapshot
Stress-induced expression in wheat of the Arabidopsis thaliana DREB1A gene delays water stress symptoms under greenhouse conditions
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112122openalex-snapshot
Abscisic Acid: Emergence of a Core Signaling Network
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112226openalex-snapshot
Guard Cell Signal Transduction Network: Advances in Understanding Abscisic Acid, CO2, and Ca2+Signaling
inferredcites →https://doi.org/10.1186/1471-2229-9-75openalex-snapshot
The HaDREB2 transcription factor enhances basal thermotolerance and longevity of seeds through functional interaction with HaHSFA9
inferredcites →https://doi.org/10.1242/dev.00993openalex-snapshot
CUPULIFORMIS establishes lateral organ boundaries in Antirrhinum
inferredcites →https://doi.org/10.1266/ggs.81.77openalex-snapshot
Differential regulation of transcript accumulation and alternative splicing of a DREB2 homolog under abiotic stress conditions in common wheat
inferredcites →https://doi.org/10.1371/journal.pone.0005154openalex-snapshot
CaZF, a Plant Transcription Factor Functions through and Parallel to HOG and Calcineurin Pathways in Saccharomyces cerevisiae to Provide Osmotolerance
inferredcites →https://doi.org/10.2307/3869643openalex-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/10.2307/3870355openalex-snapshot
Modular Nature of Abscisic Acid (ABA) Response Complexes: Composite Promoter Units That Are Necessary and Sufficient for ABA Induction of Gene Expression in Barley
inferredcites →https://doi.org/10.2307/3870530openalex-snapshot
Role of Arabidopsis MYC and MYB Homologs in Drought- and Abscisic Acid-Regulated Gene Expression
inferredcites →https://doi.org/10.2307/3871236openalex-snapshot
Activation Tagging Identifies a Conserved MYB Regulator of Phenylpropanoid Biosynthesis
inferredcites →https://doi.org/10.3724/sp.j.1006.2009.01973openalex-snapshot
Isolation and Identification of PNDREB1: A New DREB Tran-scription Factor from Peanut (Arachis hypogaea L.)
inferredcites →https://doi.org/10.5483/bmbrep.2010.43.1.034openalex-snapshot
OsAREB1, an ABRE-binding protein responding to ABA and glucose, has multiple functions in Arabidopsis
inferredcites →https://doi.org/10.5511/plantbiotechnology.23.169openalex-snapshot
The Arabidopsis DREB1A gene driven by the stress-inducible rd29A promoter increases salt-stress tolerance in proportion to its copy number in tetrasomic tetraploid potato (Solanum tuberosum)
inferredcites →https://doi.org/10.5772/1762openalex-snapshot
Abiotic Stress Response in Plants - Physiological, Biochemical and Genetic Perspectives
inferredcites →https://doi.org/10.5897/ajb2009.000-9520openalex-snapshot
Cloning and characterization of a putative transcription factor induced by abiotic stress in Zea mays
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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PGPR-Mediated Drought Tolerance in Brassica juncea by Modulating Morpho-Physiological, Biochemical, and Antioxidant Responses
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Expression analysis of cold-induced transcription factor genes in rice (Oryza sativa L.)
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Stress-Mediated cis-Element Transcription Factor Interactions Interconnecting Primary and Specialized Metabolism in planta
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A Non-specific Setaria italica Lipid Transfer Protein Gene Plays a Critical Role under Abiotic Stress
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New Insights on Plant Salt Tolerance Mechanisms and Their Potential Use for Breeding
inferred← citeshttps://doi.org/10.3389/fpls.2017.01214openalex-snapshot
Poaceae vs. Abiotic Stress: Focus on Drought and Salt Stress, Recent Insights and Perspectives
inferred← citeshttps://doi.org/10.3389/fpls.2017.01510openalex-snapshot
Bacillus amyloliquefaciens Confers Tolerance to Various Abiotic Stresses and Modulates Plant Response to Phytohormones through Osmoprotection and Gene Expression Regulation in Rice
inferred← citeshttps://doi.org/10.3389/fpls.2021.766130openalex-snapshot
Functional Characterization of Cotton C-Repeat Binding Factor Genes Reveal Their Potential Role in Cold Stress Tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2022.941026openalex-snapshot
Characterization of NAC transcription factor NtNAC028 as a regulator of leaf senescence and stress responses
inferred← citeshttps://doi.org/10.3390/agronomy7040083openalex-snapshot
Comprehensive Screening of Some West and Central African Sesame Genotypes for Drought Resistance Probing by Agromorphological, Physiological, Biochemical and Seed Quality Traits
inferred← citeshttps://doi.org/10.3390/ijms23126683openalex-snapshot
Integrated Transcriptomic and Metabolomic Analyses of Cold-Tolerant and Cold-Sensitive Pepper Species Reveal Key Genes and Essential Metabolic Pathways Involved in Response to Cold Stress
inferred← citeshttps://doi.org/10.3390/ijms232213905openalex-snapshot
Transcriptome Analysis of Two Tetraploid Potato Varieties under Water-Stress Conditions
inferred← citeshttps://doi.org/10.3390/ijms232315396openalex-snapshot
Genome and Transcriptome-Wide Analysis of OsWRKY and OsNAC Gene Families in Oryza sativa and Their Response to White-Backed Planthopper Infestation
inferred← citeshttps://doi.org/10.3390/ijms252413559openalex-snapshot
Integrated Transcriptomic, Proteomic, and Metabolomic Analyses Revealed Molecular Mechanism for Salt Resistance in Soybean (Glycine max L.) Seedlings
inferred← citeshttps://doi.org/10.3390/metabo15060416openalex-snapshot
Metabolomic Profiling Reveals PGPR-Driven Drought Tolerance in Contrasting Brassica juncea Genotypes
inferred← citeshttps://doi.org/10.3390/microorganisms9040687openalex-snapshot
Advances in Wheat Physiology in Response to Drought and the Role of Plant Growth Promoting Rhizobacteria to Trigger Drought Tolerance
inferred← citeshttps://doi.org/10.3390/plants10020387openalex-snapshot
The Foliar Application of Rice Phyllosphere Bacteria induces Drought-Stress Tolerance in Oryza sativa (L.)
inferred← citeshttps://doi.org/10.3390/plants13152111openalex-snapshot
Comparative Effects of Water Scarcity on the Growth and Development of Two Common Bean (Phaseolus vulgaris L.) Genotypes with Different Geographic Origin (Mesoamerica/Andean)
inferred← citeshttps://doi.org/10.35196/rfm.2017.2.169-180openalex-snapshot
PROTEÍNAS G HETEROTRIMÉRICAS: SEÑALIZACIÓN DE PLANTAS EN CONDICIONES DE ESTRÉS AMBIENTAL
inferred← citeshttps://doi.org/10.4236/as.2017.810087openalex-snapshot
AtDREB2A-CA Influences Root Architecture and Increases Drought Tolerance in Transgenic Cotton
inferred← citeshttps://doi.org/10.4238/2015.october.28.29openalex-snapshot
Drought-tolerant rice germplasm developed from an Oryza officinalis transformation-competent artificial chromosome clone
inferred← citeshttps://doi.org/10.47278/journal.ijab/2022.031openalex-snapshot
Applications of Crispr/Cas System in Plants
inferred← citeshttps://doi.org/10.55730/1300-008x.2741openalex-snapshot
Sorghum WRKY transcription factor SbWRKY45 enhanced seed germination under drought stress in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.70675/a94f608dzdb40z4fdez9fd4ze62eeace298fopenalex-snapshot
Sélection de rhizobactéries pour la stimulation de la croissance et l’amélioration de la tolérance au stress hydrique du blé tendre de printemps
inferred← citeshttps://doi.org/10.7287/peerj.7211v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7211v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7211v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7211v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era (v0.2)"
inferred← citeshttps://doi.org/10.9755/ejfa.v27i1.17980openalex-snapshot
Engineering crop plants against abiotic stress: Current achievements and prospects
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
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