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Revisiting the Role of Plant Transcription Factors in the Battle against Abiotic Stress
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9783527632930.ch20openalex-snapshot
Transcription Factors: Improving Abiotic Stress Tolerance in Plants
inferredcites →https://doi.org/10.1002/9783527675265.ch23openalex-snapshot
Role of Transcription Factors in Abiotic Stress Tolerance in Crop Plants
inferredcites →https://doi.org/10.1002/iub.1040openalex-snapshot
From protein interaction networks to novel therapeutic strategies
inferredcites →https://doi.org/10.1007/s00122-016-2794-zopenalex-snapshot
Transcription factors involved in drought tolerance and their possible role in developing drought tolerant cultivars with emphasis on wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.1007/s00299-014-1636-1openalex-snapshot
Overexpression of Arabidopsis MYB96 confers drought resistance in Camelina sativa via cuticular wax accumulation
inferredcites →https://doi.org/10.1007/s00299-014-1662-zopenalex-snapshot
The abiotic stress-responsive NAC-type transcription factor SlNAC4 regulates salt and drought tolerance and stress-related genes in tomato (Solanum lycopersicum)
inferredcites →https://doi.org/10.1007/s00299-015-1779-8openalex-snapshot
Molecular characterization of the basic helix-loop-helix (bHLH) genes that are differentially expressed and induced by iron deficiency in Populus
inferredcites →https://doi.org/10.1007/s00299-015-1787-8openalex-snapshot
Activated expression of AtWRKY53 negatively regulates drought tolerance by mediating stomatal movement
inferredcites →https://doi.org/10.1007/s00299-015-1907-5openalex-snapshot
CarNAC4, a NAC-type chickpea transcription factor conferring enhanced drought and salt stress tolerances in Arabidopsis
inferredcites →https://doi.org/10.1007/s00299-017-2224-yopenalex-snapshot
Overexpression of a predominantly root-expressed NAC transcription factor in wheat roots enhances root length, biomass and drought tolerance
inferredcites →https://doi.org/10.1007/s00425-011-1375-2openalex-snapshot
Arabidopsis thaliana WRKY25, WRKY26, and WRKY33 coordinate induction of plant thermotolerance
inferredcites →https://doi.org/10.1007/s00425-013-1944-7openalex-snapshot
Molecular characterization of cold-responsive basic helix-loop-helix transcription factors MabHLHs that interact with MaICE1 in banana fruit
inferredcites →https://doi.org/10.1007/s00425-016-2489-3openalex-snapshot
The Antirrhinum AmDEL gene enhances flavonoids accumulation and salt and drought tolerance in transgenic Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-016-2609-0openalex-snapshot
Arabidopsis AtNAP functions as a negative regulator via repression of AREB1 in salt stress response
inferredcites →https://doi.org/10.1007/s00425-017-2704-xopenalex-snapshot
ABP9, a maize bZIP transcription factor, enhances tolerance to salt and drought in transgenic cotton
inferredcites →https://doi.org/10.1007/s00425-017-2766-9openalex-snapshot
The maize WRKY transcription factor ZmWRKY17 negatively regulates salt stress tolerance in transgenic Arabidopsis plants
inferredcites →https://doi.org/10.1007/s00709-012-0417-3openalex-snapshot
Cloning and molecular characterization of a putative bZIP transcription factor VvbZIP23 from Vitis vinifera
inferredcites →https://doi.org/10.1007/s00709-015-0920-4openalex-snapshot
Abscisic-acid-dependent basic leucine zipper (bZIP) transcription factors in plant abiotic stress
inferredcites →https://doi.org/10.1007/s00709-016-0991-xopenalex-snapshot
Banana NAC transcription factor MusaNAC042 is positively associated with drought and salinity tolerance
inferredcites →https://doi.org/10.1007/s10126-014-9582-zopenalex-snapshot
A Dehydration-Responsive Element Binding (DREB) Transcription Factor from the Succulent Halophyte Salicornia brachiata Enhances Abiotic Stress Tolerance in Transgenic Tobacco
inferredcites →https://doi.org/10.1007/s10142-014-0394-zopenalex-snapshot
ABI-like transcription factor gene TaABL1 from wheat improves multiple abiotic stress tolerances in transgenic plants
inferredcites →https://doi.org/10.1007/s10265-011-0448-4openalex-snapshot
The Arabidopsis AtbZIP1 transcription factor is a positive regulator of plant tolerance to salt, osmotic and drought stresses
inferredcites →https://doi.org/10.1007/s10265-016-0833-0openalex-snapshot
Arabidopsis ATAF1 enhances the tolerance to salt stress and ABA in transgenic rice
inferredcites →https://doi.org/10.1007/s10265-016-0857-5openalex-snapshot
A R2R3-MYB transcription factor gene in common wheat (namely TaMYBsm1) involved in enhancement of drought tolerance in transgenic Arabidopsis
inferredcites →https://doi.org/10.1007/s11032-015-0374-6openalex-snapshot
EcbZIP60, a basic leucine zipper transcription factor from Eleusine coracana L. improves abiotic stress tolerance in tobacco by activating unfolded protein response pathway
inferredcites →https://doi.org/10.1007/s11033-010-0664-3openalex-snapshot
Abscisic acid response element binding factor 1 is required for establishment of Arabidopsis seedlings during winter
inferredcites →https://doi.org/10.1007/s11033-012-1550-yopenalex-snapshot
Over-expression of TaMYB33 encoding a novel wheat MYB transcription factor increases salt and drought tolerance in Arabidopsis
inferredcites →https://doi.org/10.1007/s11033-012-2481-3openalex-snapshot
Isolation and functional characterization of a salt responsive transcriptional factor, LrbZIP from lotus root (Nelumbo nucifera Gaertn)
inferredcites →https://doi.org/10.1007/s11033-014-3695-3openalex-snapshot
Overexpression of AtDREB1D transcription factor improves drought tolerance in soybean
inferredcites →https://doi.org/10.1007/s11033-016-4042-7openalex-snapshot
A R2R3-MYB transcription factor from Lablab purpureus induced by drought increases tolerance to abiotic stress in Arabidopsis
inferredcites →https://doi.org/10.1007/s11103-006-9119-6openalex-snapshot
Interaction network of proteins associated with abiotic stress response and development in wheat
inferredcites →https://doi.org/10.1007/s11103-010-9711-7openalex-snapshot
Functional characterization of four APETALA2-family genes (RAP2.6, RAP2.6L, DREB19 and DREB26) in Arabidopsis
inferredcites →https://doi.org/10.1007/s11103-012-9941-yopenalex-snapshot
OsWRKY30 is activated by MAP kinases to confer drought tolerance in rice
inferredcites →https://doi.org/10.1007/s11103-013-0115-3openalex-snapshot
OsbZIP71, a bZIP transcription factor, confers salinity and drought tolerance in rice
inferredcites →https://doi.org/10.1007/s11103-015-0329-7openalex-snapshot
The rice transcription factor OsWRKY47 is a positive regulator of the response to water deficit stress
inferredcites →https://doi.org/10.1007/s11103-015-0378-yopenalex-snapshot
Ectopic expression of a hot pepper bZIP-like transcription factor in potato enhances drought tolerance without decreasing tuber yield
inferredcites →https://doi.org/10.1007/s11103-015-0427-6openalex-snapshot
Molecular interactions of the γ-clade homeodomain-leucine zipper class I transcription factors during the wheat response to water deficit
inferredcites →https://doi.org/10.1007/s11103-016-0567-3openalex-snapshot
Arabidopsis ANAC069 binds to C[A/G]CG[T/G] sequences to negatively regulate salt and osmotic stress tolerance
inferredcites →https://doi.org/10.1007/s11103-017-0624-6openalex-snapshot
The function of OsbHLH068 is partially redundant with its homolog, AtbHLH112, in the regulation of the salt stress response but has opposite functions to control flowering in Arabidopsis
inferredcites →https://doi.org/10.1007/s11103-017-0643-3openalex-snapshot
The Glycine soja NAC transcription factor GsNAC019 mediates the regulation of plant alkaline tolerance and ABA sensitivity
inferredcites →https://doi.org/10.1007/s11105-012-0481-zopenalex-snapshot
AtMYB14 Regulates Cold Tolerance in Arabidopsis
inferredcites →https://doi.org/10.1007/s11240-013-0375-2openalex-snapshot
Expression of SbSNAC1, a NAC transcription factor from sorghum, confers drought tolerance to transgenic Arabidopsis
inferredcites →https://doi.org/10.1007/s11240-015-0932-yopenalex-snapshot
MpMYBS3 as a crucial transcription factor of cold signaling confers the cold tolerance of banana
inferredcites →https://doi.org/10.1007/s11248-012-9645-8openalex-snapshot
Co-expression of AtbHLH17 and AtWRKY28 confers resistance to abiotic stress in Arabidopsis
inferredcites →https://doi.org/10.1007/s11816-015-0383-2openalex-snapshot
Functional analysis of a cold-responsive rice WRKY gene, OsWRKY71
inferredcites →https://doi.org/10.1007/s12374-014-0407-4openalex-snapshot
Over-expression of SlWRKY39 leads to enhanced resistance to multiple stress factors in tomato
inferredcites →https://doi.org/10.1016/0092-8674(89)90682-xopenalex-snapshot
A new DNA binding and dimerization motif in immunoglobulin enhancer binding, daughterless, MyoD, and myc proteins
inferredcites →https://doi.org/10.1016/j.bbagrm.2011.09.002openalex-snapshot
The role of WRKY transcription factors in plant abiotic stresses
inferredcites →https://doi.org/10.1016/j.bbagrm.2015.12.008openalex-snapshot
Rice phytochrome-interacting factor protein OsPIF14 represses OsDREB1B gene expression through an extended N-box and interacts preferentially with the active form of phytochrome B
inferredcites →https://doi.org/10.1016/j.bbrc.2006.11.041openalex-snapshot
A protective role for the polyamine spermine against drought stress in Arabidopsis
inferredcites →https://doi.org/10.1016/j.bbrc.2014.05.139openalex-snapshot
A novel bHLH transcription factor PebHLH35 from Populus euphratica confers drought tolerance through regulating stomatal development, photosynthesis and growth in Arabidopsis
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.bbrc.2016.04.071openalex-snapshot
The wheat transcription factor, TabHLH39, improves tolerance to multiple abiotic stressors in transgenic plants
inferredcites →https://doi.org/10.1016/j.bbrc.2016.12.064openalex-snapshot
The role of ZmWRKY4 in regulating maize antioxidant defense under cadmium stress
inferredcites →https://doi.org/10.1016/j.bbrc.2017.06.025openalex-snapshot
The Medicago truncatula R2R3-MYB transcription factor gene MtMYBS1 enhances salinity tolerance when constitutively expressed in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.bbrc.2017.07.029openalex-snapshot
Overexpression of a novel MYB-related transcription factor, OsMYBR1 , confers improved drought tolerance and decreased ABA sensitivity in rice
inferredcites →https://doi.org/10.1016/j.bbrc.2017.07.150openalex-snapshot
The wheat salinity-induced R2R3-MYB transcription factor TaSIM confers salt stress tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.cell.2015.01.046openalex-snapshot
COLD1 Confers Chilling Tolerance in Rice
inferredcites →https://doi.org/10.1016/j.envexpbot.2015.10.007openalex-snapshot
Overexpression of MtWRKY76 increases both salt and drought tolerance in Medicago truncatula
inferredcites →https://doi.org/10.1016/j.febslet.2013.07.045openalex-snapshot
ABA‐insensitive (ABI) 4 and ABI5 synergistically regulate DGAT1 expression in Arabidopsis seedlings under stress
inferredcites →https://doi.org/10.1016/j.gene.2016.04.028openalex-snapshot
The Miscanthus NAC transcription factor MlNAC9 enhances abiotic stress tolerance in transgenic Arabidopsis
inferredcites →https://doi.org/10.1016/j.jplph.2014.09.018openalex-snapshot
An R2R3-MYB gene, LeAN2, positively regulated the thermo-tolerance in transgenic tomato
inferredcites →https://doi.org/10.1016/j.jplph.2016.06.024openalex-snapshot
Overexpression of a novel NAC-type tomato transcription factor, SlNAM1, enhances the chilling stress tolerance of transgenic tobacco
inferredcites →https://doi.org/10.1016/j.jplph.2017.04.007openalex-snapshot
Overexpression of a tartary buckwheat R2R3-MYB transcription factor gene, FtMYB9, enhances tolerance to drought and salt stresses in transgenic Arabidopsis
inferredcites →https://doi.org/10.1016/j.jplph.2017.05.002openalex-snapshot
The Reaumuria trigyna transcription factor RtWRKY1 confers tolerance to salt stress in transgenic Arabidopsis
inferredcites →https://doi.org/10.1016/j.jplph.2017.12.009openalex-snapshot
An apple NAC transcription factor negatively regulates cold tolerance via CBF-dependent pathway
inferredcites →https://doi.org/10.1016/j.jplph.2017.12.015openalex-snapshot
Transcriptional regulation of chickpea ferritin CaFer1 influences its role in iron homeostasis and stress response
inferredcites →https://doi.org/10.1016/j.molp.2014.11.022openalex-snapshot
Regulation of MYB and bHLH Transcription Factors: A Glance at the Protein Level
inferredcites →https://doi.org/10.1016/j.molp.2015.03.012openalex-snapshot
MYB Transcription Factors as Regulators of Phenylpropanoid Metabolism in Plants
inferredcites →https://doi.org/10.1016/j.pbi.2005.05.014openalex-snapshot
Functions of the respiratory burst oxidase in biotic interactions, abiotic stress and development
inferredcites →https://doi.org/10.1016/j.pbi.2011.02.001openalex-snapshot
Hormone balance and abiotic stress tolerance in crop plants
inferredcites →https://doi.org/10.1016/j.plantsci.2014.08.001openalex-snapshot
Tomato WRKY transcriptional factor SlDRW1 is required for disease resistance against Botrytis cinerea and tolerance to oxidative stress
inferredcites →https://doi.org/10.1016/j.plantsci.2015.03.023openalex-snapshot
The R2R3-type MYB gene OsMYB91 has a function in coordinating plant growth and salt stress tolerance in rice
inferredcites →https://doi.org/10.1016/j.plaphy.2014.02.022openalex-snapshot
Overexpression of a stress-responsive MYB transcription factor of Poncirus trifoliata confers enhanced dehydration tolerance and increases polyamine biosynthesis
inferredcites →https://doi.org/10.1016/j.plaphy.2015.08.013openalex-snapshot
Wheat NAC transcription factor TaNAC29 is involved in response to salt stress
inferredcites →https://doi.org/10.1016/j.plaphy.2016.03.023openalex-snapshot
TabHLH1, a bHLH-type transcription factor gene in wheat, improves plant tolerance to Pi and N deprivation via regulation of nutrient transporter gene transcription and ROS homeostasis
inferredcites →https://doi.org/10.1016/j.plaphy.2016.04.018openalex-snapshot
ZmNAC55, a maize stress-responsive NAC transcription factor, confers drought resistance in transgenic Arabidopsis
inferredcites →https://doi.org/10.1016/j.plaphy.2016.09.020openalex-snapshot
Overexpressing Arabidopsis ABF3 increases tolerance to multiple abiotic stresses and reduces leaf size in alfalfa
inferredcites →https://doi.org/10.1016/j.plaphy.2017.01.015openalex-snapshot
PacMYBA, a sweet cherry R2R3-MYB transcription factor, is a positive regulator of salt stress tolerance and pathogen resistance
inferredcites →https://doi.org/10.1016/j.plaphy.2017.02.018openalex-snapshot
A salt-stress-regulator from the Poplar R2R3 MYB family integrates the regulation of lateral root emergence and ABA signaling to mediate salt stress tolerance in Arabidopsis
inferredcites →https://doi.org/10.1016/j.plaphy.2018.01.008openalex-snapshot
Overexpression of a wheat (Triticum aestivum L.) bZIP transcription factor gene, TabZIP6, decreased the freezing tolerance of transgenic Arabidopsis seedlings by down-regulating the expression of CBFs
inferredcites →https://doi.org/10.1016/j.plaphy.2018.01.028openalex-snapshot
Overexpression of Fagopyrum tataricum FtbHLH2 enhances tolerance to cold stress in transgenic Arabidopsis
inferredcites →https://doi.org/10.1016/j.tplants.2010.02.006openalex-snapshot
WRKY transcription factors
inferredcites →https://doi.org/10.1016/j.tplants.2010.06.005openalex-snapshot
MYB transcription factors in Arabidopsis
inferredcites →https://doi.org/10.1016/j.tplants.2012.02.004openalex-snapshot
NAC proteins: regulation and role in stress tolerance
inferredcites →https://doi.org/10.1016/j.tplants.2014.09.001openalex-snapshot
Salt bladders: do they matter?
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/s1360-1385(00)01600-9openalex-snapshot
The WRKY superfamily of plant transcription factors
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(02)00289-3openalex-snapshot
Transcription factors in plant defense and stress responses
inferredcites →https://doi.org/10.1038/415977aopenalex-snapshot
MAP kinase signalling cascade in Arabidopsis innate immunity
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/10.1038/nature13593openalex-snapshot
OSCA1 mediates osmotic-stress-evoked Ca2+ increases vital for osmosensing in Arabidopsis
inferredcites →https://doi.org/10.1038/nbt.3715openalex-snapshot
Genome-scale deletion screening of human long non-coding RNAs using a paired-guide RNA CRISPR–Cas9 library
inferredcites →https://doi.org/10.1038/nplants.2016.13openalex-snapshot
Arabidopsis NAC transcription factor JUB1 regulates GA/BR metabolism and signalling
inferredcites →https://doi.org/10.1038/nrm2256openalex-snapshot
ROS as signalling molecules: mechanisms that generate specificity in ROS homeostasis
inferredcites →https://doi.org/10.1038/s41598-017-05170-xopenalex-snapshot
Chrysanthemum WRKY gene DgWRKY5 enhances tolerance to salt stress in transgenic chrysanthemum
inferredcites →https://doi.org/10.1038/s41598-017-06706-xopenalex-snapshot
The bHLH transcription factor CgbHLH001 is a potential interaction partner of CDPK in halophyte Chenopodium glaucum
inferredcites →https://doi.org/10.1038/sj.emboj.7601206openalex-snapshot
Combinatorial control of Arabidopsis proline dehydrogenase transcription by specific heterodimerisation of bZIP transcription factors
inferredcites →https://doi.org/10.1038/srep06694openalex-snapshot
A bHLH transcription factor regulates iron intake under Fe deficiency in chrysanthemum
inferredcites →https://doi.org/10.1038/srep20366openalex-snapshot
The nuclear protein GmbZIP110 has transcription activation activity and plays important roles in the response to salinity stress in soybean
inferredcites →https://doi.org/10.1038/srep23632openalex-snapshot
Banana fruit VQ motif-containing protein5 represses cold-responsive transcription factor MaWRKY26 involved in the regulation of JA biosynthetic genes
inferredcites →https://doi.org/10.1038/srep27021openalex-snapshot
Global gene expression analysis using RNA-seq uncovered a new role for SR1/CAMTA3 transcription factor in salt stress
inferredcites →https://doi.org/10.1038/srep35040openalex-snapshot
GhABF2, a bZIP transcription factor, confers drought and salinity tolerance in cotton (Gossypium hirsutum L.)
inferredcites →https://doi.org/10.1038/srep37943openalex-snapshot
Negative feedback regulation of ABA biosynthesis in peanut (Arachis hypogaea): a transcription factor complex inhibits AhNCED1 expression during water stress
inferredcites →https://doi.org/10.1073/pnas.1118876109openalex-snapshot
FLOWERING BHLH transcriptional activators control expression of the photoperiodic flowering regulator CONSTANS in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1804233115openalex-snapshot
MYB30 links ROS signaling, root cell elongation, and plant immune responses
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.86.18.7092openalex-snapshot
Lc, a member of the maize R gene family responsible for tissue-specific anthocyanin production, encodes a protein similar to transcriptional activators and contains the myc-homology region.
inferredcites →https://doi.org/10.1080/15592324.2017.1316442openalex-snapshot
The rice transcription factors OsICE confer enhanced cold tolerance in transgenic Arabidopsis
inferredcites →https://doi.org/10.1089/dna.2016.3251openalex-snapshot
A Ramie bZIP Transcription Factor BnbZIP2 Is Involved in Drought, Salt, and Heavy Metal Stress Response
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/mct205openalex-snapshot
Learning from halophytes: physiological basis and strategies to improve abiotic stress tolerance in crops
inferredcites →https://doi.org/10.1093/aob/mcu267openalex-snapshot
Plant salt tolerance: adaptations in halophytes
inferredcites →https://doi.org/10.1093/jxb/err216openalex-snapshot
A bHLH transcription factor, DvIVS, is involved in regulation of anthocyanin synthesis in dahlia (Dahlia variabilis)
inferredcites →https://doi.org/10.1093/jxb/ert298openalex-snapshot
WRKY76 is a rice transcriptional repressor playing opposite roles in blast disease resistance and cold stress tolerance
inferredcites →https://doi.org/10.1093/jxb/erv172openalex-snapshot
Interactions between cytokinin signalling and abiotic stress responses
inferredcites →https://doi.org/10.1093/jxb/erv312openalex-snapshot
Salt-induced transcription factor MYB74 is regulated by the RNA-directed DNA methylation pathway in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erv386openalex-snapshot
A stress-responsive NAC transcription factor SNAC3 confers heat and drought tolerance through modulation of reactive oxygen species in rice
inferredcites →https://doi.org/10.1093/jxb/erw122openalex-snapshot
Expression ofVitis amurensis NAC26in Arabidopsis enhances drought tolerance by modulating jasmonic acid synthesis
inferredcites →https://doi.org/10.1093/jxb/erw298openalex-snapshot
Identification and characterization of wheat drought-responsive MYB transcription factors involved in the regulation of cuticle biosynthesis
inferredcites →https://doi.org/10.1093/jxb/erx210openalex-snapshot
Chicory R2R3-MYB transcription factors CiMYB5 and CiMYB3 regulate fructan 1-exohydrolase expression in response to abiotic stress and hormonal cues
inferredcites →https://doi.org/10.1093/jxb/erx260openalex-snapshot
The OsABF1 transcription factor improves drought tolerance by activating the transcription of COR413-TM1 in rice
inferredcites →https://doi.org/10.1093/jxb/ery065openalex-snapshot
The transcription factor CsbHLH18 of sweet orange functions in modulation of cold tolerance and homeostasis of reactive oxygen species by regulating the antioxidant gene
inferredcites →https://doi.org/10.1093/mp/sss089openalex-snapshot
Requirement and Functional Redundancy of Ib Subgroup bHLH Proteins for Iron Deficiency Responses and Uptake in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/nar/gkf591openalex-snapshot
Translational fusions with the engrailed repressor domain efficiently convert plant transcription factors into dominant-negative functions
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/pct204openalex-snapshot
The NAC Family Transcription Factor OsNAP Confers Abiotic Stress Response Through the ABA Pathway
inferredcites →https://doi.org/10.1093/pcp/pcw029openalex-snapshot
Genome-Wide Identification, Evolution and Functional Divergence of MYB Transcription Factors in Chinese White Pear (Pyrus bretschneideri)
inferredcites →https://doi.org/10.1093/pcp/pcw084openalex-snapshot
Ectopic Expression of DREB Transcription Factor, AtDREB1A, Confers Tolerance to Drought in TransgenicSalvia miltiorrhiza
inferredcites →https://doi.org/10.1093/pcp/pcw118openalex-snapshot
Overexpression of a Novel NAC Domain-Containing Transcription Factor Gene (AaNAC1) Enhances the Content of Artemisinin and Increases Tolerance to Drought andBotrytis cinereainArtemisia annua
inferredcites →https://doi.org/10.1093/pcp/pcx111openalex-snapshot
Drought Tolerance Conferred in Soybean (Glycine max. L) by GmMYB84, a Novel R2R3-MYB Transcription Factor
inferredcites →https://doi.org/10.1093/pcp/pcx201openalex-snapshot
WRKY71 Acts Antagonistically Against Salt-Delayed Flowering in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcy030openalex-snapshot
CsATAF1 Positively Regulates Drought Stress Tolerance by an ABA-Dependent Pathway and by Promoting ROS Scavenging in Cucumber
inferredcites →https://doi.org/10.1093/treephys/tpv139openalex-snapshot
A bHLH gene from Tamarix hispida improves abiotic stress tolerance by enhancing osmotic potential and decreasing reactive oxygen species accumulation
inferredcites →https://doi.org/10.1104/pp.003707openalex-snapshot
Significance of the Expression of the CER6 Condensing Enzyme for Cuticular Wax Production in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.033431openalex-snapshot
When Defense Pathways Collide. The Response of Arabidopsis to a Combination of Drought and Heat Stress
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.108.129791openalex-snapshot
Transcriptional Regulatory Networks in Response to Abiotic Stresses in Arabidopsis and Grasses
inferredcites →https://doi.org/10.1104/pp.109.144220openalex-snapshot
The MYB96 Transcription Factor Mediates Abscisic Acid Signaling during Drought Stress Response in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.112.210740openalex-snapshot
A Basic Helix-Loop-Helix Transcription Factor, PtrbHLH, of Poncirus trifoliata Confers Cold Tolerance and Modulates Peroxidase-Mediated Scavenging of Hydrogen Peroxide
inferredcites →https://doi.org/10.1104/pp.113.220855openalex-snapshot
Plant Calcium-Permeable Channels
inferredcites →https://doi.org/10.1104/pp.15.00298openalex-snapshot
The Rice High-Affinity Potassium Transporter1;1 Is Involved in Salt Tolerance and Regulated by an MYB-Type Transcription Factor
inferredcites →https://doi.org/10.1104/pp.15.00962openalex-snapshot
Salt-Related MYB1 Coordinates Abscisic Acid Biosynthesis and Signaling during Salt Stress in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.15.01827openalex-snapshot
Two bHLH Transcription Factors, bHLH34 and bHLH104, Regulate Iron Homeostasis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.16.00051openalex-snapshot
Opposing control by transcription factors MYB61 and MYB3 Increases Freezing Tolerance by relieving C-repeat Binding Factor suppression
inferredcites →https://doi.org/10.1104/pp.16.00469openalex-snapshot
Feedback Regulation of ABA Signaling and Biosynthesis by a bZIP Transcription Factor Targets Drought-Resistance-Related Genes
inferredcites →https://doi.org/10.1104/pp.16.01691openalex-snapshot
A Drought-Inducible Transcription Factor Delays Reproductive Timing in Rice
inferredcites →https://doi.org/10.1105/tpc.108.064980openalex-snapshot
The WRKY6 Transcription Factor Modulates PHOSPHATE1 Expression in Response to Low Pi Stress in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.15.00163openalex-snapshot
Crosstalk between Two bZIP Signaling Pathways Orchestrates Salt-Induced Metabolic Reprogramming in Arabidopsis Roots
inferredcites →https://doi.org/10.1105/tpc.16.00171openalex-snapshot
MODD Mediates Deactivation and Degradation of OsbZIP46 to Negatively Regulate ABA Signaling and Drought Resistance in Rice
inferredcites →https://doi.org/10.1105/tpc.17.00044openalex-snapshot
A Lipid-Anchored NAC Transcription Factor Is Translocated into the Nucleus and Activates Glyoxalase I Expression during Drought Stress
inferredcites →https://doi.org/10.1105/tpc.17.00364openalex-snapshot
Arabidopsis WRKY46, WRKY54 and WRKY70 Transcription Factors Are Involved in Brassinosteroid-Regulated Plant Growth and Drought Response
inferredcites →https://doi.org/10.1105/tpc.17.00616openalex-snapshot
OPAQUE11 Is a Central Hub of the Regulatory Network for Maize Endosperm Development and Nutrient Metabolism
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.0031-9317.2004.00388.xopenalex-snapshot
Sensor types in signal transduction pathways in plant cells responding to abiotic stressors: do they depend on stress intensity?
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.2010.04459.xopenalex-snapshot
Evolutionary and comparative analysis of MYB and bHLH plant transcription factors
inferredcites →https://doi.org/10.1111/nph.12607openalex-snapshot
b HLH 122 is important for drought and osmotic stress resistance in A rabidopsis and in the repression of ABA catabolism
inferredcites →https://doi.org/10.1111/nph.13387openalex-snapshot
Arabidopsis Atb HLH 112 regulates the expression of genes involved in abiotic stress tolerance by binding to their E‐box and GCG ‐box motifs
inferredcites →https://doi.org/10.1111/nph.14952openalex-snapshot
An atypical R2R3 MYB transcription factor increases cold hardiness by CBF ‐dependent and CBF ‐independent pathways in apple
inferredcites →https://doi.org/10.1111/pbi.12498openalex-snapshot
The tomato mutant ars1 (altered response to salt stress 1) identifies an R1‐type MYB transcription factor involved in stomatal closure under salt acclimation
inferredcites →https://doi.org/10.1111/pbi.12776openalex-snapshot
NAC transcription factor JUNGBRUNNEN 1 enhances drought tolerance in tomato
inferredcites →https://doi.org/10.1111/pce.12074openalex-snapshot
TaASR1 , a transcription factor gene in wheat, confers drought stress tolerance in transgenic tobacco
inferredcites →https://doi.org/10.1111/pce.12303openalex-snapshot
Banana fruit NAC transcription factor MaNAC 1 is a direct target of MaICE 1 and involved in cold stress through interacting with MaCBF 1
inferredcites →https://doi.org/10.1111/pce.12415openalex-snapshot
AtM yb7, a subgroup 4 R 2 R 3 M yb, negatively regulates ABA ‐induced inhibition of seed germination by blocking the expression of the bZIP transcription factor ABI 5
inferredcites →https://doi.org/10.1111/pce.12978openalex-snapshot
The small ubiquitin‐like modifier E3 ligase MdSIZ1 promotes anthocyanin accumulation by sumoylating MdMYB1 under low‐temperature conditions in apple
inferredcites →https://doi.org/10.1111/plb.12524openalex-snapshot
Both Jr WRKY 2 and Jr WRKY 7 of Juglans regia mediate responses to abiotic stresses and abscisic acid through formation of homodimers and interaction
inferredcites →https://doi.org/10.1111/ppl.12261openalex-snapshot
A novel wheat bZIP transcription factor, TabZIP60 , confers multiple abiotic stress tolerances in transgenic Arabidopsis
inferredcites →https://doi.org/10.1111/ppl.12444openalex-snapshot
A stress‐associated NAC transcription factor ( SlNAC35 ) from tomato plays a positive role in biotic and abiotic stresses
inferredcites →https://doi.org/10.1111/ppl.12467openalex-snapshot
TaZAT8, a C2H2‐ZFP type transcription factor gene in wheat, plays critical roles in mediating tolerance to Pi deprivation through regulating P acquisition, ROS homeostasis and root system establishment
inferredcites →https://doi.org/10.1111/ppl.12549openalex-snapshot
AtbHLH68 transcription factor contributes to the regulation of ABA homeostasis and drought stress tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/ppl.12651openalex-snapshot
A novel cotton WRKY gene, GhWRKY6‐like, improves salt tolerance by activating the ABA signaling pathway and scavenging of reactive oxygen species
inferredcites →https://doi.org/10.1111/tpj.12159openalex-snapshot
A rabidopsis transcription factor WRKY 8 functions antagonistically with its interacting partner VQ 9 to modulate salinity stress tolerance
inferredcites →https://doi.org/10.1111/tpj.12866openalex-snapshot
The MYB 96– HHP module integrates cold and abscisic acid signaling to activate the CBF – COR pathway in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.12879openalex-snapshot
Gm WRKY 27 interacts with Gm MYB 174 to reduce expression of Gm NAC 29 for stress tolerance in soybean plants
inferredcites →https://doi.org/10.1111/tpj.13250openalex-snapshot
MID1 plays an important role in response to drought stress during reproductive development
inferredcites →https://doi.org/10.1126/science.218.4571.443openalex-snapshot
Plant Productivity and Environment
inferredcites →https://doi.org/10.1126/science.aac6014openalex-snapshot
Mechanosensitive channel MSL8 regulates osmotic forces during pollen hydration and germination
inferredcites →https://doi.org/10.1155/2015/807560openalex-snapshot
WRKY Proteins: Signaling and Regulation of Expression during Abiotic Stress Responses
inferredcites →https://doi.org/10.1155/2015/875497openalex-snapshot
TheSsDREBTranscription Factor from the Succulent HalophyteSuaeda salsaEnhances Abiotic Stress Tolerance in Transgenic Tobacco
inferredcites →https://doi.org/10.1186/1471-2164-14-216openalex-snapshot
CAMTA 1 regulates drought responses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1186/1471-2164-15-281openalex-snapshot
Genome-wide analysis and expression profile of the bZIP transcription factor gene family in grapevine (Vitis vinifera)
inferredcites →https://doi.org/10.1186/1471-2229-13-151openalex-snapshot
The bZIP protein from Tamarix hispida, ThbZIP1, is ACGT elements binding factor that enhances abiotic stress signaling in transgenic Arabidopsis
inferredcites →https://doi.org/10.1186/1471-2229-13-192openalex-snapshot
Multiple roles of the transcription factor AtMYBR1/AtMYB44 in ABA signaling, stress responses, and leaf senescence
inferredcites →https://doi.org/10.1186/s12864-016-2576-7openalex-snapshot
Genome-wide identification of the Jatropha curcas MYB family and functional analysis of the abiotic stress responsive gene JcMYB2
inferredcites →https://doi.org/10.1186/s12864-016-2659-5openalex-snapshot
Expression of OsMYB55 in maize activates stress-responsive genes and enhances heat and drought tolerance
inferredcites →https://doi.org/10.1186/s12870-016-0897-yopenalex-snapshot
Rice NAC transcription factor ONAC095 plays opposite roles in drought and cold stress tolerance
inferredcites →https://doi.org/10.1186/s12870-017-1078-3openalex-snapshot
GaMYB85, an R2R3 MYB gene, in transgenic Arabidopsis plays an important role in drought tolerance
inferredcites →https://doi.org/10.1371/journal.pgen.1006607openalex-snapshot
The Arabidopsis bZIP11 transcription factor links low-energy signalling to auxin-mediated control of primary root growth
inferredcites →https://doi.org/10.1371/journal.pone.0065120openalex-snapshot
A Wheat WRKY Transcription Factor TaWRKY10 Confers Tolerance to Multiple Abiotic Stresses in Transgenic Tobacco
inferredcites →https://doi.org/10.1371/journal.pone.0069955openalex-snapshot
Genome Wide Analysis of the Apple MYB Transcription Factor Family Allows the Identification of MdoMYB121 Gene Confering Abiotic Stress Tolerance in Plants
inferredcites →https://doi.org/10.1371/journal.pone.0070289openalex-snapshot
Ethylene Response Factor 6 Is a Regulator of Reactive Oxygen Species Signaling in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0092913openalex-snapshot
Overexpression of OsMYB48-1, a Novel MYB-Related Transcription Factor, Enhances Drought and Salinity Tolerance in Rice
inferredcites →https://doi.org/10.1371/journal.pone.0099234openalex-snapshot
Responses of a Triple Mutant Defective in Three Iron Deficiency-Induced BASIC HELIX-LOOP-HELIX Genes of the Subgroup Ib(2) to Iron Deficiency and Salicylic Acid
inferredcites →https://doi.org/10.1371/journal.pone.0120646openalex-snapshot
GhWRKY68 Reduces Resistance to Salt and Drought in Transgenic Nicotiana benthamiana
inferredcites →https://doi.org/10.1371/journal.pone.0135667openalex-snapshot
The Wheat NAC Transcription Factor TaNAC2L Is Regulated at the Transcriptional and Post-Translational Levels and Promotes Heat Stress Tolerance in Transgenic Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0136365openalex-snapshot
Tomato R2R3-MYB Proteins SlANT1 and SlAN2: Same Protein Activity, Different Roles
inferredcites →https://doi.org/10.1371/journal.pone.0137098openalex-snapshot
Overexpression of EcbHLH57 Transcription Factor from Eleusine coracana L. in Tobacco Confers Tolerance to Salt, Oxidative and Drought Stress
inferredcites →https://doi.org/10.1371/journal.pone.0143022openalex-snapshot
The Cotton WRKY Gene GhWRKY41 Positively Regulates Salt and Drought Stress Tolerance in Transgenic Nicotiana benthamiana
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Abiotic Stress Management in Cabbage
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Molecular Networks and Signaling Pathways in Halophytes
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Calcium-dependent protein kinase 2 plays a positive role in the salt stress response in potato
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Natural variation MeMYB108 associated with tolerance to stress-induced leaf abscission linked to enhanced protection against reactive oxygen species in cassava
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Functional Genomics of Salt and Drought Stress Tolerance in the Temperate Crop Apple (Malus domestica)
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Functional Diversification and Mechanistic Insights of MYB Transcription Factors in Mediating Plant Growth and Development, Secondary Metabolism, and Stress Responses
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Molecular characterization of a RING E3 ligase SbHCI1 in sorghum under heat and abscisic acid stress
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Inroads into saline-alkaline stress response in plants: unravelling morphological, physiological, biochemical, and molecular mechanisms
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Transcriptome meta-analysis of abiotic stresses-responsive genes and identification of candidate transcription factors for broad stress tolerance in wheat
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The NAC-type transcription factor GmNAC20 improves cold, salinity tolerance, and lateral root formation in transgenic rice plants
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Genome-wide profiling of drought-tolerant Arabidopsis plants over-expressing chickpea MT1 gene reveals transcription factors implicated in stress modulation
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Genome‑wide identification of CAMTA gene family members in rice (Oryza sativa L.) and in silico study on their versatility in respect to gene expression and promoter structure
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Drought induces variation in the DNA methylation status of the barley HvDME promoter
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Ion transporters and their exploration for conferring abiotic stress tolerance in plants
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Insights into molecular and biochemical approaches of multi-stress responses to horticultural crops
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The sesame SiERF054 enhances drought resistance in Arabidopsis thaliana by modulating growth, oxidation response, and expression of stress-responsive genes
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Twenty years of mining salt tolerance genes in soybean
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Molecular switches in plant stress adaptation
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CRISPR/Cas9 for Heat Stress Tolerance in Rice: A Review
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De Novo Transcriptome Sequencing and Gene Expression Profiling of Vicia hirsuta (L.) Gray in Response to Flooding Stress
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Expressional vagaries of OsCAMTA genes under differential abiotic stresses supported with protein–protein interaction study and prediction of miRNA target sites
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Transcriptional Regulation of Biotic and Abiotic Stress Responses: Challenges and Potential Mechanism for Stress Tolerance and Chickpea Improvement
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Systematic genome-wide analysis and expression profiling of the NAC transcription factor family in Nicotiana benthamiana reveal potential regulators of salt and drought stress responses
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Peroxisomal biogenesis factor 11 as a novel target to trigger lipid biosynthesis and salt stress resistance in oleaginous Tetradesmus obliquus
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Transcriptome analysis of chickpea during heat stress unveils the signatures of long intergenic non-coding RNAs (lincRNAs) and mRNAs in the heat-QTL region
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Comparative transcriptomic analysis reveals the coordinated mechanisms of Populus × canadensis ‘Neva’ leaves in response to cadmium stress
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The transcription factor GmbHLH3 confers Cl−/salt tolerance to soybean by upregulating GmCLC1 expression for maintenance of anion homeostasis
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Metallothionein (MT1): A molecular stress marker in chickpea enhances drought and heavy metal stress adaptive efficacy in transgenic plants
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Knockout of a novel salt responsive gene SlABIG1 enhance salinity tolerance in tomato
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A novel root-specific Di19 transcription factor from Glycine max compromises drought tolerance in Arabidopsis thaliana through suppression of auxin-related pathway
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105097openalex-snapshot
Integrated transcriptome and physiological analysis of rice seedlings reveals different cadmium response mechanisms between indica and japonica varieties
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Molecular Mechanism that Underlies Cotton Response To Salt and Drought Stress Revealed By Complementary Transcriptomic And Itraq Analyses
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Analysis of transcriptomic and metabolomic differences revealed the mechanism underlying the tobacco response to low-temperature
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Selenium nanoparticles induced variations in growth, morphology, anatomy, biochemistry, gene expression, and epigenetic DNA methylation in Capsicum annuum; an in vitro study
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Plant tolerance to salinity stress: Regulating transcription factors and their functional role in the cellular transcriptional network
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Uptake and toxicity of heavy metals: The protective frontiers of metal binding proteins
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SlWRKY80 and SlWRKY81 synergistically regulate the autophagy gene SlATG13b to actively resist saline-alkali stress in tomato
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.04.124openalex-snapshot
Genome wide identification, characterization and expression analysis of HD-ZIP gene family in Cucumis sativus L. under biotic and various abiotic stresses
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The SmWRKY12-SmRAP2–7-SmEXPA13 module in Salix matsudana koidz enhances plant tolerance to drought stress
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Integrative miRNA-mRNA analysis reveals key regulatory mechanisms of the miR156g-PagSPL1B module in poplar drought tolerance
inferred← citeshttps://doi.org/10.1016/j.jare.2025.03.040openalex-snapshot
MdHMGB15-MdXERICO-MdNRP module mediates salt tolerance of apple by regulating the expression of salt stress-related genes
inferred← citeshttps://doi.org/10.1016/j.jece.2021.105198openalex-snapshot
Compounds of emerging concern as new plant stressors linked to water reuse and biosolid application in agriculture
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2022.129121openalex-snapshot
Transcription factor ANAC004 enhances Cd tolerance in Arabidopsis thaliana by regulating cell wall fixation, translocation and vacuolar detoxification of Cd, ABA accumulation and antioxidant capacity
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.134245openalex-snapshot
Physiological and molecular mechanisms of ZnO quantum dots mitigating cadmium stress in Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.1016/j.jia.2022.07.022openalex-snapshot
A novel long non-coding RNA, DIR, increases drought tolerance in cassava by modifying stress-related gene expression
inferred← citeshttps://doi.org/10.1016/j.jia.2026.02.032openalex-snapshot
Grape DNA methyltransferase VvMET2b overexpression increases genome-wide methylation and enhances seed salt tolerance
inferred← citeshttps://doi.org/10.1016/j.jplph.2022.153635openalex-snapshot
LpNAC6 reversely regulates the alkali tolerance and drought tolerance of Lilium pumilum
inferred← citeshttps://doi.org/10.1016/j.molp.2019.10.012openalex-snapshot
Genetic Contribution of Paleopolyploidy to Adaptive Evolution in Angiosperms
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High-affinity potassium transporter from a mangrove tree Avicennia officinalis increases salinity tolerance of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112061openalex-snapshot
Overexpression of a plasmalemma Na+/H+ antiporter from the halophyte Nitraria sibirica enhances the salt tolerance of transgenic poplar
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109390openalex-snapshot
Genomic characterization of the NAC transcription factors in carnation and function analysis of DcNAC41 involved in thermotolerance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109759openalex-snapshot
Whole plant transpiration responses of common bean (Phaseolus vulgaris L.) to drying soil: Water channels and transcription factors
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111034openalex-snapshot
Comprehensive analysis of AP2/ERFs reveals their functional divergence in safflower flavonoid biosynthesis and stress response
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111117openalex-snapshot
Integrated transcriptomic and metabolomic analyses reveal hormone-mediated crosstalk during potato virus Y and potato spindle tuber viroid co-infection
inferred← citeshttps://doi.org/10.1016/j.plgene.2020.100257openalex-snapshot
Genome-wide identification and characterization of the bZIP gene family in potato (Solanum tuberosum)
inferred← citeshttps://doi.org/10.1016/j.plgene.2021.100315openalex-snapshot
Biotechnological interventions for inducing abiotic stress tolerance in crops
inferred← citeshttps://doi.org/10.1016/j.scienta.2021.110260openalex-snapshot
Piriformospora indica affect drought tolerance by regulation of genes expression and some morphophysiological parameters in tomato (Solanum lycopersicum L.)
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113525openalex-snapshot
PbERF2-like interacts with PbNPR1 while enhancing the resistance of pear to Alternaria alternata
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2018.11.472openalex-snapshot
Signalling molecules responsive to ozone-induced oxidative stress in Salvia officinalis
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.161751openalex-snapshot
Effects of cadmium on transcription, physiology, and ultrastructure of two tobacco cultivars
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100252openalex-snapshot
MYB transcription factor: A new weapon for biotic stress tolerance in plants
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100409openalex-snapshot
Transcription factors-golden keys to modulate the plant metabolism to develop salinity tolerance
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100447openalex-snapshot
Biogenesis to functional significance of microRNAs under drought stress in rice: Recent advances and future perspectives
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100516openalex-snapshot
Understanding abiotic stress tolerance mechanisms in non-food grass species through omics approaches
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.102039openalex-snapshot
A regulatory circuit between AGL103 and TCPs balances growth and stress tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c08261openalex-snapshot
Allelochemical from Leaves of Juglans mandshurica Maxim. And Its Transcriptomic Effects in Plants
inferred← citeshttps://doi.org/10.1038/s41598-021-03735-5openalex-snapshot
Comparative de novo transcriptome analysis identifies salinity stress responsive genes and metabolic pathways in sugarcane and its wild relative Erianthus arundinaceus [Retzius] Jeswiet
inferred← citeshttps://doi.org/10.1038/s41598-026-44868-9openalex-snapshot
Expression profiles of transcription factors and aquaporins suggest putative roles in rubber biosynthesis regulation and drought stress adaptation in guayule
inferred← citeshttps://doi.org/10.1042/bcj20190159openalex-snapshot
The signalling role of ROS in the regulation of seed germination and dormancy
inferred← citeshttps://doi.org/10.1071/fp25104openalex-snapshot
Dehydration-Responsive Element-Binding (DREB) transcription factors: a key to enhancing plant tolerance against abiotic stresses
inferred← citeshttps://doi.org/10.1080/07388551.2022.2047880openalex-snapshot
Deciphering the role of miRNA in reprogramming plant responses to drought stress
inferred← citeshttps://doi.org/10.1080/07391102.2021.1894980openalex-snapshot
Evolution and identification of DREB transcription factors in the wheat genome: modeling, docking and simulation of DREB proteins associated with salt stress
inferred← citeshttps://doi.org/10.1080/13102818.2022.2155570openalex-snapshot
Systematic identification and characterization of the soybean ( Glycine max ) B-box transcription factor family
inferred← citeshttps://doi.org/10.1093/jxb/erac194openalex-snapshot
Zinc Finger-Homeodomain and Mini Zinc Finger proteins are key players in plant growth and responses to environmental stresses
inferred← citeshttps://doi.org/10.1093/jxb/erz467openalex-snapshot
Combining phenotype, genotype and environment to uncover genetic components underlying water use efficiency in Persian walnut
inferred← citeshttps://doi.org/10.1093/plphys/kiab097openalex-snapshot
Ozone responses in Arabidopsis: beyond stomatal conductance
inferred← citeshttps://doi.org/10.1093/plphys/kiaf256openalex-snapshot
The transcription factor REM16a promotes flowering time in soybean by activating flowering-related genes
inferred← citeshttps://doi.org/10.1093/treephys/tpac107openalex-snapshot
Basic helix-loop-helix transcription factor PxbHLH02 enhances drought tolerance in Populus (Populus simonii × P. nigra)
inferred← citeshttps://doi.org/10.1094/phyto-01-23-0002-vopenalex-snapshot
CRISPR/Cas, Multiomics, and RNA Interference in Virus Disease Management
inferred← citeshttps://doi.org/10.1101/2021.09.03.458816openalex-snapshot
Evolution and functional dynamics of dehydrins in model Brachypodium grasses
inferred← citeshttps://doi.org/10.1101/2022.09.23.509270openalex-snapshot
Whole Plant Transpiration Responses of Common Bean ( Phaseolus vulgaris L.) to Drying Soil: Water Channels and Transcription Factors
inferred← citeshttps://doi.org/10.1101/2022.10.03.510673openalex-snapshot
Integrative multispecies omics reveals a hierarchy of cold-responsive regulatory network launched by circadian components in rosids
inferred← citeshttps://doi.org/10.1101/2023.02.15.528631openalex-snapshot
Genome-wide identification and characterization of major RNAi genes highlighting their regulatory factors in Cowpea ( Vigna unguiculata (L.) Walp.)
inferred← citeshttps://doi.org/10.1101/558064openalex-snapshot
Role of DNA methylation dynamics in desiccation and salinity stress responses in rice cultivars
inferred← citeshttps://doi.org/10.1111/jse.12999openalex-snapshot
Local adaptation and demographic history of vulnerable conifer Cephalotaxus oliveri in southern China
inferred← citeshttps://doi.org/10.1111/pbi.70599openalex-snapshot
Gallic Acid‐Responsive microRNAs Reprogram Lignification During Drought Acclimation Process in Spearmint
inferred← citeshttps://doi.org/10.1111/pce.14597openalex-snapshot
Pepper homeobox abscisic acid signalling‐related transcription factor 1, CaHAT1, plays a positive role in drought response
inferred← citeshttps://doi.org/10.1111/ppl.13308openalex-snapshot
Drought responsiveness in black pepper ( Piper nigrum L.): Genes associated and development of a web‐genomic resource
inferred← citeshttps://doi.org/10.1111/ppl.13451openalex-snapshot
Current status of microRNA ‐mediated regulation of drought stress responses in cereals
inferred← citeshttps://doi.org/10.1111/ppl.13892openalex-snapshot
Integrative multi‐omics analysis of three early diverged rosid species reveals an ancient hierarchical cold‐responsive regulatory network
inferred← citeshttps://doi.org/10.1111/ppl.14366openalex-snapshot
Transcription factors as molecular switches regulating plant responses to drought stress
inferred← citeshttps://doi.org/10.1111/ppl.14476openalex-snapshot
Multi‐omics integration analysis reveals the molecular mechanisms of drought adaptation in homologous tetraploid alfalfa( Medicago sativa ‘Xinjiang‐Daye’)
inferred← citeshttps://doi.org/10.1111/ppl.14547openalex-snapshot
Transcriptomics Combined with Physiology and Metabolomics Reveals the Mechanism of Tolerance to Lead Toxicity in Maize Seedling
inferred← citeshttps://doi.org/10.1111/ppl.70159openalex-snapshot
Role of pepper bZIP transcription factor CaADBZ1 in abscisic acid signalling and drought stress response
inferred← citeshttps://doi.org/10.1111/ppl.70501openalex-snapshot
Transcriptional Dynamics of Tomato Plants Under Combined Heat and Salt Stress
inferred← citeshttps://doi.org/10.1111/ppl.70537openalex-snapshot
Genome‐Wide Identification and Characterization of Circular RNAs Involved in High Night Temperature Stress at the Filling Stage of Rice
inferred← citeshttps://doi.org/10.1111/ppl.71052openalex-snapshot
Deciphering the Molecular Interplay Between Wheat and Puccinia striiformis f. sp. Tritici : Mechanisms of Interaction and Resistance Strategies
inferred← citeshttps://doi.org/10.1111/tpj.70578openalex-snapshot
Comparative analysis of DREB gene family in buckwheat: the role of FtDREB02 in the delphinidin biosynthesis and drought stress response
inferred← citeshttps://doi.org/10.1134/s1021443723600186openalex-snapshot
Efficacy of Magnesium Nanoparticles in Modifying Growth, Antioxidant Activity, Nitrogen Status, and Expression of WRKY1 and bZIP Transcription Factors in Pepper (Capsicum annuum); an In Vitro Biological Assessment
inferred← citeshttps://doi.org/10.1155/2019/6216304openalex-snapshot
Genetic Modification for Wheat Improvement: From Transgenesis to Genome Editing
inferred← citeshttps://doi.org/10.1155/2023/8832406openalex-snapshot
Genome‐Wide Identification and Characterization of Major RNAi Genes Highlighting Their Associated Factors in Cowpea (Vigna unguiculata (L.) Walp.)
inferred← citeshttps://doi.org/10.1155/2024/2924953openalex-snapshot
Genome-Wide Comprehensive Identification and In Silico Characterization of Lectin Receptor-Like Kinase Gene Family in Barley (Hordeum vulgare L.)
inferred← citeshttps://doi.org/10.1186/s12284-024-00741-9openalex-snapshot
OsWRKY70 Plays Opposite Roles in Blast Resistance and Cold Stress Tolerance in Rice
inferred← citeshttps://doi.org/10.1186/s12284-025-00774-8openalex-snapshot
The OsZHD1 and OsZHD2, Two Zinc Finger Homeobox Transcription Factor, Redundantly Control Grain Size by Influencing Cell Proliferation in Rice
inferred← citeshttps://doi.org/10.1186/s12863-024-01285-zopenalex-snapshot
Genome-wide identification, characterization and expression profiles of FORMIN gene family in cotton (Gossypium Raimondii L.)
inferred← citeshttps://doi.org/10.1186/s12864-022-08618-1openalex-snapshot
Systematic analysis and expression profiles of TCP gene family in Tartary buckwheat (Fagopyrum tataricum (L.) Gaertn.) revealed the potential function of FtTCP15 and FtTCP18 in response to abiotic stress
inferred← citeshttps://doi.org/10.1186/s12864-023-09507-xopenalex-snapshot
Identification of core genes associated with different phosphorus levels in quinoa seedlings by weighted gene co-expression network analysis
inferred← citeshttps://doi.org/10.1186/s12864-025-11657-zopenalex-snapshot
Genome-wide analysis of the Tritipyrum bHLH gene family and the response of TtbHLH310 in salt-tolerance
inferred← citeshttps://doi.org/10.1186/s12864-025-11957-4openalex-snapshot
Genome-wide identification of VOZ gene family in ten cotton species and the function analysis of GhVOZ2 involved in heat stress response
inferred← citeshttps://doi.org/10.1186/s12864-025-12134-3openalex-snapshot
Black pepper knowledge base (BlackPepKB): a centralized web resource for functional genomics of black pepper (Piper nigrum L.)
inferred← citeshttps://doi.org/10.1186/s12870-019-1686-1openalex-snapshot
Transcriptome analysis reveals regulatory framework for salt and osmotic tolerance in a succulent xerophyte
inferred← citeshttps://doi.org/10.1186/s12870-020-02341-3openalex-snapshot
Transcriptome analysis of responses in Brachypodium distachyon overexpressing the BdbZIP26 transcription factor
inferred← citeshttps://doi.org/10.1186/s12870-021-03029-yopenalex-snapshot
The NAC side of the fruit: tuning of fruit development and maturation
inferred← citeshttps://doi.org/10.1186/s12870-022-03497-wopenalex-snapshot
Comparative transcriptome analysis of heat stress responses of Clematis lanuginosa and Clematis crassifolia
inferred← citeshttps://doi.org/10.1186/s12870-022-03632-7openalex-snapshot
Genome-wide characterization and identification of candidate ERF genes involved in various abiotic stress responses in sesame (Sesamum indicum L.)
inferred← citeshttps://doi.org/10.1186/s12870-022-03767-7openalex-snapshot
Transcriptome-based gene regulatory network analyses of differential cold tolerance of two tobacco cultivars
inferred← citeshttps://doi.org/10.1186/s12870-022-03846-9openalex-snapshot
BGFD: an integrated multi-omics database of barley gene families
inferred← citeshttps://doi.org/10.1186/s12870-024-04911-1openalex-snapshot
Integrative physiology and transcriptome reveal salt-tolerance differences between two licorice species: Ion transport, Casparian strip formation and flavonoids biosynthesis
inferred← citeshttps://doi.org/10.1186/s12870-024-05204-3openalex-snapshot
Appropriate mowing can promote the growth of Anabasis aphylla through the auxin metabolism pathway
inferred← citeshttps://doi.org/10.1186/s12870-024-05429-2openalex-snapshot
TaSPL6B, a member of the Squamosa promoter binding protein-like family, regulates shoot branching and florescence in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1186/s12870-024-06028-xopenalex-snapshot
The members of zinc finger-homeodomain (ZF-HD) transcription factors are associated with abiotic stresses in soybean: insights from genomics and expression analysis
inferred← citeshttps://doi.org/10.1186/s12870-025-07243-wopenalex-snapshot
Genome-wide identification of GhEDS1 gene family members in cotton and expression analysis in response to biotic and abiotic stresses
inferred← citeshttps://doi.org/10.1186/s12870-025-07471-0openalex-snapshot
Integrated transcriptome-metabolome analysis reveals oleanolic acid as a central regulator of heat stress adaptation in Rhododendron moulmainense
inferred← citeshttps://doi.org/10.1186/s12870-025-08037-wopenalex-snapshot
Identification and functional characterization of heat shock transcription factor genes in Rhododendron Delavayi under heat stress
inferred← citeshttps://doi.org/10.1186/s12870-026-08575-xopenalex-snapshot
Integrative physiological, metabolomic, and transcriptomic analyses provide new insights into potato drought stress response
inferred← citeshttps://doi.org/10.1186/s12870-026-09107-3openalex-snapshot
CmYAB2 transcriptional module regulates fruit morphogenesis in Cucumis Melo
inferred← citeshttps://doi.org/10.1186/s12915-022-01273-8openalex-snapshot
Jasmonates and Histone deacetylase 6 activate Arabidopsis genome-wide histone acetylation and methylation during the early acute stress response
inferred← citeshttps://doi.org/10.1186/s12915-024-01852-xopenalex-snapshot
Integrative systems biology of wheat susceptibility to Fusarium graminearum uncovers a conserved gene regulatory network and identifies master regulators targeted by fungal core effectors
inferred← citeshttps://doi.org/10.1371/journal.pone.0213390openalex-snapshot
Genome-wide analysis, expansion and expression of the NAC family under drought and heat stresses in bread wheat (T. aestivum L.)
inferred← citeshttps://doi.org/10.1371/journal.pone.0227020openalex-snapshot
Heterogeneous root zone salinity mitigates salt injury to Sorghum bicolor (L.) Moench in a split-root system
inferred← citeshttps://doi.org/10.1371/journal.pone.0228233openalex-snapshot
In silico identification and characterization of AGO, DCL and RDR gene families and their associated regulatory elements in sweet orange (Citrus sinensis L.)
inferred← citeshttps://doi.org/10.1371/journal.pone.0235556openalex-snapshot
Red elemental selenium nanoparticles mediated substantial variations in growth, tissue differentiation, metabolism, gene transcription, epigenetic cytosine DNA methylation, and callogenesis in bittermelon (Momordica charantia); an in vitro experiment
inferred← citeshttps://doi.org/10.1371/journal.pone.0244207openalex-snapshot
Comparative efficacy of selenate and selenium nanoparticles for improving growth, productivity, fruit quality, and postharvest longevity through modifying nutrition, metabolism, and gene expression in tomato; potential benefits and risk assessment
inferred← citeshttps://doi.org/10.1371/journal.pone.0256873openalex-snapshot
Genome-wide identification of DCL, AGO and RDR gene families and their associated functional regulatory elements analyses in banana (Musa acuminata)
inferred← citeshttps://doi.org/10.1371/journal.pone.0294233openalex-snapshot
Genome-wide identification, classification, and characterization of lectin gene superfamily in sweet orange (Citrus sinensis L.)
inferred← citeshttps://doi.org/10.1371/journal.pone.0303065openalex-snapshot
Genome-wide identification and characterization of DTX family genes highlighting their locations, functions, and regulatory factors in banana (Musa acuminata)
inferred← citeshttps://doi.org/10.1371/journal.pone.0309353openalex-snapshot
Genome-wide identification and characterization of FORMIN gene family in potato (Solanum tuberosum L.) and their expression profiles in response to drought stress condition
inferred← citeshttps://doi.org/10.1371/journal.pone.0319176openalex-snapshot
Genome-wide identification and characterization of FORMIN gene family in cotton (Gossypium hirsutum L.) and their expression profiles in response to multiple abiotic stress treatments
inferred← citeshttps://doi.org/10.18811/ijpen.v7i01.3openalex-snapshot
Plant Metallothioneins as Regulators of Environmental Stress Responses
inferred← citeshttps://doi.org/10.20900/cbgg20260008openalex-snapshot
WRKY Transcription Factors in Disease Resistance and Environmental Stress Responses in Millets
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7702056/v1openalex-snapshot
AhDTF1, a novel R2R3-MYB transcription factor, involves in drought tolerance and seed color
inferred← citeshttps://doi.org/10.2139/ssrn.5180644openalex-snapshot
Ahdtf1, a Peanut R2r3-Myb Transcription Factor, Involves in Drought Tolerance and Seed Coat Color
inferred← citeshttps://doi.org/10.21475/ajcs.23.17.12.poj3789openalex-snapshot
Computational analysis of regulation and expression of plant DNA repair genes under various abiotic stresses reveals a stochastic correlation
inferred← citeshttps://doi.org/10.21597/jist.857775openalex-snapshot
Salvia officinalis (Tıbbi Adaçayı) Bitkisinin Bazı Abiyotik Stres Faktörlerine Yanıtları
inferred← citeshttps://doi.org/10.21638/spbu03.2020.205openalex-snapshot
The role of plant antimicrobial peptides (AMPs) in response to biotic and abiotic environmental factors
inferred← citeshttps://doi.org/10.21926/obm.genet.2402230openalex-snapshot
Molecular Plant Physiology for Model Plants under Abiotic Stress Conditions
inferred← citeshttps://doi.org/10.32604/phyton.2025.066894openalex-snapshot
Physiological and Biochemical Responses and Non-Parametric Transcriptome Analysis for the Curcumin-Induced Improvement of Saline-Alkali Resistance in Akebia trifoliate (Thunb.) Koidz
inferred← citeshttps://doi.org/10.3389/fgene.2023.1274288openalex-snapshot
The role of WRKY transcription factors in exogenous potassium (K+) response to NaCl stress in Tamarix ramosissima
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1757806openalex-snapshot
GlnR positively affects the acid resistance of Lactiplantibacillus plantarum from wine by regulating glutamate metabolism
inferred← citeshttps://doi.org/10.3389/fpls.2019.00167openalex-snapshot
Emerging Roles of LSM Complexes in Posttranscriptional Regulation of Plant Response to Abiotic Stress
inferred← citeshttps://doi.org/10.3389/fpls.2020.00936openalex-snapshot
Evidence That Phosphorylation of the α-Subunit of eIF2 Does Not Essentially Inhibit mRNA Translation in Wheat Germ Cell-Free System
inferred← citeshttps://doi.org/10.3389/fpls.2021.667458openalex-snapshot
Response Mechanisms of Plants Under Saline-Alkali Stress
inferred← citeshttps://doi.org/10.3389/fpls.2021.696919openalex-snapshot
An R2R3-MYB Transcription Factor RmMYB108 Responds to Chilling Stress of Rosa multiflora and Conferred Cold Tolerance of Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2021.759245openalex-snapshot
Regulatory Network of Cotton Genes in Response to Salt, Drought and Wilt Diseases (Verticillium and Fusarium): Progress and Perspective
inferred← citeshttps://doi.org/10.3389/fpls.2021.766999openalex-snapshot
De novo Whole-Genome Assembly of Moringa oleifera Helps Identify Genes Regulating Drought Stress Tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2022.1010314openalex-snapshot
Leaf-transcriptome profiles of phoebe bournei provide insights into temporal drought stress responses
inferred← citeshttps://doi.org/10.3389/fpls.2022.1067076openalex-snapshot
Transcriptomic and metabolic regulatory network characterization of drought responses in tobacco
inferred← citeshttps://doi.org/10.3389/fpls.2022.819658openalex-snapshot
Multidimensional Role of Silicon to Activate Resilient Plant Growth and to Mitigate Abiotic Stress
inferred← citeshttps://doi.org/10.3389/fpls.2022.888710openalex-snapshot
Low Temperature Stress Tolerance: An Insight Into the Omics Approaches for Legume Crops
inferred← citeshttps://doi.org/10.3389/fpls.2022.988505openalex-snapshot
CRISPR/Cas9 mediated gene-editing of GmHdz4 transcription factor enhances drought tolerance in soybean (Glycine max [L.] Merr.)
inferred← citeshttps://doi.org/10.3389/fpls.2023.1117507openalex-snapshot
Comparative analysis of drought stress-induced physiological and transcriptional changes of two black sesame cultivars during anthesis
inferred← citeshttps://doi.org/10.3389/fpls.2023.1126660openalex-snapshot
Transcriptomic and metabolomic insights on the molecular mechanisms of flower buds in responses to cold stress in two Camellia oleifera cultivars
inferred← citeshttps://doi.org/10.3389/fpls.2023.1136626openalex-snapshot
A MYB-related transcription factor from peanut, AhMYB30, improves freezing and salt stress tolerance in transgenic Arabidopsis through both DREB/CBF and ABA-signaling pathways
inferred← citeshttps://doi.org/10.3389/fpls.2023.1276117openalex-snapshot
Enhancing crop resilience by harnessing the synergistic effects of biostimulants against abiotic stress
inferred← citeshttps://doi.org/10.3389/fpls.2024.1352040openalex-snapshot
“Genome-wide identification of bZIP gene family in Pearl millet and transcriptional profiling under abiotic stress, phytohormonal treatments; and functional characterization of PgbZIP9”
inferred← citeshttps://doi.org/10.3389/fpls.2025.1687280openalex-snapshot
Transcriptome and WGCNA analysis revealed the molecular mechanism of drought resistance in new sugarcane varieties
inferred← citeshttps://doi.org/10.3389/fsufs.2024.1435437openalex-snapshot
Transcriptomic response of minor millets to abiotic stresses
inferred← citeshttps://doi.org/10.3389/fsufs.2025.1670566openalex-snapshot
Engineering resilience in woody plants: multi-omics, genome editing, and microbiome strategies to boost abiotic stress tolerance
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