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Phytohormones and their metabolic engineering for abiotic stress tolerance in crop plants
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9781118297674.ch34openalex-snapshot
Chemistry of Strigolactones: Why and How do Plants Produce so Many Strigolactones?
inferredcites →https://doi.org/10.1002/j.1460-2075.1984.tb02032.xopenalex-snapshot
Expression of foreign genes in regenerated plants and in their progeny
inferredcites →https://doi.org/10.1002/j.1460-2075.1984.tb02201.xopenalex-snapshot
Direct gene transfer to plants
inferredcites →https://doi.org/10.1002/ps.3257openalex-snapshot
Strigolactones—intriguing biologically active compounds: perspectives for deciphering their biological role and for proposing practical application
inferredcites →https://doi.org/10.1007/978-1-4020-2686-7openalex-snapshot
PLANT HORMONES: Biosynthesis, Signal Transduction, Action
inferredcites →https://doi.org/10.1007/978-1-4020-2686-7_4openalex-snapshot
Gibberellin Biosynthesis and Inactivation
inferredcites →https://doi.org/10.1007/978-1-4614-0634-1openalex-snapshot
Abiotic Stress Responses in Plants
inferredcites →https://doi.org/10.1007/978-1-4614-0634-1_13openalex-snapshot
Abiotic Stress and Role of Salicylic Acid in Plants
inferredcites →https://doi.org/10.1007/978-1-4614-0815-4openalex-snapshot
Environmental Adaptations and Stress Tolerance of Plants in the Era of Climate Change
inferredcites →https://doi.org/10.1007/978-1-4614-0815-4_18openalex-snapshot
Ethylene and Abiotic Stress Tolerance in Plants
inferredcites →https://doi.org/10.1007/978-1-4614-8600-8_7openalex-snapshot
Ethylene: Role in Plants Under Environmental Stress
inferredcites →https://doi.org/10.1007/978-3-319-09132-7_10openalex-snapshot
Crop Plant Hormones and Environmental Stress
inferredcites →https://doi.org/10.1007/978-3-642-25829-9openalex-snapshot
Phytohormones and Abiotic Stress Tolerance in Plants
inferredcites →https://doi.org/10.1007/978-3-642-25829-9_2openalex-snapshot
Cross-Talk Between Phytohormone Signaling Pathways Under Both Optimal and Stressful Environmental Conditions
inferredcites →https://doi.org/10.1007/978-3-642-36470-9_9openalex-snapshot
Strigolactones and the Coordinated Development of Shoot and Root
inferredcites →https://doi.org/10.1007/bf00233288openalex-snapshot
Thidiazuron promotes high frequency regeneration of peanut (Arachis hypogaea) plants in vitro
inferredcites →https://doi.org/10.1007/s00299-011-1180-1openalex-snapshot
Beyond gibberellins and abscisic acid: how ethylene and jasmonates control seed germination
inferredcites →https://doi.org/10.1007/s00299-013-1406-5openalex-snapshot
Auxin and gibberellin responsive Arabidopsis SMALL AUXIN UP RNA36 regulates hypocotyl elongation in the light
inferredcites →https://doi.org/10.1007/s00299-013-1461-yopenalex-snapshot
The phytohormone crosstalk paradigm takes center stage in understanding how plants respond to abiotic stresses
inferredcites →https://doi.org/10.1007/s00299-015-1895-5openalex-snapshot
MsZEP, a novel zeaxanthin epoxidase gene from alfalfa (Medicago sativa), confers drought and salt tolerance in transgenic tobacco
inferredcites →https://doi.org/10.1007/s00344-011-9227-7openalex-snapshot
Interaction of Brassinosteroids with Light Quality and Plant Hormones in Regulating Shoot Growth of Young Sunflower and Arabidopsis Seedlings
inferredcites →https://doi.org/10.1007/s00425-003-1037-0openalex-snapshot
Photo- and antioxidative protection, and a role for salicylic acid during drought and recovery in field-grown Phillyrea angustifolia plants
inferredcites →https://doi.org/10.1007/s00425-010-1208-8openalex-snapshot
Expression of ethylene response factor JERF1 in rice improves tolerance to drought
inferredcites →https://doi.org/10.1007/s00425-010-1310-yopenalex-snapshot
Strigolactones affect lateral root formation and root-hair elongation in Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-011-1516-7openalex-snapshot
Strigolactones promote nodulation in pea
inferredcites →https://doi.org/10.1007/s00425-011-1552-3openalex-snapshot
Activation of a flavin monooxygenase gene YUCCA7 enhances drought resistance in Arabidopsis
inferredcites →https://doi.org/10.1007/s10142-005-0013-0openalex-snapshot
Expression analysis of barley (Hordeum vulgare L.) during salinity stress
inferredcites →https://doi.org/10.1007/s10265-006-0046-zopenalex-snapshot
Development of genotype-independent regeneration system for transformation of rice (Oryza sativa ssp. indica)
inferredcites →https://doi.org/10.1007/s10725-014-0013-yopenalex-snapshot
Phytohormones and plant responses to salinity stress: a review
inferredcites →https://doi.org/10.1007/s10886-014-0474-5openalex-snapshot
The Evolution of Ethylene Signaling in Plant Chemical Ecology
inferredcites →https://doi.org/10.1007/s11103-007-9203-6openalex-snapshot
Constitutively wilted 1, a member of the rice YUCCA gene family, is required for maintaining water homeostasis and an appropriate root to shoot ratio
inferredcites →https://doi.org/10.1007/s11103-007-9213-4openalex-snapshot
T-DNA tagged knockout mutation of rice OsGSK1, an orthologue of Arabidopsis BIN2, with enhanced tolerance to various abiotic stresses
inferredcites →https://doi.org/10.1007/s11105-011-0337-yopenalex-snapshot
An Isopentyl Transferase Gene Driven by the Stress-Inducible rd29A Promoter Improves Salinity Stress Tolerance in Transgenic Tobacco
inferredcites →https://doi.org/10.1007/s11356-014-3754-2openalex-snapshot
Potential role of phytohormones and plant growth-promoting rhizobacteria in abiotic stresses: consequences for changing environment
inferredcites →https://doi.org/10.1007/s11738-005-0015-5openalex-snapshot
The effect of salicylic acid on barley response to water deficit
inferredcites →https://doi.org/10.1007/s11738-009-0297-0openalex-snapshot
Alleviation of salt stress by plant growth regulators and IAA producing bacteria in wheat
inferredcites →https://doi.org/10.1007/s11738-010-0602-yopenalex-snapshot
Growth and metabolic responses of contrasting chickpea (Cicer arietinum L.) genotypes to chilling stress at reproductive phase
inferredcites →https://doi.org/10.1007/s11738-010-0655-yopenalex-snapshot
Physiological effects and transport of 24-epibrassinolide in heat-stressed barley
inferredcites →https://doi.org/10.1007/s12892-009-0060-5openalex-snapshot
Methyl jasmonate alleviated salinity stress in soybean
inferredcites →https://doi.org/10.1016/j.bbapap.2010.01.004openalex-snapshot
Abscisic acid pretreatment enhances salt tolerance of rice seedlings: Proteomic evidence
inferredcites →https://doi.org/10.1016/j.bbrc.2008.07.128openalex-snapshot
Overexpression of Arabidopsis ZEP enhances tolerance to osmotic stress
inferredcites →https://doi.org/10.1016/j.biotechadv.2011.12.003openalex-snapshot
Genetic engineering of cytokinin metabolism: Prospective way to improve agricultural traits of crop plants
inferredcites →https://doi.org/10.1016/j.cell.2006.05.050openalex-snapshot
Different Plant Hormones Regulate Similar Processes through Largely Nonoverlapping Transcriptional Responses
inferredcites →https://doi.org/10.1016/j.chemosphere.2006.01.051openalex-snapshot
Improvement of rape (Brassica napus) plant growth and cadmium uptake by cadmium-resistant bacteria
inferredcites →https://doi.org/10.1016/j.chemosphere.2006.06.025openalex-snapshot
Variation in oxidative stress and photochemical activity in Arabidopsis thaliana leaves subjected to cadmium and excess copper in the presence or absence of jasmonate and ascorbate
inferredcites →https://doi.org/10.1016/j.copbio.2013.09.011openalex-snapshot
Novel perspectives for the engineering of abiotic stress tolerance in plants
inferredcites →https://doi.org/10.1016/j.cub.2011.03.013openalex-snapshot
Hormone Signalling Crosstalk in Plant Growth Regulation
inferredcites →https://doi.org/10.1016/j.ecoenv.2013.08.019openalex-snapshot
Methyl jasmonate as modulator of Cd toxicity in Capsicum frutescens var. fasciculatum seedlings
inferredcites →https://doi.org/10.1016/j.envexpbot.2009.09.004openalex-snapshot
Cold stress effects on reproductive development in grain crops: An overview
inferredcites →https://doi.org/10.1016/j.envexpbot.2009.11.003openalex-snapshot
An enhancing effect of exogenous brassinolide on the growth and antioxidant activity in Chlorella vulgaris cultures under heavy metals stress
inferredcites →https://doi.org/10.1016/j.envexpbot.2013.12.006openalex-snapshot
A new perspective of phytohormones in salinity tolerance: Regulation of proline metabolism
inferredcites →https://doi.org/10.1016/j.envexpbot.2015.02.010openalex-snapshot
Jasmonates counter plant stress: A Review
inferredcites →https://doi.org/10.1016/j.fcr.2005.08.018openalex-snapshot
Role of ABA in integrating plant responses to drought and salt stresses
inferredcites →https://doi.org/10.1016/j.febslet.2007.12.039openalex-snapshot
Salicylic acid production in response to biotic and abiotic stress depends on isochorismate in Nicotiana benthamiana
inferredcites →https://doi.org/10.1016/j.gene.2012.06.076openalex-snapshot
Contrapuntal role of ABA: Does it mediate stress tolerance or plant growth retardation under long-term drought stress?
inferredcites →https://doi.org/10.1016/j.jplph.2012.05.007openalex-snapshot
Cytokinin receptor-dependent and receptor-independent pathways in the dehydration response of Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.jssas.2013.01.001openalex-snapshot
Improving drought and salinity tolerance in barley by application of salicylic acid and potassium nitrate
inferredcites →https://doi.org/10.1016/j.nbt.2015.12.005openalex-snapshot
Transgenic barley overexpressing a cytokinin dehydrogenase gene shows greater tolerance to drought stress
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.2009.09.014openalex-snapshot
Ectopic expression of rice OsNCED3 in Arabidopsis increases ABA level and alters leaf morphology
inferredcites →https://doi.org/10.1016/j.plantsci.2015.02.015openalex-snapshot
Down-regulation of BdBRI1, a putative brassinosteroid receptor gene produces a dwarf phenotype with enhanced drought tolerance in Brachypodium distachyon
inferredcites →https://doi.org/10.1016/j.plantsci.2015.04.018openalex-snapshot
OsIAA6, a member of the rice Aux/IAA gene family, is involved in drought tolerance and tiller outgrowth
inferredcites →https://doi.org/10.1016/j.plaphy.2008.10.002openalex-snapshot
Effects of brassinosteroids on the plant responses to environmental stresses
inferredcites →https://doi.org/10.1016/j.plaphy.2013.03.013openalex-snapshot
Arabidopsis cysteine-rich receptor-like kinase 45 functions in the responses to abscisic acid and abiotic stresses
inferredcites →https://doi.org/10.1016/j.plaphy.2015.05.003openalex-snapshot
Transgenic poplar expressing Arabidopsis YUCCA6 exhibits auxin-overproduction phenotypes and increased tolerance to abiotic stress
inferredcites →https://doi.org/10.1016/j.soilbio.2009.11.007openalex-snapshot
First indications for the involvement of strigolactones on nodule formation in alfalfa (Medicago sativa)
inferredcites →https://doi.org/10.1016/j.tplants.2008.11.005openalex-snapshot
Jasmonate-inducible gene: what does it mean?
inferredcites →https://doi.org/10.1016/j.tplants.2011.02.004openalex-snapshot
A framework integrating plant growth with hormones and nutrients
inferredcites →https://doi.org/10.1016/j.tplants.2012.10.003openalex-snapshot
The biology of strigolactones
inferredcites →https://doi.org/10.1016/j.tplants.2014.02.004openalex-snapshot
Modelling hormonal response and development
inferredcites →https://doi.org/10.1016/j.tplants.2015.02.001openalex-snapshot
Diverse roles of jasmonates and ethylene in abiotic stress tolerance
inferredcites →https://doi.org/10.1021/jf2041164openalex-snapshot
Combined Salicyclic Acid and Ultrasound Treatments for Reducing the Chilling Injury on Peach Fruit
inferredcites →https://doi.org/10.1021/pr400689jopenalex-snapshot
Understanding the Responses of Rice to Environmental Stress Using Proteomics
inferredcites →https://doi.org/10.1023/a:1005632506230openalex-snapshot
Effects of Salinity on Endogenous Aba, Iaa, Ja, and Sa in Iris hexagona
inferredcites →https://doi.org/10.1023/a:1024894923865openalex-snapshot
Participation of Phytohormones in the Stomatal Regulation of Gas Exchange During Water Stress
inferredcites →https://doi.org/10.1023/a:1025852210937openalex-snapshot
Interaction of Cytokinins and Abscisic Acid During Regulation of Stomatal Opening in Bean Leaves
inferredcites →https://doi.org/10.1038/hortres.2015.13openalex-snapshot
Overexpression of an ABA biosynthesis gene using a stress-inducible promoter enhances drought resistance in petunia
inferredcites →https://doi.org/10.1038/nature03309openalex-snapshot
Gene transfer to plants by diverse species of bacteria
inferredcites →https://doi.org/10.1038/nature07271openalex-snapshot
Strigolactone inhibition of shoot branching
inferredcites →https://doi.org/10.1038/nature07272openalex-snapshot
Inhibition of shoot branching by new terpenoid plant hormones
inferredcites →https://doi.org/10.1038/nbt847openalex-snapshot
Genetic manipulation of gibberellin metabolism in transgenic rice
inferredcites →https://doi.org/10.1038/nrg2558openalex-snapshot
Survival of the flexible: hormonal growth control and adaptation in plant development
inferredcites →https://doi.org/10.1046/j.1365-3040.2003.01048.xopenalex-snapshot
Expression of Arabidopsis CBF1 regulated by an ABA/stress inducible promoter in transgenic tomato confers stress tolerance without affecting yield
inferredcites →https://doi.org/10.1071/ar06253openalex-snapshot
Seed priming with brassinolide improves lucerne (Medicago sativa L.) seed germination and seedling growth in relation to physiological changes under salinity stress
inferredcites →https://doi.org/10.1071/fp02076openalex-snapshot
Understanding plant responses to drought — from genes to the whole plant
inferredcites →https://doi.org/10.1073/pnas.081557298openalex-snapshot
Jasmonic acid carboxyl methyltransferase: A key enzyme for jasmonate-regulated plant responses
inferredcites →https://doi.org/10.1073/pnas.1116437108openalex-snapshot
Global food demand and the sustainable intensification of agriculture
inferredcites →https://doi.org/10.1093/aob/mcm079openalex-snapshot
Jasmonates: An Update on Biosynthesis, Signal Transduction and Action in Plant Stress Response, Growth and Development
inferredcites →https://doi.org/10.1093/aob/mct229openalex-snapshot
Auxin and the integration of environmental signals into plant root development
inferredcites →https://doi.org/10.1093/jxb/eri303openalex-snapshot
Root-ABA1, a major constitutive QTL, affects maize root architecture and leaf ABA concentration at different water regimes
inferredcites →https://doi.org/10.1093/jxb/erj212openalex-snapshot
Wounding increases salt tolerance in tomato plants: evidence on the participation of calmodulin-like activities in cross-tolerance signalling
inferredcites →https://doi.org/10.1093/jxb/ern155openalex-snapshot
The relationship of drought-related gene expression in Arabidopsis thaliana to hormonal and environmental factors
inferredcites →https://doi.org/10.1093/jxb/erp331openalex-snapshot
TaSnRK2.4, an SNF1-type serine/threonine protein kinase of wheat (Triticum aestivum L.), confers enhanced multistress tolerance in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erq053openalex-snapshot
Temperature stress and plant sexual reproduction: uncovering the weakest links
inferredcites →https://doi.org/10.1093/jxb/erq266openalex-snapshot
Root-synthesized cytokinins improve shoot growth and fruit yield in salinized tomato (Solanum lycopersicum L.) plants
inferredcites →https://doi.org/10.1093/jxb/erq340openalex-snapshot
Photosynthesis and drought: can we make metabolic connections from available data?
inferredcites →https://doi.org/10.1093/jxb/err031openalex-snapshot
Salicylic acid beyond defence: its role in plant growth and development
inferredcites →https://doi.org/10.1093/jxb/err372openalex-snapshot
Elevated cytokinin content in ipt transgenic creeping bentgrass promotes drought tolerance through regulating metabolite accumulation
inferredcites →https://doi.org/10.1093/jxb/ers091openalex-snapshot
The pathway of auxin biosynthesis in plants
inferredcites →https://doi.org/10.1093/jxb/ers148openalex-snapshot
Plant hormone interactions: innovative targets for crop breeding and management
inferredcites →https://doi.org/10.1093/jxb/ers323openalex-snapshot
Role of brassinosteroids in alleviation of phenanthrene–cadmium co-contamination-induced photosynthetic inhibition and oxidative stress in tomato
inferredcites →https://doi.org/10.1093/jxb/erv528openalex-snapshot
Increased abscisic acid levels in transgenic maize overexpressingAtLOS5mediated root ion fluxes and leaf water status under salt stress
inferredcites →https://doi.org/10.1093/jxb/erw019openalex-snapshot
Enhancing cytokinin synthesis by overexpressing ipt alleviated drought inhibition of root growth through activating ROS-scavenging systems in Agrostis stolonifera
inferredcites →https://doi.org/10.1093/mp/sss100openalex-snapshot
Overexpression of Arabidopsis YUCCA6 in Potato Results in High-Auxin Developmental Phenotypes and Enhanced Resistance to Water Deficit
inferredcites →https://doi.org/10.1093/pcp/pcr106openalex-snapshot
Achievements and Challenges in Understanding Plant Abiotic Stress Responses and Tolerance
inferredcites →https://doi.org/10.1094/mpmi-20-8-0955openalex-snapshot
The Phytotoxin Coronatine Contributes to Pathogen Fitness and Is Required for Suppression of Salicylic Acid Accumulation in Tomato Inoculated with Pseudomonas syringae pv. tomato DC3000
inferredcites →https://doi.org/10.1104/pp.105.062257openalex-snapshot
Heat Stress Phenotypes of Arabidopsis Mutants Implicate Multiple Signaling Pathways in the Acquisition of Thermotolerance
inferredcites →https://doi.org/10.1104/pp.106.091298openalex-snapshot
The coronatine-insensitive 1 Mutation Reveals the Hormonal Signaling Interaction between Abscisic Acid and Methyl Jasmonate in Arabidopsis Guard Cells. Specific Impairment of Ion Channel Activation and Second Messenger Production
inferredcites →https://doi.org/10.1104/pp.107.100560openalex-snapshot
A Putative Hydroxysteroid Dehydrogenase Involved in Regulating Plant Growth and Development
inferredcites →https://doi.org/10.1104/pp.108.134684openalex-snapshot
Methyl Jasmonate Reduces Grain Yield by Mediating Stress Signals to Alter Spikelet Development in Rice
inferredcites →https://doi.org/10.1104/pp.109.148999openalex-snapshot
Jasmonate-Dependent and -Independent Pathways Mediate Specific Effects of Solar Ultraviolet B Radiation on Leaf Phenolics and Antiherbivore Defense
inferredcites →https://doi.org/10.1104/pp.110.166645openalex-snapshot
Physiological Effects of the Synthetic Strigolactone Analog GR24 on Root System Architecture in Arabidopsis: Another Belowground Role for Strigolactones?
inferredcites →https://doi.org/10.1104/pp.110.168161openalex-snapshot
Unraveling the Evolution of Auxin Signaling
inferredcites →https://doi.org/10.1104/pp.112.195032openalex-snapshot
DELLA Signaling Mediates Stress-Induced Cell Differentiation in Arabidopsis Leaves through Modulation of Anaphase-Promoting Complex/Cyclosome Activity
inferredcites →https://doi.org/10.1104/pp.114.244939openalex-snapshot
Strigolactone Involvement in Root Development, Response to Abiotic Stress, and Interactions with the Biotic Soil Environment
inferredcites →https://doi.org/10.1104/pp.15.00780openalex-snapshot
Overexpression of ARGOS Genes Modifies Plant Sensitivity to Ethylene, Leading to Improved Drought Tolerance in Both Arabidopsis and Maize
inferredcites →https://doi.org/10.1105/tpc.107.050666openalex-snapshot
Two Calcium-Dependent Protein Kinases, CPK4 and CPK11, Regulate Abscisic Acid Signal Transduction inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.072694openalex-snapshot
Root-Specific Reduction of Cytokinin Causes Enhanced Root Growth, Drought Tolerance, and Leaf Mineral Enrichment inArabidopsisand Tobacco
inferredcites →https://doi.org/10.1105/tpc.111.084160openalex-snapshot
Pause-and-Stop: The Effects of Osmotic Stress on Cell Proliferation during Early Leaf Development in Arabidopsis and a Role for Ethylene Signaling in Cell Cycle Arrest
inferredcites →https://doi.org/10.1105/tpc.111.087395openalex-snapshot
Analysis of Cytokinin Mutants and Regulation of Cytokinin Metabolic Genes Reveals Important Regulatory Roles of Cytokinins in Drought, Salt and Abscisic Acid Responses, and Abscisic Acid Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.112.098640openalex-snapshot
Ethylene Signaling Negatively Regulates Freezing Tolerance by Repressing Expression of CBF and Type-A ARR Genes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.15.00080openalex-snapshot
Ethylene Responses in Rice Roots and Coleoptiles Are Differentially Regulated by a Carotenoid Isomerase-Mediated Abscisic Acid Pathway
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02593.xopenalex-snapshot
Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stresses that affect plant water status
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02842.xopenalex-snapshot
Ethylene‐induced stomatal closure in Arabidopsis occurs via AtrbohF‐mediated hydrogen peroxide synthesis
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02947.xopenalex-snapshot
Salicylic acid‐mediated innate immunity in Arabidopsis is regulated by SIZ1 SUMO E3 ligase
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04350.xopenalex-snapshot
De-regulation of abscisic acid contents causes abnormal endosperm development in the barley mutant seg8
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04477.xopenalex-snapshot
OsbHLH148, a basic helix‐loop‐helix protein, interacts with OsJAZ proteins in a jasmonate signaling pathway leading to drought tolerance in rice
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05121.xopenalex-snapshot
The putative auxin efflux carrier OsPIN3t is involved in the drought stress response and drought tolerance
inferredcites →https://doi.org/10.1111/nph.12797openalex-snapshot
Abiotic and biotic stress combinations
inferredcites →https://doi.org/10.1111/pbi.12066openalex-snapshot
Expression of an A rabidopsis molybdenum cofactor sulphurase gene in soybean enhances drought tolerance and increases yield under field conditions
inferredcites →https://doi.org/10.1111/pbi.12172openalex-snapshot
Transgenic alteration of ethylene biosynthesis increases grain yield in maize under field drought‐stress conditions
inferredcites →https://doi.org/10.1111/tpj.12014openalex-snapshot
SIZ1 deficiency causes reduced stomatal aperture and enhanced drought tolerance via controlling salicylic acid‐induced accumulation of reactive oxygen species in A rabidopsis
inferredcites →https://doi.org/10.1111/tpj.12508openalex-snapshot
A homolog of ETHYLENE OVERPRODUCER , O s ETOL 1, differentially modulates drought and submergence tolerance in rice
inferredcites →https://doi.org/10.1126/science.1132334openalex-snapshot
For Our Thirsty World, Efficiency or Else
inferredcites →https://doi.org/10.1126/science.1173771openalex-snapshot
Hormone (Dis)harmony Moulds Plant Health and Disease
inferredcites →https://doi.org/10.1128/mmbr.67.1.16-37.2003openalex-snapshot
Agrobacterium -Mediated Plant Transformation: the Biology behind the “Gene-Jockeying” Tool
inferredcites →https://doi.org/10.1146/annurev-phyto-073009-114453openalex-snapshot
The Strigolactone Story
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092804openalex-snapshot
Gibberellin Metabolism and its Regulation
inferredcites →https://doi.org/10.1155/2014/167681openalex-snapshot
Ethylene Response Factor Sl-ERF.B.3 Is Responsive to Abiotic Stresses and Mediates Salt and Cold Stress Response Regulation in Tomato
inferredcites →https://doi.org/10.1186/s12870-015-0415-7openalex-snapshot
Tomato (Solanum lycopersicum L.) SlIPT3 and SlIPT4 isopentenyltransferases mediate salt stress response in tomato
inferredcites →https://doi.org/10.1242/jeb.089938openalex-snapshot
The role of gibberellin signalling in plant responses to abiotic stress
inferredcites →https://doi.org/10.1371/journal.pone.0052126openalex-snapshot
Overexpression of Arabidopsis Molybdenum Cofactor Sulfurase Gene Confers Drought Tolerance in Maize (Zea mays L.)
inferredcites →https://doi.org/10.1371/journal.pone.0115418openalex-snapshot
A Hormone-Responsive C1-Domain-Containing Protein At5g17960 Mediates Stress Response in Arabidopsis thaliana
inferredcites →https://doi.org/10.1385/1-59259-774-2:329openalex-snapshot
Gene Transfer and Expression in Plants
inferredcites →https://doi.org/10.2135/cropsci2006.11.0712openalex-snapshot
Genetic Engineering of Maize with the Arabidopsis DREB1A/CBF3 Gene Using Split‐Seed Explants
inferredcites →https://doi.org/10.2174/138920211794520178openalex-snapshot
Engineering Cold Stress Tolerance in Crop Plants
inferredcites →https://doi.org/10.2174/1389202911314030001openalex-snapshot
Compatible Solute Engineering in Plants for Abiotic Stress Tolerance - Role of Glycine Betaine
inferredcites →https://doi.org/10.3389/fenvs.2014.00039openalex-snapshot
Extreme climatic events: impacts of drought and high temperature on physiological processes in agronomically important plants
inferredcites →https://doi.org/10.3389/fenvs.2014.00067openalex-snapshot
Brassinosteroids make plant life easier under abiotic stresses mainly by modulating major components of antioxidant defense system
inferredcites →https://doi.org/10.3389/fpls.2013.00397openalex-snapshot
Endogenous auxin and jasmonic acid levels are differentially modulated by abiotic stresses in rice
inferredcites →https://doi.org/10.3389/fpls.2013.00451openalex-snapshot
Cytokinin cross-talking during biotic and abiotic stress responses
inferredcites →https://doi.org/10.3389/fpls.2014.00004openalex-snapshot
Regulation of water, salinity, and cold stress responses by salicylic acid
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DNA-Delivery Methods to Produce Transgenic Plants
inferredcites →https://doi.org/10.4161/gmcr.28774openalex-snapshot
Polyamines in response to abiotic stress tolerance through transgenic approaches
inferredcites →https://doi.org/10.4172/jrr.1000e105openalex-snapshot
Biotechnology and Abiotic Stress Tolerance in Rice
inferredcites →https://doi.org/10.4236/ajps.2013.412285openalex-snapshot
Effect of Brassinosteroids on Germination and Seedling Growth of Radish (Raphanus sativus L.) under PEG-6000 Induced Water Stress
inferredcites →https://doi.org/10.5072/zenodo.34036openalex-snapshot
Abscisic acid regulated gene expression in bread wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.5772/32773openalex-snapshot
Methods to Transfer Foreign Genes to Plants
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1007/978-981-16-3364-5_9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-16-4955-4_15openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-16-6361-1_17openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-16-8538-5_10openalex-snapshot
Futuristic 2D Nanomaterial Composites Agro-Formulations for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-16-8770-9_11openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-16-9037-2_6openalex-snapshot
Plant Growth Hormones in Plants under Low-Temperature Stress: A Review
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inferred← citeshttps://doi.org/10.1007/978-981-19-4124-5_6openalex-snapshot
Plant Growth-Promoting Microorganisms: An Option for Drought and Salinity Management in Arid Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-19-4336-2_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-19-4941-8_13openalex-snapshot
Phytohormone Involvement in Plant Responses to Soil Acidity
inferred← citeshttps://doi.org/10.1007/978-981-19-4941-8_2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-19-5121-3_10openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-19-5121-3_14openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-19-5121-3_15openalex-snapshot
Cereals and Phytohormones Under Heavy Metal Stress
inferred← citeshttps://doi.org/10.1007/978-981-19-5121-3_18openalex-snapshot
Cereals and Phytohormones Under Ozone Stress
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Physiology and Abiotic Stresses
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inferred← citeshttps://doi.org/10.1007/978-981-96-7756-6_3openalex-snapshot
Exploring the Role of Nanotechnology in the Management of Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-981-96-8346-8_10openalex-snapshot
Drought Resilience in Oilseed Crops: The Role of Phytohormones in Stress Mitigation
inferred← citeshttps://doi.org/10.1007/978-981-97-0672-3_11openalex-snapshot
Plant Hormones and Their Regulatory Roles in Abiotic Stress Response
inferred← citeshttps://doi.org/10.1007/978-981-97-0840-6_1openalex-snapshot
Utilization of Agri-waste Biomass and Its Mechanism in Enhancing the Functioning of Biostimulants in Plants
inferred← citeshttps://doi.org/10.1007/978-981-97-1699-9_7openalex-snapshot
Effect on Morphology, Physiology, and Biochemistry of Plants Under Different Stresses
inferred← citeshttps://doi.org/10.1007/978-981-97-2918-0_13openalex-snapshot
Integration of Plant Hormones in the Biological System as an Opportunity for Sustainable Crop Production
inferred← citeshttps://doi.org/10.1007/978-981-97-7174-5_6openalex-snapshot
Proteomic Insights into the Impact of Au-NPs on Plants Under Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-981-97-8804-0_15openalex-snapshot
The Multifaceted Biocontrol Mechanisms of Endophytic Fungi
inferred← citeshttps://doi.org/10.1007/978-981-99-3334-1_16openalex-snapshot
Plant Phenolics and Their Versatile Promising Role in the Management of Nematode Stress
inferred← citeshttps://doi.org/10.1007/978-981-99-4669-3_8openalex-snapshot
Strategies for Improving Tolerance to the Combined Effect of Drought and Salinity Stress in Crops
inferred← citeshttps://doi.org/10.1007/978-981-99-8874-7_8openalex-snapshot
Implication of Phytohormonal Signaling and Their Molecular Cross Talk During Disease Resistance in Plants
inferred← citeshttps://doi.org/10.1007/978-981-99-9388-8_7openalex-snapshot
Beneficial Crop Microbiomes: Mitigators of Abiotic Stress
inferred← citeshttps://doi.org/10.1007/s00122-020-03764-0openalex-snapshot
Hotter, drier, CRISPR: the latest edit on climate change
inferred← citeshttps://doi.org/10.1007/s00128-021-03219-2openalex-snapshot
Individual Rather Than Simultaneous Priming with Glutathione and Putrescine Reduces Chromium Cr6+ Toxicity in Contrasting Canola (Brassica napus L.) Cultivars
inferred← citeshttps://doi.org/10.1007/s00253-022-12122-7openalex-snapshot
Gamma ray–induced tissue responses and improved secondary metabolites accumulation in Catharanthus roseus
inferred← citeshttps://doi.org/10.1007/s00284-024-03784-9openalex-snapshot
Unveiling Agricultural Biotechnological Prospects: The Draft Genome Sequence of Stenotrophomonas geniculata LGMB417
inferred← citeshttps://doi.org/10.1007/s00294-021-01199-8openalex-snapshot
Genomic assessment of Stenotrophomonas indicatrix for improved sunflower plant
inferred← citeshttps://doi.org/10.1007/s00299-020-02606-zopenalex-snapshot
ScAOC1, an allene oxide cyclase gene, confers defense response to biotic and abiotic stresses in sugarcane
inferred← citeshttps://doi.org/10.1007/s00299-020-02614-zopenalex-snapshot
Jasmonic acid: a key frontier in conferring abiotic stress tolerance in plants
inferred← citeshttps://doi.org/10.1007/s00299-021-02690-9openalex-snapshot
5-aminolevulinic acid-mediated plant adaptive responses to abiotic stress
inferred← citeshttps://doi.org/10.1007/s00299-021-02736-yopenalex-snapshot
miRNAs play critical roles in response to abiotic stress by modulating cross-talk of phytohormone signaling
inferred← citeshttps://doi.org/10.1007/s00299-022-02883-wopenalex-snapshot
VaMYB44 transcription factor from Chinese wild Vitis amurensis negatively regulates cold tolerance in transgenic Arabidopsis thaliana and V. vinifera
inferred← citeshttps://doi.org/10.1007/s00299-024-03395-5openalex-snapshot
Identification of dehydrin family genes in three Medicago species and insights into their tolerant mechanism to salt stress
inferred← citeshttps://doi.org/10.1007/s00299-025-03459-0openalex-snapshot
Genome-wide identification of SlIQMs and the regulatory effect of calcium on tomato seedlings under drought stress and phytohormone treatment
inferred← citeshttps://doi.org/10.1007/s00299-025-03673-wopenalex-snapshot
Mangrove derived coactive bacterial inoculant triggered biochemical traits rejuvenating plant cell function under salt stress
inferred← citeshttps://doi.org/10.1007/s00344-018-9875-yopenalex-snapshot
5-Aminolevulinic Acid-Induced Heavy Metal Stress Tolerance and Underlying Mechanisms in Plants
inferred← citeshttps://doi.org/10.1007/s00344-018-9886-8openalex-snapshot
Phytohormone Priming: Regulator for Heavy Metal Stress in Plants
inferred← citeshttps://doi.org/10.1007/s00344-019-09951-8openalex-snapshot
Light Stress Responses and Prospects for Engineering Light Stress Tolerance in Crop Plants
inferred← citeshttps://doi.org/10.1007/s00344-020-10157-6openalex-snapshot
Strigolactone and Methyl Jasmonate-Induced Antioxidant Defense and the Composition Alterations of Different Active Compounds in Dracocephalum kotschyi Boiss Under Drought Stress
inferred← citeshttps://doi.org/10.1007/s00344-020-10175-4openalex-snapshot
Gibberellic Acid and Sulfur-Mediated Reversal of Cadmium-Inhibited Photosynthetic Performance in Mungbean (Vigna radiata L.) Involves Nitric Oxide
inferred← citeshttps://doi.org/10.1007/s00344-020-10229-7openalex-snapshot
The Interaction Effect of Drought and Exogenous Application of Zearalenone on the Physiological, Biochemical Parameters and Yield of Legumes
inferred← citeshttps://doi.org/10.1007/s00344-020-10257-3openalex-snapshot
The key roles of salicylic acid and sulfur in plant salinity stress tolerance
inferred← citeshttps://doi.org/10.1007/s00344-020-10271-5openalex-snapshot
Salicylic Acid Modulates Antioxidant System, Defense Metabolites, and Expression of Salt Transporter Genes in Pisum sativum Under Salinity Stress
inferred← citeshttps://doi.org/10.1007/s00344-021-10350-1openalex-snapshot
Hydrogen Sulfide–Phytohormone Interaction in Plants Under Physiological and Stress Conditions
inferred← citeshttps://doi.org/10.1007/s00344-021-10362-xopenalex-snapshot
Role of Phytohormones in Regulating Heat Stress Acclimation in Agricultural Crops
inferred← citeshttps://doi.org/10.1007/s00344-022-10812-0openalex-snapshot
Phytohormones Mediated Modulation of Abiotic Stress Tolerance and Potential Crosstalk in Horticultural Crops
inferred← citeshttps://doi.org/10.1007/s00344-023-11016-wopenalex-snapshot
Abscisic Acid-Loaded ZnO Nanoparticles as Drought Tolerance Inducers in Zea mays L. with Physiological and Biochemical Attributes
inferred← citeshttps://doi.org/10.1007/s00344-023-11103-yopenalex-snapshot
Palliative Effects of Kaolin on Citrus Plants Under Controlled Stress Conditions of High Temperature and High Light Intensity
inferred← citeshttps://doi.org/10.1007/s00344-023-11119-4openalex-snapshot
Microbiological Control of Xanthomonas Induced Bacterial Leaf Streak Disease of Wheat via Phytocompounds and ROS Processing Enzymes Produced Under Biotic Stress
inferred← citeshttps://doi.org/10.1007/s00344-024-11239-5openalex-snapshot
Mitogen-Activated Protein Kinase: A Potent Signaling Protein that Combats Biotic and Abiotic Stress in Plants
inferred← citeshttps://doi.org/10.1007/s00344-024-11548-9openalex-snapshot
Effects of Rhizospheric Microbes, Growth Regulators, and Biochar in Modulating Antioxidant Machinery of Plants Under Stress
inferred← citeshttps://doi.org/10.1007/s00344-024-11568-5openalex-snapshot
Phytohormonal Regulation of Plant Development in Response to Fluctuating Light Conditions
inferred← citeshttps://doi.org/10.1007/s00344-025-11629-3openalex-snapshot
Elucidating UV-C-Induced Growth Inhibition in Seashore Paspalum and Bermudagrass from Photosynthesis and Phytohormone Changes
inferred← citeshttps://doi.org/10.1007/s00344-025-11932-zopenalex-snapshot
Transcriptional Effects of Foliar Spraying of Increasing Strigolactone on the Legume Model Medicago truncatula
inferred← citeshttps://doi.org/10.1007/s00344-026-12171-6openalex-snapshot
Salicylic Acid as a Seed Priming Agent to Alleviate Salt Stress: Integrative Insights from Morpho-Physiological and Molecular Perspectives
inferred← citeshttps://doi.org/10.1007/s00344-026-12222-yopenalex-snapshot
Are Strigolactones Relevant for Arabidopsis Co-exposed to Heat and Salt Stress? – Exploring the Role of MAX2 and MAX3 in Stress Responses and Physiological Performance
inferred← citeshttps://doi.org/10.1007/s00425-017-2786-5openalex-snapshot
Transcriptional profiling of cork oak phellogenic cells isolated by laser microdissection
inferred← citeshttps://doi.org/10.1007/s00425-018-2910-1openalex-snapshot
In vitro plant tissue culture: means for production of biological active compounds
inferred← citeshttps://doi.org/10.1007/s00425-018-2993-8openalex-snapshot
Characterization of the responses to saline stress in the symbiotic green microalga Trebouxia sp. TR9
inferred← citeshttps://doi.org/10.1007/s00425-020-03366-6openalex-snapshot
Engineering salinity tolerance in plants: progress and prospects
inferred← citeshttps://doi.org/10.1007/s00425-020-03483-2openalex-snapshot
Cytokinin activity during early kernel development corresponds positively with yield potential and later stage ABA accumulation in field-grown wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.1007/s00425-023-04146-8openalex-snapshot
Deciphering the melatonin-mediated response and signalling in the regulation of heavy metal stress in plants
inferred← citeshttps://doi.org/10.1007/s00425-023-04252-7openalex-snapshot
Plant breeding for harmony between sustainable agriculture, the environment, and global food security: an era of genomics‐assisted breeding
inferred← citeshttps://doi.org/10.1007/s00425-024-04510-2openalex-snapshot
A novel Microbacterium strain SRS2 promotes the growth of Arabidopsis and MicroTom (S. lycopersicum) under normal and salt stress conditions
inferred← citeshttps://doi.org/10.1007/s00468-020-02047-xopenalex-snapshot
Quantification of endogenous aromatic cytokinins in Pinus radiata embryonal masses after application of heat stress during initiation of somatic embryogenesis
inferred← citeshttps://doi.org/10.1007/s00709-017-1150-8openalex-snapshot
Heat or cold priming-induced cross-tolerance to abiotic stresses in plants: key regulators and possible mechanisms
inferred← citeshttps://doi.org/10.1007/s00709-019-01390-2openalex-snapshot
Functional domain analysis of LmSAP protein reveals the crucial role of the zinc-finger A20 domain in abiotic stress tolerance
inferred← citeshttps://doi.org/10.1007/s00709-020-01527-8openalex-snapshot
Cytokinin (6-benzylaminopurine) elevates lignification and the expression of genes involved in lignin biosynthesis of carrot
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