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Expression of a Bifunctional Fusion of the Escherichia coli Genes for Trehalose-6-Phosphate Synthase and Trehalose-6-Phosphate Phosphatase in Transgenic Rice Plants Increases Trehalose Accumulation and Abiotic Stress Tolerance without Stunting Growth
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Outgoing claims: the papers this work cites, builds on, or argues with.
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A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
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Protective Role of Trehalose during Heat Stress in Saccharomyces cerevisiae
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Trehalose in yeast, stress protectant rather than reserve carbohydrate
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Expression of the yeast trehalose-6-phosphate synthase gene in transgenic tobacco plants: pleiotropic phenotypes include drought tolerance
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Fluorescence emission spectra of Photosystem I, Photosystem II and the light-harvesting chlorophyll a/b complex of higher plants
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Interactions of phospholipid monolayers with carbohydrates
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Trehalose‐6‐phosphate, a new regulator of yeast glycolysis that inhibits hexokinases
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Trehalose and trehalase in plants: recent developments
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Trehalose, reserve and/or stress metabolite?
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The Metabolism of α,α-Trehalose
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Trehalose metabolism in sugar sensing and plant development
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The occurrence of trehalose in the leaves of the desiccation-tolerant angiosperm Myrothamnus flabellifolius welw.
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Trehalose affects sucrose synthase and invertase activities in soybean (Glycine max [L.] Merr.) roots
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Trehalose-producing transgenic tobacco plants show improved growth performance under drought stress
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Trehalose synthase: guard to the gate of glycolysis in yeast?
inferredcites →https://doi.org/10.1016/s1360-1385(01)01920-3openalex-snapshot
Enhancing photosynthesis with sugar signals
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Trehalose metabolism in plants
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Subcellular targeting of green fluorescent protein to plastids in transgenic rice plants provides a high-level expression system
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Transgenic rice plants harboring an introduced potato proteinase inhibitor II gene are insect resistant
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Extraordinary Stability of Enzymes Dried in Trehalose: Simplified Molecular Biology
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Trehalose‐6‐phosphate phosphatases from Arabidopsis thaliana: identification by functional complementation of the yeast tps2 mutant
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Sensing trehalose biosynthesis in plants
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Over‐expression of a single Ca 2+ ‐dependent protein kinase confers both cold and salt/drought tolerance on rice plants
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Trehalose‐6‐phosphate synthase 1, which catalyses the first step in trehalose synthesis, is essential for Arabidopsis embryo maturation
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Constitutive expression of the cold-regulated Arabidopsis thaliana COR15a gene affects both chloroplast and protoplast freezing tolerance
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Isolation of Genes for Low-Temperature-Induced Proteins in Rice by a Simple Subtractive Method
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Light-Regulated and Cell-Specific Expression of Tomato rbcS-gusA and Rice rbcS-gusA Fusion Genes in Transgenic Rice
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The Interaction of Light and Abscisic Acid in the Regulation of Plant Gene Expression
inferredcites →https://doi.org/10.1104/pp.113.1.181openalex-snapshot
Inhibition of Trehalase Activity Enhances Trehalose Accumulation in Transgenic Plants
inferredcites →https://doi.org/10.1104/pp.115.1.159openalex-snapshot
Effects of Osmoprotectants upon NaCl Stress in Rice
inferredcites →https://doi.org/10.1104/pp.124.1.105openalex-snapshot
Trehalose Induces the ADP-Glucose Pyrophosphorylase Gene,ApL3, and Starch Synthesis in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.125.2.1086openalex-snapshot
Trehalose and Trehalase in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.81.2.444openalex-snapshot
Regulation of Fructan Metabolism in Leaves of Barley (Hordeum vulgare L. cv Gerbel)
inferredcites →https://doi.org/10.1105/tpc.2.1.19openalex-snapshot
Characterization of a rice gene showing organ-specific expression in response to salt stress and drought.
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Trehalose metabolism in Escherichia coli: stress protection and stress regulation of gene expression
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Trehalose, reserve and/or stress metabolite?
inferredcites →https://doi.org/10.1126/science.223.4637.701openalex-snapshot
Preservation of Membranes in Anhydrobiotic Organisms: The Role of Trehalose
inferredcites →https://doi.org/10.1128/aem.61.10.3592-3597.1995openalex-snapshot
Trehalose and sucrose protect both membranes and proteins in intact bacteria during drying
inferredcites →https://doi.org/10.1128/aem.66.6.2484-2490.2000openalex-snapshot
Characterization of a Bifunctional Enzyme Fusion of Trehalose-6-Phosphate Synthetase and Trehalose-6-Phosphate Phosphatase of Escherichia coli
inferredcites →https://doi.org/10.2307/3869047openalex-snapshot
Characterization of a Rice Gene Showing Organ-Specific Expression in Response to Salt Stress and Drought
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Overexpression of a trehalose-6-phosphate synthase/phosphatase fusion gene enhances tolerance and photosynthesis during drought and salt stress without growth aberrations in tomato
inferred← citeshttps://doi.org/10.1007/s11240-015-0793-4openalex-snapshot
A method to identify early-stage transgenic Medicago truncatula with improved physiological response to water deficit
inferred← citeshttps://doi.org/10.1007/s11240-024-02766-wopenalex-snapshot
Cloning, purification and characterization of trehalose-6-phosphate synthase PoTPS1 and PoTPS5 from Paeonia ostii
inferred← citeshttps://doi.org/10.1007/s11248-010-9400-yopenalex-snapshot
Analysis of the Wsi18, a stress-inducible promoter that is active in the whole grain of transgenic rice
inferred← citeshttps://doi.org/10.1007/s11434-009-0645-xopenalex-snapshot
Review and prospect of transgenic rice research
inferred← citeshttps://doi.org/10.1007/s11627-006-9024-3openalex-snapshot
Trehalose and its applications in plant biotechnology
inferred← citeshttps://doi.org/10.1007/s11676-020-01224-5openalex-snapshot
Overexpression of the ThTPS gene enhanced salt and osmotic stress tolerance in Tamarix hispida
inferred← citeshttps://doi.org/10.1007/s11703-011-1148-5openalex-snapshot
Molecular characterization and roles of AP2 transcription factors on drought tolerance in plants
inferred← citeshttps://doi.org/10.1007/s11738-007-0034-5openalex-snapshot
Electroporation of maize embryogenic calli with the trehalose-6-phosphate synthase gene from Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11738-019-2813-1openalex-snapshot
Green algal molecular responses to temperature stress
inferred← citeshttps://doi.org/10.1007/s11816-008-0068-1openalex-snapshot
Arabidopsis cyclin D2 expressed in rice forms a functional cyclin-dependent kinase complex that enhances seedling growth
inferred← citeshttps://doi.org/10.1007/s11816-011-0210-3openalex-snapshot
Accumulation of trehalose increases soluble sugar contents in rice plants conferring tolerance to drought and salt stress
inferred← citeshttps://doi.org/10.1007/s11816-019-00517-4openalex-snapshot
Overexpression of OsmiR393a gene confers drought tolerance in creeping bentgrass
inferred← citeshttps://doi.org/10.1007/s11816-019-00541-4openalex-snapshot
Overexpression of the trehalose-6-phosphate phosphatase OsTPP3 increases drought tolerance in rice
inferred← citeshttps://doi.org/10.1007/s12042-020-09265-0openalex-snapshot
Mechanisms and Signaling Pathways of Salt Tolerance in Crops: Understanding from the Transgenic Plants
inferred← citeshttps://doi.org/10.1007/s12229-016-9173-yopenalex-snapshot
Plant Salt Stress: Adaptive Responses, Tolerance Mechanism and Bioengineering for Salt Tolerance
inferred← citeshttps://doi.org/10.1007/s12284-008-9006-7openalex-snapshot
Toward Understanding Molecular Mechanisms of Abiotic Stress Responses in Rice
inferred← citeshttps://doi.org/10.1007/s12298-008-0013-3openalex-snapshot
Raising salinity tolerant rice: recent progress and future perspectives
inferred← citeshttps://doi.org/10.1007/s12298-018-0517-4openalex-snapshot
Elucidating the role of osmotic, ionic and major salt responsive transcript components towards salinity tolerance in contrasting chickpea (Cicer arietinum L.) genotypes
inferred← citeshttps://doi.org/10.1007/s12298-021-00950-2openalex-snapshot
Allele mining for a drought responsive gene DRO1 determining root growth angle in donors of drought tolerance in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s12298-023-01367-9openalex-snapshot
Photosynthesis regulation, cell membrane stabilization and methylglyoxal detoxification seems major altered pathways under cold stress as revealed by integrated multi-omics meta-analysis
inferred← citeshttps://doi.org/10.1007/s12374-010-9098-7openalex-snapshot
Cloning and Characterization of Functional Trehalose-6-Phosphate Synthase Gene in Maize
inferred← citeshttps://doi.org/10.1007/s12374-018-0081-zopenalex-snapshot
Roles of Sugars in Controlling Flowering Time
inferred← citeshttps://doi.org/10.1007/s13258-013-0160-yopenalex-snapshot
Comparative transcriptome profiling of freezing stress responsiveness in two contrasting Chinese cabbage genotypes, Chiifu and Kenshin
inferred← citeshttps://doi.org/10.1007/s13580-025-00680-4openalex-snapshot
Exogenous trehalose alleviates the inhibitory effects of salt and drought stresses in okra plants
inferred← citeshttps://doi.org/10.1007/s40502-018-0418-0openalex-snapshot
Forward and reverse genetics approaches for combined stress tolerance in rice
inferred← citeshttps://doi.org/10.1007/s43538-021-00006-9openalex-snapshot
Engineering cereal crops for enhanced abiotic stress tolerance
inferred← citeshttps://doi.org/10.1007/s44281-023-00004-5openalex-snapshot
Dynamics of starch degradation and expression of related genes during chilling stress in grapevine
inferred← citeshttps://doi.org/10.1016/b978-0-12-387692-8.00004-7openalex-snapshot
Plants in Extreme Environments
inferred← citeshttps://doi.org/10.1016/b978-0-12-387692-8.00012-6openalex-snapshot
Engineering Salinity and Water-Stress Tolerance in Crop Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-813066-7.00002-4openalex-snapshot
Sugars Play a Critical Role in Abiotic Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-814332-2.00033-2openalex-snapshot
Emerging Role of Osmolytes in Enhancing Abiotic Stress Tolerance in Rice
inferred← citeshttps://doi.org/10.1016/b978-0-12-818581-0.00020-6openalex-snapshot
Transgenic approach in crop improvement
inferred← citeshttps://doi.org/10.1016/b978-0-12-820780-2.00006-6openalex-snapshot
Contribution of Genetically Modified Crops in Agricultural Production: Success Stories
inferred← citeshttps://doi.org/10.1016/b978-0-323-90943-3.00008-0openalex-snapshot
Next-generation genetic engineering tools for abiotic stress tolerance in plants
inferred← citeshttps://doi.org/10.1016/b978-0-443-33465-8.00033-5openalex-snapshot
Next-generation biotechnology for improving abiotic stress tolerance in rice
inferred← citeshttps://doi.org/10.1016/b978-0-443-40401-6.00020-0openalex-snapshot
Genic bioprospecting for stress-resistant designer crops
inferred← citeshttps://doi.org/10.1016/bs.agron.2024.05.004openalex-snapshot
Natural adaptations, tolerance mechanisms, and management concepts of crop plants against salt stress: A critical review
inferred← citeshttps://doi.org/10.1016/j.algal.2023.103121openalex-snapshot
Trehalose phosphate phosphatase overexpression for the mitigation of high-light induced stress in Parachlorella kessleri
inferred← citeshttps://doi.org/10.1016/j.apsoil.2014.07.010openalex-snapshot
Water strategy of mycorrhizal rice at low temperature through the regulation of PIP aquaporins with the involvement of trehalose
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2011.08.005openalex-snapshot
Targeting metabolic pathways for genetic engineering abiotic stress-tolerance in crops
inferred← citeshttps://doi.org/10.1016/j.bcab.2013.11.007openalex-snapshot
Metabolic engineering of cold tolerance in plants
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2009.05.026openalex-snapshot
Improving salinity tolerance of plants through conventional breeding and genetic engineering: An analytical comparison
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2009.11.005openalex-snapshot
Inducing drought tolerance in plants: Recent advances
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2011.09.006openalex-snapshot
Role of transgenic plants in agriculture and biopharming
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2013.05.004openalex-snapshot
Genomics-based precision breeding approaches to improve drought tolerance in rice
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2013.10.005openalex-snapshot
Hormonal and metabolic regulation of source–sink relations under salinity and drought: From plant survival to crop yield stability
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2018.07.007openalex-snapshot
Bacteria and archaea as the sources of traits for enhanced plant phenotypes
inferred← citeshttps://doi.org/10.1016/j.carres.2011.01.018openalex-snapshot
Inhibition of trehalose breakdown increases new carbon partitioning into cellulosic biomass in Nicotiana tabacum
inferred← citeshttps://doi.org/10.1016/j.cj.2023.09.010openalex-snapshot
Trehalose: A sugar molecule involved in temperature stress management in plants
inferred← citeshttps://doi.org/10.1016/j.copbio.2005.02.001openalex-snapshot
Recent advances in engineering plant tolerance to abiotic stress: achievements and limitations
inferred← citeshttps://doi.org/10.1016/j.devcel.2017.11.016openalex-snapshot
OsMAPK3 Phosphorylates OsbHLH002/OsICE1 and Inhibits Its Ubiquitination to Activate OsTPP1 and Enhances Rice Chilling Tolerance
inferred← citeshttps://doi.org/10.1016/j.fcr.2008.06.010openalex-snapshot
Phenotypic and genotypic analysis of drought-resistance traits for development of rice cultivars adapted to rainfed environments
inferred← citeshttps://doi.org/10.1016/j.foodcont.2006.10.007openalex-snapshot
Molecular analysis and quantitative detection of a transgenic rice line expressing a bifunctional fusion TPSP
inferred← citeshttps://doi.org/10.1016/j.gene.2013.09.016openalex-snapshot
Cloning of TPS gene from eelgrass species Zostera marina and its functional identification by genetic transformation in rice
inferred← citeshttps://doi.org/10.1016/j.gene.2019.06.006openalex-snapshot
Overexpression of the wheat trehalose 6-phosphate synthase 11 gene enhances cold tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.gene.2021.145641openalex-snapshot
Identification of the trehalose-6-phosphate synthase gene family in Medicago truncatula and expression analysis under abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2021.07.096openalex-snapshot
Characterization and expression pattern of the trehalose-6-phosphate synthase and trehalose-6-phosphate phosphatase gene families in Populus
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.135518openalex-snapshot
PagTPS1 and PagTPS10, the trehalose-6-phosphate synthase genes, increase trehalose content and enhance drought tolerance
inferred← citeshttps://doi.org/10.1016/j.jare.2024.12.025openalex-snapshot
The role of trehalose metabolism in plant stress tolerance
inferred← citeshttps://doi.org/10.1016/j.jia.2024.03.041openalex-snapshot
Integrated transcriptomics and metabolomics analysis provide insights into the alleviation of waterlogging stress in maize by exogenous spermidine application
inferred← citeshttps://doi.org/10.1016/j.plantsci.2003.10.024openalex-snapshot
Potential biochemical indicators of salinity tolerance in plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2003.11.023openalex-snapshot
HVA1, a LEA gene from barley confers dehydration tolerance in transgenic rice (Oryza sativa L.) via cell membrane protection
inferred← citeshttps://doi.org/10.1016/j.plantsci.2004.10.006openalex-snapshot
Transcriptional response of sugarcane roots to methyl jasmonate
inferred← citeshttps://doi.org/10.1016/j.plantsci.2005.02.024openalex-snapshot
Biochemical analysis of trehalose and its metabolizing enzymes in wheat under abiotic stress conditions
inferred← citeshttps://doi.org/10.1016/j.plantsci.2005.02.026openalex-snapshot
Tomato abiotic stress enhanced tolerance by trehalose biosynthesis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2011.02.008openalex-snapshot
Overexpression of OsRDCP1, a rice RING domain-containing E3 ubiquitin ligase, increased tolerance to drought stress in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/j.plantsci.2012.08.003openalex-snapshot
OsMIOX, a myo-inositol oxygenase gene, improves drought tolerance through scavenging of reactive oxygen species in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112835openalex-snapshot
Arabidopsis trehalose phosphate synthaseII (tpsII) mutants are ABA-hypersensitive during early development while tps7 to tps11 show increased drought susceptibility consistent with anomalous stomatal closure and weak post-stress recovery responses
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.04.032openalex-snapshot
Grapevine TPS (trehalose-6-phosphate synthase) family genes are differentially regulated during development, upon sugar treatment and drought stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108159openalex-snapshot
Trehalose alleviates the inhibition of adventitious root formation caused by drought stress in cucumber through regulating ROS metabolism and activating trehalose and plant hormone biosynthesis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110654openalex-snapshot
Trehalose metabolism contributed to abiotic stress tolerance of Larix gmelinii seedlings
inferred← citeshttps://doi.org/10.1016/j.rsci.2023.11.005openalex-snapshot
Drought-Tolerant Rice at Molecular Breeding Eras: An Emerging Reality
inferred← citeshttps://doi.org/10.1016/j.scienta.2011.04.018openalex-snapshot
Enhancement of stress tolerance in mulberry
inferred← citeshttps://doi.org/10.1016/j.scienta.2019.108929openalex-snapshot
Cold priming the chickpea seeds imparts reproductive cold tolerance by reprogramming the turnover of carbohydrates, osmo-protectants and redox components in leaves
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111622openalex-snapshot
Transcriptome responses to salt stress in roots and leaves of Lilium pumilum
inferred← citeshttps://doi.org/10.1016/j.stress.2021.100028openalex-snapshot
Cold acclimation and prospects for cold-resilient crops
inferred← citeshttps://doi.org/10.1016/j.tplants.2004.03.005openalex-snapshot
Bifunctional and moonlighting enzymes: lighting the way to regulatory control
inferred← citeshttps://doi.org/10.1016/s0065-2113(07)00002-8openalex-snapshot
Some Prospective Strategies for Improving Crop Salt Tolerance
inferred← citeshttps://doi.org/10.1016/s0065-2113(09)03002-8openalex-snapshot
Improvement of Drought Resistance in Rice
inferred← citeshttps://doi.org/10.1016/s1016-8478(23)13088-3openalex-snapshot
Ectopic Expression of a Cold-inducible Transcription Factor, CBF1/DREB1b, in Transgenic Rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/s1755-0408(07)01012-0openalex-snapshot
Genetic Engineering for Salinity Stress Tolerance
inferred← citeshttps://doi.org/10.1016/s1872-2075(07)60001-6openalex-snapshot
Transgenic Rice Breeding for Abiotic Stress Tolerance—Present and Future
inferred← citeshttps://doi.org/10.1016/s2095-3119(12)60022-7openalex-snapshot
Overexpression of SOS Genes Enhanced Salt Tolerance in Sweetpotato
inferred← citeshttps://doi.org/10.1016/s2095-3119(13)60534-1openalex-snapshot
Cloning and Characterization of a Salt Tolerance-Associated Gene Encoding Trehalose-6-Phosphate Synthase in Sweetpotato
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c03870openalex-snapshot
Combined Analysis of Transcriptome and Metabolome Reveals the Potential Mechanism of the Enantioselective Effect of Chiral Penthiopyrad on Tomato Fruit Flavor Quality
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c10970openalex-snapshot
Integrative Physiological, Metabolomic, and Transcriptomic Insights into MsCIPK2 Responses to Drought Stress in Alfalfa
inferred← citeshttps://doi.org/10.1021/acs.jafc.7b05990openalex-snapshot
Compound Synthesis or Growth and Development of Roots/Stomata Regulate Plant Drought Tolerance or Water Use Efficiency/Water Uptake Efficiency
inferred← citeshttps://doi.org/10.1021/jf062355topenalex-snapshot
Construction of a Recombinant Thermostable β-Amylase-Trehalose Synthase Bifunctional Enzyme for Facilitating the Conversion of Starch to Trehalose
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