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Unsaturation of Very-Long-Chain Ceramides Protects Plant from Hypoxia-Induced Damages by Modulating Ethylene Signaling in Arabidopsis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/rcm.2962openalex-snapshot
Rapid measurement of sphingolipids from Arabidopsis thaliana by reversed‐phase high‐performance liquid chromatography coupled to electrospray ionization tandem mass spectrometry
inferredcites →https://doi.org/10.1007/978-1-62703-401-2_10openalex-snapshot
Detection and Quantification of Plant Sphingolipids by LC-MS
inferredcites →https://doi.org/10.1007/bf00020987openalex-snapshot
Tissue-specific and light-responsive regulation of the promoter region of the Arabidopsis thaliana chloroplast ?-3 fatty acid desaturase gene (FAD7)
inferredcites →https://doi.org/10.1007/s10529-008-9639-zopenalex-snapshot
Fatty acid unsaturation, mobilization, and regulation in the response of plants to stress
inferredcites →https://doi.org/10.1016/0092-8674(93)90119-bopenalex-snapshot
CTR1, a negative regulator of the ethylene response pathway in arabidopsis, encodes a member of the Raf family of protein kinases
inferredcites →https://doi.org/10.1016/j.cellsig.2009.11.015openalex-snapshot
Hypoxia-induced neuronal apoptosis is mediated by de novo synthesis of ceramide through activation of serine palmitoyltransferase
inferredcites →https://doi.org/10.1016/j.pbi.2013.02.009openalex-snapshot
Plant sphingolipids: function follows form
inferredcites →https://doi.org/10.1016/j.pbi.2013.06.008openalex-snapshot
Flooding tolerance: O2 sensing and survival strategies
inferredcites →https://doi.org/10.1016/j.phytochem.2006.06.005openalex-snapshot
Quantitative profiling of polar glycerolipid species from organs of wild-type Arabidopsis and a PHOSPHOLIPASE Dα1 knockout mutant
inferredcites →https://doi.org/10.1016/j.plantsci.2013.05.008openalex-snapshot
Extending the story of very-long-chain fatty acid elongation
inferredcites →https://doi.org/10.1016/j.plipres.2010.11.002openalex-snapshot
New roles for acyl-CoA-binding proteins (ACBPs) in plant development, stress responses and lipid metabolism
inferredcites →https://doi.org/10.1016/j.tplants.2004.07.005openalex-snapshot
Plant responses to hypoxia – is survival a balancing act?
inferredcites →https://doi.org/10.1016/j.tplants.2011.12.004openalex-snapshot
Making sense of low oxygen sensing
inferredcites →https://doi.org/10.1016/s0005-2736(03)00108-1openalex-snapshot
Intracellular delivery of ceramide lipids via liposomes enhances apoptosis in vitro
inferredcites →https://doi.org/10.1016/s0092-8674(00)80183-xopenalex-snapshot
Kinase Suppressor of Ras Is Ceramide-Activated Protein Kinase
inferredcites →https://doi.org/10.1016/s0163-7827(03)00036-5openalex-snapshot
Membrane fluidity and the perception of environmental signals in cyanobacteria and plants
inferredcites →https://doi.org/10.1016/s1360-1385(03)00128-6openalex-snapshot
Sphingolipids, new players in plant signaling
inferredcites →https://doi.org/10.1016/s1369-5266(03)00038-4openalex-snapshot
Response of plant metabolism to too little oxygen
inferredcites →https://doi.org/10.1016/s1388-1981(03)00033-7openalex-snapshot
Plant sphingolipids: structural diversity, biosynthesis, first genes and functions
inferredcites →https://doi.org/10.1038/cr.2012.145openalex-snapshot
Activation of ethylene signaling is mediated by nuclear translocation of the cleaved EIN2 carboxyl terminus
inferredcites →https://doi.org/10.1038/nature10534openalex-snapshot
Homeostatic response to hypoxia is regulated by the N-end rule pathway in plants
inferredcites →https://doi.org/10.1038/nature10536openalex-snapshot
Oxygen sensing in plants is mediated by an N-end rule pathway for protein destabilization
inferredcites →https://doi.org/10.1073/pnas.0601283103openalex-snapshot
Cellular oxygen sensing: Crystal structure of hypoxia-inducible factor prolyl hydroxylase (PHD2)
inferredcites →https://doi.org/10.1073/pnas.1107161108openalex-snapshot
Integration of low temperature and light signaling during cold acclimation response in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1214848109openalex-snapshot
CTR1 phosphorylates the central regulator EIN2 to control ethylene hormone signaling from the ER membrane to the nucleus in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1307237110openalex-snapshot
Hypoxic and Ras-transformed cells support growth by scavenging unsaturated fatty acids from lysophospholipids
inferredcites →https://doi.org/10.1073/pnas.93.14.6959openalex-snapshot
Ceramide-binding and activation defines protein kinase c-Raf as a ceramide-activated protein kinase.
inferredcites →https://doi.org/10.1073/pnas.95.9.5401openalex-snapshot
Association of the Arabidopsis CTR1 Raf-like kinase with the ETR1 and ERS ethylene receptors
inferredcites →https://doi.org/10.1074/jbc.271.14.8472openalex-snapshot
Raf-1 Kinase Possesses Distinct Binding Domains for Phosphatidylserine and Phosphatidic Acid
inferredcites →https://doi.org/10.1074/jbc.274.29.20313openalex-snapshot
Long Chain Ceramides Activate Protein Phosphatase-1 and Protein Phosphatase-2A
inferredcites →https://doi.org/10.1074/jbc.m109.063586openalex-snapshot
Alkaline Ceramidase 3 (ACER3) Hydrolyzes Unsaturated Long-chain Ceramides, and Its Down-regulation Inhibits Both Cell Proliferation and Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m111.297994openalex-snapshot
Dihydroceramide-based Response to Hypoxia
inferredcites →https://doi.org/10.1074/jbc.m205375200openalex-snapshot
Profiling Membrane Lipids in Plant Stress Responses
inferredcites →https://doi.org/10.1074/jbc.m604050200openalex-snapshot
Separation and Identification of Major Plant Sphingolipid Classes from Leaves
inferredcites →https://doi.org/10.1074/jbc.m700082200openalex-snapshot
Ceramide Recruits and Activates Protein Kinase C ζ (PKCζ) within Structured Membrane Microdomains
inferredcites →https://doi.org/10.1074/jbc.m808909200openalex-snapshot
The Carboxyl-terminal Domain of Atypical Protein Kinase Cζ Binds to Ceramide and Regulates Junction Formation in Epithelial Cells
inferredcites →https://doi.org/10.1093/aob/mci217openalex-snapshot
Genome-wide Analysis of Transcript Abundance and Translation in Arabidopsis Seedlings Subjected to Oxygen Deprivation
inferredcites →https://doi.org/10.1093/aob/mci218openalex-snapshot
The Use of Microarrays to Study the Anaerobic Response in Arabidopsis
inferredcites →https://doi.org/10.1093/emboj/17.3.732openalex-snapshot
Regulation of Raf‐1 kinase by TNF via its second messenger ceramide and cross‐talk with mitogenic signalling
inferredcites →https://doi.org/10.1093/jxb/erm243openalex-snapshot
Phosphatidic acid binds to and inhibits the activity of Arabidopsis CTR1
inferredcites →https://doi.org/10.1101/gad.1140503openalex-snapshot
Ceramides modulate programmed cell death in plants
inferredcites →https://doi.org/10.1104/pp.104.055475openalex-snapshot
Global Transcription Profiling Reveals Comprehensive Insights into Hypoxic Response in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.057299openalex-snapshot
A Genome-Wide Analysis of the Effects of Sucrose on Gene Expression in Arabidopsis Seedlings under Anoxia
inferredcites →https://doi.org/10.1104/pp.107.100446openalex-snapshot
A Higher Plant Δ8 Sphingolipid Desaturase with a Preference for (Z)-Isomer Formation Confers Aluminum Tolerance to Yeast and Plants
inferredcites →https://doi.org/10.1104/pp.111.172486openalex-snapshot
The AP2/ERF Transcription Factor AtERF73/HRE1 Modulates Ethylene Responses during Hypoxia in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.176933openalex-snapshot
Overexpression of Arabidopsis ACBP3 Enhances NPR1-Dependent Plant Resistance to Pseudomonas syringe pv tomato DC3000
inferredcites →https://doi.org/10.1104/pp.112.202325openalex-snapshot
Involvement of Arabidopsis ACYL-COENZYME A DESATURASE-LIKE2 (At2g31360) in the Biosynthesis of the Very-Long-Chain Monounsaturated Fatty Acid Components of Membrane Lipids
inferredcites →https://doi.org/10.1104/pp.113.230326openalex-snapshot
Two Fatty Acid Desaturases, STEAROYL-ACYL CARRIER PROTEIN Δ9-DESATURASE6 and FATTY ACID DESATURASE3, Are Involved in Drought and Hypoxia Stress Signaling in Arabidopsis Crown Galls
inferredcites →https://doi.org/10.1104/pp.114.237990openalex-snapshot
A Shoot-Specific Hypoxic Response of Arabidopsis Sheds Light on the Role of the Phosphate-Responsive Transcription Factor PHOSPHATE STARVATION RESPONSE1
inferredcites →https://doi.org/10.1104/pp.115.3.875openalex-snapshot
Membrane Fluidity and Temperature Perception
inferredcites →https://doi.org/10.1104/pp.91.1.401openalex-snapshot
Enhanced Thermal Tolerance in a Mutant of Arabidopsis Deficient in Palmitic Acid Unsaturation
inferredcites →https://doi.org/10.1105/tpc.107.057851openalex-snapshot
Sphingolipid Long-Chain Base Hydroxylation Is Important for Growth and Regulation of Sphingolipid Content and Composition in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.060053openalex-snapshot
An Inositolphosphorylceramide Synthase Is Involved in Regulation of Plant Programmed Cell Death Associated with Defense inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.062992openalex-snapshot
Phospholipase Dα1 and Phosphatidic Acid Regulate NADPH Oxidase Activity and Production of Reactive Oxygen Species in ABA-Mediated Stomatal Closure in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.071209openalex-snapshot
Very-Long-Chain Fatty Acids Are Involved in Polar Auxin Transport and Developmental Patterning in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.110.075333openalex-snapshot
Overexpression of Arabidopsis Acyl-CoA Binding Protein ACBP3 Promotes Starvation-Induced and Age-Dependent Leaf Senescence
inferredcites →https://doi.org/10.1105/tpc.110.080473openalex-snapshot
Sphingolipids Containing Very-Long-Chain Fatty Acids Define a Secretory Pathway for Specific Polar Plasma Membrane Protein Targeting in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.089029openalex-snapshot
A Small-Molecule Screen Identifies l -Kynurenine as a Competitive Inhibitor of TAA1/TAR Activity in Ethylene-Directed Auxin Biosynthesis and Root Growth in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.093880openalex-snapshot
Plant Oxygen Sensing Is Mediated by the N-End Rule Pathway: A Milestone in Plant Anaerobiosis
inferredcites →https://doi.org/10.1105/tpc.113.111179openalex-snapshot
ACYL-LIPID DESATURASE2Is Required for Chilling and Freezing Tolerance inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.115741openalex-snapshot
COPPER RESPONSE REGULATOR1–Dependent and –Independent Responses of theChlamydomonas reinhardtiiTranscriptome to Dark Anoxia
inferredcites →https://doi.org/10.1105/tpc.113.120162openalex-snapshot
Phosphatidic Acid Interacts with a MYB Transcription Factor and Regulates Its Nuclear Localization and Function in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02536.xopenalex-snapshot
Modulated fatty acid desaturation via overexpression of two distinctω‐3 desaturases differentially alters tolerance to various abiotic stresses in transgenic tobacco cells and plants
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03642.xopenalex-snapshot
Selective mRNA translation coordinates energetic and metabolic adjustments to cellular oxygen deprivation and reoxygenation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03765.xopenalex-snapshot
Functional association of cell death suppressor, Arabidopsis Bax inhibitor‐1, with fatty acid 2‐hydroxylation through cytochrome b5
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04829.xopenalex-snapshot
Sphingolipid Δ8 unsaturation is important for glucosylceramide biosynthesis and low‐temperature performance in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.00992.xopenalex-snapshot
An introduction to plant sphingolipids and a review of recent advances in understanding their metabolism and function
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03287.xopenalex-snapshot
As simple as ACB – new insights into the role of acyl‐CoA‐binding proteins in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03451.xopenalex-snapshot
Hypoxia responsive gene expression is mediated by various subsets of transcription factors and miRNAs that are determined by the actual oxygen availability
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03590.xopenalex-snapshot
Molecular characterization of the submergence response of the Arabidopsis thaliana ecotype Columbia
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03852.xopenalex-snapshot
Disruption of the ceramide synthase LOH1 causes spontaneous cell death inArabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04351.xopenalex-snapshot
A rabidopsis mutants of sphingolipid fatty acid α‐hydroxylases accumulate ceramides and salicylates
inferredcites →https://doi.org/10.1111/nph.12774openalex-snapshot
Transcriptomic and lipidomic profiles of glycerolipids during A rabidopsis flower development
inferredcites →https://doi.org/10.1111/plb.12014openalex-snapshot
Ethylene – and oxygen signalling – drive plant survival during flooding
inferredcites →https://doi.org/10.1111/tpj.12692openalex-snapshot
Arabidopsis acyl‐ C o A ‐binding protein ACBP 3 participates in plant response to hypoxia by modulating very‐long‐chain fatty acid metabolism
inferredcites →https://doi.org/10.1126/science.1071505openalex-snapshot
RopGAP4-Dependent Rop GTPase Rheostat Control of Arabidopsis Oxygen Deprivation Tolerance
inferredcites →https://doi.org/10.1126/science.1168532openalex-snapshot
Protection of C. elegans from Anoxia by HYL-2 Ceramide Synthase
inferredcites →https://doi.org/10.1126/science.1173278openalex-snapshot
Ceramides--Friend or Foe in Hypoxia?
inferredcites →https://doi.org/10.1126/science.1225974openalex-snapshot
Processing and Subcellular Trafficking of ER-Tethered EIN2 Control Response to Ethylene Gas
inferredcites →https://doi.org/10.1126/science.287.5452.476openalex-snapshot
Trienoic Fatty Acids and Plant Tolerance of High Temperature
inferredcites →https://doi.org/10.1186/1471-2229-4-17openalex-snapshot
Regulation of membrane fatty acid composition by temperature in mutants of Arabidopsis with alterations in membrane lipid composition
inferredcites →https://doi.org/10.1194/jlr.m025395openalex-snapshot
Identification and characterization of protein phosphatase 2C activation by ceramide
inferredcites →https://doi.org/10.1371/journal.pone.0030355openalex-snapshot
Arabidopsis Fatty Acid Desaturase FAD2 Is Required for Salt Tolerance during Seed Germination and Early Seedling Growth
inferredcites →https://doi.org/10.3389/fpls.2012.00068openalex-snapshot
Sphingolipids and Plant Defense/Disease: The “Death” Connection and Beyond
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/1873-3468.13987openalex-snapshot
Sphingolipids in plants: a guidebook on their function in membrane architecture, cellular processes, and environmental or developmental responses
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0623openalex-snapshot
Signalling Interactions in Flooding Tolerance
inferred← citeshttps://doi.org/10.1002/9783527836512.ch22openalex-snapshot
Lipidomics in Plant Science
inferred← citeshttps://doi.org/10.1002/cppb.20109openalex-snapshot
Liquid Chromatography–Mass Spectrometry (LC‐MS)‐Based Analysis for Lipophilic Compound Profiling in Plants
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Complexity of Abiotic Stress Stimuli: Mimicking Hypoxic Conditions Experimentally on the Basis of Naturally Occurring Environments
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Omics Technologies for Abiotic Stress Tolerance in Plants: Current Status and Prospects
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Microbial Metabolites: A Potential Weapon Against Phytopathogens
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Repressors: the gatekeepers of phytohormone signaling cascades
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Hydrogen sulfide reduces cell death through regulating autophagy during submergence in Arabidopsis
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Beyond the surface: delving into plant signaling during flooding stress
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Association mapping for traits related to nitrogen use efficiency in tropical maize lines under field conditions
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Understanding lipid-mediated defense mechanisms in plant responses to abiotic stress
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Overexpression of the Arabidopsis ceramide synthase gene AtLOH1 enhances plant cold stress tolerance
inferred← citeshttps://doi.org/10.1007/s44281-025-00088-1openalex-snapshot
Molecular mechanisms and adaptive strategies for hypoxia tolerance in horticultural crops: beyond model systems
inferred← citeshttps://doi.org/10.1016/b978-0-443-15313-6.00023-5openalex-snapshot
Role of phospholipase D in abiotic stress tolerance
inferred← citeshttps://doi.org/10.1016/j.bbalip.2016.04.003openalex-snapshot
Plant sphingolipids: Their importance in cellular organization and adaption
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Using lipidomics for expanding the knowledge on lipid metabolism in plants
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A new era in plant functional genomics
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The significance and functions of ethylene in flooding stress tolerance in plants
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Multi-class polar lipid profiling in fresh and roasted hazelnut (Corylus avellana cultivar “Tonda di Giffoni”) by LC-ESI/LTQOrbitrap/MS/MSn
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Lipidomic profiling reveals the protective mechanism of nitrogen-controlled atmosphere on brown rice quality during storage
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Lipids signaling and unsaturation of fatty acids participate in ramie response to submergence stress and hypoxia-responsive gene regulation
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Down-regulating a fiber-specific KCR like gene GhKCRL1 suppressed fiber elongation through blocking the synthesis of sphingolipids in fiber cell
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Hypoxia-induced modulation of ceramide metabolism: Implications for potential biomarkers and intervention targets
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OsPLDα1 mediates cadmium stress response in rice by regulating reactive oxygen species accumulation and lipid remodeling
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Integrated transcriptomics and metabolomics analysis provide insights into the alleviation of waterlogging stress in maize by exogenous spermidine application
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Growth of Arabidopsis thaliana and Eutrema salsugineum in a closed growing system designed for quantification of plant water use
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Calcium deprivation enhances non-selective fluid-phase endocytosis and modifies membrane lipid profiles in Arabidopsis roots
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SWATH-MS quantitative proteomic investigation of nitrogen starvation in Arabidopsis reveals new aspects of plant nitrogen stress responses
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Emerging Roles of Sphingolipid Signaling in Plant Response to Biotic and Abiotic Stresses
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Calcium-dependent activation of CPK12 facilitates its cytoplasm-to-nucleus translocation to potentiate plant hypoxia sensing by phosphorylating ERF-VII transcription factors
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Function of ceramide synthases on growth, ganoderic acid biosynthesis and sphingolipid homeostasis in Ganoderma lucidum
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Submergence induced changes of molecular species in membrane lipids in Arabidopsis thaliana
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Plant acyl-CoA-binding proteins: An emerging family involved in plant development and stress responses
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Lipidomic studies of membrane glycerolipids in plant leaves under heat stress
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New insights into the role of lipids in plant hypoxia responses
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Phosphatidic acid signaling and function in nuclei
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Plant and algal lipidomes: Analysis, composition, and their societal significance
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Plant Class III acyl-CoA binding proteins can protect against necrotrophs: A review
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Adjustments of both phospholipids and sphingolipids contribute to cold tolerance in stony hard peach fruit by continuous ethylene
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Surviving under ice: Gene expression changes during ice encasement in timothy (Phleum pratense L.) overlap with freezing and hypoxia stress responses
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Differential leaf flooding resilience in Arabidopsis thaliana is controlled by ethylene signaling-activated and age-dependent phosphorylation of ORESARA1
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Ethylene-mediated nitric oxide depletion pre-adapts plants to hypoxia stress
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The SnRK1–RAP2.4h–PIP2 module contributes to the trade-off between growth and hypoxia tolerance in plants
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Endophytic Flavobacterium promotes root hair development and enhances drought tolerance via an ERF–CEP5 hormonal regulatory module
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Differential metabolic responses of shrubs and grasses to water additions in arid karst region, southwestern China
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Phosphatidic acid directly activates mTOR and then regulates SREBP to promote ganoderic acid biosynthesis under heat stress in Ganoderma lingzhi
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The sphingolipid biosynthetic enzyme Sphingolipid delta8 desaturase is important for chilling resistance of tomato
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Sphingolipid biosynthesis in man and microbes
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The mechanisms behind the contrasting responses to waterlogging in black-grass (Alopecurus myosuroides) and wheat (Triticum aestivum)
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Membrane lipids are involved in plant response to oxygen deprivation
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NAC-mediated membrane lipid remodeling negatively regulates fruit cold tolerance
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The β-ketoacyl-CoA synthase KCS13 regulates the cold response in cotton by modulating lipid and oxylipin biosynthesis
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The hypoxia–reoxygenation stress in plants
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How plant roots respond to waterlogging
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The SALT OVERLY SENSITIVE 2–CONSTITUTIVE TRIPLE RESPONSE1 module coordinates plant growth and salt tolerance in Arabidopsis
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Sphingolipids in plant abiotic stress responses
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Alternative splicing and translation play important roles in hypoxic germination in rice
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Transcription Factor WRKY62 Plays a Role in Pathogen Defense and Hypoxia-Responsive Gene Expression in Rice
inferred← citeshttps://doi.org/10.1093/plcell/koab289openalex-snapshot
Phosphatidic acid modulates MPK3- and MPK6-mediated hypoxia signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plcell/koad060openalex-snapshot
Brassinosteroids regulate cotton fiber elongation by modulating very-long-chain fatty acid biosynthesis
inferred← citeshttps://doi.org/10.1093/plcell/koaf257openalex-snapshot
MPK3- and MPK6-mediated phosphorylation of STOP1 triggers its nuclear stabilization to modulate hypoxia responses in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiaa015openalex-snapshot
GENOMES UNCOUPLED1-independent retrograde signaling targets the ethylene pathway to repress photomorphogenesis
inferred← citeshttps://doi.org/10.1093/plphys/kiab064openalex-snapshot
Plasma and vacuolar membrane sphingolipidomes: composition and insights on the role of main molecular species
inferred← citeshttps://doi.org/10.1101/2021.03.22.436362openalex-snapshot
α1-COP delivers sphingolipid modifiers and controls plasmodesmal callose deposition in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2022.11.23.517613openalex-snapshot
Differential leaf flooding resilience in Arabidopsis thaliana is controlled by age-dependent ORESARA1 activity
inferred← citeshttps://doi.org/10.1101/2024.04.11.589102openalex-snapshot
Surviving under Ice: Insights into gene expression changes during ice encasement in timothy ( Phleum pratense L.)
inferred← citeshttps://doi.org/10.1101/2025.08.13.669664openalex-snapshot
Autophagic degradation of EIN3 ensures developmental plasticity and recovery from environmental stress in Arabidopsis
inferred← citeshttps://doi.org/10.1101/371583openalex-snapshot
Alternative splicing and translation play important roles in parallel with transcriptional regulation during rice hypoxic germination
inferred← citeshttps://doi.org/10.1104/pp.16.00985openalex-snapshot
Ethylene-Regulated Glutamate Dehydrogenase Fine-Tunes Metabolism during Anoxia-Reoxygenation
inferred← citeshttps://doi.org/10.1104/pp.16.01803openalex-snapshot
Jasmonate Regulates Plant Responses to Postsubmergence Reoxygenation through Transcriptional Activation of Antioxidant Synthesis
inferred← citeshttps://doi.org/10.1104/pp.17.01225openalex-snapshot
Group VII Ethylene Response Factors in Arabidopsis: Regulation and Physiological Roles
inferred← citeshttps://doi.org/10.1104/pp.19.01220openalex-snapshot
Brassinosteroids Antagonize Jasmonate-Activated Plant Defense Responses through BRI1-EMS-SUPPRESSOR1 (BES1)
inferred← citeshttps://doi.org/10.1104/pp.20.00401openalex-snapshot
Sphingolipids Modulate Secretion of Glycosylphosphatidylinositol-Anchored Plasmodesmata Proteins and Callose Deposition
inferred← citeshttps://doi.org/10.1111/1462-2920.13928openalex-snapshot
Phospholipase D and phosphatidic acid mediate heat stress induced secondary metabolism in Ganoderma lucidum
inferred← citeshttps://doi.org/10.1111/jipb.12875openalex-snapshot
Polyunsaturated linolenoyl‐CoA modulates ERF‐VII‐mediated hypoxia signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1111/jipb.13028openalex-snapshot
Ethylene signaling in rice and Arabidopsis: New regulators and mechanisms
inferred← citeshttps://doi.org/10.1111/jipb.13711openalex-snapshot
α1‐COP modulates plasmodesmata function through sphingolipid enzyme regulation
inferred← citeshttps://doi.org/10.1111/jipb.13880openalex-snapshot
Survival mechanisms of plants under hypoxic stress: Physiological acclimation and molecular regulation
inferred← citeshttps://doi.org/10.1111/nph.15997openalex-snapshot
Sphingolipids: towards an integrated view of metabolism during the plant stress response
inferred← citeshttps://doi.org/10.1111/nph.18674openalex-snapshot
MYB30 integrates light signals with antioxidant biosynthesis to regulate plant responses during postsubmergence recovery
inferred← citeshttps://doi.org/10.1111/nph.19006openalex-snapshot
Hypoxia response protein HRM1 modulates the activity of mitochondrial electron transport chain in Arabidopsis under hypoxic stress
inferred← citeshttps://doi.org/10.1111/pbi.13944openalex-snapshot
Multi‐stress resilience in plants recovering from submergence
inferred← citeshttps://doi.org/10.1111/pce.15290openalex-snapshot
Autophagy Regulates Plant Tolerance to Submergence by Modulating Photosynthesis
inferred← citeshttps://doi.org/10.1111/ppl.12620openalex-snapshot
Phospholipases AtPLDζ1 and AtPLDζ2 function differently in hypoxia
inferred← citeshttps://doi.org/10.1111/ppl.12874openalex-snapshot
Arabidopsis PLDs with C2‐domain function distinctively in hypoxia
inferred← citeshttps://doi.org/10.1111/tpj.14997openalex-snapshot
Identification of potential post‐ethylene events in the signaling cascade induced by stimuli of bud dormancy release in grapevine
inferred← citeshttps://doi.org/10.1146/annurev-arplant-070225-043435openalex-snapshot
RAF-Like Protein Kinases in Plants
inferred← citeshttps://doi.org/10.11606/d.11.2017.tde-18052017-153422openalex-snapshot
Associação genômica ampla para caracteres relacionados à eficiência no uso de nitrogênio em linhagens de milho tropical
inferred← citeshttps://doi.org/10.1186/s12862-024-02304-4openalex-snapshot
Spatially heterogeneous selection and inter-varietal differentiation maintain population structure and local adaptation in a widespread conifer
inferred← citeshttps://doi.org/10.1186/s12870-024-05234-xopenalex-snapshot
Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.1186/s12870-024-05578-4openalex-snapshot
Hypoxia increases triacylglycerol levels and unsaturation in tomato roots
inferred← citeshttps://doi.org/10.1360/ssv-2024-0140openalex-snapshot
Plant biology research at Sun Yat-sen University: past and present
inferred← citeshttps://doi.org/10.21273/jashs05287-22openalex-snapshot
Waterlogging-responsive Genes Revealed by Transcriptome Sequencing in Leaves of Two Crabapple Species with Contrasting Waterlogging Tolerance
inferred← citeshttps://doi.org/10.21894/jopr.2022.0013openalex-snapshot
CELL WALL-GLYCOLIPIDS PROFILING OF OIL PALM ROOTS DURING Ganoderma boninense INFECTION USING GAS CHROMATOGRAPHYMASS SPECTROMETRY
inferred← citeshttps://doi.org/10.22215/etd/2024-16102openalex-snapshot
Exploring the gene expression patterns of plant ACYL LIPID THIOESTERASEs (ALTs) through various analyses
inferred← citeshttps://doi.org/10.3126/jnba.v4i1.53448openalex-snapshot
Lipids: A Key Regulatory Hub in Plant Stress Adaptation
inferred← citeshttps://doi.org/10.33540/1802openalex-snapshot
Flooding resilience is determined by leaf age in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fgene.2023.1113470openalex-snapshot
Metabolomic and transcriptomic responses of Adiantum (Adiantum nelumboides) leaves under drought, half-waterlogging, and rewater conditions
inferred← citeshttps://doi.org/10.3389/fpls.2017.01302openalex-snapshot
Metabolomics for Plant Improvement: Status and Prospects
inferred← citeshttps://doi.org/10.3389/fpls.2020.00080openalex-snapshot
Primary Metabolism in Fresh Fruits During Storage
inferred← citeshttps://doi.org/10.3389/fpls.2020.600458openalex-snapshot
Fumonisin B1: A Tool for Exploring the Multiple Functions of Sphingolipids in Plants
inferred← citeshttps://doi.org/10.3390/antiox11101869openalex-snapshot
Nitrated Fatty-Acids Distribution in Storage Biomolecules during Arabidopsis thaliana Development
inferred← citeshttps://doi.org/10.3390/biom11050756openalex-snapshot
Sweet Modifications Modulate Plant Development
inferred← citeshttps://doi.org/10.3390/biom11091352openalex-snapshot
Sphingolipid Profile during Cotton Fiber Growth Revealed That a Phytoceramide Containing Hydroxylated and Saturated VLCFA Is Important for Fiber Cell Elongation
inferred← citeshttps://doi.org/10.3390/cells10020346openalex-snapshot
Metabolomics Intervention Towards Better Understanding of Plant Traits
inferred← citeshttps://doi.org/10.3390/cells10051064openalex-snapshot
Plant Acyl-CoA-Binding Proteins—Their Lipid and Protein Interactors in Abiotic and Biotic Stresses
inferred← citeshttps://doi.org/10.3390/cells10061284openalex-snapshot
Biosynthesis and Functions of Very-Long-Chain Fatty Acids in the Responses of Plants to Abiotic and Biotic Stresses
inferred← citeshttps://doi.org/10.3390/ijms21197361openalex-snapshot
The Anaerobic Product Ethanol Promotes Autophagy-Dependent Submergence Tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms23063237openalex-snapshot
Full-Length Transcriptome and RNA-Seq Analyses Reveal the Mechanisms Underlying Waterlogging Tolerance in Kiwifruit (Actinidia valvata)
inferred← citeshttps://doi.org/10.3390/ijms23073572openalex-snapshot
Regulatory Mechanisms of Mitogen-Activated Protein Kinase Cascades in Plants: More than Sequential Phosphorylation
inferred← citeshttps://doi.org/10.3390/plants6020015openalex-snapshot
Lipid Raft, Regulator of Plasmodesmal Callose Homeostasis
inferred← citeshttps://doi.org/10.3390/plants9010019openalex-snapshot
Plant-Unique cis/trans Isomerism of Long-Chain Base Unsaturation is Selectively Required for Aluminum Tolerance Resulting from Glucosylceramide-Dependent Plasma Membrane Fluidity
inferred← citeshttps://doi.org/10.3390/plants9020262openalex-snapshot
Long-Chain acyl-CoA Synthetase LACS2 Contributes to Submergence Tolerance by Modulating Cuticle Permeability in Arabidopsis
inferred← citeshttps://doi.org/10.3410/f.736552447.793566743openalex-snapshot
Faculty Opinions recommendation of Ethylene-mediated nitric oxide depletion pre-adapts plants to hypoxia stress.
inferred← citeshttps://doi.org/10.48130/ph-0025-0015openalex-snapshot
Ethylene signaling in Arabidopsis: a journey from historical discoveries to modern insights
inferred← citeshttps://doi.org/10.53846/goediss-8396openalex-snapshot
The role of plasma membrane lipids in plant stresses adaptation
inferred← citeshttps://doi.org/10.6084/m9.figshare.26019584openalex-snapshot
Additional file 1 of Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26019754openalex-snapshot
Additional file 2 of Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26732749openalex-snapshot
Additional file 3 of Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26732752openalex-snapshot
Additional file 4 of Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26732755openalex-snapshot
Additional file 5 of Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26732758openalex-snapshot
Additional file 6 of Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26732761openalex-snapshot
Additional file 7 of Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26732764openalex-snapshot
Additional file 8 of Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26732767openalex-snapshot
Additional file 9 of Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26732770openalex-snapshot
Additional file 10 of Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26732773openalex-snapshot
Additional file 11 of Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.27140784openalex-snapshot
Additional file 1 of Hypoxia increases triacylglycerol levels and unsaturation in tomato roots
inferred← citeshttps://doi.org/10.70675/0313d2a3z230cz4c49zbe1bzfd1f8f562105openalex-snapshot
Elucidating the functional redundancy of the Fatty Acid Elongase complexes in Arabidopsis
inferred← citeshttps://doi.org/10.70675/143e03c5zd07bz4a8fz8049z0e7c66c2dd08openalex-snapshot
Rôle des rhamnolipides bactériens dans la tolérance des plantes aux stress abiotiques
inferred← citeshttps://doi.org/10.70675/2cdd8fc6z23c8z4aa0zb375z039394d96aadopenalex-snapshot
Rôle des sphingolipides dans l'interaction entre Pseudomonas syringae et Arabidopsis thaliana
inferred← citeshttps://doi.org/10.70675/e4cda680z4981z411cza18az85481fb84a09openalex-snapshot
Role of the most abundant plant sphingolipids, Glycosyl Inositol Phosphoryl Ceramides GIPCs, in membrane structure and host/pathogen interactions
inferred← citeshttps://doi.org/10.7287/peerj.15404v0.1/reviews/1openalex-snapshot
Peer Review #1 of "The relationship between ethylene-induced autophagy and reactive oxygen species in Arabidopsis root cells during the early stages of waterlogging stress (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15404v0.1/reviews/2openalex-snapshot
Peer Review #2 of "The relationship between ethylene-induced autophagy and reactive oxygen species in Arabidopsis root cells during the early stages of waterlogging stress (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15404v0.2/reviews/1openalex-snapshot
Peer Review #1 of "The relationship between ethylene-induced autophagy and reactive oxygen species in Arabidopsis root cells during the early stages of waterlogging stress (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.15404v0.2/reviews/2openalex-snapshot
Peer Review #2 of "The relationship between ethylene-induced autophagy and reactive oxygen species in Arabidopsis root cells during the early stages of waterlogging stress (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.15404openalex-snapshot
The relationship between ethylene-induced autophagy and reactive oxygen species in Arabidopsis root cells during the early stages of waterlogging stress
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