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Host lipid alterations after Macrophomina phaseolina infection contribute to charcoal rot disease susceptibility in grain sorghum: Evidence from transcriptomic and lipidomic data
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s003440010006openalex-snapshot
Regulation of Tracheary Element Differentiation
inferredcites →https://doi.org/10.1007/s12155-016-9775-6openalex-snapshot
Stalk Rot Diseases Impact Sweet Sorghum Biofuel Traits
inferredcites →https://doi.org/10.1007/s12600-014-0451-0openalex-snapshot
Integrating resistance and tolerance for improved evaluation of sorghum lines against Fusarium stalk rot and charcoal rot
inferredcites →https://doi.org/10.1016/0163-7827(90)90002-3openalex-snapshot
The role of alterations in membrane lipid composition in enabling physiological adaptation of organisms to their physical environment
inferredcites →https://doi.org/10.1016/0304-4157(76)90008-3openalex-snapshot
The function of sterols in membranes
inferredcites →https://doi.org/10.1016/0968-0004(83)90366-3openalex-snapshot
Monogalactosyldiacylglycerol: The most abundant polar lipid in nature
inferredcites →https://doi.org/10.1016/j.bbabio.2013.09.007openalex-snapshot
Glycerolipids in photosynthesis: Composition, synthesis and trafficking
inferredcites →https://doi.org/10.1016/j.cropro.2016.12.018openalex-snapshot
Stalk rot fungi affect grain sorghum yield components in an inoculation stage-specific manner
inferredcites →https://doi.org/10.1016/j.febslet.2007.10.053openalex-snapshot
The diacylglycerol forming pathways differ among floral organs of Petunia hybrida
inferredcites →https://doi.org/10.1016/j.fgb.2010.05.005openalex-snapshot
The lipid language of plant–fungal interactions
inferredcites →https://doi.org/10.1016/j.mib.2006.06.003openalex-snapshot
Lipid signaling in pathogenic fungi
inferredcites →https://doi.org/10.1016/j.pbi.2013.06.011openalex-snapshot
Fatty acids and early detection of pathogens
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.plaphy.2009.01.004openalex-snapshot
Surface lipids and plant defenses
inferredcites →https://doi.org/10.1016/j.plipres.2009.10.003openalex-snapshot
Chloroplast proteomics highlights the subcellular compartmentation of lipid metabolism
inferredcites →https://doi.org/10.1016/j.tplants.2004.06.008openalex-snapshot
Learning the lipid language of plant signalling
inferredcites →https://doi.org/10.1016/j.tplants.2005.06.002openalex-snapshot
Phosphatidic acid: a multifunctional stress signaling lipid in plants
inferredcites →https://doi.org/10.1016/s0005-2728(09)91002-7openalex-snapshot
Biochemical and biophysical properties of thylakoid acyl lipids
inferredcites →https://doi.org/10.1016/s0014-5793(03)00109-1openalex-snapshot
Phosphate‐deficient oat replaces a major portion of the plasma membrane phospholipids with the galactolipid digalactosyldiacylglycerol
inferredcites →https://doi.org/10.1016/s0021-9258(17)42293-9openalex-snapshot
A dual role for phosphatidylglycerol in protein translocation across the Escherichia coli inner membrane.
inferredcites →https://doi.org/10.1016/s0163-7827(01)00027-3openalex-snapshot
Mutants of Arabidopsis reveal many roles for membrane lipids
inferredcites →https://doi.org/10.1016/s0163-7827(02)00047-4openalex-snapshot
The role of sterols in plant growth and development
inferredcites →https://doi.org/10.1016/s0968-0004(99)01532-7openalex-snapshot
Signal transduction in the plant immune response
inferredcites →https://doi.org/10.1016/s1360-1385(01)01918-5openalex-snapshot
Phosphatidic acid: an emerging plant lipid second messenger
inferredcites →https://doi.org/10.1016/s1369-5266(00)00122-9openalex-snapshot
Xylogenesis: the birth of a corpse
inferredcites →https://doi.org/10.1016/s1369-5266(02)00268-6openalex-snapshot
Phospholipid signalling in plant defence
inferredcites →https://doi.org/10.1016/s1388-1981(02)00268-8openalex-snapshot
Oxylipin profiling in pathogen-infected potato leaves
inferredcites →https://doi.org/10.1023/a:1026532223173openalex-snapshot
Programmed cell death of tracheary elements as a paradigm in plants
inferredcites →https://doi.org/10.1034/j.1399-3054.2003.00131.xopenalex-snapshot
Activation of phospholipases by N‐acetylchitooligosaccharide elicitor in suspension‐cultured rice cells mediates reactive oxygen generation
inferredcites →https://doi.org/10.1038/nature07723openalex-snapshot
The Sorghum bicolor genome and the diversification of grasses
inferredcites →https://doi.org/10.1038/nrm2330openalex-snapshot
Membrane lipids: where they are and how they behave
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01730.xopenalex-snapshot
Cyclopentenone isoprostanes induced by reactive oxygen species trigger defense gene activation and phytoalexin accumulation in plants
inferredcites →https://doi.org/10.1073/pnas.180320497openalex-snapshot
DGD1-independent biosynthesis of extraplastidic galactolipids after phosphate deprivation in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.88.16.6926openalex-snapshot
Differential effects of plant sterols on water permeability and on acyl chain ordering of soybean phosphatidylcholine bilayers.
inferredcites →https://doi.org/10.1074/jbc.274.52.36827openalex-snapshot
Lipid-assisted Protein Folding
inferredcites →https://doi.org/10.1074/jbc.m205375200openalex-snapshot
Profiling Membrane Lipids in Plant Stress Responses
inferredcites →https://doi.org/10.1074/jbc.m604820200openalex-snapshot
Oxylipin Profiling of the Hypersensitive Response in Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/jbc.m706692200openalex-snapshot
Differential Degradation of Extraplastidic and Plastidic Lipids during Freezing and Post-freezing Recovery in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/bioinformatics/bti310openalex-snapshot
GMAP: a genomic mapping and alignment program for mRNA and EST sequences
inferredcites →https://doi.org/10.1094/pdis-02-16-0171-reopenalex-snapshot
Stalk Rot Fungi Affect Leaf Greenness (SPAD) of Grain Sorghum in a Genotype- and Growth-Stage-Specific Manner
inferredcites →https://doi.org/10.1094/pdis-02-17-0238-reopenalex-snapshot
Impacts of Fungal Stalk Rot Pathogens on Physicochemical Properties of Sorghum Grain
inferredcites →https://doi.org/10.1094/pdis-09-10-0631openalex-snapshot
First Report of Charcoal Rot Caused by Macrophomina phaseolina in Sunflower in Turkey
inferredcites →https://doi.org/10.1094/pdis-93-6-0666copenalex-snapshot
First Report of Charcoal Rot on Canola Caused by Macrophomina phaseolina in Western Australia
inferredcites →https://doi.org/10.1094/phyto-70-13openalex-snapshot
Survival ofMacrophomina phaseolinain Soil and in Residue of Soybean
inferredcites →https://doi.org/10.1096/fj.08-111070openalex-snapshot
Depletion of phytosterols from the plant plasma membrane provides evidence for disruption of lipid rafts
inferredcites →https://doi.org/10.1104/pp.008722openalex-snapshot
An Early C-22 Oxidation Branch in the Brassinosteroid Biosynthetic Pathway
inferredcites →https://doi.org/10.1104/pp.102.017954openalex-snapshot
Nod Factor and Elicitors Activate Different Phospholipid Signaling Pathways in Suspension-Cultured Alfalfa Cells
inferredcites →https://doi.org/10.1104/pp.105.4.1239openalex-snapshot
Chemically Induced Cuticle Mutation Affecting Epidermal Conductance to Water Vapor and Disease Susceptibility in Sorghum bicolor (L.) Moench
inferredcites →https://doi.org/10.1104/pp.109.1.15openalex-snapshot
Cold Acclimation of Arabidopsis thaliana (Effect on Plasma Membrane Lipid Composition and Freeze-Induced Lesions)
inferredcites →https://doi.org/10.1104/pp.109.138230openalex-snapshot
Reactive Oxygen Species Are Involved in Brassinosteroid-Induced Stress Tolerance in Cucumber
inferredcites →https://doi.org/10.1104/pp.111.189217openalex-snapshot
Phytosterols Play a Key Role in Plant Innate Immunity against Bacterial Pathogens by Regulating Nutrient Efflux into the Apoplast
inferredcites →https://doi.org/10.1104/pp.111.190280openalex-snapshot
Direct Infusion Mass Spectrometry of Oxylipin-Containing Arabidopsis Membrane Lipids Reveals Varied Patterns in Different Stress Responses
inferredcites →https://doi.org/10.1104/pp.112.202846openalex-snapshot
Lipid Profiling of the Arabidopsis Hypersensitive Response Reveals Specific Lipid Peroxidation and Fragmentation Processes: Biogenesis of Pimelic and Azelaic Acid
inferredcites →https://doi.org/10.1104/pp.114.250050openalex-snapshot
Inducible Knockdown of MONOGALACTOSYLDIACYLGLYCEROL SYNTHASE1 Reveals Roles of Galactolipids in Organelle Differentiation in Arabidopsis Cotyledons
inferredcites →https://doi.org/10.1104/pp.123.4.1507openalex-snapshot
Elicitation of Suspension-Cultured Tomato Cells Triggers the Formation of Phosphatidic Acid and Diacylglycerol Pyrophosphate
inferredcites →https://doi.org/10.1104/pp.124.3.1293openalex-snapshot
Analysis of Oxidative Stress and Wound-Inducible Dinor Isoprostanes F1 (Phytoprostanes F1) in Plants
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/10.1111/j.1365-3040.2006.01527.xopenalex-snapshot
Characterization of the Arabidopsis thermosensitive mutant atts02 reveals an important role for galactolipids in thermotolerance
inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02341.xopenalex-snapshot
Plant adaptation to frequent alterations between high and low temperatures: remodelling of membrane lipids and maintenance of unsaturation levels
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02110.xopenalex-snapshot
Phosphatidic acid accumulation is an early response in theCf‐4/Avr4interaction
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04235.xopenalex-snapshot
A role for β‐sitosterol to stigmasterol conversion in plant–pathogen interactions
inferredcites →https://doi.org/10.1111/j.2517-6161.1995.tb02031.xopenalex-snapshot
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
inferredcites →https://doi.org/10.1111/tpj.12659openalex-snapshot
Lipid changes after leaf wounding in Arabidopsis thaliana: expanded lipidomic data form the basis for lipid co‐occurrence analysis
inferredcites →https://doi.org/10.1126/science.1191803openalex-snapshot
Freezing Tolerance in Plants Requires Lipid Remodeling at the Outer Chloroplast Membrane
inferredcites →https://doi.org/10.1126/science.294.5548.1871openalex-snapshot
Prostaglandins and Leukotrienes: Advances in Eicosanoid Biology
inferredcites →https://doi.org/10.1146/annurev-phyto-080508-081820openalex-snapshot
Fatty Acid–Derived Signals in Plant Defense
inferredcites →https://doi.org/10.1146/annurev.arplant.55.031903.141616openalex-snapshot
BIOSYNTHESIS AND ACCUMULATION OF STEROLS
inferredcites →https://doi.org/10.1146/annurev.phyto.43.040204.135923openalex-snapshot
Contrasting Mechanisms of Defense Against Biotrophic and Necrotrophic Pathogens
inferredcites →https://doi.org/10.1146/annurev.phyto.43.040204.135951openalex-snapshot
Lipids, Lipases, and Lipid-Modifying Enzymes in Plant Disease Resistance
inferredcites →https://doi.org/10.1186/1471-2164-13-1openalex-snapshot
Optimizing illumina next-generation sequencing library preparation for extremely at-biased genomes
inferredcites →https://doi.org/10.1186/1471-2164-13-493openalex-snapshot
Tools to kill: Genome of one of the most destructive plant pathogenic fungi Macrophomina phaseolina
inferredcites →https://doi.org/10.1186/bcr1678openalex-snapshot
Inflammation and breast cancer. Cyclooxygenase/prostaglandin signaling and breast cancer
inferredcites →https://doi.org/10.1194/jlr.r700020-jlr200openalex-snapshot
Thematic Review Series: Glycerolipids. Phosphatidylserine and phosphatidylethanolamine in mammalian cells: two metabolically related aminophospholipids
inferredcites →https://doi.org/10.14806/ej.17.1.200openalex-snapshot
Cutadapt removes adapter sequences from high-throughput sequencing reads
inferredcites →https://doi.org/10.2135/cropsci2004.1195openalex-snapshot
Estimation of Combining Ability for Resistance to Fusarium Stalk Rot in Grain Sorghum
inferredcites →https://doi.org/10.2741/2250openalex-snapshot
Plant lipidomics: Discerning biological function by profiling plant complex lipids using mass spectrometry
inferredcites →https://doi.org/10.3109/10409238309102790openalex-snapshot
Sterol, Structure and Membrane Function
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/2021.06.28.450227openalex-snapshot
Plant lipid metabolism in susceptible and tolerant soybean ( Glycine max ) cultivars in response to Phytophthora sojae colonization and infection
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