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Overexpression of Arabidopsis Acyl-CoA Binding Protein ACBP3 Promotes Starvation-Induced and Age-Dependent Leaf Senescence

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/abbi.1996.0282openalex-snapshot
Characterization of an Acyl-CoA-Binding Protein fromArabidopsis thaliana
inferredcites →https://doi.org/10.1007/s00425-005-0139-2openalex-snapshot
Arabidopsis ACBP3 is an extracellularly targeted acyl-CoA-binding protein
inferredcites →https://doi.org/10.1007/s11103-004-0642-zopenalex-snapshot
ACBP4 and ACBP5, novel Arabidopsis acyl-CoA-binding proteins with kelch motifs that bind oleoyl-CoA
inferredcites →https://doi.org/10.1007/s11103-008-9392-7openalex-snapshot
Arabidopsis acyl-CoA-binding proteins ACBP4 and ACBP5 are subcellularly localized to the cytosol and ACBP4 depletion affects membrane lipid composition
inferredcites →https://doi.org/10.1016/j.cell.2007.12.032openalex-snapshot
Oncogenic BRAF Induces Senescence and Apoptosis through Pathways Mediated by the Secreted Protein IGFBP7
inferredcites →https://doi.org/10.1016/j.cell.2008.03.038openalex-snapshot
Chemokine Signaling via the CXCR2 Receptor Reinforces Senescence
inferredcites →https://doi.org/10.1016/j.cell.2008.03.039openalex-snapshot
Oncogene-Induced Senescence Relayed by an Interleukin-Dependent Inflammatory Network
inferredcites →https://doi.org/10.1016/j.pbi.2004.03.012openalex-snapshot
Lipid signaling
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.2008.12.002openalex-snapshot
An Arabidopsis family of six acyl-CoA-binding proteins has three cytosolic members
inferredcites →https://doi.org/10.1016/j.plaphy.2008.12.011openalex-snapshot
Oxylipins: Structurally diverse metabolites from fatty acid oxidation
inferredcites →https://doi.org/10.1016/j.plaphy.2008.12.014openalex-snapshot
Delayed leaf senescence by exogenous lyso-phosphatidylethanolamine: Towards a mechanism of action
inferredcites →https://doi.org/10.1016/j.plaphy.2009.06.007openalex-snapshot
Light-regulated Arabidopsis ACBP4 and ACBP5 encode cytosolic acyl-CoA-binding proteins that bind phosphatidylcholine and oleoyl-CoA ester
inferredcites →https://doi.org/10.1016/s0040-4039(03)01148-1openalex-snapshot
Arabidopsides A and B, two new oxylipins from Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s0163-7827(98)00006-xopenalex-snapshot
Lipid metabolism during plant senescence
inferredcites →https://doi.org/10.1016/s0958-1669(97)80103-6openalex-snapshot
The molecular genetic analysis of leaf senescence
inferredcites →https://doi.org/10.1016/s1360-1385(00)01655-1openalex-snapshot
Molecular aspects of leaf senescence
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/s1360-1385(02)02282-3openalex-snapshot
Recollections and reflections of a plant physiologist
inferredcites →https://doi.org/10.1021/np0495938openalex-snapshot
Oxylipins Arabidopsides C and D from Arabidopsis thaliana
inferredcites →https://doi.org/10.1023/a:1006052108468openalex-snapshot
Arabidopsis cDNA encoding a membrane-associated protein with an acyl-CoA binding domain
inferredcites →https://doi.org/10.1023/a:1026524108095openalex-snapshot
Single amino acid substitutions at the acyl-CoA-binding domain interrupt 14[C]palmitoyl-CoA binding of ACBP2, an Arabidopsis acyl-CoA-binding protein with ankyrin repeats
inferredcites →https://doi.org/10.1023/b:plan.0000028790.75090.abopenalex-snapshot
Arabidopsis Acyl-CoA-Binding Protein ACBP2 Interacts With an Ethylene-Responsive Element-Binding Protein, AtEBP, via its Ankyrin Repeats
inferredcites →https://doi.org/10.1038/26506openalex-snapshot
A protein conjugation system essential for autophagy
inferredcites →https://doi.org/10.1038/35044114openalex-snapshot
A ubiquitin-like system mediates protein lipidation
inferredcites →https://doi.org/10.1038/embor.2008.255openalex-snapshot
The M‐type receptor PLA2R regulates senescence through the p53 pathway
inferredcites →https://doi.org/10.1038/sj.emboj.7600086openalex-snapshot
An extracellular aspartic protease functions in Arabidopsis disease resistance signaling
inferredcites →https://doi.org/10.1042/0300-5127:0280775openalex-snapshot
Altered membrane lipase expression delays leaf senescence
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00443.xopenalex-snapshot
Isolation of a gene encoding Arabidopsis membrane‐associated acyl‐CoA binding protein and immunolocalization of its gene product
inferredcites →https://doi.org/10.1073/pnas.140213697openalex-snapshot
An ethylene-induced cDNA encoding a lipase expressed at the onset of senescence
inferredcites →https://doi.org/10.1074/jbc.273.8.4783openalex-snapshot
Analysis of Chimeric Proteins Identifies the Regions in the Carbohydrate Recognition Domains of Rat Lung Collectins That Are Essential for Interactions with Phospholipids, Glycolipids, and Alveolar Type II Cells
inferredcites →https://doi.org/10.1074/jbc.m010743200openalex-snapshot
A Novel Class of Oxylipins,sn1-O-(12-Oxophytodienoyl)-sn2-O-(hexadecatrienoyl)-monogalactosyl Diglyceride, from Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/jbc.m109.061432openalex-snapshot
Velocity Estimates for Signal Propagation Leading to Systemic Jasmonic Acid Accumulation in Wounded Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m204630200openalex-snapshot
The APG8/12-activating Enzyme APG7 Is Required for Proper Nutrient Recycling and Senescence in Arabidopsis thaliana
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.m706214200openalex-snapshot
In Vitro Reconstitution of Plant Atg8 and Atg12 Conjugation Systems Essential for Autophagy
inferredcites →https://doi.org/10.1083/jcb.147.2.435openalex-snapshot
Formation Process of Autophagosome Is Traced with Apg8/Aut7p in Yeast
inferredcites →https://doi.org/10.1091/mbc.e06-01-0035openalex-snapshot
MAA-1, a Novel Acyl-CoA–binding Protein Involved in Endosomal Vesicle Transport inCaenorhabditis elegans
inferredcites →https://doi.org/10.1093/jxb/48.2.181openalex-snapshot
The molecular biology of leaf senescence
inferredcites →https://doi.org/10.1093/jxb/eri276openalex-snapshot
The autophagy-associated Atg8 gene family operates both under favourable growth conditions and under starvation stresses in Arabidopsis plants
inferredcites →https://doi.org/10.1093/jxb/ern241openalex-snapshot
Ethylene- and pathogen-inducible Arabidopsis acyl-CoA-binding protein 4 interacts with an ethylene-responsive element binding protein
inferredcites →https://doi.org/10.1093/jxb/ern244openalex-snapshot
An autophagy-associated Atg8 protein is involved in the responses of Arabidopsis seedlings to hormonal controls and abiotic stresses
inferredcites →https://doi.org/10.1104/pp.010843openalex-snapshot
Evidence Supporting a Role of Jasmonic Acid in Arabidopsis Leaf Senescence
inferredcites →https://doi.org/10.1104/pp.103.031393openalex-snapshot
Phosphatidic Acid Induces Leaf Cell Death in Arabidopsis by Activating the Rho-Related Small G Protein GTPase-Mediated Pathway of Reactive Oxygen Species Generation
inferredcites →https://doi.org/10.1104/pp.105.060673openalex-snapshot
Autophagic Nutrient Recycling in Arabidopsis Directed by the ATG8 and ATG12 Conjugation Pathways
inferredcites →https://doi.org/10.1104/pp.106.079293openalex-snapshot
Transcription Analysis of Arabidopsis Membrane Transporters and Hormone Pathways during Developmental and Induced Leaf Senescence
inferredcites →https://doi.org/10.1104/pp.106.082115openalex-snapshot
Wounding Stimulates the Accumulation of Glycerolipids Containing Oxophytodienoic Acid and Dinor-Oxophytodienoic Acid in Arabidopsis Leaves
inferredcites →https://doi.org/10.1104/pp.106.090811openalex-snapshot
Characterization of a Plastid Triacylglycerol Lipase from Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.104752openalex-snapshot
Oxo-Phytodienoic Acid-Containing Galactolipids in Arabidopsis: Jasmonate Signaling Dependence
inferredcites →https://doi.org/10.1104/pp.108.123331openalex-snapshot
Overexpression of the Arabidopsis 10-Kilodalton Acyl-Coenzyme A-Binding Protein ACBP6 Enhances Freezing Tolerance
inferredcites →https://doi.org/10.1104/pp.108.126714openalex-snapshot
The ATG Autophagic Conjugation System in Maize: ATG Transcripts and Abundance of the ATG8-Lipid Adduct Are Regulated by Development and Nutrient Availability
inferredcites →https://doi.org/10.1105/tpc.001701openalex-snapshot
Silencing of Phosphoethanolamine N-Methyltransferase Results in Temperature-Sensitive Male Sterility and Salt Hypersensitivity in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.010422openalex-snapshot
A Gene Encoding an Acyl Hydrolase Is Involved in Leaf Senescence in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.020370openalex-snapshot
COS1: An Arabidopsis coronatine insensitive1 Suppressor Essential for Regulation of Jasmonate-Mediated Plant Defense and Senescence
inferredcites →https://doi.org/10.1105/tpc.104.025395openalex-snapshot
Processing of ATG8s, Ubiquitin-Like Proteins, and Their Deconjugation by ATG4s Are Essential for Plant Autophagy
inferredcites →https://doi.org/10.1105/tpc.107.054718openalex-snapshot
Tocopherols Modulate Extraplastidic Polyunsaturated Fatty Acid Metabolism inArabidopsisat Low Temperature
inferredcites →https://doi.org/10.1105/tpc.109.068635openalex-snapshot
Autophagy Negatively Regulates Cell Death by Controlling NPR1-Dependent Salicylic Acid Signaling during Senescence and the Innate Immune Response inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.11.2.191openalex-snapshot
The Arabidopsis ssi1 Mutation Restores Pathogenesis-Related Gene Expression in npr1 Plants and Renders Defensin Gene Expression Salicylic Acid Dependent
inferredcites →https://doi.org/10.1105/tpc.9.12.2183openalex-snapshot
Antisense suppression of phospholipase D alpha retards abscisic acid- and ethylene-promoted senescence of postharvest Arabidopsis leaves.
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02396.xopenalex-snapshot
Visualization of autophagy in Arabidopsis using the fluorescent dye monodansylcadaverine and a GFP‐AtATG8e fusion protein
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02397.xopenalex-snapshot
AtATG18a is required for the formation of autophagosomes during nutrient stress and senescence in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03402.xopenalex-snapshot
Overexpression of membrane‐associated acyl‐CoA‐binding protein ACBP1 enhances lead tolerance in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1467-7652.2009.00427.xopenalex-snapshot
A 10‐kDa acyl‐CoA‐binding protein (ACBP) from Brassica napus enhances acyl exchange between acyl‐CoA and phosphatidylcholine
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02118.xopenalex-snapshot
Regulation and execution of molecular disassembly and catabolism during senescence
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02631.xopenalex-snapshot
Arabidopsis thaliana acyl‐CoA‐binding protein ACBP2 interacts with heavy‐metal‐binding farnesylated protein AtFP6
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03231.xopenalex-snapshot
The Arabidopsis acbp1acbp2 double mutant lacking acyl‐CoA‐binding proteins ACBP1 and ACBP2 is embryo lethal
inferredcites →https://doi.org/10.1139/b84-392openalex-snapshot
The biochemistry and regulation of senescence in chloroplasts
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105316openalex-snapshot
Leaf Senescence
inferredcites →https://doi.org/10.1177/43.9.7543914openalex-snapshot
Fluorescent conjugates of brefeldin A selectively stain the endoplasmic reticulum and Golgi complex of living cells.
inferredcites →https://doi.org/10.1515/znc-2006-5-611openalex-snapshot
Senescence-Promoting Effect of Arabidopside A
inferredcites →https://doi.org/10.1534/genetics.107.086199openalex-snapshot
The ATG12-Conjugating Enzyme ATG10 Is Essential for Autophagic Vesicle Formation in Arabidopsis thaliana
inferredcites →https://doi.org/10.2307/3870578openalex-snapshot
Antisense Suppression of Phospholipase Da Retards Abscisic Acid- and Ethylene-Promoted Senescence of Postharvest Arabidopsis Leaves

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4659296openalex-extracted
Salicylic Acid Priming Before Cadmium Exposure Increases Wheat Growth But Does Not Uniformly Reverse Cadmium Effects on Membrane Glycerolipid
inferred← citeshttps://doi.org/10.1002/1873-3468.13923openalex-snapshot
Crystal structure of the rice acyl‐CoA‐binding protein OsACBP2 in complex with C18:3‐CoA reveals a novel pattern of binding to acyl‐CoA esters
inferred← citeshttps://doi.org/10.1002/pld3.182openalex-snapshot
Arabidopsis cytosolic acyl‐CoA‐binding proteins function in determining seed oil composition
inferred← citeshttps://doi.org/10.1002/pmic.201800368openalex-snapshot
Overexpression of a Monocot Acyl‐CoA‐Binding Protein Confers Broad‐Spectrum Pathogen Protection in a Dicot
inferred← citeshttps://doi.org/10.1007/978-1-4939-2540-7_13openalex-snapshot
Signaling Pathways in Eukaryotic Stress, Aging, and Senescence: Common and Distinct Pathways
inferred← citeshttps://doi.org/10.1007/978-1-61779-995-2_13openalex-snapshot
Arabidopsis thaliana Membrane Lipid Molecular Species and Their Mass Spectral Analysis
inferred← citeshttps://doi.org/10.1007/978-3-319-25979-6_15openalex-snapshot
Acyl-CoA-Binding Proteins (ACBPs) in Plant Development
inferred← citeshttps://doi.org/10.1007/978-3-319-31703-8_20openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00360-019-01207-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00360-020-01339-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00425-010-1293-8openalex-snapshot
An Arabidopsis senescence-associated protein SAG29 regulates cell viability under high salinity
inferred← citeshttps://doi.org/10.1007/s00425-013-1904-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00425-021-03721-1openalex-snapshot
Phylogeny and subcellular localization analyses reveal distinctions in monocot and eudicot class IV acyl-CoA-binding proteins
inferred← citeshttps://doi.org/10.1007/s00709-015-0882-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00709-018-1310-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10059-012-0098-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10495-014-0981-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10725-021-00718-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10863-021-09905-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11101-018-9595-8openalex-snapshot
New insights into the biosynthesis of esterified oxylipins and their involvement in plant defense and developmental mechanisms
inferred← citeshttps://doi.org/10.1007/s11103-013-0043-2openalex-snapshot
Hormonal regulation of leaf senescence through integration of developmental and stress signals
inferred← citeshttps://doi.org/10.1007/s11103-016-0541-0openalex-snapshot
Arabidopsis acyl-CoA-binding protein ACBP6 localizes in the phloem and affects jasmonate composition
inferred← citeshttps://doi.org/10.1007/s11103-016-0557-5openalex-snapshot
Kelch-motif containing acyl-CoA binding proteins AtACBP4 and AtACBP5 are differentially expressed and function in floral lipid metabolism
inferred← citeshttps://doi.org/10.1007/s11103-021-01234-9openalex-snapshot
Root-specific CLE3 expression is required for WRKY33 activation in Arabidopsis shoots
inferred← citeshttps://doi.org/10.1007/s11104-018-3794-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11120-013-9862-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11306-011-0318-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11676-022-01485-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11745-015-4103-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13258-011-0044-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13562-024-00928-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s44307-023-00002-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s44307-025-00078-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-813187-9.00004-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-813187-9.00005-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-1-893997-98-1.00010-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbabio.2022.148596openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbalip.2015.12.018openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbalip.2021.158922openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bcab.2013.09.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biotechadv.2013.02.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cbpb.2019.05.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cbpb.2020.110539openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cj.2021.01.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cryobiol.2016.02.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.foodchem.2020.126684openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.foodres.2018.06.038openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jlr.2025.100790openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jplph.2012.11.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.meatsci.2020.108065openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.meatsci.2022.109091openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molp.2015.06.009openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molp.2021.03.021openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.pbi.2026.102964openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2013.09.026openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plantsci.2012.12.009openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.06.026openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111859openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plaphy.2012.02.013openalex-snapshot
Oxidative stress-induced autophagy in plants: The role of mitochondria
inferred← citeshttps://doi.org/10.1016/j.plipres.2010.11.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plipres.2015.04.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plipres.2016.06.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plipres.2019.100990openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plipres.2022.101156openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plipres.2026.101384openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.pmpp.2024.102459openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.postharvbio.2020.111315openalex-snapshot
Melatonin ameliorates chilling injury in green bell peppers during storage by regulating membrane lipid metabolism and antioxidant capacity
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2022.111986openalex-snapshot
SGR mutation in pak choi prolongs its shelf life by retarding chlorophyll degradation and maintaining membrane function
inferred← citeshttps://doi.org/10.1016/j.scienta.2020.109308openalex-snapshot
Methyl jasmonate alleviates chilling injury by regulating membrane lipid composition in green bell pepper
inferred← citeshttps://doi.org/10.1016/j.scienta.2025.114520openalex-snapshot
BnACBP1-like in regulating JA-dependent leaf senescence via lipid remodeling and interaction with PLA2β in Brassica napus
inferred← citeshttps://doi.org/10.1016/j.tplants.2015.10.011openalex-snapshot
Fatty Acid and Lipid Transport in Plant Cells
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c06867openalex-snapshot
Characteristics of Metabolites by Seed-Specific Inhibition of FAD2 in Brassica napus L
inferred← citeshttps://doi.org/10.1021/acsomega.7b01934openalex-snapshot
High-Temperature Stress Alleviation by Selenium Nanoparticle Treatment in Grain Sorghum
inferred← citeshttps://doi.org/10.1021/jf401537qopenalex-snapshot
A Vigna radiata 8S Globulin α′ Promoter Drives Efficient Expression of GUS in Arabidopsis Cotyledonary Embryos
inferred← citeshttps://doi.org/10.1038/mt.2013.64openalex-snapshot
Grape Exosome-like Nanoparticles Induce Intestinal Stem Cells and Protect Mice From DSS-Induced Colitis
inferred← citeshttps://doi.org/10.1038/ncomms2886openalex-snapshot
Delivery of therapeutic agents by nanoparticles made of grapefruit-derived lipids
inferred← citeshttps://doi.org/10.1038/s41419-024-06633-6openalex-snapshot
Inhibition of acyl-CoA binding protein (ACBP) by means of a GABAARγ2-derived peptide
inferred← citeshttps://doi.org/10.1038/s41438-020-00356-3openalex-snapshot
PuMYB21/PuMYB54 coordinate to activate PuPLDβ1 transcription during peel browning of cold-stored “Nanguo” pears
inferred← citeshttps://doi.org/10.1038/s41477-019-0429-5openalex-snapshot
Sphingolipid biosynthesis modulates plasmodesmal ultrastructure and phloem unloading
inferred← citeshttps://doi.org/10.1038/s41598-017-05925-6openalex-snapshot
Positioning of the SCRAMBLED receptor requires UDP-Glc:sterol glucosyltransferase 80B1 in Arabidopsis roots
inferred← citeshttps://doi.org/10.1038/s41598-020-71851-9openalex-snapshot
The overexpression of OsACBP5 protects transgenic rice against necrotrophic, hemibiotrophic and biotrophic pathogens
inferred← citeshttps://doi.org/10.1038/srep20309openalex-snapshot
Precocious leaf senescence by functional loss of PROTEIN S-ACYL TRANSFERASE14 involves the NPR1-dependent salicylic acid signaling
inferred← citeshttps://doi.org/10.1042/bsr20140139openalex-snapshot
Arabidopsis cytosolic acyl-CoA-binding proteins ACBP4, ACBP5 and ACBP6 have overlapping but distinct roles in seed development
inferred← citeshttps://doi.org/10.1071/cp22347openalex-snapshot
Overexpression of rice acyl-CoA-binding protein OsACBP5 protects Brassica napus against seedling infection by fungal phytopathogens
inferred← citeshttps://doi.org/10.1071/fp19150openalex-snapshot
Lipid remodelling plays an important role in wheat (Triticum aestivum) hypoxia stress
inferred← citeshttps://doi.org/10.1073/pnas.1805855115openalex-snapshot
Structure of a lipid-bound viral membrane assembly protein reveals a modality for enclosing the lipid bilayer
inferred← citeshttps://doi.org/10.1073/pnas.1918539117openalex-snapshot
COST1 regulates autophagy to control plant drought tolerance
inferred← citeshttps://doi.org/10.1073/pnas.2207344119openalex-snapshot
ACBP/DBI protein neutralization confers autophagy-dependent organ protection through inhibition of cell loss, inflammation, and fibrosis
inferred← citeshttps://doi.org/10.1074/jbc.m111.274274openalex-snapshot
Connections between Sphingosine Kinase and Phospholipase D in the Abscisic Acid Signaling Pathway in Arabidopsis
inferred← citeshttps://doi.org/10.1080/15548627.2015.1112483openalex-snapshot
Autophagy contributes to regulation of the hypoxia response during submergence in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1080/15548627.2018.1520547openalex-snapshot
Autophagy regulates glucose-mediated root meristem activity by modulating ROS production inArabidopsis
inferred← citeshttps://doi.org/10.1080/15548627.2020.1847797openalex-snapshot
Hydrogen peroxide mediates spermidine-induced autophagy to alleviate salt stress in cucumber
inferred← citeshttps://doi.org/10.1080/15548627.2022.2046449openalex-snapshot
Phosphatidic acid suppresses autophagy through competitive inhibition by binding GAPC (glyceraldehyde-3-phosphate dehydrogenase) and PGK (phosphoglycerate kinase) proteins
inferred← citeshttps://doi.org/10.1080/15548627.2022.2127240openalex-snapshot
VAMP724 and VAMP726 are involved in autophagosome formation inArabidopsis thaliana
inferred← citeshttps://doi.org/10.1080/15548627.2026.2668859openalex-snapshot
SINAT proteins modulate autophagic vesicle degradation by regulating V-ATPase subunit proteolysis in Arabidopsis
inferred← citeshttps://doi.org/10.1080/15592324.2017.1359365openalex-snapshot
Arabidopsis thaliana Acyl-CoA-binding protein ACBP6 interacts with plasmodesmata-located protein PDLP8
inferred← citeshttps://doi.org/10.1093/hr/uhac039openalex-snapshot
NAC-mediated membrane lipid remodeling negatively regulates fruit cold tolerance
inferred← citeshttps://doi.org/10.1093/jxb/erab107openalex-snapshot
Retracted: Glycosyltransferase UGT79B7 negatively regulates hypoxia response through γ-aminobutyric acid homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erab362openalex-snapshot
Retraction to: Glycosyltransferase UGT79B7 negatively regulates hypoxia response through γ-aminobutyric acid homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erab499openalex-snapshot
Roles of acyl-CoA-binding proteins in plant reproduction
inferred← citeshttps://doi.org/10.1093/jxb/err031openalex-snapshot
Salicylic acid beyond defence: its role in plant growth and development
inferred← citeshttps://doi.org/10.1093/jxb/err454openalex-snapshot
Metabolic engineering of the omega-3 long chain polyunsaturated fatty acid biosynthetic pathway into transgenic plants
inferred← citeshttps://doi.org/10.1093/jxb/ers009openalex-snapshot
The gene encoding Arabidopsis acyl-CoA-binding protein 3 is pathogen inducible and subject to circadian regulation
inferred← citeshttps://doi.org/10.1093/jxb/eru304openalex-snapshot
Arabidopsis membrane-associated acyl-CoA-binding protein ACBP1 is involved in stem cuticle formation
inferred← citeshttps://doi.org/10.1093/jxb/eru410openalex-snapshot
Functional diversification of two UGT80 enzymes required for steryl glucoside synthesis in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erv402openalex-snapshot
Patatin-related phospholipase A, pPLAIIIα, modulates the longitudinal growth of vegetative tissues and seeds in rice
inferred← citeshttps://doi.org/10.1093/jxb/erx392openalex-snapshot
Lipids in membrane dynamics during autophagy in plants
inferred← citeshttps://doi.org/10.1093/jxb/erz463openalex-snapshot
Transcription factor CaNAC1 regulates low-temperature-induced phospholipid degradation in green bell pepper
inferred← citeshttps://doi.org/10.1093/mp/ssr118openalex-snapshot
The Patatin-Containing Phospholipase A pPLAIIα Modulates Oxylipin Formation and Water Loss in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/pcp/pcac088openalex-snapshot
Lipidomic Analysis of Arabidopsis T-DNA Insertion Lines Leads to Identification and Characterization of C-Terminal Alterations in FATTY ACID DESATURASE 6
inferred← citeshttps://doi.org/10.1093/pcp/pcu163openalex-snapshot
The Arabidopsis Cytosolic Acyl-CoA-Binding Proteins Play Combinatory Roles in Pollen Development
inferred← citeshttps://doi.org/10.1093/pcp/pcx171openalex-snapshot
Changes in Membrane Lipid Composition and Function Accompanying Chilling Injury in Bell Peppers
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/koac251openalex-snapshot
Type one protein phosphatase regulates fixed-carbon starvation-induced autophagy in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plcell/koac273openalex-snapshot
14-3-3 proteins contribute to autophagy by modulating SINAT-mediated degradation of ATG13
inferred← citeshttps://doi.org/10.1093/plcell/koad252openalex-snapshot
HOOKLESS1 acetylates AUTOPHAGY-RELATED PROTEIN18a to promote autophagy during nutrient starvation in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plcell/koae153openalex-snapshot
The calcium-dependent protein kinase CPK16 regulates hypoxia-induced ROS production by phosphorylating the NADPH oxidase RBOHD in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiad525openalex-snapshot
Acyl-CoA binding protein is required for lipid droplet degradation in the diatom Phaeodactylum tricornutum
inferred← citeshttps://doi.org/10.1094/mpmi-01-12-0022-ropenalex-snapshot
Rapid Mobilization of Membrane Lipids in Wheat Leaf Sheaths During Incompatible Interactions with Hessian Fly
inferred← citeshttps://doi.org/10.1094/phyto-05-12-0099-ropenalex-snapshot
Lipid Profiles in Wheat Cultivars Resistant and Susceptible to Tan Spot and the Effect of Disease on the Profiles
inferred← citeshttps://doi.org/10.1097/cm9.0000000000004305openalex-snapshot
Extracellular matrix targeting peptide functionalized plant-derived lipid nanoparticles for gene therapy in osteoarthritis
inferred← citeshttps://doi.org/10.1101/2022.04.10.487768openalex-snapshot
Type One Protein Phosphatase Regulates Fixed-Carbon Starvation-Induced Autophagy by Dephosphorylating ATG13a to Facilitate ATG1a-ATG13a Formation in Arabidopsis
inferred← citeshttps://doi.org/10.1101/854067openalex-snapshot
Host lipid alterations after Macrophomina phaseolina infection contribute to charcoal rot disease susceptibility in grain sorghum: Evidence from transcriptomic and lipidomic data
inferred← citeshttps://doi.org/10.1104/pp.111.176933openalex-snapshot
Overexpression of Arabidopsis ACBP3 Enhances NPR1-Dependent Plant Resistance to Pseudomonas syringe pv tomato DC3000
inferred← citeshttps://doi.org/10.1104/pp.111.185132openalex-snapshot
Theglossyhead1Allele ofACC1Reveals a Principal Role for Multidomain Acetyl-Coenzyme A Carboxylase in the Biosynthesis of Cuticular Waxes by Arabidopsis
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1104/pp.18.00402openalex-snapshot
DIACYLGLYCEROL ACYLTRANSFERASE and DIACYLGLYCEROL KINASE Modulate Triacylglycerol and Phosphatidic Acid Production in the Plant Response to Freezing Stress
inferred← citeshttps://doi.org/10.1104/pp.18.01312openalex-snapshot
The Role of Gβ Protein in Controlling Cell Expansion via Potential Interaction with Lipid Metabolic Pathways
inferred← citeshttps://doi.org/10.1104/pp.19.01552openalex-snapshot
Seedling Chloroplast Responses Induced by N-Linolenoylethanolamine Require Intact G-Protein Complexes
inferred← citeshttps://doi.org/10.1105/tpc.109.071720openalex-snapshot
Nonspecific Phospholipase C NPC4 Promotes Responses to Abscisic Acid and Tolerance to Hyperosmotic Stress inArabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.110.081240openalex-snapshot
Patatin-Related Phospholipase pPLAIIIβ-Induced Changes in Lipid Metabolism Alter Cellulose Content and Cell Elongation in Arabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.111.094946openalex-snapshot
Cytosolic Glyceraldehyde-3-Phosphate Dehydrogenases Interact with Phospholipase Dδ to Transduce Hydrogen Peroxide Signals in the Arabidopsis Response to Stress
inferred← citeshttps://doi.org/10.1105/tpc.114.127050openalex-snapshot
Loss of Ceramide Kinase in Arabidopsis Impairs Defenses and Promotes Ceramide Accumulation and Mitochondrial H2O2 Bursts
inferred← citeshttps://doi.org/10.1105/tpc.17.00056openalex-snapshot
TRAF Family Proteins Regulate Autophagy Dynamics by Modulating AUTOPHAGY PROTEIN6 Stability in Arabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.19.00413openalex-snapshot
Arabidopsis SINAT Proteins Control Autophagy by Mediating Ubiquitylation and Degradation of ATG13
inferred← citeshttps://doi.org/10.1107/s2059798317004193openalex-snapshot
The first plant acyl-CoA-binding protein structures: the close homologues OsACBP1 and OsACBP2 from rice
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/acel.13751openalex-snapshot
High plasma concentrations of acyl‐coenzyme A binding protein ( ACBP ) predispose to cardiovascular disease: Evidence for a phylogenetically conserved proaging function of ACBP
inferred← citeshttps://doi.org/10.1111/acel.13910openalex-snapshot
Acyl coenzyme A binding protein ( ACBP ): An aging‐ and disease‐relevant “autophagy checkpoint”
inferred← citeshttps://doi.org/10.1111/cns.12005openalex-snapshot
A Double‐Edged Sword with Therapeutic Potential: An Updated Role of Autophagy in Ischemic Cerebral Injury
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2010.03546.xopenalex-snapshot
The rice acyl‐CoA‐binding protein gene family: phylogeny, expression and functional analysis
inferred← citeshttps://doi.org/10.1111/jipb.12005openalex-snapshot
Regulation of Leaf Senescence and Crop Genetic ImprovementF
inferred← citeshttps://doi.org/10.1111/jipb.13343openalex-snapshot
The plant circadian clock regulates autophagy rhythm through transcription factor LUX ARRHYTHMO
inferred← citeshttps://doi.org/10.1111/nph.12809openalex-snapshot
Subcellular localization of rice acyl‐CoA‐binding proteins (ACBPs) indicates that Os ACBP 6:: GFP is targeted to the peroxisomes
inferred← citeshttps://doi.org/10.1111/nph.15707openalex-snapshot
Arabidopsis acyl‐CoA‐binding proteins regulate the synthesis of lipid signals
inferred← citeshttps://doi.org/10.1111/nph.19924openalex-snapshot
A promoter polymorphism defines distinct roles in anther development for Col‐0 and Ler‐0 alleles of Arabidopsis ACYL‐COA BINDING PROTEIN3
inferred← citeshttps://doi.org/10.1111/nph.70142openalex-snapshot
Acyl‐ CoA ‐binding proteins: bridging long‐chain acyl‐ CoA metabolism to gene regulation
inferred← citeshttps://doi.org/10.1111/pbi.12012openalex-snapshot
The modification of plant oil composition via metabolic engineering—better nutrition by design
inferred← citeshttps://doi.org/10.1111/pbi.12304openalex-snapshot
Overexpression of patatin‐related phospholipase AIII δ altered plant growth and increased seed oil content in camelina
inferred← citeshttps://doi.org/10.1111/pbi.12446openalex-snapshot
Phospholipase Dε enhances Braasca napus growth and seed production in response to nitrogen availability
inferred← citeshttps://doi.org/10.1111/pbi.12799openalex-snapshot
Development of iFOX ‐hunting as a functional genomic tool and demonstration of its use to identify early senescence‐related genes in the polyploid Brassica napus
inferred← citeshttps://doi.org/10.1111/pbi.12828openalex-snapshot
Improved fruit α‐tocopherol, carotenoid, squalene and phytosterol contents through manipulation of Brassica juncea 3‐ HYDROXY ‐3‐ METHYLGLUTARYL ‐ COA SYNTHASE 1 in transgenic tomato
inferred← citeshttps://doi.org/10.1111/pce.12382openalex-snapshot
Expression of A rabidopsis acyl‐ CoA ‐binding proteins AtACBP 1 and AtACBP 4 confers P b( II ) accumulation in B rassica juncea roots
inferred← citeshttps://doi.org/10.1111/pce.12649openalex-snapshot
Wheat leaf lipids during heat stress: I. High day and night temperatures result in major lipid alterations
inferred← citeshttps://doi.org/10.1111/pce.13089openalex-snapshot
Sensitivity of sorghum pollen and pistil to high‐temperature stress
inferred← citeshttps://doi.org/10.1111/pce.13148openalex-snapshot
Loss of alkaline ceramidase inhibits autophagy in Arabidopsis and plays an important role during environmental stress response
inferred← citeshttps://doi.org/10.1111/pce.13502openalex-snapshot
Molecular signatures associated with increased freezing tolerance due to low temperature memory in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.15290openalex-snapshot
Autophagy Regulates Plant Tolerance to Submergence by Modulating Photosynthesis
inferred← citeshttps://doi.org/10.1111/pce.70012openalex-snapshot
HIPP33 Contributes to Selective Autophagy‐Mediated Vacuolar Sequestration of Cadmium in Arabidopsis
inferred← citeshttps://doi.org/10.1111/plb.13736openalex-snapshot
Salicylic acid priming before cadmium exposure increases wheat growth but does not uniformly reverse cadmium effects on membrane glycerolipids
inferred← citeshttps://doi.org/10.1111/ppl.12132openalex-snapshot
Head‐group acylation of monogalactosyldiacylglycerol is a common stress response, and the acyl‐galactose acyl composition varies with the plant species and applied stress
inferred← citeshttps://doi.org/10.1111/ppl.12601openalex-snapshot
Does triacylglycerol (TAG) serve a photoprotective function in plant leaves? An examination of leaf lipids under shading and drought
inferred← citeshttps://doi.org/10.1111/tpj.12043openalex-snapshot
Calmodulin‐related CML 24 interacts with ATG 4b and affects autophagy progression in A rabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.12121openalex-snapshot
Arabidopsis acyl‐CoA‐binding protein ACBP 1 participates in the regulation of seed germination and seedling development
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/tpj.13165openalex-snapshot
Non‐specific phospholipase C1 affects silicon distribution and mechanical strength in stem nodes of rice
inferred← citeshttps://doi.org/10.1111/tpj.14503openalex-snapshot
The overexpression of rice ACYL ‐ CoA ‐ BINDING PROTEIN 2 increases grain size and bran oil content in transgenic rice
inferred← citeshttps://doi.org/10.1111/tpj.70088openalex-snapshot
Inducible expression of DEFECTIVE IN ANTHER DEHISCENCE 1 enhances triacylglycerol accumulation and lipid droplet formation in vegetative tissues
inferred← citeshttps://doi.org/10.1186/1471-2229-14-96openalex-snapshot
Arabidopsis genes, AtNPR1, AtTGA2 and AtPR-5, confer partial resistance to soybean cyst nematode (Heterodera glycines) when overexpressed in transgenic soybean roots
inferred← citeshttps://doi.org/10.1186/s12284-020-00435-yopenalex-snapshot
RICE ACYL-COA-BINDING PROTEIN6 Affects Acyl-CoA Homeostasis and Growth in Rice
inferred← citeshttps://doi.org/10.1186/s12864-017-4419-6openalex-snapshot
Acyl-CoA-binding protein family members in laticifers are possibly involved in lipid and latex metabolism of Hevea brasiliensis (the Para rubber tree)
inferred← citeshttps://doi.org/10.1186/s12870-014-0332-1openalex-snapshot
Patatin-related phospholipase pPLAIIIδ influences auxin-responsive cell morphology and organ size in Arabidopsis and Brassica napus
inferred← citeshttps://doi.org/10.1186/s12870-018-1263-zopenalex-snapshot
Decreased photosynthetic rate under high temperature in wheat is due to lipid desaturation, oxidation, acylation, and damage of organelles
inferred← citeshttps://doi.org/10.1186/s12870-019-1930-8openalex-snapshot
Proximity-dependent biotinylation screening identifies NbHYPK as a novel interacting partner of ATG8 in plants
inferred← citeshttps://doi.org/10.1186/s12870-020-2257-1openalex-snapshot
Dynamic changes in membrane lipid composition of leaves of winter wheat seedlings in response to PEG-induced water stress
inferred← citeshttps://doi.org/10.1186/s12870-021-03189-xopenalex-snapshot
Alterations in the leaf lipidome of Brassica carinata under high-temperature stress
inferred← citeshttps://doi.org/10.1186/s12870-024-04944-6openalex-snapshot
Acyl-CoA-binding protein (ACBP) genes involvement in response to abiotic stress and exogenous hormone application in barley (Hordeum vulgare L.)
inferred← citeshttps://doi.org/10.1186/s12870-024-05854-3openalex-snapshot
14-3-3 proteins inhibit autophagy by regulating SINAT-mediated proteolysis of ATG6 in Arabidopsis
inferred← citeshttps://doi.org/10.1186/s12870-025-07066-9openalex-snapshot
Autophagy deficiency confers freezing tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1186/s12915-025-02149-3openalex-snapshot
Proteomics revealed novel functions and drought tolerance of Arabidopsis thaliana protein kinase ATG1
inferred← citeshttps://doi.org/10.1186/s13007-018-0282-yopenalex-snapshot
An efficient modified method for plant leaf lipid extraction results in improved recovery of phosphatidic acid
inferred← citeshttps://doi.org/10.1186/s13007-018-0299-2openalex-snapshot
Bioorthogonal click chemistry for fluorescence imaging of choline phospholipids in plants
inferred← citeshttps://doi.org/10.1186/s43897-021-00006-9openalex-snapshot
Leaf senescence: progression, regulation, and application
inferred← citeshttps://doi.org/10.1371/journal.pbio.2002978openalex-snapshot
A new vesicle trafficking regulator CTL1 plays a crucial role in ion homeostasis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005143openalex-snapshot
Unsaturation of Very-Long-Chain Ceramides Protects Plant from Hypoxia-Induced Damages by Modulating Ethylene Signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1371/journal.pone.0048138openalex-snapshot
Functional and Transcriptome Analysis Reveals an Acclimatization Strategy for Abiotic Stress Tolerance Mediated by Arabidopsis NF-YA Family Members
inferred← citeshttps://doi.org/10.1371/journal.pone.0098264openalex-snapshot
Transgenic Tobacco Overexpressing Brassica juncea HMG-CoA Synthase 1 Shows Increased Plant Growth, Pod Size and Seed Yield
inferred← citeshttps://doi.org/10.1371/journal.pone.0107372openalex-snapshot
Gene Expression in Plant Lipid Metabolism in Arabidopsis Seedlings
inferred← citeshttps://doi.org/10.1371/journal.pone.0129650openalex-snapshot
Computational Prediction of acyl-coA Binding Proteins Structure in Brassica napus
inferred← citeshttps://doi.org/10.1603/ec14286openalex-snapshot
Impact of Transient Heat Stress on Polar Lipid Metabolism in Seedlings of Wheat Near-Isogenic Lines Contrasting in Resistance to Hessian Fly (Cecidomyiidae) Infestation
inferred← citeshttps://doi.org/10.1615/critreveukargeneexpr.v21.i1.50openalex-snapshot
Autophagy in tumor suppression and cancer therapy
inferred← citeshttps://doi.org/10.2135/cropsci2012.07.0441openalex-snapshot
High Day‐ or Nighttime Temperature Alters Leaf Assimilation, Reproductive Success, and Phosphatidic Acid of Pollen Grain in Soybean [Glycine max (L.) Merr.]
inferred← citeshttps://doi.org/10.2147/ijn.s293067openalex-snapshot
Engineering Exosome-Like Nanovesicles Derived from Asparagus cochinchinensis Can Inhibit the Proliferation of Hepatocellular Carcinoma Cells with Better Safety Profile
inferred← citeshttps://doi.org/10.25148/etd.fidc010220openalex-snapshot
High and Low Toxin Producing Strains of Karenia Brevis Differ Significantly in the Redox Proteome, Lipid Profiles, and Xanthophyll Cycle Pigments
inferred← citeshttps://doi.org/10.3233/jbr-200528openalex-snapshot
Evolution of Acyl-CoA-binding protein gene family in plants provides insights into potential functions of grapevine (Vitis vinifera L.)
inferred← citeshttps://doi.org/10.3389/fcell.2020.616434openalex-snapshot
Rheostatic Balance of Circadian Rhythm and Autophagy in Metabolism and Disease
inferred← citeshttps://doi.org/10.3389/fgene.2018.00182openalex-snapshot
Functional and Structural Diversity of Acyl-coA Binding Proteins in Oil Crops
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