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Dosage differences in 12-OXOPHYTODIENOATE REDUCTASE genes modulate wheat root growth.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36248-y
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Dosage differences in 12-OXOPHYTODIENOATE REDUCTASE genes modulate wheat root growth.
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- Nature Communications, 2023, v. 14, p. 1, doi. 10.1038/s41467-023-36248-y
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- Article
A Facile and Efficient Method for the Synthesis of Labeled and Unlabeled Very Long Chain Polyunsaturated Fatty Acids.
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- Journal of the American Oil Chemists' Society (JAOCS), 2021, v. 98, n. 5, p. 489, doi. 10.1002/aocs.12484
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Selective inhibition of prostaglandin D<sub>2</sub> biosynthesis in human mast cells to overcome need for multiple receptor antagonists: Biochemical consequences.
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- Clinical & Experimental Allergy, 2021, v. 51, n. 4, p. 594, doi. 10.1111/cea.13831
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- Article
Protein Profiles of Lipid Droplets during the Hypersensitive Defense Response of Arabidopsis against Pseudomonas Infection.
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- Plant & Cell Physiology, 2020, v. 61, n. 6, p. 1144, doi. 10.1093/pcp/pcaa041
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- Article
Charge migration fragmentation in the negative ion mode of cyclopentenone and cyclopentanone intermediates in the biosynthesis of jasmonates.
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- Rapid Communications in Mass Spectrometry: RCM, 2020, v. 34, n. 8, p. 1, doi. 10.1002/rcm.8665
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- Article
Biosynthesis of Jasmonates from Linoleic Acid by the Fungus Fusarium oxysporum. Evidence for a Novel Allene Oxide Cyclase.
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- Lipids, 2019, v. 54, n. 9, p. 543, doi. 10.1002/lipd.12180
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Arabidopsis nonresponding to oxylipins locus NOXY7 encodes a yeast GCN1 homolog that mediates noncanonical translation regulation and stress adaptation.
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- Plant, Cell & Environment, 2018, v. 41, n. 6, p. 1438, doi. 10.1111/pce.13182
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The activity of HYDROPEROXIDE LYASE 1 regulates accumulation of galactolipids containing 12-oxo-phytodienoic acid in Arabidopsis.
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- Journal of Experimental Botany, 2016, v. 67, n. 17, p. 5133, doi. 10.1093/jxb/erw278
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Screen Identifying Arabidopsis Transcription Factors Involved in the Response to 9-Lipoxygenase-Derived Oxylipins.
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- PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0153216
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9-Lipoxygenase-Derived Oxylipins Activate Brassinosteroid Signaling to Promote Cell Wall-Based Defense and Limit Pathogen Infection.
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- Plant Physiology, 2015, v. 169, n. 3, p. 2324, doi. 10.1104/pp.15.00992
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- Article
Oxylipins in moss development and defense.
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- Frontiers in Plant Science, 2015, p. 1, doi. 10.3389/fpls.2015.00483
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Oxylipins in moss development and defense.
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- Frontiers in Plant Science, 2015, p. 1, doi. 10.3389/fpls.2015.00483
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- Article
The Physcomitrella patens unique alpha-dioxygenase participates in both developmental processes and defense responses.
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- BMC Plant Biology, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12870-015-0439-z
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- Article
Involvement of the Electrophilic Isothiocyanate Sulforaphane in Arabidopsis Local Defense Responses.
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- Plant Physiology, 2015, v. 167, n. 1, p. 251, doi. 10.1104/pp.114.251892
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Rational design of a ligand-based antagonist of jasmonate perception.
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- Nature Chemical Biology, 2014, v. 10, n. 8, p. 671, doi. 10.1038/nchembio.1575
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- Article
An Iron 13<i>S</i>-Lipoxygenase with an α-Linolenic Acid Specific Hydroperoxidase Activity from <i>Fusarium oxysporum</i>
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- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0064919
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- Article
Defense Activated by 9-Lipoxygenase-Derived Oxylipins Requires Specific Mitochondrial Proteins.
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- Plant Physiology, 2013, v. 161, n. 2, p. 617, doi. 10.1104/pp.112.207514
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- Article
Crystal Structures of Physcomitrella patens AOC1 and AOC2: Insights into the Enzyme Mechanism and Differences in Substrate Specificity.
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- Plant Physiology, 2012, v. 160, n. 3, p. 1251, doi. 10.1104/pp.112.205138
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Applications of Stereospecifically-Labeled Fatty Acids in Oxygenase and Desaturase Biochemistry.
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- Lipids, 2012, v. 47, n. 2, p. 101, doi. 10.1007/s11745-011-3612-7
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Identification of avian wax synthases.
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- BMC Biochemistry, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2091-13-4
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- Article
Linolenate 9 R-Dioxygenase and Allene Oxide Synthase Activities of Lasiodiplodia theobromae.
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- Lipids, 2012, v. 47, n. 1, p. 65, doi. 10.1007/s11745-011-3622-5
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A prokaryotic acyl-CoA reductase performing reduction of fatty acyl-CoA to fatty alcohol
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- FEBS Letters, 2011, v. 585, n. 22, p. 3538, doi. 10.1016/j.febslet.2011.10.016
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Efficient and Specific Conversion of 9-Lipoxygenase Hydroperoxides in the Beetroot. Formation of Pinellic Acid.
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- Lipids, 2011, v. 46, n. 9, p. 873, doi. 10.1007/s11745-011-3592-7
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Antagonistic role of 9-lipoxygenase-derived oxylipins and ethylene in the control of oxidative stress, lipid peroxidation and plant defence.
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- Plant Journal, 2011, v. 67, n. 3, p. 447, doi. 10.1111/j.1365-313X.2011.04608.x
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- Article
Omega-3 fatty acid supplementation delays the progression of neuroblastoma in vivo.
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- International Journal of Cancer, 2011, v. 128, n. 7, p. 1703, doi. 10.1002/ijc.25473
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- Article
Stereochemistry of Hydrogen Removal During Oxygenation of Linoleic Acid by Singlet Oxygen and Synthesis of 11( S)-Deuterium-Labeled Linoleic Acid.
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- Lipids, 2011, v. 46, n. 2, p. 201, doi. 10.1007/s11745-010-3510-4
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Biosynthesis of 14,15-Hepoxilins in Human L1236 Hodgkin Lymphoma Cells and Eosinophils.
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- Lipids, 2011, v. 46, n. 1, p. 69, doi. 10.1007/s11745-010-3485-1
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Emerging Complexity in Reactive Oxygen Species Production and Signaling during the Response of Plants to Pathogens.
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- Plant Physiology, 2010, v. 154, n. 2, p. 444, doi. 10.1104/pp.110.161273
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- Article
Thromboxane synthase expression and thromboxane A<sub>2</sub> production in the atherosclerotic lesion.
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- Journal of Molecular Medicine, 2010, v. 88, n. 8, p. 795, doi. 10.1007/s00109-010-0621-6
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- Article
A tomato enzyme synthesizes (+)-7- iso-jasmonoyl- l-isoleucine in wounded leaves.
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- Planta: An International Journal of Plant Biology, 2010, v. 231, n. 3, p. 717, doi. 10.1007/s00425-009-1080-6
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(+)-7-iso-Jasmonoyl-L-isoleucine is the endogenous bioactive jasmonate.
- Published in:
- Nature Chemical Biology, 2009, v. 5, n. 5, p. 344, doi. 10.1038/nchembio.161
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- Article
Diversity of the Enzymatic Activity in the Lipoxygenase Gene Family of Arabidopsis thaliana.
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- Lipids, 2009, v. 44, n. 2, p. 85, doi. 10.1007/s11745-008-3245-7
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- Article
Cover Picture: Tomato CYP74C3 is a Multifunctional Enzyme not only Synthesizing Allene Oxide but also Catalyzing its Hydrolysis and Cyclization (ChemBioChem 15/2008).
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- ChemBioChem, 2008, v. 9, n. 15, p. 2341, doi. 10.1002/cbic.200890057
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Tomato CYP74C3 is a Multifunctional Enzyme not only Synthesizing Allene Oxide but also Catalyzing its Hydrolysis and Cyclization.
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- ChemBioChem, 2008, v. 9, n. 15, p. 2498, doi. 10.1002/cbic.200800331
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Structural insights into the evolutionary paths of oxylipin biosynthetic enzymes.
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- Nature, 2008, v. 455, n. 7211, p. 363, doi. 10.1038/nature07307
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Evidence for communality in the primary determinants of CYP74 catalysis and of structural similarities between CYP74 and classical mammalian P450 enzymes.
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- Proteins, 2008, v. 72, n. 4, p. 1199, doi. 10.1002/prot.22012
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Enzymatic, but not non-enzymatic, <sup>1</sup>O<sub>2</sub>-mediated peroxidation of polyunsaturated fatty acids forms part of the EXECUTER1-dependent stress response program in the flu mutant of Arabidopsis thaliana.
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- Plant Journal, 2008, v. 54, n. 2, p. 236, doi. 10.1111/j.1365-313X.2008.03409.x
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- Article
Synthesis of 3-oxalinolenic acid and β-oxidation-resistant 3-oxa-oxylipins.
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- Lipids, 2006, v. 41, n. 5, p. 499, doi. 10.1007/s11745-006-5123-5
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- Article
Conversion of linoleic acid into novel oxylipins by the mushroom Agaricus bisporus.
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- Lipids, 2005, v. 40, n. 11, p. 1163, doi. 10.1007/s11745-005-1481-2
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- Article
Novel oxylipins formed from docosahexaenoic acid by potato lipoxygenase—10( S)-hydroxydocosahexaenoic acid and 10,20-dihydroxydocosahexaenoic acid.
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- Lipids, 2005, v. 40, n. 3, p. 249, doi. 10.1007/s11745-005-1379-z
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- Article
Hidden stereospecificity in the biosynthesis of divinyl ether fatty acids.
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- FEBS Journal, 2005, v. 272, n. 3, p. 736, doi. 10.1111/j.1742-4658.2004.04510.x
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Isolation and structures of two divinyl ether fatty acids from Clematis vitalba.
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- Lipids, 2004, v. 39, n. 6, p. 565, doi. 10.1007/s11745-004-1264-9
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Biosynthesis and isomerization of 11-hydroperoxylinoleates by manganese- and iron-dependent lipoxygenases.
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- Lipids, 2004, v. 39, n. 4, p. 319, doi. 10.1007/s11745-004-1235-1
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- Article
Detection of an enol intermediate in the hydroperoxide lyase chain cleavage reaction
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- FEBS Letters, 2003, v. 549, n. 1-3, p. 31, doi. 10.1016/S0014-5793(03)00758-0
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Separation of conjugated linoleic acid isomers and parinaric fatty acid isomers by capillary electrophoresis.
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- Journal of Separation Science, 2002, v. 25, n. 8, p. 499, doi. 10.1002/1615-9314(20020601)25:8<499::AID-JSSC499>3.0.CO;2-X
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- Article
Biosynthesis of new divinyl ether oxylipins in Ranunculus plants.
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- Lipids, 2002, v. 37, n. 4, p. 427, doi. 10.1007/s1145-002-0911-5
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- Article
Involvement of the Arabidopsis α-DOX1 fatty acid dioxygenase in protection against oxidative stress and cell death.
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- Plant Journal, 2002, v. 29, n. 1, p. 61, doi. 10.1046/j.1365-313x.2002.01195.x
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- Article
Separation of divinyl ether fatty acid isomers by micellar electrokinetic chromatography.
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- Electrophoresis, 2001, v. 22, n. 6, p. 1163, doi. 10.1002/1522-2683()22:6<1163::AID-ELPS1163>3.0.CO;2-M
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- Article
Evidence for the mitochondrial biosynthesis of 3 R-hydroxy-5 Z,8 Z,11 Z,14 Z-eicosatetraenoic acid in the yeast Dipodascopsis uninucleata.
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- Lipids, 2000, v. 35, n. 11, p. 1205, doi. 10.1007/s11745-000-0637-4
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- Article