| P50 | author | Philippe Potin | Q43075850 |
| P2093 | author name string | Didier Andrivon | |
| | Dominique Barloy | |
| | Sophie Goulitquer | |
| | Florence Val | |
| | Guillaume Saubeau | |
| P2860 | cites work | Defective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in Tlr4 Gene | Q22299417 |
| | Oxylipins produced by the 9-lipoxygenase pathway in Arabidopsis regulate lateral root development and defense responses through a specific signaling cascade | Q24685959 |
| | A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 |
| | Fatty acid-derived signals in plants | Q28216660 |
| | Oxylipin profiling reveals the preferential stimulation of the 9-lipoxygenase pathway in elicitor-treated potato cells | Q30321056 |
| | Enzymes of the biosynthesis of octadecanoid-derived signalling molecules | Q31960792 |
| | In vivo substrates and the contribution of the common phospholipase D, PLDalpha, to wound-induced metabolism of lipids in Arabidopsis | Q32142657 |
| | Isolation and characterization of NgRLK1, a receptor-like kinase of Nicotiana glutinosa that interacts with the elicitin of Phytophthora capsici | Q33556168 |
| | Quantitative resistance of potato to Pectobacterium atrosepticum and Phytophthora infestans: integrating PAMP-triggered response and pathogen growth | Q33997086 |
| | A pathogen-inducible divinyl ether synthase (CYP74D) from elicitor-treated potato suspension cells. | Q34100620 |
| | Oxylipin profiling in pathogen-infected potato leaves. | Q34147868 |
| | Are elicitins cryptograms in plant-Oomycete communications? | Q34158551 |
| | The phospholipase A2 superfamily and its group numbering system | Q34566140 |
| | Early signaling events induced by elicitors of plant defenses. | Q34569067 |
| | Characterization of a divinyl ether biosynthetic pathway specifically associated with pathogenesis in tobacco | Q34579358 |
| | Impact of phyto-oxylipins in plant defense | Q34740978 |
| | The lipoxygenase pathway. | Q34833694 |
| | Lipoxygenases: occurrence, functions and catalysis. | Q36357140 |
| | PAMP recognition and the plant-pathogen arms race | Q36579673 |
| | Activation of defence reactions in Solanaceae: where is the specificity? | Q36642822 |
| | Strategies of attack and defense in plant-oomycete interactions, accentuated for Phytophthora parasitica Dastur (syn. P. Nicotianae Breda de Haan). | Q36927127 |
| | Oxylipins: structurally diverse metabolites from fatty acid oxidation. | Q37376645 |
| | Lipoxygenases - Structure and reaction mechanism. | Q37600460 |
| | The role of lipopolysaccharide and peptidoglycan, two glycosylated bacterial microbe-associated molecular patterns (MAMPs), in plant innate immunity. | Q37897286 |
| | Spatio-temporal expression of patatin-like lipid acyl hydrolases and accumulation of jasmonates in elicitor-treated tobacco leaves are not affected by endogenous levels of salicylic acid | Q38972046 |
| | The enzymic deacylation of phospholipids and galactolipids in plants. Purification and properties of a lipolytic acyl-hydrolase from potato tubers | Q42061231 |
| | Activation of the fatty acid alpha-dioxygenase pathway during bacterial infection of tobacco leaves. Formation of oxylipins protecting against cell death | Q42450982 |
| | Lipid hydroperoxide levels in plant tissues | Q42492034 |
| | Coordinated transcriptional regulation of the divinyl ether biosynthetic genes in tobacco by signal molecules related to defense | Q43170743 |
| | Nicotiana attenuata SIPK, WIPK, NPR1, and fatty acid-amino acid conjugates participate in the induction of jasmonic acid biosynthesis by affecting early enzymatic steps in the pathway | Q43246237 |
| | From elicitins to lipid-transfer proteins: a new insight in cell signalling involved in plant defence mechanisms | Q44064861 |
| | NbLRK1, a lectin-like receptor kinase protein of Nicotiana benthamiana, interacts with Phytophthora infestans INF1 elicitin and mediates INF1-induced cell death | Q44637094 |
| | Human CYP4F3s are the main catalysts in the oxidation of fatty acid epoxides | Q44897935 |
| | A leaf lipoxygenase of potato induced specifically by pathogen infection | Q45015545 |
| | Role of chloroplast trienoic fatty acids in plant disease defense responses | Q45177815 |
| | Endocytosis of Xanthomonas campestris pathovar campestris lipopolysaccharides in non-host plant cells of Nicotiana tabacum | Q45273631 |
| | Direct fungicidal activities of C6-aldehydes are important constituents for defense responses in Arabidopsis against Botrytis cinerea. | Q46538355 |
| | Evaluation of the antimicrobial activities of plant oxylipins supports their involvement in defense against pathogens | Q46813388 |
| | A culture filtrate of Phytophthora infestans primes defense reaction in potato cell suspensions | Q47281224 |
| | Lipid peroxidation during the hypersensitive response in potato in the absence of 9-lipoxygenases | Q47449841 |
| | Sequential Induction of Phenylalanine Ammonia-lyase and a Lyase-inactivating System in Potato Tuber Disks | Q47946530 |
| | Evidence for oxylipin synthesis and induction of a new polyunsaturated fatty acid hydroxylase activity in Chondrus crispus in response to methyljasmonate. | Q50699060 |
| | Divinyl ether fatty acid synthesis in late blight-diseased potato leaves. | Q51471197 |
| | The RPM1 plant disease resistance gene facilitates a rapid and sustained increase in cytosolic calcium that is necessary for the oxidative burst and hypersensitive cell death. | Q54038128 |
| | The combined action of 9 lipoxygenase and galactolipase is sufficient to bring about programmed cell death during tobacco hypersensitive response | Q57642973 |
| | Lipoxygenase-mediated production of fatty acid hydroperoxides is a specific signature of the hypersensitive reaction in plants | Q57643010 |
| | Characterization of the Cryptogein Binding Sites on Plant Plasma Membranes | Q57643039 |
| | Elicitin–membrane interaction is driven by a positive charge on the protein surface: Role of Lys13 residue in lipids loading and resistance induction | Q62274611 |
| | omega-Hydroxylation of Z9-octadecenoic, Z9,10-epoxystearic and 9,10-dihydroxystearic acids by microsomal cytochrome P450 systems from Vicia sativa | Q68099237 |
| | Involvement of lipoxygenase-dependent production of fatty acid hydroperoxides in the development of the hypersensitive cell death induced by cryptogein on tobacco leaves | Q73263476 |
| | Intracellular Levels of Free Linolenic and Linoleic Acids Increase in Tomato Leaves in Response to Wounding | Q74776559 |
| | Increase in free linolenic and linoleic acids associated with phospholipase D-mediated hydrolysis of phospholipids in wounded castor bean leaves | Q77136092 |
| | Stereochemistry of hydrogen removal during oxygenation of linoleic acid by singlet oxygen and synthesis of 11(S)-deuterium-labeled linoleic acid | Q82907315 |
| | Antagonistic role of 9-lipoxygenase-derived oxylipins and ethylene in the control of oxidative stress, lipid peroxidation and plant defence | Q83825653 |
| | Lipopolysaccharides of Pectobacterium atrosepticum and Pseudomonas corrugata induce different defence response patterns in tobacco, tomato, and potato | Q83931700 |
| P433 | issue | 5 | |
| P921 | main subject | 9(S)-HOTrE | Q27149496 |
| P304 | page(s) | 579-589 | |
| P577 | publication date | 2013-03-12 | |
| P1433 | published in | Plant Cell Reports | Q7201465 |
| P1476 | title | Differential induction of oxylipin pathway in potato and tobacco cells by bacterial and oomycete elicitors | |
| P478 | volume | 32 | |