scholarly article | Q13442814 |
P2093 | author name string | Nancy P. Keller | |
Gregory J. Fischer | |||
P2860 | cites work | Prostaglandin E(2) production by high and low virulent strains of Paracoccidioides brasiliensis | Q79962488 |
Thallphytic alleopathy: isolation and identification of laetisaric Acid | Q81002212 | ||
Multifrequency electron paramagnetic resonance characterization of PpoA, a CYP450 fusion protein that catalyzes fatty acid dioxygenation | Q84054110 | ||
Isolation of lipoxygenase-like enzyme from Fusarium oxysporum. | Q105125721 | ||
Stereochemical assignment, antiinflammatory properties, and receptor for the omega-3 lipid mediator resolvin E1 | Q24297600 | ||
Inhibition of arachidonate 5-lipoxygenase triggers massive apoptosis in human prostate cancer cells | Q24643373 | ||
Identification of PpoA from Aspergillus nidulans as a fusion protein of a fatty acid heme dioxygenase/peroxidase and a cytochrome P450 | Q24655007 | ||
The Crystal Structure of α-Dioxygenase Provides Insight into Diversity in the Cyclooxygenase-Peroxidase Superfamily | Q27676108 | ||
Cyclooxygenase isozymes: the biology of prostaglandin synthesis and inhibition. | Q27863328 | ||
Prostaglandins and leukotrienes: advances in eicosanoid biology | Q28208246 | ||
Identification of 9-hydroxyoctadecadienoic acid and other oxidized free fatty acids as ligands of the G protein-coupled receptor G2A | Q28278018 | ||
Inducible endothelium-derived hyperpolarizing factor: role of the 15-lipoxygenase-EDHF pathway | Q28281647 | ||
A review on leukotrienes and their receptors with reference to asthma | Q28294597 | ||
Cytochrome P450 eicosanoids are activators of peroxisome proliferator-activated receptor alpha | Q28297822 | ||
Prostaglandin E2 synthesis and secretion: the role of PGE2 synthases | Q28302274 | ||
Quantitative profiling method for oxylipin metabolome by liquid chromatography electrospray ionization tandem mass spectrometry | Q28397076 | ||
Candida albicans modulates host defense by biosynthesizing the pro-resolving mediator resolvin E1 | Q28471781 | ||
Action of jasmonates in plant stress responses and development--applied aspects | Q30317703 | ||
Characterization of oxylipins and dioxygenase genes in the asexual fungus Aspergillus niger | Q33421113 | ||
Oxygenation by COX-2 (cyclo-oxygenase-2) of 3-HETE (3-hydroxyeicosatetraenoic acid), a fungal mimetic of arachidonic acid, produces a cascade of novel bioactive 3-hydroxyeicosanoids | Q33433330 | ||
20-HETE mediates ozone-induced, neutrophil-independent airway hyper-responsiveness in mice | Q33565645 | ||
Nuclear localization of prostaglandin E2 receptors | Q33614279 | ||
Lipoxygenase-catalyzed oxygenation of storage lipids is implicated in lipid mobilization during germination | Q33728480 | ||
Sporogenic effect of polyunsaturated fatty acids on development of Aspergillus spp. | Q33985668 | ||
Pathogenic yeasts Cryptococcus neoformans and Candida albicans produce immunomodulatory prostaglandins | Q34007207 | ||
Reaction mechanism of 5,8-linoleate diol synthase, 10R-dioxygenase, and 8,11-hydroperoxide isomerase of Aspergillus clavatus. | Q34090748 | ||
Plant stress hormones suppress the proliferation and induce apoptosis in human cancer cells | Q34124352 | ||
Prostaglandins and inflammation | Q34179727 | ||
Cyclooxygenases and lipoxygenases in cancer | Q34224752 | ||
The role of leukotrienes in inflammation | Q34324567 | ||
Purification and characterization of linoleate 8-dioxygenase from the fungus Gaeumannomyces graminis as a novel hemoprotein | Q34384336 | ||
Characterization and differentiation of filamentous fungi based on Fatty Acid composition | Q34423797 | ||
Significance of inducible defense-related proteins in infected plants. | Q34511918 | ||
Identification of rice Allene Oxide Cyclase mutants and the function of jasmonate for defence against Magnaporthe oryzae. | Q45812869 | ||
Phenothiazine is a potent inhibitor of prostaglandin E2 production by Candida albicans biofilms. | Q46011666 | ||
Bronchodilatory effect of the PPAR-gamma agonist rosiglitazone in smokers with asthma | Q46055749 | ||
Fusarium oxysporum hijacks COI1-mediated jasmonate signaling to promote disease development in Arabidopsis. | Q46120432 | ||
A novel class of fungal lipoxygenases | Q46365902 | ||
Microbial conversion of jasmonates-hydroxylations by Aspergillus niger | Q46539751 | ||
Efficient production of arachidonic acid by Mortierella alpina through integrating fed-batch culture with a two-stage pH control strategy | Q46775820 | ||
Aspergillus infection inhibits the expression of peanut 13S-HPODE-forming seed lipoxygenases | Q46778966 | ||
Reciprocal oxylipin-mediated cross-talk in the Aspergillus-seed pathosystem | Q46817806 | ||
Identification of dioxygenases required for Aspergillus development. Studies of products, stereochemistry, and the reaction mechanism. | Q46974011 | ||
A peanut seed lipoxygenase responsive to Aspergillus colonization | Q47861118 | ||
Biological dynamics and distribution of 3-hydroxy fatty acids in the yeast Dipodascopsis uninucleata as investigated by immunofluorescence microscopy. Evidence for a putative regulatory role in the sexual reproductive cycle | Q47937966 | ||
Oxygenase coordination is required for morphological transition and the host-fungus interaction of Aspergillus flavus | Q48069612 | ||
Three putative oxylipin biosynthetic genes integrate sexual and asexual development in Aspergillus nidulans | Q48134966 | ||
A fungal monooxygenase-derived jasmonate attenuates host innate immunity | Q48148323 | ||
Independently silencing two JAR family members impairs levels of trypsin proteinase inhibitors but not nicotine. | Q51713943 | ||
(3R)-hydroxy-oxylipins--a novel family of oxygenated polyenoic fatty acids of fungal origin. | Q52974298 | ||
The plant growth regulator methyl jasmonate inhibits aflatoxin production by Aspergillus flavus. | Q53460192 | ||
13-Hydroxy-linoleic acid induces airway hyperresponsiveness to histamine and methacholine in guinea pigs in vivo. | Q54168904 | ||
Lipoperoxidase activity of Pityrosporum: characterisation of by-products and possible role in pityriasis versicolor | Q62660035 | ||
Lipoxygenase Activity of Pityrosporum In Vitro and In Vivo | Q62660075 | ||
An endogenous inducer of sexual development in Aspergillus nidulans | Q68189726 | ||
Do specific linoleate 13-lipoxygenases initiate beta-oxidation? | Q73240718 | ||
Lipoxygenase-dependent degradation of storage lipids | Q73937998 | ||
An acetylsalicylic acid-sensitive aggregation phenomenon in Dipodascopsis uninucleata | Q78064165 | ||
Resolvin E2: identification and anti-inflammatory actions: pivotal role of human 5-lipoxygenase in resolvin E series biosynthesis | Q79369903 | ||
Biosynthesis of eicosanoids and transcellular metabolism of leukotrienes in murine bone marrow cells | Q79441685 | ||
Jasmonates: novel anticancer agents acting directly and selectively on human cancer cell mitochondria | Q34555806 | ||
LDS1-produced oxylipins are negative regulators of growth, conidiation and fumonisin synthesis in the fungal maize pathogen Fusarium verticillioides | Q34677867 | ||
Transcellular biosynthesis contributes to the production of leukotrienes during inflammatory responses in vivo | Q34791616 | ||
Production of eicosanoids and other oxylipins by pathogenic eukaryotic microbes | Q35139747 | ||
The distribution of 3-hydroxy oxylipins in fungi | Q35547030 | ||
Paracoccidioides brasiliensis interferes on dendritic cells maturation by inhibiting PGE2 production | Q35582660 | ||
Prostaglandin E2 suppresses antifungal immunity by inhibiting interferon regulatory factor 4 function and interleukin-17 expression in T cells. | Q35907174 | ||
Inactivation of the lipoxygenase ZmLOX3 increases susceptibility of maize to Aspergillus spp. | Q35983605 | ||
Comparative effects of inhaled leukotriene C4, leukotriene D4, and histamine in normal human subjects | Q36138245 | ||
Isolation of a sexual sporulation hormone from Aspergillus nidulans | Q36179997 | ||
Inflammation and immune regulation by 12/15-lipoxygenases | Q36469920 | ||
Eicosanoid transcellular biosynthesis: from cell-cell interactions to in vivo tissue responses | Q36591942 | ||
Oxylipins as developmental and host-fungal communication signals | Q36727293 | ||
Defects in conidiophore development and conidium-macrophage interactions in a dioxygenase mutant of Aspergillus fumigatus. | Q36747080 | ||
Transcellular biosynthesis of cysteinyl leukotrienes in vivo during mouse peritoneal inflammation | Q37208628 | ||
Oxylipins in fungi. | Q37833673 | ||
Biosynthesis and analysis of plant oxylipins | Q38299105 | ||
The role of laccase in prostaglandin production by Cryptococcus neoformans | Q38595824 | ||
Leukotrienes: their formation and role as inflammatory mediators | Q39492661 | ||
Aspergillus oxylipin signaling and quorum sensing pathways depend on g protein-coupled receptors | Q39529541 | ||
Identification of a cluster of PR4-like genes involved in stress responses in rice | Q39575119 | ||
Production of prostaglandins and leukotrienes by pathogenic fungi | Q39653627 | ||
Endogenous lipogenic regulators of spore balance in Aspergillus nidulans | Q40737343 | ||
Lipids in Aspergillus flavus-maize interaction. | Q41897172 | ||
Cryptococcus neoformans produces authentic prostaglandin E2 without a cyclooxygenase | Q41908929 | ||
Global survey of canonical Aspergillus flavus G protein-coupled receptors | Q41956744 | ||
Silencing threonine deaminase and JAR4 in Nicotiana attenuata impairs jasmonic acid-isoleucine-mediated defenses against Manduca sexta | Q42035573 | ||
Morphological transitions governed by density dependence and lipoxygenase activity in Aspergillus flavus | Q42604134 | ||
Aspergillus cyclooxygenase-like enzymes are associated with prostaglandin production and virulence. | Q42623369 | ||
Expression analysis for genes involved in arachidonic acid biosynthesis in Mortierella alpina CBS 754.68. | Q42883415 | ||
Gene deletion of 7,8-linoleate diol synthase of the rice blast fungus: studies on pathogenicity, stereochemistry, and oxygenation mechanisms. | Q42918047 | ||
Methyl jasmonate induces ganoderic acid biosynthesis in the basidiomycetous fungus Ganoderma lucidum | Q43098074 | ||
Paracoccidioides brasiliensis uses endogenous and exogenous arachidonic acid for PGE x production | Q43110051 | ||
Quantitative profiling of oxylipins through comprehensive LC-MS/MS analysis of Fusarium verticillioides and maize kernels | Q43323665 | ||
Genetic connection between fatty acid metabolism and sporulation in Aspergillus nidulans | Q43607732 | ||
Methyl jasmonate stimulates aflatoxin B1 biosynthesis by Aspergillus parasiticus | Q43674365 | ||
Cultivar-dependent expression of a maize lipoxygenase responsive to seed infesting fungi | Q43702614 | ||
Isolation of a novel arachidonic acid metabolite 3-hydroxy-5,8,11,14-eicosatetraenoic acid (3-HETE) from the yeast Dipodascopsis uninucleata UOFs-Y128. | Q43879642 | ||
A gene that encodes a product with similarity to dioxygenases is highly expressed in teliospores of Ustilago maydis | Q44122284 | ||
Chronic hypoxia activates lung 15-lipoxygenase, which catalyzes production of 15-HETE and enhances constriction in neonatal rabbit pulmonary arteries | Q44400021 | ||
The lipid body protein, PpoA, coordinates sexual and asexual sporulation in Aspergillus nidulans | Q44709078 | ||
Linoleate diol synthase of the rice blast fungus Magnaporthe grisea | Q44761130 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 254-64 | |
P577 | publication date | 2016-03-01 | |
P1433 | published in | The Journal of Microbiology | Q15749838 |
P1476 | title | Production of cross-kingdom oxylipins by pathogenic fungi: An update on their role in development and pathogenicity | |
P478 | volume | 54 |
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