-
1
-
-
0036633804
-
Impact of phyto-oxylipins in plant defense
-
Blee E. Impact of phyto-oxylipins in plant defense. Trends Plant Sci. 7:2002;315-322
-
(2002)
Trends Plant Sci.
, vol.7
, pp. 315-322
-
-
Blee, E.1
-
2
-
-
0346434165
-
Activation of the fatty acid alpha-dioxygenase pathway during bacterial infection of tobacco leaves. Formation of oxylipins protecting against cell death
-
Hamberg M., Sanz A., Rodriguez M.J., Calvo A.P., Castresana C. Activation of the fatty acid alpha-dioxygenase pathway during bacterial infection of tobacco leaves. Formation of oxylipins protecting against cell death. J Biol Chem. 278:2003;51796-51805
-
(2003)
J Biol Chem
, vol.278
, pp. 51796-51805
-
-
Hamberg, M.1
Sanz, A.2
Rodriguez, M.J.3
Calvo, A.P.4
Castresana, C.5
-
3
-
-
10744230800
-
Rapid induction of distinct stress responses after the release of singlet oxygen in Arabidopsis
-
op den Camp R.G., Przybyla D., Ochsenbein C., Laloi C., Kim C., Danon A., Wagner D., Hideg E., Gobel C., Feussner I., et al. Rapid induction of distinct stress responses after the release of singlet oxygen in Arabidopsis. Plant Cell. 15:2003;2320-2332
-
(2003)
Plant Cell
, vol.15
, pp. 2320-2332
-
-
Op Den Camp, R.G.1
Przybyla, D.2
Ochsenbein, C.3
Laloi, C.4
Kim, C.5
Danon, A.6
Wagner, D.7
Hideg, E.8
Gobel, C.9
Feussner, I.10
-
5
-
-
0038367940
-
Cyclopentenone isoprostanes induced by reactive oxygen species trigger defense gene activation and phytoalexin accumulation in plants
-
This work reveals novel cyclopentenone phytoprostanes that can be formed by free-radical-catalyzed oxidation of linolenic acid in vitro and in vivo. These novel phytoprostanes are induced by oxidative stress and display biological activities that are probably due to their electrophilicity.
-
Thoma I., Loeffler C., Sinha A.K., Gupta M., Steffan B., Krischke M., Roitsch T., Mueller M.J. Cyclopentenone isoprostanes induced by reactive oxygen species trigger defense gene activation and phytoalexin accumulation in plants. Plant J. 34:2003;363-375 This work reveals novel cyclopentenone phytoprostanes that can be formed by free-radical-catalyzed oxidation of linolenic acid in vitro and in vivo. These novel phytoprostanes are induced by oxidative stress and display biological activities that are probably due to their electrophilicity.
-
(2003)
Plant J
, vol.34
, pp. 363-375
-
-
Thoma, I.1
Loeffler, C.2
Sinha, A.K.3
Gupta, M.4
Steffan, B.5
Krischke, M.6
Roitsch, T.7
Mueller, M.J.8
-
7
-
-
0025814980
-
Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes
-
Esterbauer H., Schaur R.J., Zollner H. Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes. Free Radic Biol Med. 11:1991;81-128
-
(1991)
Free Radic Biol Med
, vol.11
, pp. 81-128
-
-
Esterbauer, H.1
Schaur, R.J.2
Zollner, H.3
-
10
-
-
0037308057
-
1 pathway
-
2, is the most reactive Michael-addition acceptor and the most potent electrophile in the prostanoid series.
-
2, is the most reactive Michael-addition acceptor and the most potent electrophile in the prostanoid series.
-
(2003)
Phytochemistry
, vol.62
, pp. 351-358
-
-
Krischke, M.1
Loeffler, C.2
Mueller, M.J.3
-
11
-
-
0035980746
-
Enzymatic and nonenzymatic lipid peroxidation in leaf development
-
Berger S., Weichert H., Porzel A., Wasternack C., Kühn H., Feussner I. Enzymatic and nonenzymatic lipid peroxidation in leaf development. Biochim Biophys Acta. 1533:2001;266-276
-
(2001)
Biochim Biophys Acta
, vol.1533
, pp. 266-276
-
-
Berger, S.1
Weichert, H.2
Porzel, A.3
Wasternack, C.4
Kühn, H.5
Feussner, I.6
-
12
-
-
0346732279
-
Lipid peroxidation during the hypersensitive response in potato in the absence of 9-lipoxygenases
-
i transgenic plants that lack 9-lipoxygenase, autoxidatively formed fatty acid hydroperoxides dramatically increase and possibly compensate the loss of 9-lipoxygenase products. The mechanism by which autoxidation is upregulated is not clear. It seems possible, however, that 9-lipoxygenase products and electrophilic fragments thereof trigger antioxidative defense mechanisms, thereby limiting autoxidation in wildtype plants but not in transgenic plants that lack 9-lipoxygenase.
-
i transgenic plants that lack 9-lipoxygenase, autoxidatively formed fatty acid hydroperoxides dramatically increase and possibly compensate the loss of 9-lipoxygenase products. The mechanism by which autoxidation is upregulated is not clear. It seems possible, however, that 9-lipoxygenase products and electrophilic fragments thereof trigger antioxidative defense mechanisms, thereby limiting autoxidation in wildtype plants but not in transgenic plants that lack 9-lipoxygenase.
-
(2003)
J Biol Chem
, vol.278
, pp. 52834-52840
-
-
Gobel, C.1
Feussner, I.2
Rosahl, S.3
-
13
-
-
18644384146
-
Lipid peroxidation in cotton: Xanthomonas interactions and the role of lipoxygenases during the hypersensitive reaction
-
Jalloul A., Montillet J.L., Assigbetse K., Agnel J.P., Delannoy E., Triantaphylides C., Daniel J.F., Marmey P., Geiger J.P., Nicole M. Lipid peroxidation in cotton: Xanthomonas interactions and the role of lipoxygenases during the hypersensitive reaction. Plant J. 32:2002;1-12
-
(2002)
Plant J
, vol.32
, pp. 1-12
-
-
Jalloul, A.1
Montillet, J.L.2
Assigbetse, K.3
Agnel, J.P.4
Delannoy, E.5
Triantaphylides, C.6
Daniel, J.F.7
Marmey, P.8
Geiger, J.P.9
Nicole, M.10
-
14
-
-
0024354775
-
Oxygen radical chemistry of polyunsaturated fatty acids
-
Gardner H.W. Oxygen radical chemistry of polyunsaturated fatty acids. Free Radic Biol Med. 7:1989;65-86
-
(1989)
Free Radic Biol Med
, vol.7
, pp. 65-86
-
-
Gardner, H.W.1
-
15
-
-
1642323692
-
Selective and powerful stress gene expression in Arabidopsis in response to malondialdehyde
-
1-phytoprostanes, occurs in high abundance in Arabidopsis and is rapidly turned over, suggesting that it is formed constitutively at a high rate in healthy plants. Genetic confirmation of the hypothesis that malondialdehyde originates predominantly (up to 75%) from triunsaturated fatty acids is provided. Malondialdehyde is shown to encode complex regulatory information, implicating this electrophile as mediator in abiotic stress signaling.
-
1-phytoprostanes, occurs in high abundance in Arabidopsis and is rapidly turned over, suggesting that it is formed constitutively at a high rate in healthy plants. Genetic confirmation of the hypothesis that malondialdehyde originates predominantly (up to 75%) from triunsaturated fatty acids is provided. Malondialdehyde is shown to encode complex regulatory information, implicating this electrophile as mediator in abiotic stress signaling.
-
(2004)
Plant J
, vol.37
, pp. 877-888
-
-
Weber, H.1
Chetelat, A.2
Reymond, P.3
Farmer, E.E.4
-
16
-
-
0037064036
-
A novel family of atherogenic oxidized phospholipids promotes macrophage foam cell formation via the scavenger receptor CD36 and is enriched in atherosclerotic lesions
-
Podrez E.A., Poliakov E., Shen Z., Zhang R., Deng Y., Sun M., Finton P.J., Shan L., Febbraio M., Hajjar D.P., et al. A novel family of atherogenic oxidized phospholipids promotes macrophage foam cell formation via the scavenger receptor CD36 and is enriched in atherosclerotic lesions. J Biol Chem. 277:2002;38517-38523
-
(2002)
J Biol Chem
, vol.277
, pp. 38517-38523
-
-
Podrez, E.A.1
Poliakov, E.2
Shen, Z.3
Zhang, R.4
Deng, Y.5
Sun, M.6
Finton, P.J.7
Shan, L.8
Febbraio, M.9
Hajjar, D.P.10
-
17
-
-
0037064120
-
Identification of a novel family of oxidized phospholipids that serve as ligands for the macrophage scavenger receptor CD36
-
Podrez E.A., Poliakov E., Shen Z., Zhang R., Deng Y., Sun M., Finton P.J., Shan L., Gugiu B., Fox P.L., et al. Identification of a novel family of oxidized phospholipids that serve as ligands for the macrophage scavenger receptor CD36. J Biol Chem. 277:2002;38503-38516
-
(2002)
J Biol Chem
, vol.277
, pp. 38503-38516
-
-
Podrez, E.A.1
Poliakov, E.2
Shen, Z.3
Zhang, R.4
Deng, Y.5
Sun, M.6
Finton, P.J.7
Shan, L.8
Gugiu, B.9
Fox, P.L.10
-
18
-
-
0042031044
-
Receptors involved in the oxidized 1-palmitoyl-2-arachidonoyl-sn-glycero- 3-phosphorylcholine-mediated synthesis of interleukin-8. A role for Toll-like receptor 4 and a glycosylphosphatidylinositol-anchored protein
-
Toll-like receptors (TLRs) play an essential role in the activation of innate immunity by recognizing specific patterns of microbial components in animals and plants. This study suggests that oxidized phospholipids (isoprostane and fragmented fatty-acid-containing phospholipids) initially bind to a glycosylphosphatidyinositol-anchored protein, which interacts with TLR4 and activates the TLR4 signal pathway in animals.
-
Walton K.A., Hsieh X., Gharavi N., Wang S., Wang G., Yeh M., Cole A.L., Berliner J.A. Receptors involved in the oxidized 1-palmitoyl-2-arachidonoyl-sn- glycero-3-phosphorylcholine-mediated synthesis of interleukin-8. A role for Toll-like receptor 4 and a glycosylphosphatidylinositol-anchored protein. J Biol Chem. 278:2003;29661-29666 Toll-like receptors (TLRs) play an essential role in the activation of innate immunity by recognizing specific patterns of microbial components in animals and plants. This study suggests that oxidized phospholipids (isoprostane and fragmented fatty-acid-containing phospholipids) initially bind to a glycosylphosphatidyinositol-anchored protein, which interacts with TLR4 and activates the TLR4 signal pathway in animals.
-
(2003)
J Biol Chem
, vol.278
, pp. 29661-29666
-
-
Walton, K.A.1
Hsieh, X.2
Gharavi, N.3
Wang, S.4
Wang, G.5
Yeh, M.6
Cole, A.L.7
Berliner, J.A.8
-
19
-
-
0344667546
-
Isolevuglandins, a novel class of isoprostenoid derivatives, function as integrated sensors of oxidant stress and are generated by myeloperoxidase in vivo
-
Poliakov E., Brennan M.L., Macpherson J., Zhang R., Sha W., Narine L., Salomon R.G., Hazen S.L. Isolevuglandins, a novel class of isoprostenoid derivatives, function as integrated sensors of oxidant stress and are generated by myeloperoxidase in vivo. FASEB J. 17:2003;2209-2220
-
(2003)
FASEB J
, vol.17
, pp. 2209-2220
-
-
Poliakov, E.1
Brennan, M.L.2
MacPherson, J.3
Zhang, R.4
Sha, W.5
Narine, L.6
Salomon, R.G.7
Hazen, S.L.8
-
20
-
-
0033574541
-
Formation of reactive cyclopentenone compounds in vivo as products of the isoprostane pathway
-
Chen Y., Morrow J.D., Jackson Roberts L. II Formation of reactive cyclopentenone compounds in vivo as products of the isoprostane pathway. J Biol Chem. 274:1999;10863-10868
-
(1999)
J Biol Chem
, vol.274
, pp. 10863-10868
-
-
Chen, Y.1
Morrow, J.D.2
Jackson Roberts II, L.3
-
21
-
-
0037026527
-
Protective role of phospholipid oxidation products in endotoxin-induced tissue damage
-
Bochkov V.N., Kadl A., Huber J., Gruber F., Binder B.R., Leitinger N. Protective role of phospholipid oxidation products in endotoxin-induced tissue damage. Nature. 419:2002;77-81
-
(2002)
Nature
, vol.419
, pp. 77-81
-
-
Bochkov, V.N.1
Kadl, A.2
Huber, J.3
Gruber, F.4
Binder, B.R.5
Leitinger, N.6
-
22
-
-
0242320191
-
Anti-inflammatory properties of lipid oxidation products
-
Bochkov V.N., Leitinger N. Anti-inflammatory properties of lipid oxidation products. J Mol Med. 81:2003;613-626
-
(2003)
J Mol Med
, vol.81
, pp. 613-626
-
-
Bochkov, V.N.1
Leitinger, N.2
-
23
-
-
0036791022
-
C-reactive protein binds to both oxidized LDL and apoptotic cells through recognition of a common ligand: Phosphorylcholine of oxidized phospholipids
-
Chang M.K., Binder C.J., Torzewski M., Witztum J.L. C-reactive protein binds to both oxidized LDL and apoptotic cells through recognition of a common ligand: phosphorylcholine of oxidized phospholipids. Proc Natl Acad Sci USA. 99:2002;13043-13048
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 13043-13048
-
-
Chang, M.K.1
Binder, C.J.2
Torzewski, M.3
Witztum, J.L.4
-
24
-
-
0037942895
-
The autoreactivity of anti-phosphorylcholine antibodies for atherosclerosis-associated neo-antigens and apoptotic cells
-
Shaw P.X., Goodyear C.S., Chang M.K., Witztum J.L., Silverman G.J. The autoreactivity of anti-phosphorylcholine antibodies for atherosclerosis- associated neo-antigens and apoptotic cells. J Immunol. 170:2003;6151-6157
-
(2003)
J Immunol
, vol.170
, pp. 6151-6157
-
-
Shaw, P.X.1
Goodyear, C.S.2
Chang, M.K.3
Witztum, J.L.4
Silverman, G.J.5
-
25
-
-
0036790973
-
Oxidized phosphatidylcholines: Pattern recognition for multiple pathways of the innate immune response
-
Hazen S.L., Chisolm G.M. Oxidized phosphatidylcholines: pattern recognition for multiple pathways of the innate immune response. Proc Natl Acad Sci USA. 99:2002;12515-12517
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 12515-12517
-
-
Hazen, S.L.1
Chisolm, G.M.2
-
26
-
-
0038352228
-
Inflammation, bioactive lipids and atherosclerosis: Potential roles of a lipoprotein-associated phospholipase A2, platelet activating factor-acetylhydrolase
-
Tselepis A.D., John Chapman M. Inflammation, bioactive lipids and atherosclerosis: potential roles of a lipoprotein-associated phospholipase A2, platelet activating factor-acetylhydrolase. Atheroscler Suppl. 3:2002;57-68
-
(2002)
Atheroscler Suppl
, vol.3
, pp. 57-68
-
-
Tselepis, A.D.1
John Chapman, M.2
-
27
-
-
0036669403
-
Platelet-activating factor acetylhydrolase
-
Arai H. Platelet-activating factor acetylhydrolase. Prostaglandins Other Lipid Mediat. 68-69:2002;83-94
-
(2002)
Prostaglandins Other Lipid Mediat
, vol.6869
, pp. 83-94
-
-
Arai, H.1
-
28
-
-
0037348464
-
Plasma platelet activating factor-acetylhydrolase (PAF-AH)
-
Karasawa K., Harada A., Satoh N., Inoue K., Setaka M. Plasma platelet activating factor-acetylhydrolase (PAF-AH). Prog Lipid Res. 42:2003;93-114
-
(2003)
Prog Lipid Res
, vol.42
, pp. 93-114
-
-
Karasawa, K.1
Harada, A.2
Satoh, N.3
Inoue, K.4
Setaka, M.5
-
29
-
-
0035901524
-
Platelet-activating factor acetylhydrolases: Broad substrate specificity and lipoprotein binding does not modulate the catalytic properties of the plasma enzyme
-
Min J.H., Wilder C., Aoki J., Arai H., Inoue K., Paul L., Gelb M.H. Platelet-activating factor acetylhydrolases: broad substrate specificity and lipoprotein binding does not modulate the catalytic properties of the plasma enzyme. Biochemistry. 40:2001;4539-4549
-
(2001)
Biochemistry
, vol.40
, pp. 4539-4549
-
-
Min, J.H.1
Wilder, C.2
Aoki, J.3
Arai, H.4
Inoue, K.5
Paul, L.6
Gelb, M.H.7
-
30
-
-
0031449808
-
Protection against oxidative stress-induced cell death by intracellular platelet-activating factor-acetylhydrolase II
-
Matsuzawa A., Hattori K., Aoki J., Arai H., Inoue K. Protection against oxidative stress-induced cell death by intracellular platelet-activating factor-acetylhydrolase II. J Biol Chem. 272:1997;32315-32320
-
(1997)
J Biol Chem
, vol.272
, pp. 32315-32320
-
-
Matsuzawa, A.1
Hattori, K.2
Aoki, J.3
Arai, H.4
Inoue, K.5
-
31
-
-
18744403354
-
Identification of platelet-activating factor acetylhydrolase II in human skin
-
Marques M., Pei Y., Southall M.D., Johnston J.M., Arai H., Aoki J., Inoue T., Seltmann H., Zouboulis C.C., Travers J.B. Identification of platelet-activating factor acetylhydrolase II in human skin. J Invest Dermatol. 119:2002;913-919
-
(2002)
J Invest Dermatol
, vol.119
, pp. 913-919
-
-
Marques, M.1
Pei, Y.2
Southall, M.D.3
Johnston, J.M.4
Arai, H.5
Aoki, J.6
Inoue, T.7
Seltmann, H.8
Zouboulis, C.C.9
Travers, J.B.10
-
32
-
-
0037709808
-
Recombinant platelet-activating factor acetylhydrolase to prevent acute respiratory distress syndrome and mortality in severe sepsis: Phase IIb, multicenter, randomized, placebo-controlled, clinical trial
-
Schuster D.P., Metzler M., Opal S., Lowry S., Balk R., Abraham E., Levy H., Slotman G., Coyne E., Souza S., et al. Recombinant platelet-activating factor acetylhydrolase to prevent acute respiratory distress syndrome and mortality in severe sepsis: Phase IIb, multicenter, randomized, placebo-controlled, clinical trial. Crit Care Med. 31:2003;1612-1619
-
(2003)
Crit Care Med
, vol.31
, pp. 1612-1619
-
-
Schuster, D.P.1
Metzler, M.2
Opal, S.3
Lowry, S.4
Balk, R.5
Abraham, E.6
Levy, H.7
Slotman, G.8
Coyne, E.9
Souza, S.10
-
33
-
-
0041384469
-
Platelet-activating factor acetylhydrolase inhibits alveolar macrophage activation in vivo
-
Bulger E.M., Gourlay D., Cuschieri J., Jelacic S., Staudenmeyer K., Garcia I., Maier R.V. Platelet-activating factor acetylhydrolase inhibits alveolar macrophage activation in vivo. Shock. 20:2003;17-22
-
(2003)
Shock
, vol.20
, pp. 17-22
-
-
Bulger, E.M.1
Gourlay, D.2
Cuschieri, J.3
Jelacic, S.4
Staudenmeyer, K.5
Garcia, I.6
Maier, R.V.7
-
34
-
-
0043011490
-
Molecular characterization of a novel lipase-like pathogen-inducible gene family of Arabidopsis
-
Jakab G., Manrique A., Zimmerli L., Metraux J.P., Mauch-Mani B. Molecular characterization of a novel lipase-like pathogen-inducible gene family of Arabidopsis. Plant Physiol. 132:2003;2230-2239
-
(2003)
Plant Physiol
, vol.132
, pp. 2230-2239
-
-
Jakab, G.1
Manrique, A.2
Zimmerli, L.3
Metraux, J.P.4
Mauch-Mani, B.5
-
35
-
-
0036697124
-
Isoprostanes as a biomarker of lipid peroxidation in humans: Physiology, pharmacology and clinical implications
-
Cracowski J.L., Durand T., Bessard G. Isoprostanes as a biomarker of lipid peroxidation in humans: physiology, pharmacology and clinical implications. Trends Pharmacol Sci. 23:2002;360-366
-
(2002)
Trends Pharmacol Sci
, vol.23
, pp. 360-366
-
-
Cracowski, J.L.1
Durand, T.2
Bessard, G.3
-
36
-
-
0842303252
-
Isoprostanes: An emerging role in vascular physiology and disease
-
Cracowski J.L. Isoprostanes: an emerging role in vascular physiology and disease. Chem Phys Lipids. 128:2004;75-83
-
(2004)
Chem Phys Lipids
, vol.128
, pp. 75-83
-
-
Cracowski, J.L.1
-
37
-
-
0842346332
-
The pulmonary biology of isoprostanes
-
Janssen L.J. The pulmonary biology of isoprostanes. Chem Phys Lipids. 128:2004;101-116
-
(2004)
Chem Phys Lipids
, vol.128
, pp. 101-116
-
-
Janssen, L.J.1
-
38
-
-
0842303253
-
Molecular pharmacology of isoprostanes in vascular smooth muscle
-
Habib A., Badr K.F. Molecular pharmacology of isoprostanes in vascular smooth muscle. Chem Phys Lipids. 128:2004;69-73
-
(2004)
Chem Phys Lipids
, vol.128
, pp. 69-73
-
-
Habib, A.1
Badr, K.F.2
-
40
-
-
0034543482
-
Fatty acid ketodienes and fatty acid ketotrienes: Michael addition acceptors that accumulate in wounded and diseased Arabidopsis leaves
-
Vollenweider S., Weber H., Stolz S., Chetelat A., Farmer E.E. Fatty acid ketodienes and fatty acid ketotrienes: Michael addition acceptors that accumulate in wounded and diseased Arabidopsis leaves. Plant J. 24:2000;467-476
-
(2000)
Plant J
, vol.24
, pp. 467-476
-
-
Vollenweider, S.1
Weber, H.2
Stolz, S.3
Chetelat, A.4
Farmer, E.E.5
-
41
-
-
0037696318
-
Reactive electrophile species activate defense gene expression in Arabidopsis
-
Unsaturated carbonyls that can be derived by either non-enzymatic or hydroperoxide-lyase-catalyzed breakdown of hydroperoxy fatty acids are shown to represent electrophiles that can act as mediators of both genetic and biochemical effects on core defense signal transduction.
-
Almeras E., Stolz S., Vollenweider S., Reymond P., Mene-Saffrane L., Farmer E.E. Reactive electrophile species activate defense gene expression in Arabidopsis. Plant J. 34:2003;205-216 Unsaturated carbonyls that can be derived by either non-enzymatic or hydroperoxide-lyase-catalyzed breakdown of hydroperoxy fatty acids are shown to represent electrophiles that can act as mediators of both genetic and biochemical effects on core defense signal transduction.
-
(2003)
Plant J
, vol.34
, pp. 205-216
-
-
Almeras, E.1
Stolz, S.2
Vollenweider, S.3
Reymond, P.4
Mene-Saffrane, L.5
Farmer, E.E.6
-
42
-
-
0035940424
-
Plant defense in the absence of jasmonic acid: The role of cyclopentenones
-
Stintzi A., Weber H., Reymond P., Browse J., Farmer E.E. Plant defense in the absence of jasmonic acid: the role of cyclopentenones. Proc Natl Acad Sci USA. 98:2001;12837-12842
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 12837-12842
-
-
Stintzi, A.1
Weber, H.2
Reymond, P.3
Browse, J.4
Farmer, E.E.5
-
43
-
-
0041762551
-
Overexpression of a stress-inducible aldehyde dehydrogenase gene from Arabidopsis thaliana in transgenic plants improves stress tolerance
-
Sunkar R., Bartels D., Kirch H.H. Overexpression of a stress-inducible aldehyde dehydrogenase gene from Arabidopsis thaliana in transgenic plants improves stress tolerance. Plant J. 35:2003;452-464
-
(2003)
Plant J
, vol.35
, pp. 452-464
-
-
Sunkar, R.1
Bartels, D.2
Kirch, H.H.3
-
44
-
-
0035983888
-
Probing the diversity of the Arabidopsis glutathione S-transferase gene family
-
Wagner U., Edwards R., Dixon D.P., Mauch F. Probing the diversity of the Arabidopsis glutathione S-transferase gene family. Plant Mol Biol. 49:2002;515-532
-
(2002)
Plant Mol Biol
, vol.49
, pp. 515-532
-
-
Wagner, U.1
Edwards, R.2
Dixon, D.P.3
Mauch, F.4
-
45
-
-
0032216816
-
C6-volatiles derived from the lipoxygenase pathway induce a subset of defense-related genes
-
Bate N.J., Rothstein S.J. C6-volatiles derived from the lipoxygenase pathway induce a subset of defense-related genes. Plant J. 16:1998;561-569
-
(1998)
Plant J
, vol.16
, pp. 561-569
-
-
Bate, N.J.1
Rothstein, S.J.2
-
46
-
-
1242297047
-
Airborne signals prime plants against insect herbivore attack
-
Volatile six-carbon aldehydes and alcohols that are formed via the hydroperoxide lyase pathway prime plants to produce more jasmonates and secondary metabolites (i.e. sesquiterpenes) after attacks by caterpillars. Interestingly, hexenal (an electrophil) and hexenol are equally active. Notably, both of these six-carbon volatiles can also be formed non-enzymatically.
-
Engelberth J., Alborn H.T., Schmelz E.A., Tumlinson J.H. Airborne signals prime plants against insect herbivore attack. Proc Natl Acad Sci USA. 101:2004;1781-1785 Volatile six-carbon aldehydes and alcohols that are formed via the hydroperoxide lyase pathway prime plants to produce more jasmonates and secondary metabolites (i.e. sesquiterpenes) after attacks by caterpillars. Interestingly, hexenal (an electrophil) and hexenol are equally active. Notably, both of these six-carbon volatiles can also be formed non-enzymatically.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 1781-1785
-
-
Engelberth, J.1
Alborn, H.T.2
Schmelz, E.A.3
Tumlinson, J.H.4
-
47
-
-
0041569777
-
Jasmonates and related oxylipins in plant responses to pathogenesis and herbivory
-
Farmer E.E., Almeras E., Krishnamurthy V. Jasmonates and related oxylipins in plant responses to pathogenesis and herbivory. Curr Opin Plant Biol. 6:2003;372-378
-
(2003)
Curr Opin Plant Biol
, vol.6
, pp. 372-378
-
-
Farmer, E.E.1
Almeras, E.2
Krishnamurthy, V.3
-
48
-
-
1642579640
-
The cyclopentenone product of lipid peroxidation, 15-A(2t)-isoprostane, is efficiently metabolized by HepG2 cells via conjugation with glutathione
-
Milne G.L., Zanoni G., Porta A., Sasi S., Vidari G., Musiek E.S., Freeman M.L., Morrow J.D. The cyclopentenone product of lipid peroxidation, 15-A(2t)-isoprostane, is efficiently metabolized by HepG2 cells via conjugation with glutathione. Chem Res Toxicol. 17:2004;17-25
-
(2004)
Chem Res Toxicol
, vol.17
, pp. 17-25
-
-
Milne, G.L.1
Zanoni, G.2
Porta, A.3
Sasi, S.4
Vidari, G.5
Musiek, E.S.6
Freeman, M.L.7
Morrow, J.D.8
-
49
-
-
0036964718
-
Contribution of covalent protein modification to the antiinflammatory effects of cyclopentenone prostaglandins
-
Perez-Sala D., Cerunda-Morollon E., Pineda-Molina E., Canada F.J. Contribution of covalent protein modification to the antiinflammatory effects of cyclopentenone prostaglandins. Ann NY Acad Sci. 973:2002;533-536
-
(2002)
Ann NY Acad Sci
, vol.973
, pp. 533-536
-
-
Perez-Sala, D.1
Cerunda-Morollon, E.2
Pineda-Molina, E.3
Canada, F.J.4
-
53
-
-
0037428454
-
Electrophilic prostaglandins and lipid aldehydes repress redox-sensitive transcription factors p53 and hypoxia-inducible factor by impairing the selenoprotein thioredoxin reductase
-
Moos P.J., Edes K., Cassidy P., Massuda E., Fitzpatrick F.A. Electrophilic prostaglandins and lipid aldehydes repress redox-sensitive transcription factors p53 and hypoxia-inducible factor by impairing the selenoprotein thioredoxin reductase. J Biol Chem. 278:2003;745-750
-
(2003)
J Biol Chem
, vol.278
, pp. 745-750
-
-
Moos, P.J.1
Edes, K.2
Cassidy, P.3
Massuda, E.4
Fitzpatrick, F.A.5
-
54
-
-
0038600719
-
Thioredoxin as a molecular target of cyclopentenone prostaglandins
-
Shibata T., Yamada T., Ishii T., Kumazawa S., Nakamura H., Masutani H., Yodoi J., Uchida K. Thioredoxin as a molecular target of cyclopentenone prostaglandins. J Biol Chem. 278:2003;26046-26054
-
(2003)
J Biol Chem
, vol.278
, pp. 26046-26054
-
-
Shibata, T.1
Yamada, T.2
Ishii, T.3
Kumazawa, S.4
Nakamura, H.5
Masutani, H.6
Yodoi, J.7
Uchida, K.8
-
55
-
-
0034610759
-
Anti-inflammatory cyclopentenone prostaglandins are direct inhibitors of IκB kinase
-
Rossi A., Kapahi P., Natoli G., Takahashi T., Chen Y., Karin M., Santoro M.G. Anti-inflammatory cyclopentenone prostaglandins are direct inhibitors of IκB kinase. Nature. 403:2000;103-108
-
(2000)
Nature
, vol.403
, pp. 103-108
-
-
Rossi, A.1
Kapahi, P.2
Natoli, G.3
Takahashi, T.4
Chen, Y.5
Karin, M.6
Santoro, M.G.7
-
56
-
-
1642282736
-
Cellular mechanisms of redox cell signaling: The role of cysteine modification in controlling antioxidant defenses in response to electrophilic lipid oxidation products
-
Levonen A.L., Landar A., Ramachandran A., Ceaser E.K., Dickinson D.A., Zanoni G., Morrow J.D., Darley-Usmar V.M. Cellular mechanisms of redox cell signaling: the role of cysteine modification in controlling antioxidant defenses in response to electrophilic lipid oxidation products. Biochem J. 378:2003;373-382
-
(2003)
Biochem J
, vol.378
, pp. 373-382
-
-
Levonen, A.L.1
Landar, A.2
Ramachandran, A.3
Ceaser, E.K.4
Dickinson, D.A.5
Zanoni, G.6
Morrow, J.D.7
Darley-Usmar, V.M.8
-
57
-
-
0345707597
-
2 on proteasome
-
2 on proteasome. Biochemistry. 42:2003;13960-13968
-
(2003)
Biochemistry
, vol.42
, pp. 13960-13968
-
-
Shibata, T.1
Yamada, T.2
Kondo, M.3
Tanahashi, N.4
Tanaka, K.5
Nakamura, H.6
Masutani, H.7
Yodoi, J.8
Uchida, K.9
-
58
-
-
0035053973
-
Cyclopentenone prostaglandins: New insights on biological activities and cellular targets
-
Straus D.S., Glass C.K. Cyclopentenone prostaglandins: new insights on biological activities and cellular targets. Med Res Rev. 21:2001;185-210
-
(2001)
Med Res Rev
, vol.21
, pp. 185-210
-
-
Straus, D.S.1
Glass, C.K.2
-
60
-
-
0042260801
-
First total synthesis of the e type I phytoprostanes
-
Rodriguez A.R., Spur B.W. First total synthesis of the E type I phytoprostanes. Tetrahedron Lett. 44:2003;7411-7415
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 7411-7415
-
-
Rodriguez, A.R.1
Spur, B.W.2
-
61
-
-
0032401897
-
Radically novel prostaglandins in animals and plants: The isoprostanes
-
Mueller M.J. Radically novel prostaglandins in animals and plants: the isoprostanes. Chem Biol. 5:1998;R323-R333
-
(1998)
Chem Biol
, vol.5
, pp. 323-R333
-
-
Mueller, M.J.1
-
62
-
-
0029817359
-
Nonenzymatic free radical-catalyzed generation of thromboxane-like compounds (isothromboxanes) in vivo
-
Morrow J.D., Awad J.A., Wu A., Zackert W.E., Daniel V.C., Roberts L.J. II Nonenzymatic free radical-catalyzed generation of thromboxane-like compounds (isothromboxanes) in vivo. J Biol Chem. 271:1996;23185-23190
-
(1996)
J Biol Chem
, vol.271
, pp. 23185-23190
-
-
Morrow, J.D.1
Awad, J.A.2
Wu, A.3
Zackert, W.E.4
Daniel, V.C.5
Roberts II, L.J.6
-
63
-
-
0029154210
-
Isoleukotrienes are biologically active free radical products of lipid peroxidation
-
Harrison K.A., Murphy R.C. Isoleukotrienes are biologically active free radical products of lipid peroxidation. J Biol Chem. 270:1995;17273-17278
-
(1995)
J Biol Chem
, vol.270
, pp. 17273-17278
-
-
Harrison, K.A.1
Murphy, R.C.2
-
64
-
-
0041563683
-
Detection of an enol intermediate in the hydroperoxide lyase chain cleavage reaction
-
Grechkin A.N., Mukhtarova L.S., Hamberg M. Detection of an enol intermediate in the hydroperoxide lyase chain cleavage reaction. FEBS Lett. 549:2003;31-34
-
(2003)
FEBS Lett
, vol.549
, pp. 31-34
-
-
Grechkin, A.N.1
Mukhtarova, L.S.2
Hamberg, M.3
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