Isoprostane nomenclature: inherent problems may cause setbacks for the development of the isoprostanoid field.

[1]  Martin J. Mueller,et al.  Reactive electrophilic oxylipins: pattern recognition and signalling. , 2009, Phytochemistry.

[2]  Martin J. Mueller,et al.  Impact of cyclopentenone-oxylipins on the proteome of Arabidopsis thaliana. , 2008, Biochimica et biophysica acta.

[3]  J. Schwabe,et al.  Structural basis for the activation of PPARγ by oxidized fatty acids , 2008, Nature Structural &Molecular Biology.

[4]  U. Jahn,et al.  Beyond prostaglandins--chemistry and biology of cyclic oxygenated metabolites formed by free-radical pathways from polyunsaturated fatty acids. , 2008, Angewandte Chemie.

[5]  Martin J. Mueller,et al.  General Detoxification and Stress Responses Are Mediated by Oxidized Lipids through TGA Transcription Factors in Arabidopsis[W] , 2008, The Plant Cell Online.

[6]  F. Ni,et al.  A profile of the residues in the second extracellular loop that are critical for ligand recognition of human prostacyclin receptor , 2008, The FEBS journal.

[7]  Abdelazize Laoui,et al.  Prediction of the 3D structure and dynamics of human DP G-protein coupled receptor bound to an agonist and an antagonist. , 2007, Journal of the American Chemical Society.

[8]  J. Morrow,et al.  Regiochemistry of Neuroprostanes Generated from the Peroxidation of Docosahexaenoic Acid in Vitro and in Vivo* , 2005, Journal of Biological Chemistry.

[9]  Martin J. Mueller,et al.  B1-Phytoprostanes Trigger Plant Defense and Detoxification Responses1[w] , 2005, Plant Physiology.

[10]  J. Morrow,et al.  Identification of a Novel Class of Endoperoxides from Arachidonate Autoxidation* , 2004, Journal of Biological Chemistry.

[11]  L. Roberts,et al.  Isomer-specific contractile effects of a series of synthetic f2-isoprostanes on retinal and cerebral microvasculature. , 2004, Free radical biology & medicine.

[12]  Martin J. Mueller,et al.  Biosynthesis of 14,15-dehydro-12-oxo-phytodienoic acid and related cyclopentenones via the phytoprostane D(1) pathway. , 2003, Phytochemistry.

[13]  L. Janssen,et al.  Involvement of TP and EP3 receptors in vasoconstrictor responses to isoprostanes in pulmonary vasculature. , 2002, The Journal of pharmacology and experimental therapeutics.

[14]  D. Denis,et al.  Key structural features of prostaglandin E(2) and prostanoid analogs involved in binding and activation of the human EP(1) prostanoid receptor. , 2001, Molecular pharmacology.

[15]  C. Glass,et al.  Cyclopentenone prostaglandins: New insights on biological activities and cellular targets , 2001, Medicinal research reviews.

[16]  M. J. Mueller,et al.  Analysis of oxidative stress and wound-inducible dinor isoprostanes F(1) (phytoprostanes F(1)) in plants. , 2000, Plant physiology.

[17]  L. Janssen,et al.  Isoprostanes: generation, pharmacology, and roles in free-radical-mediated effects in the lung. , 2000, Pulmonary pharmacology & therapeutics.

[18]  L. Hitchingham,et al.  The nature and composition of 15-deoxy-Delta(12,14)PGJ(2). , 2000, Prostaglandins & other lipid mediators.

[19]  Martin J. Mueller,et al.  Formation of isoprostane F(2)-like compounds (phytoprostanes F(1)) from alpha-linolenic acid in plants. , 2000, Free radical biology & medicine.

[20]  S. Parchmann,et al.  Evidence for the Formation of Dinor Isoprostanes E1from α-Linolenic Acid in Plants* , 1998, The Journal of Biological Chemistry.

[21]  M. J. Mueller Radically novel prostaglandins in animals and plants: the isoprostanes. , 1998, Chemistry & biology.

[22]  T. Montine,et al.  Formation of Isoprostane-like Compounds (Neuroprostanes) in Vivo from Docosahexaenoic Acid* , 1998, The Journal of Biological Chemistry.

[23]  G. FitzGerald,et al.  Nomenclature of isoprostanes: a proposal. , 1997, Prostaglandins.

[24]  J. Morrow,et al.  A nomenclature system for the isoprostanes. , 1997, Prostaglandins.

[25]  Y. Sugimoto,et al.  Molecular mechanisms of diverse actions of prostanoid receptors. , 1995, Biochimica et biophysica acta.

[26]  F. Fitzpatrick,et al.  Albumin-catalyzed metabolism of prostaglandin D2. Identification of products formed in vitro. , 1983, The Journal of biological chemistry.

[27]  B. Fredholm,et al.  Isomerization of prostaglandin H2 into prostaglandin D2 in the presence of serum albumin. , 1976, Biochimica et biophysica acta.

[28]  M. Hamberg,et al.  Isolation and structure of two prostaglandin endoperoxides that cause platelet aggregation. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[29]  K. Uchida,et al.  15-Deoxy-Δ12,14-prostaglandin J2: An Electrophilic Trigger of Cellular Responses , 2008 .

[30]  J. Schwabe,et al.  Structural Basis for the Activation of Pparg by Oxidised Fatty Acids , 2008 .

[31]  R. J. Waugh,et al.  Identification and relative quantitation of F2-isoprostane regioisomers formed in vivo in the rat. , 1997, Free radical biology & medicine.