Lipid Essentials Literature - Highlights - 2011
This list was created by means of a weekly literature search with a highly subjective scan to select those papers that appeared helpful to me for updating the Lipid Essentials or Blog pages on this site. They are mainly review articles dealing with the chemistry, occurrence and biochemistry of lipids, and the nutritional/clinical literature is under represented here. Please note that I select references mainly from journals to which I have direct access, or will have access after a period specified by the journal (usually 6 to 24 months). Further references may be added at any time as I become aware of them. References are listed alphabetically by the first author.
- Abdel-Mawgoud, M., Hausmann, R., Lépine, F., Müller, M. and Déziel, E. Rhamnolipids: detection, analysis, biosynthesis, genetic regulation, and bioengineering of production. In: Biosurfactants: from genes to applications, Microbiology Monographs 20, pp. 13-55 (edited by G. Soberón-Chávez, Springer, Berlin) (2011); DOI.
- Acehan, D., Malhotra, A., Xu, Y., Ren M, Stokes, D.L. and Schlame, M. Cardiolipin affects the supramolecular organization of ATP synthase in mitochondria. Biophys. J., 100, 2184-2192 (2011); DOI.
- Aicart-Ramos, C., Valero, R.A. and Rodriguez-Crespo, I. Protein palmitoylation and subcellular trafficking. Biochim. Biophys. Acta, 1808, 2981-2994 (2011).
- Aid, S. and Bosetti, F. Targeting cyclooxygenases-1 and-2 in neuroinflammation: Therapeutic implications. Biochimie, 93, 46-51 (2011).
- Alger, B.E. and Kim, J. Supply and demand for endocannabinoids. Trends Neurosci., 34, 304-315 (2011).
- Almena, M. and Merida, I. Shaping up the membrane: diacylglycerol coordinates spatial orientation of signalling. Trends Biochem. Sci., 36, 593-603 (2011).
- Aresta-Branco, F., Cordeiro, A.M., Marinho, H.S., Cyrne, L., Antunes, F. and de Almeida, R.F.M. Gel domains in the plasma membrane of Saccharomyces cerevisiae: highly ordered, ergosterol-free, and sphingolipid-enriched lipid rafts. J. Biol. Chem., 286, 5043-5054 (2011).
- Arutchelvi, J. and Doble, M. Mannosylerythritol lipids: microbial production and their applications. In: Biosurfactants: from genes to applications, Microbiology Monographs 20, pp. 145-177 (edited by G. Soberón-Chávez, Springer, Berlin) (2011); DOI.
- Augustin, J.M., Kuzina, V., Andersen, S.B. and Bak, S. Molecular activities, biosynthesis and evolution of triterpenoid saponins. Phytochemistry, 72, 435-457 (2011).
- Aureli, M., Loberto,N., Chigorno,V., Prinetti,A. and Sonnino,S. Remodeling of sphingolipids by plasma membrane associated enzymes. Neurochem. Res., 36, 1636-1644 (2011).
- Bab, I., Smoum,R., Bradshaw,H. and Mechoulam,R. Skeletal lipidomics: regulation of bone metabolism by fatty acid amide family. Brit. J. Pharm., 163, 1441-1446 (2011).
- Barcelo-Coblijn, G., Martin, M.L., de Almeida, R.F.M., Noguera-Salva, M.A., Marcilla-Etxenike, A., Guardiola-Serrano, F., Luth, A., Kleuser, B., Halver, J.E. and Escriba, P.V. Sphingomyelin and sphingomyelin synthase (SMS) in the malignant transformation of glioma cells and in 2-hydroxyoleic acid therapy. PNAS, 108, 19569-19574 (2011); DOI.
- Bedke, D.K. and Vanderwal,C.D. Chlorosulfolipids: Structure, synthesis, and biological relevance. Nat. Prod. Rep., 28, 15-25 (2011).
- Bikman, B.T. and Summers,S.A. Ceramides as modulators of cellular and whole-body metabolism. J. Clin. Invest., 121, 4222-4230 (2011).
- Blaho, V.A. and Hla,T. Regulation of mammalian physiology, development, and disease by the sphingosine 1-phosphate and lysophosphatidic acid receptors. Chem. Rev., 111, 6299-6320 (2011).
- Blom, T., Somerharju, P. and Ikonen, E. Synthesis and biosynthetic trafficking of membrane lipids. Cold Spring Harbor Persp. Biol., 3, a004713 (2011).
- Blomqvist, M., Gieselmann, V. and Mansson, J.-E. Accumulation of lysosulfatide in the brain of arylsulfatase A-deficient mice. Lipids Health Dis., 10, 28 (2011); DOI.
- Bornancin, F. Ceramide kinase: The first decade. Cellular Signalling, 23, 999-1008 (2011).
- Botté, C.Y., Yamaryo-Botté, Y., Janouskovec, J., Rupasinghe, T., Keeling, P.J., Crellin, P., Coppel, R.L., Maréchal, E., McConville, M.J. and McFadden, G.I. Identification of plant-like galactolipids in Chromera velia, a photosynthetic relative of malaria parasites. J. Biol. Chem., 286, 29893-29903 (2011).
- Bozza, P.T., Bakker-Abreu, I., Navarro-Xavier, R.A. and Bandeira-Melo, C. Lipid body function in eicosanoid synthesis: An update. Prostaglandins, Leukotrienes Essential Fatty Acids, 85, 205-213 (2011).
- Brodhun, F. and Feussner,I. Oxylipins in fungi. FEBS J., 278, 1047-1063 (2011).
- Broniec, A., Klosinski,R., Pawlak,A., Wrona-Krol,M., Thompson,D. and Sarna,T. Interactions of plasmalogens and their diacyl analogs with singlet oxygen in selected model systems. Free Rad. Biol. Med., 50, 892-898 (2011).
- Butinar, B., Bucar-Miklavcic,M., Mariani,C. and Raspor,P. New vitamin E isomers (gamma-tocomonoenol and alpha-tocomonoenol) in seeds, roasted seeds and roasted seed oil from the Slovenian pumpkin variety ‘Slovenska golica’. Food Chemistry, 128, 505-512 (2011).
- Butovich, I.A. Lipidomics of human Meibomian gland secretions: Chemistry, biophysics, and physiological role of Meibomian lipids. Prog. Lipid Res., 50, 278-301 (2011).
- Chaves, V.E., Frasson,D. and Kawashita,N.H. Several agents and pathways regulate lipolysis in adipocytes. Biochimie, 93, 1631-1640 (2011).
- Chen, P., Véricel E., Lagarde M. and Guichardant M. Poxytrins, a class of oxygenated products from polyunsaturated fatty acids, potently inhibit blood platelet aggregation. FASEB J., 25, 382-388 (2011); DOI.
- Christensen, S.A. and Kolomiets,M.V. The lipid language of plant-fungal interactions. Fungal Genetics Biol., 48, 4-14 (2011).
- Coleman, R.A. and Mashek, D.G. Mammalian triacylglycerol metabolism: synthesis, lipolysis, and signalling. Chem. Rev., 111, 6359-6386 (2011).
- D'Ambrosio, D.N. Clugston, R.D. and Blaner, W.S. Vitamin A metabolism: an update. Nutrients, 3, 63-103 (2011).
- Davies, S.S. and Roberts, L.J. F-2-isoprostanes as an indicator and risk factor for coronary heart disease. Free Rad. Biol. Med., 50, 559-566 (2011).
- Dennis, E.A., Cao,J., Hsu,Y.-H., Magrioti,V. and Kokotos,G. Phospholipase A2 enzymes: physical structure, biological function, disease implication, chemical inhibition, and therapeutic intervention. Chem. Rev., 111, 6130-6185 (2011).
- Di Marzo, V. Endocannabinoid signaling in the brain: biosynthetic mechanisms in the limelight. Nature Neuro., 14, 9-15 (2011).
- Dobrian, A.D., Lieb,D.C., Cole,B.K., Taylor-Fishwick,D.A., Chakrabarti,S.K. and Nadler,J.L. Functional and pathological roles of the 12- and 15-lipoxygenases. Prog. Lipid Res., 50, 115-131 (2011).
- Dolganiuc, A. Role of lipid rafts in liver health and disease. World J. Gastroenterol., 17, 2520-2535 (2011).
- Dominguez, E., Heredia-Guerrero,J.A. and Heredia,A. The biophysical design of plant cuticles: an overview. New Phytologist, 189, 938-948 (2011).
- Duan, R.D. Physiological functions and clinical implications of sphingolipids in the gut. J. Digestive Diseases, 12, 60-70 (2011).
- Durand, T., Bultel-Ponce,V., Guy,A., El Fangour,S., Rossi,J.C. and Galano,J.M. Isoprostanes and phytoprostanes: Bioactive lipids. Biochimie, 93, 52-60 (2011).
- Fujimoto, T. and Parton, R.G. Not just fat: the structure and function of the lipid droplet. Cold Spring Harbor Persp. Biol., 3, a004838 (2011).
- Fukuda, S., Terasawa,M. and Shiomi,K. Phosphatidylarsenocholine, one of the major arsenolipids in marine organisms: Synthesis and metabolism in mice. Food Chem. Toxicol., 49, 1598-1603 (2011).
- Gallala, H.D. and Sandhoff,K. Biological function of the cellular lipid BMP-BMP as a key activator for cholesterol sorting and membrane digestion. Neurochem. Res., 36, 1594-1600 (2011).
- Garcia-Llatas, G. and Rodriguez-Estrada,M.T. Current and new insights on phytosterol oxides in plant sterol-enriched food. Chem. Phys. Lipids, 164, 607-624 (2011).
- Gharbi, S.I., Rincon, E., Avila-Flores, A., Torres-Ayuso, P., Almena, M., Cobos, M.A., Albar, J.P. and Merida, I. Diacylglycerol kinase zeta controls diacylglycerol metabolism at the immunological synapse. Mol. Biol. Cell, 22, 4406-4414 (2011); DOI.
- Gordon, S.M., Hofmann,S., Askew,D.S. and Davidson,W.S. High density lipoprotein: it's not just about lipid transport anymore. Trends Endocrinol. Metab., 22, 9-15 (2011).
- Greene, E.R., Huang,S., Serhan,C.N. and Panigrahy,D. Regulation of inflammation in cancer by eicosanoids. Prostaglandins Other Lipid Mediators, 96, 27-36 (2011).
- Haeggström, J.Z. and Funk, C.D. Lipoxygenase and leukotriene pathways: biochemistry, biology, and roles in disease. Chem. Rev., 111, 5866-5898 (2011).
- Hang, H.C. and Linder, M.E. Exploring protein lipidation with chemical biology. Chem. Rev., 111, 6341-6358 (2011).
- Hannich, J.T., Umebayashi, K. and Riezman, H. Distribution and functions of sterols and sphingolipids. Cold Spring Harbor Persp. Biol., 3, a004762 (2011).
- Hannun, Y.A. and Obeid,L.M. Many ceramides. J. Biol. Chem., 286, 27855-27862 (2011).
- Harden, T.K., Waldo,G.L., Hicks,S.N. and Sondek,J. Mechanism of activation and inactivation of Gq/phospholipase C-ß signaling nodes. Chem. Rev., 111, 6120-6129 (2011).
- Harmon, G.S., Lam,M.T. and Glass,C.K. PPARs and lipid ligands in inflammation and metabolism. Chem. Rev., 111, 6321-6340 (2011).
- Harris, T.E. and Finck,B.N. Dual function lipin proteins and glycerolipid metabolism. Trends Endocrinol. Metab., 22, 226-233 (2011).
- Hauser, P.S., Narayanaswami,V. and Ryan,R.O. Apolipoprotein E: From lipid transport to neurobiology. Prog. Lipid Res., 50, 62-74 (2011).
- Heaton, N.S. and Randall,G. Multifaceted roles for lipids in viral infection. Trends Microbiol., 19, 368-375 (2011).
- Hennessy, A.A., Ross, R.P., Devery, R. and Stanton, C. The health promoting properties of the conjugated isomers of alpha-linolenic acid. Lipids, 46, 105-119 (2011).
- Hirata, T. and Narumiya, S. Prostanoid receptors. Chem. Rev., 111, 6209-6230 (2011).
- Huang, W.-C., Chen, C.-L., Lin, Y.-S. and Lin,C.-F. Apoptotic sphingolipid ceramide in cancer therapy. J. Lipids, 565316 (2011).
- Ikushiro, H. and Hayashi, H. Mechanistic enzymology of serine palmitoyltransferase. Biochim. Biophys. Acta, 1814, 1474-1480 (2011).
- Inokuchi, J. Physiopathological function of hematoside (GM3 ganglioside). Proc. Japan Acad., Series B, 87, 179-198 (2011).
- Iuliano, L. Pathways of cholesterol oxidation via non-enzymatic mechanisms. Chem. Phys. Lipids, 164, 457-468 (2011).
- Jacques, P. Surfactin and other lipopeptides from Bacillus spp. In: Biosurfactants: from genes to applications, Microbiology Monographs 20, pp. 57-91 (edited by G. Soberón-Chávez, Springer, Berlin) (2011); DOI.
- Ji, R.-J., Xu,Z.-Z., Strichartz,G. and Serhan,C.N. Emerging roles of resolvins in the resolution of inflammation and pain. Trends Neurosci., 34, 599-609 (2011).
- Kaur, G., Cameron-Smith,D., Garg,M. and Sinclair,A.J. Docosapentaenoic acid (22:5n-3): A review of its biological effects. Prog. Lipid Res., 50, 28-34 (2011).
- Kay, J.G. and Grinstein,S. Sensing phosphatidylserine in cellular membranes. Sensors, 11, 1744-1755 (2011).
- Kerr, W.G. and Colucci,F. Inositol phospholipid signaling and the biology of natural killer cells. J. Innate Immunity, 3, 249-257 (2011).
- Koga, Y. Early evolution of membrane lipids: how did the lipid divide occur? J. Mol. Evol., 72, 274-282 (2011).
- Kolter, T. A view on sphingolipids and disease. Chem. Phys. Lipids, 164, 590-606 (2011).
- Konkel, A. and Schunck,W.H. Role of cytochrome P450 enzymes in the bioactivation of polyunsaturated fatty acids. Biochim. Biophys. Acta, 1814, 210-222 (2011).
- Kovacs-Simon, A., Titball, R.W. and Michell, S.L. Lipoproteins of bacterial pathogens. Infect Immun., 79, 548-561 (2011).
- Kraut, R. Roles of sphingolipids in Drosophila development and disease. J. Neurochem., 116, 764-778 (2011).
- Kruk, J., Pisarski, A. and Szymanska, R. Novel vitamin E forms in leaves of Kalanchoe daigremontiana and Phaseolus coccineus. J. Plant Physiol., 168, 2021-2027 (2011); DOI.
- Kulkarni, C.V., Wachter,W., Iglesias-Salto,G., Engelskirchen,S. and Ahualli,S. Monoolein: a magic lipid? Phys. Chem. Chem. Phys., 13, 3004-3021 (2011).
- Kumar, A., Byun, H.S., Bittman, R. and Saba, J.D. The sphingolipid degradation product trans-2-hexadecenal induces cytoskeletal reorganization and apoptosis in a JNK-dependent manner. Cell Signal., 23, 1144-1152 (2011); DOI.
- Lass, A., Zimmermann,R., Oberer,M. and Zechner,R. Lipolysis - A highly regulated multi-enzyme complex mediates the catabolism of cellular fat stores. Prog. Lipid Res., 50, 14-27 (2011).
- Lee, A.G. Biological membranes: the importance of molecular detail. Trends Biochem. Sci., 36, 493-500 (2011).
- Lee, W.S. Integral hair lipid in human hair follicle. J. Dermatol. Sci., 64, 153-158 (2011); DOI.
- Leoni, V. and Caccia,C. Oxysterols as biomarkers in neurodegenerative diseases. Chem. Phys. Lipids, 164, 515-524 (2011).
- Li, C.J., Guan,Z.Q., Liu,D. and Raetz,C.R.H. Pathway for lipid A biosynthesis in Arabidopsis thaliana resembling that of Escherichia coli. Proc. Natl. Acad. Sci. USA, 108, 11387-11392 (2011).
- Lingwood, C.A. Glycosphingolipid functions. Cold Spring Harbor Persp. Biol., 3, a004788 (2011).
- Littarru, G.P. and Lambrechts,P. Coenzyme Q10: multiple benefits in one ingredient. Oléag. Corps Gras, Lipides, 18, 76-82 (2011).
- Long, J.Z. and Cravatt, B.F. The metabolic serine hydrolases and their functions in mammalian physiology and disease. Chem. Rev., 111, 6022-6063 (2011).
- Maccioni, H.J.F., Quiroga, R. and Ferrari, M.L. Cellular and molecular biology of glycosphingolipid glycosylation. J. Neurochem., 117, 589-602 (2011).
- Maccioni, H.J.F., Quiroga, R. and Spessott, W. Organization of the synthesis of glycolipid oligosaccharides in the Golgi complex. FEBS Letts, 585, 1691-1698 (2011); DOI.
- Maeda, Y. and Kinoshita,T. Structural remodeling, trafficking and functions of glycosylphosphatidylinositol-anchored proteins. Prog. Lipid Res., 50, 411-424 (2011).
- Magnusson, C.D. and Haraldsson,G.G. Ether lipids. Chem. Phys. Lipids, 164, 315-340 (2011).
- Marechal, E., Riou,M., Kerboeuf,D., Beugnet,F., Chaminade,P. and Loiseau,P.M. Membrane lipidomics for the discovery of new antiparasitic drug targets. Trends Parasitol., 27, 496-504 (2011).
- Martin, D.O., Beauchamp,E. and Berthiaume,L.G. Post-translational myristoylation: Fat matters in cellular life and death. Biochimie, 93, 18-31 (2011).
- Matsumi, R., Atomi,H., Driessen,A.J.M. and van der Oost,J. Isoprenoid biosynthesis in Archaea - Biochemical and evolutionary implications. Res. Microbiol., 162, 39-52 (2011).
- Matsuyama, T., Tanikawa, T. and Nakagawa, Y. Serrawettins and other surfactants produced by Serratia. In: Biosurfactants: from genes to applications, Microbiology Monographs 20, pp. 93-120 (edited by G. Soberón-Chávez, Springer, Berlin) (2011); DOI.
- Merrill, A.H. Sphingolipid and glycosphingolipid metabolic pathways in the era of sphingolipidomics. Chem. Rev., 111, 6387-6422 (2011).
- Miller, W.L. and Bose,H.S. Early steps in steroidogenesis: intracellular cholesterol trafficking. J. Lipid Res., 52, 2111-2135 (2011).
- Milne, G.L., Yin,H., Hardy,K.D., Davies,S.S. and Roberts,L.J. Isoprostane generation and function. Chem. Rev., 111, 5973-5996 (2011).
- Mishra, A.K., Driessen,N.N., Appelmelk,BJ. and Besra,G.S. Lipoarabinomannan and related glycoconjugates: structure, biogenesis and role in Mycobacterium tuberculosis physiology and host-pathogen interaction. FEMS Microbiol. Rev., 35, 1126-1157 (2011).
- Moellering, E.R. and Benning, C. Galactoglycerolipid metabolism under stress: a time for remodelling. Trends Plant Sci., 16, 98-107 (2011).
- Morita, Y.S., Fukuda,T., Sena,C.B.C., Yamaryo-Botte,Y., McConville,M.J. and Kinoshita,T. Inositol lipid metabolism in mycobacteria: Biosynthesis and regulatory mechanisms. Biochim. Biophys. Acta, 1810, 630-641 (2011).
- Mouritsen, O.G. Model answers to lipid membrane questions. Cold Spring Harbor Persp. Biol., 3, a004622 (2011).
- Munnik, T. and Nielsen, E. Green light for polyphosphoinositide signals in plants. Curr. Opinion Plant Biol., 14, 489-497 (2011).
- Nakamura, M. and Shimizu,T. Leukotriene receptors. Chem. Rev., 111, 6231-6298 (2011).
- Nes, W.D. Biosynthesis of cholesterol and other sterols. Chem. Rev., 111, 6423-6451 (2011).
- Nikolaidis, M.G., Kyparos,A. and Vrabas,I.S. F2-isoprostane formation, measurement and interpretation: The role of exercise. Prog. Lipid Res., 50, 89-103 (2011).
- Nomura, D.K., Morrison,B.E., Blankman,J.L., Long,J.Z., Kinsey,S.G., Marcondes,M.C.G., Ward,A.M., Hahn,Y.K., Lichtman,A.H., Conti,B. and Cravatt,B.F. Endocannabinoid hydrolysis generates brain prostaglandins that promote neuroinflammation. Science, 334, 809-813 (2011).
- Osman, C., Voelker, D.R. and Langer, T. Making heads or tails of phospholipids in mitochondria. J. Cell Biol., 192, 7-16 (2011).
- Pilch, P.F. and Liu,L.B. Fat caves: caveolae, lipid trafficking and lipid metabolism in adipocytes. Trends Endocrinol. Metab., 22, 318-324 (2011).
- Pitson, S.M. Regulation of sphingosine kinase and sphingolipid signalling. Trends Biochem. Sci., 36, 97-107 (2011).
- Porter, F.D. and Herman,G.E. Malformation syndromes caused by disorders of cholesterol synthesis J. Lipid Res., 52, 6-34 (2011).
- Prinetti, A., Prioni,S., Chiricozzi,E., Schuchman,E.H., Chigorno,V. and Sonnino,S. Secondary alterations of sphingolipid metabolism in lysosomal storage diseases. Neurochem. Res., 36, 1654-1668 (2011).
- Pyne, S. and Pyne, N.J. Translational aspects of sphingosine 1-phosphate biology. Trends Mol. Med., 17, 463-472 (2011).
- Quiroga, A.D. and Lehner,R. Role of endoplasmic reticulum neutral lipid hydrolases. Trends Endocrinol. Metab., 22, 218-225 (2011).
- Ramazzotti, G., Faenza,I., Fiume,R., Matteucci,A., Piazzi,M., Follo,M.Y. and Cocco,L. The physiology and pathology of inositide signaling in the nucleus. J. Cell. Physiol., 226, 14-20 (2011).
- Reichmann, N.T. and Grundling,A. Location, synthesis and function of glycolipids and polyglycerolphosphate lipoteichoic acid in Gram-positive bacteria of the phylum Firmicutes. FEMS Microbiol. Letts, 319, 97-105 (2011).
- Ricciotti, E. and FitzGerald, G.A. Prostaglandins and inflammation. Arterioscler. Thromb. Vasc. Biol., 31, 986-1000 (2011).
- Ringseis, R. and Eder,K. Regulation of genes involved in lipid metabolism by dietary oxidized fat. Mol. Nutr. Food Res., 55, 109-121 (2011).
- Rioux, V., Pédrono,F. and Legrand,P Regulation of mammalian desaturases by myristic acid: N-terminal myristoylation and other modulations. Biochim. Biophys. Acta, 1811, 1-8 (2011).
- Roongsawang, N., Washio,K. and Morikawa,M. Diversity of nonribosomal peptide synthetases involved in the biosynthesis of lipopeptide biosurfactants. Int. J. Mol. Sci., 12, 141-172 (2011).
- Ross, R.A. L-alpha-Lysophosphatidylinositol meets GPR55: a deadly relationship. Trends Pharm. Sci., 32, 265-269 (2011).
- Rouzer, C.A. and Marnett,L.J. Endocannabinoid oxygenation by cyclooxygenases, lipoxygenases, and cytochromes P450: Cross-talk between the eicosanoid and endocannabinoid signaling pathways. Chem. Rev., 111, 5899–5921 (2011).
- Ryland, L.K., Fox,T.E., Liu,X., Loughran,T.P. and Kester,M. Dysregulation of sphingolipid metabolism in cancer. Cancer Biology Therapy, 11, 138-149 (2011).
- Schopfer, F.J., Cipollina,C. and Freeman,B.A. Formation and signaling actions of electrophilic lipids. Chem. Rev., 111, 5997-6021 (2011).
- Schulze, H. and Sandhoff, K. Lysosomal lipid storage diseases. Cold Spring Harbor Persp. Biol., 3, a004804 (2011).
- Selvy, P.E., Lavieri,R.R., Lindsley,C.W. and Brown,H.A. Phospholipase D: enzymology, functionality, and chemical modulation. Chem. Rev., 111, 6064–6119 (2011).
- Serhan, C.N. and Petasis, N.A. Resolvins and protectins in inflammation resolution. Chem. Rev., 111, 5922-5943 (2011).
- Shahidi, F. and Zhong,Y. Revisiting the polar paradox theory: a critical overview. J. Agric. Food Chem., 59, 3499-3504 (2011).
- Shao, Z. Trehalolipids. In: Biosurfactants: from genes to applications, Microbiology Monographs 20, pp. 121-143 (edited by G. Soberón-Chávez, Springer, Berlin) (2011); DOI.
- Shewan, A., Eastburn, D.J. and Mostov, K. Phosphoinositides in cell architecture. Cold Spring Harbor Persp. Biol., 3, a004796 (2011).
- Shimojima, M. Biosynthesis and functions of the plant sulfolipid. Prog. Lipid Res., 50, 234-239 (2011).
- Shimojima, M. and Ohta,H. Critical regulation of galactolipid synthesis controls membrane differentiation and remodeling in distinct plant organs and following environmental changes. Prog. Lipid Res., 50, 258-266 (2011).
- Shimozu, Y., Hirano,K., Shibata,T., Shibata,N. and Uchida,K. 4-Hydroperoxy-2-nonenal is not just an intermediate but a reactive molecule that covalently modifies proteins to generate unique intramolecular oxidation products. J. Biol. Chem., 286, 29313-29324 (2011).
- Shipston, M.J. Ion channel regulation by protein palmitoylation. J. Biol. Chem., 286, 8709-8716 (2011).
- Shulga, Y.V., Topham, M.K. and Epand,R.M. Regulation and functions of diacylglycerol kinases. Chem. Rev., 111, 6186-6208 (2011).
- Simon-Plas, F., Perraki, A., Bayer, E., Gerbeau-Pissot, P. and Mongrand, S. An update on plant membrane rafts. Curr. Opinion Plant Biol., 14, 642-649 (2011).
- Simons, K. and Sampaio, J.L. Membrane organization and lipid rafts. Cold Spring Harbor Persp. Biol., 3, a004697 (2011).
- Singh, A. and Del Poeta, M. Lipid signalling in pathogenic fungi. Cell. Microbiol., 13, 177-185 (2011).
- Smith, W.L., Urade, Y. and Jakobsson, P.-J. Enzymes of the cyclooxygenase pathways of prostanoid biosynthesis. Chem. Rev., 111, 5821-5865 (2011).
- Soberón-Chávez, G. and Maier, R.M. Biosurfactants: a general overview. In: Biosurfactants: from genes to applications, Microbiology Monographs 20, pp. 1-11 (edited by G. Soberón-Chávez, Springer, Berlin) (2011); DOI.
- Sookwong, P., Nakagawa,K., Fujita,I., Shoji,N. and Miyazawa,T. Amadori-glycated phosphatidylethanolamine, a potential marker for hyperglycemia, in streptozotocin-induced diabetic rats. Lipids, 46, 943-952 (2011).
- Spanova, M. and Daum,G. Squalene - biochemistry, molecular biology, process biotechnology, and applications. Eur. J. Lipid Sci. Technol., 113, 1299-1320 (2011).
- Stables, M.J. and Gilroy,D.W. Old and new generation lipid mediators in acute inflammation and resolution. Prog. Lipid Res., 50, 35-51 (2011).
- Staubach, S. and Hanisch,F.G. Lipid rafts: signaling and sorting platforms of cells and their roles in cancer. Expert Rev. Proteomics, 8, 263-277 (2011).
- Surmacz, L. and Swiezewska,E. Polyisoprenoids - secondary metabolites or physiologically important superlipids? Biochem. Biophys. Res. Commun., 407, 627-632 (2011).
- Tanaka, K., Fujimura-Kamada,K. and Yamamoto,T. Functions of phospholipid flippases. J. Biochem. (Tokyo), 149, 131-143 (2011).
- Ternes, P., Wobbe,T., Schwarz,M., Albrecht,S., Feussner,K., Riezman,I., Cregg,J.M., Heinz,E., Riezman,H., Feussner,I. and Warnecke,D. Two pathways of sphingolipid biosynthesis are separated in the yeast Pichia pastoris. J. Biol. Chem., 286, 11401-11414 (2011).
- Testerink, C. and Munnik,T. Molecular, cellular, and physiological responses to phosphatidic acid formation in plants. J. Exp. Botany, 62, 2349-2361 (2011).
- Trostchansky, A., Bonilla, L., Thomas, C.P., O’Donnell, V.B., Marnett, L.J., Radi, R. and Rubbo, H. Nitroarachidonic acid, a novel peroxidase inhibitor of prostaglandin endoperoxide H synthases 1 and 2. J. Biol. Chem., 286, 12891-12900 (2011); DOI.
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