Synaptic lipid signaling

Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs

Markram, H., Lübke, J., Frotscher, M., & Sakmann, B. (1997) · Science · doi:10.1126/science.275.5297.213 · Cited by 3,832 · see citing works

COX-3, a cyclooxygenase-1 variant inhibited by acetaminophen and other analgesic/antipyretic drugs: Cloning, structure, and expression

Chandrasekharan, N. V., Dai, H., Roos, K. L. T., Evanson, N. K., Tomsik, J., Elton, T. S., & Simmons, D. L. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.162468699 · Cited by 1,989 · see citing works

The molecular logic of endocannabinoid signalling

Piomelli, D. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1247 · Cited by 1,957 · see citing works

A series of prostaglandin F2-like compounds are produced in vivo in humans by a non-cyclooxygenase, free radical-catalyzed mechanism.

Morrow, J. D., Hill, K. E., Burk, R. F., Nammour, T., Badr, K. F., & Roberts, L. J. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.23.9383 · Cited by 1,898 · see citing works

Resolvins

Serhan, C. N., Hong, S., Gronert, K., Colgan, S. P., Devchand, P. R., Mirick, G., & Moussignac, R.-L. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20020760 · Cited by 1,650 · see citing works

Endogenous cannabinoids mediate retrograde signalling at hippocampal synapses

Wilson, R. I., & Nicoll, R. A. (2001) · Nature · doi:10.1038/35069076 · Cited by 1,607 · see citing works

Synaptic Modification by Correlated Activity: Hebb's Postulate Revisited

Bi, G., & Poo, M. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.139 · Cited by 1,476 · see citing works

Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation

Zonta, M., Angulo, M. C., Gobbo, S., Rosengarten, B., Hossmann, K.-A., Pozzan, T., & Carmignoto, G. (2002) · Nature Neuroscience · doi:10.1038/nn980 · Cited by 1,446 · see citing works

Diversity of group types, regulation, and function of phospholipase A2.

Dennis, E. A. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)36794-7 · Cited by 1,435 · see citing works

The expanding superfamily of phospholipase A2 enzymes: classification and characterization

Six, D. A., & Dennis, E. A. (2000) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/s1388-1981(00)00105-0 · Cited by 1,359 · see citing works

A Synaptically Controlled, Associative Signal for Hebbian Plasticity in Hippocampal Neurons

Magee, J. C., & Johnston, D. (1997) · Science · doi:10.1126/science.275.5297.209 · Cited by 1,303 · see citing works

Endocannabinoid Signaling in the Brain

Wilson, R. I., & Nicoll, R. A. (2002) · Science · doi:10.1126/science.1063545 · Cited by 1,260 · see citing works

Expression of a mitogen-inducible cyclooxygenase in brain neurons: Regulation by synaptic activity and glucocorticoids

Yamagata, K., Andreasson, K. I., Kaufmann, W. E., Barnes, C. A., & Worley, P. F. (1993) · Neuron · doi:10.1016/0896-6273(93)90192-t · Cited by 1,224 · see citing works

Presynaptically Located CB1 Cannabinoid Receptors Regulate GABA Release from Axon Terminals of Specific Hippocampal Interneurons

Katona, I., Sperlágh, B., Sı́k, A., Käfalvi, A., Vizi, E. S., Mackie, K., & Freund, T. F. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-11-04544.1999 · Cited by 1,218 · see citing works

Novel Functional Sets of Lipid-Derived Mediators with Antiinflammatory Actions Generated from Omega-3 Fatty Acids via Cyclooxygenase 2–Nonsteroidal Antiinflammatory Drugs and Transcellular Processing

Serhan, C. N., Clish, C. B., Brannon, J., Colgan, S. P., Chiang, N., & Gronert, K. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.8.1197 · Cited by 1,189 · see citing works

Prostaglandins stimulate calcium-dependent glutamate release in astrocytes

Bezzi, P., Carmignoto, G., Pasti, L., Vesce, S., Rossi, D., Rizzini, B. L., Pozzan, T., & Volterra, A. (1998) · Nature · doi:10.1038/34651 · Cited by 1,143 · see citing works

Tests of the roles of two diffusible substances in long-term potentiation: evidence for nitric oxide as a possible early retrograde messenger.

O’Dell, T. J., Hawkins, R. D., Kandel, E. R., & Arancio, O. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.24.11285 · Cited by 1,034 · see citing works

Direct Signaling from Astrocytes to Neurons in Cultures of Mammalian Brain Cells

Nedergaard, M. (1994) · Science · doi:10.1126/science.8134839 · Cited by 1,006 · see citing works

Novel Docosatrienes and 17S-Resolvins Generated from Docosahexaenoic Acid in Murine Brain, Human Blood, and Glial Cells

Hong, S., Gronert, K., Devchand, P. R., Moussignac, R.-L., & Serhan, C. N. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300218200 · Cited by 1,000 · see citing works

Global analyses of cellular lipidomes directly from crude extracts of biological samples by ESI mass spectrometry: a bridge to lipidomics

Han, X., & Gross, R. W. (2003) · Journal of Lipid Research · doi:10.1194/jlr.r300004-jlr200 · Cited by 914 · see citing works

Effects of ischemia and electroconvulsive shock on free fatty acid pool in the brain

Bazán, N. G. (1970) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/0005-2760(70)90086-x · Cited by 855 · see citing works

Reduced fertility and postischaemic brain injury in mice deficient in cytosolic phospholipase A2

Bonventre, J. V., Huang, Z., Taheri, M. R., O’Leary, E., Li, E., Moskowitz, M. A., & Sapirstein, A. (1997) · Nature · doi:10.1038/37635 · Cited by 846 · see citing works

Endogenous Cannabinoids Mediate Retrograde Signals from Depolarized Postsynaptic Neurons to Presynaptic Terminals

Ohno‐Shosaku, T., Maejima, T., & Kano, M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00247-1 · Cited by 846 · see citing works

Novel docosanoids inhibit brain ischemia-reperfusion-mediated leukocyte infiltration and pro-inflammatory gene expression

Marcheselli, V. L., Hong, S., Lukiw, W. J., Tian, X. H., Gronert, K., Musto, A., Hardy, M., Gimenez, J. M., Chiang, N., Serhan, C. N., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m305841200 · Cited by 802 · see citing works

Platelet-Activating Factor and Related Lipid Mediators

Prescott, S. M., Zimmerman, G. A., Stafforini, D. M., & McIntyre, T. M. (2000) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.69.1.419 · Cited by 747 · see citing works

Arachidonic acid induces a long-term activity-dependent enhancement of synaptic transmission in the hippocampus

Williams, J. H. H., Errington, M. L., Lynch, M. A., & Bliss, T. V. P. (1989) · Nature · doi:10.1038/341739a0 · Cited by 627 · see citing works

COX-2, a synaptically induced enzyme, is expressed by excitatory neurons at postsynaptic sites in rat cerebral cortex.

Kaufmann, W. E., Worley, P. F., Pegg, J. A., Bremer, M., & Isakson, P. C. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.6.2317 · Cited by 593 · see citing works

NMDA receptors activate the arachidonic acid cascade system in striatal neurons

Dumuis, A., Sebben, M., Haynes, L., Pin, J., & Bockaert, J. (1988) · Nature · doi:10.1038/336068a0 · Cited by 593 · see citing works

Cloning by functional expression of platelet-activating factor receptor from guinea-pig lung

Honda, Z., Nakamura, M., Miki, I., Minami, M., Watanabe, T., Seyama, Y., Okado, H., Toh, H., Ito, K., Miyamoto, T., et al. (1991) · Nature · doi:10.1038/349342a0 · Cited by 586 · see citing works

Microglia as effector cells in brain damage and repair: focus on prostanoids and nitric oxide

Minghetti, L. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00052-x · Cited by 566 · see citing works

Anti-inflammatory properties of a platelet-activating factor acetylhydrolase

Tjoelker, L. W., Wilder, C., Eberhardt, C., Stafforinit, D. M., Dietsch, G., Schimpf, B. A., Hooper, S., Trong, H. L., Cousens, L. S., Zimmerman, G. A., et al. (1995) · Nature · doi:10.1038/374549a0 · Cited by 525 · see citing works

Receptor-mediated activation of phospholipase A2 via GTP-binding proteins: arachidonic acid and its metabolites as second messengers

Axelrod, J., Burch, R. M., & Jelsema, C. L. (1988) · Trends in Neurosciences · doi:10.1016/0166-2236(88)90157-9 · Cited by 504 · see citing works

Membrane docosahexaenoate is supplied to the developing brain and retina by the liver.

Scott, B. L., & Bazan, N. (1989) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.86.8.2903 · Cited by 445 · see citing works

Formation of Isoprostane-like Compounds (Neuroprostanes) in Vivo from Docosahexaenoic Acid*

Roberts, L., Montine, T., Markesbery, W., Tapper, A. R., Hardy, P., Chemtob, S., Dettbarn, W., & Morrow, J. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.22.13605 · Cited by 430 · see citing works

Modulation of rhodopsin function by properties of the membrane bilayer

Brown, M. F. (1994) · Chemistry and Physics of Lipids · doi:10.1016/0009-3084(94)90180-5 · Cited by 422 · see citing works

Modulation of TTX-RINaby PKC and PKA and Their Role in PGE2-Induced Sensitization of Rat Sensory NeuronsIn Vitro

Gold, M. S., Levine, J. D., & Correa, A. M. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-24-10345.1998 · Cited by 421 · see citing works

Cerebrovascular Disease: Pathophysiology, Diagnosis and Management

Ginsberg, M. D., & Bogousslavsky, J. (1998) · Medical Entomology and Zoology · Cited by 392 · see citing works

Calcium dynamics in single spines during coincident pre- and postsynaptic activity depend on relative timing of back-propagating action potentials and subthreshold excitatory postsynaptic potentials

Koester, H. J., & Sakmann, B. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.16.9596 · Cited by 338 · see citing works

Endocannabinoids facilitate the induction of LTP in the hippocampus

Carlson, G. C., Wang, Y., & Alger, B. E. (2002) · Nature Neuroscience · doi:10.1038/nn879 · Cited by 336 · see citing works

A new perspective on cannabinoid signalling: complimentary localization of fatty acid amide hydrolase and the CB1 receptor in rat brain.

Egertová, M., Giang, D. K., Cravatt, B. F., & Elphick, M. R. (1998) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1998.0543 · Cited by 333 · see citing works

Glial neuronal signaling in the central nervous system

Hansson, E., & Rönnbäck, L. (2003) · The FASEB Journal · doi:10.1096/fj.02-0429rev · Cited by 326 · see citing works

Arachidonic Acid Is Preferentially Metabolized by Cyclooxygenase-2 to Prostacyclin and Prostaglandin E2

Brock, T. G., McNish, R. W., & Peters-Golden, M. L. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.17.11660 · Cited by 306 · see citing works

Role of the CNS microvascular pericyte in the blood-brain barrier

Balabanov, R. D., & Dore‐Duffy, P. (1998) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19980915)53:6 · Cited by 304 · see citing works

Cyclooxygenase-2 Regulates Prostaglandin E2Signaling in Hippocampal Long-Term Synaptic Plasticity

Chen, C., Magee, J. C., & Bazan, N. G. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.87.6.2851 · Cited by 293 · see citing works

Diacylglycerols and phosphatidates: which molecular species are intracellular messengers?

Hodgkin, M. N., Pettitt, T. R., Martin, A., Michell, R. H., Pemberton, A. J., & Wakelam, M. J. O. (1998) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(98)01200-6 · Cited by 286 · see citing works

Cloning and expression of a membrane receptor for secretory phospholipases A2.

Lambeau, G. J., Ancian, P., Barhanin, J., & Lazdunski, M. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)42060-6 · Cited by 279 · see citing works

Fatty acid amide hydrolase is located preferentially in large neurons in the rat central nervous system as revealed by immunohistochemistry

Tsou, K., Nogueron, M. I., Muthian, S., Sañudo-Peña, M. C., Hillard, C. J., Deutsch, D. G., & Walker, J. M. (1998) · Neuroscience Letters · doi:10.1016/s0304-3940(98)00700-9 · Cited by 240 · see citing works

Neuroregulatory and Neuropathological Actions of the Ether-Phospholipid Platelet-Activating Factor

Kornecki, E., & Ehrlich, Y. H. (1988) · Science · doi:10.1126/science.3381103 · Cited by 240 · see citing works

Platelet-activating factor as a potential retrograde messenger in CA1 hippocampal long-term potentiation

Kato, K., Clark, G. D., Bazan, N., & Zorumski, C. (1994) · Nature · doi:10.1038/367175a0 · Cited by 239 · see citing works

Functional Hyperemia in the Brain

Harder, D. R., Alkayed, N. J., Lange, A. R., Gebremedhin, D., & Roman, R. J. (1998) · Stroke · doi:10.1161/01.str.29.1.229 · Cited by 220 · see citing works

Enhancement of hippocampal excitatory synaptic transmission by platelet-activating factor.

Clark, G. D., Happel, L., Zorumski, C., & Bazan, N. (1992) · Neuron · doi:10.1016/0896-6273(92)90078-r · Cited by 214 · see citing works

Distinct platelet-activating factor binding sites in synaptic endings and in intracellular membranes of rat cerebral cortex.

Marcheselli, V. L., Rossowska, M. J., Domingo, M. T., Braquet, P. G., & Bazan, N. G. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)38822-2 · Cited by 211 · see citing works

Modulation of the hyperpolarization‐activated current (Ih) by cyclic nucleotides in guinea‐pig primary afferent neurons.

Ingram, S., & Williams, J. T. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021292 · Cited by 201 · see citing works

Identification and Properties of Very High Affinity Brain Membrane-binding Sites for a Neurotoxic Phospholipase from the Taipan Venom

Lambeau, G. J., Barhanin, J., Schweitz, H., Qar, J., & Lazdunski, M. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)60492-2 · Cited by 187 · see citing works

Increased Seizure Susceptibility and Proconvulsant Activity of Anandamide in Mice Lacking Fatty Acid Amide Hydrolase

Clement, A. B., Hawkins, E. G., Lichtman, A. H., & Cravatt, B. F. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-09-03916.2003 · Cited by 187 · see citing works

F₄ ‐ Isoprostanes as Specific Marker of Docosahexaenoic Acid Peroxidation in Alzheimer's Disease

Nourooz‐Zadeh, J., Liu, E. H. C., Yhlen, B., Änggåard, E. E., & Halliwell, B. (1999) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1999.0720734.x · Cited by 187 · see citing works

The human leukocyte platelet-activating factor receptor. cDNA cloning, cell surface expression, and construction of a novel epitope-bearing analog.

Kunz, D., Gerard, N. P., & Gerard, C. J. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)50394-5 · Cited by 186 · see citing works

Interleukin‐1β Induces Prostaglandin G/H Synthase‐2 (Cyclooxygenase‐2) in Primary Murine Astrocyte Cultures

O’Banion, M. K., Miller, J. C., Chang, J. W., Kaplan, M. D., & Coleman, P. D. (1996) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1996.66062532.x · Cited by 185 · see citing works

Astrocyte-mediated control of cerebral microcirculation

Anderson, C. M., & Nedergaard, M. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00141-3 · Cited by 183 · see citing works

Rapid production of diacylglycerols enriched in arachidonate and stearate during early brain ischemia

Aveldaño, M. I., & Bazan, N. G. (1975) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1975.tb04432.x · Cited by 178 · see citing works

Platelet-activating factor (PAF) receptor in rat brain: PAF mobilizes intracellular Ca2+ in hippocampal neurons

Bito, H., Nakamura, M., Honda, Z., Izumi, T., Iwatsubo, T., Seyama, Y., Ogura, A., Kudo, Y., & Shimizu, T. (1992) · Neuron · doi:10.1016/0896-6273(92)90167-c · Cited by 175 · see citing works

Diacylglycerol kinase ɛ regulates seizure susceptibility and long-term potentiation through arachidonoyl– inositol lipid signaling

Turco, E., Tang, W., Topham, M. K., Sakane, F., Marcheselli, V. L., Chen, C., Taketomi, A., Prescott, S. M., & Bazan, N. G. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081536298 · Cited by 160 · see citing works

The Biodisposition and Metabolism of Anandamide in Mice

Willoughby, K. A., Moore, S. F., Martin, B. R., & Ellis, E. F. (1997) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)36812-0 · Cited by 159 · see citing works

Production of platelet-activating factor by chick retina.

Bussolino, F., Gremo, F., Tetta, C., Pescarmona, G., & Camussi, G. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)66594-9 · Cited by 158 · see citing works

Identification and purification of a very high affinity binding protein for toxic phospholipases A2 in skeletal muscle.

Lambeau, G. J., Schmid‐Alliana, A., Lazdunski, M., & Barhanin, J. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)38881-7 · Cited by 157 · see citing works

Effects of a platelet activating factor antagonist (BN 52021) on free fatty acids, diacylglycerols, polyphosphoinositides and blood flow in the gerbil brain: Inhibition of ischemia-reperfusion induced cerebral injury

Panetta, T. F., Marcheselli, V. L., Braquet, P. G., Spinnewyn, B., & Bazan, N. G. (1987) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(87)90407-4 · Cited by 155 · see citing works

Platelet-activating factor and retinoic acid synergistically activate the inducible prostaglandin synthase gene.

Bazan, N. G., Fletcher, B. S., Herschman, H. R., & Mukherjee, P. K. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.12.5252 · Cited by 153 · see citing works

Phospholipid species containing long and very long polyenoic fatty acids remain with rhodopsin after hexane extraction of photoreceptor membranes

Aveldano, M. I. (1988) · Biochemistry · doi:10.1021/bi00404a024 · Cited by 149 · see citing works

Long-term potentiation in the hippocampus induced by platelet-activating factor

Wieraszko, A., Li, G., Kornecki, E., Hogan, M. V., & Ehrlich, Y. H. (1993) · Neuron · doi:10.1016/0896-6273(93)90342-o · Cited by 148 · see citing works

Prostaglandins Suppress an Outward Potassium Current in Embryonic Rat Sensory Neurons

Nicol, G. D., Vasko, M. R., & Evans, A. R. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.1.167 · Cited by 136 · see citing works

PAF Antagonist Ginkgolide B Reduces Postischemic Neuronal Damage in Rat Brain Hippocampus

Oberpichler-Schwenk, H., Sauer, D., Roßberg, C., Mennel, H.-D., & Krieglstein, J. (1990) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1990.17 · Cited by 130 · see citing works

Structural Elements of Secretory Phospholipases A2 Involved in the Binding to M-type Receptors

Lambeau, G. J., Ancian, P., Nicolas, J., Beiboer, S. H. W., Moinier, D., Verheij, H. M., & Lazdunski, M. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.10.5534 · Cited by 128 · see citing works

Role of PKC and MAPK in cytosolic PLA2 phosphorylation and arachadonic acid release in primary murine astrocytes

Xu, J., Weng, Y., Simonyi, Á., Krugh, B. W., Liao, Z., Weisman, G. A., & Sun, G. Y. (2002) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2002.01145.x · Cited by 127 · see citing works

The fatty acid composition of phosphatidylinositol from thrombin-stimulated human platelets.

Prescott, S. M., & Majerus, P. W. (1981) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)70010-6 · Cited by 125 · see citing works

Mechanisms of prostaglandin E2‐induced interleukin‐6 release in astrocytes: possible involvement of EP4‐like receptors, p38 mitogen‐activated protein kinase and protein kinase C

Fiebich, B. L., Schleicher, S., Spleiss, O., Czygan, M., & Hüll, M. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00652.x · Cited by 122 · see citing works

Proinflammatory Gene Induction by Platelet-Activating Factor Mediated Via Its Cognate Nuclear Receptor

Marrache, A. M., Gobeil, F., Bernier, S. G., Staňková, J., Rola‐Pleszczynski, M., Choufani, S., Bkaily, G., Bourdeau, A., Sirois, M. G., Vazquez‐Tello, A., et al. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.11.6474 · Cited by 121 · see citing works

Memory enhancement by intrahippocampal, intraamygdala, or intraentorhinal infusion of platelet-activating factor measured in an inhibitory avoidance task.

Izquierdo, I., Fin, C. A., Schmitz, P. K., Silva, R. C. D., Jerusalinsky, D. A., Quillfeldt, J. A., Ferreira, M. B. C., Medina, J. H., & Bazan, N. G. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.11.5047 · Cited by 117 · see citing works

Platelet-Activating Factor Acetylhydrolase (PAF-AH)

Arai, H., Koizumi, H., Aoki, J., & Inoue, K. (2002) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a003145 · Cited by 110 · see citing works

Platelet‐activating factor stimulates a Fos/Jun/AP‐1 transcriptional signaling system in human neuroblastoma cells

Squinto, S. P., Block, A. L., Braquet, P. G., & Bazan, N. G. (1989) · Journal of Neuroscience Research · doi:10.1002/jnr.490240414 · Cited by 110 · see citing works

Hippocampal kindling epileptogenesis upregulates neuronal cyclooxygenase-2 expression in neocortex☆☆Grant support: United States Public Health Service Grant NS23002 from the National Institute of Neurologic Disorders and Stroke, National Institutes of Health, Bethesda, MD.

Tu, B., & Bazan, N. G. (2003) · Experimental Neurology · doi:10.1016/s0014-4886(02)00019-5 · Cited by 108 · see citing works

Valproic acid down‐regulates the conversion of arachidonic acid to eicosanoids via cyclooxygenase‐1 and ‐2 in rat brain

Bosetti, F., Weerasinghe, G. R., Rosenberger, T. A., & Rapoport, S. I. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01701.x · Cited by 108 · see citing works

Docosahexaenoic acid (22:6, n-3) is metabolized to lipoxygenase reaction products in the retina

Bazan, N. G., Birkle, D. L., & Reddy, T. S. (1984) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(84)90601-6 · Cited by 107 · see citing works

Genes encoding multiple forms of phospholipase A2 are expressed in rat brain

Molloy, G. Y., Rattray, M., & Williams, R. J. (1998) · Neuroscience Letters · doi:10.1016/s0304-3940(98)00838-6 · Cited by 105 · see citing works

Evidence for platelet-activating factor as a novel mediator in experimental stroke in rabbits.

Lindsberg, P. J., Yue, T. L., Frerichs, K. U., Hallenbeck, J. M., & FEUERSTEIN, G. Z. (1990) · Stroke · doi:10.1161/01.str.21.10.1452 · Cited by 105 · see citing works

A monoclonal antibody shows discrete cellular and subcellular localizations of mGluR1α metabotropic glutamate receptors

Petralia, R. S., Wang, Y., Singh, S., Wu, C., Shi, L., Wei, J., & Wenthold, R. J. (1997) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(97)00023-9 · Cited by 104 · see citing works

Increased Brain Synthesis of Prostaglandin E2and F2-Isoprostane in Human and Experimental Transmissible Spongiform Encephalopathies

Minghetti, L., Greco, A., Cardone, F., Puopolo, M., Ladogana, A., Almonti, S., Cunningham, C. M., Perry, V. H., Pocchiari, M., & Levi, G. (2000) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/59.10.866 · Cited by 101 · see citing works

F4-Isoprostanes: A Novel Class of Prostanoids Formed during Peroxidation of Docosahexaenoic Acid (DHA)

Nourooz‐Zadeh, J., Liu, E. H. C., Änggård, E., & Halliwell, B. B. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.7883 · Cited by 101 · see citing works

Release of secretory phospholipase A2 from rat neuronal cells and its possible function in the regulation of catecholamine secretion

Matsuzawa, A., Murakami, M., Atsumi, G.-I., Kazuhiro, I. M. A. I., Prados, P., Inoue, K., & Kudo, I. (1996) · Biochemical Journal · doi:10.1042/bj3180701 · Cited by 99 · see citing works

Synergy by Secretory Phospholipase A2 and Glutamate on Inducing Cell Death and Sustained Arachidonic Acid Metabolic Changes in Primary Cortical Neuronal Cultures

Kolko, M., DeCoster, M. A., Turco, E., & Bazan, N. G. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.51.32722 · Cited by 97 · see citing works

Platelet‐activating factor and polyunsaturated fatty acids in cerebral ischemia or convulsions: Intracellular PAF‐binding sites and activation of a fos/jun/AP‐1 transcriptional signaling system

Bazan, N. G., Squinto, S. P., Braquet, P. G., Panetta, T. F., & Marcheselli, V. L. (1991) · Lipids · doi:10.1007/bf02536539 · Cited by 96 · see citing works

Dietary deficiency of N-3 fatty acids alters rhodopsin content and function in the rat retina.

Bush, R. A., Malnoë, A., Remé, C. E., & Williams, T. P. (1994) · PubMed · Cited by 90 · see citing works

Retinal pigment epithelial cells play a central role in the conservation of docosahexaenoic acid by photoreceptor cells after shedding and phagocytosis

Gordon, W. C., de Turco, E. B. R., & Bazan, N. G. (1992) · Current Eye Research · doi:10.3109/02713689209069169 · Cited by 89 · see citing works

Molecular cloning and characterization of the platelet-activating factor receptor gene expressed in the human heart

Sugimoto, T., Tsuchimochi, H., McGregor, C. G. A., Mutoh, H., Shimizu, T., & Kurachi, Y. (1992) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(92)92245-s · Cited by 89 · see citing works

Neuroprotective effects of prostaglandin E2 or cAMP against microglial and neuronal free radical mediated toxicity associated with inflammation

Kim, E. J., Kwon, K. J., Park, J., Lee, S., Moon, C., & Baik, E. J. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10373 · Cited by 89 · see citing works

Synthesis of docosahexaenoic acid by retina and retinal pigment epithelium

Wang, N., & Anderson, R. E. (1993) · Biochemistry · doi:10.1021/bi00212a040 · Cited by 86 · see citing works

Recovery of Postischemic Brain Metabolism and Function Following Treatment with a Free Radical Scavenger and Platelet‐Activating Factor Antagonists

Gilboe, D. D., Kintner, D. B., Fitzpatric, J. H., Emoto, S. E., Esanu, A., Braquet, P. G., & Bazan, N. G. (1991) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1991.tb02597.x · Cited by 82 · see citing works

Effect of Bicuculline‐Induced Status Epilepticus on Prostaglandins and Hydroxyeicosatetraenoic Acids in Rat Brain Subcellular Fractions

Birkle, D. L., & Bazan, N. G. (1987) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1987.tb05735.x · Cited by 81 · see citing works

Platelet‐activating factor antagonists reduce excitotoxic damage in cultured neurons from embryonic chick telencephalon and protect the rat hippocampus and neocortex from ischemic injury in vivo

Prehn, J. H. M., & Krieglstein, J. (1993) · Journal of Neuroscience Research · doi:10.1002/jnr.490340205 · Cited by 80 · see citing works

Brain lipid metabolism in the cPLA2 knockout mouse

Rosenberger, T. A., Villacreses, N. E., Contreras, M. A., Bonventre, J. V., & Rapoport, S. I. (2003) · Journal of Lipid Research · doi:10.1194/jlr.m200298-jlr200 · Cited by 80 · see citing works

Lipocalin-Type Prostaglandin D Synthase (β-Trace) Is Located in Pigment Epithelial Cells of Rat Retina and Accumulates within Interphotoreceptor Matrix

Beuckmann, C. T., Gordon, W. C., Kanaoka, Y., Eguchi, N., Marcheselli, V. L., Gerashchenko, D. Y., Urade, Y., Hayaishi, O., & Bazan, N. G. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-19-06119.1996 · Cited by 80 · see citing works

Essential Fatty Acids and Eicosanoids: Invited Papers from the Third International Congress

Eicosanoids, Sinclair, A. H., & Gibson, R. B. (1993) · Medical Entomology and Zoology · Cited by 75 · see citing works

Bioactive lipids in excitatory neurotransmission and neuronal plasticity

Bazan, N. G., Packard, M. G., Teather, L. A., & Allan, G. (1997) · Neurochemistry International · doi:10.1016/s0197-0186(96)00020-4 · Cited by 75 · see citing works

Plasma docosahexaenoic acid levels in various genetic forms of retinitis pigmentosa.

Gong, J., ROSNER, B. A., Rees, D., Berson, E. L., Weigel-DiFranco, C., & Schaefer, E. J. (1992) · PubMed · Cited by 74 · see citing works

Oxidant-mediated AA release from astrocytes involves cPLA(2) and iPLA(2).

Xu, J.-F., Yu, S., Sun, A. Y., & Sun, G. Y. (2003) · Free Radical Biology & Medicine · doi:10.1016/s0891-5849(03)00152-7 · Cited by 74 · see citing works

A signal terminator

Bazan, N. G. (1995) · Nature · doi:10.1038/374501a0 · Cited by 72 · see citing works

Fatty acids and lipids: biological aspects.

Galli, C., Simopoulos, A. P., & Tremoli, E. (1994) · Cited by 70 · see citing works

Rapid kindling with recurrent hippocampal seizures

Lothman, E. W., & Williamson, J. M. (1993) · Epilepsy Research · doi:10.1016/0920-1211(93)90045-9 · Cited by 69 · see citing works

Differential expression of rat and human type 1 metabotropic glutamate receptor splice variant messenger RNAs

Berthele, A., Laurie, D. J., Platzer, S., Zieglgänsberger, W., Tölle, T. R., & Sommer, B. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00670-2 · Cited by 67 · see citing works

Attenuated LTP in Hippocampal Dentate Gyrus Neurons of Mice Deficient in the PAF Receptor

Chen, C., Magee, J. C., Marcheselli, V., Hardy, M., & Bazan, N. G. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.1.384 · Cited by 67 · see citing works

Platelet activating factor receptor blockade enhances recovery after multifocal brain ischemia

Kochanek, P. M., Dutka, A. J., Kumaroo, K. K., & Hallenbeck, J. M. (1987) · Life Sciences · doi:10.1016/0024-3205(87)90278-5 · Cited by 65 · see citing works

Diacylglycerol Kinase ε, but Not ζ, Selectively Removes Polyunsaturated Diacylglycerol, Inducing Altered Protein Kinase C Distribution in Vivo

Pettitt, T. R., & Wakelam, M. J. O. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.51.36181 · Cited by 62 · see citing works

Effects of Intrastriatal Injections of Platelet-Activating Factor and the PAF Antagonist BN 52021 on Memory

Packard, M. G., Teather, L. A., & Bazan, N. G. (1996) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1996.0058 · Cited by 59 · see citing works

Abnormal plasma levels of polyunsaturated fatty acid in autosomal dominant retinitis pigmentosa

Anderson, R. E., Maude, M. B., Lewis, R. A., Newsome, D. A., & Fishman, G. A. (1987) · Experimental Eye Research · doi:10.1016/s0014-4835(87)80034-9 · Cited by 59 · see citing works

Transport of n-3 fatty acids from the intestine to the retina in rats.

Li, J., Wetzel, M., & O'Brien, P. (1992) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)41619-0 · Cited by 59 · see citing works

Both arachidonic acid and 1-oleoyl-2-acetyl glycerol in low magensium solution induce long-term potentiation in hippocampal CA1 neurons in vitro

Katō, K., Uruno, K., Saito, K., & Kato, H. (1991) · Brain Research · doi:10.1016/0006-8993(91)91519-7 · Cited by 58 · see citing works

Effect of K+ depolarization on the synthesis of prostaglandins and hydroxyeicosatetra(5,8,11,14)enoic acids (HETE) in the rat retina

Birkle, D. L., & Bazan, N. G. (1984) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/0005-2760(84)90187-5 · Cited by 57 · see citing works

G protein regulation of phospholipase A2

Burch, R. M. (1989) · Molecular Neurobiology · doi:10.1007/bf02935629 · Cited by 57 · see citing works

Antagonists of the Platelet‐activating Factor Receptor Block Long‐term Potentiation in Hippocampal Slices

Arai, A., & LYNCH, G. S. (1992) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1992.tb00890.x · Cited by 55 · see citing works

Dominant Expression of Rat Prostanoid DP Receptor mRNA in Leptomeninges, Inner Segments of Photoreceptor Cells, Iris Epithelium, and Ciliary Processes

Gerashchenko, D., Beuckmann, C. T., Kanaoka, Y., Eguchi, N., Gordon, W. C., Urade, Y., Bazan, N. G., & Hayaishi, O. (1998) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1998.71030937.x · Cited by 53 · see citing works

Plasma lipid abnormalities in retinitis pigmentosa and related conditions.

Converse, C. A., Hammer, H. M., Packard, C. J., & Shepherd, J. (1983) · PubMed · Cited by 53 · see citing works

Secreted phospholipase A2 potentiates glutamate‐induced calcium increase and cell death in primary neuronal cultures

DeCoster, M. A., Lambeau, G. J., Lazdunski, M., & Bazan, N. G. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10131 · Cited by 51 · see citing works

Diets enriched in docosahexaenoic acid fail to correct progressive rod-cone degeneration (prcd) phenotype.

Aguirre, G. K., Acland, G. M., Maude, M. B., & Anderson, R. E. (1997) · PubMed · Cited by 49 · see citing works

Imaging brain phospholipase A2 activation in awake rats in response to the 5-HT2A/2C agonist (±)2,5-dimethoxy-4-iodophenyl-2-aminopropane (DOI)

Qu, Y., Chang, L., Klaff, J., Balbo, A., & Rapoport, S. I. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300022 · Cited by 46 · see citing works

α-Methyl-p-tyrosine inhibits the production of free arachidonic acid and diacylglycerols in brain after a single electroconvulsive shock

de Caldironi, M. I. A., & Bazan, N. G. (1979) · Neurochemical Research · doi:10.1007/bf00964145 · Cited by 44 · see citing works

Visualization of [3H]docosahexaenoic acid trafficking through photoreceptors and retinal pigment epithelium by electron microscopic autoradiography.

Gordon, W. C., & Bazan, N. G. (1993) · PubMed · Cited by 43 · see citing works

Chronic lithium administration potentiates brain arachidonic acid signaling at rest and during cholinergic activation in awake rats

Basselin, M., Chang, L., Seemann, R., Bell, J. M., & Rapoport, S. I. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01811.x · Cited by 42 · see citing works

Lipid signals in pain control

Bazan, N. G., & Flower, R. (2002) · Nature · doi:10.1038/420135a · Cited by 42 · see citing works

What is a glial cell?

Barres, B. A. (2003) · Glia · doi:10.1002/glia.10252 · Cited by 39 · see citing works

Neuronal damage by secretory phospholipase A2: modulation by cytosolic phospholipase A2, platelet-activating factor, and cyclooxygenase-2 in neuronal cells in culture

Kolko, M., Turco, E., Diemer, N. H., & Bazan, N. G. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(02)01385-x · Cited by 38 · see citing works

Transport of 22:6n-3 in the Plasma and Uptake into Retinal Pigment Epithelium and Retina

Wang, N., & Anderson, R. E. (1993) · Experimental Eye Research · doi:10.1006/exer.1993.1118 · Cited by 38 · see citing works

Potassium-evoked Glutamate Release Liberates Arachidonic Acid from Cortical Neurons

Taylor, A. L., & Hewett, S. J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m205872200 · Cited by 38 · see citing works

Secretory phospholipase A2 potentiates glutamate-induced rat striatal neuronal cell death in vivo

Kolko, M., Bruhn, T., Christensen, T., Lazdunski, M., Lambeau, G. J., Bazan, N. G., & Diemer, N. H. (1999) · Neuroscience Letters · doi:10.1016/s0304-3940(99)00709-0 · Cited by 37 · see citing works

Localization of lipocalin-type prostaglandin D synthase (beta-trace) in iris, ciliary body, and eye fluids.

Gerashchenko, D. Y., Beuckmann, C. T., Marcheselli, V. L., Gordon, W. C., Kanaoka, Y., Eguchi, N., Urade, Y., Hayaishi, O., & Bazan, N. G. (1998) · PubMed · Cited by 37 · see citing works

Platelet‐activating factor receptor is not required for long‐term potentiation in the hippocampal CA1 region

Kobayashi, K., Ishii, S., Kume, K., Takahashi, T., Shimizu, T., & Manabe, T. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00538.x · Cited by 32 · see citing works

Developmental maturation of hepatic n-3 polyunsaturated fatty acid metabolism: Supply of docosahexaenoic acid to retina and brain

Martin, R. E., Turco, E., & Bazan, N. G. (1994) · The Journal of Nutritional Biochemistry · doi:10.1016/0955-2863(94)90087-6 · Cited by 32 · see citing works

Platelet activating factor receptor (PAF-R) is found in a large endosomal compartment in human umbilical vein endothelial cells

Ihida, K., Predescu, D. N., Czekay, R., & Palade, G. E. (1999) · Journal of Cell Science · doi:10.1242/jcs.112.3.285 · Cited by 32 · see citing works

Docosahexaenoic Acid Supply to the Retina and Its Conservation in Photoreceptor Cells by Active Retinal Pigment Epithelium-Mediated Recycling

Bazan, N. G., Turco, E., & Gordon, W. C. (2015) · World review of nutrition and dietetics · doi:10.1159/000423564 · Cited by 31 · see citing works

Effects of Posttraining Intrahippocampal Injections of Platelet-Activating Factor and PAF Antagonists on Memory

Teather, L. A., Packard, M. G., & Bazan, N. G. (1998) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1998.3862 · Cited by 30 · see citing works

Platelet-activating factor activates HIV promoter in transfected SH-SY5Y neuroblastoma cells and MOLT-4 T lymphocytes

Squinto, S. P., Braquet, P. G., Block, A. L., & Bazan, N. G. (1990) · Journal of Molecular Neuroscience · doi:10.1007/bf02876914 · Cited by 26 · see citing works

GLIA: A reassessment based on novel data on the developing and mature central nervous system

Villegas, S. N., Poletta, F. A., & Carri, N. G. (2003) · Cell Biology International · doi:10.1016/s1065-6995(03)00119-7 · Cited by 25 · see citing works

A hypothesis to explain the reduced blood levels of docosahexaenoic acid in inherited retinal degenerations caused by mutations in genes encoding retina‐specific proteins

Anderson, R. E., Maude, M. B., Alvarez, R., Acland, G. M., & Aguirre, G. K. (1999) · Lipids · doi:10.1007/bf02562304 · Cited by 25 · see citing works

Platelet-activating factor production occurs through stimulation of cholinergic and dopaminergic receptors in the chick retina.

Bussolino, F., Torelli, S., Stefanini, E., & Gremo, F. (1989) · PubMed · Cited by 23 · see citing works

Effect of antagonists of platelet-activating factor receptors on memory of inhibitory avoidance in rats

Jerusalinsky, D. A., Fin, C. A., Quillfeldt, J. A., Ferreira, M. B. C., Schmitz, P. K., da Silva, R. C., Walz, R., Bazan, N. G., Medina, J. H., & Izquierdo, I. (1994) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(05)80052-4 · Cited by 23 · see citing works

Polyunsaturated fatty acids are lower in blood lipids of Usher's type I but not Usher's type II.

Maude, M. B., Anderson, E., & Anderson, R. E. (1998) · PubMed · Cited by 22 · see citing works

ω3 Fatty Acid Status in Patients with Retinitis pigmentosa

Hoffman, D. R., & Birch, D. G. (1998) · KARGER eBooks · doi:10.1159/000059653 · Cited by 22 · see citing works

Differential Interaction of Platelet-Activating Factor and NMDA Receptor Function in Hippocampal and Dorsal Striatal Memory Processes

Teather, L. A., Packard, M. G., & Bazan, N. G. (2001) · Neurobiology of Learning and Memory · doi:10.1006/nlme.2000.3974 · Cited by 20 · see citing works

Involvement of lipid mediators on cytokine signaling and induction of secretory phospholipase A2 in immortalized astrocytes (DITNC)

Tong, W., Shah, D., Xu, J., Diehl, J. A., Hans, A., Hannink, M., & Sun, G. Y. (1999) · Journal of Molecular Neuroscience · doi:10.1007/bf02736923 · Cited by 19 · see citing works

Platelet-activating factor inhibits ionotropic GABA receptor activity in cultured hippocampal neurons

Chen, C., & Bazan, N. G. (1999) · Neuroreport · doi:10.1097/00001756-199912160-00020 · Cited by 16 · see citing works

Strong Association of Unesterified [3H]Docosahexaenoic Acid and [3H-Docosahexaenoyl]Phosphatidate to Rhodopsin During In Vivo Labeling of Frog Retinal Rod Outer Segments

de Turco, E. B. R., Jackson, F. R., Parkins, N., & Gordon, W. C. (2000) · Neurochemical Research · doi:10.1023/a:1007571305987 · Cited by 15 · see citing works

Synthesis and release of docosahexaenoic acid by the RPE cells of prcd-affected dogs.

Chen, H., Ray, J., Scarpino, V., Acland, G. M., Aguirre, G. K., & Anderson, R. E. (1999) · PubMed · Cited by 15 · see citing works

A role for docosahexaenoic acid-derived neuroprotectin D1 in neural cell survival and Alzheimer disease

Lukiw, W. J. (2005) · Journal of Clinical Investigation · doi:10.1172/jci25420 · Cited by 873 · see citing works

Cyclooxygenase-2 (COX-2) in Inflammatory and Degenerative Brain Diseases

Minghetti, L. (2004) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/63.9.901 · Cited by 780 · see citing works

Docosahexaenoic acid protects from dendritic pathology in an Alzheimer's disease mouse model

Calon, F., Lim, G. P., Yang, F., Morihara, T., Teter, B., Ubeda, O., Rostaing, P., Triller, A., Salem, N., Ashe, K. H., et al. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.013 · Cited by 707 · see citing works

Dietary omega 3 fatty acids and the developing brain

Innis, S. M. (2008) · Brain Research · doi:10.1016/j.brainres.2008.08.078 · Cited by 671 · see citing works

Docosahexaenoic acid signalolipidomics in nutrition: significance in aging, neuroinflammation, macular degeneration, Alzheimer’s, and other neurodegenerative diseases

Bazan, N. G., Molina, M. F., & Gordon, W. C. (2011) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.012809.104635 · Cited by 441 · see citing works

Neuroprotectin D1 (NPD1): A DHA-Derived Mediator that Protects Brain and Retina Against Cell Injury-Induced Oxidative Stress

Bazan, N. G. (2006) · Brain Pathology · doi:10.1111/j.1750-3639.2005.tb00513.x · Cited by 367 · see citing works

Cell survival matters: docosahexaenoic acid signaling, neuroprotection and photoreceptors

Bazan, N. G. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.03.005 · Cited by 353 · see citing works

Resolvin D Series and Protectin D1 Mitigate Acute Kidney Injury

Duffield, J. S., Hong, S., Vaidya, V. S., Lu, Y., Fredman, G., Serhan, C. N., & Bonventre, J. V. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.9.5902 · Cited by 335 · see citing works

Effects of dietary omega-3 polyunsaturated fatty acids on brain gene expression

Kitajka, K., Sinclair, A. J., Weisinger, R. S., Weisinger, H. S., Mathai, M. L., Jayasooriya, A. P., Halver, J. E., & Puskás, L. G. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402342101 · Cited by 313 · see citing works

DHA- and EPA-derived resolvins, protectins, and maresins in airway inflammation

Duvall, M. G., & Levy, B. D. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.11.001 · Cited by 287 · see citing works

Polyunsaturated fatty acids in the central nervous system: evolution of concepts and nutritional implications throughout life

Alessandri, J., Guesnet, P., Vancassel, S., Astorg, P., Denis, I., Goustard, B., Aïd, S., Poumès‐Ballihaut, C., Champeil‐Potokar, G., & Lavialle, M. (2004) · annales de biologie animale biochimie biophysique · doi:10.1051/rnd:2004063 · Cited by 283 · see citing works

DOCOSAHEXAENOIC ACID, FATTY ACID–INTERACTING PROTEINS, AND NEURONAL FUNCTION: Breastmilk and Fish Are Good for You

Marszalek, J. R., & Lodish, H. F. (2005) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.21.122303.120624 · Cited by 270 · see citing works

Neuroprotectin D1-mediated anti-inflammatory and survival signaling in stroke, retinal degenerations, and Alzheimer's disease

Bazan, N. G. (2009) · Journal of Lipid Research · doi:10.1194/jlr.r800068-jlr200 · Cited by 256 · see citing works

Docosahexaenoic Acid and the Aging Brain

Lukiw, W. J., & Bazan, N. G. (2008) · Journal of Nutrition · doi:10.3945/jn.108.096016 · Cited by 247 · see citing works

Lipid Signaling in Neural Plasticity, Brain Repair, and Neuroprotection

Bazan, N. G. (2005) · Molecular Neurobiology · doi:10.1385/mn:32:1:089 · Cited by 235 · see citing works

Ceramide and neurodegeneration: Susceptibility of neurons and oligodendrocytes to cell damage and death

Jana, A., Hogan, E. L., & Pahan, K. (2009) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2008.12.010 · Cited by 233 · see citing works

Glycerophospholipids and glycerophospholipid-derived lipid mediators: A complex meshwork in Alzheimer’s disease pathology

Frisardi, V., Panza, F., Seripa, D., Farooqui, T., & Farooqui, A. A. (2011) · Progress in Lipid Research · doi:10.1016/j.plipres.2011.06.001 · Cited by 230 · see citing works

Lipid signaling: Sleep, synaptic plasticity, and neuroprotection

Chen, C., & Bazan, N. G. (2005) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2005.07.001 · Cited by 193 · see citing works

Cyclooxygenase-2 in synaptic signaling

Yang, H., & Chen, C. (2008) · Current Pharmaceutical Design · doi:10.2174/138161208784480144 · Cited by 195 · see citing works

Postsynaptically Synthesized Prostaglandin E2 (PGE2) Modulates Hippocampal Synaptic Transmission via a Presynaptic PGE2 EP2 Receptor

Sang, N., Zhang, J., Marcheselli, V., Bazan, N. G., & Chen, C. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2392-05.2005 · Cited by 191 · see citing works

Cytidine 5?-Diphosphocholine (CDP-Choline) in Stroke and Other CNS Disorders

Rao, A. M., & Hatcher, J. F. (2005) · Neurochemical Research · doi:10.1007/s11064-004-9681-8 · Cited by 193 · see citing works

Lipids and lipidomics in brain injury and diseases

Rao, A. M., Hatcher, J. F., & Dempsey, R. J. (2006) · The AAPS Journal · doi:10.1007/bf02854902 · Cited by 187 · see citing works

Retinal energy demands control vascular supply of the retina in development and disease: The role of neuronal lipid and glucose metabolism

Joyal, J., Gantner, M. L., & Smith, L. E. H. (2017) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2017.11.002 · Cited by 186 · see citing works

Untitled work

Menzies (2007) · doi:10.1093/brain/awm223 · Cited by 177 · see citing works

Robust docosahexaenoic acid-mediated neuroprotection in a rat model of transient, focal cerebral ischemia

Belayev, L., Khoutorova, L., Atkins, K. D., & Bazan, N. G. (2009) · Stroke · doi:10.1161/strokeaha.109.555979 · Cited by 170 · see citing works

Cellular and molecular events mediated by docosahexaenoic acid-derived neuroprotectin D1 signaling in photoreceptor cell survival and brain protection

Bazan, N. G. (2009) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2009.05.024 · Cited by 171 · see citing works

Receptor-independent actions of cannabinoids on cell membranes: Focus on endocannabinoids

Öz, M. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2005.09.009 · Cited by 164 · see citing works

Histone-Methyltransferase MLL2 (KMT2B) Is Required for Memory Formation in Mice

Kerimoglu, C., Agís‐Balboa, R. C., Kranz, A., Stilling, R. M., Bahari‐Javan, S., Benito, E., Halder, R., Burkhardt, S., Stewart, A. F., & Fischer, A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3356-12.2013 · Cited by 155 · see citing works

Lipid changes in the aged brain: Effect on synaptic function and neuronal survival

Ledesma, M. D., Martín, M. G., & Dotti, C. G. (2011) · Progress in Lipid Research · doi:10.1016/j.plipres.2011.11.004 · Cited by 148 · see citing works

Docosanoids and elovanoids from omega-3 fatty acids are pro-homeostatic modulators of inflammatory responses, cell damage and neuroprotection

Bazan, N. G. (2018) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2018.09.003 · Cited by 148 · see citing works

Rescue and repair during photoreceptor cell renewal mediated by docosahexaenoic acid-derived neuroprotectin D1

Bazan, N. G., Calandria, J. M., & Serhan, C. N. (2010) · Journal of Lipid Research · doi:10.1194/jlr.r001131 · Cited by 140 · see citing works

Plasmalogens, platelet-activating factor and beyond – Ether lipids in signaling and neurodegeneration

Dorninger, F., Forss‐Petter, S., Wimmer, I., & Berger, J. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105061 · Cited by 139 · see citing works

Maternal Fatty Acid Metabolism in Pregnancy and Its Consequences in the Feto-Placental Development

Duttaroy, A. K., & Basak, S. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2021.787848 · Cited by 139 · see citing works

Secretory PLA2-IIA: a new inflammatory factor for Alzheimer's disease

Moses, G. S. D., Jensen, M. D., Lue, L., Walker, D. G., Sun, A. Y., Simonyi, Á., & Sun, G. Y. (2006) · Journal of Neuroinflammation · doi:10.1186/1742-2094-3-28 · Cited by 136 · see citing works

Docosahexaenoic Acid Complexed to Albumin Elicits High-Grade Ischemic Neuroprotection

Belayev, L., Marcheselli, V. L., Khoutorova, L., Turco, E., Busto, R., Ginsberg, M. D., & Bazan, N. G. (2004) · Stroke · doi:10.1161/01.str.0000149620.74770.2e · Cited by 132 · see citing works

Brain Response to Injury and Neurodegeneration: Endogenous Neuroprotective Signaling

Bazan, N. G. (2005) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1344.011 · Cited by 130 · see citing works

The neurovascular unit and its growth factors: coordinated response in the vascular and nervous systems

Ward, N. L., & Lamanna, J. C. (2004) · Neurological Research · doi:10.1179/016164104x3798 · Cited by 122 · see citing works

Endogenous signaling by omega-3 docosahexaenoic acid-derived mediators sustains homeostatic synaptic and circuitry integrity

Bazan, N. G., Musto, A. E., & Knott, E. J. (2011) · Molecular Neurobiology · doi:10.1007/s12035-011-8200-6 · Cited by 125 · see citing works

Homeostatic Regulation of Photoreceptor Cell Integrity: Significance of the Potent Mediator Neuroprotectin D1 Biosynthesized from Docosahexaenoic Acid The Proctor Lecture

Bazan, N. G. (2007) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.07-0918 · Cited by 116 · see citing works

(n-3) Polyunsaturated Fatty Acid Deficiency Reduces the Expression of Both Isoforms of the Brain Glucose Transporter GLUT1 in Rats

Pifferi, F., Roux, F. S., Goustard, B., Alessandri, J., Vancassel, S., Jouin, M., Lavialle, M., & Guesnet, P. (2005) · Journal of Nutrition · doi:10.1093/jn/135.9.2241 · Cited by 116 · see citing works

The Neurobiology of Lipid Metabolism in Autism Spectrum Disorders

Tamiji, J., & Crawford, D. A. (2010) · Neurosignals · doi:10.1159/000323189 · Cited by 114 · see citing works

Identification of disease markers in human cerebrospinal fluid using lipidomic and proteomic methods

Fonteh, A. N., Harrington, R. J., Huhmer, A. F., Biringer, R. G., Riggins, J. N., & Harrington, M. G. (2006) · Disease Markers · doi:10.1155/2006/202938 · Cited by 113 · see citing works

Sphingolipids in Multiple Sclerosis

Jana, A., & Pahan, K. (2010) · NeuroMolecular Medicine · doi:10.1007/s12017-010-8128-4 · Cited by 111 · see citing works

Resolvins: Natural agonists for resolution of pulmonary inflammation

Uddin, M., & Levy, B. D. (2010) · Progress in Lipid Research · doi:10.1016/j.plipres.2010.09.002 · Cited by 110 · see citing works

Neurolipidomics: challenges and developments

Han, X. (2006) · Frontiers in bioscience · doi:10.2741/2258 · Cited by 110 · see citing works

Role of COX-2 in Inflammatory and Degenerative Brain Diseases

Minghetti, L. (2007) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/1-4020-5688-5_5 · Cited by 104 · see citing works

An (n-3) Polyunsaturated Fatty Acid–Deficient Diet Disturbs Daily Locomotor Activity, Melatonin Rhythm, and Striatal Dopamine in Syrian Hamsters13

Lavialle, M., Champeil‐Potokar, G., Alessandri, J. M. J. M., Balasse, L., Guesnet, P., Papillon, C., Pévet, P., Vancassel, S., VIVIEN‐ROELS, B., & Denis, I. (2008) · Journal of Nutrition · doi:10.1093/jn/138.9.1719 · Cited by 99 · see citing works

Lipid Signaling and Synaptic Plasticity

Sang, N., & Chen, C. (2006) · The Neuroscientist · doi:10.1177/1073858406290794 · Cited by 96 · see citing works

Prostaglandins are powerful inducers of NGF and BDNF production in mouse astrocyte cultures

Toyomoto, M., Ohta, M., Okumura, K., Yano, H., Matsumoto, K., Inoue, S., Hayashi, K., & Ikeda, K. (2004) · FEBS Letters · doi:10.1016/s0014-5793(04)00246-7 · Cited by 98 · see citing works

Docosahexaenoic Acid Production and Lipid-Body Formation in Schizochytrium limacinum SR21

Morita, E., Kumon, Y., Nakahara, T., Kagiwada, S., & Noguchi, T. (2006) · Marine Biotechnology · doi:10.1007/s10126-005-5060-y · Cited by 97 · see citing works

Prolonged Exposure of Cortical Neurons to Oligomeric Amyloid-β Impairs NMDA Receptor Function Via NADPH Oxidase-Mediated ROS Production: Protective Effect of Green Tea (-)-Epigallocatechin-3-Gallate

He, Y., Cui, J., Lee, J. C., Ding, S., Chalimoniuk, M., Simonyi, Á., Sun, A. Y., Gu, Z., Weisman, G. A., Wood, W. G., et al. (2011) · ASN NEURO · doi:10.1042/an20100025 · Cited by 92 · see citing works

The potential role of sigma-1 receptors in lipid transport and lipid raft reconstitution in the brain: Implication for drug abuse

Hayashi, T., & Su, T. (2005) · Life Sciences · doi:10.1016/j.lfs.2005.05.009 · Cited by 92 · see citing works

Effects of maternal malnutrition and postnatal nutritional rehabilitation on brain fatty acids, learning, and memory

de Souza, A. S., Fernandes, F. S., & do Carmo, M. D. G. T. (2011) · Nutrition Reviews · doi:10.1111/j.1753-4887.2011.00374.x · Cited by 92 · see citing works

Topical Combination of NGF and DHA Increases Rabbit Corneal Nerve Regeneration after Photorefractive Keratectomy

Esquenazi, S., Bazán, H. E. P., Bui, V., He, J., Kim, D. B., & Bazan, N. G. (2005) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.05-0241 · Cited by 91 · see citing works

Docosahexaenoic acid neurolipidomics

Niemoller, T. D., & Bazan, N. G. (2009) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2009.09.005 · Cited by 89 · see citing works

Acyl-CoA Synthetase 2 Overexpression Enhances Fatty Acid Internalization and Neurite Outgrowth

Marszalek, J. R., Kitidis, C., Dararutana, A., & Lodish, H. F. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313460200 · Cited by 89 · see citing works

Exercise contributes to the effects of DHA dietary supplementation by acting on membrane-related synaptic systems

Chytrova, G., Ying, Z., & Gómez‐Pinilla, F. (2009) · Brain Research · doi:10.1016/j.brainres.2009.05.018 · Cited by 89 · see citing works

Dietary manipulation implicates lipid signaling in the regulation of germ cell maintenance in C. elegans

Watts, J. L., & Browse, J. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.01.013 · Cited by 86 · see citing works

The Onset of Brain Injury and Neurodegeneration Triggers the Synthesis of Docosanoid Neuroprotective Signaling

Bazan, N. G. (2006) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-006-9064-6 · Cited by 88 · see citing works

Synaptic and Vascular Associations of Neurons Containing Cyclooxygenase-2 and Nitric Oxide Synthase in Rat Somatosensory Cortex

Wang, H., Hitron, I. M., Iadecola, C., & Pickel, V. M. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhi008 · Cited by 88 · see citing works

Docosahexaenoic Acid Signaling Modulates Cell Survival in Experimental Ischemic Stroke Penumbra and Initiates Long-Term Repair in Young and Aged Rats

Eady, T. N., Belayev, L., Khoutorova, L., Atkins, K. D., Zhang, C., & Bazan, N. G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046151 · Cited by 85 · see citing works

Docosahexaenoic acid (DHA) incorporation into the brain from plasma, as an in vivo biomarker of brain DHA metabolism and neurotransmission

Rapoport, S. I., Ramadan, E., & Basselin, M. (2011) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2011.06.003 · Cited by 84 · see citing works

Acyl-CoA Synthetase Activity Links Wild-Type but Not Mutant α-Synuclein to Brain Arachidonate Metabolism

Golovko, M. Y., Rosenberger, T. A., Færgeman, N. J., Feddersen, S., Cole, N. B., Pribill, I., Berger, J., Nussbaum, R. L., & Murphy, E. J. (2006) · Biochemistry · doi:10.1021/bi0600289 · Cited by 85 · see citing works

Neuroprotective effect of nimesulide, a preferential COX-2 inhibitor, against pentylenetetrazol (PTZ)-induced chemical kindling and associated biochemical parameters in mice

Dhir, A., Naidu, P. S., & Kulkarni, S. K. (2007) · Seizure · doi:10.1016/j.seizure.2007.05.016 · Cited by 85 · see citing works

High‐fat diet ameliorates neurological deficits caused by defective astrocyte lipid metabolism

Camargo, N., Brouwers, J. F. H. M., Loos, M., Gutmann, D. H., Smit, A. B., & Verheijen, M. H. G. (2012) · The FASEB Journal · doi:10.1096/fj.12-205807 · Cited by 84 · see citing works

Docosahexaenoic acid: brain accretion and roles in neuroprotection after brain hypoxia and ischemia

Mayurasakorn, K., Williams, J. J., Ten, V. S., & Deckelbaum, R. J. (2010) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e328342cba5 · Cited by 83 · see citing works

Identification of protein biomarkers for schizophrenia and bipolar disorder in the postmortem prefrontal cortex using SELDI-TOF-MS ProteinChip profiling combined with MALDI-TOF-PSD-MS analysis

Novikova, S. I., He, F., Cutrufello, N. J., & Lidow, M. S. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.02.002 · Cited by 82 · see citing works

Catalytic Nanoceria Are Preferentially Retained in the Rat Retina and Are Not Cytotoxic after Intravitreal Injection

Wong, L., Hirst, S. M., Pye, Q. N., Reilly, C. M., Seal, S., & McGinnis, J. F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058431 · Cited by 82 · see citing works

Effect of cyclooxygenase inhibitors on pentylenetetrazol (PTZ)-induced convulsions: Possible mechanism of action

Dhir, A., Naidu, P. S., & Kulkarni, S. K. (2006) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2006.06.003 · Cited by 81 · see citing works

Linoleic and α-linolenic acid as precursor and inhibitor for the synthesis of long-chain polyunsaturated fatty acids in liver and brain of growing pigs

Smink, W., Gerrits, W. J. J., Gloaguen, M., Ruiter, A., & van Baal, J. (2012) · animal · doi:10.1017/s1751731111001479 · Cited by 80 · see citing works

Brain Response to Injury and Neurodegeneration

Bazan, N. G., Marcheselli, V. L., & Cole-Edwards, K. K. (2005) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2005.tb00018.x · Cited by 80 · see citing works

The role of α-synuclein in brain lipid metabolism: a downstream impact on brain inflammatory response

Golovko, M. Y., Barceló‐Coblijn, G., Castagnet, P. I., Austin, S. A., Combs, C. K., & Murphy, E. J. (2008) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-008-0008-y · Cited by 79 · see citing works

Synaptic and Extrasynaptic NMDA Receptors Differentially Modulate Neuronal Cyclooxygenase-2 Function, Lipid Peroxidation, and Neuroprotection

Stark, D. T., & Bazan, N. G. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3544-11.2011 · Cited by 76 · see citing works

Inhibition of astroglial glutamate transport by polyunsaturated fatty acids: Evidence for a signalling role of docosahexaenoic acid

Grintal, B., Champeil‐Potokar, G., Lavialle, M., Vancassel, S., Breton, S., & Denis, I. (2009) · Neurochemistry International · doi:10.1016/j.neuint.2009.02.018 · Cited by 74 · see citing works

Altered hippocampal long‐term synaptic plasticity in mice deficient in the PGE2 EP2 receptor

Yang, H., Zhang, J., BREYER, R. M., & Chen, C. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05766.x · Cited by 70 · see citing works

Docosahexaenoic acid (22:6n‐3) enrichment of membrane phospholipids increases gap junction coupling capacity in cultured astrocytes

Champeil‐Potokar, G., Chaumontet, C., Guesnet, P., Lavialle, M., & Denis, I. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05185.x · Cited by 72 · see citing works

The omega-3 fatty acid-derived neuroprotectin D1 limits hippocampal hyperexcitability and seizure susceptibility in kindling epileptogenesis: NPD1 Limits Kindling Epileptogenesis

Musto, A. E., Gjorstrup, P., & Bazan, N. G. (2011) · Epilepsia · doi:10.1111/j.1528-1167.2011.03081.x · Cited by 71 · see citing works

Oxidized phospholipid: POVPC binds to platelet-activating-factor receptor on human macrophages

Pégorier, S., Stengel, D., Durand, H., Croset, M., & Ninio, E. (2005) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2005.11.015 · Cited by 71 · see citing works

Chemical Determinants Involved in Anandamide-induced Inhibition of T-type Calcium Channels

Chemin, J., Nargeot, J., & Lory, P. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m610033200 · Cited by 70 · see citing works

Oxidative stress‐induced death in the nervous system: Cell cycle dependent or independent?

Langley, B. C., & Ratan, R. R. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20210 · Cited by 68 · see citing works

SREBPs: SREBP function in glia–neuron interactions

Camargo, N., Smit, A. B., & Verheijen, M. H. G. (2008) · FEBS Journal · doi:10.1111/j.1742-4658.2008.06808.x · Cited by 69 · see citing works

Endocannabinoid Signaling Dynamics Probed with Optical Tools

Heinbockel, T., Brager, D. H., Reich, C. G., Zhao, J., Muralidharan, S., Alger, B. E., & Kao, J. P. Y. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2078-05.2005 · Cited by 69 · see citing works

Cellular and molecular events in corneal wound healing: significance of lipid signalling

Bazán, H. E. P. (2005) · Experimental Eye Research · doi:10.1016/j.exer.2004.12.023 · Cited by 68 · see citing works

Docosahexaenoic acid confers enduring neuroprotection in experimental stroke

Hong, S., Belayev, L., Khoutorova, L., Obenaus, A., & Bazan, N. G. (2014) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2013.12.033 · Cited by 66 · see citing works

Docosahexaenoic acid and arachidonic acid are fundamental supplements for the induction of neuronal differentiation

Kan, I., Melamed, E., Offen, D., & Green, P. (2006) · Journal of Lipid Research · doi:10.1194/jlr.c600022-jlr200 · Cited by 64 · see citing works

Abundance of triacylglycerols in ganglia and their depletion in diabetic mice: implications for the role of altered triacylglycerols in diabetic neuropathy

Cheng, H., Guan, S., & Han, X. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03794.x · Cited by 62 · see citing works

Dietary Docosahexaenoic Acid [22: 6(n-3)] as a Phospholipid or a Triglyceride Enhances the Potassium Chloride–Evoked Release of Acetylcholine in Rat Hippocampus

Aïd, S., Vancassel, S., Linard, A., Lavialle, M., & Guesnet, P. (2005) · Journal of Nutrition · doi:10.1093/jn/135.5.1008 · Cited by 62 · see citing works

Estrogen Interactions With Lipid Rafts Related to Neuroprotection. Impact of Brain Ageing and Menopause

Marín, R., & Díaz, M. L. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00128 · Cited by 58 · see citing works

Effect of acute administration of Pistacia lentiscus L. essential oil on rat cerebral cortex following transient bilateral common carotid artery occlusion

Quartu, M., Serra, M. P., Boi, M., Pillolla, G., Melis, T., Poddighe, L., Fiacco, M. D., Falconieri, D., Carta, G., Murru, E., et al. (2012) · Lipids in Health and Disease · doi:10.1186/1476-511x-11-8 · Cited by 57 · see citing works

PUFA and their derivatives in neurotransmission and synapses: a new hallmark of synaptopathies

Miceli, M. D., Bosch‐Bouju, C., & Layé, S. (2020) · Proceedings of The Nutrition Society · doi:10.1017/s0029665120000129 · Cited by 56 · see citing works

Resolution of Inflammation in Asthma

Levy, B. D., Vachier, I., & Serhan, C. N. (2012) · Clinics in Chest Medicine · doi:10.1016/j.ccm.2012.06.006 · Cited by 56 · see citing works

Platelet-activating factor (PAF) mediates NLRP3-NEK7 inflammasome induction independently of PAFR

Deng, M., Guo, H., Tam, J. W., Johnson, B. M., Brickey, W. J., New, J. S., Lenox, A. R., Shi, H., Golenbock, D. T., Koller, B. H., et al. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20190111 · Cited by 56 · see citing works

Long-term treatment with fish oil prevents memory impairments but not hippocampal damage in rats subjected to transient, global cerebral ischemia

Fernandes, J. S., Mori, M., Ekuni, R., de Oliveira, R. M. W., & Milani, H. (2008) · Nutrition Research · doi:10.1016/j.nutres.2008.09.004 · Cited by 53 · see citing works

Tranylcypromine

Frieling, H., & Bleich, S. (2006) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-006-0660-8 · Cited by 52 · see citing works

Lipids and Lipidomics in Brain Injury and Diseases

Adibhatla, R. M., Hatcher, J. F., & Dempsey, R. J. (2006) · The AAPS Journal · doi:10.1208/aapsj080236 · Cited by 52 · see citing works

Lipid Signaling in Experimental Epilepsy

Cole-Edwards, K. K., & Bazan, N. G. (2005) · Neurochemical Research · doi:10.1007/s11064-005-6878-4 · Cited by 50 · see citing works

Brain Protection in Schizophrenia, Mood and Cognitive Disorders

Ritsner, M. S. (2010) · Springer eBooks · doi:10.1007/978-90-481-8553-5 · Cited by 52 · see citing works

Eicosanomics: targeted lipidomics of eicosanoids in biological systems

Balazy, M. (2004) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2004.03.003 · Cited by 51 · see citing works

Nutritional aspects modulating brain development and the responses to stress in early neonatal life

Walker, C. (2005) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2005.08.010 · Cited by 47 · see citing works

Neuroprotectin D1 Induces Neuronal Survival and Downregulation of Amyloidogenic Processing in Alzheimer’s Disease Cellular Models

Stark, D. T., & Bazan, N. G. (2011) · Molecular Neurobiology · doi:10.1007/s12035-011-8174-4 · Cited by 49 · see citing works

Synaptic Signaling by Lipids in the Life and Death of Neurons

Bazan, N. G. (2005) · Molecular Neurobiology · doi:10.1385/mn:31:1-3:219 · Cited by 45 · see citing works

Lipid Signaling and Synaptic Plasticity

Sang, N., & Chen, C. (2006) · The Neuroscientist · doi:10.1177/1073858406290794 · Cited by 96 · see citing works

Lipid Signaling in Neural Plasticity, Brain Repair, and Neuroprotection

Bazan, N. G. (2005) · Molecular Neurobiology · doi:10.1385/mn:32:1:089 · Cited by 235 · see citing works

The Onset of Brain Injury and Neurodegeneration Triggers the Synthesis of Docosanoid Neuroprotective Signaling

Bazan, N. G. (2006) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-006-9064-6 · Cited by 88 · see citing works

Brain Response to Injury and Neurodegeneration: Endogenous Neuroprotective Signaling

Bazan, N. G. (2005) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1344.011 · Cited by 130 · see citing works