Oligodendrocytes and Ischemic Brain Injury
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[1] P. Lopresti,et al. Functional implications for the microtubule-associated protein tau: Localization in oligodendrocytes , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[2] S. Scherer,et al. Expression and regulation of kainate and AMPA receptors in uncommitted and committed neural progenitors , 1995, Neurochemical Research.
[3] J. Goldman. Lineage, migration, and fate determination of postnatal subventricular zone cells in the mammalian CNS , 2005, Journal of Neuro-Oncology.
[4] J. Ávila,et al. Tau Dephosphorylation at Tau-1 Site Correlates with its Association to Cell Membrane , 2004, Neurochemical Research.
[5] Pietro Mazzoni,et al. The Behavioral Neurology of White Matter , 2003 .
[6] J. Mcculloch,et al. Grey Matter and White Matter Ischemic Damage is Reduced by the Competitive AMPA Receptor Antagonist, SPD 502 , 2002, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[7] T. Wood,et al. Insulin-like Growth Factor I, but Not Neurotrophin-3, Sustains Akt Activation and Provides Long-Term Protection of Immature Oligodendrocytes from Glutamate-Mediated Apoptosis , 2002, Molecular and Cellular Neuroscience.
[8] G. Almazan,et al. AMPA receptor‐mediated toxicity in oligodendrocyte progenitors involves free radical generation and activation of JNK, calpain and caspase 3 , 2002, Journal of neurochemistry.
[9] M. Shibata,et al. Temporal Profiles of the Subcellular Localization of Bim, a BH3-Only Protein, during Middle Cerebral Artery Occlusion in Mice , 2002, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[10] H. Kinney,et al. Arrested Oligodendrocyte Lineage Progression During Human Cerebral White Matter Development: Dissociation Between the Timing of Progenitor Differentiation and Myelinogenesis , 2002, Journal of neuropathology and experimental neurology.
[11] M. Goldberg,et al. Cerebrovascular Disease: Cellular mechanisms of white matter ischemia: what can we learn from culture models? , 2002 .
[12] J. Volpe,et al. Neurobiology of Periventricular Leukomalacia in the Premature Infant , 2001, Pediatric Research.
[13] S. Levison,et al. Perinatal Hypoxia-Ischemia Induces Apoptotic and Excitotoxic Death of Periventricular White Matter Oligodendrocyte Progenitors , 2001, Developmental Neuroscience.
[14] Kortaro Tanaka,et al. Phosphorylation of Cyclic Adenosine Monophosphate Response Element Binding Protein in Oligodendrocytes in the Corpus Callosum after Focal Cerebral Ischemia in the Rat , 2001, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[15] M. Fini,et al. Effects of Matrix Metalloproteinase-9 Gene Knock-Out on the Proteolysis of Blood–Brain Barrier and White Matter Components after Cerebral Ischemia , 2001, The Journal of Neuroscience.
[16] G. Konat,et al. Hydrogen peroxide induces transient dephosphorylation of tau protein in cultured rat oligodendrocytes , 2001, Neuroscience Letters.
[17] D. Graham,et al. Ebselen Protects Both Gray and White Matter in a Rodent Model of Focal Cerebral Ischemia , 2001, Stroke.
[18] Irving Ea,et al. Assessment of white matter injury following prolonged focal cerebral ischaemia in the rat. , 2001 .
[19] T N Behar,et al. Analysis of fractal dimension of O2A glial cells differentiating in vitro. , 2001, Methods.
[20] E. E. Kelland,et al. Group I metabotropic glutamate receptors limit AMPA receptor-mediated oligodendrocyte progenitor cell death. , 2001, European journal of pharmacology.
[21] Kortaro Tanaka,et al. Activation of NG2-positive oligodendrocyte progenitor cells during post-ischemic reperfusion in the rat brain , 2001, Neuroreport.
[22] M. Goldberg,et al. AMPA/Kainate Receptor Activation Mediates Hypoxic Oligodendrocyte Death and Axonal Injury in Cerebral White Matter , 2001, The Journal of Neuroscience.
[23] E. Lehrmann,et al. Focal cerebral ischemia induces increased myelin basic protein and growth-associated protein-43 gene transcription in peri-infarct areas in the rat brain , 2001, Experimental Brain Research.
[24] F. Sharp,et al. Microglia/Macrophages Proliferate in Striatum and Neocortex but Not in Hippocampus after Brief Global Ischemia That Produces Ischemic Tolerance in Gerbil Brain , 2001, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[25] N. Baumann,et al. Biology of oligodendrocyte and myelin in the mammalian central nervous system. , 2001, Physiological reviews.
[26] A. Pérez-Samartín,et al. The link between excitotoxic oligodendroglial death and demyelinating diseases , 2001, Trends in Neurosciences.
[27] H. Kinney,et al. Late Oligodendrocyte Progenitors Coincide with the Developmental Window of Vulnerability for Human Perinatal White Matter Injury , 2001, The Journal of Neuroscience.
[28] Richard Reynolds,et al. The oligodendrocyte precursor cell in health and disease , 2001, Trends in Neurosciences.
[29] Pamela L. Follett,et al. NBQX Attenuates Excitotoxic Injury in Developing White Matter , 2000, The Journal of Neuroscience.
[30] G. Feng,et al. Imaging Neuronal Subsets in Transgenic Mice Expressing Multiple Spectral Variants of GFP , 2000, Neuron.
[31] H. Okano,et al. Caspases determine the vulnerability of oligodendrocytes in the ischemic brain. , 2000, The Journal of clinical investigation.
[32] P. Stys,et al. Important role of reverse Na(+)-Ca(2+) exchange in spinal cord white matter injury at physiological temperature. , 2000, Journal of neurophysiology.
[33] T. Sundt,et al. White matter injury in spinal cord ischemia: protection by AMPA/kainate glutamate receptor antagonism. , 2000, Stroke.
[34] M. Goldberg,et al. Oxygen-glucose deprivation induces inducible nitric oxide synthase and nitrotyrosine expression in cerebral endothelial cells. , 2000, Stroke.
[35] M. Hori,et al. Contribution of microglia/macrophages to expansion of infarction and response of oligodendrocytes after focal cerebral ischemia in rats. , 2000, Stroke.
[36] M. Wegner. Transcriptional control in myelinating glia: Flavors and spices , 2000, Glia.
[37] D. Pleasure,et al. Neurotrophin‐3 (NT‐3) diminishes susceptibility of the oligodendroglial lineage to AMPA glutamate receptor‐mediated excitotoxicity , 2000, Journal of neuroscience research.
[38] T. Uchihara,et al. Appearance of tau-2 immunoreactivity in glial cells in human brain with cerebral infarction , 2000, Neuroscience Letters.
[39] J. Mcculloch,et al. Quantitative Assessment of Ischemic Pathology in Axons, Oligodendrocytes, and Neurons: Attenuation of Damage after Transient Ischemia , 2000, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[40] A. Reith,et al. Differential activation of MAPK/ERK and p38/SAPK in neurones and glia following focal cerebral ischaemia in the rat. , 2000, Brain research. Molecular brain research.
[41] A. Shah,et al. BDNF Blocks Caspase-3 Activation in Neonatal Hypoxia–Ischemia , 2000, Neurobiology of Disease.
[42] D. Pleasure,et al. Non-N-methyl-d-aspartate glutamate receptors mediate oxygen–glucose deprivation-induced oligodendroglial injury , 2000, Brain Research.
[43] P. Casaccia‐Bonnefil. Cell death in the oligodendrocyte lineage: A molecular perspective of life/death decisions in development and disease , 2000, Glia.
[44] M. Schwab,et al. NI‐35/250/nogo‐a: A neurite growth inhibitor restricting structural plasticity and regeneration of nerve fibers in the adult vertebrate CNS , 2000, Glia.
[45] T. Möller,et al. Rapid Ischemic Cell Death in Immature Oligodendrocytes: A Fatal Glutamate Release Feedback Loop , 2000, The Journal of Neuroscience.
[46] M. Beattie,et al. Cell death and plasticity after experimental spinal cord injury. , 2000, Progress in brain research.
[47] L. Turski,et al. Autoimmune encephalomyelitis ameliorated by AMPA antagonists , 2000, Nature Medicine.
[48] D. Pitt,et al. Glutamate excitotoxicity in a model of multiple sclerosis , 2000, Nature Medicine.
[49] C. Matute,et al. AMPA and Kainate Receptors Each Mediate Excitotoxicity in Oligodendroglial Cultures , 1999, Neurobiology of Disease.
[50] Merrill,et al. Mechanisms of damage to myelin and oligodendrocytes and their relevance to disease , 1999, Neuropathology and applied neurobiology.
[51] F. Barone,et al. Inflammatory Mediators and Stroke: New Opportunities for Novel Therapeutics , 1999, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[52] G. Mealing,et al. Novel Injury Mechanism in Anoxia and Trauma of Spinal Cord White Matter: Glutamate Release via Reverse Na+-dependent Glutamate Transport , 1999, The Journal of Neuroscience.
[53] J. Wrathall,et al. Effects of the Sodium Channel Blocker Tetrodotoxin on Acute White Matter Pathology After Experimental Contusive Spinal Cord Injury , 1999, The Journal of Neuroscience.
[54] C. Mathiesen,et al. SPD 502: a water-soluble and in vivo long-lasting AMPA antagonist with neuroprotective activity. , 1999, The Journal of pharmacology and experimental therapeutics.
[55] Joseph J. Volpe,et al. Maturation-Dependent Vulnerability of Oligodendrocytes to Oxidative Stress-Induced Death Caused by Glutathione Depletion , 1998, The Journal of Neuroscience.
[56] G. Drewes,et al. MAPs, MARKs and microtubule dynamics. , 1998, Trends in biochemical sciences.
[57] H. Kettenmann,et al. Oligodendrocytes and Microglia Are Selectively Vulnerable to Combined Hypoxia and Hypoglycemia Injury in Vitro , 1998, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[58] L. Hertz,et al. Peroxide‐scavenging deficit underlies oligodendrocyte susceptibility to oxidative stress , 1998, Glia.
[59] J. Mcdonald,et al. Oligodendrocytes from forebrain are highly vulnerable to AMPA/kainate receptor-mediated excitotoxicity , 1998, Nature Medicine.
[60] C. Petito,et al. Selective Glial Vulnerability following Transient Global Ischemia in Rat Brain , 1998, Journal of neuropathology and experimental neurology.
[61] R. Miledi,et al. Glutamate receptor-mediated toxicity in optic nerve oligodendrocytes. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[62] M. Chopp,et al. Immunoreactivity of Cyclin D1/cdk4 in Neurons and Oligodendrocytes After Focal Cerebral Ischemia in Rat , 1997, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[63] J. Mcculloch,et al. Rapid Alteration of Tau in Oligodendrocytes After Focal Ischemic Injury in the Rat: Involvement of Free Radicals , 1997, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[64] J. Wrathall,et al. Delayed Antagonism of AMPA/Kainate Receptors Reduces Long-Term Functional Deficits Resulting from Spinal Cord Trauma , 1997, Experimental Neurology.
[65] C. Richter-Landsberg,et al. Expression of microtubule-associated proteins MAP2 and tau in cultured rat brain oligodendrocytes , 1997, Cell and Tissue Research.
[66] T. Yanagihara,et al. Ischemic damage and subsequent proliferation of oligodendrocytes in focal cerebral ischemia , 1997, Neuroscience.
[67] M. Fehlings,et al. Role of NMDA and Non-NMDA Ionotropic Glutamate Receptors in Traumatic Spinal Cord Axonal Injury , 1997, The Journal of Neuroscience.
[68] D. Pleasure,et al. Expression of N‐methyl‐D‐aspartate (NMDA) and non‐NMDA glutamate receptor genes in neuroblastoma, medulloblastoma, and other cell lines , 1996, Journal of neuroscience research.
[69] C. Sato-Bigbee,et al. Treatment of oligodendrocytes with antisense deoxyoligonucleotide directed against CREB mRNA: Effect on the cyclic AMP‐dependent induction of myelin basic protein expression , 1996, Journal of neuroscience research.
[70] J. Garcìa,et al. Cerebral white matter is highly vulnerable to ischemia. , 1996, Stroke.
[71] B. Juurlink,et al. Low Glutathione and High Iron Govern the Susceptibility of Oligodendroglial Precursors to Oxidative Stress , 1996, Journal of neurochemistry.
[72] D. Graham,et al. Increased tau immunoreactivity in oligodendrocytes following human stroke and head injury , 1996, Neuroscience Letters.
[73] J. Mcculloch,et al. Intracortical perfusion of glutamate in vivo induces alterations of tau and microtubule-associated protein 2 immunoreactivity in the rat , 1996, Acta Neuropathologica.
[74] P. Contreras,et al. Increased Expression of IL-1β Converting Enzyme in Hippocampus after Ischemia: Selective Localization in Microglia , 1996, The Journal of Neuroscience.
[75] Robert H Miller. Oligodendrocyte origins , 1996, Trends in Neurosciences.
[76] J. Wrathall,et al. Amelioration of Functional Deficits from Spinal Cord Trauma with Systemically Administered NBQX, an Antagonist of Non-N-methyl-D-aspartate receptors , 1996, Experimental Neurology.
[77] J. Levine,et al. The NG2 chondroitin sulfate proteoglycan: a multifunctional proteoglycan associated with immature cells. , 1996, Perspectives on developmental neurobiology.
[78] G. Almazan,et al. Glutamate Induces c‐fos Proto‐oncogene Expression and Inhibits Proliferation in Oligodendrocyte Progenitors: Receptor Characterization , 1995, The European journal of neuroscience.
[79] B. Juurlink,et al. Oligodendroglial precursor cell susceptibility to hypoxia is related to poor ability to cope with reactive oxygen species , 1995, Brain Research.
[80] V. Gallo,et al. Excitatory amino acid receptors in glia: Different subtypes for distinct functions? , 1995, Journal of neuroscience research.
[81] R. Osathanondh,et al. Oligodendroglial development in human fetal cerebrum , 1995, Annals of neurology.
[82] J. Garcìa,et al. The significance of cerebral white matter abnormalities 100 years after Binswanger's report. A review. , 1995, Stroke.
[83] D. Dewar,et al. Tau protein is altered by focal cerebral ischaemia in the rat: an immunohistochemical and immunoblotting study , 1995, Brain Research.
[84] D. Pleasure,et al. α‐Amino‐3‐Hydroxy‐5‐Methyl‐4‐Isoxazolepropionate (AMPA) Receptors Mediate Excitotoxicity in the Oligodendroglial Lineage , 1995 .
[85] K. Borges,et al. Ampa/kainate receptor activation in murine oligodendrocyte precursor cells leads to activation of a cation conductance, calcium influx and blockade of delayed rectifying K+ channels , 1994, Neuroscience.
[86] J. Wrathall,et al. Dose-dependent reduction of tissue loss and functional impairment after spinal cord trauma with the AMPA/kainate antagonist NBQX , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[87] B. Barres,et al. Control of oligodendrocyte number in the developing rat optic nerve , 1994, Neuron.
[88] V. Gallo,et al. Glutamate regulates intracellular calcium and gene expression in oligodendrocyte progenitors through the activation of DL-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[89] J. Holzwarth,et al. Glutamate receptor agonists stimulate diverse calcium responses in different types of cultured rat cortical glial cells , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[90] M. Mayer,et al. Glial cells of the oligodendrocyte lineage express both kainate- and AMPA-preferring subtypes of glutamate receptor , 1994, Neuron.
[91] M. Goldberg,et al. Combined oxygen and glucose deprivation in cortical cell culture: calcium-dependent and calcium-independent mechanisms of neuronal injury , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[92] Virginia M. Y. Lee,et al. Even in culture, oligodendrocytes myelinate solely axons. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[93] K. McCarthy,et al. Oligodendroglial lineage cells express neuroligand receptors , 1993, Glia.
[94] J. Volpe,et al. Vulnerability of oligodendroglia to glutamate: pharmacology, mechanisms, and prevention , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[95] B. Barres,et al. Proliferation of oligodendrocyte precursor cells depends on electrical activity in axons , 1993, Nature.
[96] W. Cammer,et al. A Pi Form of Glutathione‐S‐Transferase Is a Myelin‐and Oligodendrocyte‐Associated Enzyme in Mouse Brain , 1991, Journal of neurochemistry.
[97] Seung U. Kim,et al. Oligodendroglial cell death induced by oxygen radicals and its protection by catalase , 1991, Journal of neuroscience research.
[98] T. Iwaki,et al. Hydrated autoclave pretreatment enhances tau immunoreactivity in formalin-fixed normal and Alzheimer's disease brain tissues. , 1991, Laboratory investigation; a journal of technical methods and pathology.
[99] A. Mathie,et al. Activation of glutamate receptors and glutamate uptake in identified macroglial cells in rat cerebellar cultures. , 1991, The Journal of physiology.
[100] D. Corey,et al. Ion channels in vertebrate glia. , 1990, Annual review of neuroscience.
[101] M. Dąmbska,et al. Early and Late Neuropathological Changes in Perinatal White Matter Damage , 1989, Journal of child neurology.
[102] M. Raff. Glial cell diversification in the rat optic nerve. , 1989, Science.
[103] S. Hockfield,et al. In situ demonstration of mature oligodendrocytes and their processes: An immunocytochemical study with a new monoclonal antibody, Rip , 1989, Glia.
[104] M. Shelanski,et al. Light and electron microscope localization of the microtubule- associated tau protein in rat brain , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[105] J. Levine,et al. Light and electron microscopic localization of a cell surface antigen (NG2) in the rat cerebellum: association with smooth protoplasmic astrocytes , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[106] C. Petito. Transformation of Postischemic Perineuronal Glial Cells. I. Electron Microscopic Studies , 1986, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[107] M. Noble,et al. Purified astrocytes promote the in vitro division of a bipotential glial progenitor cell. , 1984, The EMBO journal.
[108] F. Gilles,et al. Acquired perinatal leukoencephalopathy , 1984, Annals of neurology.
[109] S. Ludwin. THE FUNCTION OF PERINEURONAL SATELLITE OLIGODENDROCYTES: AN IMMUNOHISTOCHEMICAL STUDY , 1984, Neuropathology and applied neurobiology.
[110] M. Raff,et al. A glial progenitor cell that develops in vitro into an astrocyte or an oligodendrocyte depending on culture medium , 1983, Nature.
[111] I. Griffiths,et al. Nerve fibres in spinal cord impact injuries Part 1. Changes in the myelin sheath during the initial 5 weeks , 1983, Journal of the Neurological Sciences.
[112] K. McCarthy,et al. Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue , 1980, The Journal of cell biology.
[113] J A Corsellis,et al. VARIATION WITH AGE IN THE VOLUMES OF GREY AND WHITE MATTER IN THE CEREBRAL HEMISPHERES OF MAN: MEASUREMENTS WITH AN IMAGE ANALYSER , 1980, Neuropathology and applied neurobiology.
[114] P. Mandel,et al. Demonstration of a specific localization of carbonic anhydrase C in the glial cells of rat CNS by an immunohistochemical method , 1979, Brain Research.
[115] L. Caplan,et al. Clinical features of subcortical arteriosclerotic encephalopathy (Binswanger disease) , 1978, Neurology.
[116] D. Silberberg,et al. Galactocerebroside is a specific cell-surface antigenic marker for oligodendrocytes in culture , 1978, Nature.
[117] B. Trump,et al. Cellular events during partial cerebral ischemia , 1977, Virchows Archiv B Cell Pathology.
[118] J. Garcìa,et al. Cellular events during partial cerebral ischemia. I. Electron microscopy of feline cerebral cortex after middle-cerebral-artery occlusion. , 1977, Virchows Archiv. B, Cell pathology.
[119] P. Prior,et al. Cyanide intoxication in Macaca mulatta Physiological and neuropathological aspects , 1977, Journal of the Neurological Sciences.
[120] W. Mcdonald,et al. Demyelination and remyelination after acute spinal cord compression. , 1973, Experimental neurology.
[121] J. Poirier,et al. [The oligodendrocyte]. , 1972, La Nouvelle presse medicale.
[122] F. Gilles,et al. Morphologic correlates of age at death of infants with perinatal telencephalic leukoencephalopathy. , 1971, The American journal of pathology.
[123] F. Gilles,et al. Perinatal telencephalic leucoencephalopathy. , 1969, Journal of neurology, neurosurgery, and psychiatry.