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Nature, ISSN 0028-0836, 07/2012, Volume 487, Issue 7408, pp. 443 - 448
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 10/2011, Volume 31, Issue 42, pp. 14899 - 14909
Multiple sclerosis is a demyelinating disease that affects similar to 2,000,000 people worldwide. In the advanced stages of the disease, endogenous... 
OLIGODENDROCYTE PRECURSORS | FIBROBLAST GROWTH FACTOR-2 | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | IN-VIVO | DEMYELINATED LESIONS | MIRROR MOVEMENTS | CENTRAL-NERVOUS-SYSTEM | EXTRACELLULAR-MATRIX | BLOOD-BRAIN-BARRIER | LINKED KALLMANNS-SYNDROME | NEUROSCIENCES | Oligodendroglia - metabolism | Cricetulus | Humans | Middle Aged | Cerebral Cortex - pathology | Receptor, Fibroblast Growth Factor, Type 1 - metabolism | Male | Glial Fibrillary Acidic Protein - metabolism | Phosphoproteins - metabolism | Cerebral Cortex - metabolism | Antigens, CD - metabolism | Oligodendroglia - drug effects | Transfection - methods | Basic Helix-Loop-Helix Transcription Factors - metabolism | Gangliosides - metabolism | Up-Regulation - physiology | Aged, 80 and over | Fibroblast Growth Factor 2 - metabolism | Adult | Female | Membrane Proteins - metabolism | HLA-DR Antigens - metabolism | Extracellular Matrix Proteins - metabolism | Adult Stem Cells - drug effects | Multiple Sclerosis - metabolism | Cricetinae | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Cells, Cultured | Enzyme Inhibitors - pharmacology | Proteoglycans - metabolism | Antigens - metabolism | Multiple Sclerosis - classification | Nerve Tissue Proteins - metabolism | Oligodendroglia - pathology | Up-Regulation - drug effects | Adult Stem Cells - metabolism | Pyrroles - pharmacology | Animals | Zonula Occludens-1 Protein | Antigens, Differentiation, Myelomonocytic - metabolism | Multiple Sclerosis - pathology | Aged | Mice | Postmortem Changes | Index Medicus
Journal Article
Neuron, ISSN 0896-6273, 2010, Volume 65, Issue 5, pp. 597 - 611
To investigate the role of microRNAs in regulating oligodendrocyte (OL) differentiation and myelination, we utilized transgenic mice in which microRNA... 
DEVBIO | MOLNEURO | TRANSCRIPTION FACTORS | NERVOUS-SYSTEM | GLIAL PROGENITOR-CELL | PROTEIN | CYCLE EXIT | NEURONS | GROWTH-FACTOR | IDENTIFICATION | MICRORNA EXPRESSION | LINEAGE | NEUROSCIENCES | Central Nervous System - metabolism | MicroRNAs - metabolism | Green Fluorescent Proteins - genetics | S100 Proteins - genetics | Oligodendroglia - drug effects | Basic Helix-Loop-Helix Transcription Factors - metabolism | Animals, Newborn | Basic Helix-Loop-Helix Transcription Factors - genetics | Receptor, Platelet-Derived Growth Factor alpha - metabolism | S100 Calcium Binding Protein beta Subunit | Oligonucleotide Array Sequence Analysis - methods | Rats | Mice, Transgenic | Oligodendrocyte Transcription Factor 2 | Myelin Proteins - genetics | Rats, Sprague-Dawley | Nerve Growth Factors - genetics | Mice | MicroRNAs - genetics | Myelin Proteins - metabolism | SOXD Transcription Factors - genetics | Optic Nerve - metabolism | Age Factors | SOXD Transcription Factors - metabolism | Gene Expression Regulation, Developmental - genetics | Sciatic Nerve - growth & development | Myelin Sheath - metabolism | Central Nervous System - growth & development | DNA-Binding Proteins - metabolism | Sciatic Nerve - metabolism | Oligodendroglia - physiology | Transfection | DEAD-box RNA Helicases - metabolism | Cell Differentiation - physiology | Optic Nerve - growth & development | Brain - cytology | 2',3'-Cyclic-Nucleotide Phosphodiesterases - genetics | Ribonuclease III - genetics | Ribonuclease III - metabolism | Mice, Inbred C57BL | Cells, Cultured | Gene Expression Profiling - methods | Transcription Factors - genetics | 2',3'-Cyclic-Nucleotide Phosphodiesterases - metabolism | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | DEAD-box RNA Helicases - genetics | Animals | Cell Differentiation - drug effects | Receptor, Platelet-Derived Growth Factor alpha - genetics | Stem Cells - drug effects | Stem Cells - physiology | Proteins | Genotype & phenotype | Gene expression | Experiments | Rodents | Cell cycle | Index Medicus
Journal Article
Neuron, ISSN 0896-6273, 2003, Volume 40, Issue 3, pp. 485 - 499
The CNS is thought to develop from self-renewing stem cells that generate neurons, astrocytes, and oligodendrocytes. Other data, however, have suggested that... 
OLIGODENDROCYTE LINEAGE | PROGENITOR CELLS | TRANSCRIPTION FACTORS | GLIAL-RESTRICTED PRECURSORS | RAT CEREBRAL-CORTEX | SONIC HEDGEHOG | EMBRYONIC SPINAL-CORD | NEURAL-TUBE | CENTRAL-NERVOUS-SYSTEM | MAMMALIAN FOREBRAIN | NEUROSCIENCES | Immunohistochemistry | Green Fluorescent Proteins | O Antigens - metabolism | Embryo, Mammalian | Cell Count | Homeodomain Proteins - metabolism | Fibroblast Growth Factor 2 - pharmacology | Glial Fibrillary Acidic Protein - metabolism | Hedgehog Proteins | RNA, Messenger - biosynthesis | Time Factors | SOXE Transcription Factors | Neurons - metabolism | Basic Helix-Loop-Helix Transcription Factors | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Enzyme Inhibitors - pharmacology | Proteoglycans - metabolism | Rats | Oligodendrocyte Transcription Factor 2 | Mice | Astrocytes - metabolism | Oligodendroglia - metabolism | Flow Cytometry - methods | Epithelial Cells - metabolism | Epithelial Cells - drug effects | PAX7 Transcription Factor | Carbocyanines - metabolism | DNA-Binding Proteins - metabolism | Dose-Response Relationship, Drug | Tubulin - metabolism | Transfection | Reverse Transcriptase Polymerase Chain Reaction - methods | beta-Galactosidase - metabolism | Fibroblast Growth Factor 2 - physiology | Bromodeoxyuridine - metabolism | Spinal Cord - cytology | Cell Differentiation - physiology | High Mobility Group Proteins - metabolism | Cells, Cultured | Antigens - metabolism | Body Patterning - physiology | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Spinal Cord - embryology | Blotting, Northern | Animals | Cell Aggregation | Stem Cells - physiology | Trans-Activators - metabolism | Epidermal Growth Factor - pharmacology | In Vitro Techniques | Luminescent Proteins - metabolism | Spinal cord | Scholarships & fellowships | Neurosciences | Rodents | Stem cells | Experiments | Neurogenesis | Index Medicus
Journal Article
Glia, ISSN 0894-1491, 01/2016, Volume 64, Issue 1, pp. 21 - 34
Journal Article
Nature, ISSN 0028-0836, 05/2012, Volume 485, Issue 7399, pp. 517 - 521
Oligodendrocytes, the myelin-forming glial cells of the central nervous system, maintain long-term axonal integrity(1-3). However, the underlying support... 
CYTOCHROME-C-OXIDASE | RAT OLIGODENDROCYTES | OPTIC-NERVE | CELL-DEVELOPMENT | GLUCOSE | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | LACTATE | MICE LACKING | BRAIN | DEFICIENCY | Protons | Mitochondria - enzymology | Oligodendroglia - metabolism | Electron Transport Complex IV - antagonists & inhibitors | Demyelinating Diseases - genetics | Alkyl and Aryl Transferases - metabolism | Axons - physiology | Demyelinating Diseases - metabolism | Electron Transport Complex IV - metabolism | Myelin Sheath - metabolism | Action Potentials | Brain - metabolism | Membrane Proteins - deficiency | Oligodendroglia - drug effects | Cell Respiration | Mitochondria - genetics | Time Factors | Alkyl and Aryl Transferases - genetics | Membrane Proteins - metabolism | Oligodendroglia - cytology | Demyelinating Diseases - pathology | Alkyl and Aryl Transferases - deficiency | Brain - cytology | Demyelinating Diseases - enzymology | Magnetic Resonance Spectroscopy | Cell Survival | Membrane Proteins - genetics | Lactic Acid - metabolism | Mutant Proteins - genetics | Mutant Proteins - metabolism | Mitochondria - metabolism | Schwann Cells - metabolism | Electron Transport Complex IV - genetics | Mitochondria - pathology | Animals | Glycolysis | Oligodendroglia - enzymology | Mice | Schwann Cells - enzymology | Physiological aspects | Oligodendroglia | Axons | Health aspects | Electrodes | Medical research | Mitochondria | Metabolites | Rodents | Nervous system | Apoptosis | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2012, Volume 7, Issue 11, pp. e49023 - e49023
Intrauterine infection and inflammation are major reasons for preterm birth. The switch from placenta-mediated to lung-mediated oxygen supply during birth is... 
INDUCED CELL-DEATH | ISCHEMIC TOLERANCE | MICROGLIAL TOXICITY | NITRIC-OXIDE SYNTHASE | MULTIDISCIPLINARY SCIENCES | PERIVENTRICULAR LEUKOMALACIA | DEVELOPING OLIGODENDROCYTES | NECROSIS-FACTOR-ALPHA | EXCITOTOXIC INJURY | INDUCED BRAIN-INJURY | BACTERIAL-ENDOTOXIN SENSITIZES | Inflammation - chemically induced | Inflammation - pathology | Microglia - metabolism | Oligodendroglia - metabolism | Rats, Wistar | Apoptosis - drug effects | Caspase 3 - metabolism | Brain - metabolism | Inflammation - metabolism | Oligodendroglia - drug effects | Nerve Fibers, Myelinated - pathology | Hyperoxia - metabolism | Microglia - pathology | Animals, Newborn | Nerve Fibers, Myelinated - metabolism | Leukoencephalopathies - pathology | Microglia - drug effects | Nerve Fibers, Myelinated - drug effects | Cells, Cultured | Rats | Leukoencephalopathies - metabolism | Rats, Sprague-Dawley | Brain - drug effects | Hyperoxia - pathology | Oligodendroglia - pathology | Animals | Lipopolysaccharides - pharmacology | Brain - pathology | Apoptosis - physiology | Immunohistochemistry | Brain | Cell death | Infants (Premature) | Inflammation | Research | Mitogens | Health aspects | Injuries | Neuroimaging | Neonates | Cell culture | Pediatrics | Transcription factors | Traumatic brain injury | Lung | Premature birth | Interleukin | Superoxide dismutase | Infants | Infections | Birth | Western blotting | Lipopolysaccharides | Head injuries | Newborn babies | Ischemia | Rodents | Oligodendrocytes | Oxygen | Pain perception | Cytokines | Maturation | Incubation | Mortality | Superoxide | Gene expression | Substantia alba | Microglia | Hospitals | Placenta | Magnetic resonance imaging | Magnetic permeability | Hyperoxia | Interleukin 10 | Brain damage | Hypoxia | Oxygen tension | Brain injury | Apoptosis | Index Medicus | pathology | Leukoencephalopathies | Sprague-Dawley | pharmacology | Caspase 3 | Cultured | Basic Medicine | chemically induced | Myelinated | physiology | drug effects | Cells | Newborn | Wistar | Medicinska grundvetenskaper | Oligodendroglia | metabolism | Nerve Fibers
Journal Article
Brain, Behavior, and Immunity, ISSN 0889-1591, 2015, Volume 52, pp. 106 - 119
Highlights • Fingolimod (FTY720) improves long-term cognitive deficits after neonatal hyperoxia. • Hyperoxia-related long-term microstructural abnormalities... 
Psychiatry | Allergy and Immunology | White matter development | Oligodendrocyte | Fingolimod | Hyperoxia | Neonatal brain injury | SURVIVAL | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | RAT | IMMUNOLOGY | NEUROSCIENCES | CELL-DEATH | MULTIPLE-SCLEROSIS | OLIGODENDROCYTE PROGENITORS | FTY720 | INFANTS | ISCHEMIC BRAIN-INJURY | MODULATION | Lysophospholipids - metabolism | Microglia - metabolism | Oligodendroglia - metabolism | Receptors, Lysosphingolipid - antagonists & inhibitors | Rats, Wistar | White Matter - metabolism | Cognition Disorders - metabolism | Male | Brain - metabolism | Cognition Disorders - prevention & control | Oligodendroglia - drug effects | Microglia - pathology | Female | Sphingosine - metabolism | Receptors, Lysosphingolipid - metabolism | Fingolimod Hydrochloride - therapeutic use | Animals, Newborn | Microglia - drug effects | Nerve Fibers, Myelinated - drug effects | Cognition Disorders - pathology | Rats | White Matter - drug effects | Random Allocation | White Matter - pathology | Hyperoxia - pathology | Oligodendroglia - pathology | Pregnancy | Oxygen - administration & dosage | Sphingosine - analogs & derivatives | Animals | Diffusion Magnetic Resonance Imaging | Hyperoxia - drug therapy | Infants (Newborn) | Brain | Multiple sclerosis | Analysis | Injuries | Sphingosine | Index Medicus
Journal Article
Journal Article
Neuron, ISSN 0896-6273, 02/2012, Volume 73, Issue 4, pp. 713 - 728
Myelination by oligodendrocytes in the central nervous system (CNS) is essential for proper brain function, yet the molecular determinants that control this... 
TRANSCRIPTION FACTORS | IN-VITRO | MULTIPLE-SCLEROSIS | BONE MORPHOGENETIC PROTEIN | OLIGODENDROCYTE PRECURSOR CELLS | DEMYELINATED LESIONS | MOWAT-WILSON-SYNDROME | DIFFERENTIATION | BETA-CATENIN | CNS MYELINATION | NEUROSCIENCES | Central Nervous System - ultrastructure | Microcephaly - genetics | Oligonucleotide Array Sequence Analysis | Embryo, Mammalian | Homeodomain Proteins - metabolism | Humans | Nerve Tissue Proteins - deficiency | Caspase 3 - metabolism | Ki-67 Antigen - metabolism | Gene Expression Profiling | Green Fluorescent Proteins - genetics | RNA, Messenger - metabolism | Zinc Finger E-box Binding Homeobox 2 | Central Nervous System - physiology | Bone Morphogenetic Proteins - metabolism | Basic Helix-Loop-Helix Transcription Factors - metabolism | Facies | Repressor Proteins - metabolism | Smad7 Protein - metabolism | Animals, Newborn | Basic Helix-Loop-Helix Transcription Factors - genetics | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Hirschsprung Disease - pathology | Intellectual Disability - pathology | Models, Molecular | Smad Proteins - genetics | Oligodendrocyte Transcription Factor 2 | Signal Transduction - genetics | Mice, Knockout | Central Nervous System - cytology | Mice | Optic Nerve - metabolism | Receptor-Interacting Protein Serine-Threonine Kinases - metabolism | Oligodendroglia - metabolism | Immunoprecipitation | Age Factors | Hirschsprung Disease - genetics | Gene Expression Regulation, Developmental - genetics | Intellectual Disability - genetics | Myelin Sheath - metabolism | Cell Differentiation - genetics | Transfection | Microcephaly - pathology | Optic Nerve - embryology | Smad7 Protein - genetics | Optic Nerve - growth & development | Microscopy, Elec