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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
Journal Article
Nature Neuroscience, ISSN 1097-6256, 06/2006, Volume 9, Issue 6, pp. 843 - 852
The optic nerve, like most mature CNS pathways, does not regenerate after injury. Through unknown mechanisms, however, macrophage activation in the eye... 
SURVIVAL | GROWTH-STATE | INHIBITION | INJURY | DEATH IN-VIVO | CALCIUM-BINDING | ADULT-RATS | RAT OPTIC-NERVE | CILIARY NEUROTROPHIC FACTOR | NEUROSCIENCES | SENSORY NEURONS | Growth Substances - secretion | Optic Nerve - cytology | Calcium - metabolism | Calcium Signaling - physiology | Nerve Regeneration - physiology | Rats, Inbred F344 | Cell Communication - physiology | Culture Media, Conditioned - pharmacology | Male | Ganglia, Spinal - cytology | Nerve Growth Factors - metabolism | Retinal Ganglion Cells - metabolism | Retinal Ganglion Cells - cytology | Macrophages - secretion | Calcium-Calmodulin-Dependent Protein Kinase Type 1 | Cyclic AMP - metabolism | Calcium-Binding Proteins - metabolism | Nerve Growth Factors - secretion | Cells, Cultured | Rats | Rats, Sprague-Dawley | Macrophages - metabolism | Animals | Growth Cones - metabolism | Growth Cones - ultrastructure | Signal Transduction - drug effects | Calcium Signaling - drug effects | Calcium-Binding Proteins - secretion | Calcium-Binding Proteins - physiology | Cell Communication - drug effects | Nerve Regeneration - drug effects | Signal Transduction - physiology | Transcriptional Activation - physiology | Growth Cones - drug effects | Ganglia, Spinal - drug effects | Optic Nerve - drug effects | Calcium-Calmodulin-Dependent Protein Kinases - metabolism | Retinal Ganglion Cells - drug effects | Ganglia, Spinal - metabolism | Growth Substances - metabolism | Optic Nerve - metabolism | Regeneration | Nervous system | Optic nerve | Research | Apoptosis | Index Medicus
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, Electron, Transmission | Cells, Cultured | Nerve Tissue Proteins - genetics | Organogenesis | Nerve Tissue Proteins - metabolism | Animals | Signal Transduction - physiology | Smad Proteins - metabolism | Medical colleges | Neurosciences | Neurons | Central nervous system | Bone morphogenetic proteins | Universities and colleges | DNA binding proteins | Proteins | Multiple sclerosis | Transcription factors | Rodents | Nervous system | Genomes | Kinases | Gene expression | Index Medicus | Antagonism
Journal Article
Acta Ophthalmologica, ISSN 1755-375X, 10/2016, Volume 94, Issue S256, p. n/a
Glycogen is a glucose storage molecule. We studied the physiology and functions of glycogen in CNS white matter using acutely isolated mouse optic nerve (MON),... 
Physiological aspects | Lactates | Glucose metabolism | Glycogen | Energy metabolism | Optic nerve | Astrocytes | Oxidative metabolism | Central nervous system | Action potential | Glucose | Metabolism | Tissues | Substantia alba | Discharge | Latency | Axons | Inhibitors | Energy | Exhaustion | Oligodendrocytes | Breakdown | Lactic acid | Axonal transport
Journal Article
Neuron, ISSN 0896-6273, 12/2016, Volume 92, Issue 6, pp. 1294 - 1307
Journal Article