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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
Nature Immunology, ISSN 1529-2908, 02/2006, Volume 7, Issue 2, pp. 148 - 155
Journal Article
Cell, ISSN 0092-8674, 2006, Volume 124, Issue 3, pp. 573 - 586
How is the characteristic shape of a membrane bound organelle achieved? We have used an in vitro system to address the mechanism by which the tubular network... 
YEAST | LOCALIZATION | NEURITE OUTGROWTH | POLYPOSIS LOCUS | INTERACTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | NOGO-A | FUNCTIONAL DOMAINS | GENE FAMILY | IDENTIFICATION | SACCHAROMYCES-CEREVISIAE | CELL BIOLOGY | Saccharomyces cerevisiae - genetics | Humans | Cercopithecus aethiops | Endoplasmic Reticulum - metabolism | Intracellular Signaling Peptides and Proteins - metabolism | Saccharomyces cerevisiae - metabolism | Transfection | Membrane Transport Proteins - genetics | Female | Membrane Transport Proteins - metabolism | Membrane Proteins - metabolism | Nogo Proteins | Membrane Proteins - classification | Intracellular Signaling Peptides and Proteins - genetics | Calcium Signaling | Recombinant Proteins - metabolism | Membrane Proteins - genetics | Oocytes - metabolism | Rats | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Saccharomyces cerevisiae Proteins - genetics | Membrane Transport Proteins - chemistry | Animals | Membrane Proteins - chemistry | Intracellular Signaling Peptides and Proteins - chemistry | Saccharomyces cerevisiae Proteins - metabolism | Myelin Proteins | In Vitro Techniques | COS Cells | Saccharomyces cerevisiae Proteins - chemistry | Usage | Physiological aspects | Immunoblotting | Research | Brewer's yeast | Endoplasmic reticulum | Membrane proteins | Lipids | Aquaporins | Synthesis | 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
Nature Neuroscience, ISSN 1097-6256, 08/2011, Volume 14, Issue 8, pp. 1009 - 1016
Permanent damage to white matter tracts, comprising axons and myelinating oligodendrocytes, is an important component of brain injuries of the newborn that... 
FUNCTIONAL INTERACTION | MULTIPLE-SCLEROSIS | CNS REMYELINATION | MYELINATION | SIGNALING PATHWAY | TRANSCRIPTION | DIFFERENTIATION | BETA-CATENIN | NEUROSCIENCES | WHITE-MATTER INJURY | NEGATIVE REGULATOR | Humans | Ki-67 Antigen - metabolism | Male | Brain Injuries - metabolism | Wnt Proteins - metabolism | Oligodendroglia - drug effects | Hypoxia-Ischemia, Brain - therapy | Infant, Newborn | Organ Culture Techniques | Disease Models, Animal | Animals, Newborn | Basic Helix-Loop-Helix Transcription Factors - genetics | Mice, Transgenic | Oligodendrocyte Transcription Factor 2 | Brain Injuries - therapy | Multiple Sclerosis - therapy | Myelin Proteins - genetics | beta Catenin - metabolism | Heterocyclic Compounds, 3-Ring - therapeutic use | Spinal Cord - physiology | Axin Protein | Mice | Myelin Sheath - ultrastructure | beta-Galactosidase - genetics | Cerebellum - ultrastructure | Myelin Proteins - metabolism | Corpus Callosum - metabolism | Spinal Cord - drug effects | Heterocyclic Compounds, 3-Ring - pharmacology | Myelin Proteins - therapeutic use | Cerebellum - drug effects | Myelin Sheath - drug effects | Hypoxia-Ischemia, Brain - pathology | Cerebral Cortex - cytology | Cytoskeletal Proteins - deficiency | Dose-Response Relationship, Drug | Oligodendroglia - physiology | Wnt Proteins - genetics | beta-Galactosidase - metabolism | Adult | Cytoskeletal Proteins - metabolism | Female | Demyelinating Diseases - chemically induced | Demyelinating Diseases - pathology | Neurons - drug effects | Cell Differentiation - physiology | Hypoxia-Ischemia, Brain - metabolism | Microscopy, Electron, Transmission | Myelin Sheath - pathology | Gene Expression Regulation - genetics | Cerebellum - metabolism | Cells, Cultured | Gene Expression Regulation - physiology | Corpus Callosum - drug effects | Nerve Tissue Proteins - genetics | beta Catenin - genetics | Multiple Sclerosis - complications | Nerve Tissue Proteins - metabolism | Animals | Cell Differentiation - drug effects | Multiple Sclerosis - pathology | Stem Cells - drug effects | Brain Injuries - etiology | Lysophosphatidylcholines - toxicity | Postmortem Changes | Infants (Newborn) | Brain | Care and treatment | Physiological aspects | Research | Binding proteins | Health aspects | Injuries | Index Medicus
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 12/2011, Volume 365, Issue 25, pp. 2377 - 2388
The authors report that INF2 mutations are present in patients with focal segmental glomerulosclerosis (FSGS) associated with Charcot–Marie–Tooth neuropathy.... 
GLOMERULOSCLEROSIS | MEDICINE, GENERAL & INTERNAL | MYELIN | PROTEIN | NEUROPATHY | EPITHELIAL-CELLS | GENE | RHO | MEDIATED TRANSPORT | FORMIN | NEPHROPATHY | Humans | Middle Aged | Proteolipids - metabolism | Actins - metabolism | Male | Charcot-Marie-Tooth Disease - genetics | Young Adult | Kidney - metabolism | Glomerulosclerosis, Focal Segmental - etiology | Myelin and Lymphocyte-Associated Proteolipid Proteins | Adult | Female | Membrane Transport Proteins - metabolism | Microfilament Proteins - metabolism | Child | Microfilament Proteins - genetics | Charcot-Marie-Tooth Disease - complications | Schwann Cells - metabolism | Phenotype | Animals | Adolescent | Age of Onset | Heterozygote | Mice | Mutation | Myelin Proteins - metabolism | Glomerulonephritis | Gene mutations | Charcot-Marie-Tooth disease | Causes of | Genetic aspects | Research | Myelin proteins | Cdc42 protein | Disease | Exons | Genes | Amino acids | Nervous system | Neuropathy | Guanine nucleotide-binding protein | Proteins | Myelin P0 protein | Localization | Peripheral myelin protein 22 | Deoxyribonucleic acid--DNA | Kidneys | Schwann cells | Polymerization | Myelination | Genotyping | Biopsy | Glomerulus | Cytoskeleton | Genetic testing | Cytoplasm | Guanosinetriphosphatase | Index Medicus | Abridged Index Medicus | Schwann Cells | Genomics | Kidney | Charcot-Marie-Tooth Disease | Life Sciences | Proteolipids | Biochemistry, Molecular Biology | Actins | Microfilament Proteins | Membrane Transport Proteins | Myelin Proteins | Glomerulosclerosis, Focal Segmental
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
The Journal of Cell Biology, ISSN 0021-9525, 4/2010, Volume 189, Issue 2, pp. 223 - 232
Journal Article
PLoS Biol, ISSN 1544-9173, 05/2017, Volume 15, Issue 5, pp. e1002605 - e1002605
In the vertebrate nervous system, myelination of axons for rapid impulse propagation requires the synthesis of large amounts of lipids and proteins by... 
CHOLESTEROL-METABOLISM | NERVOUS-SYSTEM | PROMOTE MYELINATION | IN-VITRO | ACID | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOLOGY | NEURONS | SCHWANN-CELLS | RAT-BRAIN | GLIAL-CELLS | MATURATION | Glial Fibrillary Acidic Protein - genetics | Oligodendroglia - metabolism | Humans | Astrocytes - pathology | Intracellular Signaling Peptides and Proteins - metabolism | Demyelinating Diseases - metabolism | Glial Fibrillary Acidic Protein - metabolism | Oligodendroglia - ultrastructure | Myelin Sheath - metabolism | Diet, High-Fat | Gene Deletion | Membrane Proteins - metabolism | Sterol Regulatory Element Binding Protein 2 - genetics | Sterol Regulatory Element Binding Protein 2 - metabolism | Demyelinating Diseases - pathology | Intracellular Signaling Peptides and Proteins - genetics | Biomarkers - metabolism | Microscopy, Electron, Transmission | Myelin Sheath - pathology | Membrane Proteins - genetics | Mice, Inbred C57BL | Lipid Metabolism | Mice, Transgenic | Demyelinating Diseases - prevention & control | Organ Specificity | Fatty Acid Synthase, Type I - metabolism | Nerve Tissue Proteins - genetics | Astrocytes - ultrastructure | Nerve Tissue Proteins - metabolism | Oligodendroglia - pathology | Animals | Myelin Sheath - ultrastructure | Protein Processing, Post-Translational | Mutation | Astrocytes - metabolism | Crosses, Genetic | Enrichment | Brain | Membranes | Propagation | Central nervous system | Neurobiology | Lipids | Nervous system | Biosynthesis | Glial cells | Gene deletion | Inactivation | Proteins | Clonal deletion | Oligodendrocytes | Sterol regulatory element-binding protein | Deletion | Cleavage | Inhibition | Age | Fluctuations | Deactivation | Astrocytes | Myelin | Neurons | Developmental biology | Schwann cells | Flux | Embryos | Mutants | Axons | Myelination | Brain research | Index Medicus
Journal Article
Nature Neuroscience, ISSN 1097-6256, 05/2012, Volume 15, Issue 5, pp. 703 - 712
In the adult mammalian CNS, chondroitin sulfate proteoglycans (CSPGs) and myelin-associated inhibitors (MAIs) stabilize neuronal structure and restrict... 
RETINAL GANGLION-CELLS | NEURITE GROWTH | AXON REGENERATION | OPTIC-NERVE REGENERATION | SPINAL-CORD-INJURY | TYROSINE-PHOSPHATASE-SIGMA | CORTICOSPINAL TRACT REGENERATION | NOGO RECEPTOR | OLIGODENDROCYTE-MYELIN GLYCOPROTEIN | FUNCTIONAL RECEPTOR | NEUROSCIENCES | Protein Binding - genetics | Embryo, Mammalian | Humans | Myelin Proteins - deficiency | Nerve Regeneration - physiology | Myelin-Associated Glycoprotein - genetics | Myelin-Associated Glycoprotein - metabolism | Ganglia, Spinal - cytology | Dose-Response Relationship, Drug | Tubulin - metabolism | Transfection | GPI-Linked Proteins - deficiency | Receptor-Like Protein Tyrosine Phosphatases, Class 4 - pharmacology | Protein Binding - drug effects | Optic Nerve Injuries - metabolism | Neurons - metabolism | Nogo Receptor 1 | Neurons - drug effects | Receptors, Tumor Necrosis Factor - genetics | Animals, Newborn | Receptors, Tumor Necrosis Factor - metabolism | Gene Expression Regulation - genetics | Cells, Cultured | Chondroitin Sulfate Proteoglycans - metabolism | Gene Expression Regulation - physiology | Rats | Receptors, Cell Surface - metabolism | Mutation - genetics | Myelin Proteins - genetics | GPI-Linked Proteins - metabolism | Mice, Knockout | Gene Expression Regulation - drug effects | Animals | Analysis of Variance | Central Nervous System - cytology | Receptors, Cell Surface - deficiency | Mice | Myelin Proteins - metabolism | GPI-Linked Proteins - genetics | Receptors, Cell Surface - genetics | Neuroplasticity | Physiological aspects | Proteoglycans | Research | Chondroitin | Index Medicus
Journal Article