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1. Full Text HDAC1 and HDAC2 regulate oligodendrocyte differentiation by disrupting the beta-catenin-TCF interaction
by Ye, F and Chen, Y and Hoang, T and Montgomery, R.L and Zhao, X.H and Bu, H and Hu, T and Taketo, M.M and van Es, J.H and Clevers, H and Hsieh, J and Bassel-Duby, R and Olson, E.N and Lu, Q.R
Nature Neuroscience, ISSN 1097-6256, 2009, Volume 12, Issue 7, pp. 829 - 838
Oligodendrocyte development is regulated by the interaction of repressors and activators in a complex transcriptional network. We found that two... 
PROGENITOR CELLS | STEM-CELLS | PROTEIN | GENE | DEVELOPING RAT-BRAIN | SPINAL-CORD | MICE | HISTONE DEACETYLASE INHIBITORS | WNT SIGNALING CONTROLS | NEUROSCIENCES | COLON-CARCINOMA | Rats, Inbred F344 | Wnt Proteins - metabolism | Brain - physiology | TCF Transcription Factors - metabolism | Oligodendroglia - physiology | Female | Cell Differentiation | Oligodendroglia - cytology | Repressor Proteins - metabolism | Motor Neurons - physiology | Histone Deacetylases - genetics | Signal Transduction | Cells, Cultured | Rats | Repressor Proteins - genetics | Histone Deacetylase 2 | Histone Deacetylases - metabolism | Mice, Transgenic | Chick Embryo | Transcription Factor 7-Like 2 Protein | beta Catenin - metabolism | Histone Deacetylase 1 | Astrocytes - physiology | Animals | Spinal Cord - physiology | Mice | Mutation | β-catenin | conditional mutagenesis | TCF | LEF factors | chromatin remodeling | ID proteins | Olig2 | Wnt | oligodendrocyte differentiation | Olig1 | epigenetic regulation
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2. Full Text Mesenchymal Differentiation Mediated by NF-κB Promotes Radiation Resistance in Glioblastoma
by Bhat, Krishna P.L and Balasubramaniyan, Veerakumar and Vaillant, Brian and Ezhilarasan, Ravesanker and Hummelink, Karlijn and Hollingsworth, Faith and Wani, Khalida and Heathcock, Lindsey and James, Johanna D and Goodman, Lindsey D and Conroy, Siobhan and Long, Lihong and Lelic, Nina and Wang, Suzhen and Gumin, Joy and Raj, Divya and Kodama, Yoshinori and Raghunathan, Aditya and Olar, Adriana and Joshi, Kaushal and Pelloski, Christopher E and Heimberger, Amy and Kim, Se Hoon and Cahill, Daniel P and Rao, Ganesh and Den Dunnen, Wilfred F.A and Boddeke, Hendrikus W.G.M and Phillips, Heidi S and Nakano, Ichiro and Lang, Frederick F and Colman, Howard and Sulman, Erik P and Aldape, Kenneth
Cancer Cell, ISSN 1535-6108, 09/2013, Volume 24, Issue 3, pp. 331 - 346
Despite extensive study, few therapeutic targets have been identified for glioblastoma (GBM). Here we show that patient-derived glioma sphere cultures (GSCs)... 
INITIATING CELLS | MALIGNANT GLIOMA | HETEROGENEITY | STEM-CELLS | ONCOLOGY | SENESCENCE | CANCER | EXPRESSION | TUMOR MICROENVIRONMENT | MODULATION | BRAIN-TUMORS | CELL BIOLOGY | Prognosis | Epigenesis, Genetic | Humans | Gene Expression Regulation, Neoplastic | Transcriptome | NF-kappa B - metabolism | Gene Expression Profiling | Cell Differentiation - genetics | DNA Methylation | Basic Helix-Loop-Helix Transcription Factors - metabolism | Glioblastoma - genetics | Hyaluronan Receptors - metabolism | Glioblastoma - metabolism | Disease Models, Animal | Basic Helix-Loop-Helix Transcription Factors - genetics | Signal Transduction | Radiation Tolerance - genetics | Oligodendrocyte Transcription Factor 2 | Hyaluronan Receptors - genetics | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Xenograft Model Antitumor Assays | Tumor Necrosis Factor-alpha - pharmacology | Animals | NF-kappa B - genetics | Mice | Glioblastoma - mortality | Cluster Analysis
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3. Full Text M2 microglia and macrophages drive oligodendrocyte differentiation during CNS remyelination
by Miron, Veronique E and Boyd, Amanda and Zhao, Jing-Wei and Yuen, Tracy J and Ruckh, Julia M and Shadrach, Jennifer L and Van Wijngaarden, Peter and Wagers, Amy J and Williams, Anna and Franklin, Robin J.M and Ffrench-Constant, Charles
Nature Neuroscience, ISSN 1097-6256, 09/2013, Volume 16, Issue 9, pp. 1211 - 1218
The lack of therapies for progressive multiple sclerosis highlights the need to understand the regenerative process of remyelination that can follow CNS... 
PROGENITOR CELLS | ACTIVIN-A | REGENERATION | GENE-EXPRESSION | MONOCYTES | INJURY | GADOLINIUM CHLORIDE | IDENTIFICATION | NEUROSCIENCES | PROGRESSION | BETA | Clodronic Acid - pharmacology | Humans | Middle Aged | Central Nervous System - pathology | Culture Media, Conditioned - pharmacology | Male | Cell Differentiation - genetics | Microglia - physiology | Oligodendroglia - drug effects | Oligodendroglia - physiology | Aged, 80 and over | Adult | Female | Cadmium Chloride - pharmacology | Demyelinating Diseases - pathology | Cell Differentiation - physiology | Animals, Newborn | Macrophages - physiology | Mice, Inbred C57BL | Cells, Cultured | Rats | Mice, Transgenic | Regeneration - physiology | Rats, Sprague-Dawley | Regeneration - drug effects | Animals | Cell Differentiation - drug effects | Central Nervous System - drug effects | Aged | Mice | In Vitro Techniques | Myelin Proteins - metabolism | Physiological aspects | Multiple sclerosis | Myelination | Research | Regeneration (Biology) | Macrophages
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4. Full Text MicroRNA-Mediated Control of Oligodendrocyte Differentiation
by Zhao, Xianghui and He, Xuelian and Han, Xiaolei and Yu, Yang and Ye, Feng and Chen, Ying and Hoang, ThaoNguyen and Xu, Xiaomei and Mi, Qing-Sheng and Xin, Mei and Wang, Fan and Appel, Bruce and Lu, Q. Richard
Neuron, ISSN 0896-6273, 2010, Volume 65, Issue 5, pp. 612 - 626
MicroRNAs (miRNAs) regulate various biological processes, but evidence for miRNAs that control the differentiation program of specific neural cell types has... 
MOLNEURO | CELLS | MULTIPLE-SCLEROSIS | GENE | CNS | NEUROGENESIS | DICER | SPECIFICATION | IDENTIFICATION | EXPRESSION | NEUROSCIENCES | REQUIREMENT | Spinal Cord - metabolism | Embryo, Mammalian | Spinal Cord - growth & development | SOXD Transcription Factors - metabolism | Gene Expression Regulation, Developmental - genetics | MicroRNAs - metabolism | Cerebral Cortex - cytology | Myelin Sheath - metabolism | Cell Differentiation - genetics | Oligodendroglia - drug effects | Oligodendroglia - physiology | Basic Helix-Loop-Helix Transcription Factors - metabolism | DEAD-box RNA Helicases - deficiency | Neurons - physiology | Endoribonucleases - deficiency | Neurons - drug effects | Basic Helix-Loop-Helix Transcription Factors - genetics | RNA, Small Interfering - pharmacology | Cells, Cultured | Rats | Zebrafish | Electroporation - methods | Hippocampus - cytology | Chick Embryo | Mice, Knockout | Spinal Cord - embryology | Animals | Cell Differentiation - drug effects | Models, Biological | Ribonuclease III | Embryo, Nonmammalian | Stem Cells - drug effects | Stem Cells - physiology | Mice | SOXD Transcription Factors - genetics | Enzymes | Spinal cord | Mutagenesis | Rodents | Hybridization | Gene expression | Embryos | Myelination | Dicer | transcriptional regulation | oligodendrocytes | small non-coding RNAs | differentiation inhibitors | miR-338 | miR-219
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5. Full Text Self‐organized developmental patterning and differentiation in cerebral organoids
by Renner, Magdalena and Lancaster, Madeline A and Bian, Shan and Choi, Heejin and Ku, Taeyun and Peer, Angela and Chung, Kwanghun and Knoblich, Juergen A
The EMBO Journal, ISSN 0261-4189, 05/2017, Volume 36, Issue 10, pp. 1316 - 1329
Cerebral organoids recapitulate human brain development at a considerable level of detail, even in the absence of externally added signaling factors. The... 
neurogenesis | development | signaling | patterning | human brain development | organoid | DEVELOPING HUMAN BRAIN | HUMAN ES | BIOCHEMISTRY & MOLECULAR BIOLOGY | CORTICAL HEM | CELL BIOLOGY | PLURIPOTENT STEM-CELLS | NEOCORTEX | EVOLUTION | CORTEX | WNT GENES | NEURONS | EXPRESSION | Brain - embryology | Cell Proliferation | Organoids - growth & development | Humans | Body Patterning | Spatio-Temporal Analysis | Cell Differentiation | Neurochemistry | Clearing | Brain | Pattern formation | Astrocytes | Regional analysis | Cortex | Spatial discrimination | Forebrain | Tissues | Neurogenesis | Organoids | Oligodendrocytes | Differentiation | Growth factors | In vitro methods and tests | Development & Differentiation
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6. Full Text Olig2 Targets Chromatin Remodelers to Enhancers to Initiate Oligodendrocyte Differentiation
by Yu, Yang and Chen, Ying and Kim, Bongwoo and Wang, Haibo and Zhao, Chuntao and He, Xuelian and Liu, Lei and Liu, Wei and Wu, Lai Man N and Wu, Jiang and Mao, Meng and Chan, Jonah R and Lu, Q. Richard
Cell, ISSN 0092-8674, 01/2013, Volume 152, Issue 1-2, pp. 248 - 261
Establishment of oligodendrocyte identity is crucial for subsequent events of myelination in the CNS. Here, we demonstrate that activation of ATP-dependent... 
CELLS | COMPLEX | THERAPY | MULTIPLE-SCLEROSIS | MYELINATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | BIOLOGY | CNS | SWITCH | LESIONS | CELL BIOLOGY | Oligodendroglia - metabolism | Brain - cytology | Cells, Cultured | Gene Expression Regulation | Chromatin Assembly and Disassembly | Rats | Nuclear Proteins - metabolism | Oligodendrocyte Transcription Factor 2 | Mice, Knockout | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | DNA Helicases - metabolism | Animals | Basic Helix-Loop-Helix Transcription Factors - metabolism | Enhancer Elements, Genetic | Cell Differentiation | Mice | Oligodendroglia - cytology | Spinal Cord - cytology | Enzymes | Neurosciences | Chromatin | Genes | Genomics | Stem cells | Physiological aspects | Birth defects
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7. Full Text GSK3β negatively regulates oligodendrocyte differentiation and myelination in vivo
by Azim, Kasum and Butt, Arthur M
Glia, ISSN 0894-1491, 04/2011, Volume 59, Issue 4, pp. 540 - 553
Glycogen synthase kinase 3β (GSK3β) is an essential integrating molecule for multiple proliferation and differentiation signals that regulate cell fate. Here,... 
oligodendrocyte precursor | myelination | GSK3β | demyelination | oligodendrocyte | Myelination | Oligodendrocyte | Demyelination | Oligodendrocyte precursor | PROGENITOR CELLS | MOUSE SUBVENTRICULAR ZONE | CYCLIN D1 | BETA-CATENIN | TAU-PHOSPHORYLATION | NEUROSCIENCES | GLYCOGEN-SYNTHASE KINASE-3-BETA | FIBROBLAST GROWTH FACTOR-2 | CENTRAL-NERVOUS-SYSTEM | GSK3 beta | LITHIUM | EXPRESSION | Immunohistochemistry | Oligodendroglia - metabolism | Rats, Wistar | Myelin Sheath - drug effects | Glycogen Synthase Kinase 3 beta | Wnt Proteins - metabolism | Myelin Sheath - metabolism | Oligodendroglia - drug effects | Lithium Chloride - pharmacology | Cell Differentiation - physiology | Organ Culture Techniques | Glycogen Synthase Kinase 3 - antagonists & inhibitors | Mice, Inbred C57BL | Rats | Mice, Transgenic | Glycogen Synthase Kinase 3 - metabolism | beta Catenin - metabolism | Blotting, Western | Animals | Wnt Proteins - agonists | Signal Transduction - drug effects | Cell Differentiation - drug effects | Signal Transduction - physiology | Cell Proliferation - drug effects | Mice | Oligopeptides - pharmacology | Optic Nerve - drug effects | Optic Nerve - metabolism
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8. Full Text Extracellular cues influencing oligodendrocyte differentiation and (re)myelination
by Wheeler, Natalie A and Fuss, Babette
Experimental Neurology, ISSN 0014-4886, 09/2016, Volume 283, Issue Pt B, pp. 512 - 530
There is an increasing number of neurologic disorders found to be associated with loss and/or dysfunction of the CNS myelin sheath, ranging from the classic... 
Regeneration | Signaling | Multiple sclerosis | Oligodendrocyte | Myelin | CNS injury | Neuropsychiatric diseases | Extracellular | Remyelination | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | MULTIPLE-SCLEROSIS LESIONS | CELL-ADHESION MOLECULE | CHONDROITIN SULFATE PROTEOGLYCANS | BONE MORPHOGENETIC PROTEINS | FIBROBLAST-GROWTH-FACTOR | NEUROSCIENCES | SPHINGOSINE 1-PHOSPHATE RECEPTOR | APPEARING WHITE-MATTER | CENTRAL-NERVOUS-SYSTEM | CUPRIZONE-INDUCED DEMYELINATION | Demyelinating Diseases - physiopathology | Animals | Oligodendroglia - physiology | Humans | Nerve Regeneration - physiology | Extracellular Matrix - metabolism | Stem Cells - physiology | Demyelinating Diseases - metabolism | Cell Differentiation - physiology | Nervous system diseases | extracellular | signaling | regeneration | multiple sclerosis | oligodendrocyte | neuropsychiatric diseases | remyelination
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