Biology of Oligodendrocyte and Myelin in the Mammalian Central Nervous System

Generation of Neurons and Astrocytes from Isolated Cells of the Adult Mammalian Central Nervous System

Reynolds, B. A., & Weiss, S. (1992) · Science · doi:10.1126/science.1553558 · Cited by 5,413 · see citing works

Axonal transection in the lesions of multiple sclerosis

Trapp, B. D., Peterson, J., Ransohoff, R. M., Rudick, R., Mörk, S., & Bö, L. (1998) · New England Journal of Medicine · doi:10.1056/nejm199801293380502 · Cited by 4,029 · see citing works

CNS stem cells express a new class of intermediate filament protein

Lendahl, U., Zimmerman, L. B., & McKay, R. D. G. (1990) · Cell · doi:10.1016/0092-8674(90)90662-x · Cited by 3,164 · see citing works

Degeneration and Regeneration of the Nervous System.

(1929) · JAMA · doi:10.1001/jama.1929.02710220063037 · Cited by 2,920 · see citing works

Cellular Composition and Three-Dimensional Organization of the Subventricular Germinal Zone in the Adult Mammalian Brain

Doetsch, F. K., García‐Verdugo, J. M., & Álvarez-Buylla, A. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-13-05046.1997 · Cited by 1,909 · see citing works

Identification of a Neural Stem Cell in the Adult Mammalian Central Nervous System

Johansson, C. B., Momma, S., Clarke, D. L., Risling, M., Lendahl, U., & Frisén, J. (1999) · Cell · doi:10.1016/s0092-8674(00)80956-3 · Cited by 1,875 · see citing works

Reactive astrocytes: cellular and molecular cues to biological function

Ridet, J., Privat, A., Malhotra, S. K., & Gage, F. H. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01139-9 · Cited by 1,766 · see citing works

Axonal Elongation into Peripheral Nervous System "Bridges" After Central Nervous System Injury in Adult Rats

David, S., & Aguayo, A. J. (1981) · Science · doi:10.1126/science.6171034 · Cited by 1,698 · see citing works

Axonal damage in acute multiple sclerosis lesions

Ferguson, B. (1997) · Brain · doi:10.1093/brain/120.3.393 · Cited by 1,532 · see citing works

Nogo-A is a myelin-associated neurite outgrowth inhibitor and an antigen for monoclonal antibody IN-1

Chen, M. S., Huber, A. B., van der Haar, M. E., Frank, M., Schnell, L., Spillmann, A. A., Christ, F., & Schwab, M. E. (2000) · Nature · doi:10.1038/35000219 · Cited by 1,445 · see citing works

MYELINATION IN RAT BRAIN: METHOD OF MYELIN ISOLATION¹

Norton, W. T., & Poduslo, S. E. (1973) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1973.tb07519.x · Cited by 1,413 · see citing works

Tumor necrosis factor mediates myelin and oligodendrocyte damage in vitro

Selmaj, K. W., & Raine, C. S. (1988) · Annals of Neurology · doi:10.1002/ana.410230405 · Cited by 1,357 · see citing works

Cell death and control of cell survival in the oligodendrocyte lineage

Barres, B. A., Hart, I. K., Coles, H. S. R., Burne, J. F., Voyvodic, J. T., Richardson, W. D., & Raff, M. C. (1992) · Cell · doi:10.1016/0092-8674(92)90531-g · Cited by 1,345 · see citing works

Proliferating subventricular zone cells in the adult mammalian forebrain can differentiate into neurons and glia.

Lois, C., & Álvarez-Buylla, A. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.5.2074 · Cited by 1,339 · see citing works

Notch Signaling

Artavanis‐Tsakonas, S., Matsuno, K., & Fortini, M. (1995) · Science · doi:10.1126/science.7716513 · Cited by 1,305 · see citing works

Multipotent CNS Stem Cells Are Present in the Adult Mammalian Spinal Cord and Ventricular Neuroaxis

Weiss, S., Dunne, C., Hewson, J., Wohl, C. A., Wheatley, M., Peterson, A. C., & Reynolds, B. A. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-23-07599.1996 · Cited by 1,219 · see citing works

Single factors direct the differentiation of stem cells from the fetal and adult central nervous system.Preprint

Johe, K. K., Hazel, T. G., Müller, T. H., Dugich‐Djordjevic, M. M., & McKay, R. D. G. (1996) · Genes & Development · doi:10.1101/gad.10.24.3129 · Cited by 1,154 · see citing works

Identification of the Nogo inhibitor of axon regeneration as a Reticulon protein

GrandPré, T., Nakamura, F., Vartanian, T. K., & Strittmatter, S. M. (2000) · Nature · doi:10.1038/35000226 · Cited by 1,139 · see citing works

Monoclonal antibodies (O1 to O4) to oligodendrocyte cell surfaces: An immunocytological study in the central nervous system

Sommer, I., & Schachner, M. (1981) · Developmental Biology · doi:10.1016/0012-1606(81)90477-2 · Cited by 1,136 · see citing works

Identification of myelin-associated glycoprotein as a major myelin-derived inhibitor of neurite growth

McKerracher, L. J., David, S., Jackson, D. L., Kottis, V., Dunn, R. J., & Braun, P. E. (1994) · Neuron · doi:10.1016/0896-6273(94)90247-x · Cited by 1,125 · see citing works

Degeneration and regeneration of axons in the lesioned spinal cord

Schwab, M. E., & Bartholdi, D. (1996) · Physiological Reviews · doi:10.1152/physrev.1996.76.2.319 · Cited by 1,124 · see citing works

A theory of the effects of fibre size in medullated nerve

Rushton, W. A. H. (1951) · The Journal of Physiology · doi:10.1113/jphysiol.1951.sp004655 · Cited by 1,075 · see citing works

Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease

Bergoffen, J., Scherer, S. S., Wang, S., Scott, M. O., Bone, L. J., Paul, D. L., CHEN, K., Lensch, M. W., Chance, P. F., & Fischbeck, K. H. (1993) · Science · doi:10.1126/science.8266101 · Cited by 1,064 · see citing works

A novel role for myelin-associated glycoprotein as an inhibitor of axonal regeneration

Mukhopadhyay, G., Doherty, P., Walsh, F. S., Crocker, P. R., & Filbin, M. T. (1994) · Neuron · doi:10.1016/0896-6273(94)90042-6 · Cited by 1,061 · see citing works

Embryonic Stem Cell-Derived Glial Precursors: A Source of Myelinating Transplants

Brüstle, O., Jones, K. N., Learish, R. D., Karram, K., Choudhary, K., Wiestler, O. D., Duncan, I. D., & McKay, R. D. G. (1999) · Science · doi:10.1126/science.285.5428.754 · Cited by 976 · see citing works

Monoclonal antibody to a plasma membrane antigen of neurons.

Eisenbarth, G. S., Walsh, F. S., & Nirenberg, M. W. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.10.4913 · Cited by 969 · see citing works

Axons from CNS neurones regenerate into PNS grafts

Richardson, P. M., Mcguinness, U. M., & Aguayo, A. J. (1980) · Nature · doi:10.1038/284264a0 · Cited by 938 · see citing works

Antibody against myelin associated inhibitor of neurite growth neutralizes nonpermissive substrate properties of CNS white matter

Caroni, P., & Schwab, M. E. (1988) · Neuron · doi:10.1016/0896-6273(88)90212-7 · Cited by 892 · see citing works

Identification of autoantibodies associated with myelin damage in multiple sclerosis

Genain, C. P., Cannella, B., Hauser, S. L., & Raine, C. S. (1999) · Nature Medicine · doi:10.1038/5532 · Cited by 891 · see citing works

Axonal Swellings and Degeneration in Mice Lacking the Major Proteolipid of Myelin

Griffiths, I., Klugmann, M., Anderson, T., Yool, D., Thomson, C., Schwab, M. H., Schneider, A., Zimmermann, F., McCulloch, M., Nadon, N., et al. (1998) · Science · doi:10.1126/science.280.5369.1610 · Cited by 889 · see citing works

Two membrane protein fractions from rat central myelin with inhibitory properties for neurite growth and fibroblast spreading.

Caroni, P., & Schwab, M. E. (1988) · The Journal of Cell Biology · doi:10.1083/jcb.106.4.1281 · Cited by 880 · see citing works

Glutamate excitotoxicity in a model of multiple sclerosis

Pitt, D., Werner, P., & Raine, C. S. (2000) · Nature Medicine · doi:10.1038/71555 · Cited by 855 · see citing works

The oligodendrocyte and its many cellular processes

Pfeiffer, S. E., Warrington, A. E., & Bansal, R. (1993) · Trends in Cell Biology · doi:10.1016/0962-8924(93)90213-k · Cited by 852 · see citing works

Development of oligodendrocytes and Schwann cells studied with a monoclonal antibody against galactocerebroside.

Ranscht, B., Clapshaw, P. A., Price, J., Noble, M., & Seifert, W. E. (1982) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.79.8.2709 · Cited by 834 · see citing works

Galactocerebroside is a specific cell-surface antigenic marker for oligodendrocytes in culture

RAFF, M. C., Mirsky, R., Fields, K. L., Lisak, R. P., Dorfman, S. H., Silberberg, D. H., Gregson, N. A., Leibowitz, S., & KENNEDY, M. C. (1978) · Nature · doi:10.1038/274813a0 · Cited by 808 · see citing works

Cell-type-specific markers for distinguishing and studying neurons and the major classes of glial cells in culture

RAFF, M. C., Fields, K. L., Hakomori, S., Mirsky, R., Pruss, R. M., & Winter, J. (1979) · Brain Research · doi:10.1016/0006-8993(79)90851-5 · Cited by 800 · see citing works

Organization of projections from the basomedial nucleus of the amygdala: A PHAL study in the rat

Petrovich, G., Risold, P., & Swanson, L. (1996) · The Journal of comparative neurology · doi:10.1002/(sici)1096-9861(19961021)374:3 · Cited by 793 · see citing works

Identification of major cell classes in the developing mammalian nervous system

Hockfield, S. J., & McKay, R. D. G. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-12-03310.1985 · Cited by 792 · see citing works

PROTEOLIPIDES, A NEW TYPE OF TISSUE LIPOPROTEINS

Folch, J., & Lees, M. B. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)55985-8 · Cited by 782 · see citing works

A role for platelet-derived growth factor in normal gliogenesis in the central nervous system

Richardson, W. D., Pringle, N. P., Mosley, M. J., Westermark, B., & Dubois-Dalcg, M. (1988) · Cell · doi:10.1016/0092-8674(88)90392-3 · Cited by 774 · see citing works

Platelet-derived growth factor from astrocytes drives the clock that times oligodendrocyte development in culture

RAFF, M. C., Lillien, L. E., Richardson, W. D., Burne, J. F., & Noble, M. (1988) · Nature · doi:10.1038/333562a0 · Cited by 761 · see citing works

In vivo growth factor expansion of endogenous subependymal neural precursor cell populations in the adult mouse brain

Craig, C., Tropepe, V., Morshead, C., Reynolds, B. A., Weiss, S., & van der Kooy, D. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-08-02649.1996 · Cited by 752 · see citing works

Regeneration of adult axons in white matter tracts of the central nervous system

Davies, S. J. A., Fitch, M. T., Memberg, S. P., Hall, A. K., Raisman, G., & Silver, J. (1997) · Nature · doi:10.1038/37776 · Cited by 737 · see citing works

Distinct Patterns of Multiple Sclerosis Pathology Indicates Heterogeneity in Pathogenesis

Lucchinetti, C. F., Brück, W., Rodriguez, M., & Lassmann, H. (1996) · Brain Pathology · doi:10.1111/j.1750-3639.1996.tb00854.x · Cited by 733 · see citing works

Both oligodendrocytes and astrocytes develop from progenitors in the subventricular zone of postnatal rat forebrain

Levison, S. W., & Goldman, J. E. (1993) · Neuron · doi:10.1016/0896-6273(93)90311-e · Cited by 725 · see citing works

Identification of a multipotent astrocytic stem cell in the immature and adult mouse brain

Laywell, E. D., RAKIC, P. T., Kukekov, V. G., Holland, E. C., & Steindler, D. A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.250471697 · Cited by 722 · see citing works

Multiple extracellular signals are required for long-term oligodendrocyte survival

Barres, B. A., Schmid, R., Sendnter, M., & Raff, M. C. (1993) · Development · doi:10.1242/dev.118.1.283 · Cited by 712 · see citing works

Augmentation of demyelination in rat acute allergic encephalomyelitis by circulating mouse monoclonal antibodies directed against a myelin/oligodendrocyte glycoprotein.

Linington, C., Bradl, M., Lassmann, H., Brunner, C., & Vass, K. (1988) · PubMed Central · Cited by 711 · see citing works

Long-Distance Axonal Regeneration in the Transected Adult Rat Spinal Cord Is Promoted by Olfactory Ensheathing Glia Transplants

Ramón‐Cueto, A., Plant, G. W., Ávila, J., & Bunge, M. B. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03803.1998 · Cited by 710 · see citing works

Notch Receptor Activation Inhibits Oligodendrocyte Differentiation

Wang, S., Sdrulla, A. D., diSibio, G., Bush, G., Nofziger, D., Hicks, C. D., Weinmaster, G., & Barres, B. A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80515-2 · Cited by 706 · see citing works

CNS Myelin and Sertoli Cell Tight Junction Strands Are Absent in Osp/Claudin-11 Null Mice

Gow, A., Southwood, C. M., Li, J. S., Pariali, M., Riordan, G. P., Brodie, S. E., Danias, J., Bronstein, J. M., Kachar, B., & Lazzarini, R. A. (1999) · Cell · doi:10.1016/s0092-8674(00)81553-6 · Cited by 699 · see citing works

Bone Morphogenetic Proteins Promote Astroglial Lineage Commitment by Mammalian Subventricular Zone Progenitor Cells

Gross, R. E., Mehler, M. F., Mabie, P. C., Zang, Z., Santschi, L. A., & Kessler, J. A. (1996) · Neuron · doi:10.1016/s0896-6273(00)80193-2 · Cited by 696 · see citing works

Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

Brenner, M., Johnson, T., Boespflug‐Tanguy, O., Rodriguez, D., Goldman, J. E., & Messing, A. (2001) · Nature Genetics · doi:10.1038/83679 · Cited by 689 · see citing works

Induction of myelination in the central nervous system by electrical activity

Demerens, C., Stankoff, B., Logak, M., Anglade, P., Allinquant, B., Couraud, F., Zalc, B., & Lubetzki, C. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.18.9887 · Cited by 678 · see citing works

Proliferation of oligodendrocyte precursor cells depends on electrical activity in axons

Barres, B. A., & Raff, M. C. (1993) · Nature · doi:10.1038/361258a0 · Cited by 673 · see citing works

MYELINATION IN RAT BRAIN: CHANGES IN MYELIN COMPOSITION DURING BRAIN MATURATION1

Norton, W. T., & Poduslo, S. E. (1973) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1973.tb07520.x · Cited by 668 · see citing works

Igf1 gene disruption results in reduced brain size, CNS hypomyelination, and loss of hippocampal granule and striatal parvalbumin-containing neurons

Beck, K. D., Powell-Braxtont, L., Widmer, H.-R., Valverde, J., & Hefti, F. (1995) · Neuron · doi:10.1016/0896-6273(95)90216-3 · Cited by 636 · see citing works

Matrix metalloproteinases and diseases of the CNS

Yong, V. W., Forsyth, P. A., Bell, R. B., Krekoski, C. A., & Edwards, D. R. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01169-7 · Cited by 635 · see citing works

Myelination in the Absence of Galactocerebroside and Sulfatide: Normal Structure with Abnormal Function and Regional Instability

Coetzee, T., Fujita, N., Dupree, J. L., Shi, R., Blight, A. R., Suzuki, K., Suzuki, K., & Popko, B. (1996) · Cell · doi:10.1016/s0092-8674(00)80093-8 · Cited by 624 · see citing works

Mutant Mice (Quaking and Jimpy) with Deficient Myelination in the Central Nervous System

Sidman, R. L., Dickie, M. M., & Appel, S. H. (1964) · Science · doi:10.1126/science.144.3616.309 · Cited by 603 · see citing works

FGF modulates the PDGF-driven pathway of oligodendrocyte development

McKinnon, R. D., Matsui, T., Dubois-Dalcq, M. E., & Aaronsont, S. A. (1990) · Neuron · doi:10.1016/0896-6273(90)90215-2 · Cited by 596 · see citing works

Molecular mimicry and immune‐mediated diseases

Oldstone, M. B. A. (1998) · The FASEB Journal · doi:10.1096/fasebj.12.13.1255 · Cited by 594 · see citing works

A novel role for thyroid hormone, glucocorticoids and retinoic acid in timing oligodendrocyte development

Barrès, A., Lazar, M. A., & RAFF, M. C. (1994) · Development · doi:10.1242/dev.120.5.1097 · Cited by 593 · see citing works

Neurotrophin-3 and Brain-Derived Neurotrophic Factor Induce Oligodendrocyte Proliferation and Myelination of Regenerating Axons in the Contused Adult Rat Spinal Cord

McTigue, D. M., Horner, P. J., Stokes, B. T., & Gage, F. H. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-14-05354.1998 · Cited by 592 · see citing works

GD3, a prominent ganglioside of human melanoma. Detection and characterisation by mouse monoclonal antibody.

Pukel, C., Lloyd, K. O., Travassos, L. R., et al. (1982) · The Journal of Experimental Medicine · doi:10.1084/jem.155.4.1133 · Cited by 579 · see citing works

Cooperation between two growth factors promotes extended self-renewal and inhibits differentiation of oligodendrocyte-type-2 astrocyte (O-2A) progenitor cells.

Bögler, O., Wren, D. R., Barnett, S. C., Land, H., & Noble, M. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.16.6368 · Cited by 577 · see citing works

Multiple sclerosis: Remyelination of nascent lesions: Remyelination of nascent lesions

Prineas, J. W., Barnard, R. O., Kwon, E. E., Sharer, L. R., & Cho, E. ‐. (1993) · Annals of Neurology · doi:10.1002/ana.410330203 · Cited by 574 · see citing works

Autoimmunity to Myelin Oligodendrocyte Glycoprotein in Rats Mimics the Spectrum of Multiple Sclerosis Pathology

Storch, M., Stefferl, A., Brehm, U., Weissert, R., Wallström, E., Kerschensteiner, M., Olsson, T., Linington, C., & Lassmann, H. (1998) · Brain Pathology · doi:10.1111/j.1750-3639.1998.tb00194.x · Cited by 566 · see citing works

Cell lineage in the cerebral cortex of the mouse studied in vivo and in vitro with a recombinant retrovirus.

Luskin, M. B., Pearlman, A., & Sanes, J. (1988) · Neuron · doi:10.1016/0896-6273(88)90163-8 · Cited by 554 · see citing works

αB-crystallin is expressed in non-lenticular tissues and accumulates in Alexander's disease brain

Iwaki, T., Kume-Iwaki, A., Liem, R. K. H., & Goldman, J. E. (1989) · Cell · doi:10.1016/0092-8674(89)90173-6 · Cited by 549 · see citing works

Oligodendrocytes from forebrain are highly vulnerable to AMPA/kainate receptor-mediated excitotoxicity

McDonald, J. W., Althomsons, S. P., Hyrc, K. L., Choi, D. W., & Goldberg, M. P. (1998) · Nature Medicine · doi:10.1038/nm0398-291 · Cited by 545 · see citing works

Endogenous progenitors remyelinate demyelinated axons in the adult CNS

Gensert, J. M., & Goldman, J. E. (1997) · Neuron · doi:10.1016/s0896-6273(00)80359-1 · Cited by 544 · see citing works

Glial cells and the central myelin sheath.

Bunge, R. P. (1968) · Physiological Reviews · doi:10.1152/physrev.1968.48.1.197 · Cited by 539 · see citing works

GFAP Is Necessary for the Integrity of CNS White Matter Architecture and Long-Term Maintenance of Myelination

(1996) · doi:10.1016/s0896-6273(00)80194-4 · Cited by 538 · see citing works

Polysialic acid in the vertebrate nervous system: a promoter of plasticity in cell-cell interactions

Rutishauser, U. S. (1996) · Trends in Neurosciences · doi:10.1016/0166-2236(96)10041-2 · Cited by 515 · see citing works

A singularity of PDGF alpha-receptor expression in the dorsoventral axis of the neural tube may define the origin of the oligodendrocyte lineage

Pringle, N. P., & Richardson, W. D. (1993) · Development · doi:10.1242/dev.117.2.525 · Cited by 510 · see citing works

Vulnerability of oligodendroglia to glutamate: pharmacology, mechanisms, and prevention

Oka, A., Belliveau, M. J., Rosenberg, P. A., & Volpe, J. J. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-04-01441.1993 · Cited by 504 · see citing works

Specific Expression of N‐Acetylaspartate in Neurons, Oligodendrocyte‐Type‐2 Astrocyte Progenitors, and Immature Oligodendrocytes In Vitro

Urenjak, J., Williams, S. R., Gadian, D. G., & Noble, M. (1992) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1992.tb08875.x · Cited by 503 · see citing works

Oligodendrocyte Population Dynamics and the Role of PDGF In Vivo

Calver, A. R., Hall, A. C., Yu, W., Walsh, F. S., Heath, J. K., Betsholtz, C., & Richardson, W. D. (1998) · Neuron · doi:10.1016/s0896-6273(00)80469-9 · Cited by 501 · see citing works

Gap junctions in the brain: where, what type, how many and why?

Dermietzel, R., & Spray, D. C. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90151-b · Cited by 501 · see citing works

Myelin-Associated Glycoprotein Is a Myelin Signal that Modulates the Caliber of Myelinated Axons

Yin, X., Crawford, T. O., Griffin, J. W., Tu, P., Lee, V. M. ‐., Li, C. C., Roder, J., & Trapp, B. D. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-06-01953.1998 · Cited by 491 · see citing works

Ankyrin

Kordeli, E., Lambert, S., & Bennett, V. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.5.2352 · Cited by 489 · see citing works

Adrenoleukodystrophy: phenotype, genetics, pathogenesis and therapy

Moser, H. (1997) · Brain · doi:10.1093/brain/120.8.1485 · Cited by 478 · see citing works

Evidence for migration of oligodendrocyte–type-2 astrocyte progenitor cells into the developing rat optic nerve

Small, R. K., Riddle, P. N., & Noble, M. A. (1987) · Nature · doi:10.1038/328155a0 · Cited by 474 · see citing works

Insulin-like growth factor I increases brain growth and central nervous system myelination in tTransgenic mice

Carson, M. J., Behringer, R. R., Brinster, R. L., & McMorris, F. A. (1993) · Neuron · doi:10.1016/0896-6273(93)90173-o · Cited by 474 · see citing works

Assembly of CNS Myelin in the Absence of Proteolipid Protein

Klugmann, M., Schwab, M. H., Pühlhofer, A., Schneider, A., Zimmermann, F., Griffiths, I. R., & Nave, K. (1997) · Neuron · doi:10.1016/s0896-6273(01)80046-5 · Cited by 472 · see citing works

Immunogold evidence suggests that coupling of K+ siphoning and water transport in rat retinal M�ller cells is mediated by a coenrichment of Kir4.1 and AQP4 in specific membrane domains

Nagelhus, E. A., Horio, Y., Inanobe, A., Fujita, A., Haug, F. Š., Nielsen, S., Kurachi, Y., & Ottersen, O. P. (1999) · Glia · doi:10.1002/(sici)1098-1136(199903)26:1 · Cited by 472 · see citing works

Electron microscopic identification of three classes of oligodendrocytes and a preliminary study of their proliferative activity in the corpus callosum of young rats

Mori, S., & Leblond, C. P. (1970) · The Journal of Comparative Neurology · doi:10.1002/cne.901390102 · Cited by 466 · see citing works

A quantitative analysis of oligodendrocytes in multiple sclerosis lesions

Lucchinetti, C., Brück, W., Parisi, J., Scheithauer, B., Rodriguez, M., & Lassmann, H. (1999) · Brain · doi:10.1093/brain/122.12.2279 · Cited by 464 · see citing works

Clonal analysis of oligodendrocyte development in culture: Evidence for a developmental clock that counts cell divisions

Temple, S., & RAFF, M. C. (1986) · Cell · doi:10.1016/0092-8674(86)90843-3 · Cited by 455 · see citing works

FGF2 Concentration Regulates the Generation of Neurons and Glia from Multipotent Cortical Stem Cells

Qian, X., Davis, A. A., Goderie, S. K., & Temple, S. (1997) · Neuron · doi:10.1016/s0896-6273(01)80048-9 · Cited by 454 · see citing works

glial cells missing: a genetic switch that controls glial versus neuronal fate

Jones, B. W., Fetter, R. D., Tear, G., & Goodman, C. S. (1995) · Cell · doi:10.1016/0092-8674(95)90280-5 · Cited by 450 · see citing works

Claudin-11/OSP-based Tight Junctions of Myelin Sheaths in Brain and Sertoli Cells in Testis

Morita, K., Sasaki, H., Fujimoto, K., Furuse, M., & Tsukita, S. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.145.3.579 · Cited by 444 · see citing works

Defective oligodendrocyte development and severe hypomyelination in PDGF-A knockout mice

Fruttiger, M., Karlsson, L. K., Hall, A. C., Abramsson, A., Calver, A. R., Boström, H., Willetts, K. E., Bertold, C.-H., Heath, J. K., Betsholtz, C., et al. (1999) · Development · doi:10.1242/dev.126.3.457 · Cited by 440 · see citing works

Structure of sulfated glucuronyl glycolipids in the nervous system reacting with HNK-1 antibody and some IgM paraproteins in neuropathy.

Chou, D. K. H., Ilyas, A. A., Evans, J. E., et al. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)67303-x · Cited by 437 · see citing works

Recognition of myelin-associated glycoprotein by the monoclonal antibody HNK-1

McGarry, R. C., Helfand, S. L., Quarles, R. H., & Roder, J. (1983) · Nature · doi:10.1038/306376a0 · Cited by 430 · see citing works

Cell lineage in the rat cerebral cortex: a study using retroviral-mediated gene transfer

Price, J., & Thurlow, L. (1988) · Development · doi:10.1242/dev.104.3.473 · Cited by 424 · see citing works

Glial cells missing: A binary switch between neuronal and glial determination in drosophila

Hosoya, T., Takizawa, K., Nitta, K., & Hotta, Y. (1995) · Cell · doi:10.1016/0092-8674(95)90281-3 · Cited by 424 · see citing works

Synthesis and incorporation of myelin polypeptides into CNS myelin.

Colman, D., Kreibich, G., Frey, A. B., & Sabatini, D. D. (1982) · The Journal of Cell Biology · doi:10.1083/jcb.95.2.598 · Cited by 424 · see citing works

Multiple and novel specificities of monoclonal antibodies O1, O4, and R‐mAb used in the analysis of oligodendrocyte development

Bansal, R., Warrington, A. E., Gard, A. L., Ranscht, B., & Pfeiffer, S. E. (1989) · Journal of Neuroscience Research · doi:10.1002/jnr.490240413 · Cited by 418 · see citing works

CG‐4, A new bipotential glial cell line from rat brain, is capable of differentiating in vitro into either mature oligodendrocytes or type‐2 astrocytes

Louis, J., Magal, E., Muir, D., Manthorpe, M., & Varon, S. S. (1992) · Journal of Neuroscience Research · doi:10.1002/jnr.490310125 · Cited by 414 · see citing works

Dissociated neurons regenerate into sciatic but not optic nerve explants in culture irrespective of neurotrophic factors

Schwab, M. E., & Thoenen, H. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-09-02415.1985 · Cited by 413 · see citing works

Connexin32 is a myelin-related protein in the PNS and CNS

Scherer, S., Deschênes, S. M., Xu, Y., Grinspan, J. B., Fischbeck, K. H., & Paul, D. L. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-12-08281.1995 · Cited by 410 · see citing works

Differential Ultrastructural Localization of Myelin Basic Protein, Myelin/Oligodendroglial Glycoprotein, and 2′,3′‐Cyclic Nucleotide 3′‐Phosphodiesterase in the CNS of Adult Rats

Brunner, C., Lassmann, H., Waehneldt, T. V., Matthieu, J., & Linington, C. (1989) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1989.tb10930.x · Cited by 409 · see citing works

Oligodendrocyte progenitor cell proliferation and lineage progression are regulated by glutamate receptor-mediated K+ channel block

Gallo, V., Jm, Z., McBain, C. J., Wright, P., Knutson, P. L., & Armstrong, R. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-08-02659.1996 · Cited by 406 · see citing works

The small heat-shock protein αB-crystallin as candidate autoantigen in multiple sclerosis

van Noort, J. M., van Sechel, A. C., Bajramovic, J. J., Ouagmiri, M. E., Polman, C. H., Lassmann, H., & Ravid, R. (1995) · Nature · doi:10.1038/375798a0 · Cited by 402 · see citing works

“Global” cell replacement is feasible via neural stem cell transplantation: Evidence from the dysmyelinated shiverer mouse brain

Yandava, B. D., Billinghurst, L. L., & Snyder, E. Y. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.12.7029 · Cited by 399 · see citing works

Expression of a myelin basic protein gene in transgenic shiverer mice: Correction of the dysmyelinating phenotype

Readhead, C. W., Popko, B., Takahashi, N., Shine, H. D., Saavedra, R. A., Sidman, R. L., & Hood, L. (1987) · Cell · doi:10.1016/0092-8674(87)90248-0 · Cited by 397 · see citing works

ULTRASTRUCTURAL STUDY OF REMYELINATION IN AN EXPERIMENTAL LESION IN ADULT CAT SPINAL CORD

Bunge, M. B., Bunge, R. P., & Ris, H. (1961) · The Journal of Cell Biology · doi:10.1083/jcb.10.1.67 · Cited by 397 · see citing works

Differentiation and death of premyelinating oligodendrocytes in developing rodent brain

Trapp, B. D., Nishiyama, A., Cheng, D., & Macklin, W. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.137.2.459 · Cited by 395 · see citing works

Shaping of the autoreactive T-cell repertoire by a splice variant of self protein expressed in thymic epithelial cells

Klein, L., Klugmann, M., Nave, K., Tuohy, V. K., & Kyewski, B. (2000) · Nature Medicine · doi:10.1038/71540 · Cited by 392 · see citing works

A new leukoencephalopathy with vanishing white matter

van der Knaap, M. S., Barth, P. G., Gabreëls, F. J. M., Franzonı, E., Begeer, J. H., Stroink, H., Rotteveel, J. J., & Valk, J. (1997) · Neurology · doi:10.1212/wnl.48.4.845 · Cited by 389 · see citing works

Initial events of myelination involve Fyn tyrosine kinase signalling

Umemori, H., Satot, S., Yagi, T., Aizawal, S., & Yamamoto, T. S. (1994) · Nature · doi:10.1038/367572a0 · Cited by 387 · see citing works

Control of oligodendrocyte number in the developing rat optic nerve

Barres, B. A., & RAFF, M. C. (1994) · Neuron · doi:10.1016/0896-6273(94)90305-0 · Cited by 385 · see citing works

Neurite growth inhibitors restrict plasticity and functional recovery following corticospinal tract lesions

Thallmair, M., Metz, G. A. S., Z'Graggen, W. J., Raineteau, O., Kartje, G. L., & Schwab, M. E. (1998) · Nature Neuroscience · doi:10.1038/373 · Cited by 382 · see citing works

Identification of epitopes of myelin oligodendrocyte glycoprotein for the induction of experimental allergic encephalomyelitis in SJL and Biozzi AB/H mice.

Amor, S., Groome, N. P., Linington, C., Morris, M. M., Dornmair, K., Gardinier, M. V., Matthieu, J., & Baker, D. (1994) · The Journal of Immunology · doi:10.4049/jimmunol.153.10.4349 · Cited by 381 · see citing works

Persistent functional deficit in multiple sclerosis and autosomal dominant cerebellar ataxia is associated with axon loss.

Davie, C., Barker, G., Webb, S., Tofts, P., Thompson, A. J., Harding, A., Mcdonald, W., & Miller, D. (1995) · Brain : a journal of neurology · doi:10.1093/brain/118.6.1583 · Cited by 381 · see citing works

Myelination in the absence of myelin-associated glycoprotein

Li, C. C., Tropak, M. B., Gerlai, R. T., Clapoff, S., Abramow-Newerly, W., Trapp, B. D., Peterson, A. C., & Roder, J. (1994) · Nature · doi:10.1038/369747a0 · Cited by 380 · see citing works

Characterization of cloned cDNA representing rat myelin basic protein: Absence of expression in brain of shiverer mutant mice

Roach, A., Boylan, K., Horvath, S. J., Prusiner, S. B., & Hood, L. (1983) · Cell · doi:10.1016/0092-8674(83)90536-6 · Cited by 379 · see citing works

Mice deficient for the glycoprotein show subtle abnormalities in myelin

Montag, D., Giese, K.-P., Bartsch, U., Martini, R., Lang, Y., Blüthmann, H., Karthigasan, J., Kirschner, D. A., Wintergerst, E. S., Nave, K., et al. (1994) · Neuron · doi:10.1016/0896-6273(94)90472-3 · Cited by 377 · see citing works

Myelinated nerve fibres in the CNS

Hildebrand, C., Remahl, S., Persson, H., & Bjartmar, C. (1993) · Progress in Neurobiology · doi:10.1016/0301-0082(93)90015-k · Cited by 376 · see citing works

GGF/Neuregulin Is a Neuronal Signal That Promotes the Proliferation and Survival and Inhibits the Differentiation of Oligodendrocyte Progenitors

Canoll, P., Musacchio, J. M., Hardy, R., Reynolds, R., Marchionni, M. A., & Salzer, J. L. (1996) · Neuron · doi:10.1016/s0896-6273(00)80155-5 · Cited by 374 · see citing works

The amino acid sequences of the myelin-associated glycoproteins: homology to the immunoglobulin gene superfamily

Salzer, J. L., Holmes, W., & Colman, D. (1987) · The Journal of Cell Biology · doi:10.1083/jcb.104.4.957 · Cited by 371 · see citing works

The axonal membrane protein Caspr, a homologue of neurexin IV, is a component of the septate-like paranodal junctions that assemble during myelination

Einheber, S., Zanazzi, G., Ching, W., Scherer, S., Milner, T. A., Peles, E., & Salzer, J. L. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.139.6.1495 · Cited by 369 · see citing works

Insulin‐like growth factor I promotes cell proliferation and oligodendroglial commitment in rat glial progenitor cells developing in vitro

McMorris, F. A., & Dubois-Dalcq, M. E. (1988) · Journal of Neuroscience Research · doi:10.1002/jnr.490210212 · Cited by 366 · see citing works

PDGF A-chain gene is expressed by mammalian neurons during development and in maturity

Yeh, H.-J., Ruit, K. G., Wang, Y.-X., Parks, W. C., Snider, W. D., & Deuel, T. F. (1991) · Cell · doi:10.1016/0092-8674(91)90222-k · Cited by 364 · see citing works

Electron microscopic autoradiographic studies of gliogenesis in rat optic nerve I. Cell proliferation

Skoff, R. P., Price, D. L., & Stocks, A. (1976) · The Journal of Comparative Neurology · doi:10.1002/cne.901690303 · Cited by 362 · see citing works

Axonal Control of Oligodendrocyte Development

Barres, B. A., & Raff, M. C. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.147.6.1123 · Cited by 360 · see citing works

A crucial role for neurotrophin-3 in oligodendrocyte development

Barres, B. A., RAFF, M. C., Gaese, F., Bartke, I., Dechant, G., & Barde, Y. (1994) · Nature · doi:10.1038/367371a0 · Cited by 357 · see citing works

Axonal changes in chronic demyelinated cervical spinal cord plaques

Lovas, G., Szilágyi, N., Majtényi, K., Palkovits, M., & Komoly, S. (2000) · Brain · doi:10.1093/brain/123.2.308 · Cited by 356 · see citing works

Basic A1 Protein of the Myelin Membrane

EYLAR, E. H., Brostoff, S. W., Hashim, G. A., et al. (1971) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)61872-1 · Cited by 352 · see citing works

Functional breakdown of the lipid bilayer of the myelin membrane in central and peripheral nervous system by disrupted galactocerebroside synthesis

Bosio, A., Binczek, E., & Stoffel, W. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.23.13280 · Cited by 347 · see citing works

Molecular composition of the node of Ranvier: identification of ankyrin-binding cell adhesion molecules neurofascin (mucin+/third FNIII domain-) and NrCAM at nodal axon segments.

Davis, J. Q., Lambert, S., & Bennett, V. (1996) · The Journal of Cell Biology · doi:10.1083/jcb.135.5.1355 · Cited by 347 · see citing works

Emergence of three myelin proteins in oligodendrocytes cultured without neurons.

Dubois-Dalcq, M. E., Behar, T. N., Hudson, L. D., & Lazzarini, R. A. (1986) · The Journal of Cell Biology · doi:10.1083/jcb.102.2.384 · Cited by 342 · see citing works

The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteins

Ebersole, T. A., Chen, Q., Justice, M. J., & Artzt, K. (1996) · Nature Genetics · doi:10.1038/ng0396-260 · Cited by 340 · see citing works

Transplanted Olfactory Ensheathing Cells Remyelinate and Enhance Axonal Conduction in the Demyelinated Dorsal Columns of the Rat Spinal Cord

Imaizumi, T., Lankford, K. L., Waxman, S. G., Greer, C. A., & Kocsis, J. D. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-16-06176.1998 · Cited by 336 · see citing works

Myelin-associated glycoprotein, a member of the L2/HNK-1 family of neural cell adhesion molecules, is involved in neuron-oligodendrocyte and oligodendrocyte-oligodendrocyte interaction.

Półtorak, M., Sadoul, R., Keilhauer, G., Landa, C., Fahrig, T., & Schachner, M. (1987) · The Journal of Cell Biology · doi:10.1083/jcb.105.4.1893 · Cited by 336 · see citing works

Chromosomal mapping of mouse myelin basic protein gene and structure and transcription of the partially deleted gene in shiverer mutant mice

ROACH, A., TAKAHASHI, N., PRAVTCHEVA, D., RUDDLE, F., & HOOD, L. (1985) · Cell · doi:10.1016/s0092-8674(85)80110-0 · Cited by 336 · see citing works

Cerebral white matter changes in acquired immunodeficiency syndrome dementia: Alterations of the blood‐brain barrier

Power, C., Kong, P., Crawford, T. O., Wesselingh, S. L., Glass, J. D., McArthur, J. C., & Trapp, B. D. (1993) · Annals of Neurology · doi:10.1002/ana.410340307 · Cited by 335 · see citing works

News on glutamate receptors in glial cells

Steinhäuser, C., & Gallo, V. (1996) · Trends in Neurosciences · doi:10.1016/0166-2236(96)10043-6 · Cited by 334 · see citing works

Induction of sodium channel clustering by oligodendrocytes

Kaplan, M. R., Meyer‐Franke, A., Lambert, S., Bennett, V., Duncan, I. D., Levinson, S. R., & Barres, B. A. (1997) · Nature · doi:10.1038/386724a0 · Cited by 332 · see citing works

Transport and Localization Elements in Myelin Basic Protein mRNA

Ainger, K. J., Avossa, D., Diana, A. S., Barry, C. T., Barbarese, E., & Carson, J. H. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.138.5.1077 · Cited by 323 · see citing works

A novel myelin-associated glycoprotein defined by a mouse monoclonal antibody

Linington, C., Webb, M. H., & Woodhams, P. L. (1984) · Journal of Neuroimmunology · doi:10.1016/0165-5728(84)90064-x · Cited by 323 · see citing works

Rapid Ischemic Cell Death in Immature Oligodendrocytes: A Fatal Glutamate Release Feedback Loop

Fern, R. F., & Möller, T. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-01-00034.2000 · Cited by 321 · see citing works

Late Complications of Immune Deviation Therapy in a Nonhuman Primate

Genain, C. P., Abel, K., Belmar, N. A., Villinger, F. J., Rosenberg, D. P., Linington, C., Raine, C. S., & Hauser, S. L. (1996) · Science · doi:10.1126/science.274.5295.2054 · Cited by 320 · see citing works

Absence of the major dense line in myelin of the mutant mouse ‘shiverer’

Privat, A., Jacque, C., Bourre, J. M., Dupouey, P., & Baumann, N. (1979) · Neuroscience Letters · doi:10.1016/0304-3940(79)91489-7 · Cited by 308 · see citing works

Alternative splicing accounts for the four forms of myelin basic protein

de Ferra, F., Engh, H., Hudson, L. D., Kamholz, J. A., Robinson, C. P., Molineaux, S. M., & Lazzarini, R. A. (1985) · Cell · doi:10.1016/0092-8674(85)90245-4 · Cited by 303 · see citing works

Oligodendrocytes originate in a restricted zone of the embryonic ventral neural tube defined by DM-20 mRNA expression

Timsit, S., Martı́nez, S., Allinquant, B., Peyron, F., Puelles, L., & Zalc, B. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-02-01012.1995 · Cited by 302 · see citing works

Splice site selection in the proteolipid protein (PLP) gene transcript and primary structure of the DM-20 protein of central nervous system myelin.

Nave, K., Lai, C., Bloom, F. E., & Milner, R. J. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.16.5665 · Cited by 302 · see citing works

Multiple Restricted Origin of Oligodendrocytes

Spassky, N., Goujet‐Zalc, C., Parmantier, E., Olivier, C., Martı́nez, S., Ivanova, A., Ikenaka, K., Macklin, W., Cerruti, I., Zalc, B., et al. (1998) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(98)91253-x · Cited by 301 · see citing works

NG2+ Glial Cells: A Novel Glial Cell Population in the Adult Brain

Nishiyama, A., Chang, A., & Trapp, B. D. (1999) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-199911000-00001 · Cited by 297 · see citing works

Untitled work

(1978) · PubMed · Cited by 297 · see citing works

Gangliosides are neuronal ligands for myelin-associated glycoprotein.

Yang, L. J., Zeller, C. B., Shaper, N. L., Kiso, M., Hasegawa, A., Shapiro, R. E., & Schnaar, R. L. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.2.814 · Cited by 295 · see citing works

Matrix metalloproteinases degrade myelin basic protein

Chandler, S., Coates, R. E., Gearing, A. J. H., Lury, J., Wells, G., & Bone, E. A. (1995) · Neuroscience Letters · doi:10.1016/0304-3940(95)12173-0 · Cited by 294 · see citing works

A mouse model for X-linked adrenoleukodystrophy

Lu, J.-F., Lawler, A. M., Watkins, P. A., Powers, J. M., Moser, A. B., Moser, H. W., & Smith, K. D. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.17.9366 · Cited by 293 · see citing works

Matrix Metalloproteinases in the Normal Human Central Nervous System, Microglial Nodules, and Multiple Sclerosis Lesions

Maeda, A., & Sobel, R. A. (1996) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-199603000-00005 · Cited by 293 · see citing works

Oligodendrocyte progenitors are present in the normal adult human CNS and in the lesions of multiple sclerosis

Scolding, N. J. (1998) · Brain · doi:10.1093/brain/121.12.2221 · Cited by 293 · see citing works

Multiple Sclerosis: Remyelination in Acute Lesions

Raine, C. S., & WU, E. (1993) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/00005072-199305000-00003 · Cited by 285 · see citing works

Oligodendrocytes arrest neurite growth by contact inhibition

Bandtlow, C. E., Zachleder, T., & Schwab, M. E. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-12-03837.1990 · Cited by 283 · see citing works

Twenty Five Years of the “Psychosine Hypothesis”: A Personal Perspective of its History and Present Status

Suzuki, K. (1998) · Neurochemical Research · doi:10.1023/a:1022436928925 · Cited by 282 · see citing works

Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage

Readhead, C. W., Schneider, A., Griffiths, I. R., & Nave, K. (1994) · Neuron · doi:10.1016/0896-6273(94)90214-3 · Cited by 281 · see citing works

Determination of Neuroepithelial Cell Fate: Induction of the Oligodendrocyte Lineage by Ventral Midline Cells and Sonic Hedgehog

Pringle, N. P., Yu, W., Guthrie, S., Roelink, H., Lumsden, A., Peterson, A. C., & Richardson, W. D. (1996) · Developmental Biology · doi:10.1006/dbio.1996.0142 · Cited by 281 · see citing works

The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein

Mosser, J., Lutz, Y., Stoeckel, M. E., Sarde, C. O., Kretz, C., Douar, A. M., Lopez, J., Aubourg, P., & Mandel, J. L. (1994) · Human Molecular Genetics · doi:10.1093/hmg/3.2.265 · Cited by 281 · see citing works

Development and differentiation of glial precursor cells in the rat cerebellum

Levine, J. M., Stincone, F., & Lee, Y. (1993) · Glia · doi:10.1002/glia.440070406 · Cited by 279 · see citing works

Myelin Formation, Structure and Biochemistry

Morell, P., & Quarles, R. H. (1999) · Cited by 272 · see citing works

Evidence for the ventral origin of oligodendrocyte precursors in the rat spinal cord

Warf, B. C., Fok‐Seang, J., & Miller, R. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-08-02477.1991 · Cited by 270 · see citing works

Myelin basic protein demonstrated immunocytochemically in oligodendroglia prior to myelin sheath formation.

Sternberger, N. H., Itoyama, Y., Kies, M. W., & Webster, H. D. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.5.2521 · Cited by 270 · see citing works

Myelin oligodendrocyte glycoprotein: a novel candidate autoantigen in multiple sclerosis

Bernard, C. C. A., Johns, T. G., Slavin, A., Ichikawa, M., Ewing, C., Liu, J., & Bettadapura, J. (1997) · Journal of Molecular Medicine · doi:10.1007/s001090050092 · Cited by 270 · see citing works

Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene

Kagawa, T., Ikenaka, K., Inoue, Y., Kuriyama, S., Tsujii, T., Nakao, J., Nakajima, K., Aruga, J., Okano, H., & Mikoshiba, K. (1994) · Neuron · doi:10.1016/0896-6273(94)90358-1 · Cited by 269 · see citing works

High Frequency of Autoreactive Myelin Proteolipid Protein–Specific T Cells in the Periphery of Naive Mice

Anderson, A. C., Nicholson, L. B., Legge, K. L., Turchin, V., Zaghouani, H., & Kuchroo, V. K. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.191.5.761 · Cited by 269 · see citing works

The vimentin‐GFA protein transition in rat neuroglia cytoskeleton occurs at the time of myelination

Dahl, D. (1981) · Journal of Neuroscience Research · doi:10.1002/jnr.490060608 · Cited by 267 · see citing works

Matrix Metalloproteinase-9/Gelatinase B Is Required for Process Outgrowth by Oligodendrocytes

Oh, L. Y. S., Larsen, P. H., Krekoski, C. A., Edwards, D. R., Donovan, F. M., Werb, Z., & Yong, V. W. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-19-08464.1999 · Cited by 267 · see citing works

Persistent infection of oligodendrocytes in Theiler's virus‐induced encephalomyelitis

Rodriguez, M., Leibowitz, J. L., & Lampert, P. W. (1983) · Annals of Neurology · doi:10.1002/ana.410130409 · Cited by 266 · see citing works

T cells specific for the myelin oligodendrocyte glycoprotein mediate an unusual autoimmune inflammatory response in the central nervous system

Linington, C., Berger, T., Perry, L., Weerth, S., Hinze‐Selch, D., Zhang, Y., Lu, H., Lassmann, H., & Wekerle, H. (1993) · European Journal of Immunology · doi:10.1002/eji.1830230627 · Cited by 266 · see citing works

Sonic hedgehog signaling is required during the appearance of spinal cord oligodendrocyte precursors

Orentas, D. M., Hayes, J. E., Dyer, K. L., & Miller, R. H. (1999) · Development · doi:10.1242/dev.126.11.2419 · Cited by 265 · see citing works

Phenotype of arylsulfatase A-deficient mice: Relationship to human metachromatic leukodystrophy

Heß, B., Säftig, P., Hartmann, D., Coenen, R., Lüllmann‐Rauch, R., Goebel, H. H., Evers, M., FIGURA, K. V., D’Hooge, R., Nagels, G., et al. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.25.14821 · Cited by 263 · see citing works

Paranodin, a glycoprotein of neuronal paranodal membranes.

Menegoz, M., Gaspar, P., Bert, M. L., Galvez, T., Burgaya, F., Palfrey, C., Ezan, P., Arnos, F., & Girault, J. (1997) · Neuron · doi:10.1016/s0896-6273(00)80942-3 · Cited by 262 · see citing works

Childhood ataxia with diffuse central nervous system hypomyelination

Schiffmann, R., Möller, J. R., Trapp, B. D., Shih, H., Farrer, R. G., Katz, D. A., Alger, J. R., Parker, C. C., Hauer, P. E., Kaneski, C. R., et al. (1994) · Annals of Neurology · doi:10.1002/ana.410350314 · Cited by 260 · see citing works

B Lymphocytes Producing Demyelinating Autoantibodies: Development and Function in Gene-targeted Transgenic Mice

Litzenburger, T., Fässler, R., Bauer, J., Lassmann, H., Linington, C., Wekerle, H., & Iglesias, A. H. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.188.1.169 · Cited by 257 · see citing works

Oligodendroglial progenitors labeled with the O4 antibody persist in the adult rat cerebral cortex in vivo

Reynolds, R., & Hardy, R. (1997) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19970301)47:5 · Cited by 257 · see citing works

Development of macroglial cells in rat cerebellum II. An in situ immunohistochemical study of oligodendroglial lineage from precursor to mature myelinating cell

Reynolds, R., & Wilkin, G. P. (1988) · Development · doi:10.1242/dev.102.2.409 · Cited by 256 · see citing works

MHC haplotype-dependent regulation of MOG-induced EAE in rats.

Weissert, R., Wallström, E., Storch, M. K., Stefferl, A., Lorentzen, J. C., Lassmann, H., Linington, C., & Olsson, T. P. (1998) · Journal of Clinical Investigation · doi:10.1172/jci3022 · Cited by 256 · see citing works

Sprouting and Regeneration of Lesioned Corticospinal Tract Fibres in the Adult Rat Spinal Cord

Schnell, L., & Schwab, M. E. (1993) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1993.tb00970.x · Cited by 256 · see citing works

ELECTRON MICROSCOPIC DEMONSTRATION OF CONNECTIONS BETWEEN GLIA AND MYELIN SHEATHS IN THE DEVELOPING MAMMALIAN CENTRAL NERVOUS SYSTEM

Bunge, M. B., Bunge, R. P., & Pappas, G. D. (1962) · The Journal of Cell Biology · doi:10.1083/jcb.12.2.448 · Cited by 255 · see citing works

Mechanism Involved in Initiation and Propagation of Receptor-Induced Intercellular Calcium Signaling in Cultured Rat Astrocytes

Venance, L., Stella, N., Glowinski, J., & Giaume, C. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-06-01981.1997 · Cited by 254 · see citing works

Channel expression correlates with differentiation stage during the development of Oligodendrocytes from their precursor cells in culture

Sontheimer, H. W., Trotter, J., Schachner, M., & Kettenmann, H. (1989) · Neuron · doi:10.1016/0896-6273(89)90180-3 · Cited by 254 · see citing works

Proliferation and differentiation potential of rat forebrain oligodendroglial progenitors both in vitro and in vivo

Hardy, R., & Reynolds, R. (1991) · Development · doi:10.1242/dev.111.4.1061 · Cited by 251 · see citing works

Myelin acquisition in the central nervous system of the mouse revealed by an MBP-Lac Z transgene

Foran, D., & Peterson, A. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-12-04890.1992 · Cited by 250 · see citing works

Oligodendroglia Regulate the Regional Expansion of Axon Caliber and Local Accumulation of Neurofilaments during Development Independently of Myelin Formation

Sánchez, I., Hassinger, L. C., Paskevich, P. A., Shine, H. D., & Nixon, R. A. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05095.1996 · Cited by 250 · see citing works

Restoration of Normal Conduction Properties in Demyelinated Spinal Cord Axons in the Adult Rat by Transplantation of Exogenous Schwann Cells

Honmou, O., Felts, P. A., Waxman, S. G., & Kocsis, J. D. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-10-03199.1996 · Cited by 249 · see citing works

In situ demonstration of mature oligodendrocytes and their processes: An immunocytochemical study with a new monoclonal antibody, Rip

Friedman, B., Hockfield, S. J., Black, J. A., Woodruff, K., & Waxman, S. G. (1989) · Glia · doi:10.1002/glia.440020510 · Cited by 248 · see citing works

Embryonic expression of myelin genes: Evidence for a focal source of oligodendrocyte precursors in the ventricular zone of the neural tube

Yu, W. (1994) · Neuron · doi:10.1016/0896-6273(94)90450-2 · Cited by 247 · see citing works

The myelin-associated glycoprotein is enriched in multivesicular bodies and periaxonal membranes of actively myelinating oligodendrocytes.

Trapp, B. D., Andrews, S., Cootauco, C., & Quarles, R. H. (1989) · The Journal of Cell Biology · doi:10.1083/jcb.109.5.2417 · Cited by 247 · see citing works

Myelin/oligodendrocyte glycoprotein is a unique member of the immunoglobulin superfamily

Gardinier, M. V., Amiguet, P., Linington, C., & Matthieu, J. (1992) · Journal of Neuroscience Research · doi:10.1002/jnr.490330123 · Cited by 244 · see citing works

Fatal encephalopathy with astrocyte inclusions in GFAP transgenic mice.

Messing, A., Head, M. W., Galles, K., Galbreath, E. J., Goldman, J. E., & Brenner, M. (1998) · Europe PMC (PubMed Central) · Cited by 242 · see citing works

Mechanisms of Immune Injury in Multiple Sclerosis

Brosnan, C. F., & Raine, C. S. (1996) · Brain Pathology · doi:10.1111/j.1750-3639.1996.tb00853.x · Cited by 242 · see citing works

Expression and Activity of the POU Transcription Factor SCIP

Monuki, E. S., Kuhn, R., Weinmaster, G., Trapp, B. D., & Lemke, G. (1990) · Science · doi:10.1126/science.1975954 · Cited by 239 · see citing works

Interaction between NG2 proteoglycan and PDGF ?-receptor on O2A progenitor cells is required for optimal response to PDGF

Nishiyama, A., Lin, X., Giese, N. A., Heldin, C., & Stallcup, W. B. (1996) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19960201)43:3 · Cited by 239 · see citing works

CD22, a B cell-specific immunoglobulin superfamily member, is a sialic acid-binding lectin.

Sgroi, D. C., Varki, A. P., Braesch‐Andersen, S., & Stamenkovic, I. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)53139-2 · Cited by 238 · see citing works

Regional modulation of neurofilament organization by myelination in normal axons

Hsieh, S., Kidd, G. J., Crawford, T., Xu, Z., Lin, W., Trapp, B., Cleveland, D. W., & Griffin, J. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-11-06392.1994 · Cited by 238 · see citing works

The search for true numbers of neurons and glial cells in the human brain: A review of 150 years of cell counting

von Bartheld, C. S., Bahney, J., & Herculano‐Houzel, S. (2016) · Journal of Comparative Neurology · doi:10.1002/cne.24040 · Cited by 1,063 · see citing works

Origin of oligodendrocytes in the subventricular zone of the adult brain

Menn, B., Garcia-Verdugo, J. M., Yaschine, C., Gonzalez-Perez, O., Rowitch, D., & Alvarez-Buylla, A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1299-06.2006 · Cited by 972 · see citing works

Oligodendrocytes: biology and pathology

Bradl, M., & Lassmann, H. (2010) · Acta Neuropathologica · doi:10.1007/s00401-009-0601-5 · Cited by 933 · see citing works

The early development of brain white matter: a review of imaging studies in fetuses, newborns and infants

Dubois, J., Dehaene-Lambertz, G., Kulikova, S., Poupon, C., Hüppi, P. S., & Hertz-Pannier, L. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2013.12.044 · Cited by 851 · see citing works

White matter changes in Alzheimer’s disease: A focus on myelin and oligodendrocytes

Nasrabady, S. E., Rizvi, B., Goldman, J. E., & Brickman, A. M. (2018) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0515-3 · Cited by 723 · see citing works

Neocortical glial cell numbers in human brains

Pelvig, D. P., Pakkenberg, H., Stark, A. K., & Pakkenberg, B. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.04.013 · Cited by 601 · see citing works

Distinct Profiles of Myelin Distribution Along Single Axons of Pyramidal Neurons in the Neocortex

Tomassy, G. S., Berger, D. R., Chen, H.-H., Kasthuri, N., Hayworth, K. J., Vercelli, A., Seung, H. S., Lichtman, J. W., & Arlotta, P. (2014) · Science · doi:10.1126/science.1249766 · Cited by 600 · see citing works

Cellular and molecular neuropathology of the cuprizone mouse model: Clinical relevance for multiple sclerosis

Praet, J., Guglielmetti, C., Berneman, Z., Van der Linden, A., & Ponsaerts, P. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.10.004 · Cited by 435 · see citing works

Oligodendrocytes and Ischemic Brain Injury

Dewar, D., Underhill, S. M., & Goldberg, M. P. (2003) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/01.wcb.0000053472.41007.f9 · Cited by 335 · see citing works

Central nervous system myelin: structure, synthesis and assembly

Aggarwal, S., Yurlova, L., & Simons, M. (2011) · Trends in Cell Biology · doi:10.1016/j.tcb.2011.06.004 · Cited by 301 · see citing works

The Prefrontal Cortex: Functional Neural Development During Early Childhood

Tsujimoto, S. (2008) · The Neuroscientist · doi:10.1177/1073858408316002 · Cited by 291 · see citing works

Conservation and divergence of cortical cell organization in human and mouse revealed by MERFISH

Fang, R., Xia, C., Close, J. L., Zhang, M., He, J., Huang, Z., Halpern, A. R., Long, B., Miller, J. A., Lein, E. S., et al. (2022) · Science · doi:10.1126/science.abm1741 · Cited by 277 · see citing works

Regional differences between grey and white matter in cuprizone induced demyelination

Gudi, V., Moharregh-Khiabani, D., Skripuletz, T., Koutsoudaki, P. N., Kotsiari, A., Skuljec, J., Trebst, C., & Stangel, M. (2009) · Brain Research · doi:10.1016/j.brainres.2009.06.005 · Cited by 252 · see citing works

BCAS1 expression defines a population of early myelinating oligodendrocytes in multiple sclerosis lesions

Fard, M. K., van der Meer, F., Sánchez, P., Cantuti-Castelvetri, L., Mandad, S., Jäkel, S., Fornasiero, E. F., Schmitt, S., Ehrlich, M., Starost, L., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aam7816 · Cited by 247 · see citing works

Neurite outgrowth inhibitor Nogo-A establishes spatial segregation and extent of oligodendrocyte myelination

Chong, S. Y. C., Rosenberg, S. S., Fancy, S. P. J., Zhao, C., Shen, Y.-A. A., Hahn, A. T., McGee, A. W., Xu, X., Zheng, B., Zhang, L. I., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1113540109 · Cited by 232 · see citing works

Early Oligodendrocyte/Myelin Pathology in Alzheimer's Disease Mice Constitutes a Novel Therapeutic Target

Desai, M. K., Mastrangelo, M. A., Ryan, D. A., Sudol, K. L., Narrow, W. C., & Bowers, W. J. (2010) · The American Journal of Pathology · doi:10.2353/ajpath.2010.100087 · Cited by 232 · see citing works

Act1 mediates IL-17-induced EAE pathogenesis selectively in NG2+ glial cells

Kang, Z., Wang, C., Zepp, J., Wu, L., Sun, K., Zhao, J., Chandrasekharan, U., DiCorleto, P. E., Trapp, B. D., Ransohoff, R. M., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3505 · Cited by 218 · see citing works

The role of myelin damage in Alzheimer’s disease pathology

Papuć, E., & Rejdak, K. (2020) · Archives of Medical Science · doi:10.5114/aoms.2018.76863 · Cited by 188 · see citing works

The role of myelination in measures of white matter integrity: Combination of diffusion tensor imaging and two-photon microscopy of CLARITY intact brains

Chang, E. H., Argyelan, M., Aggarwal, M., Chandon, T.-S. S., Karlsgodt, K. H., Mori, S., & Malhotra, A. K. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2016.11.068 · Cited by 186 · see citing works

Expanded Repertoire of AAV Vector Serotypes Mediate Unique Patterns of Transduction in Mouse Brain

Cearley, C. N., Vandenberghe, L. H., Parente, M. K., Carnish, E. R., Wilson, J. M., & Wolfe, J. H. (2008) · Molecular Therapy · doi:10.1038/mt.2008.166 · Cited by 182 · see citing works

Fungal brain infection modelled in a human-neurovascular-unit-on-a-chip with a functional blood–brain barrier

Kim, J., Lee, K.-T., Lee, J. S., Shin, J., Cui, B., Yang, K., Choi, Y. S., Choi, N., Lee, S. H., Lee, J.-H., et al. (2021) · Nature Biomedical Engineering · doi:10.1038/s41551-021-00743-8 · Cited by 172 · see citing works

Antidepressant Effects of Fibroblast Growth Factor-2 in Behavioral and Cellular Models of Depression

Elsayed, M., Banasr, M., Duric, V., Fournier, N. M., Licznerski, P., & Duman, R. S. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.03.003 · Cited by 169 · see citing works

Myelination and mTOR

Figlia, G., Gerber, D., & Suter, U. (2018) · Glia · doi:10.1002/glia.23273 · Cited by 165 · see citing works

Exploring the Early Organization and Maturation of Linguistic Pathways in the Human Infant Brain

Dubois, J., Poupon, C., Thirion, B., Simonnet, H., Kulikova, S., Leroy, F., Hertz-Pannier, L., & Dehaene-Lambertz, G. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv082 · Cited by 165 · see citing works

Adolescent Neurodevelopment and Vulnerability to Psychosis

Patel, P. K., Leathem, L. D., Currin, D. L., & Karlsgodt, K. H. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.06.028 · Cited by 152 · see citing works

Genetically Induced Adult Oligodendrocyte Cell Death Is Associated with Poor Myelin Clearance, Reduced Remyelination, and Axonal Damage

Pohl, H. B. F., Porcheri, C., Mueggler, T., Bachmann, L. C., Martino, G., Riethmacher, D., Franklin, R. J. M., Rudin, M., & Suter, U. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5035-10.2011 · Cited by 145 · see citing works

Schizophrenia, myelination, and delayed corollary discharges: a hypothesis

Whitford, T. J., Ford, J. M., Mathalon, D. H., Kubicki, M., & Shenton, M. E. (2012) · Schizophrenia Bulletin · doi:10.1093/schbul/sbq105 · Cited by 140 · see citing works

The molecular physiology of the axo-myelinic synapse

Micu, I., Plemel, J. R., Lachance, C., Proft, J., Jansen, A. J., Cummins, K., van Minnen, J., & Stys, P. K. (2016) · Experimental Neurology · doi:10.1016/j.expneurol.2015.10.006 · Cited by 140 · see citing works

A unique role for DNA (hydroxy)methylation in epigenetic regulation of human inhibitory neurons

Kozlenkov, A., Li, J., Apontes, P., Hurd, Y. L., Byne, W. M., Koonin, E. V., Wegner, M., Mukamel, E. A., & Dracheva, S. (2018) · Science Advances · doi:10.1126/sciadv.aau6190 · Cited by 103 · see citing works

Progesterone and Nestorone Facilitate Axon Remyelination: A Role for Progesterone Receptors

Hussain, R., El-Etr, M., Gaci, O., Rakotomamonjy, J., Macklin, W. B., Kumar, N., Sitruk-Ware, R., Schumacher, M., & Ghoumari, A. M. (2011) · Endocrinology · doi:10.1210/en.2011-1219 · Cited by 123 · see citing works

Oligodendroglial differentiation induces mitochondrial genes and inhibition of mitochondrial function represses oligodendroglial differentiation

Schoenfeld, R., Wong, A., Silva, J., Li, M., Itoh, A., Horiuchi, M., Itoh, T., Pleasure, D., & Cortopassi, G. (2010) · Mitochondrion · doi:10.1016/j.mito.2009.12.141 · Cited by 112 · see citing works

Identification of a Gene Regulatory Network Necessary for the Initiation of Oligodendrocyte Differentiation

Swiss, V. A., Nguyen, T., Dugas, J., Ibrahim, A., Barres, B., Androulakis, I. P., & Casaccia, P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018088 · Cited by 112 · see citing works

Assessment of normal fetal brain maturation in utero by proton magnetic resonance spectroscopy

Girard, N., Gouny, S. C., Viola, A., Le Fur, Y., Viout, P., Chaumoitre, K., D'Ercole, C., Gire, C., Figarella‐Branger, D., & Cozzone, P. J. (2006) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21017 · Cited by 111 · see citing works

Aerobic glycolysis in the primate brain: Reconsidering the implications for growth and maintenance

Bauernfeind, A. L., Barks, S. K., Duka, T., Grossman, L. I., Hof, P. R., & Sherwood, C. C. (2014) · Brain Structure and Function · doi:10.1007/s00429-013-0662-z · Cited by 105 · see citing works

Sox10 is necessary for oligodendrocyte survival following axon wrapping

Takada, N., Kucenas, S., & Appel, B. (2010) · Glia · doi:10.1002/glia.20981 · Cited by 91 · see citing works

Mechanisms of oligodendrocyte regeneration from ventricular-subventricular zone-derived progenitor cells in white matter diseases

Maki, T., Liang, A. C., Miyamoto, N., Lo, E. H., & Arai, K. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00275 · Cited by 99 · see citing works

Oligodendrocyte progenitor cells in Alzheimer's disease: from physiology to pathology

Zou, P., Wu, C., Liu, T. C.-Y., Duan, R., & Yang, L. (2023) · Translational Neurodegeneration · doi:10.1186/s40035-023-00385-7 · Cited by 97 · see citing works

Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy

Vanni, N., Fruscione, F., Ferlazzo, E., Striano, P., Robbiano, A., Traverso, M., Sander, T., Falace, A., Gazzerro, E., Bramanti, P., et al. (2014) · Annals of Neurology · doi:10.1002/ana.24170 · Cited by 94 · see citing works

Altered lipid levels provide evidence for myelin dysfunction in multiple system atrophy

Don, A. S., Hsiao, J.-H. T., Bleasel, J. M., Couttas, T. A., Halliday, G. M., & Kim, W. S. (2014) · Acta Neuropathologica Communications · doi:10.1186/s40478-014-0150-6 · Cited by 88 · see citing works

A correlative light and electron microscopic study of postnatal myelination in the murine corpus callosum

Vincze, A., Mázló, M., Seress, L., Komoly, S., & Ábrahám, H. (2008) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2008.05.003 · Cited by 85 · see citing works

Alcohol-induced apoptosis of oligodendrocytes in the fetal macaque brain

Creeley, C. E., Dikranian, K. T., Johnson, S. A., Farber, N. B., & Olney, J. W. (2013) · Acta Neuropathologica Communications · doi:10.1186/2051-5960-1-23 · Cited by 84 · see citing works

Predicting inter-hemispheric transfer time from the diffusion properties of the corpus callosum in healthy individuals and schizophrenia patients: A combined ERP and DTI study

Whitford, T. J., Kubicki, M., Ghorashi, S., Schneiderman, J. S., Hawley, K. J., McCarley, R. W., Shenton, M. E., & Spencer, K. M. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.10.048 · Cited by 83 · see citing works

Liver X receptors regulate cholesterol homeostasis in oligodendrocytes

Nelissen, K., Mulder, M., Smets, I., Timmermans, S., Smeets, K., Ameloot, M., & Hendriks, J. J. A. (2012) · Journal of Neuroscience Research · doi:10.1002/jnr.22743 · Cited by 80 · see citing works

Tubulin polymerization promoting protein (TPPP/p25) as a marker for oligodendroglial changes in multiple sclerosis

Höftberger, R., Fink, S., Aboul‐Enein, F., Botond, G., Olah, J., Berki, T., Ovadi, J., Lassmann, H., Budka, H., & Kovacs, G. G. (2010) · Glia · doi:10.1002/glia.21054 · Cited by 79 · see citing works

Quantitative Analysis of the Detergent-Insoluble Brain Proteome in Frontotemporal Lobar Degeneration Using SILAC Internal Standards

Seyfried, N. T., Gozal, Y. M., Donovan, L. E., Herskowitz, J. H., Dammer, E. B., Xia, Q., Ku, L., Chang, J., Duong, D. M., Rees, H. D., et al. (2012) · Journal of Proteome Research · doi:10.1021/pr2010814 · Cited by 64 · see citing works

Differential expression of peroxisomal matrix and membrane proteins during postnatal development of mouse brain

Ahlemeyer, B., Neubert, I., Kovacs, W. J., & Baumgart‐Vogt, E. (2007) · Journal of Comparative Neurology · doi:10.1002/cne.21448 · Cited by 68 · see citing works

The metalloprotease ADAMTS4 generates N-truncated Aβ4–x species and marks oligodendrocytes as a source of amyloidogenic peptides in Alzheimer’s disease

Walter, S., Jumpertz, T., Hüttenrauch, M., Ogorek, I., Gerber, H., Storck, S. E., Zampar, S., Dimitrov, M., Lehmann, S., Lepka, K., et al. (2019) · Acta Neuropathologica · doi:10.1007/s00401-018-1929-5 · Cited by 65 · see citing works

Scientific Validation of Human Neurosphere Assays for Developmental Neurotoxicity Evaluation

Koch, K., Bartmann, K., Hartmann, J., Kapr, J., Klose, J., Kuchovská, E., Pahl, M., Schlüppmann, K., Zühr, E., & Fritsche, E. (2022) · Frontiers in Toxicology · doi:10.3389/ftox.2022.816370 · Cited by 48 · see citing works

MRI and M/EEG studies of the White Matter Development in Human Fetuses and Infants: Review and Opinion

Dubois, J., Adibpour, P., Poupon, C., Hertz-Pannier, L., & Dehaene-Lambertz, G. (2016) · Brain Plasticity · doi:10.3233/bpl-160031 · Cited by 40 · see citing works

Development of the Cell Population in the Brain White Matter of Young Children

Sigaard, R. K., Kjær, M., & Pakkenberg, B. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhu178 · Cited by 43 · see citing works

Incidence of Abcd1 level on the induction of cell death and organelle dysfunctions triggered by very long chain fatty acids and TNF-α on oligodendrocytes and astrocytes

Baarine, M., Ragot, K., Athias, A., Nury, T., Kattan, Z., Genin, E. C., Andreoletti, P., Ménétrier, F., Riedinger, J.-M., Bardou, M., et al. (2012) · NeuroToxicology · doi:10.1016/j.neuro.2011.10.007 · Cited by 43 · see citing works

Minocycline promotes remyelination in aggregating rat brain cell cultures after interferon-γ plus lipopolysaccharide-induced demyelination

Defaux, A., Zurich, M.-G., Honegger, P., & Monnet-Tschudi, F. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.04.053 · Cited by 40 · see citing works

The polarity protein Scribble regulates myelination and remyelination in the central nervous system

Jarjour, A. A., Boyd, A., Dow, L. E., Holloway, R. K., Goebbels, S., Humbert, P. O., Williams, A., & ffrench-Constant, C. (2015) · PLOS Biology · doi:10.1371/journal.pbio.1002107 · Cited by 39 · see citing works

Selective expression of <i>LDLR</i> and <i>VLDLR</i> in myelinating oligodendrocytes

Zhao, S., Hu, X., Park, J., Zhu, Y., Zhu, Q., Li, H., Luo, C., Han, R., Cooper, N., & Qiu, M. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21283 · Cited by 39 · see citing works

Lack of interferon-beta leads to accelerated remyelination in a toxic model of central nervous system demyelination

Trebst, C., Heine, S., Lienenklaus, S., Lindner, M., Baumgärtner, W., Weiss, S., & Stangel, M. (2007) · Acta Neuropathologica · doi:10.1007/s00401-007-0300-z · Cited by 38 · see citing works

Novel in vitro Experimental Approaches to Study Myelination and Remyelination in the Central Nervous System

Marangon, D., Caporale, N., Boccazzi, M., Abbracchio, M. P., Testa, G., & Lecca, D. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.748849 · Cited by 34 · see citing works

The progeroid gene BubR1 regulates axon myelination and motor function

Choi, C.-I., Yoo, K. H., Hussaini, S. M. Q., Jeon, B. T., Welby, J., Gan, H., Scarisbrick, I. A., Zhang, Z., Baker, D. J., van Deursen, J. M., et al. (2016) · Aging · doi:10.18632/aging.101032 · Cited by 26 · see citing works

Oligodendrocyte precursor cells express a functional chemokine receptor CCR3: Implications for myelination

Maysami, S., Nguyen, D., Zobel, F., Heine, S., Höpfner, M., & Stangel, M. (2006) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.05.021 · Cited by 25 · see citing works

Remyelinating and neuroprotective treatments in multiple sclerosis

Stangel, M. (2004) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.13.4.331 · Cited by 22 · see citing works

High Dose Pharmaceutical Grade Biotin (MD1003) Accelerates Differentiation of Murine and Grafted Human Oligodendrocyte Progenitor Cells In Vivo

Levy, M. J. F., Garcia-Diaz, B., Sedel, F., Baron-Van Evercooren, A., & Mozafari, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232415733 · Cited by 7 · see citing works

Myelin protein expression in the myelin-deficient rat brain and cultured oligodendrocytes

Zeller, N. K., Dubois-Dalcq, M. E., & Lazzarini, R. A. (1989) · Journal of Molecular Neuroscience · doi:10.1007/bf02918900 · Cited by 20 · see citing works

Progress in the research of molecular genetics of Pelizaeus-Merzbacher disease

Cao, F.-L., & Lan, F. (2010) · Int J Genet · doi:10.3760/cma.j.issn.1673-4386.2010.04.008

Tissue culture techniques applied to demyelinating disease

Bornstein, M. B. (1981) · Trends in Neurosciences · doi:10.1016/0166-2236(81)90074-6 · Cited by 4 · see citing works

Tumefactive Demyelinating Lesions in Multiple Sclerosis and Associated Disorders

Frederick, M. C., & Cameron, M. H. (2016) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-016-0626-9 · Cited by 59 · see citing works

Pelizaeus-Merzbacher Disease: A Case Report

Soufi, G. J., & Iravani, S. (2020) · Case Reports in Clinical Practice · doi:10.18502/crcp.v5i2.3841