Axonal Control of Oligodendrocyte Development

Integrin signaling

Giancotti, F. G., & Ruoslahti, E. (1999) · Science · doi:10.1126/science.285.5430.1028 · Cited by 3,869

A glial progenitor cell that develops in vitro into an astrocyte or an oligodendrocyte depending on culture medium

RAFF, M. C., Miller, R. H., & Noble, M. (1983) · Nature · doi:10.1038/303390a0 · Cited by 2,030

Programmed Cell Death and the Control of Cell Survival: Lessons from the Nervous System

RAFF, M. C., Barres, B. A., Burne, J. F., Coles, H., Ishizaki, Y., & Jacobson, M. D. (1993) · Science · doi:10.1126/science.8235590 · Cited by 1,450

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

Multiple essential functions of neuregulin in development

Meyer, D., & Birchmeier, C. (1995) · Nature · doi:10.1038/378386a0 · Cited by 1,273

Anchorage dependence, integrins, and apoptosis

Ruoslahti, E. I., & Reed, J. C. (1994) · Cell · doi:10.1016/0092-8674(94)90209-7 · Cited by 1,001

Platelet-derived growth factor promotes division and motility and inhibits premature differentiation of the oligodendrocyte/type-2 astrocyte progenitor ceil

Noble, M., Murray, K., Stroobant, P., Waterfield, M. D., & Riddle, P. (1988) · Nature · doi:10.1038/333560a0 · Cited by 830

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

A BDNF autocrine loop in adult sensory neurons prevents cell death

Acheson, A., Conover, J. C., Fandl, J. P., DeChiara, T. M., Russell, M., Thadani, A., Squinto, S. P., Yancopoulos, G. D., & Lindsay, R. M. (1995) · Nature · doi:10.1038/374450a0 · Cited by 765

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 762

Programmed Cell Death in Animal Development and Disease

Fuchs, Y., & Steller, H. (2011) · Cell · doi:10.1016/j.cell.2011.10.033 · Cited by 1,915

Biology of Oligodendrocyte and Myelin in the Mammalian Central Nervous System

Baumann, N., & Pham-Dinh, D. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.2.871 · Cited by 1,828

Spinal-cord injury

McDonald, J. W., & Sadowsky, C. L. (2002) · The Lancet · doi:10.1016/s0140-6736(02)07603-1 · Cited by 1,858

Astroglia induce neurogenesis from adult neural stem cells

Song, H., Stevens, C. F., & Gage, F. H. (2002) · Nature · doi:10.1038/417039a · Cited by 1,452

Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia

Hakak, Y., Walker, J. R., Li, C., Wong, W. H., Davis, K. L., Buxbaum, J. D., Haroutunian, V., & Fienberg, A. A. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081071198 · Cited by 1,192

Neuregulins: functions, forms, and signaling strategies

Falls, D. L. (2003) · Experimental Cell Research · doi:10.1016/s0014-4827(02)00102-7 · Cited by 1,071

Apoptosis in development

Meier, P., Finch, A. J., & Evan, G. I. (2000) · Nature · doi:10.1038/35037734 · Cited by 1,027

Oligodendrocytes: Myelination and Axonal SupportPreprint

Simons, M., & Nave, K. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020479 · Cited by 929

Timing of CNS Cell Generation

Qian, X., Shen, Q., Goderie, S. K., He, W., Capela, A., Davis, A. A., & Temple, S. (2000) · Neuron · doi:10.1016/s0896-6273(00)00086-6 · Cited by 860

Localization of white matter volume increase in autism and developmental language disorder

Herbert, M. R., Ziegler, D. A., Makris, N., Filipek, P. A., Kemper, T. L., Normandin, J. J., Sanders, H. A., Kennedy, D. N., & Caviness, V. S. (2004) · Annals of Neurology · doi:10.1002/ana.20032 · Cited by 663

Oligodendrocytes in development, myelin generation and beyond

Kuhn, S., Gritti, L., Crooks, D., & Dombrowski, Y. (2019) · Cells · doi:10.3390/cells8111424 · Cited by 625

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

Untitled work

Stevens (2002) · doi:10.1016/s0896-6273(02)01067-x · Cited by 543

Dissociations of cerebral cortex, subcortical and cerebral white matter volumes in autistic boys

Herbert, M. R., Ziegler, D. A., Deutsch, C., O’Brien, L. M., LANGE, N. D., Bakardjiev, A. I., Hodgson, J. M., Adrien, K. T., Steele, S., Makris, N., et al. (2003) · Brain · doi:10.1093/brain/awg110 · Cited by 505

A Mouse Model of Tuberous Sclerosis: Neuronal Loss of Tsc1 Causes Dysplastic and Ectopic Neurons, Reduced Myelination, Seizure Activity, and Limited Survival

Meikle, L., Talos, D. M., Onda, H., Pollizzi, K., Rotenberg, A., Sahin, M., Jensen, F. E., & Kwiatkowski, D. J. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5540-06.2007 · Cited by 462

The life, death, and replacement of oligodendrocytes in the adult CNS

McTigue, D. M., & Tripathi, R. B. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05570.x · Cited by 474

Polarized Domains of Myelinated Axons

Salzer, J. L. (2003) · Neuron · doi:10.1016/s0896-6273(03)00628-7 · Cited by 416

Unwrapping Glial Biology

Freeman, M. R., Delrow, J. J., Kim, J., Johnson, E. A., & Doe, C. Q. (2003) · Neuron · doi:10.1016/s0896-6273(03)00289-7 · Cited by 395

Dysmaturation of Premature Brain: Importance, Cellular Mechanisms, and Potential Interventions

Volpe, J. J. (2019) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2019.02.016 · Cited by 390

Evolution of increased glia–neuron ratios in the human frontal cortex

Sherwood, C. C., Stimpson, C. D., Raghanti, M. A., Wildman, D. E., Uddin, M., Grossman, L. I., Goodman, M., Redmond, J. C., Bonar, C. J., Erwin, J. M., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605843103 · Cited by 342

Neuregulin and BDNF Induce a Switch to NMDA Receptor-Dependent Myelination by Oligodendrocytes

Lundgaard, I., Luzhynskaya, A., Stockley, J. H., Wang, Z., Evans, K. A., Swire, M., Volbracht, K., Gautier, H. O. B., Franklin, R. J. M., ffrench‐Constant, C., et al. (2013) · PLoS Biology · doi:10.1371/journal.pbio.1001743 · Cited by 351

Functional Genomic Analysis of Oligodendrocyte Differentiation

Dugas, J. C., Tai, Y. C., Speed, T. P., Ngai, J., & Barres, B. A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2572-06.2006 · Cited by 324

Neuronal activity regulates remyelination via glutamate signalling to oligodendrocyte progenitors

Gautier, H. O. B., Evans, K. A., Volbracht, K., James, R., Sitnikov, S., Lundgaard, I., James, F., Lao‐Peregrín, C., Reynolds, R., Franklin, R. J. M., et al. (2015) · Nature Communications · doi:10.1038/ncomms9518 · Cited by 316

Neural activity promotes long-distance, target-specific regeneration of adult retinal axons

Lim, J.-H. A., Stafford, B. K., Nguyen, P. L., Lien, B. V., Wang, C., Zukor, K., He, Z., & Huberman, A. D. (2016) · Nature Neuroscience · doi:10.1038/nn.4340 · Cited by 296

Kir4.1 Potassium Channel Subunit Is Crucial for Oligodendrocyte Development and In Vivo Myelination

Neusch, C., Rozengurt, N., Jacobs, R. E., Lester, H. A., & Kofuji, P. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-15-05429.2001 · Cited by 298

Opposing Extracellular Signal-Regulated Kinase and Akt Pathways Control Schwann Cell Myelination

Ogata, T., Iijima, S., Hoshikawa, S., Miura, T., Yamamoto, S.-I., Oda, H., Nakamura, K., & Tanaka, S. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5520-03.2004 · Cited by 264

CNS integrins switch growth factor signalling to promote target-dependent survival

Colognato, H., Baron, W., Avellana‐Adalid, V., Relvas, J. B., Evercooren, A. B., Georges‐Labouesse, E., & ffrench‐Constant, C. (2002) · Nature Cell Biology · doi:10.1038/ncb865 · Cited by 250

Cells of the oligodendroglial lineage, myelination, and remyelination

Miron, V. E., Kuhlmann, T., & Antel, J. P. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2010.09.010 · Cited by 249

Cell proliferation and replacement following contusive spinal cord injury

Zai, L. J., & Wrathall, J. R. (2005) · Glia · doi:10.1002/glia.20176 · Cited by 240

Glial Cells and Neurotransmission

Auld, D. S., & Robitaille, R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00607-x · Cited by 239

Brain-Derived Neurotrophic Factor Promotes Central Nervous System Myelination via a Direct Effect upon Oligodendrocytes

Xiao, J., Wong, A. W., Willingham, M. M., van den Buuse, M., Kilpatrick, T. J., & Murray, S. S. (2010) · Neurosignals · doi:10.1159/000323170 · Cited by 242

Knockout mice reveal a contribution of the extracellular matrix molecule tenascin-C to neural precursor proliferation and migration

Garcion, E., Faissner, A., & ffrench‐Constant, C. (2001) · Development · doi:10.1242/dev.128.13.2485 · Cited by 241

Contrasting the Glial Response to Axon Injury in the Central and Peripheral Nervous Systems

Lutz, A. B., & Barres, B. A. (2014) · Developmental Cell · doi:10.1016/j.devcel.2013.12.002 · Cited by 233

Wrapping it up: the cell biology of myelination

Simons, M., & Trotter, J. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.08.003 · Cited by 187

On Myelinated Axon Plasticity and Neuronal Circuit Formation and Function

Almeida, R. G., & Lyons, D. A. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.3185-16.2017 · Cited by 221

Neuron-glia communication in the control of oligodendrocyte function and myelin biogenesis

Simons, M., & Trajković, K. (2006) · Journal of Cell Science · doi:10.1242/jcs.03242 · Cited by 233

Individual axons regulate the myelinating potential of single oligodendrocytes in vivo

Almeida, R. G., Czopka, T., ffrench-Constant, C., & Lyons, D. A. (2011) · Development · doi:10.1242/dev.071001 · Cited by 214

Notch1 control of oligodendrocyte differentiation in the spinal cord

Genoud, S., Lappe-Siefke, C., Goebbels, S., Radtke, F., Aguet, M., Scherer, S. S., Suter, U., Nave, K.-A., & Mantei, N. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200202002 · Cited by 211

Inflammation stimulates remyelination in areas of chronic demyelination

Foote, A. K. (2005) · Brain · doi:10.1093/brain/awh417 · Cited by 230

Synantocytes: New functions for novel NG2 expressing glia

Butt, A. M., Kiff, J., Hubbard, P. S., & Berry, M. (2002) · Journal of Neurocytology · doi:10.1023/a:1025751900356 · Cited by 203

Glutamate Stimulates Oligodendrocyte Progenitor Migration Mediated via an αvIntegrin/Myelin Proteolipid Protein Complex

Gudz, T. I., Komuro, H., & Macklin, W. B. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4054-05.2006 · Cited by 213

Molecular and Cellular Evidence for an Oligodendrocyte Abnormality in Schizophrenia

Hof, P. R., Haroutunian, V., Copland, C., Davis, K. L., & Buxbaum, J. D. (2002) · Neurochemical Research · doi:10.1023/a:1020981510759 · Cited by 199

Effects of erythropoietin on glial cell development; oligodendrocyte maturation and astrocyte proliferation

Sugawa, M., Sakurai, Y., Ishikawa-Ieda, Y., Suzuki, H., & Asou, H. (2002) · Neuroscience Research · doi:10.1016/s0168-0102(02)00161-x · Cited by 197

Type III neuregulin‐1 promotes oligodendrocyte myelination

Taveggia, C., Thaker, P., Petrylak, A., Caporaso, G. L., Toews, A. D., Falls, D. L., Einheber, S., & Salzer, J. L. (2007) · Glia · doi:10.1002/glia.20612 · Cited by 201

Lysolecithin induces demyelination in vitro in a cerebellar slice culture system

Birgbauer, E., Rao, T. S., & Webb, M. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20248 · Cited by 202

Neuron to glia signaling triggers myelin membrane exocytosis from endosomal storage sites

Trajkovic, K., Dhaunchak, A. S., Goncalves, J. T., Wenzel, D., Schneider, A., Bunt, G., Nave, K.-A., & Simons, M. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200509022 · Cited by 186

Absence of fibroblast growth factor 2 promotes oligodendroglial repopulation of demyelinated white matter

Armstrong, R. C., Le, T. Q., Frost, E. E., Borke, R. C., & Vana, A. C. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-19-08574.2002 · Cited by 178

Integrins: versatile integrators of extracellular signals

ffrench‐Constant, C., & Colognato, H. (2004) · Trends in Cell Biology · doi:10.1016/j.tcb.2004.10.005 · Cited by 174

Evidence that Axon-Derived Neuregulin Promotes Oligodendrocyte Survival in the Developing Rat Optic Nerve

Fernandez, P.-A., Tang, D. G., Cheng, L., Prochiantz, A., Mudge, A. W., & RAFF, M. C. (2000) · Neuron · doi:10.1016/s0896-6273(00)00087-8 · Cited by 174

Activation of sphingosine‐1‐phosphate receptor S1P5 inhibits oligodendrocyte progenitor migration

Novgorodov, A. S., El‐Awani, M., Bielawski, J., Obeid, L. M., & Gudz, T. I. (2007) · The FASEB Journal · doi:10.1096/fj.06-7420com · Cited by 174

Connectivity-driven white matter scaling and folding in primate cerebral cortex

Herculano‐Houzel, S., Mota, B., Wong, P., & Kaas, J. H. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1012590107 · Cited by 166

Regulation of Kv1 subunit expression in oligodendrocyte progenitor cells and their role in G 1 /S phase progression of the cell cycle

Chittajallu, R., Chen, Y., Wang, H., Yuan, X., Ghiani, C. A., Heckman, T., McBain, C. J., & Gallo, V. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.042698399 · Cited by 165

Inside-Out versus Outside-In models for virus induced demyelination: axonal damage triggering demyelination

Tsunoda, I., & Fujinami, R. S. (2002) · Springer Seminars in Immunopathology · doi:10.1007/s00281-002-0105-z · Cited by 164

Sigma-1 receptors at galactosylceramide-enriched lipid microdomains regulate oligodendrocyte differentiation

Hayashi, T., & Su, T. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402890101 · Cited by 160

The ERK2 Mitogen-Activated Protein Kinase Regulates the Timing of Oligodendrocyte Differentiation

Fyffe-Maricich, S. L., Karlo, J. C., Landreth, G. E., & Miller, R. H. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3239-10.2011 · Cited by 164

Demyelination and Remyelination after Spinal Cord Injury

McDonald, J. W., & Belegu, V. (2006) · Journal of Neurotrauma · doi:10.1089/neu.2006.23.345 · Cited by 158

Demyelination as a rational therapeutic target for ischemic or traumatic brain injury

Shi, H., Hu, X., Leak, R. K., Shi, Y., An, C., Suenaga, J., Chen, J., & Gao, Y. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.03.017 · Cited by 159

Regulation of Integrin Growth Factor Interactions in Oligodendrocytes by Lipid Raft Microdomains

Baron, W., Decker, L., Colognato, H., & ffrench‐Constant, C. (2003) · Current Biology · doi:10.1016/s0960-9822(02)01437-9 · Cited by 152

Oligodendrocyte precursor cells ingest axons in the mouse neocortex

Buchanan, J., Elabbady, L., Collman, F., Jorstad, N. L., Bakken, T. E., Ott, C. M., Glatzer, J. C., Bleckert, A., Bodor, Á. L., Brittain, D., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2202580119 · Cited by 162

NB-3/Notch1 Pathway via Deltex1 Promotes Neural Progenitor Cell Differentiation into Oligodendrocytes

Cui, X., Hu, Q., Tekaya, M., Shimoda, Y., Ang, B.-T., Nie, D. A., Sun, L. J., Hu, W.-P., Karsak, M., Duka, T., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313505200 · Cited by 144

Progesterone increases oligodendroglial cell proliferation in rat cerebellar slice cultures

Ghoumari, A. M., Baulieu, E. E., & Schumacher, M. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.05.023 · Cited by 161

Control of progenitor cell number by mitogen supply and demand

van Heyningen, P., Calver, A. R., & Richardson, W. D. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00075-6 · Cited by 138

Semaphorins in Adult Nervous System Plasticity and Disease

Carulli, D., de Winter, F., & Verhaagen, J. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.672891 · Cited by 137

Cell death in development: shaping the embryo

Penaloza, C. G., Lin, L., Lockshin, R. A., & Zakeri, Z. F. (2006) · Histochemistry and Cell Biology · doi:10.1007/s00418-006-0214-1 · Cited by 136

Glaucomatous optic nerve injury involves early astrocyte reactivity and late oligodendrocyte loss

Son, J. L., Soto, I., Oglesby, E., López-Roca, T., Pease, M. E., Quigley, H. A., & Marsh‐Armstrong, N. (2010) · Glia · doi:10.1002/glia.20962 · Cited by 132

Central nervous system myelination in mice with deficient expression of Notch1 receptor

Givogri, M. I., Costa, R. M., Schonmann, V., Silva, A. J., Campagnoni, A. T., & Bongarzone, E. R. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10128 · Cited by 140

Maturation-dependent sensitivity of oligodendrocyte lineage cells to apoptosis: implications for normal development and disease

Butts, B. D., Houde, C., & Mehmet, H. (2008) · Cell Death and Differentiation · doi:10.1038/cdd.2008.70 · Cited by 132

Glial cells are born with synapses

Kukley, M., Kiladze, M., Tognatta, R., Hans, M., Swandulla, D., Schramm, J., & Dietrich, D. (2008) · The FASEB Journal · doi:10.1096/fj.07-090985 · Cited by 137

Different scaling of white matter volume, cortical connectivity, and gyrification across rodent and primate brains

Ventura-Antunes, L., Mota, B., & Herculano-Houzel, S. (2013) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2013.00003 · Cited by 129

Cdk5 Phosphorylation of WAVE2 Regulates Oligodendrocyte Precursor Cell Migration through Nonreceptor Tyrosine Kinase Fyn

Miyamoto, Y., Yamauchi, J., & Tanoue, A. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1482-08.2008 · Cited by 126

The Absolute Number of Oligodendrocytes in the Adult Mouse Brain

Valério‐Gomes, B., Guimarães, D. M., Szczupak, D., & Lent, R. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00090 · Cited by 129

Integrin‐growth factor interactions as regulators of oligodendroglial development and function

Baron, W., Colognato, H., & ffrench‐Constant, C. (2004) · Glia · doi:10.1002/glia.20132 · Cited by 126

Neuregulins and the neuromuscular system: 10 years of answers and questions

Falls, D. L. (2003) · Journal of Neurocytology · doi:10.1023/b:neur.0000020614.83883.be · Cited by 120

Oligodendrocytes in a Nutshell

Michalski, J., & Kothary, R. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00340 · Cited by 124

Towards improved animal models of neonatal white matter injury associated with cerebral palsy

Silbereis, J. C., Huang, E. J., Back, S. A., & Rowitch, D. H. (2010) · Disease Models & Mechanisms · doi:10.1242/dmm.002915 · Cited by 120

Proteomic mapping provides powerful insights into functional myelin biology

Taylor, C. M., Marta, C. B., Claycomb, R. J., Han, D. K., Rasband, M. N., Coetzee, T., & Pfeiffer, S. E. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400922101 · Cited by 118

Myelin regulatory factor drives remyelination in multiple sclerosis

Duncan, G. J., Plemel, J. R., Assinck, P., Manesh, S. B., Muir, F. G. W., Hirata, R., Berson, M., Liu, J., Wegner, M., Emery, B., et al. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1741-7 · Cited by 120

The erbB2 gene is required for the development of terminally differentiated spinal cord oligodendrocytes

Park, S., Miller, R. H., Krane, I. M., & Vartanian, T. K. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.200104025 · Cited by 113

Contactin-1 regulates myelination and nodal/paranodal domain organization in the central nervous system

Çolakoğlu, G., Bergstrom-Tyrberg, U., Berglund, E. O., & Ranscht, B. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1313769110 · Cited by 115

Myelin inhibits oligodendroglial maturation and regulates oligodendrocytic transcription factor expression

Plemel, J. R., Manesh, S. B., Sparling, J. S., & Tetzlaff, W. (2013) · Glia · doi:10.1002/glia.22535 · Cited by 107

The extracellular matrix glycoprotein Tenascin‐C is expressed by oligodendrocyte precursor cells and required for the regulation of maturation rate, survival and responsiveness to platelet‐derived growth factor

Garwood, J., Garcion, E., Dobbertin, A., Heck, N., Calco, V., ffrench‐Constant, C., & Faissner, A. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03727.x · Cited by 104

Adenomatous Polyposis Coli Regulates Oligodendroglial Development

Lang, J., Maeda, Y., Bannerman, P. G. C., Xu, J., Horiuchi, M., Pleasure, D., & Guo, F. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3467-12.2013 · Cited by 106

Axon‐oligodendrocyte interactions during developmental myelination, demyelination and repair

Piaton, G., Gould, R. M., & Lubetzki, C. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06831.x · Cited by 107

Overexpression of nerve growth factor in skin causes preferential increases among innervation to specific sensory targets

Davis, B. M., Fundín, B. T., Albers, K. M., Goodness, T. P., Cronk, K. M., & Rice, F. L. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19971103)387:4 · Cited by 90

Axon-glia interaction and membrane traffic in myelin formation

White, R., & Krämer‐Albers, E. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00284 · Cited by 109

Platelet-Derived Growth Factor Promotes Repair of Chronically Demyelinated White Matter

Vana, A. C., Flint, N. C., Harwood, N. E., Le, T. Q., Fruttiger, M., & Armstrong, R. C. (2007) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e3181587d46 · Cited by 101

Neuronal and glial cell biology

Barres, B. A., & Barde, Y. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00134-3 · Cited by 101

The NG2 proteoglycan promotes oligodendrocyte progenitor proliferation and developmental myelination

Kuchárová, K., & Stallcup, W. B. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.12.014 · Cited by 107

Developmentally Regulated Ceramide Synthase 6 Increases Mitochondrial Ca2+ Loading Capacity and Promotes Apoptosis

Novgorodov, S. A., Chudakova, D. A., Wheeler, B. W., Bielawski, J., Kindy, M. S., Obeid, L. M., & Gudz, T. I. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.164392 · Cited by 97

Oligodendrocyte Generation Is Differentially Influenced by Toll-Like Receptor (TLR) 2 and TLR4-Mediated Intraspinal Macrophage Activation

Schonberg, D. L., Popovich, P. G., & McTigue, D. M. (2007) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31815c2530 · Cited by 97

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