Cited by 360Neurogenesis and neuroplasticity mechanismsNeuroscience and Neuropharmacology ResearchNeuroinflammation and Neurodegeneration Mechanisms

The DOI matches its Crossref record; 70 of the 70 references it cites were found in a registry or an index.

Axonal Control of Oligodendrocyte Development

Open access

Barres, Ben A., Raff, Martin C.·1999·The Journal of Cell Biology

DOI 10.1083/jcb.147.6.1123PMC PMC2168096

Open this paper in CoChat — free account

Abstract

How are the numbers of different cell types matched together during tissue development? The nervous system has provided an excellent model system for understanding this question as it contains two main classes of cell types, neurons and glia. Presynaptic neurons are believed to be precisely matched

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1083/jcb.147.6.1123

Cites

70 of 70 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

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
Self-citation
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
Self-citation
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
Self-citation
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
Self-citation

Flagged first, then by citations

Show all 69 references

Research works printed but not linked: 2

Barres, 1993, Does oligodendrocyte survival depend on axons?, Curr. Biol., 3, 489, 10.1016/0960-9822(93)90039-Q · DOI
Purves, 1988, Body and BrainA Trophic Theory of Neural Connections

Sorted by citations

Items 101–200 of 360

Myelin Proteolipid Protein Forms a Complex with Integrins and May Participate in Integrin Receptor Signaling in Oligodendrocytes
Gudz, T. I., Schneider, T. E., Haas, T. A., & Macklin, W. B. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-17-07398.2002 · Cited by 93
Destruction and reconstruction: Hypoxia and the developing brain
Barrett, R. D., Bennet, L., Davidson, J. O., Dean, J. M., George, S. A., Emerald, B. S., & Gunn, A. J. (2007) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.20095 · Cited by 89
Oligodendroglia in Developmental Neurotoxicity
Deng, W., & Poretz, R. D. (2003) · NeuroToxicology · doi:10.1016/s0161-813x(02)00196-1 · Cited by 85
How Do Cells of the Oligodendrocyte Lineage Affect Neuronal Circuits to Influence Motor Function, Memory and Mood?
Pepper, R., Pitman, K. A., Cullen, C. L., & Young, K. M. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00399 · Cited by 86
Activity‐dependent central nervous system myelination throughout life
de Faria, O., Gonsalvez, D. G., Nicholson, M., & Xiao, J. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14592 · Cited by 90
Axonal loss in multiple sclerosis
Criste, G. A., Trapp, B. D., & Dutta, R. (2014) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52001-2.00005-4 · Cited by 86
Novel Treatment Strategies Targeting Myelin and Oligodendrocyte Dysfunction in Schizophrenia
Junqueira, D. G., Falvella, A. C. B., Antunes, A. S. L. M., Seabra, G., Brandão‐Teles, C., Martins‐de‐Souza, D., & Crunfli, F. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00379 · Cited by 80
Oligodendrogenesis and myelination regulate cortical development, plasticity and circuit function
Fletcher, J. L., Makowiecki, K., Cullen, C. L., & Young, K. M. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.03.017 · Cited by 82
Extracellular signal‐regulated kinase 1/2 signaling promotes oligodendrocyte myelination in vitro
Xiao, J., Ferner, A. H., Wong, A. W., Denham, M., Kilpatrick, T. J., & Murray, S. S. (2012) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2012.07871.x · Cited by 84
How the Cortex Gets Its Folds: An Inside-Out, Connectivity-Driven Model for the Scaling of Mammalian Cortical Folding
Mota, B., & Herculano‐Houzel, S. (2012) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2012.00003 · Cited by 80
Mechanical Strain Promotes Oligodendrocyte Differentiation by Global Changes of Gene Expression
Jagielska, A., Lowe, A. L., Makhija, E., Wróblewska, L., Guck, J. R., Franklin, R. J. M., Shivashankar, G. V., & Vliet, K. J. V. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00093 · Cited by 80
Perturbed Myelination Process of Premyelinating Oligodendrocyte in Niemann-PickType C Mouse
Takikita, S., Fukuda, T., Mohri, I., Yagi, T., & Suzuki, K. (2004) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/63.6.660 · Cited by 78
Astrocytes promote TNF-mediated toxicity to oligodendrocyte precursors
Kim, S.-J., Steelman, A. J., Koito, H., & Li, J. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.07084.x · Cited by 77
The Lysosomal Sialic Acid Transporter Sialin Is Required for Normal CNS Myelination
Prolo, L. M., Vogel, H. S., & Reimer, R. J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3005-09.2009 · Cited by 76
The Importance of NAD in Multiple Sclerosis
Penberthy, W. T., & Tsunoda, I. (2009) · Current Pharmaceutical Design · doi:10.2174/138161209787185751 · Cited by 77
Increased growth factor expression and cell proliferation after contusive spinal cord injury
Zai, L. J., Yoo, S., & Wrathall, J. R. (2005) · Brain Research · doi:10.1016/j.brainres.2005.05.071 · Cited by 75
Functional electrical stimulation helps replenish progenitor cells in the injured spinal cord of adult rats
Becker, D., Gary, D. S., Rosenzweig, E. S., Grill, W. M., & McDonald, J. W. (2010) · Experimental Neurology · doi:10.1016/j.expneurol.2009.12.029 · Cited by 75
Dysregulation of the neuregulin‐1– E rb B network modulates endogenous oligodendrocyte differentiation and preservation after spinal cord injury
Gauthier, M., Kosciuczyk, K., Tapley, L., & Karimi‐Abdolrezaee, S. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12268 · Cited by 74
Cyfip1 haploinsufficient rats show white matter changes, myelin thinning, abnormal oligodendrocytes and behavioural inflexibility
Silva, A. I., Haddon, J. E., Ahmed Syed, Y., Trent, S., Lin, T.-C. E., Patel, Y., Carter, J., Haan, N., Honey, R. C., Humby, T., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11119-7 · Cited by 71
Microglia Diversity in Health and Multiple Sclerosis
Zia, S., Rawji, K. S., Michaels, N. J., Burr, M. K., Kerr, B. J., Healy, L. M., & Plemel, J. R. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.588021 · Cited by 70
Roles of Voltage-Dependent Sodium Channels in Neuronal Development, Pain, and Neurodegeneration
Wada, A. (2006) · Journal of Pharmacological Sciences · doi:10.1254/jphs.crj06012x · Cited by 70
Neuregulin‐2 is developmentally regulated and targeted to dendrites of central neurons
Longart, M., Liu, Y., Karavanova, I. D., & Buonanno, A. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20016 · Cited by 70
The Role of Oligodendroglial Dysfunction in Amyotrophic Lateral Sclerosis
Nonneman, A., Robberecht, W., & Bosch, L. V. D. (2014) · Neurodegenerative Disease Management · doi:10.2217/nmt.14.21 · Cited by 76
Diffusion Imaging of White Matter in Schizophrenia: Progress and Future Directions
Karlsgodt, K. H. (2015) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2015.12.001 · Cited by 71
Characterization of a neural-specific splicing form of the human neuregulin 3 gene involved in oligodendrocyte survival
Carteron, C., Ferrer-Montiel, A. V., & Cabedo, H. (2006) · Journal of Cell Science · doi:10.1242/jcs.02799 · Cited by 67
Retinal organization in the bcl‐2‐overexpressing transgenic mouse
Strettoi, E., & Volpini, M. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10177 · Cited by 67
Evidence that perinatal and adult NG2-glia are not conventional oligodendrocyte progenitors and do not depend on axons for their survival
Greenwood, K. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00176-3 · Cited by 66
Integrin Signaling in Oligodendrocytes and Its Importance in CNS Myelination
O'Meara, R. W., Michalski, J.-P., & Kothary, R. (2010) · Journal of signal transduction · doi:10.1155/2011/354091 · Cited by 77
Oligodendrocyte Progenitor Cells Promote Neovascularization in Glioma by Disrupting the Blood–Brain Barrier
Huang, Y., Hoffman, C. E., Rajappa, P., Kim, J. H., Hu, W., Huse, J. T., Tang, Z., Li, X., Weksler, B. B., Bromberg, J., et al. (2013) · Cancer Research · doi:10.1158/0008-5472.can-13-1072 · Cited by 64
Growth Factor Control of CNS Myelination
Park, S.-K., Solomon, D., & Vartanian, T. K. (2001) · Developmental Neuroscience · doi:10.1159/000048716 · Cited by 65
Not being the wrong size
Gomer, R. H. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35048058 · Cited by 64
A novel type of glial cell in the retina is stimulated by insulin‐like growth factor 1 and may exacerbate damage to neurons and Müller glia
Fischer, A. J., Scott, M. A., Zelinka, C. P., & Sherwood, P. (2009) · Glia · doi:10.1002/glia.20950 · Cited by 62
High-Frequency Microdomain Ca2+ Transients and Waves during Early Myelin Internode Remodeling
Battefeld, A., Popovic, M. A., de Vries, S. I., & Kole, M. H. P. (2019) · Cell Reports · doi:10.1016/j.celrep.2018.12.039 · Cited by 64
Modulating astrogliosis after neurotrauma
McGraw, J., Hiebert, G. W., & Steeves, J. D. (2001) · Journal of Neuroscience Research · doi:10.1002/1097-4547(20010115)63:2 · Cited by 277
Alterations of myelin morphology and oligodendrocyte development in early stage of Alzheimer’s disease mouse model
Wu, Y. C., Ma, Y., Liu, Z., Geng, Q., Chen, Z., & Zhang, Y. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.02.007 · Cited by 67
Oligodendrogliopathy in neurodegenerative diseases with abnormal protein aggregates: The forgotten partner
Ferrer, I. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.07.004 · Cited by 65
Rho Regulates Membrane Transport in the Endocytic Pathway to Control Plasma Membrane Specialization in Oligodendroglial Cells
Kippert, A., Trajković, K., Rajendran, L., Ries, J., & Simons, M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4926-06.2007 · Cited by 58
Loss of Fyn tyrosine kinase on the C57BL/6 genetic background causes hydrocephalus with defects in oligodendrocyte development
Goto, J., Tezuka, T., Nakazawa, T., Sagara, H., & Yamamoto, T. S. (2008) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2008.02.009 · Cited by 60
Axonal Signals and Oligodendrocyte Differentiation
Bozzali, M., & Wrabetz, L. G. (2004) · Neurochemical Research · doi:10.1023/b:nere.0000021242.12455.75 · Cited by 57
The concept of space and competition in immune regulation
Stockinger, B., Barthlott, T., & Kassiotis, G. (2004) · Immunology · doi:10.1111/j.1365-2567.2004.01831.x · Cited by 59
Netrin-1 Is Required for the Normal Development of Spinal Cord Oligodendrocytes
Tsai, H., Macklin, W. B., & Miller, R. H. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3571-05.2006 · Cited by 57
C5b-9 Terminal Complex Protects Oligodendrocytes from Apoptotic Cell Death by Inhibiting Caspase-8 Processing and Up-Regulating FLIP
Cudrici, C. D., Niculescu, F. I., Jensen, T., Zafranskaia, E., Fosbrink, M. D., Rus, V., Shin, M. L., & Rus, H. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.5.3173 · Cited by 57
Developmental expression of genes involved in neurosteroidogenesis: 3β-hydroxysteroid dehydrogenase/Δ5-Δ4 isomerase in the rat brain
Ibanez, C., Guennoun, R., Liere, P., Eychenne, B., Pianos, A., El-Etr, M., Baulieu, E.-E., & Schumacher, M. (2003) · Endocrinology · doi:10.1210/en.2002-0073 · Cited by 56
Control of glial precursor cell development in the mouse optic nerve by sonic hedgehog from retinal ganglion cells
Dakubo, G. D., Beug, S. T., Mazerolle, C. J., Thurig, S., Wang, Y., & Wallace, V. A. (2008) · Brain Research · doi:10.1016/j.brainres.2008.06.058 · Cited by 56
Theiler's virus infection: Pathophysiology of demyelination and neurodegeneration
Sato, F., Tanaka, H., Hasanovic, F., & Tsunoda, I. (2010) · Pathophysiology · doi:10.1016/j.pathophys.2010.04.011 · Cited by 55
Response of Ependymal Progenitors to Spinal Cord Injury or Enhanced Physical Activity in Adult Rat
Čı́žková, D., Nagyová, M., Slovinská, L., Novotna, I., Radoňak, J., Čížek, M., Mechírová, E., Tomori, Z., Juhásová, J., Motlík, J., et al. (2009) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-009-9387-1 · Cited by 54
Selective Cell-Cycle Arrest and Induction of Apoptosis in Proliferating Neural Cells by Ganglioside GM3
Nakatsuji, Y., & Miller, R. H. (2001) · Experimental Neurology · doi:10.1006/exnr.2000.7602 · Cited by 54
Potential Role of Neuroactive Tryptophan Metabolites in Central Fatigue: Establishment of the Fatigue Circuit
Yamashita, M. (2020) · International Journal of Tryptophan Research · doi:10.1177/1178646920936279 · Cited by 54
Dorsal Spinal Cord Inhibits Oligodendrocyte Development
Wada, T., Kagawa, T., Ivanova, A. N., Zalc, B., Shirasaki, R., Murakami, F., Iemura, S.-I., Ueno, N., & Ikenaka, K. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9869 · Cited by 53
nsf Is Essential for Organization of Myelinated Axons in Zebrafish
Woods, I. G., Lyons, D. A., Voas, M. G., Pogoda, H., & Talbot, W. S. (2006) · Current Biology · doi:10.1016/j.cub.2006.02.067 · Cited by 51
In vivo analysis of oligodendrocyte lineage development in postnatal FGF2 null mice
Murtie, J. C., Zhou, Y., Le, T. Q., & Armstrong, R. C. (2004) · Glia · doi:10.1002/glia.20142 · Cited by 51
Identification of Tmem10/Opalin as a novel marker for oligodendrocytes using gene expression profiling
Kippert, A., Trajković, K., Fitzner, D., Opitz, L., & Simons, M. (2008) · BMC Neuroscience · doi:10.1186/1471-2202-9-40 · Cited by 46
Natural Polyphenols and Apoptosis Induction in Cancer Therapy
Estrela, L. R. M. (2013) · Journal of Carcinogenesis & Mutagenesis · doi:10.4172/2157-2518.s6-004 · Cited by 50
AMPA/kainate receptors in mouse spinal cord cell‐specific display of receptor subunits by oligodendrocytes and astrocytes and at the nodes of Ranvier
Brand‐Schieber, E., & Werner, P. (2003) · Glia · doi:10.1002/glia.10136 · Cited by 50
Dpp and Hedgehog mediate neuron–glia interactions in Drosophila eye development by promoting the proliferation and motility of subretinal glia
Rangarajan, R., Courvoisier, H., & Gaul, U. (2001) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00501-9 · Cited by 50
Remyelination in multiple sclerosis: Cellular mechanisms and novel therapeutic approaches
Olsen, J. A., & Akirav, E. M. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23493 · Cited by 51
Epidermal Growth Factor in the CNS: A Beguiling Journey from Integrated Cell Biology to Multiple Sclerosis. An Extensive Translational Overview
Scalabrino, G. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00989-x · Cited by 49
Neural progenitors, neurons and oligodendrocytes from human umbilical cord blood cells in a serum-free, feeder-free cell culture
Chua, S. J., Bielecki, R., Wong, C. J., Yamanaka, N., Rogers, I. M., & Casper, R. F. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.12.045 · Cited by 47
Targeting Glia Cells: Novel Perspectives for the Treatment of Neuropsychiatric Diseases
Benedetto, B. D., & Rupprecht, R. (2013) · Current Neuropharmacology · doi:10.2174/1570159x11311020004 · Cited by 50
Regulating Axonal Responses to Injury: The Intersection between Signaling Pathways Involved in Axon Myelination and The Inhibition of Axon Regeneration
Rao, S. N. R., & Pearse, D. D. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00033 · Cited by 45
The Rules of Attraction in Central Nervous System Myelination
Almeida, R. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00367 · Cited by 50
Novel role for aspartoacylase in regulation of BDNF and timing of postnatal oligodendrogenesis
Francis, J. S., Olariu, A., McPhee, S., & Leone, P. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.20866 · Cited by 45
Constitutional mislocalization of Pten drives precocious maturation in oligodendrocytes and aberrant myelination in model of autism spectrum disorder
Lee, H., Thacker, S., Sarn, N., Dutta, R., & Eng, C. (2019) · Translational Psychiatry · doi:10.1038/s41398-018-0364-7 · Cited by 45
Insulin-like growth factor-1 promotes neuronal glucose utilization during brain development and repair processes
Bondy, C. A., & Cheng, C. M. (2002) · International review of neurobiology · doi:10.1016/s0074-7742(02)51006-0 · Cited by 43
Sema4D as an inhibitory regulator in oligodendrocyte development
Yamaguchi, W., Tamai, R., Kageura, M., Furuyama, T., & Inagaki, S. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.12.004 · Cited by 43
NF-κB signaling regulates myelination in the CNS
Blank, T., & Prinz, M. (2014) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2014.00047 · Cited by 44
SHANK3 deficiency leads to myelin defects in the central and peripheral nervous system
Malara, M., Lutz, A.-K., Incearap, B., Bauer, H. F., Cursano, S., Volbracht, K., Lerner, J. J., Pandey, R., Delling, J. P., Ioannidis, V., et al. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04400-4 · Cited by 49
Human umbilical cord blood cells directly suppress ischemic oligodendrocyte cell death
Hall, A. A., Guyer, A. G., Leonardo, C. C., Ajmo, C. T., Collier, L. A., Willing, A. E., & Pennypacker, K. R. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21857 · Cited by 43
Multiple Sclerosis and Aging: The Dynamics of Demyelination and Remyelination
Correale, J. D., & Ysrraelit, M. C. (2022) · ASN NEURO · doi:10.1177/17590914221118502 · Cited by 45
Sema4D deficiency results in an increase in the number of oligodendrocytes in healthy and injured mouse brains
Taniguchi, Y., Amazaki, M., Furuyama, T., Yamaguchi, W., Takahara, M., Saino, O., Wada, T., Niwa, H., Tashiro, F., Miyazaki, J., et al. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.22124 · Cited by 42
Regional variation, hemispheric asymmetries and gender differences in pericortical white matter
Kang, X., Herron, T. J., & Woods, D. L. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.03.016 · Cited by 41
On the resemblance of synapse formation and CNS myelination
Almeida, R., & Lyons, D. A. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.062 · Cited by 42
Tryptophan circuit in fatigue: From blood to brain and cognition.
Yamashita, M., & Yamamoto, T. (2017) · Brain Research · doi:10.1016/j.brainres.2017.09.002 · Cited by 37
Oligodendrocyte Development in the Absence of Their Target Axons In Vivo
Almeida, R., & Lyons, D. A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0164432 · Cited by 41
Extrinsic Factors Driving Oligodendrocyte Lineage Cell Progression in CNS Development and Injury
Baydyuk, M., Morrison, V. E., Gross, P. S., & Huang, J. K. (2020) · Neurochemical Research · doi:10.1007/s11064-020-02967-7 · Cited by 42
Temporal analysis of growth factor mRNA expression in myelinating rat brain aggregate cultures: Increments in CNTF, FGF-2, IGF-I, and PDGF-AA mRNA are induced by antibody-mediated demyelination
Copelman, C. A., Cuzner, M. L., Groome, N. P., & Diemel, L. T. (2000) · Glia · doi:10.1002/(sici)1098-1136(200006)30:4 · Cited by 35
Neuronal network structuring induces greater neuronal activity through enhanced astroglial development
Chang, J. C. S., Brewer, G. J., & Wheeler, B. C. (2006) · Journal of Neural Engineering · doi:10.1088/1741-2560/3/3/004 · Cited by 39
Implication of γ-secretase in neuregulin-induced maturation of oligodendrocytes
Lai, C., & Feng, L. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2003.12.131 · Cited by 41
Effects of axon degeneration on oligodendrocyte lineage cells: Dorsal rhizotomy evokes a repair response while axon degeneration rostral to spinal contusion induces both repair and apoptosis
Sun, F., Lin, C. G., Mctigue, D., Shan, X., Tovar, C. A., Bresnahan, J. C., & Beattie, M. S. (2010) · Glia · doi:10.1002/glia.21009 · Cited by 38
Biomaterial Approaches to Enhancing Neurorestoration after Spinal Cord Injury: Strategies for Overcoming Inherent Biological Obstacles
Siebert, J. R., Eade, A. M., & Osterhout, D. J. (2015) · BioMed Research International · doi:10.1155/2015/752572 · Cited by 40
The Relationship of Developmental Changes in White Matter to the Onset of Psychosis
Karlsgodt, K. H., Jacobson, S. C., Seal, M. L., & Fusar‐Poli, P. (2012) · Current Pharmaceutical Design · doi:10.2174/138161212799316073 · Cited by 35
Erythropoietin promotes oligodendrogenesis and myelin repair following lysolecithin-induced injury in spinal cord slice culture
Cho, Y. K., Kim, G.-H., Park, S., Sim, J. H., Won, Y. J., Hwang, C. H., Yoo, J. Y., & Hong, H. N. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.12.029 · Cited by 37
JC Virus Agnoprotein Inhibits In Vitro Differentiation of Oligodendrocytes and Promotes Apoptosis
Merabova, N., Kaniowska, D., Kaminski, R., Deshmane, S. L., White, M. K., Amini, S., Darbinyan, A., & Khalili, K. (2007) · Journal of Virology · doi:10.1128/jvi.01680-07 · Cited by 37
Glial ensheathment of peripheral axons in Drosophila
Banerjee, S., & Bhat, M. A. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21574 · Cited by 36
The intellectual disability protein PAK3 regulates oligodendrocyte precursor cell differentiation
Renkilaraj, M. R. L. M., Baudouin, L., Wells, C. M., Doulazmi, M., Wehrlé, R., Cannaya, V., Bachelin, C., Barnier, J., Jia, Z., Nait‐Oumesmar, B., et al. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.12.004 · Cited by 33
A role for Sec8 in oligodendrocyte morphological differentiation
Anitei, M., Ifrim, M. F., Ewart, M., Cowan, A. E., Carson, J. H., Bansal, R., & Pfeiffer, S. E. (2006) · Journal of Cell Science · doi:10.1242/jcs.02785 · Cited by 35
Autosomal Dominant Leukodystrophy Caused by Lamin B1 Duplications: A Clinical and Molecular Case Study of Altered Nuclear Function and Disease
Padiath, Q. S., & Fu, Y. (2010) · Methods in cell biology · doi:10.1016/s0091-679x(10)98014-x · Cited by 35
Hypoxia and myelination deficits in the developing brain
Singh, D. K., Ling, E., & Kaur, C. (2018) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2018.06.012 · Cited by 34
Studies on Integrins in the Nervous System
Denda, S., & Reichardt, L. F. (2007) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(07)26010-0 · Cited by 32
Abnormal gene expression in cerebellum of Npc1−/− mice during postnatal development
Liao, G., Wen, Z., Irizarry, K. J. L., Huang, Y. S., Mitsouras, K., Darmani, M., Leon, T. L., Shi, L. M., & Bi, X. (2010) · Brain Research · doi:10.1016/j.brainres.2010.02.019 · Cited by 31
Glutamate Signaling via the AMPAR Subunit GluR4 Regulates Oligodendrocyte Progenitor Cell Migration in the Developing Spinal Cord
Piller, M., Werkman, I. L., Brown, R. I., Latimer, A. J., & Kucenas, S. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2562-20.2021 · Cited by 29
Eccentric rehabilitation induces white matter plasticity and sensorimotor recovery in chronic spinal cord injury
Faw, T. D., Lakhani, B., Schmalbrock, P., Knopp, M. V., Lohse, K. R., Kramer, J. L. K., Liu, H., Nguyen, H. T., Phillips, E. G., Bratasz, A., et al. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113853 · Cited by 29
Sonic Hedgehog Is a Potent Inducer of Rat Oligodendrocyte Development from Cortical Precursors in Vitro
Murray, K., Calaora, V., Rottkamp, C. A., Guicherit, O. M., & Dubois-Dalcq, M. E. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2001.1079 · Cited by 29
Live imaging of remyelination after antibody-mediated demyelination in an ex-vivo model for immune mediated CNS damage
Harrer, M. D., von Büdingen, H. ‐., Stoppini, L., Alliod, C., Pouly, S., Fischer, K., & Goebels, N. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2008.12.027 · Cited by 28
Myelin under construction—teamwork required
Boiko, T., & Winckler, B. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200602101 · Cited by 28
Oligodendrocyte precursor cells prune axons in the mouse neocortexPreprint
Buchanan, J., Elabbady, L., Collman, F., Jorstad, N. L., Bakken, T. E., Ott, C. M., Glatzer, J. C., Bleckert, A., Bodor, Á. L., Brittan, D., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.29.446047 · Cited by 28
Expression and localization of myosin-1d in the developing nervous system
Benesh, A. E., Fleming, J. T., Chiang, C. C., Carter, B. D., & Tyska, M. J. (2012) · Brain Research · doi:10.1016/j.brainres.2011.12.054 · Cited by 27
Hes1 functions downstream of growth factors to maintain oligodendrocyte lineage cells in the early progenitor stage
Ogata, T., Ueno, T., Hoshikawa, S., Ito, J., Okazaki, R., Hayakawa, K., Morioka, K., Yamamoto, S., Nakamura, K., Tanaka, S., et al. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.12.015 · Cited by 28
Cellular Environment Directs Differentiation of Human Umbilical Cord Blood–Derived Neural Stem Cells In Vitro
Markiewicz, I., Sypecka, J., Domańska‐Janik, K., Wyszomirski, T., & Łukomska, B. (2011) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155410397997 · Cited by 26
How big is the myelinating orchestra? Cellular diversity within the oligodendrocyte lineage: facts and hypotheses
Tomassy, G. S., & Fossati, V. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00201 · Cited by 27

Authors: Barres, B. A., & Raff, M. C.
Affiliations: Stanford Medicine (US)
MRC Laboratory for Molecular Cell Biology (GB)
ORCID: Barres, Ben A.
Venue: The Journal of Cell Biology
Publisher: Rockefeller University Press
Published: 1999-12-13
Volume: 147
Issue: 6
Pages: 1123-1128
ISSN: 0021-9525 (ISSN-L)
1540-8140
DOI: 10.1083/jcb.147.6.1123
PMC: PMC2168096
OpenAlex: W1993097534
Cited by: 360
References: 69
Citations by year: 2026: 2 · 2025: 6 · 2024: 28 · 2023: 5 · 2022: 9 · 2021: 13 · 2020: 16 · 2019: 8 · 2018: 12 · 2017: 14 · 2016: 9 · 2015: 10 · 2014: 17 · 2013: 17 · 2012: 9
FWCI: 1.28
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: cc-by-nc-sa
Locations: The Journal of Cell Biology (publishedVersion)
PubMed Central (publishedVersion, cc-by-nc-sa)
PubMed (publishedVersion)
UCL Discovery (University College London) (submittedVersion)
Topics: Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
Keywords: oligodendrocyte development, axon-glia interaction, brain development, glial differentiation
MeSH terms: Animals, Axons, Cell Count, Cell Differentiation, Cell Division, Cell Survival, Myelin Sheath, Oligodendroglia, Neuregulins

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Axonal Control of Oligodendrocyte Development

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks