Increased number of unmyelinated axons in optic nerves of adult mice deficient in the myelin-associated glycoprotein (MAG)

Immunoelectron microscopic localization of neural cell adhesion molecules (L1, N-CAM, and MAG) and their shared carbohydrate epitope and myelin basic protein in developing sciatic nerve.

Martini, R., & Schachner, M. (1986) · The Journal of Cell Biology · doi:10.1083/jcb.103.6.2439 · Cited by 488 · 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

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

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

Myelin-associated glycoprotein demonstrated immunocytochemically in myelin and myelin-forming cells of developing rat.

Sternberger, N. H., Quarles, R. H., Itoyama, Y., & Webster, H. D. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.3.1510 · Cited by 370 · 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

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

Immunohistological localization of the adhesion molecules L1, N‐CAM, and MAG in the developing and adult optic nerve of mice

Bartsch, U., Kirchhoff, F., & Schachner, M. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902840310 · Cited by 234 · see citing works

Crucial Role for the Myelin‐associated Glycoprotein in the Maintenance of Axon‐Myelin Integrity

Fruttiger, M., Montag, D., Schachner, M., & Martini, R. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb00347.x · Cited by 231 · see citing works

Myelin‐Associated Glycoprotein Location and Potential Functions^a

TRAPP, B. D. (1990) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1990.tb42378.x · Cited by 172 · see citing works

Evidence for an early role for myelin‐associated glycoprotein in the process of myelination

Owens, G. C., & Bunge, R. P. (1989) · Glia · doi:10.1002/glia.440020208 · Cited by 101 · see citing works

Schwann cells infected with a recombinant retrovirus expressing myelin-associated glycoprotein antisense RNA do not form myelin

Owens, G. C., & Bunge, R. P. (1991) · Neuron · doi:10.1016/0896-6273(91)90369-b · Cited by 98 · see citing works

Expression of recombinant myelin-associated glycoprotein in primary Schwann cells promotes the initial investment of axons by myelinating Schwann cells.

Owens, G. C., Boyd, C. J., Bunge, R. P., & Salzer, J. L. (1990) · The Journal of Cell Biology · doi:10.1083/jcb.111.3.1171 · Cited by 75 · see citing works

Myelination and axonal regeneration in the central nervous system of mice deficient in the myelin-associated glycoprotein

Bartsch, U. (1996) · Journal of Neurocytology · doi:10.1007/bf02284804 · Cited by 55 · see citing works

Multiply myelinated axons in the optic nerve of mice deficient for the myelin‐associated glycoprotein

Bartsch, U., Montag, D., Bartsch, S., & Schachner, M. (1995) · Glia · doi:10.1002/glia.440140206 · Cited by 47 · see citing works

Axon Myelination: Myelination without myelin-associated glycoprotein

Meyer‐Franke, A., & Barres, B. A. (1994) · Current Biology · doi:10.1016/s0960-9822(00)00190-1 · Cited by 18 · see citing works

Different voltage-gated sodium currents are expressed by human neuroblastoma NB69 cells when cultured in defined serum-free and in astroglial-conditioned media

Urbano, F. J., Sierra, F., Colombo, J. A., Velasco, J. M., & Bu�o, W. (1997) · Glia · doi:10.1002/(sici)1098-1136(199702)19:2 · Cited by 9 · see citing works

Oligodendrocyte Dynamics in the Healthy Adult CNS: Evidence for Myelin Remodeling

Young, K. M., Psachoulia, K., Tripathi, R. B., Dunn, S.-J., Cossell, L., Attwell, D., Tohyama, K., & Richardson, W. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.006 · Cited by 872 · see citing works

White Matter Changes in Schizophrenia: Evidence for Myelin-Related Dysfunction

Davis, K. L., Stewart, D. G., Friedman, J. I., Buchsbaum, M., Harvey, P. D., Hof, P. R., Buxbaum, J., & Haroutunian, V. (2003) · Archives of General Psychiatry · doi:10.1001/archpsyc.60.5.443 · Cited by 793 · see citing works

Axon-Glial Signaling and the Glial Support of Axon Function

Nave, K., & Trapp, B. D. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094309 · Cited by 659 · see citing works

Mice lacking complex gangliosides develop Wallerian degeneration and myelination defects

Sheikh, K. A., Sun, J., Liu, Y., Kawai, H., Crawford, T. O., Proia, R. L., Griffin, J. W., & Schnaar, R. L. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.13.7532 · Cited by 396 · see citing works

Diabetic neuropathy and nerve regeneration

Yasuda, H., Terada, M., Maeda, K., Kogawa, S., Sanada, M., Haneda, M., Kashiwagi, A., & Kikkawa, R. (2003) · Progress in Neurobiology · doi:10.1016/s0301-0082(03)00034-0 · Cited by 241 · see citing works

The Pathobiology of Amyotrophic Lateral Sclerosis: A Proteinopathy?

Strong, M. J., Kesavapany, S., & Pant, H. C. (2005) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/01.jnen.0000173889.71434.ea · Cited by 206 · see citing works

Myelin-associated glycoprotein and complementary axonal ligands, gangliosides, mediate axon stability in the CNS and PNS: Neuropathology and behavioral deficits in single- and double-null mice

Pan, B., Fromholt, S., Hess, E. J., Crawford, T. O., Griffin, J. W., Sheikh, K. A., & Schnaar, R. L. (2005) · Experimental Neurology · doi:10.1016/j.expneurol.2005.04.017 · Cited by 195 · see citing works

X-linked adrenoleukodystrophy enigma: How does the ALD peroxisomal transporter mutation affect CNS glia?

Aubourg, P. R., & Dubois-Dalcq, M. E. (2000) · Glia · doi:10.1002/(sici)1098-1136(20000115)29:2 · Cited by 42 · see citing works

White matter plasticity in adulthood

Wang, S., & Young, K. M. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.10.018 · Cited by 172 · see citing works

New Aspects of Siglec Binding Specificities, Including the Significance of Fucosylation and of the Sialyl-Tn Epitope

der Linden, E. C. M. B.-V., & Varki, A. P. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.12.8625 · Cited by 168 · see citing works

Myelin sheaths: glycoproteins involved in their formation, maintenance and degeneration

Quarles, R. H. (2002) · Cellular and Molecular Life Sciences · doi:10.1007/pl00012510 · Cited by 160 · see citing works

Myelin‐associated glycoprotein and its axonal receptors

Schnaar, R. L., & López, P. H. H. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.21992 · Cited by 153 · see citing works

The raft-associated protein MAL is required for maintenance of proper axon–glia interactions in the central nervous system

Schaeren‐Wiemers, N., Bonnet, A., Erb, M., Erne, B., Bartsch, U., Kern, F., Mantei, N., Sherman, D. L., & Suter, U. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200406092 · Cited by 141 · see citing works

Myelin-associated glycoprotein and myelin galactolipids stabilize developing axo-glial interactions

Marcus, J., Dupree, J., & Popko, B. (2002) · Journal of Cell Biology · doi:10.1083/jcb.200111047 · Cited by 138 · see citing works

ERK1/2 Activation in Preexisting Oligodendrocytes of Adult Mice Drives New Myelin Synthesis and Enhanced CNS Function

Jeffries, M. A., Urbanek, K., Torres, L., Wendell, S. G., Rubio, M. E., & Fyffe-Maricich, S. L. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1444-16.2016 · Cited by 119 · see citing works

Glycolipid-mediated cell?cell recognition in inflammation and nerve regeneration*1

Schnaar, R. L. (2004) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2004.02.019 · Cited by 112 · see citing works

Conversion of cellular sialic acid expression from N-acetyl- to N-glycolylneuraminic acid using a synthetic precursor, N-glycolylmannosamine pentaacetate: inhibition of myelin-associated glycoprotein binding to neural cells

Collins, B. E. (2000) · Glycobiology · doi:10.1093/glycob/10.1.11 · Cited by 103 · see citing works

Abnormal Indices of Cell Cycle Activity in Schizophrenia and their Potential Association with Oligodendrocytes

Katsel, P., Davis, K. L., Li, C., Tan, W., Greenstein, E., Hoffman, L. B., & Haroutunian, V. H. (2008) · Neuropsychopharmacology · doi:10.1038/npp.2008.19 · Cited by 102 · see citing works

Myelin‐associated glycoprotein modulates expression and phosphorylation of neuronal cytoskeletal elements and their associated kinases

Dashiell, S. M., Tanner, S. L., Pant, H. C., & Quarles, R. H. (2002) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2002.00927.x · Cited by 98 · see citing works

The Cytoplasmic Domain of the Large Myelin-Associated Glycoprotein Isoform Is Needed for Proper CNS But Not Peripheral Nervous System Myelination

Fujita, N., Kemper, A., Dupree, J. L., Nakayasu, H., Bartsch, U., Schachner, M., Maeda, N., Suzuki, K., Suzuki, K., & Popko, B. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-06-01970.1998 · Cited by 85 · see citing works

Maternal separation with early weaning: a rodent model providing novel insights into neglect associated developmental deficits

Carlyle, B. C., Duque, A., Kitchen, R. R., Bordner, K. A., Coman, D., Doolittle, E., Papademetris, X., Hyder, F., Taylor, J. R., & Simen, A. A. (2012) · Development and Psychopathology · doi:10.1017/s095457941200079x · Cited by 80 · see citing works

Severe Hypomyelination of the Murine CNS in the Absence of Myelin-Associated Glycoprotein and Fyn Tyrosine Kinase

Biffiger, K., Bartsch, S., Montag, D., Aguzzi, A., Schachner, M., & Bartsch, U. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-19-07430.2000 · Cited by 77 · see citing works

Central Nervous System Regeneration Inhibitors and their Intracellular Substrates

Nash, M., Pribiag, H., Fournier, A. E., & Jacobson, C. (2009) · Molecular Neurobiology · doi:10.1007/s12035-009-8083-y · Cited by 74 · see citing works

Neuronal cyclin-dependent kinase 5: role in nervous system function and its specific inhibition by the Cdk5 inhibitory peptide

Kesavapany, S., Li, B., Amin, N. D., Zheng, Y.-L., Grant, P. G., & Pant, H. C. (2003) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2003.11.020 · Cited by 69 · see citing works

Novel molecular insights into the critical role of sulfatide in myelin maintenance/function

Palavicini, J. P., Wang, C., Chen, L., Ahmar, S., Higuera, J. D., Dupree, J. L., & Han, X. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13738 · Cited by 69 · see citing works

Functional Genomic and Proteomic Analysis Reveals Disruption of Myelin-Related Genes and Translation in a Mouse Model of Early Life Neglect

Bordner, K. A., George, E. D., Carlyle, B. C., Duque, A., Kitchen, R. R., Lam, T. T., Colangelo, C. M., Stone, K. L., Abbott, T. B., Mane, S., et al. (2011) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2011.00018 · Cited by 65 · see citing works

Myelin proteolipid proteins promote the interaction of oligodendrocytes and axons

Yool, D. A., Klugmann, M., McLaughlin, M., Vouyiouklis, D. A., Dimou, L., Barrie, J. A., McCulloch, M. C., Nave, K., & Griffiths, I. R. (2001) · Journal of Neuroscience Research · doi:10.1002/1097-4547(20010115)63:2 · Cited by 63 · see citing works

Sialometabolism in Brain Health and Alzheimer’s Disease

Rawal, P., & Zhao, L. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.648617 · Cited by 62 · see citing works

Molecular dissection of the myelin-associated glycoprotein receptor complex reveals cell type–specific mechanisms for neurite outgrowth inhibition

Venkatesh, K., Chivatakarn, O., Sheu, S., & Giger, R. J. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200702102 · Cited by 61 · see citing works

Mouse Models of Myelin Diseases

Werner, H. B., Jung, M., Klugmann, M., Sereda, M. W., Griffiths, I. R., & Nave, K. (1998) · Brain Pathology · doi:10.1111/j.1750-3639.1998.tb00200.x · Cited by 57 · see citing works

Sensing the neuronal glycocalyx by glial sialic acid binding immunoglobulin-like lectins

Linnartz-Gerlach, B., Mathews, M., & Neumann, H. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.05.061 · Cited by 54 · see citing works

Cyclin-Dependent Kinase 5 in Neurofilament Function and Regulation

Kesavapany, S., Li, B.-S., & Pant, H. C. (2003) · Neurosignals · doi:10.1159/000074627 · Cited by 54 · see citing works

Possible Contributions of Myelin and Oligodendrocyte Dysfunction to Schizophrenia

Stewart, D. G., & Davis, K. L. (2004) · International review of neurobiology · doi:10.1016/s0074-7742(04)59015-3 · Cited by 53 · see citing works

Activity-Dependent and Experience-Driven Myelination Provide New Directions for the Management of Multiple Sclerosis

Jensen, S. K., & Yong, V. W. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.04.003 · Cited by 44 · see citing works

Comparison of myelin, axon, lipid, and immunopathology in the central nervous system of differentially myelin-compromised mutant mice: a morphological and biochemical study

Loers, G., Aboul‐Enein, F., Bartsch, U., Lassmann, H., & Schachner, M. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.06.006 · Cited by 42 · see citing works

Myelin Plasticity and Repair: Neuro-Glial Choir Sets the Tuning

Ronzano, R., Thétiot, M., Lubetzki, C., & Desmazières, A. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00042 · Cited by 38 · see citing works

Neurofibromatosis type 1 I. General overview

Lakkis, M. M., & Tennekoon, G. I. (2000) · Journal of Neuroscience Research · doi:10.1002/1097-4547(20001215)62:6 · Cited by 55 · see citing works

Complexity of Generating Mouse Models to Study the Upper Motor Neurons: Let Us Shift Focus from Mice to Neurons

Genç, B., Gözütok, Ö., & Özdi̇nler, P. H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20163848 · Cited by 35 · see citing works

Sequence requirements for formation of conformational variants of tau similar to those found in Alzheimer's disease

Jicha, G. A., Berenfeld, B., & Davies, P. (1999) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19990315)55:6 · Cited by 123 · see citing works

Neural CAMs and their role in the development and organization of myelin sheaths

Bartsch, U. (2003) · Frontiers in bioscience · doi:10.2741/1028 · Cited by 34 · see citing works

Subtle roles of neural cell adhesion molecule and myelin-associated glycoprotein during Schwann cell spiralling in P0-deficient mice

Carenini, S., Montag, D., Schachner, M., & Martini, R. (1999) · Glia · doi:10.1002/(sici)1098-1136(199909)27:3 · Cited by 32 · see citing works

Many facets of the peripheral myelin protein PMP22 in myelination and disease

Naef, R., & Suter, U. (1998) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(19980601)41:5 · Cited by 123 · see citing works

Axon regeneration inhibitors

Yang, L. J. ‐., & Schnaar, R. L. (2008) · Neurological Research · doi:10.1179/174313208x362523 · Cited by 25 · see citing works

Establishment and characterization of adenoviral E1A immortalized cell lines derived from the rat suprachiasmatic nucleus

Earnest, D. J., Liang, F.-Q., DiGiorgio, S., Gallagher, M., Harvey, B. K., Earnest, B. J., & Seigel, G. M. (1999) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199904)39:1 · Cited by 49 · see citing works

Axonopathy precedes cell death in ocular damage mediated by blast exposure

Boehme, N., Hedberg‐Buenz, A., Tatro, N. J., Bielecki, M., Castonguay, W. C., Scheetz, T. E., Anderson, M. G., & Dutca, L. M. (2021) · Scientific Reports · doi:10.1038/s41598-021-90412-2 · Cited by 25 · see citing works

Focused ion beam‐scanning electron microscopy links pathological myelin outfoldings to axonal changes in mice lacking Plp1 or Mag

Steyer, A. M., Buscham, T. J., Lorenz, C., Hümmert, S., Eichel‐Vogel, M. A., Schadt, L. C., Edgar, J. M., Köster, S., Möbius, W., Nave, K., et al. (2022) · Glia · doi:10.1002/glia.24290 · Cited by 24 · see citing works

Early myelination involves the dynamic and repetitive ensheathment of axons which resolves through a low and consistent stabilization rate

Almeida, A. R., & Macklin, W. B. (2023) · eLife · doi:10.7554/elife.82111 · Cited by 24 · see citing works

White Matter Abnormalities and Animal Models Examining a Putative Role of Altered White Matter in Schizophrenia

Xu, H., & Li, X. (2011) · Schizophrenia Research and Treatment · doi:10.1155/2011/826976 · Cited by 23 · see citing works

Epstein–Barr and other viral mimicry of autoantigens, myelin and vitamin D-related proteins and of EIF2B, the cause of vanishing white matter disease: massive mimicry of multiple sclerosis relevant proteins by the Synechococcus phage

Carter, C. J. (2011) · Immunopharmacology and Immunotoxicology · doi:10.3109/08923973.2011.572262 · Cited by 20 · see citing works

hnRNP A1 and secondary structure coordinate alternative splicing of Mag

Zearfoss, N. R., Johnson, E. S., & Ryder, S. (2013) · RNA · doi:10.1261/rna.036780.112 · Cited by 20 · see citing works

Astrocytes protect neurons from neurotoxic injury by serum glutamate

Ye, Z., & Sontheimer, H. W. (1998) · Glia · doi:10.1002/(sici)1098-1136(199803)22:3 · Cited by 94 · see citing works

Process extension and myelin sheet formation in maturing oligodendrocytes

Buttery, P. C., & ffrench‐Constant, C. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)32070-8 · Cited by 19 · see citing works

Insufficient Oligodendrocyte Turnover in Optic Nerve Contributes to Age-Related Axon Loss and Visual Deficits

Zhi, J.-J., Wu, S.-L., Wu, H., Ran, Q., Gao, X., Chen, J., Gu, X., Li, T., Wang, F., Xiao, L., et al. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.2130-22.2023 · Cited by 20 · see citing works

Glycobiology of the Nervous System

Schnaar, R. L. (2000) · Carbohydrates in Chemistry and Biology · doi:10.1002/9783527618255.ch101 · Cited by 18 · see citing works

Myelin-Associated Glycoprotein Gene

Georgiou, J., Tropak, M. B., & Roder, J. (2004) · Elsevier eBooks · doi:10.1016/b978-012439510-7/50070-x · Cited by 17 · see citing works

Real-time multi-site multi-parametric monitoring of rat brain subjected to traumatic brain injury

Manor, T., Barbiro‐Michaely, E., Gg, R., & Mayevsky, A. (2008) · Neurological Research · doi:10.1179/174313208x346107 · Cited by 16 · see citing works

Cell Adhesion Molecules of the Immunoglobulin Superfamily in the Nervous System

Walmod, P. S., Pedersen, M. V., Berezin, V., & Bock, E. (2007) · Springer eBooks · doi:10.1007/978-0-387-30379-6_2 · Cited by 15 · see citing works

Cell recognition molecules of the immunoglobulin superfamily in the nervous system

(1996) · Biomembranes · doi:10.1016/s1874-5342(96)80017-1 · Cited by 10 · see citing works

Hereditary spastic paraplegia and prominent sensorial involvement: think MAG mutations!

Roubertie, A., Charif, M., Meyer, P., Manès, G., Meunier, I., Taïeb, G., Morales, R. J., Guichet, A., Delettre, C., Sarzi, E., et al. (2019) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.50860 · Cited by 9 · see citing works

Nerve growth factor modulates myelin‐associatedglycoprotein binding to sensory neurons

Turnley, A. M., & Bartlett, P. F. (1999) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(98)00068-9 · Cited by 8 · see citing works

Evidence for Cooperative Selection of Axons for Myelination by Adjacent Oligodendrocytes in the Optic Nerve

Walsh, D. M., Merson, T. D., Landman, K. A., & Hughes, B. D. (2016) · PLoS ONE · doi:10.1371/journal.pone.0165673 · Cited by 6 · see citing works

Myelin Molecules Limiting Nervous System Plasticity

Schnaar, R. L. (2003) · Progress in molecular and subcellular biology · doi:10.1007/978-3-642-55557-2_6 · Cited by 6 · see citing works

Microanatomy of the cerebellum in Persian squirrel (Sciurus anomalus), a transmission electron microscopy, and immunohistochemical study

Nowrozi, M., & Goodarzi, N. (2022) · Microscopy Research and Technique · doi:10.1002/jemt.24234 · Cited by 5 · see citing works

Central Axonal Development and Pathology in Early Life

Haynes, R. L., & Kinney, H. C. (2010) · Advances in neurobiology · doi:10.1007/978-1-4419-6787-9_1 · Cited by 5 · see citing works

Endoplasmic reticulum quality control and dysmyelination

Kraus, A., & Michalak, M. (2011) · BioMolecular Concepts · doi:10.1515/bmc.2011.028 · Cited by 3 · see citing works

The X‐Linked Intellectual Disability Gene, ZDHHC9 , Is Important for Oligodendrocyte Subtype Determination and Myelination

White, R., Wild, A., O’Leary, T. P., Thompson, A. J., Flibotte, S., Peng, A., Rogalski, J. C., Mair, M., Derhami, N., & Bamji, S. (2024) · bioRxiv · doi:10.1002/glia.70016 · Cited by 2 · see citing works

Major Components of Myelin in the Mammalian Central and Peripheral Nervous Systems

Kálmán, B., & Gow, A. (2007) · doi:10.1002/9780470692363.ch2 · Cited by 2 · see citing works

Potential Drug Targets for Neuroregeneration and Repair

Saikia, D. (2017) · Journal of Analytical & Pharmaceutical Research · doi:10.15406/japlr.2017.04.00109 · Cited by 1 · see citing works

Transduction of Inhibitory Signals by the Axonal Growth Cone

Wang, L., Fournier, A. E., Nakamura, F., Takahashi, T., Kalb, R. G., & Strittmatter, S. M. (2000) · Humana Press eBooks · doi:10.1007/978-1-59259-200-5_6 · Cited by 1 · see citing works

Psychiatric Disorders

Sambataro, F., & Bertolino, A. (2005) · Springer eBooks · doi:10.1007/3-540-27644-0_30 · Cited by 1 · see citing works

The septin cytoskeleton is associated with distinct myelin structures of the central and peripheral nervous system

Buser, A. (2008) · edoc (University of Basel) · doi:10.5451/unibas-004587317

I-Type Lectins: Sialoadhesin Family

Gupta, G. (2012) · Springer eBooks · doi:10.1007/978-3-7091-1065-2_16

Stickoxidmetabolite als Ursache einer differentiellen Myelingenexpression in MS-Läsionen?

Beck, A. K. (2011) · doi:10.53846/goediss-1091

Quantification of Retinal Ganglion Cell Axons in a Murine Model of Diabetic Retinopathy

Keenan, E. (2008) · OhioLink ETD Center (Ohio Library and Information Network)

Molecular Interactions between Neurons and Oligodendrocytes during Myelin Formation

Timmler, S. (2019) · doi:10.53846/goediss-7396

Neurofilaments

Kesavapany, S., Quarles, R. H., & Pant, H. C. (2007) · Springer eBooks · doi:10.1007/0-387-33781-4_4

Histological and Immunohistochemical Investigation of the Cerebellum in Porcupine and Guinea Pig

Goodarzi, N., Nowrozi, M., & Baharan, O. (2023) · Microscopy and Microanalysis · doi:10.1093/micmic/ozad043

Role of clathrin-mediated endocytosis in myelinating oligodendrocytes

Siems, S. B. (2024) · doi:10.53846/goediss-10475

Adaptor protein complex 2 (AP2) participates in biogenesis and homeostasis of myelin sheaths in the central nervous systemPreprint

Siems, S. B., Jung, R. B., Jahn, O., Meschkat, M., Michanski, S., Łukasik, N., Hümmert, S., Sasmita, A. O., Möbius, W., Benseler, F., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.02.673641

Early reduction and impaired targeting of myelin-associated glycoprotein to myelin membranes in Huntington’s diseasePreprint

Boudi, A., Sapp, E., Li, Y. Y., Shing, K., Kegel-Gleason, K. B., Petrozziello, T., Sadri‐Vakili, G., D, N. A. M., DiFiglia, M., & Li, X. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.15.682629

Guidage axonal des cellules ganglionnaires de la rétine en cours de régénération dans le noyau suprachiasmatique

Tardy, C. (2021) · doi:10.70675/1622b534z9107z40c2z85eez2caf8cc3454c

Early reduction of myelin-associated glycoprotein at myelin membranes in Huntington's disease

Boudi, A., Sapp, E., Li, Y. Y., Shing, K., Kegel-Gleason, K. B., Petrozziello, T., Sadri‐Vakili, G., D, N. A. M., DiFiglia, M., & Li, X. (2026) · Experimental Neurology · doi:10.1016/j.expneurol.2026.115995

Involvement of amyloid precursor protein in functional synapse formation in cultured hippocampal neurons

Morimoto, T., Ohsawa, I., Takamura, C., Ishiguro, M., & Kohsaka, S. (1998) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19980115)51:2 · Cited by 85 · see citing works

Myelination and axonal regeneration in the central nervous system of mice deficient in the myelin-associated glycoprotein

Bartsch, U. (1996) · Journal of Neurocytology · doi:10.1007/bf02284804 · Cited by 55 · 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

Astrocytes protect neurons from neurotoxic injury by serum glutamate

Ye, Z., & Sontheimer, H. W. (1998) · Glia · doi:10.1002/(sici)1098-1136(199803)22:3 · Cited by 94 · 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