Klugmann, M.; Schwab, M. H.; Schneider, A.; Zimmermann, F.; Griffiths, I. R.; Nave, K.-A.: Assembly of CNS Myelin in the Absence of Proteolipid Protein. Neuron 18 (1), pp. 59 - 70 (1997)

Rossner, M. J.; Dörr, J.; Gass, P.; Schwab, M. H.; Nave, K.-A.: SHARPs: MammalianEnhancer-of-Split- and Hairy-Related Proteins Coupled to Neuronal Stimulation. Molecular and Cellular Neuroscience 9 (5-6), pp. 460 - 475 (1997)

Jung, M.; Sommer, I.; Schachner, M.; Nave, K.-A.: Monoclonal Antibody O10 Defines a Conformationally Sensitive Cell-Surface Epitope of Proteolipid Protein (PLP): Evidence that PLP Misfolding Underlies Dysmyelination in Mutant Mice. The Journal of Neuroscience 16 (24), pp. 7920 - 7929 (1996)

Sereda, M.; Griffiths, I.; Pühlhofer, A.; Stewart, H.; Rossner, M. J.; Zimmermann, F.; Magyar, J. P.; Schneider, A.; Hund, E.; Meinck, H.-M. et al.; Suter, U.; Nave, K.-A.: A Transgenic Rat Model of Charcot-Marie-Tooth Disease. Neuron 16 (5), pp. 1049 - 1060 (1996)

Griffiths, I.R.; Schneider, A.; Anderson, J.; Nave, K.-A.: Transgenic and Natural Mouse Models of Proteolipid Protein (PLP)-Related Dysmyelination and Demyelination. Brain Pathology 5 (3), pp. 275 - 281 (1995)

Nave, K.-A.: Myelin Genetics: New Insight Into Old Diseases. Brain Pathology 5 (3), pp. 231 - 232 (1995)

Schneider, A. M.; Griffiths, I. R.; Readhead, C.; Nave, K.-A.: Dominant-negative action of the jimpy mutation in mice complemented with an autosomal transgene for myelin proteolipid protein. Proceedings of the National Academy of Sciences of the United States of America 92 (10), pp. 4447 - 4451 (1995)

Vellutini, C.; Horschowski, N.; Philippon, V.; Gambarelli, D.; Nave, K.-A.; Filippi, P.: Development of Lymphoid Hyperplasia in Transgenic Mice Expressing the HIV tat Gene. AIDS Research and Human Retroviruses 11 (1), pp. 21 - 29 (1995)

Bartholomä, A.; Nave, K.-A.: NEX-1: a novel brain-specific helix-loop-helix protein with autoregulation and sustained expression in mature cortical neurons. Mechanisms of Development 48 (3), pp. 217 - 228 (1994)

Nave, K.-A.: Neurological mouse mutants and the genes of myelin. Journal of Neuroscience Research 38 (6), pp. 607 - 612 (1994)

Vellutini, C.; Philippon, V.; Gambarelli, D.; Horschowski, N.; Nave, K.-A.; Navarro, J. M.; Auphan, M.; Courcoul, M. A.; Filippi, P.: The maedi-visna virus Tat protein induces multiorgan lymphoid hyperplasia in transgenic mice. Journal of Virology 68 (8), pp. 4955 - 4962 (1994)

Montag, D.; Giese, K. P.; Bartsch, U.; Martini, R.; Lang, Y.; Blüthmann, H.; Karthigasan, J.; Kirschner, D. A.; Wintergerst, E. S.; Nave, K.-A. et al.; Zielasek, J.; Toyka, K. V.; Lipp, H.-P.; Schachner, M.: Mice deficient for the glycoprotein show subtle abnormalities in myelin. Neuron 13 (1), pp. 229 - 246 (1994)

Readhead, C.; Schneider, A.; Griffiths, I.; Nave, K.-A.: Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage. Neuron 12 (3), pp. 583 - 595 (1994)

Fanarraga, M. L.; Sommer, I. U.; Griffiths, I. R.; Montague, P.; Groome, N. P.; Nave, K.-A.; Schneider, A.; Brophy, P. J.; Kennedy, P. G. E.: Oligodendrocyte development and differentiation in the rumpshaker mutation. Glia 9 (2), pp. 146 - 156 (1993)

Schneider, A.; Montague, P.; Griffiths, I.; Fanarraga, M.; Kennedy, P.; Brophy, P.; Nave, K.-A.: Uncoupling of hypomyelination and glial cell death by a mutation in the proteolipid protein gene. Nature 358, pp. 758 - 761 (1992)

Nave, K.-A.; Lemke, G.: Induction of the myelin proteolipid protein (PLP) gene in C6 glioblastoma cells: functional analysis of the PLP promotor. The Journal of Neuroscience 11 (10), pp. 3060 - 3069 (1991)

Milner, R. J.; Lai, C.; Nave, K.-A.; Montag, D.; Farber, L.; Sutcliffe, J. G.: Organization of Myelin Protein Genes: Myelin-Associated Glycoprotein. Annals of the New York Academy of Sciences 605 (1), pp. 254 - 261 (1990)

Nave, K.-A.; Milner, R. J.: Proteolipid proteins: structure and genetic expression in normal and myelin-deficient mutant mice. Critical Reviews in Neurobiology 5 (1), pp. 65 - 91 (1989)

Nave, K.-A.; Bloom,, F. E.; Milner, R. J.: A Single Nucleotide Difference in the Gene for Myelin Proteolipid Protein Defines the Jimpy Mutation in Mouse. Journal of Neurochemistry 49 (6), pp. 1873 - 1877 (1987)

Nave, K.-A.; Lai, C.; Bloom, F. E.; Milner, R. J.: Splice site selection in the proteolipid protein (PLP) gene transcript and primary structure of the DM-20 protein of central nervous system myelin. Proceedings of the National Academy of Sciences of the United States of America 84 (16), pp. 5665 - 5669 (1987)

Lai, C.; Brow, M. A.; Nave, K.-A.; Noronha, A. B.; Quarles, R. H.; Bloom, F. E.; Milner, R. J.; Sutcliffe, J. G.: Two forms of 1B236/myelin-associated glycoprotein, a cell adhesion molecule for postnatal neural development, are produced by alternative splicing. Proceedings of the National Academy of Sciences of the United States of America 84 (12), pp. 4337 - 4341 (1987)

Nave, K.-A.; Lai, C.; Bloom, F. E.; Milner, R. J.: Jimpy mutant mouse: a 74-base deletion in the mRNA for myelin proteolipid protein and evidence for a primary defect in RNA splicing. Proceedings of the National Academy of Sciences of the United States of America 83 (23), pp. 9264 - 9268 (1986)

Milner, R. J.; Lai, C.; Nave, K.-A.; Lenoir, D.; Ogata, J.; Sutcliffe, J.G.: Nucleotide sequences of two mRNAs for rat brain myelin proteolipid protein. Cell 42 (3), pp. 931 - 939 (1985)

Nave, K.-A.; Probstmeier, R.; Schachner, M.: Epidermal growth factor does not cross the blood-brain barrier. Cell and Tissue Research 241, pp. 453 - 457 (1985)

Lazzarini, R. A.; Griffin, J. W.; Lassman, H.; Nave, K.-A.; Miller, R.; Trapp, B. D. (Eds.): Myelin Biology and Disorders. Academic Press, London [u.a.] (2004), 1182 pp.

Steyer, A. M.; Schertel, A.; Nardis, C.; Möbius, W.: FIB-SEM of mouse nervous tissue: Fast and slow sample preparation. In: Methods in Cell Biology, Vol. 152, Bd. 152 Ed., pp. 1 - 21. Academic Press, San Diego [etc.] (2019)

Erwig, M. S.; Hesse, D.; Jung, R. B.; Uecker, M.; Kusch, K.; Tenzer , S.; Jahn, O.; Werner, H. B.: Myelin: Methods for Purification and Proteome Analysis. In: Oligodendrocytes: Methods and protocols, pp. 37 - 63 (Eds. Lyons, D. A.; Kegel, L.). Humana Press, New York, NY (2019)

Goebbels, S.; Nave, K.-A.: Conditional Mutagenesis in Oligodendrocyte Lineage Cells. In: Oligodendrocytes: Methods and protocols, pp. 249 - 274 (Eds. Lyons, D. A.; Kegel, L.). Humana Press, New York, NY (2019)

Weil, M.-T.; Ruhwedel, T.; Meschkat, M.; Sadowski, B.; Möbius, W.: Transmission Electron Microscopy of Oligodendrocytes and Myelin. In: Oligodendrocytes: Methods and protocols, pp. 343 - 375 (Eds. Lyons, D. A.; Kegel, L.). Humana Press,, New York, NY (2019)

Wehr, M. C.; Galinski, S.; Rossner, M. J.: Monitoring G protein-coupled receptor activation using the protein fragment complementation technique split TEV. In: G-protein-coupled receptor screening assays, pp. 107 - 118 (Eds. Prazeres, D. M. F.; Martins, S. A. M.). Springer Science and Business Media, New York (2015)

Jahn, O.; Tenzer, S.; Bartsch, N.; Patzig, J.; Werner, H. B.: Myelin proteome analysis: methods and implications for the myelin cytoskeleton. In: The Cytoskeleton: Imaging, isolation, and interaction, pp. 335 - 353 (Ed. Dermietzel, R.). Springer Science + Business Media, New York [usw.] (2013)

Schwab, M. H.; Sereda, M. W.; Nave, K.-A.: Neuron-glial interactions: Schwann cells. In: Patterning and cell type specification developing CNS and PNS: Comprehensive developmental neuroscience, Chapter 44 Ed., pp. 851 - 869 (Eds. Rubenstein, J. L.; Rakic, P.). Elsevier, Amsterdam [et al.] (2013)

Botvinnik, A.; Rossner, M. J.: Linking cellular signalling to gene expression using EXT-encoded reporter libraries. In: Gene Regulatory Networks, pp. 151 - 166 (Eds. Deplancke, B.; Gheldof, N.). Springer Science+Media, New York (2012)

Botvinnik, A.; Rossner, M. J.: Integrated measurement of Split TEV and Cis-regulatory assays using EXT encoded reporter libraries. In: Two Hybrid Technologies, pp. 309 - 323 (Eds. Suter, B.; Wanker, E. E.). Springer Science+Business Media, New York (2012)

Möbius, W.; Cooper, B.; Kaufmann, W. A.; Imig, C.; Ruhwedel, T.; Snaidero, N.; Saab, A. S.; Varoqueaux, F.: Electron microscopy of the mouse central nervous system. In: Electron microscopy of model systems, pp. 475 - 512 (Ed. Müller-Reichert, T.). Elsevier Acad.Pr., Amsterdam [et.al.] (2010)

Saher, G.; Simons, M.: Cholesterol and myelin biogenesis. In: Cholesterol Binding and Cholesterol Transport Proteins: Structure and Function in Health and Disease, 10.1007/978-90-481-8622-8_18, pp. 489 - 508 (Ed. Harris, J. R.). Springer, Dordrecht (2010)

Hirrlinger, J.; Dringen, R.: Multidrug resistance protein 1-mediated export of glutathione and glutathione disulfide from brain astrocytes. In: Phase II Conjugation Enzymes and Transport Systems, pp. 395 - 409 (Eds. Sies, H.; Packer, L.). Elsevier, Amsterdam (2005)

Nave, K.-A.; Werner, H. B.: Mutations of Myelination-Associated Genes That Affect Axonal Integrity. In: Multiple Sclerosis as a Neuronal Disease, pp. 305 - 315 (Ed. Waxman, S. G.). Elsevier, Amsterdam (2005)

Nave, K.-A.; Griffiths, I. R.: Models of Pelizeaus-Merzbacher-Disease. In: Myelin Biology and Disorders, Vol. 2 Ed., pp. 1125 - 1142 (Eds. Lazzarini, R. R.; Griffin, J. W.; Lassman, H.; Nave, K.-A.; Miller, R. et al.). Academic Press, London [u.a.] (2004)

Sereda, M. W.; Schöls, L.; Nave, K.-A.: Molekulargenetische Grundlagen der Charcot-Marie-Tooth Neuropathie (CMT/HMSN). In: Neurogenetik: molekulargenetische Diagnostik neurologischer und psychiatrischer Erkrankungen, 2. Aufl. Ed., pp. 459 - 469 (Eds. Rieß, O.; Schöls, L.). Kohlhammer, Stuttgart (2002)

Dimou, L.; Klugmann, M.; Werner, H.; Jung, M.; Nave, K.-A.; Griffiths, I. R.: Dysmyelination In Mice and the Proteolipid Protein Gene Family. In: The Functional Roles of Glial Cells in Health and Disease, pp. 261 - 271 (Eds. Matsas, R.; Tsacopoulos, M.). Springer US, Boston, MA (1999)

Nave, K.-A.; Trapp, B.: Foreword. Glia 29 (2), p. 103 - 103 (2000)

Sasmita, A. O.; Depp, C.; Nazarenko, T.; Sun, T.; Siems, S. B.; Yu, X.; Böhler, C.; Ong, E. C.; Bues, B.; Evangelista, L. et al.; Morgado, B.; Wu, Z.; Ruhwedel, T.; Subramanian, S.; Börensen, F.; Overhoff, K.; Spieth, L.; Berghoff, S. A.; Sadleir, K. R.; Vassar, R.; Eggert, S.; Goebbels, S.; Saito, T.; Saido, T.; Möbius, W.; Castelo-Branco, G.; Klafki, H.-W.; Wirths, O.; Wiltfang, J.; Jäkel, S.; Yan, R.; Nave, K.-A.: Oligodendrocytes and neurons contribute to amyloid-β deposition in Alzheimer’s disease. (2023)

Singh, M.; Zhao, Y.; Daguano Gastaldi, V.; Wojcik, S. M.; Curto, Y.; Kawaguchi, R.; Merino, R. M.; Garcia-Agudo, L. F.; Taschenberger, H.; Brose, N. et al.; Geschwind, D.; Nave, K.-A.; Ehrenreich, H.: Transcriptional networks predating cognition-associated pyramidal lineages are restructured by erythropoietin. (2023)

Asadollahi, E.; Trevisiol, A.; Saab, A. S.; Looser, Z.J.; Dibaj, P.; Kusch, K.; Ruhwedel, T.; Möbius, W.; Jahn, O.; Baes, M. et al.; Weber, B.; Abel, E.D.; Balabio, A.; Popko, B.; Kassmann, C. M.; Ehrenreich, H.; Hirrlinger, J.; Nave, K.-A.: Myelin lipids as nervous system energy reserves. (2022)

Schäffner, E.; Edgar, J. M.; Lehning, M.; Strauß, J.; Bosch-Queralt, M.; Wieghofer, P.; Berghoff, S. A.; Krueger, M.; Morawski, M.; Reinert, T. et al.; Möbius, W.; Barrantes-Freer, A.; Prinz, M.; Reich, D.S.; Flügel, A.; Stadelmann, C.; Fledrich, R.; Stassart, R. M.; Nave, K.-A.: Myelin insulation as a risk factor for axonal degeneration in autoimmune demyelinating disease. (2021)

Depp, C.; Sun, T.; Sasmita, A. O.; Spieth, L.; Berghoff, S. A.; Steixner-Kumar, A. A.; Subramanian, S.; Möbius, W.; Göbbels, S.; Saher, G. et al.; Zampar, S.; Wirths, O.; Thalmann, M.; Saito, T.; Saido, T.; Krüger-Burg, D. D.; Kawaguchi, R.; Willem, M.; Haass, C.; Geschwind, D.; Ehrenreich, H.; Stassart, R.; Nave, K.-A.: Ageing-associated myelin dysfunction drives amyloid deposition in mouse models of Alzheimer's disease. (2021)

Altas, B.; Ju, A.; Cruces Solís, H.; Karaca, S.; Winchenbach, J.; Kaplan, Ö.; Schwark, M.; Wieser, G. L.; Chaugule, V. K.; Majoul, I. et al.; Hassan, M. A.; Goel, R.; Wojcik, S. M.; Pichler, A.; Mitkovski, M.; de Hoz, L.; Urlaub, H.; Jahn, O.; Saher, G.; Rhee, J. S.; Kawabe, H.: Physiological and pathophysiological homeostasis of astroglial channel proteins by Nedd4-2. (2019)