Publikationen von K.-A. Nave

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), S. 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), S. 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), S. 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), S. 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, S. 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), S. 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), S. 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), S. 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), S. 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), S. 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), S. 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), S. 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), S. 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, S. 453 - 457 (1985)

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

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

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 Aufl., S. 851 - 869 (Hg. Rubenstein, J. L.; Rakic, P.). Elsevier, Amsterdam [et al.] (2013)

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

Nave, K.-A.; Griffiths, I. R.: Models of Pelizeaus-Merzbacher-Disease. In: Myelin Biology and Disorders, Vol. 2 Aufl., S. 1125 - 1142 (Hg. 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. Aufl., S. 459 - 469 (Hg. Rieß, O.; Schöls, L.). Kohlhammer, Stuttgart (2002)