Publikationen von K.-A. Nave

Schwab, M. H.; Druffel-Augustin, S.; Gass, P.; Jung, M.; Klugmann, M.; Bartholomae, A.; Rossner, M. J.; Nave, K.-A.: Neuronal Basic Helix-Loop-Helix Proteins (NEX, neuroD, NDRF): Spatiotemporal Expression and Targeted Disruption of the NEX Gene in Transgenic Mice. The Journal of Neuroscience 18 (4), S. 1408 - 1418 (1998)

Forss-Petter, S.; Werner, H.; Berger, J.; Lassmann, H.; Molzer, B.; Schwab, M. H.; Bernheimer, H.; Zimmermann, F.; Nave, K.-A.: Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice. Journal of Neuroscience Research 50 (5), S. 829 - 843 (1997)

Stewart, H.J.S.; Zoidl, G.; Rossner, M.; Brennan, A.; Zoidl, C.; Nave, K.-A.; Mirsky, R.; Jessen, K.R.: Helix-loop-helix proteins in Schwann cells: A study of regulation and subcellular localization of Ids, REB, and E12/47 during embryonic and postnatal development. Journal of Neuroscience Research 50 (5), S. 684 - 701 (1997)

Anderson, T. J.; Montague, P.; Nadon, N.; Nave, K.-A.; Griffiths, I. R.: Modification of Schwann cell phenotype withPlp transgenes: Evidence that the PLP and DM20 isoproteins are targeted to different cellular domains. Journal of Neuroscience Research 50 (1), S. 13 - 22 (1997)

Thomson, C.E.; Montague, P.; Jung, M.; Nave, K.-A.; Griffiths, I.R.: Phenotypic severity of murinePlp mutants reflects in vivo and in vitro variatioans in transport of PLP isoproteins. Glia 20 (4), S. 322 - 332 (1997)

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), S. 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), S. 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), S. 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), S. 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), S. 275 - 281 (1995)

Nave, K.-A.: Myelin Genetics: New Insight Into Old Diseases. Brain Pathology 5 (3), S. 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), S. 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), S. 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), S. 217 - 228 (1994)

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