Publikationen (Abteilung Neurogenetik)

Yool, D.; Montague, P.; McLaughlin, M.; McCulloch, M. C.; Edgar, J. M.; Nave, K.-A.; Davies, R. W.; Griffiths, I. R.; McCallion, A. S.: Phenotypic analysis of mice deficient in the major myelin protein MOBP, and evidence for a novel Mobp isoform. Glia 39 (3), S. 256 - 267 (2002)

Edgar, J. M.; Anderson, T. J.; Dickinson, P. J.; Barrie, J. A.; McCulloch, M. C.; Nave, K.-A.; Griffiths, I. R.: Survival of, and competition between, oligodendrocytes expressing different alleles of the Plp gene. Journal of Cell Biology 158 (4), S. 719 - 729 (2002)

Genoud, S.; Lappe-Siefke, C.; Goebbels, S.; Radtke, F.; Aguet, M.; Scherer, S. S.; Suter, U.; Nave, K.-A.; Mantei, N.: Notch1 control of oligodendrocyte differentiation in the spinal cord. Journal of Cell Biology 158 (4), S. 709 - 718 (2002)

Maier, M.; Berger, P.; Nave, K.-A.; Suter, U.: Identification of the Regulatory Region of the Peripheral Myelin Protein 22 (PMP22) Gene That Directs Temporal and Spatial Expression in Development and Regeneration of Peripheral Nerves. Molecular and Cellular Neuroscience 20 (1), S. 93 - 109 (2002)

Simons, M.; Kramer, E. M.; Macchi, P.; Rathke-Hartlieb, S.; Trotter, J.; Nave, K.-A.; Schulz, J. B.: Overexpression of the myelin proteolipid protein leads to accumulation of cholesterol and proteolipid protein in endosomes/lysosomes: implications for Pelizaeus-Merzbacher disease. The Journal of Cell Biology: JCB 157 (2), S. 327 - 336 (2002)

Garbern, J. Y.; Yool, D. A.; Moore, G. J.; Wilds, I. B.; Faulk, M. W.; Klugmann, M.; Nave, K.-A.; Sistermans, E. A.; van der Knaap, M. S.; Bird, T. D. et al.; Shy, M. E.; Kamholz, J. A.; Griffiths, I. R.: Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation. Brain 125 (3), S. 551 - 561 (2002)

Atanasoski, S.; Scherer, S. S.; Nave, K.-A.; Suter, U.: Proliferation of Schwann cells and regulation of cyclin D1 expression in an animal model of Charcot-Marie-Tooth disease type 1A. Journal of Neuroscience Research 67 (4), S. 443 - 449 (2002)

Schipke, C. G.; Boucsein, C.; Ohlemeyer, C.; Kirchhoff, F.; Kettenmann, H.: Astrocyte Ca²⁺ waves trigger responses in microglial cells in brain slices. The FASEB Journal 16 (2), S. 1 - 16 (2002)

Schoen, C.; Reichard, U.; Monod, M.; Kratzin, H. D.; Ruchel, R.: Molecular cloning of an extracellular aspartic proteinase from Rhizopus microsporus and evidence for its expression during infection. Medical Mycology 40 (1), S. 61 - 71 (2002)

Yool, D.; Klugmann, M.; Barrie, J. A.; McCulloch, M. C.; Nave, K.-A.; Griffiths, I. R.: Observations on the structure of myelin lacking the major proteolipid protein. Neuropathology and Applied Neurobiology 28 (1), S. 75 - 78 (2002)

Ntefidou, M.; Elsner, C.; Spreer, A.; Weinstock, N.; Kratzin, H. D.; Rüchel, R.: Blood coagulation with domestic deep-seated mycoses. Mycoses 45 (S1), S. 53 - 56 (2002)

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)