Detailseite
A reverse genetic approach to define physiologically important functional domains of APP family proteins: analysis in APP/APLP knockout mice
Antragstellerin
Professorin Dr. Ulrike Müller
Fachliche Zuordnung
Molekulare Biologie und Physiologie von Nerven- und Gliazellen
Förderung
Förderung von 2000 bis 2007
Projektkennung
Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 5247598
Erstellungsjahr
2008
Zusammenfassung der Projektergebnisse
Keine Zusammenfassung vorhanden
Projektbezogene Publikationen (Auswahl)
- (2004). Cortical Dysplasia Resembling Human Type 2 Lissencephaly in Mice Lacking all Three APP-Family Members. The EMBO J. 23: 4106 - 4115
Herms, J., Anliker, B., Heber, S., Ring, S., Fuhrmann, M., Kretzschmar, H., Sisodia, S. and Müller, U.
- (2005) Homo- and hetero-dimerization of APP family members promotes intercellular adhesion. EMBO J. 24: 3624-3634
Soba, P. , Eggert, S., Zentgraf, H., Siehl, K., Kreger, S., Löwer, A., Langer, A., Merdes, G., Paro, R., Masters, C. L., Müller, U., Kins, S. and Konrad Beyreuther
- (2005). Lengthening of G2/mitosis in cortical precursors from mice lacking ß-amyloid precursor protein. Neuroscience 130:51-60
Lopez-Sanchez, M., Müller, U. and Frade, J. M.
- (2005). Regulation of cholesterol and sphingomyelin metabolism by amyloid-ß and presenilin. Nat. Cell. Biol. 7: 1118-1123
Grimm, M. O. W., Grimm, H. S., Pätzold, A. J., Zinser, E. G., Halonen, R., Duering, M., Tschäpe, J.-A., De Strooper, B., Müller, U., Shen, J. and Hartmann, T.
- (2005). Shedding of the amyloid precursor protein-like protein APLP2 by disintegrin-metalloproteinases. FEBS J. 272: 5808-5820
Endres, K., Postina, R., Schröder, A., Müller, U. and Fahrenholz, F.
- (2007) Beta-amyloid precursor protein can be transported independent of any sorting signal to the axonal and dendritic compartment. J Neurosci Res. 85: 2580-2590
Back S, Haas P, Tschape JA, Gruebl T, Kirsch J, Müller U, Beyreuther K, and Kins S
- (2007) The secreted APPsα domain is sufficient to rescue the anatomical, behavioral, and electrophysiological abnormalities of APP deficient mice. J. Neuroscience 27: 7817-7826
Ring. S, Weyer, S., Kilian, S. B., Waldron, E., Pietrzik, C. U., Filippov, M., Herms, J., Buchholz, C., Eckman, C. B., Martin Korte, M., Wolfer, D. P. and Müller, U.