Publikationen von B. Anliker

Müller, U.; Anliker, B.; Heber, S.; Fuhrmann, M.; Kretzschmar, H.; Sisodia, S.; Herms, J.: Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP-family members. Neurobiology of Aging 25 (Suppl. Suppl. 2), S. S81 - S82 (2004)

Herms, J.; Anliker, B.; Heber, S.; Ring, S.; Fuhrmann, M.; Kretzschmar, H.; Sisodia, S.; Müller, U.: Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members. EMBO Journal 23 (20), S. 4106 - 4115 (2004)

Birkenfeld, J.; Kartmann, B.; Anliker, B.; Ono, K.; Schlotcke, B.; Betz, H.; Roth, D.: Characterization of zetin 1/rBSPRY, a novel binding partner of 14-3-3 proteins. Biochemical and Biophysical Research Communications 302 (3), S. 526 - 533 (2003)

Leissring, M. A.; Murphy, M. P.; Mead, T. R.; Akbari, Y.; Sugarman, M. C.; Jannatipour, M.; Anliker, B.; Müller, U.; Saftig, P.; De Strooper, B. et al.; Wolfe, M. S.; Golde, T. E.; LaFerla, F. M.: A physiologic signaling role for the γ-secretase-derived intracellular fragment of APP. Proceedings of the National Academy of Sciences of the United States of America 99 (7), S. 4697 - 4702 (2002)