Publikationen von Annett Boeddrich

Ehrnhoefer, D. E.; Bieschke, J.; Boeddrich, A.; Herbst, M.; Masino, L.; Lurz, R.; Engemann, S.; Pastore, A.; Wanker, E. E.: EGCG redirects amyloidogenic polypeptides into unstructured, off-pathway oligomers. Nature Structural & Molecular Biology 15 (6), S. 558 - 56 (2008)

Albrecht, A. N.; Kornak, U.; Böddrich, A.; Süring, K.; Robinson, P. N.; Stiege, A. C.; Lurz, R.; Stricker, S.; Wanker, E. E.; Mundlos, S.: A molecular pathogenesis for transcription factor associated poly-alanine tract expansions. Human Molecular Genetics 13 (20), S. 2351 - 2359 (2004)

Heiser, V.; Engernann, S.; Brocker, W.; Dunkel, I.; Boeddrich, A.; Waelter, S.; Nordhoff, E.; Lurz, R.; Schugardt, N.; Rautenberg, S. et al.; Herhaus, C.; Barnickel, G.; Boettcher, H.; Lehrach, H.; Wanker, E. E.: Identification of benzothiazoles as potential polyglutamine aggregation inhibitors of Huntington's disease by using an automated filter retardation assay. Proceedings of the National Academy of Sciences of the United States of America 99 (Suppl. 4), S. 16400 - 16406 (2002)

Heiser, V.; Engemann, S.; Bröcker, W.; Dunke, I.; Boeddrich, A.; Waelter, S.; Nordhoff, E.; Lurz, R.; Schugardt, N.; Rautenberg, S. et al.; Herhaus, C.; Barnickel, G.; Böttcher, H.; Lehrach, H.; Wanker, E. E.: Identification of benzothiazoles as potential polyglutamine aggregation inhibitors of Huntington's disease by using an automated filter retardation assay. Proceedings of the National Academy of Sciences 99 (Suppl. 4), S. 16400 - 16406 (2002)

Heiser, V.; Engemann, S.; Bröcker, W.; Dunkel, I.; Boeddrich, A.; Waelter, S.; Nordhoff, E.; Lurz, R.; Schugardt, N.; Rautenberg, S. et al.; Herhaus, C.; Barnickel, G.; Böttcher, H.; Lehrach, H.; Wanker, E. E.: Identification of benzothiazoles as potential polyglutamine aggregation inhibitors of Huntington’s disease by using an automated filter retardation assay. Self-Perpetuating Structural States in Biology, Disease, and Genetics, S. 16400 - 16406 (2002)

Albrecht, A. N.; Schwabe, G. C.; Stricker, S.; Böddrich, A.; Wanker, E. E.; Mundlos, S.: The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development 112 (1-2), S. 53 - 67 (2002)

Albrecht, A. N.; Schwabe, G. C.; Stricker, S.; Böddrich, A.; Wanker, E. E.; Mundlos, S.: The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development 112 (1-2), S. 53 - 67 (2002)

Boeddrich, A.; Lurz, R.; Wanker, E. E.: Huntingtin fragments form aggresome-like inclusion bodies in mammalian cells. In: Protein misfolding and disease: principles and protocols, S. 217 - 229 (Hg. Bross, P.; Gregersen, N.). Humana Press, Totowa, New Jersey (2003)