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Januar 2003 / J Biol Chem Lithostathine quadruple-helical filaments form proteinase K-resistant deposits in Creutzfeldt-Jakob disease E. Laurine C. Gregoire M. Faendrich S. Engemann S. Marchal L. Thion M. Mohr B. Monsarrat B. Michel C.M. Dobson E.E. Wanker M. Erard J.M. Verdier 01. Januar 2003 / J Neurochem Histone deacetylase activity is retained in primary neurons expressing mutant huntingtin protein M. Hoshino K. Tagawa T. Okuda M. Murata K. Oyanagi N. Arai T. Mizutani I. Kanazawa E.E. Wanker H. Okazawa 07. Januar 2003 / Proc Natl Acad Sci U S A Polyglutamine fibrillogenesis: The pathway unfolds C.A. Ross M.A. Poirier E.E. Wanker M. Amzel 01. Juni 2003 / Hum Mol Genet Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p M. Gong H.Y. Zhang H. Schulz Y.A. Lee K. Sun S. Bähring F.C. Luft P. Nürnberg A. Reis K. Rohde D. Ganten R.T. Hui N. Hübner 2003 / Methods Mol Med The study of gene polymorphisms - How complex is complex genetic disease? S. Bähring A. Aydin F.C. Luft August 2003 / Trends Biochem Sci The hunt for huntingtin function: interaction partners tell many different stories P. Harjes E.E. Wanker 01. Oktober 2003 / Am J Physiol Regul Integr Comp Physiol Mendelian hypertension with brachydactyly as a molecular genetic lesson in regulatory physiology F.C. Luft O. Toka H.R. Toka J. Jordan S. Bähring 05. September 2003 / Circ Res A splice mutation in a Syrian autosomal recessive hypercholesterolemia family causes a two-nucleotide deletion of mRNA H. Al Kateb E.K.F. Bautz F.C. Luft S. Bähring 17. Oktober 2003 / J Biol Chem Mutant huntingtin promotes the fibrillogenesis of wild-type huntingtin - A potential mechanism for loss of huntingtin function in Huntington's disease A. Busch S. Engemann R. Lurz H. Okazawa H. Lehrach E.E. Wanker 2003 / Methods Mol Biol Huntingtin fragments form aggresome-like inclusion bodies in mammalian cells A. Boeddrich R. Lurz E.E. Wanker
01. Januar 2003 / J Biol Chem Lithostathine quadruple-helical filaments form proteinase K-resistant deposits in Creutzfeldt-Jakob disease E. Laurine C. Gregoire M. Faendrich S. Engemann S. Marchal L. Thion M. Mohr B. Monsarrat B. Michel C.M. Dobson E.E. Wanker M. Erard J.M. Verdier
01. Januar 2003 / J Neurochem Histone deacetylase activity is retained in primary neurons expressing mutant huntingtin protein M. Hoshino K. Tagawa T. Okuda M. Murata K. Oyanagi N. Arai T. Mizutani I. Kanazawa E.E. Wanker H. Okazawa
07. Januar 2003 / Proc Natl Acad Sci U S A Polyglutamine fibrillogenesis: The pathway unfolds C.A. Ross M.A. Poirier E.E. Wanker M. Amzel
01. Juni 2003 / Hum Mol Genet Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p M. Gong H.Y. Zhang H. Schulz Y.A. Lee K. Sun S. Bähring F.C. Luft P. Nürnberg A. Reis K. Rohde D. Ganten R.T. Hui N. Hübner
2003 / Methods Mol Med The study of gene polymorphisms - How complex is complex genetic disease? S. Bähring A. Aydin F.C. Luft
August 2003 / Trends Biochem Sci The hunt for huntingtin function: interaction partners tell many different stories P. Harjes E.E. Wanker
01. Oktober 2003 / Am J Physiol Regul Integr Comp Physiol Mendelian hypertension with brachydactyly as a molecular genetic lesson in regulatory physiology F.C. Luft O. Toka H.R. Toka J. Jordan S. Bähring
05. September 2003 / Circ Res A splice mutation in a Syrian autosomal recessive hypercholesterolemia family causes a two-nucleotide deletion of mRNA H. Al Kateb E.K.F. Bautz F.C. Luft S. Bähring
17. Oktober 2003 / J Biol Chem Mutant huntingtin promotes the fibrillogenesis of wild-type huntingtin - A potential mechanism for loss of huntingtin function in Huntington's disease A. Busch S. Engemann R. Lurz H. Okazawa H. Lehrach E.E. Wanker
2003 / Methods Mol Biol Huntingtin fragments form aggresome-like inclusion bodies in mammalian cells A. Boeddrich R. Lurz E.E. Wanker