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Evidence for a pathogenic role of different mutations at codon 188 of PRNP.
Roeber S, Grasbon-Frodl EM, Windl O, Krebs B, Xiang W, Vollmert C, Illig T, Schröter A, Arzberger T, Weber P, Zerr I, Kretzschmar HA. Roeber S, et al. Among authors: illig t. PLoS One. 2008 May 14;3(5):e2147. doi: 10.1371/journal.pone.0002147. PLoS One. 2008. PMID: 18478114 Free PMC article.
Prion protein codon 129 polymorphism and risk of Alzheimer disease.
Riemenschneider M, Klopp N, Xiang W, Wagenpfeil S, Vollmert C, Müller U, Förstl H, Illig T, Kretzschmar H, Kurz A. Riemenschneider M, et al. Among authors: illig t. Neurology. 2004 Jul 27;63(2):364-6. doi: 10.1212/01.wnl.0000130198.72589.69. Neurology. 2004. PMID: 15277640
A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with Alzheimer's disease.
Riemenschneider M, Konta L, Friedrich P, Schwarz S, Taddei K, Neff F, Padovani A, Kölsch H, Laws SM, Klopp N, Bickeböller H, Wagenpfeil S, Mueller JC, Rosenberger A, Diehl-Schmid J, Archetti S, Lautenschlager N, Borroni B, Müller U, Illig T, Heun R, Egensperger R, Schlegel J, Förstl H, Martins RN, Kurz A. Riemenschneider M, et al. Among authors: illig t. Hum Mol Genet. 2006 Aug 15;15(16):2446-56. doi: 10.1093/hmg/ddl167. Epub 2006 Jul 6. Hum Mol Genet. 2006. PMID: 16825285
Calpain-10 variants and haplotypes are associated with polycystic ovary syndrome in Caucasians.
Vollmert C, Hahn S, Lamina C, Huth C, Kolz M, Schöpfer-Wendels A, Mann K, Bongardt F, Mueller JC, Kronenberg F, Wichmann HE, Herder C, Holle R, Löwel H, Illig T, Janssen OE; KORA group. Vollmert C, et al. Among authors: illig t. Am J Physiol Endocrinol Metab. 2007 Mar;292(3):E836-44. doi: 10.1152/ajpendo.00584.2005. Epub 2006 Nov 14. Am J Physiol Endocrinol Metab. 2007. PMID: 17106059 Free article.
711 results