Glas, J., J. Seiderer, J. Wagner, T. Olszak, C. Fries, C. Tillack, M. Friedrich, F. Beigel, J. Stallhofer, C. Steib, M. Wetzke, B. Göke, T. Ochsenkühn, J. Diegelmann, D. Czamara and S. Brand: Analysis of IL12B Gene Variants in Inflammatory Bowel Disease. In: PLoS ONE 7, 3, Seq. No.: e34349 (2012).
Glas, J., J. Wagner, J. Seiderer, T. Olszak, M. Wetzke, F. Beigel, C. Tillack, J. Stallhofer, M. Friedrich, C. Steib, B. Göke, T. Ochsenkühn, N. Karbalai, J. Diegelmann, D. Czamara and S. Brand: PTPN2 Gene Variants Are Associated with Susceptibility to Both Crohn's Disease and Ulcerative Colitis Supporting a Common Genetic Disease Background. In: PLoS ONE 7, 3, Seq. No.: e33682 (2012).
Glas, J., J. Seiderer, C. Bayrle, M. Wetzke, C. Fries, C. Tillack, T. Olszak, F. Beigel, C. Steib, M. Friedrich, J. Diegelmann, D. Czamara and S. Brand: The Role of Osteopontin (OPN/SPP1) Haplotypes in the Susceptibility to Crohn's Disease. In: PLoS ONE 6, 12, Seq. No.: e29309 (2011).
Glas, J., J. Seiderer, C. Tillack, E. Paschos, M. Wetzke, J. Diegelmann, D. Czamara and S. Brand: Functional SFTPD Gene Variants Are Not Associated with Susceptibility to Inflammatory Bowel Disease in the German Population. In: Inflammatory Bowel Diseases 17, 6, 1439-1440 (2011).
Glas, J., J. Seiderer, C. Fries, C. Tillack, S. Pfennig, M. Weidinger, F. Beigel, T. Olszak, U. Lass, B. Göke, T. Ochsenkühn, C. Wolf, P. Lohse, B. Müller-Myhsok, J. Diegelmann, D. Czamara and S. Brand: CEACAM6 Gene Variants in Inflammatory Bowel Disease. In: PLoS ONE 6, 4, Seq. No.: e19319 (2011).
Glas, J., J. Seiderer, C. Tillack, S. Pfennig, F. Beigel, M. Jürgens, T. Olszak, R. P. Laubender, M. Weidinger, B. Müller-Myhsok, B. Göke, T. Ochsenkühn, P. Lohse, J. Diegelmann, D. Czamara and S. Brand: The NOD2 Single Nucleotide Polymorphisms rs2066843 and rs2076756 Are Novel and Common Crohn's Disease Susceptibility Gene Variants. In: PLoS ONE 5, 12, Seq. No.: e14466 (2010).
Glas, J., J. Seiderer, G. Pasciuto, C. Tillack, J. Diegelmann, S. Pfennig, A. Konrad, S. Schmechel, M. Wetzke, H. P. Torok, J. Stallhofer, M. Jürgens, T. Griga, W. Klein, J. T. Epplen, U. Schiemann, T. Mussack, P. Lohse, B. Göke, T. Ochsenkühn, M. Folwaczny, B. Müller-Myhsok and S. Brand: rs224136 on Chromosome 10q21.1 and Variants in PHOX2B, NCF4, and FAM92B Are Not Major Genetic Risk Factors for Susceptibility to Crohn's Disease in the German Population. In: American Journal of Gastroenterology 104, 3, 665-672 (2009).
Seiderer, J., J. Dambacher, D. Leistner, C. Tillack, J. Glas, J. H. Niess, S. Pfennig, M. Jürgens, B. Müller-Myhsok, B. Göke, T. Ochsenkühn, P. Lohse, H. C. Reinecker and S. Brand: Genotype-phenotype analysis of the CXCL 16 p.Ala181Val polymorphism in inflammatory bowel disease. In: Clinical Immunology 127, 1, 49-55 (2008).
Seiderer, J., I. Elben, J. Diegelmann, J. Glas, J. Stallhofer, C. Tillack, S. Pfennig, M. Jürgens, S. Schmechel, A. Konrad, B. Göke, T. Ochsenkühn, B. Müller-Myhsok, P. Lohse and S. Brand: Role of the novel th17 cytokine IL-17F in inflammatory bowel disease (IBD): Upregulated colonic IL-17F expression in active Crohn's disease and analysis of the IL17F p.Hisl6lArg polymorphism in IBD. In: Inflammatory Bowel Diseases 14, 4, 437-445 (2008).
Torok, H. P., J. Glas, L. Tonenchi, P. Lohse, B. Müller-Myhsok, O. Limbersky, C. Neugebauer, F. Schnitzler, J. Seiderer, C. Tillack, S. Brand, G. Brunnler, P. Jagiello, J. T. Epplen, T. Griga, W. Klein, U. Schiemann, M. Folwaczny, T. Ochsenkuhn and C. Folwaczny: Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease. In: Gut 54, 10, 1421-1427 (2005).
http://edoc.mpg.de
The Max Planck Society does not take any responsibility for the content of this export.