Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Melanie Hudler"'
Autor:
Caroline End, Philip Rosenstiel, Annemarie Poustka, Antoon J. M. Ligtenberg, Gaby Bergmann, Melanie Hudler, Christian Sina, Floris J. Bikker, Frank Autschbach, Nikolaus Gassler, Arie V. Nieuw Amerongen, Marcus Renner, Uffe Holmskov, Axel Benner, Andre Franke, Stefan Lyer, Stefan Schreiber, Jan Mollenhauer, Mathias Hafner, Peter Schirmacher, Burkhard Helmke, Petra Kioschis, Stephanie Blaich
Publikováno v:
European Journal of Immunology. 39:833-842
Deleted in malignant brain tumors 1 (DMBT1) is a secreted glycoprotein displaying a broad bacterial-binding spectrum. Recent functional and genetic studies linked DMBT1 to the suppression of LPS-induced TLR4-mediated NF-kappaB activation and to the p
Autor:
Annemarie Poustka, Gaby Bergmann, Arie V. Nieuw Amerongen, Vito Annese, Uffe Holmskov, Antoon J. M. Ligtenberg, Mauro D'Amato, Stefan Lyer, Inge Krebs, Frank Autschbach, Jens Madsen, Stephanie Blaich, Anna Latiano, Petra Kioschis, Floris J. Bikker, Rainer Wittig, Melanie Hudler, Sabine Gronert-Sum, Olga Strobel-Freidekind, Peter Schirmacher, Marcus Renner, Jan Mollenhauer, Caroline End, Burkhard Helmke, Nikolaus Gassler, Frank Hilberg, Axel Benner, Mathias Hafner
Publikováno v:
Renner, M, Bergmann, G, Krebs, I, End, C, Lyer, S, Hilberg, F, Helmke, B, Gassler, N, Autschbach, F, Bikker, F, Strobel-Freidekind, O, Gronert-Sum, S, Benner, A, Blaich, S, Wittig, R, Hudler, M, Ligtenberg, A J, Madsen, J, Holmskov, U, Annese, V, Latiano, A, Schirmacher, P, Amerongen, A V N, D'Amato, M, Kioschis, P, Hafner, M, Poustka, A & Mollenhauer, J 2007, ' DMBT1 confers mucosal protection in vivo and a deletion variant is associated with Crohn's disease ', Gastroenterology, vol. 133, no. 5, pp. 1499-509 . https://doi.org/10.1053/j.gastro.2007.08.007
Gastroenterology, 133, 1499-1509. W.B. Saunders Ltd
Renner, M, Bergmann, G, Krebs, I, End, C, Lyer, S, Hillberg, F, Helmke, B, Gassler, N, Autschbach, F, Bikker, F J, Strobel-Freidekind, O, Gronert-Sum, S, Benner, A, Blaich, S, Wittig, R, Hudler, M, Ligtenberg, A J M, Madsen, J, Holmskov, U, Annese, V, Latiano, A, Schirmacher, P, van Nieuw Amerongen, A, D'Amato, M, Kioschis, P, Hafner, M, Poustka, A & Mollenhauer, J 2007, ' DMBT1 confers mucosal protection in vivo and a deletion variant is associated with Crohn's disease ', Gastroenterology, vol. 133, pp. 1499-1509 . https://doi.org/10.1053/j.gastro.2007.08.007
Gastroenterology, 133, 1499-1509. W.B. Saunders Ltd
Renner, M, Bergmann, G, Krebs, I, End, C, Lyer, S, Hillberg, F, Helmke, B, Gassler, N, Autschbach, F, Bikker, F J, Strobel-Freidekind, O, Gronert-Sum, S, Benner, A, Blaich, S, Wittig, R, Hudler, M, Ligtenberg, A J M, Madsen, J, Holmskov, U, Annese, V, Latiano, A, Schirmacher, P, van Nieuw Amerongen, A, D'Amato, M, Kioschis, P, Hafner, M, Poustka, A & Mollenhauer, J 2007, ' DMBT1 confers mucosal protection in vivo and a deletion variant is associated with Crohn's disease ', Gastroenterology, vol. 133, pp. 1499-1509 . https://doi.org/10.1053/j.gastro.2007.08.007
Udgivelsesdato: 2007-Nov BACKGROUND & AIMS: Impaired mucosal defense plays an important role in the pathogenesis of Crohn's disease (CD), one of the main subtypes of inflammatory bowel disease (IBD). Deleted in malignant brain tumors 1 (DMBT1) is a s
Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndrome
Autor:
Jürgen Kunz, Karl-Heinz Grzeschik, Inge Krebs, Kazushiro Tsuji, Steven W. Scherer, Isabel Weis, H. Roth, Lap-Chee Tsui, Ernst-Martin Füchtbauer, Melanie Hudler, Johanna M. Rommens
Publikováno v:
Human Molecular Genetics. 6:1079-1086
Saethre-Chotzen syndrome, a common autosomal dominant craniosynostosis in humans, is characterized by brachydactyly, soft tissue syndactyly and facial dysmorphism including ptosis, facial asymmetry, and prominent ear crura. Previously, we identified
Publikováno v:
Journal of Medical Genetics. 36:650-652
Editor—The original report by Robinow and Sorauf1 described a large family with autosomal dominant craniosynostosis and hallucal duplication. The clinical features include craniosynostosis, plagiocephaly, flat face, hypertelorism, thin, long, and p
Autor:
Jan Mollenhauer, Stephanie Blaich, Lukasz A. Kacprzyk, Holger Sültmann, Melanie Hudler, Rainer Wittig
Publikováno v:
Cancer Research. 69:A51-A51
Microarray analyses of global changes in gene expression patterns have recovered a large number of genes, which are deregulated in prostate cancer, when compared to normal prostate tissue. In order to successfully translate these data into clinical i