Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Billurvan Taskin"'
Autor:
Frank Jacobsen, Billurvan Taskin, Nathaniel Melling, Charlotte Sauer, Corinna Wittmer, Claudia Hube-Magg, Martina Kluth, Ronald Simon, Dirk Pehrke, Burkhard Beyer, Thomas Steuber, Imke Thederan, Guido Sauter, Thorsten Schlomm, Waldemar Wilczak, Katharina Möller, Sören A. Weidemann, Susanne Burdak-Rothkamm
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-11 (2017)
Abstract Background Animal model experiments have suggested a role of the DNA repair protein ERCC1 (Excision Repair Cross-Complementation Group 1) in prostate cancer progression. Methods To better understand the impact of ERCC1 protein expression in
Externí odkaz:
https://doaj.org/article/c2dfda6de6ee4ff5b74f18521aae0709
Autor:
Billurvan, Taskin, Christopher, Kloth, Veronika, Hechler, Tobias, Benz, Meinrad, Beer, Daniel, Vogele
Publikováno v:
Radiologie (Heidelberg, Germany)Literatur.
Autor:
Sohall Frogh, Thorsten Schlomm, Guido Sauter, Frank Jacobsen, Mohammad Hussein, Christina Möller-Koop, Sarah Minner, Billurvan Taskin, Andreas M. Lübke, Ronald Simon, Heinke Volta, Hartwig Huland, Hans Heinzer, Till S. Clauditz, Franziska Büscheck, Martina Kluth, Waldemar Wilczak, Markus Graefen, Andrea Hinsch, Maria Christina Tsourlakis
Publikováno v:
Cancer Management and Research. 10:5909-5917
Introduction Deletion of 3p13 is one of the most common alterations in prostate cancer preferentially occurring in tumors with TMPRSS2:ERG fusion. The cause for the striking association between 3p13 loss and ERG fusion is unknown. Methods Here, we ma
Autor:
Martina, Kluth, Heinke, Volta, Mohammad, Hussein, Billurvan, Taskin, Sohall, Frogh, Christina, Möller-Koop, Franziska, Büscheck, Frank, Jacobsen, Maria Christina, Tsourlakis, Andreas M, Lübke, Andrea, Hinsch, Till, Clauditz, Markus, Graefen, Hans, Heinzer, Hartwig, Huland, Sarah, Minner, Guido, Sauter, Waldemar, Wilczak, Thorsten, Schlomm, Ronald, Simon
Publikováno v:
Cancer Management and Research
Introduction Deletion of 3p13 is one of the most common alterations in prostate cancer preferentially occurring in tumors with TMPRSS2:ERG fusion. The cause for the striking association between 3p13 loss and ERG fusion is unknown. Methods Here, we ma
Autor:
Sven Mahner, Katharina Möller, Stefan Geist, Cansu Özden, Patrick Lebok, Guido Sauter, Uwe Heilenkötter, A von der Assen, Rainer Krech, M. Kluth, Volkmar Müller, Annette Lebeau, Khakan Hussein, Christian Wilke, Fritz Jänicke, A Hartmann, Ronald Simon, A. Mittenzwei, Linn Wölber, Peter Paluchowski, Luigi Terracciano, E Burandt, Billurvan Taskin, Isabell Witzel
Publikováno v:
Cancer Biology & Therapy. 16:1080-1087
Deletions of chromosome 8p occur frequently in breast cancers, but analyses of its clinical relevance have been limited to small patient cohorts and provided controversial results. A tissue microarray with 2,197 breast cancers was thus analyzed by fl
Autor:
Jacobsen, Frank, Billurvan Taskin, Melling, Nathaniel, Sauer, Charlotte, Wittmer, Corinna, Hube-Magg, Claudia, Kluth, Martina, Simon, Ronald, Pehrke, Dirk, Beyer, Burkhard, Steuber, Thomas, Thederan, Imke, Sauter, Guido, Schlomm, Thorsten, Wilczak, Waldemar, MĂśller, Katharina, SĂśren Weidemann, Burdak-Rothkamm, Susanne
Association between ERCC1 immunostaining results and prostate cancer phenotype in ERG-negative tumors. Table S2. Association between ERCC1 immunostaining results and prostate cancer phenotype in ERG-positive tumors. (PDF 112Â kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::287c5ca80092a7a8f4b852581b561220
Autor:
M. Kluth, A. Mittenzwei, Ronald Simon, Patrick Lebok, Khakan Hussein, Volkmar Müller, Claudia Hube-Magg, Christian Wilke, Isabell Witzel, Uwe Heilenkötter, Fritz Jänicke, Annette Lebeau, V. Kopperschmidt, Luigi Terracciano, Stefan Geist, Cansu Özden, Sven Mahner, Billurvan Taskin, A von der Assen, Guido Sauter, Rainer Krech, E Burandt, Linn Wölber, Peter Paluchowski
Publikováno v:
BMC Cancer
Background Deletions of chromosome 10q23, including the PTEN (phosphatase and tensin homolog) locus, are known to occur in breast cancer, but systematic analyses of its clinical relevance are lacking. Methods We thus analyzed a tissue microarray (TMA