Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Konstantin Weber"'
Autor:
Julika Borde, Yael Laitman, Britta Blümcke, Dieter Niederacher, Konstantin Weber-Lassalle, Christian Sutter, Andreas Rump, Norbert Arnold, Shan Wang-Gohrke, Judit Horváth, Andrea Gehrig, Gunnar Schmidt, Véronique Dutrannoy, Juliane Ramser, Julia Hentschel, Alfons Meindl, Christopher Schroeder, Barbara Wappenschmidt, Christoph Engel, Karoline Kuchenbaecker, Rita K. Schmutzler, Eitan Friedman, Eric Hahnen, Corinna Ernst
Publikováno v:
BMC Cancer, Vol 22, Iss 1, Pp 1-9 (2022)
Abstract Background Clinical management of women carrying a germline pathogenic variant (PV) in the BRCA1/2 genes demands for accurate age-dependent estimators of breast cancer (BC) risks, which were found to be affected by a variety of intrinsic and
Externí odkaz:
https://doaj.org/article/d015c012069441ee82eb7df529d64307
Autor:
Nana Weber-Lassalle, Julika Borde, Konstantin Weber-Lassalle, Judit Horváth, Dieter Niederacher, Norbert Arnold, Silke Kaulfuß, Corinna Ernst, Victoria G. Paul, Ellen Honisch, Kristina Klaschik, Alexander E. Volk, Christian Kubisch, Steffen Rapp, Nadine Lichey, Janine Altmüller, Louisa Lepkes, Esther Pohl-Rescigno, Holger Thiele, Peter Nürnberg, Mirjam Larsen, Lisa Richters, Kerstin Rhiem, Barbara Wappenschmidt, Christoph Engel, Alfons Meindl, Rita K. Schmutzler, Eric Hahnen, Jan Hauke
Publikováno v:
Breast Cancer Research, Vol 21, Iss 1, Pp 1-6 (2019)
Abstract Background The role of the BARD1 gene in breast cancer (BC) and ovarian cancer (OC) predisposition remains elusive, as published case-control investigations have revealed controversial results. We aimed to assess the role of deleterious BARD
Externí odkaz:
https://doaj.org/article/6542c7dcf6614ef1973c45fb57592c84
Autor:
Jan Hauke, Judit Horvath, Eva Groß, Andrea Gehrig, Ellen Honisch, Karl Hackmann, Gunnar Schmidt, Norbert Arnold, Ulrike Faust, Christian Sutter, Julia Hentschel, Shan Wang‐Gohrke, Mateja Smogavec, Bernhard H. F. Weber, Nana Weber‐Lassalle, Konstantin Weber‐Lassalle, Julika Borde, Corinna Ernst, Janine Altmüller, Alexander E. Volk, Holger Thiele, Verena Hübbel, Peter Nürnberg, Katharina Keupp, Beatrix Versmold, Esther Pohl, Christian Kubisch, Sabine Grill, Victoria Paul, Natalie Herold, Nadine Lichey, Kerstin Rhiem, Nina Ditsch, Christian Ruckert, Barbara Wappenschmidt, Bernd Auber, Andreas Rump, Dieter Niederacher, Thomas Haaf, Juliane Ramser, Bernd Dworniczak, Christoph Engel, Alfons Meindl, Rita K. Schmutzler, Eric Hahnen
Publikováno v:
Cancer Medicine, Vol 7, Iss 4, Pp 1349-1358 (2018)
Abstract The prevalence of germ line mutations in non‐BRCA1/2 genes associated with hereditary breast cancer (BC) is low, and the role of some of these genes in BC predisposition and pathogenesis is conflicting. In this study, 5589 consecutive BC i
Externí odkaz:
https://doaj.org/article/ef20fad57668492e8e5c076a0c75dc32
Autor:
Nana Weber-Lassalle, Jan Hauke, Juliane Ramser, Lisa Richters, Eva Groß, Britta Blümcke, Andrea Gehrig, Anne-Karin Kahlert, Clemens R. Müller, Karl Hackmann, Ellen Honisch, Konstantin Weber-Lassalle, Dieter Niederacher, Julika Borde, Holger Thiele, Corinna Ernst, Janine Altmüller, Guido Neidhardt, Peter Nürnberg, Kristina Klaschik, Christopher Schroeder, Konrad Platzer, Alexander E. Volk, Shan Wang-Gohrke, Walter Just, Bernd Auber, Christian Kubisch, Gunnar Schmidt, Judit Horvath, Barbara Wappenschmidt, Christoph Engel, Norbert Arnold, Bernd Dworniczak, Kerstin Rhiem, Alfons Meindl, Rita K. Schmutzler, Eric Hahnen
Publikováno v:
Breast Cancer Research, Vol 20, Iss 1, Pp 1-6 (2018)
Abstract Background Germline mutations in the BRIP1 gene have been described as conferring a moderate risk for ovarian cancer (OC), while the role of BRIP1 in breast cancer (BC) pathogenesis remains controversial. Methods To assess the role of delete
Externí odkaz:
https://doaj.org/article/951e74b0cfc6446ab5113f955636b95b
Autor:
Konstantin Weber-Lassalle, Corinna Ernst, Alexander Reuss, Kathrin Möllenhoff, Klaus Baumann, Christian Jackisch, Jan Hauke, Dimo Dietrich, Julika Borde, Tjoung-Won Park-Simon, Lars Hanker, Katharina Prieske, Sandra Schmidt, Nana Weber-Lassalle, Esther Pohl-Rescigno, Stefan Kommoss, Frederik Marmé, Florian Heitz, Julia C Stingl, Rita K Schmutzler, Philipp Harter, Eric Hahnen
Publikováno v:
JNCI: Journal of the National Cancer Institute. 114:565-570
Background Cancer patients are at risk of secondary therapy–related myeloid neoplasms (t-MNs). Acquired blood-specific mutations in clonal hematopoiesis (CH)–associated genes are t-MN risk factors, and their occurrence associated with cancer ther
Autor:
Dorothee Bleisch, Konstantin Weber
Publikováno v:
Zeitschrift für philosophische Forschung. 75:591-594
Mit From Value to Rightness liefert Vuko Andrić einen innovativen, scharfsinnigen und erfreulich klaren Beitrag zur Frage nach der Perspektivabhängigkeit moralischer Pflichten im Allgemeinen und dem angemessenen Verständnis des Konsequentialismus
Autor:
Deborah J. Jones, Marta Zaton, Jacques Rozière, Sara Cavaliere, Silvain Buche, Jonathan Sharman, Alejandro M. Bonastre, Adam Hodgkinson, Emily Nesling, Albert Albert, Olav Finkenwirth, Stefan Zink, Sylvain Brimaud, Ludwig Joerissen, Hannes Barsch, Mark Muggli, Ivan Ponomarev, Martina Spackova, Hubert Andreas Gasteiger, Konstantin Weber, Paulette A. Loichet, Peter Strasser, Fabio Dionigi, Lujin Pan
Publikováno v:
ECS Meeting Abstracts. :2560-2560
The European GAIA project focussed on the development of novel ionomer, membrane, reinforcement, catalyst, catalyst support, gas diffusion and microporous layers, and layer constructions for high power density, high current density automotive membran
Autor:
Konstantin Weber
Publikováno v:
Grazer Philosophische Studien. 96:620-628
Every theory of rationality worth taking seriously implies that it is in some way irrational to accept contradictions. In this essay, the author examines how exactly this basic idea should be spelled out. He argues for two claims. First, it is not pr
Diagnosis of Li-Fraumeni Syndrome: Differentiating TP53 germline mutations from clonal hematopoiesis
Autor:
Jan Hauke, Christoph Engel, Esther Pohl-Rescigno, Stefan Kommoss, Philipp Harter, Julia C. Stingl, Julika Borde, Frederik Marmé, Dimo Dietrich, Nana Weber-Lassalle, Eric Hahnen, Katharina Prieske, Rita K. Schmutzler, Corinna Ernst, Beyhan Ataseven, Konstantin Weber-Lassalle, Alexander Reuss
Publikováno v:
Human Mutation. 39:2040-2046
The Li-Fraumeni cancer predisposition syndrome (LFS1) presents with a variety of tumor types and the TP53 gene is covered by most diagnostic cancer gene panels. We demonstrate that deleterious TP53 variants identified in blood-derived DNA of 523 pati