Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Daniela Baus"'
Autor:
Florian M. Corvinus, Carina Orth, Richard Moriggl, Svetlana A. Tsareva, Stefan Wagner, Edith B. Pfitzner, Daniela Baus, Roland Kaufman, Lukas A. Huber, Kurt Zatloukal, Hartmut Beug, Peter Öhlschläger, Alexander Schütz, Karl-Jürgen Halbhuber, Karlheinz Friedrich
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 7, Iss 6, Pp 545-555 (2005)
Colorectal carcinoma (CRC) is a major cause of morbidity and mortality in Western countries. It has so far been molecularly defined mainly by alterations of the Wnt pathway. We show here for the first time that aberrant activities of the signal trans
Externí odkaz:
https://doaj.org/article/01d811dc532a4aa7bc1d7367ab5b615f
Autor:
Manuel Grez, Oliver G. Ottmann, Martin Zörnig, Edith Pfitzner, Daniela Baus, Markus Heinrich, Linping Chen, Christian Wichmann
Supplementary Figure 4 from Targeting the Oligomerization Domain of ETO Interferes with RUNX1/ETO Oncogenic Activity in t(8;21)-Positive Leukemic Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fab70119c997855a572aeff4731f9db
https://doi.org/10.1158/0008-5472.22366013
https://doi.org/10.1158/0008-5472.22366013
Autor:
Manuel Grez, Oliver G. Ottmann, Martin Zörnig, Edith Pfitzner, Daniela Baus, Markus Heinrich, Linping Chen, Christian Wichmann
About 12% of all de novo acute myeloid leukemias are characterized by the translocation t(8;21), which generates the oncogenic fusion protein RUNX1/ETO. RUNX1/ETO has a modular structure and contains several docking sites for heterologous proteins, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd7aeb3fcd9a816f0a66678ca426c404
https://doi.org/10.1158/0008-5472.c.6494951
https://doi.org/10.1158/0008-5472.c.6494951
Autor:
Manuel Grez, Oliver G. Ottmann, Martin Zörnig, Edith Pfitzner, Daniela Baus, Markus Heinrich, Linping Chen, Christian Wichmann
Supplementary Figure 1 from Targeting the Oligomerization Domain of ETO Interferes with RUNX1/ETO Oncogenic Activity in t(8;21)-Positive Leukemic Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1095ae6ca9536d31e2ee1e16d3314130
https://doi.org/10.1158/0008-5472.22366022
https://doi.org/10.1158/0008-5472.22366022
Autor:
Manuel Grez, Oliver G. Ottmann, Martin Zörnig, Edith Pfitzner, Daniela Baus, Markus Heinrich, Linping Chen, Christian Wichmann
Supplementary Figure 2 from Targeting the Oligomerization Domain of ETO Interferes with RUNX1/ETO Oncogenic Activity in t(8;21)-Positive Leukemic Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2795c6f43f0044fb606eb03d81d279e7
https://doi.org/10.1158/0008-5472.22366019.v1
https://doi.org/10.1158/0008-5472.22366019.v1
Autor:
Manuel Grez, Oliver G. Ottmann, Martin Zörnig, Edith Pfitzner, Daniela Baus, Markus Heinrich, Linping Chen, Christian Wichmann
Supplementary Figure 3 from Targeting the Oligomerization Domain of ETO Interferes with RUNX1/ETO Oncogenic Activity in t(8;21)-Positive Leukemic Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62df260ee55b9ae0a4677d303be5c3bc
https://doi.org/10.1158/0008-5472.22366016
https://doi.org/10.1158/0008-5472.22366016
Publikováno v:
Analytical Biochemistry. 397:233-240
Muscle and fat cells translocate GLUT4 (glucose transporter 4) to the plasma membrane when stimulated by insulin. Usually, this event is measured in differentiated adipocytes, myotubes, or cell lines overexpressing tagged GLUT4 by immunostaining. How
Autor:
Martin Zörnig, Oliver G. Ottmann, Markus Heinrich, Linping Chen, Daniela Baus, Edith Pfitzner, Christian Wichmann, Manuel Grez
Publikováno v:
Cancer Research. 67:2280-2289
About 12% of all de novo acute myeloid leukemias are characterized by the translocation t(8;21), which generates the oncogenic fusion protein RUNX1/ETO. RUNX1/ETO has a modular structure and contains several docking sites for heterologous proteins, i
Publikováno v:
Current Signal Transduction Therapy. 1:337-351
Publikováno v:
The FASEB Journal. 20:1074-1081
Glucocorticoids mediate a variety of biological effects via binding their intracellular receptor. Ligand-bound glucocorticoid receptor (GR) translocates to the nucleus and regulates gene transcription in a DNA binding-dependent or independent manner.