Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Christoph Heyder"'
Autor:
Nataliia Beztsinna, Maria B.C. de Matos, Bárbara S. Miranda, Robbert J. Kok, Christoph Heyder, Gero Leneweit, Enrico Mastrobattista
Publikováno v:
Phytomedicine. 61:3-4
Autor:
D. Trapin, Ursula Denk, Alexander Egle, Christoph Heyder, Daniela Asslaber, Inge Tinhofer, Thomas Kocher, J. Piñón Hofbauer, Richard Greil, Claudia Holler
Publikováno v:
Leukemia. 25:1452-1458
Chronic lymphocytic leukemia (CLL) cells require complex microenvironmental and immunologic interactions to survive and proliferate. Such interactions might be best recreated in animal models; however, this needs extensive verification. We therefore
Autor:
Ursula Denk, Christoph Heyder, Sebastian W. Hofbauer, Richard Greil, Alexander Egle, Josefina D. Piñón, Claudia Holler
Publikováno v:
Blood. 113:2791-2794
The development and the propagation of chronic lymphocytic leukemia (CLL) has been linked to signaling via the B-cell receptor (BCR). Protein kinase C β (PKCβ) is an essential signaling element of the BCR and was recently shown to be overexpressed
Autor:
Christoph Heyder, Zlatko Trajanoski, Richard Greil, Daniela Asslaber, Christine Papak, Olaf Merkel, Claudia Holler, Inge Tinhofer, Andreas Prokesch, Markus Stöcher, Frank Hamacher, Marcel Scheideler
Publikováno v:
Journal of Molecular Medicine. 86:541-552
In the last decade, arsenic trioxide (As2O3) has been used very successfully to treat acute promyelocytic leukaemia (APL). Much less is known about the effectiveness of As2O3 in other neoplastic disorders. In this paper, we report that after 18 h in
Autor:
Christoph Heyder, Karin Fromell, Kristina Nilsson Ekdahl, Gero Leneweit, Claudia Duehrkop, Katarina Edwards, Bo Nilsson
Publikováno v:
Colloids and surfaces. B, Biointerfaces. 141
Liposomes have been recognized as excellent drug delivery systems, but when they come in direct contact with different blood components they may trigger an immediate activation of the innate immune system. The aim of the present study was to produce
Autor:
Eva Gloria-Maercker, Frank Entschladen, Dirk Kemming, Thomas Dittmar, Christoph Heyder, Wolfgang Hatzmann, Burkhard Brandt, Kurt S. Zänker, Antje Rötger
Publikováno v:
Seminars in Cancer Biology. 15:387-395
Extravasation has been described as a rate-limiting step in the process of hematogeneous metastasis formation. Thereby, transendothelial migration of tumor cells consists of a complex series of events involving multiple cell-cell and cell-matrix inte
Autor:
Thomas Dittmar, Bernd Niggemann, Eva Gloria-Maercker, Wolfgang Hatzmann, Kurt S. Zänker, Christoph Heyder
Publikováno v:
Clinical & Experimental Metastasis. 22:99-106
The abilities of tumor cells to extravasate from the blood vessel system and to migrate through the connective tissue are prerequisites in metastasis formation. Both processes are chiefly mediated by integrins, which mediate both cell-cell and cell-m
Liposomal formulations of mistletoe produced by centrifugal technologies suitable for cancer therapy
Autor:
Robbert J. Kok, Christoph Heyder, Maria B.C. de Matos, Gero Leneweit, Hermann Nirschl, Kristina Nilsson Ekdahl, Jan-Hendrik Sommerling, Alberto Dessy, Ellen Hildebrandt, Bo Nilsson, Yvonne Klapper, Claudia Duehrkop, Illya Fedotenko
Publikováno v:
Phytomedicine. 22:S9-S10
Liposomal formulations of mistletoe produced by centrifugal technologies suitable for cancer therapy
Publikováno v:
Clinicalexperimental metastasis. 25(1)
To date, cancer is still the second most prevalent cause of death after cardiovascular diseases in the industrialized word, whereby the primary cause of cancer is not attributed to primary tumor formation, but rather to the growth of metastases at di
Autor:
Christoph, Heyder, Eva, Gloria-Maercker, Wolfgang, Hatzmann, Kurt S, Zaenker, Thomas, Dittmar
Publikováno v:
Contributions to microbiology. 13
In cancer the blood-borne spread of tumor cells leads to the formation of secondary tumors at distant loci, whereby the extravasation of tumor cells is a prerequisite step during hematogenous metastasis. In regard to the fate of endothelial cells loc