Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Katrin, Goldhahn"'
Autor:
Klaus G. Schmetterer, Katrin Goldhahn, Liesa S. Ziegler, Marlene C. Gerner, Ralf L. J. Schmidt, Madeleine Themanns, Eva Zebedin-Brandl, Doris Trapin, Judith Leitner, Winfried F. Pickl, Peter Steinberger, Ilse Schwarzinger, Rodrig Marculescu
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Malignant cells acquire physiological mechanisms of immunosuppression to escape immune surveillance. Strategies to counteract this suppression could help to improve adoptive immunotherapy regimen. The intracellular second messenger cyclic AMP (cAMP)
Externí odkaz:
https://doaj.org/article/3106358779e54303bd074a2d14a619de
Autor:
Katrin Goldhahn, Burkhard Kloesch, Farid Aldawsari, Carlos Velazques-Martinez, Klaus Schmetterer, Guenter Steiner
Publikováno v:
Novel technologies.
Autor:
Katrin Goldhahn, Georg Greiner, Doris Trapin, Nadine Witzeneder, Peter Steinberger, Franz Ratzinger, Klaus G. Schmetterer, Guenter Steiner, Sabrina Jutz, Winfried F. Pickl, Gregor Hoermann, Marlene C. Gerner, Ralf Schmidt, Heinz Burgmann
Publikováno v:
Scientific Reports
Chloroquine (CQ) is widely used as an anti-inflammatory therapeutic for rheumatic diseases. Although its modes of action on the innate immune system are well described, there is still insufficient knowledge about its direct effects on the adaptive im
Autor:
Katrin, Goldhahn, Michael, Hintersteininger, Guenter, Steiner, Thomas, Erker, Burkhard, Kloesch
Publikováno v:
Anticancer research. 35(5)
Inhibition of arachidonic acid metabolism by curcumin has been suggested to be a key mechanism for its anti-carcinogenic action. Recently, we reported on the synthesis of curcumin analogues and their evaluation as selective COX1 inhibitors. Two compo
Autor:
Norbert Handler, Jenny Breitenbach, Katrin Goldhahn, Silvia Loebsch, Thomas Erker, Burkhard Kloesch, Philipp Schreppel
Publikováno v:
Natural Product Communications. 11:1934578X1601101
Genistein, a naturally occurring isoflavone, possesses many beneficial health effects. To improve the bioactivity of the natural compound, we designed and synthesized the genistein prodrug FEHH6-1. In the present study, we evaluated the biological ef