Publications

 

 

Germany

 

16. Kozlova, D., Chernousova, S., Knuschke, T., Buer, J., Westendorf, A. M., and Epple, M. (2012). Cell targeting by antibody-functionalized calcium phosphate nanoparticles. J Mater Chem 22, 396-404.

 

15. Zhang, E., Zhang, X., Liu, J., Wang, B., Tian, Y., Kosinska, A. D., Ma, Z., Xu, Y., Dittmer, U., Roggendorf, M., et al. (2011). The expression of PD-1 ligands and their involvement in regulation of T cell functions in acute and chronic woodchuck hepatitis virus infection. PLoS One 6, e26196.

 

14. Zelinskyy, G., Myers, L., Dietze, K. K., Gibbert, K., Roggendorf, M., Liu, J., Lu, M., Kraft, A. R., Teichgraber, V., Hasenkrug, K. J., and Dittmer, U. (2011). Virus-specific CD8+ T cells upregulate programmed death-1 expression during acute friend retrovirus infection but are highly cytotoxic and control virus replication. J Immunol 187, 3730-3737.

 

13. Sokolova, V., Knuschke, T., Buer, J., Westendorf, A. M., and Epple, M. (2011). Quantitative determination of the composition of multi-shell calcium phosphate-oligonucleotide nanoparticles and their application for the activation of dendritic cells. Acta Biomater 7, 4029-4036.

 

12. Ruhl, M., Knuschke, T., Schewior, K., Glavinic, L., Neumann-Haefelin, C., Chang, D. I., Klein, M., Heinemann, F. M., Tenckhoff, H., Wiese, M., et al. (2011). CD8+ T-cell response promotes evolution of hepatitis C virus nonstructural proteins. Gastroenterology 140, 2064-2073.

 

11. in revision.

 

10. Zhang, X., et al. Modulation of hepatitis B virus replication and hepatocyte differentiation by MicroRNA-1. Hepatology 53, 1476-1485 (2011).

 

9.  Dietze, K.K., et al. Transient depletion of regulatory T cells in transgenic mice reactivates virus-specific CD8+ T cells and reduces chronic retroviral set points. Proc Natl Acad Sci U S A 108, 2420-2425 (2011).

 

8.  Winning, S., Splettstoesser, F., Fandrey, J. & Frede, S. Acute hypoxia induces HIF-independent monocyte adhesion to endothelial cells through increased intercellular adhesion molecule-1 expression: the role of hypoxic inhibition of prolyl hydroxylase activity for the induction of NF-kappa B. J Immunol 185, 1786-1793 (2010).

 

7.   Dybowski, J.N., Heider, D. & Hoffmann, D. Prediction of co-receptor usage of HIV-1 from genotype. PLoS Comput Biol 6, e1000743 (2010).

 

6.   Dybowski, J.N., Heider, D. & Hoffmann, D. Structure of HIV-1 quasi-species as early indicator for switches of co-receptor tropism. AIDS Res Ther 7, 41 (2010).

 

5.   Banki, Z., et al. Complement as an endogenous adjuvant for dendritic cell-mediated induction of retrovirus-specific CTLs. PLoS Pathog 6, e1000891 (2010).

 

4.   Sokolova, V., et al. The use of calcium phosphate nanoparticles encapsulating Toll-like receptor ligands and the antigen hemagglutinin to induce dendritic cell maturation and T cell activation. Biomaterials 31, 5627-5633 (2010).

 

3.   Nair, S.R., et al. Mechanisms of control of acute Friend virus infection by CD4+ T helper cells and their functional impairment by regulatory T cells. J Gen Virol 91, 440-451 (2010).

 

2.   Heider, D., Verheyen, J. & Hoffmann, D. Predicting Bevirimat resistance of HIV-1 from genotype. BMC Bioinformatics 11, 37 (2010).

 

1.    Zelinskyy, G., et al. The regulatory T-cell response during acute retroviral infection is locally defined and controls the magnitude and duration of the virus-specific cytotoxic T-cell response. Blood 114, 3199-3207 (2009).

 

 

 

China

 

8. Yin, Y., Wu, C., Song, J., Wang, J., Zhang, E., Liu, H., Yang, D., Chen, X., Lu, M., and Xu, Y. (2011). DNA immunization with fusion of CTLA-4 to hepatitis B virus (HBV) core protein enhanced Th2 type responses and cleared HBV with an accelerated kinetic. PLoS One 6, e22524.

 

7. Wang, B. J., Bao, J. J., Wang, J. Z., Wang, Y., Jiang, M., Xing, M. Y., Zhang, W. G., Qi, J. Y., Roggendorf, M., Lu, M. J., and Yang, D. L. (2011). Immunostaining of PD-1/PD-Ls in liver tissues of patients with hepatitis and hepatocellular carcinoma. World J Gastroenterol 17, 3322-3329.

 

6.   Wang, B.J., et al. Establishing a new animal model for hepadnaviral infection: susceptibility of Chinese Marmota-species to woodchuck hepatitis virus infection. J Gen Virol 92, 681-691 (2011).

5.   Li, Y., et al. Infection of mouse bone marrow-derived dendritic cells by live attenuated Japanese encephalitis virus induces cells maturation and triggers T cells activation. Vaccine 29, 855-862 (2011).

4.   Cao, S., et al. Japanese encephalitis Virus wild strain infection suppresses dendritic cells maturation and function, and causes the expansion of regulatory T cells. Virol J 8, 39 (2011).

3.   Li, Y., et al. Development of a convenient immunochromatographic strip for the diagnosis of infection with Japanese encephalitis virus in swine. J Virol Methods 168, 51-56 (2010).

2.   Li, Y., et al. Evaluation of murine bone marrow-derived dendritic cells loaded with inactivated virus as a vaccine against Japanese encephalitis virus. Vaccine 27, 6004-6010 (2009).

1.   Zhu, W., et al. The wild-type hepatitis C virus core inhibits initiation of antigen-specific T- and B-cell immune responses in BALB/c mice. Clin Vaccine Immunol 17, 1139-1147 (2010).