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Wolff, G.* et al.: Diet-dependent function of the extracellular matrix proteoglycan Lumican in obesity and glucose homeostasis. Mol. Metab. 19, 97-106 (2019)
Kunze, C. et al.: Synthetic AAV/CRISPR vectors for blocking HIV-1 expression in persistently infected astrocytes. Glia 66, 413-427 (2018)
Michler, T. et al.: Suppression of hepatitis B virus antigens by RNA interference enables therapeutic vaccination to achieve immune control in high-titer virus carriers. Hepatology 68, 49A-50A (2018)
Michler, T. et al.: Combinatorial RNAi/vaccination therapy for chronic hepatitis B achieves long-term functional cure in preclinical mouse model. J. Hepatol. 68, S16-S16 (2018)
Michler, T. et al.: Preclinical study of a combinatorial RNAi/vaccination therapy as a potential cure for chronic hepatitis B. J. Hepatol. 66, S112-S112 (2017)
Senís, E.* et al.: TALEN/CRISPR-mediated engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus. Nucleic Acids Res. 45:e3 (2017)
Michler, T. et al.: Blocking sense-strand activity improves potency, safety and specificity of anti-hepatitis B virus short hairpin RNA. EMBO Mol. Med. 8, 1082-1098 (2016)
Michler, T. et al.: RNA interference mediated suppression of HBV transcripts restores HBV-specific immunity and enhances the efficacy of therapeutic vaccination. J. Hepatol. 64, S148-S149 (2016)
Michler, T.* et al.: RNAi-based gene therapy for chronic hepatitis B: Evaluation in a murine model. L. J. Hepatol. 62, S526 (2015)
Hentzschel, F.* et al.: AAV8-mediated in vivo overexpression of miR-155 enhances the protective capacity of genetically-attenuated malarial parasites. Mol. Ther. 22, 2130-2141 (2014)
Parameswaran, P.* et al.: Six RNA viruses and forty-one hosts: Viral small RNAs and modulation of small RNA repertoires in vertebrate and invertebrate systems. PLoS Pathog. 6:e1000764 (2010)