Simone Backes

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Herpes simplex virus 1 (HSV-1) is one of nine herpesviruses known to infect humans

T. Hennig, L. Dölken, C. Friedel, 2022 .

Protein-prime/modified vaccinia virus Ankara vector-boost vaccination overcomes tolerance in high-antigenemic HBV-transgenic mice.

D. Busch, L. Babiuk, U. Protzer, 2016, Vaccine.

Neutralizing antibody responses 300 days after SARS‐CoV‐2 infection and induction of high antibody titers after vaccination

N. Babel, S. Raunser, M. Hoffmann, 2022, European journal of immunology.

Performance of Three SARS-CoV-2 Immunoassays, Three Rapid Lateral Flow Tests, and a Novel Bead-Based Affinity Surrogate Test for the Detection of SARS-CoV-2 Antibodies in Human Serum

L. Dölken, J. Wischhusen, O. Kurzai, 2021, medRxiv.

Degradation of host microRNAs by poxvirus poly(A) polymerase reveals terminal RNA methylation as a protective antiviral mechanism.

B. Moss, S. Cherry, B. tenOever, 2012, Cell host & microbe.

Influenza A virus transmission bottlenecks are defined by infection route and recipient host.

Marshall Crumiller, Adolfo García-Sastre, Nicole M. Bouvier, 2014, Cell host & microbe.

The Mammalian response to virus infection is independent of small RNA silencing.

D. Sachs, R. Langlois, B. tenOever, 2014, Cell reports.

Targeted protein degradation reveals a direct role of SPT6 in RNAPII elongation and termination

Florian Erhard, L. Dölken, M. Eilers, 2021, Molecular cell.

Viral host-range factor C7 or K1 is essential for modified vaccinia virus Ankara late gene expression in human and murine cells, irrespective of their capacity to inhibit protein kinase R-mediated phosphorylation of eukaryotic translation initiation factor 2alpha.

E. Kremmer, C. Staib, G. Sutter, 2010, The Journal of general virology.

HSV-1 and influenza infection induce linear and circular splicing of the long NEAT1 isoform

T. Hennig, L. Dölken, C. Friedel, 2021, bioRxiv.