Professur für Innere Medizin mit dem Schwerpunkt Immundefizienz


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Cytotoxic effect of Efavirenz in BxPC-3 pancreatic cancer cells is based on oxidative stress and is synergistic with ionizing radiation (2018) Hecht M, Harrer T, Koeber V, Sarpong EO, Moser F, Fiebig N, Schwegler M, et al. Journal article HIV Activates the Tyrosine Kinase Hck to Secrete ADAM Protease-Containing Extracellular Vesicles (2018) Lee JH, Zhao Z, Ostalecki C, Kesti T, Bruns H, Simon B, Harrer T, et al. Journal article Experimental lupus is aggravated in mouse strains with impaired induction of neutrophil extracellular traps (2017) Kienhofer D, Hahn J, Stoof J, Csepregi JZ, Reinwald C, Urbonaviciute V, Johnsson C, et al. Journal article ROS is the boss (2017) Hahn J, Kienhofer D, Stoof J, Csepregi JZ, Reinwald C, Maueröder C, Urbonaviciute V, et al. Conference contribution T-cell receptor transfer for boosting HIV-1-specific T-cell immunity in HIV-1-infected patients (2016) Mummert C, Hofmann C, Hueckelhoven AG, Bergmann S, Mueller-Schmucker SM, Harrer EG, Dörrie J, et al. Journal article Sequence-function analysis of three T cell receptors targeting the HIV-1 p17 (2016) Mummert C, Hofmann C, Hueckelhoven AG, Bergmann S, Müller-Schmucker S, Harrer EG, Dörrie J, et al. Conference contribution HIV Nef- and Notch1-dependent Endocytosis of ADAM17 Induces Vesicular TNF Secretion in Chronic HIV Infection (2016) Ostalecki C, Wittki S, Lee JH, Geist MM, Tibroni N, Harrer T, Schuler G, et al. Journal article Efficacy, safety, tolerability and pharmacokinetics of a novel human immune globulin subcutaneous, 20%: a Phase 2/3 study in Europe in patients with primary immunodeficiencies (2016) Borte M, Krivan G, Derfalvi B, Marodi L, Harrer T, Jolles S, Bourgeois C, et al. Journal article Improved tag-switch method reveals that thioredoxin acts as depersulfidase and controls the intracellular levels of protein persulfidation (2016) Wedmann R, Onderka C, Wei S, Szijarto IA, Miljkovic J, Mitrovic A, Lange M, et al. Journal article A Multiplex Kindred with Hennekam Syndrome due to Homozygosity for a CCBE1 Mutation that does not Prevent Protein Expression (2016) Jackson CC, Best L, Lorenzo L, Casanova JL, Wacker J, Bertz S, Agaimy A, Harrer T Journal article
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