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Karin Hahnke

Researcher at Max Planck Society

Publications -  15
Citations -  880

Karin Hahnke is an academic researcher from Max Planck Society. The author has contributed to research in topics: Immune system & RNase P. The author has an hindex of 11, co-authored 15 publications receiving 747 citations.

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In vivo 3′-to-5′ exoribonuclease targetomes of Streptococcus pyogenes

TL;DR: It is determined that YhaM is an unspecific enzyme that trims a few nucleotides and targets the majority of transcript ends, generated either by transcription termination or by endonucleolytic activity, which sheds light on the very distinct features of S. pyogenes 3′-to-5′ exoRNases.
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Neonatal Fc Receptor Regulation of Lung Immunoglobulin and CD103+ Dendritic Cells Confers Transient Susceptibility to Tuberculosis.

TL;DR: It is found that FcRn expression maintains homeostatic IgG levels in lung and leads to preferential secretion of low-affinity IgG ligands into the lumen, which sheds light on the role of mucosal IgG in immune responses in the lung during homeostasis and bacterial disease.
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Striptease on glass: Validation of an improved stripping procedure for in situ microarrays

TL;DR: It is shown that stripping of commercial in situ arrays is feasible and that reuse of stripped arrays gave similar results compared to unused ones, and that the stripping procedure does not significantly influence data quality derived from post-primary hybridizations.
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RNase Y-mediated regulation of the streptococcal pyrogenic exotoxin B.

TL;DR: It is demonstrated for the first time that RNase Y processing of an mRNA target requires the presence of a G, which is essential for the processing of the 5′ untranslated region of speB mRNA 5′ UTR byRNase Y.
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Restricted expression of C-type lectin-like natural killer receptors by CD8 T cells in the murine small intestine

TL;DR: In the intestinal mucosa, conventional CD8αβ+ T cells lack NKR expression and thereby lose responsiveness to NKR ligands, which otherwise could possibly cause adverse activation or inhibition of T cells in this environment.