P
Peter Steinlein
Researcher at Research Institute of Molecular Pathology
Publications - 48
Citations - 4042
Peter Steinlein is an academic researcher from Research Institute of Molecular Pathology. The author has contributed to research in topics: Progenitor cell & Haematopoiesis. The author has an hindex of 28, co-authored 47 publications receiving 3931 citations. Previous affiliations of Peter Steinlein include Boehringer Ingelheim & Erasmus University Rotterdam.
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Journal ArticleDOI
The profile of repeat‐associated histone lysine methylation states in the mouse epigenome
Joost H.A. Martens,Roderick J. O'Sullivan,Ulrich Braunschweig,Susanne Opravil,Martin Radolf,Peter Steinlein,Thomas Jenuwein +6 more
TL;DR: A profile of repressive histone lysine methylation states for the repetitive complement of four distinct mouse epigenomes is defined and tandem repeats and dsRNA are suggested as primary triggers for more stable chromatin imprints.
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The size of DNA/transferrin-PEI complexes is an important factor for gene expression in cultured cells.
Manfred Ogris,Peter Steinlein,Malgorzata Kursa,Karl Mechtler,Ralf Kircheis,Ernst Wagner,Ernst Wagner +6 more
TL;DR: Application of the small particles in more concentrated form and over extended periods of time improves transfection activity, and analysis of gene expression at the cellular level revealed that the differences in overall gene expression largely result from different intensities per expressing cell, while the difference in the percentage of expressing cells is less substantial.
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Receptor-mediated endocytosis of transferrin-polycation conjugates: an efficient way to introduce DNA into hematopoietic cells.
TL;DR: It is shown here that transferrin-polylysine andtransferrin-protamine, when complexed to plasmid DNA containing a luciferase reporter gene, is efficiently bound and moved into avian erythroblasts by endocytosis.
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The glucocorticoid receptor is required for stress erythropoiesis
Anton Bauer,François Tronche,Oliver Wessely,Oliver Wessely,Christoph Kellendonk,Holger M. Reichardt,Peter Steinlein,Günther Schütz,Hartmut Beug +8 more
TL;DR: The impact of the GR on erythropoiesis in vivo is analyzed, using GR-deficient mice or mice expressing a GR defective for transactivation to determine whether a particular, GR-sensitive progenitor could be identified as being responsible for the stress response.
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DNA/polyethylenimine transfection particles: Influence of ligands, polymer size, and PEGylation on internalization and gene expression
TL;DR: Receptor-mediated uptake of ligand-containing DNA/PEI (molecular weight, 800 kd) complexes was found to occur quickly (within 1 hour), whereas unspecific uptake through adsorptive endocytosis is less efficient or requires extended periods to reach the same degree of internalization.