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Rainer G. Ulrich

Researcher at Friedrich Loeffler Institute

Publications -  287
Citations -  9468

Rainer G. Ulrich is an academic researcher from Friedrich Loeffler Institute. The author has contributed to research in topics: Hantavirus & Puumala virus. The author has an hindex of 46, co-authored 250 publications receiving 7911 citations.

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The feasibility of developing a risk assessment for the impact of climate change on the emergence of Crimean-Congo haemorrhagic fever in livestock in Europe: a review.

TL;DR: The pathways and data requirements for a qualitative risk assessment for the emergence of CCHFV in livestock in Europe are discussed and a risk map approach is proposed based on layers that include the potential routes of release together with the main components for exposure, namely the distributions of the tick vectors, the small vertebrate host reservoirs and the livestock.
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HBV core particles allow the insertion and surface exposure of the entire potentially protective region of Puumala hantavirus nucleocapsid protein.

TL;DR: A suppressable stop codon located between the HBV core and the C-terminally fused hantavirus sequence restored the ability to form particles (‘mosaic particles’) and allowed the formation of particles built up by the core protein itself and theHBV core-Puumala nucleocapsid- readthrough protein.
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Mapping of B-cell epitopes in the nucleocapsid protein of Puumala hantavirus.

TL;DR: Mapping by overlapping peptides (PEPSCAN) confirmed a complex recognition pattern for most analyzed mAbs and revealed the existence of several, partially overlapping, and discontinuous B-cell epitopes of Puumala hantavirus N.
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Age-related and regional differences in the prevalence of hepatitis E virus-specific antibodies in pigs in Germany.

TL;DR: The present study clearly demonstrates that a high percentage of domestic pigs in Germany have had contact with HEV, and the presence of anti-HEV-free herds may indicate that it is feasible to establish and sustain HEV- free pig herds.
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Inactivation of Hantaan virus-containing samples for subsequent investigations outside biosafety level 3 facilities.

TL;DR: The virus inactivation and depletion methods described herein are suitable to prepare non-infectious samples for further use in immunological, virological and cell-biological assays.