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Eva Loepfe

Researcher at University of Zurich

Publications -  6
Citations -  321

Eva Loepfe is an academic researcher from University of Zurich. The author has contributed to research in topics: Golgi apparatus & Viral envelope. The author has an hindex of 5, co-authored 6 publications receiving 311 citations.

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The genome of bovine herpesvirus 1 (BHV-1) strains exhibiting a neuropathogenic potential compared to known BHV-1 strains by restriction site mapping and cross-hybridization.

TL;DR: The structural genome characteristics of BHV-1.3 compared to those of the other BHv-1 strains, examined by means of restriction site mapping, electron microscopy and cross-hybridization are described.
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Impairment of Nuclear Pores in Bovine Herpesvirus 1-Infected MDBK Cells

TL;DR: High-resolution scanning and transmission electron microscopy proved the distortions to be related to enlargement of nuclear pores through which nuclear content including capsids protrudes into the cytoplasm, suggesting that capsid-membrane interaction of high identity to the budding process at the inner nuclear membrane.
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The genome of caprine herpesvirus 1: genome structure and relatedness to bovine herpesvirus 1.

TL;DR: Caprine herpesvirus 1 (CapHV-1) DNA was examined by electron microscopy, restriction site mapping and homology studies and it was shown that the genome structures were identical and that the DNAs shared a high degree of base sequence homology.
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The significance of the Golgi complex in envelopment of bovine herpesvirus 1 (BHV-1) as revealed by cryobased electron microscopy

TL;DR: The data strongly indicate an intracisternal transport of enveloped virus particles from the budding site to the packaging site, and Glycoprotein K is discussed to likely play a role in the intrac isternal transportation of virions.
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Novel Entry Pathway of Bovine Herpesvirus 1 and 5

TL;DR: This work visualized the crucial steps of the entry pathway of bovine herpesvirus 1 and BHV-5 by transmission and scanning electron microscopy, employing cryotechniques that include time monitoring, ultrarapid freezing, and freeze substitution of cultured cells inoculated with virus.