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Caveolin- and clathrin-independent entry of BKPyV into primary human proximal tubule epithelial cells.
Abstract BK polyomavirus (BKPyV) is a human pathogen that causes polyomavirus-associated nephropathy and hemorrhagic cystitis in transplant patients. Gangliosides and caveolin proteins have previously been reported to be required for BKPyV infection in animal cell models. Recent studies from our lab and others, however, have indicated that the identity of the cells used for infection studies can greatly influence the behavior of the virus. We therefore wished to re-examine BKPyV entry in a physiologically relevant primary cell culture model, human renal proximal tubule epithelial cells. Using siRNA knockdowns, we ...
Source: Virology - February 19, 2016 Category: Virology Authors: Zhao L, Marciano AT, Rivet CR, Imperiale MJ Tags: Virology Source Type: research