Nicholas R Faunce
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Nicholas R Faunce has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Michele E. Hardy
Veterinary Molecular Biology, Montana State University, Bozeman, MT 59717, USA
2 shared publications - Brian Bothner
Department of Chemistry and Biochemistry, Montana State University, Bozeman, USA
1 shared publication - Jay M Hendricks
Immunology and Infectious Diseases, Montana State University, PO Box 173610, Bozeman, MT 59718, USA
1 shared publication - Jeana M Paulson
Immunology and Infectious Diseases, Montana State University, PO Box 173610, Bozeman, MT 59718, USA
1 shared publication - José Luis Zambrano
Laboratorio de Virología Celular, Centro de Microbiología y Biología Celular, Instituto Venezolano de Investigaciones Científicas, Caracas, Miranda, Venezuela
1 shared publication - Khalil Ettayebi
Immunology and Infectious Diseases, Montana State University, Bozeman MT, 59718, USA
1 shared publication
Latest Publications
- Open Access
- 22 May 2012
- Published by Springer Nature in Virology Journal
- Vol. 9 (1) , 96
18 β-glycyrrhetinic acid inhibits rotavirus replication in culture
Glycyrrhizin (GA) and primary metabolite 18β-glycyrrhetinic acid (GRA) are pharmacologically active components of the medicinal licorice root, and both have been shown to have antiviral and immunomodulatory properties. Although these properties are well established, the mechanisms of action are not completely understood. In this study, GA and GRA were tested for the ability to inhibit rotavirus replication in cell culture, toward a long term goal of discovering natural compounds that may complement existing vaccines.
- 22 May 2012
- Published by Springer Nature in Virology Journal
- Vol. 9 (1) , 96
Open Access18 β-glycyrrhetinic acid inhibits rotavirus replication in culture
Glycyrrhizin (GA) and primary metabolite 18β-glycyrrhetinic acid (GRA) are pharmacologically active components of the medicinal licorice root, and both have been shown to have antiviral and immunomodulatory properties. Although these properties are well established, the mechanisms of action are not completely understood. In this study, GA and GRA were tested for the ability to inhibit rotavirus replication in cell culture, toward a long term goal of discovering natural compounds that may complement existing vaccines.
- Open Access
- 20 July 2011
- Published by Springer Nature in Virology Journal
- Vol. 8 (1) , 359
Rotavirus infection activates the UPR but modulates its activity
Rotaviruses are known to modulate the innate antiviral defense response driven by IFN. The purpose of this study was to identify changes in the cellular proteome in response to rotavirus infection in the context of the IFN response. We also sought to identify proteins outside the IFN induction and signaling pathway that were modulated by rotavirus infection.
- 20 July 2011
- Published by Springer Nature in Virology Journal
- Vol. 8 (1) , 359
Open AccessRotavirus infection activates the UPR but modulates its activity
Rotaviruses are known to modulate the innate antiviral defense response driven by IFN. The purpose of this study was to identify changes in the cellular proteome in response to rotavirus infection in the context of the IFN response. We also sought to identify proteins outside the IFN induction and signaling pathway that were modulated by rotavirus infection.