William E. Miller

William E. Miller

Department of Molecular Genetics, University of Cincinnati College of Medicine

Affiliated withUniversity of Cincinnati College of Medicine

Research Area

Biography

William Miller is a Professor in the Department of Molecular Genetics, Biochemistry, and Microbiology at the University of Cincinnati College of Medicine. He earned his undergraduate degree in Genetics and Development from the Pennsylvania State University and obtained his Ph.D. in Microbiology and Immunology from the University of North Carolina at Chapel Hill under the guidance of Dr. Nancy Raab-Traub. Drs. Miller and Raab-Traub investigated the role of the Epstein-Barr Virus Latent Membrane Protein 1 in epithelial cell transformation and demonstrated that signaling through TNF receptor associated factors (TRAFs) played a central role in LMP1’s mechanisms of action.

After receiving his Ph.D. he pursued postdoctoral work with Dr. Robert J. Lefkowitz at Duke University in Durham, North Carolina where his work investigated mechanisms of G-protein Coupled Receptor (GPCR) Signaling and uncovered novel roles for the beta-arrestin proteins in GPCR signaling.

Dr. Miller joined the Department of Molecular Genetics, Biochemistry, and Microbiology in 2002 and established a laboratory focused on understanding the role of herpesvirus encoded GPCRs (vGPCRs) in promoting viral replication. His laboratory is currently focused on understanding how these vGPCRs facilitate replication in the salivary epithelium where it positions itself for efficient horizontal transmission. To that end, the laboratory has recently pursued the use of novel primary salivary cell systems to explore the roles of these vGPCRs within this tissue type.

JoVE Journal Publications

ArticleTotal : 1
Year
Isolation of Salivary Epithelial Cells from Human Salivary Glands for In Vitro Growth as Salispheres or Monolayers
Publication title

Cited by 5

2019

Other Publications

Article
Year
G-protein-coupled receptor (GPCR) kinase phosphorylation and beta-arrestin recruitment regulate the constitutive signaling activity of the human cytomegalovirus US28 GPCR.

The Journal of biological chemistry| PubMed ID: 12668664

2003
beta-Arrestin inhibits NF-kappaB activity by means of its interaction with the NF-kappaB inhibitor IkappaBalpha.

Proceedings of the National Academy of Sciences of the United States of America| PubMed ID: 15173580

2004
2004
Signaling and regulation of G-protein coupled receptors encoded by cytomegaloviruses.

Biochemistry and cell biology = Biochimie et biologie cellulaire| PubMed ID: 15674431

2004
2006
2007
2008
Functional analysis of human cytomegalovirus pUS28 mutants in infected cells.

The Journal of general virology| PubMed ID: 18089733

2008
2009
2009
2009
2009
2012
2012
2013
2013
2014
2015
2016
2016
2016
2017
2019
Human cytomegalovirus G protein-coupled receptor US28 promotes latency by attenuating c-fos.

Proceedings of the National Academy of Sciences of the United States of America| PubMed ID: 30647114

2019
2019