Kellogg Eye Center,
Cellular and Molecular Biology Program
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.
A platform for assessing outer segment fate in primary human fetal RPE cultures.
Experimental eye research Jan, 2019 | Pubmed ID: 30336126
Retinal artery occlusion in young patients without typical cardiovascular risk factors: etiologies, prognosis, and suggested work-up.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie Jun, 2024 | Pubmed ID: 38847894
Reassessing retinal pigment epithelial ketogenesis: Enzymatic assays for ketone body levels provide inaccurate results.
Experimental eye research Aug, 2024 | Pubmed ID: 38857822
Basic science observations link subretinal drusenoid deposit formation to retinal pigment epithelial hypoxia.
Eye (London, England) Jun, 2024 | Pubmed ID: 38871936
Qitao Zhang*,1,
Daisy Y. Shu*,2,
Richard A. Bryan3,
John Y. S. Han1,
Gillian A. Gulette1,
Kin Lo3,
Leo A. Kim4,
Jason M. L. Miller1,5
1Kellogg Eye Center, University of Michigan, Ann Arbor,
2School of Optometry and Vision Science, University of New South Wales,
3, Lucid Scientific,
4Schepens Eye Research Institute of Mass. Eye and Ear, Department of Ophthalmology, Harvard Medical School,
5Cellular and Molecular Biology Program, University of Michigan, Ann Arbor
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