![]() ![]() Here we describe a model system, SELective Expression and Controlled Transduction In Vivo (SELECTIV), that enables efficient and specific expression of transgenes by coupling adeno-associated virus (AAV) vectors with Cre-inducible overexpression of the multi-serotype AAV receptor, AAVR. ![]() However, generating these models is time- and resource-intensive. The development of transgenic mouse models that express genes of interest in specific cell types has transformed our understanding of basic biology and disease. These colloborative studies include dengue virus, zika virus, adeno-associated virus, coxsackie virus, enterovirus 71, enterohepatic helicobacters, campylobacters, and anaplasma. His research focuses on using mouse models to study murine and human infectious diseases. in Ecology from the University of California, Davis (1979), obtained postdoctoral training in endocrinology, developmental genetics, immunology, and molecular biology of the mouse at the Memorial Sloan-Kettering Cancer Center (NYC), Institut Pasteur (France), and the Howard Hughes Medical Institute at the University of California, San Francisco and was an Assistant Professor of Cell Biology at the Vanderbilt University School of Medicine. He joined the Department of Comparative Medicine at Stanford in 2008. from the University of Tennessee in 2004 and completed his residency training in Laboratory Animal Medicine at the Massachusetts Institute of Technology in 2007. Nagamine, DVM, PhD Associate Professor received his D.V.M.
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |