Alphaviruses are small, enveloped positive-strand RNA viruses that have been successfully transformed into expression vectors in the case of Semliki Forest virus (SFV), Sindbis virus (SIN), and Venezuelan equine encephalitis virus. Compared to other viral vectors, their advantages are easy and fast generation of recombinant viral particles, rapid onset, and high-level transgene expression. When applied to neuronal tissue, SFV and SIN vectors possess the additional advantage of efficiently and preferentially transducing neurons rather than non-neuronal cells. This article gives an overview of the biology of SFV and SIN, their generation into expression vectors, and their application in neurobiology, with particular emphasis on the transducti...
Gene therapy is a promising approach for treating a spectrum of neurological and neurodegenerative d...
Lentiviral-mediated gene transfer in vivo or in cultured mammalian neurons can be used to address a ...
Thesis (Ph.D.)--University of Washington, 2015The development of novel therapies to treat diseases o...
Alphaviruses are small, enveloped positive-strand RNA viruses that have been successfully transforme...
Alphaviruses are small, enveloped positive-strand RNA viruses that have been successfully transforme...
The options available for genetic modification of cells of the central nervous system (CNS) have gre...
Manipulation of gene expression in developing or in mature central nervous systems (CNS) holds a pro...
Preface The use of viral vectors as gene transfer tools for the central nervous system has seen a s...
The last two decades have witnessed the increasing instrumentalization of viruses, which have progre...
AbstractDuring the last decade, alphaviruses became widely used for expression of heterologous genet...
Effective gene delivery to the central nervous system (CNS) is vital for development of novel gene t...
The potential benefits of gene therapy for neurological diseases such as Parkinson’s, Amyotrophic La...
Lentiviruses have been extensively used as gene delivery vectors since the mid-1990s. Usually derive...
AbstractSindbis virus (SIN) expression vectors offer the opportunity for studying neuropathogenesis ...
The ability of herpes simplex virus (HSV) to establish lifelong latency in neurons suggests that HSV...
Gene therapy is a promising approach for treating a spectrum of neurological and neurodegenerative d...
Lentiviral-mediated gene transfer in vivo or in cultured mammalian neurons can be used to address a ...
Thesis (Ph.D.)--University of Washington, 2015The development of novel therapies to treat diseases o...
Alphaviruses are small, enveloped positive-strand RNA viruses that have been successfully transforme...
Alphaviruses are small, enveloped positive-strand RNA viruses that have been successfully transforme...
The options available for genetic modification of cells of the central nervous system (CNS) have gre...
Manipulation of gene expression in developing or in mature central nervous systems (CNS) holds a pro...
Preface The use of viral vectors as gene transfer tools for the central nervous system has seen a s...
The last two decades have witnessed the increasing instrumentalization of viruses, which have progre...
AbstractDuring the last decade, alphaviruses became widely used for expression of heterologous genet...
Effective gene delivery to the central nervous system (CNS) is vital for development of novel gene t...
The potential benefits of gene therapy for neurological diseases such as Parkinson’s, Amyotrophic La...
Lentiviruses have been extensively used as gene delivery vectors since the mid-1990s. Usually derive...
AbstractSindbis virus (SIN) expression vectors offer the opportunity for studying neuropathogenesis ...
The ability of herpes simplex virus (HSV) to establish lifelong latency in neurons suggests that HSV...
Gene therapy is a promising approach for treating a spectrum of neurological and neurodegenerative d...
Lentiviral-mediated gene transfer in vivo or in cultured mammalian neurons can be used to address a ...
Thesis (Ph.D.)--University of Washington, 2015The development of novel therapies to treat diseases o...