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Ilya Frolov

Researcher at University of Alabama at Birmingham

Publications -  115
Citations -  8216

Ilya Frolov is an academic researcher from University of Alabama at Birmingham. The author has contributed to research in topics: Alphavirus & Viral replication. The author has an hindex of 51, co-authored 112 publications receiving 7587 citations. Previous affiliations of Ilya Frolov include University of Washington & Washington University in St. Louis.

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Sindbis virus expression vectors: packaging of RNA replicons by using defective helper RNAs.

TL;DR: A series of defective Sind Bis virus helper RNAs are described which can be used for packaging Sindbis virus RNA replicons and would be useful under conditions in which extensive amplification is advantageous.
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Alphavirus-based expression vectors : strategies and applications

TL;DR: Alphaviruses are positive-strand RNA viruses that can mediate efficient cytoplasmic gene expression in insect and vertebrate cells that have been engineered for high-level expression of heterologous RNAs and proteins through recombinant DNA technology.
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The Old World and New World Alphaviruses Use Different Virus-Specific Proteins for Induction of Transcriptional Shutoff

TL;DR: These data provide new insights into alphavirus evolution and present a plausible explanation for the particular recombination events that led to the formation of western equine encephalitis virus (WEEV) from SINV- and EEEV-like ancestors.
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Noncytopathic Sindbis virus RNA vectors for heterologous gene expression

TL;DR: These vectors should prove to be flexible tools for the rapid expression of heterologous genes under conditions in which cellular metabolism is not perturbed, and they illustrate their utility with a number of foreign proteins.
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Roles of Nonstructural Protein nsP2 and Alpha/Beta Interferons in Determining the Outcome of Sindbis Virus Infection

TL;DR: It is demonstrated that a viral nonstructural protein, nsP2, is a significant regulator of Sindbis virus-host cell interactions and has implications for the development of improved alphavirus expression systems with better antigen-presenting potential.