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Virginia Chu

Researcher at University of California, Los Angeles

Publications -  8
Citations -  461

Virginia Chu is an academic researcher from University of California, Los Angeles. The author has contributed to research in topics: Induced pluripotent stem cell & Embryonic stem cell. The author has an hindex of 7, co-authored 7 publications receiving 391 citations. Previous affiliations of Virginia Chu include National Institutes of Health.

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Engrafted human stem cell–derived hepatocytes establish an infectious HCV murine model

TL;DR: It is determined that, despite an immature phenotype, differentiated HLCs are permissive to hepatitis C virus (HCV) infection and mount an interferon response to HCV infection in vitro.
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Repurposing of the antihistamine chlorcyclizine and related compounds for treatment of hepatitis C virus infection

TL;DR: Chlorcyclizine HCl (CCZ), an over-the-counter drug for allergy symptoms, is identified and characterized as an anti-HCV drug in vitro and in vivo, and represents a promising candidate for drug repurposing and further development as an effective and accessible agent for treatment of HCV infection.
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A quantitative high-resolution genetic profile rapidly identifies sequence determinants of hepatitis C viral fitness and drug sensitivity.

TL;DR: This high-resolution profiling methodology will be useful for next-generation drug development to select drugs with higher fitness costs to resistance, and also for informing the rational use of drugs based on viral variant spectra from patients.
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Hepatic differentiation of human pluripotent stem cells in miniaturized format suitable for high-throughput screen.

TL;DR: This protocol affords the unique opportunity to miniaturize the hPSC-based differentiation technology and facilitates screening for molecules in modulating liver differentiation, metabolism, genetic network, and response to infection or other external stimuli.
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Systematic identification of anti-interferon function on hepatitis C virus genome reveals p7 as an immune evasion protein.

TL;DR: In this paper, a high-throughput profiling platform was developed to enable mapping of hepatitis C virus (HCV) sequences critical for anti-IFN function at high resolution, and it was found that p7 is a critical immune evasion protein that suppresses the antiviral IFN function by counteracting the function of IFI6-16.