Education
Ph.D. in Human
Retrovirology, Division of Antiviral Chemotherapy, Center for Chronic
Viral Diseases, Graduate School of Medical and Dental Sciences,
Kagoshima University, 2003
Current position
He
is a Research Associate in Department of Genetics, Stanford University
School of Medicine. His research focuses on the profiling of novel
protein-metabolite interaction for antiviral & anticancer
therapeutics development.
Publications
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Li,
X.*, Wang, X.* and Snyder, M. (2013). Systematic investigation of
protein-small molecule interactions. IUBMB Life 65(1): 2-8. (*These
authors made equal contributions to the work)
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Wang, X., Tanaka, H., Baba, M. and
Cheng, Y.-C. (2009). Study
of the retention of metabolites of 4′-Ed4T, a novel anti-HIV-1 thymidine
analog, in cells. Antiviral Research 82(2): A27.
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Wang, X., Uto, T., Akagi, T., Akashi, M.
and Baba, M. (2008). Induction of Potent and Specific Humoral and Cellular
Immune Responses by Poly(γ-Glutamic Acid) Nanoparticles as an Efficient Antigen
Delivery System and Adjuvant. J Med Virol 80: 11-19.
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Wang,
X., Akagi, T., Akashi, M. and Baba, M. (2007). Development
of core-corona type polymeric nanoparticles as an anti-HIV-1 vaccine. Mini-Reviews in Organic Chemistry 4(1):
51-59.
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Wang, X., Uto, T., Akagi, T., Akashi, M. and Baba, M. (2007). Induction
of potent CD8+ T-cell responses by novel biodegradable nanoparticles
carrying human immunodeficiency virus type 1 gp120. J Virol 81(18): 10009-10016.
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Wang, X. and Baba, M. (2005). The role of breast cancer
resistance protein (BCRP/ABCG2) in cellular resistance to HIV-1 nucleoside
reverse transcriptase inhibitors. Antivir Chem Chemother 16(4):
213-216.
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Wang, X., Uto, T., Sato, K., Ide, K., Akagi, T., Okamoto, M., Kaneko, T., Akashi, M. and Baba, M. (2005). Potent activation of antigen-specific T cells by antigen-loaded nanospheres. Immunol Lett 98(1): 123-130.
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Wang, X., Nitanda, T., Shi, M.,
Okamoto, M., Furukawa, T., Sugimoto, Y., Akiyama, S. and Baba, M. (2004). Induction of cellular
resistance to nucleoside reverse transcriptase inhibitors by the wild-type
breast cancer resistance protein. Biochem Pharmacol 68(7):
1363-1370.
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Wang, X., Furukawa, T., Nitanda, T.,
Okamoto, M., Sugimoto, Y., Akiyama, S. and Baba, M. (2003). Breast cancer resistance
protein (BCRP/ABCG2) induces cellular resistance to HIV-1 nucleoside reverse
transcriptase inhibitors. Mol Pharmacol 63(1): 65-72.
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Wang, X., Miyake, H., Okamoto, M.,
Saito, M., Fujisawa, J.-I., Tanaka, Y., Izumo, S. and Baba, M. (2002). Inhibition of
the tax-dependent human T-lymphotropic virus type I replication in persistently
infected cells by the fluoroquinolone derivative K-37. Molecular
pharmacology 61(6): 1359-1365.