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Vershkov, D., & Benvenisty, N. (2017). Human pluripotent stem cells in modeling human disorders: the case of fragile X syndrome. Regen Med, 12(1), 53–68.
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Li, M., Zhao, H., Ananiev, G. E., Musser, M. T., Ness, K. H., Maglaque, D. L., et al. (2017). Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells. Stem Cells, 35(1), 158–169.
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Tahara, T., Hirata, I., Nakano, N., Nagasaka, M., Nakagawa, Y., Shibata, T., et al. (2017). Comprehensive DNA Methylation Profiling of Inflammatory Mucosa in Ulcerative Colitis. Inflamm Bowel Dis, 23(1), 165–173.
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Miranda, A., Blanco-Prieto, M., Sousa, J., Pais, A., & Vitorino, C. (2017). Breaching barriers in glioblastoma. Part I: Molecular pathways and novel treatment approaches. Int J Pharm, 531(1), 372–388.
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Voss, D. M., Spina, R., Carter, D. L., Lim, K. S., Jeffery, C. J., & Bar, E. E. (2017). Disruption of the monocarboxylate transporter-4-basigin interaction inhibits the hypoxic response, proliferation, and tumor progression. Sci Rep, 7(1), 4292.
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