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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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Fogel, O., Richard-Miceli, C., & Tost, J. (2017). Epigenetic Changes in Chronic Inflammatory Diseases. Adv Protein Chem Struct Biol, 106, 139–189.
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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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Heffernan, J. M., McNamara, J. B., Borwege, S., Vernon, B. L., Sanai, N., Mehta, S., et al. (2017). PNIPAAm-co-Jeffamine(R) (PNJ) scaffolds as in vitro models for niche enrichment of glioblastoma stem-like cells. Biomaterials, 143, 149–158.
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