Warren Laboratory

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Publications - 2002   D’Agata, V, Warren, ST, Zhao, W, Torre, E, Alkon, D and Cavallaro, S: Gene expression profiles in a transgenic animal model of fragile X syndrome. Neurobiology of Disease 10:211-218 (2002). O’Donnell, WT and Warren, ST: A decade of molecular studies of fragile X syndrome. Annual Review of Neuroscience 25:315-338 (2002). Coffee, B, Zhang, F, Ceman, S, Warren,ST and Reines, D: Epigenetic histone modifications depict an aberrantly heterochromatized FMR1 gene in fragile X syndrome. American Journal of Human Genetics 71:923-932 (2002). Huber, KM, Gallagher, S, Warren, ST and Bear, MF: Altered synaptic plasticity in a mouse model of fragile-X mental retardation. Proceedings of the National Academy of Sciences, USA 99:7746-7750 (2002). Tarleton, J, Kenneson, A, Taylor, A, Crandall, K, Fletcher, R, Casey, R, Hart, S, Hatton, D, Bailey, D, Fisch, D, and Warren, ST: A single base alteration in the CGG repeat region of FMR1: Possible effects on gene expression and phenotype. Journal of Medical Genetics 39:196-200 (2002).

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