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Conway, KE, McConnell, BB, Bowring, CE, Donald, CD, Warren, ST and Vertino, PM:TMS1, a novel proapoptotic CARD protein, is a target of methylation-induced gene silencing in human breast cancers. Cancer Research 60:6236-6242 (2000). |
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Fryns, J-P, Borghgraef, M, Brown, WT, Chelly, J, Fisch, GS, Hamel, B, Hanauer, A, Lacombe, D, Luo, L, MacPherson, JN, Mandel, J-L, Moraine, C, Mulley, J, Nelson, D, Oostra, B, Partington, M, Ramakers, GJA, Roper, H-H, Rousseau, F, Schwartz, C, Steinbach, P, Stoll, C, Tranebjaerg, L, Turner, G, Van Bokhoven, HV, Vianna-Morgante, A, Villard, L and Warren, ST: Conference report: 9th international workshop on fragile X syndrome and X-linked mental retardation. American Journal of Medical Genetics 94:345-360 (2000). |
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Peier, AM, McIlwain, KL, Kenneson, A, Warren, ST, Paylor, R and Nelson, DL: (Over)correction of the FMR1 deficiency with YAC transgenics: Behavioral and physical features. Human Molecular Genetics 9:1145-1159 (2000). |
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Dongsheng, D, Boekhoudt, G, Zhou, F, Morris, A, Philipson, S, Warren, ST and Boss, JM: Sp1 binding is critical for promoter assembly and activation of the MCP-1 gene. Journal of Biological Chemistry 275:1708-1714 (2000). |
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Crawford, DC, Schwartz, CE, Meadows, KL, Newman, JL, Taft, LF, Gunter, C, Bailey, DB, Brown, WT, Carpender, NJ, Howard-Peebles, P, Mazzocco, MM, Monaghan, KG, Nolin, SL, Reiss, AL, Roberson, J, Rohlfs, EM, Taylor, AK, Warren, ST and Sherman, SL: Survey of the fragile X syndrome CGG repeat and STR- and SNP- haplotypes in an African-American population. American Journal of Human Genetics 66:480-493 (2000). |
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