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Selected References for Raymond L. White: Neufeld, K. L., Zhang, F., Cullen, B. R., White, R. L. APC-mediated downregulation of beta-catenin activity involves nuclear sequestration and nuclear export. EMBO Rep 1(6):519-23, 2000. Satterwhite, D. J., White, R. L., Matsunami, N., Neufeld, K. L. Inhibition of topoisomerase IIalpha expression by transforming growth factor-beta1 is abrogated by the papillomavirus E7 protein. Cancer Res 15;60(24):6989-94, 2000. Zhang, F., White, R. L., Neufeld, K. L. Phosphorylation near nuclear localization signal regulates nuclear import of adenomatous polyposis coli protein. Proc Natl Acad Sci USA 97(23):12577-82, 2000. Neufeld, K. L. , Nix, D. A., Bogerd, H., Kang, Y., Beckerle, M. C., Cullen, B. R., White, R. L. Adenomatous polyposis coli protein contains two nuclear export signals and shuttles between the nucleus and cytoplasm. Proc Natl Acad Sci USA 97(22):12085-90, 2000. Satterwhite, D. J., Matsunami, N., White, R. L. TGF-beta1 inhibits BRCA1 expression through a pathway that requires pRb. Biochem Biophys Res Commun 276(2):686-92, 2000. Branscomb, A., Seger, J., White, R.L. Evolution of odorant receptors expressed in mammalian testes. Genetics 156(2):785-97, 2000. Spancake, K. M., Anderson, C. B., Weaver, V. M., Matsunami, N., Bissell, M. J., White, R. L. E7-transduced human breast epithelial cells show partial differentiation in three-dimensional culture. Cancer Res 59(24):6042-5, 1999. White, R.L. Colon polyps: a damaged developmental system and a precursor to cancer. Cytogenet Cell Genet 86(2):95-8, 1999. Hsu, L. C., White, R. L. BRCA1 is associated with the centrosome during mitosis. Proc Natl Acad Sci USA 95(22):12983-8, 1998. White, R. L. Excess risk of colon cancer associated with a polymorphism of the APC gene? Cancer Res 58(18):4038-9, 1998. Broman, K. W., Murray, J. C., Sheffield, V. C., White, R. L., Weber, J. L. Comprehensive human genetic maps: individual and sex-specific variation in recombination. Am J Hum Genet 63(3):861-9, 1998. White, R. L. Tumor suppressing pathways. Cell 92(5):591-2, 1998. Utah Marker Development Group: Adamson, D., Albertsen, H., Ballard, L., Bradley, P., Carlson, M., Cartwright, P., Elsner, T., Fuhrman, D., Gerken, S., Harris, L., Holik, P., Kimball, A., Knell, J., Lawrence, E., Lu, J., Marks, A., Matsunami, N., Melis, R., Milner, B., Moore, M., Nelson, L., Odelberg, S., Peters, G., Plaetke, R., Riley, R., Robertson, M., Sargent, R., Staker, G., Tinge, A., Ward, K., Zhao, X. and White, R. A collection of ordered tetra-nucleotide repeat markers from the human genome. Am J Hum Genet 57(3):619-628, 1995. Groden, J., Thliveris, A., Samowitz, W., Carlson, M., Gelbert, L., Albertsen, H., Joslyn, G., Stevens, J., Spirio, L., Robertson, M., Sargeant, L., Krapcho, K., Wolff, E., Burt, R., Hughes, J.P., Warrington, J., McPherson, J., Wasmuth, J., Le Paslier, D., Abderrahim, H., Cohen, D., Leppert, M. and White, R. Identification and characterization of the familial adenomatous polyposis coli gene. Cell 66(3):589-600, 1991. Joslyn, G., Carlson, M., Thliveris, A., Albertsen, H., Gelbert, L., Samowitz, W., Groden, J., Stevens, J., Spirio, L., Robertson, M., Sargeant, L., Krapcho, K., Wolff, E., Burt, R., Hughes, J.P., Warrington, J., McPherson, J., Wasmuth, J., Le Paslier, D., Abderrahim, H., Cohen, D., Leppert, M. and White, R. Identification of deletion mutations and three new genes at the familial polyposis locus. Cell 66(3):601-613, 1991. Cawthon, R., Weiss, R., Xu, G., Viskochil, D., Culver, M., Stevens, J., Robertson, M., Dunn, D., Gesteland, R., O'Connell, P. and White, R. A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations. Cell 62(1):193-201, 1990. Viskochil, D., Buchberg, A., Xu, G., Cawthon, R., Stevens, J., Wolff, R., Culver, M., Carey, J., Copeland, N., Jenkins, N., White, R. and O'Connell, P. Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus. Cell 62(1):187-192, 1990. Nakamura, Y., Leppert, M., O'Connell, P., Wolff, R., Culver, M., Martin, C., Fujimoto, E., Hoff, M., Kumlin, E. and White, R. Variable number of tandem repeat (VNTR) markers for human gene mapping. Science 235(4796):1616-1622, 1987. Drayna, D., Davies, K., Hartley, D., Mandel, J L., Camerino, G., Williamson R. and White, R.L. Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms. Proc Natl Acad Sci USA 81(9):2836-2839, 1984. Cavenee, W., Dryja, T., Phillips, R., Benedict, R., Godbout, B., Gallie, B., Murphree, A.L. and White, R.L. Expression of recessive alleles by chromosomal mechanisms in retinoblastoma. Nature 305(5937), pp. 779-784, 1983. Wyman, A. and White, R.L. A highly polymorphic locus in human DNA. Proc Natl Acad Sci USA 77:6754-6758, 1980. |


