List of Faculty Publications

Below is a list of Faculty publications imported from PubMed or manually added. By default, publications are sorted by year with titles displayed in ascending alphabetical order.
Shortcuts: Wühr, Martin | Wingreen, Ned | Wieschaus, Eric | Troyanskaya, Olga | Tilghman, Shirley | Storey, John | Singh, Mona | Shvartsman, Stanislav | Shaevitz, Joshua | Rabinowitz, Joshua | Murphy, Coleen | Levine, Michael {Levine, Michael S.} | Gregor, Thomas | Botstein, David | Bialek, William | Ayroles, Julien | Andolfatto, Peter | Akey, Joshua

Filters: Keyword is Homozygote  [Clear All Filters]
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Homozygote
T. J. Vasicek, Zeng, L., Guan, X. J., Zhang, T., Costantini, F., and Tilghman, S. M., Two dominant mutations in the mouse fused gene are the result of transposon insertions., Genetics, vol. 147, no. 2, pp. 777-86, 1997.
E. Wieschaus and Nöthiger, R., The role of the transformer genes in the development of genitalia and analia of Drosophila melanogaster., Dev Biol, vol. 90, no. 2, pp. 320-34, 1982.
K. Ranade, Jorgenson, E., Sheu, W. H. - H., Pei, D., Hsiung, C. Agnes, Chiang, F. -tien, Chen, Y. - D. I., Pratt, R., Olshen, R. A., Curb, D., Cox, D. R., Botstein, D., and Risch, N., A polymorphism in the beta1 adrenergic receptor is associated with resting heart rate., Am J Hum Genet, vol. 70, no. 4, pp. 935-42, 2002.
L. J. Kurihara, Kikuchi, T., Wada, K., and Tilghman, S. M., Loss of Uch-L1 and Uch-L3 leads to neurodegeneration, posterior paralysis and dysphagia., Hum Mol Genet, vol. 10, no. 18, pp. 1963-70, 2001.
E. Wieschaus, Nusslein-Volhard, C., and Kluding, H., Krüppel, a gene whose activity is required early in the zygotic genome for normal embryonic segmentation., Dev Biol, vol. 104, no. 1, pp. 172-86, 1984.
D. L. Metallinos, Oppenheimer, A. J., Rinchik, E. M., Russell, L. B., Dietrich, W., and Tilghman, S. M., Fine structure mapping and deletion analysis of the murine piebald locus., Genetics, vol. 136, no. 1, pp. 217-23, 1994.
T. Schupbach and Wieschaus, E., Female sterile mutations on the second chromosome of Drosophila melanogaster. I. Maternal effect mutations., Genetics, vol. 121, no. 1, pp. 101-17, 1989.
L. J. Kurihara, Semenova, E., Levorse, J. M., and Tilghman, S. M., Expression and functional analysis of Uch-L3 during mouse development., Mol Cell Biol, vol. 20, no. 7, pp. 2498-504, 2000.
E. Semenova, Wang, X. F., Jablonski, M. M., Levorse, J., and Tilghman, S. M., An engineered 800 kilobase deletion of Uchl3 and Lmo7 on mouse chromosome 14 causes defects in viability, postnatal growth and degeneration of muscle and retina., Hum Mol Genet, vol. 12, no. 11, pp. 1301-12, 2003.
T. P. O'Brien, Metallinos, D. L., Chen, H., Shin, M. K., and Tilghman, S. M., Complementation mapping of skeletal and central nervous system abnormalities in mice of the piebald deletion complex., Genetics, vol. 143, no. 1, pp. 447-61, 1996.
E. Wieschaus, A combined genetic and mosaic approach to the study of oogenesis in Drosophila., Basic Life Sci, vol. 16, pp. 85-94, 1980.
E. Wieschaus, Audit, C., and Masson, M., A clonal analysis of the roles of somatic cells and germ line during oogenesis in Drosophila., Dev Biol, vol. 88, no. 1, pp. 92-103, 1981.