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

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A. S. Putnam, J Scriber, M., and Andolfatto, P., Discordant divergence times among Z-chromosome regions between two ecologically distinct swallowtail butterfly species., Evolution, vol. 61, no. 4, pp. 912-27, 2007.
J. G. Purdy, Shenk, T., and Rabinowitz, J. D., Fatty acid elongase 7 catalyzes lipidome remodeling essential for human cytomegalovirus replication., Cell Rep, vol. 10, no. 8, pp. 1375-85, 2015.
P. F. Przytycki and Singh, M., Differential Allele-Specific Expression Uncovers Breast Cancer Genes Dysregulated by Cis Noncoding Mutations., Cell Syst, vol. 10, no. 2, pp. 193-203.e4, 2020.
P. F. Przytycki and Singh, M., Differential analysis between somatic mutation and germline variation profiles reveals cancer-related genes., Genome Med, vol. 9, no. 1, p. 79, 2017.
Y. Pritykin and Singh, M., Simple topological features reflect dynamics and modularity in protein interaction networks., PLoS Comput Biol, vol. 9, no. 10, p. e1003243, 2013.
Y. Pritykin, Ghersi, D., and Singh, M., Genome-Wide Detection and Analysis of Multifunctional Genes., PLoS Comput Biol, vol. 11, no. 10, p. e1004467, 2015.
Y. Pritykin, Brito, T., Schüpbach, T., Singh, M., and Pane, A., Integrative analysis unveils new functions for the Drosophila Cutoff protein in noncoding RNA biogenesis and gene regulation., RNA, vol. 23, no. 7, pp. 1097-1109, 2017.
M. Pribyl, Muratov, C. B., and Shvartsman, S. Y., Long-range signal transmission in autocrine relays., Biophys J, vol. 84, no. 2 Pt 1, pp. 883-96, 2003.
M. Pribyl, Muratov, C. B., and Shvartsman, S. Y., Transitions in the model of epithelial patterning., Dev Dyn, vol. 226, no. 1, pp. 155-9, 2003.
M. Pribyl, Muratov, C. B., and Shvartsman, S. Y., Discrete models of autocrine cell communication in epithelial layers., Biophys J, vol. 84, no. 6, pp. 3624-35, 2003.
M. O. Press, McCoy, R. C., Hall, A. N., Akey, J. M., and Queitsch, C., Massive variation of short tandem repeats with functional consequences across strains of Arabidopsis thaliana., Genome Res, vol. 28, no. 8, pp. 1169-1178, 2018.
M. A. Postner, Miller, K. G., and Wieschaus, E. F., Maternal effect mutations of the sponge locus affect actin cytoskeletal rearrangements in Drosophila melanogaster embryos., J Cell Biol, vol. 119, no. 5, pp. 1205-18, 1992.
M. A. Postner and Wieschaus, E. F., The nullo protein is a component of the actin-myosin network that mediates cellularization in Drosophila melanogaster embryos., J Cell Sci, vol. 107 ( Pt 7), pp. 1863-73, 1994.
A. Pop, Huttenhower, C., Iyer-Pascuzzi, A., Benfey, P. N., and Troyanskaya, O. G., Integrated functional networks of process, tissue, and developmental stage specific interactions in Arabidopsis thaliana., BMC Syst Biol, vol. 4, p. 180, 2010.
A. J. Pompeani, Irgon, J. J., Berger, M. F., Bulyk, M. L., Wingreen, N. S., and Bassler, B. L., The Vibrio harveyi master quorum-sensing regulator, LuxR, a TetR-type protein is both an activator and a repressor: DNA recognition and binding specificity at target promoters., Mol Microbiol, vol. 70, no. 1, pp. 76-88, 2008.
O. Polyakov, He, B., Swan, M., Shaevitz, J. W., Kaschube, M., and Wieschaus, E., Passive mechanical forces control cell-shape change during Drosophila ventral furrow formation., Biophys J, vol. 107, no. 4, pp. 998-1010, 2014.
J. R. Pollack, Sørlie, T., Perou, C. M., Rees, C. A., Jeffrey, S. S., Lonning, P. E., Tibshirani, R., Botstein, D., Børresen-Dale, A. - L., and Brown, P. O., Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors., Proc Natl Acad Sci U S A, vol. 99, no. 20, pp. 12963-8, 2002.
J. R. Pollack, van de Rijn, M., and Botstein, D., Challenges in developing a molecular characterization of cancer., Semin Oncol, vol. 29, no. 3, pp. 280-5, 2002.
L. Poillet-Perez, Xie, X., Zhan, L., Yang, Y., Sharp, D. W., Hu, Z. Sherrie, Su, X., Maganti, A., Jiang, C., Lu, W., Zheng, H., Bosenberg, M. W., Mehnert, J. M., Guo, J. Yanxiang, Lattime, E., Rabinowitz, J. D., and White, E., Autophagy maintains tumour growth through circulating arginine., Nature, vol. 563, no. 7732, pp. 569-573, 2018.
T. Pilizota and Shaevitz, J. W., Fast, multiphase volume adaptation to hyperosmotic shock by Escherichia coli., PLoS One, vol. 7, no. 4, p. e35205, 2012.
T. Pilizota and Shaevitz, J. W., Plasmolysis and cell shape depend on solute outer-membrane permeability during hyperosmotic shock in E. coli., Biophys J, vol. 104, no. 12, pp. 2733-42, 2013.
T. Pilizota and Shaevitz, J. W., Origins of Escherichia coli Growth Rate and Cell Shape Changes at High External Osmolality., Biophys J, vol. 107, no. 8, pp. 1962-9, 2014.
M. Piazza, Feng, X. - J., Rabinowitz, J. D., and Rabitz, H., Diverse metabolic model parameters generate similar methionine cycle dynamics., J Theor Biol, vol. 251, no. 4, pp. 628-39, 2008.
K. Pfeifer, Leighton, P. A., and Tilghman, S. M., The structural H19 gene is required for transgene imprinting., Proc Natl Acad Sci U S A, vol. 93, no. 24, pp. 13876-83, 1996.
K. Pfeifer and Tilghman, S. M., Allele-specific gene expression in mammals: the curious case of the imprinted RNAs., Genes Dev, vol. 8, no. 16, pp. 1867-74, 1994.
A. A. Petti, Crutchfield, C. A., Rabinowitz, J. D., and Botstein, D., Survival of starving yeast is correlated with oxidative stress response and nonrespiratory mitochondrial function., Proc Natl Acad Sci U S A, vol. 108, no. 45, pp. E1089-98, 2011.
A. A. Petti, R McIsaac, S., Ho-Shing, O., Bussemaker, H. J., and Botstein, D., Combinatorial control of diverse metabolic and physiological functions by transcriptional regulators of the yeast sulfur assimilation pathway., Mol Biol Cell, vol. 23, no. 15, pp. 3008-24, 2012.
M. D. Petkova, Little, S. C., Liu, F., and Gregor, T., Maternal origins of developmental reproducibility., Curr Biol, vol. 24, no. 11, pp. 1283-8, 2014.
C. N. Peterson, Levchenko, I., Rabinowitz, J. D., Baker, T. A., and Silhavy, T. J., RpoS proteolysis is controlled directly by ATP levels in Escherichia coli., Genes Dev, vol. 26, no. 6, pp. 548-53, 2012.
A. V. Persikov, Wetzel, J. L., Rowland, E. F., Oakes, B. L., Xu, D. J., Singh, M., and Noyes, M. B., A systematic survey of the Cys2His2 zinc finger DNA-binding landscape., Nucleic Acids Res, vol. 43, no. 3, pp. 1965-84, 2015.
A. V. Persikov and Singh, M., An expanded binding model for Cys2His2 zinc finger protein-DNA interfaces., Phys Biol, vol. 8, no. 3, p. 035010, 2011.
A. V. Persikov, Rowland, E. F., Oakes, B. L., Singh, M., and Noyes, M. B., Deep sequencing of large library selections allows computational discovery of diverse sets of zinc fingers that bind common targets., Nucleic Acids Res, vol. 42, no. 3, pp. 1497-508, 2014.
A. V. Persikov and Singh, M., De novo prediction of DNA-binding specificities for Cys2His2 zinc finger proteins., Nucleic Acids Res, vol. 42, no. 1, pp. 97-108, 2014.
A. V. Persikov, Osada, R., and Singh, M., Predicting DNA recognition by Cys2His2 zinc finger proteins., Bioinformatics, vol. 25, no. 1, pp. 22-9, 2009.
M. W. Perry, Boettiger, A. N., Bothma, J. P., and Levine, M., Shadow enhancers foster robustness of Drosophila gastrulation., Curr Biol, vol. 20, no. 17, pp. 1562-7, 2010.
M. W. Perry, Bothma, J. P., Luu, R. D., and Levine, M., Precision of hunchback expression in the Drosophila embryo., Curr Biol, vol. 22, no. 23, pp. 2247-52, 2012.
M. W. Perry, Boettiger, A. N., and Levine, M., Multiple enhancers ensure precision of gap gene-expression patterns in the Drosophila embryo., Proc Natl Acad Sci U S A, vol. 108, no. 33, pp. 13570-5, 2011.
L. Peña-Castillo, Tasan, M., Myers, C. L., Lee, H., Joshi, T., Zhang, C., Guan, Y., Leone, M., Pagnani, A., Kim, W. Kyu, Krumpelman, C., Tian, W., Obozinski, G., Qi, Y., Mostafavi, S., Lin, G. Ning, Berriz, G. F., Gibbons, F. D., Lanckriet, G., Qiu, J., Grant, C., Barutcuoglu, Z., Hill, D. P., Warde-Farley, D., Grouios, C., Ray, D., Blake, J. A., Deng, M., Jordan, M. I., Noble, W. S., Morris, Q., Klein-Seetharaman, J., Bar-Joseph, iv, Z., Chen, T., Sun, F., Troyanskaya, O. G., Marcotte, E. M., Xu, D., Hughes, T. R., and Roth, F. P., A critical assessment of Mus musculus gene function prediction using integrated genomic evidence., Genome Biol, vol. 9 Suppl 1, p. S2, 2008.
R. J. Pelham, Rodgers, L., Hall, I., Lucito, R., Nguyen, K. C. Q., Navin, N., Hicks, J., Mu, D., Powers, S., Wigler, M., and Botstein, D., Identification of alterations in DNA copy number in host stromal cells during tumor progression., Proc Natl Acad Sci U S A, vol. 103, no. 52, pp. 19848-53, 2006.
M. Peifer, Sweeton, D., Casey, M., and Wieschaus, E., wingless signal and Zeste-white 3 kinase trigger opposing changes in the intracellular distribution of Armadillo., Development, vol. 120, no. 2, pp. 369-80, 1994.
M. Peifer, McCrea, P. D., Green, K. J., Wieschaus, E., and Gumbiner, B. M., The vertebrate adhesive junction proteins beta-catenin and plakoglobin and the Drosophila segment polarity gene armadillo form a multigene family with similar properties., J Cell Biol, vol. 118, no. 3, pp. 681-91, 1992.
M. Peifer, Rauskolb, C., Williams, M., Riggleman, B., and Wieschaus, E., The segment polarity gene armadillo interacts with the wingless signaling pathway in both embryonic and adult pattern formation., Development, vol. 111, no. 4, pp. 1029-43, 1991.
M. Peifer and Wieschaus, E., The segment polarity gene armadillo encodes a functionally modular protein that is the Drosophila homolog of human plakoglobin., Cell, vol. 63, no. 6, pp. 1167-76, 1990.
M. Peifer, Orsulic, S., Sweeton, D., and Wieschaus, E., A role for the Drosophila segment polarity gene armadillo in cell adhesion and cytoskeletal integrity during oogenesis., Development, vol. 118, no. 4, pp. 1191-207, 1993.
M. Peifer and Wieschaus, E., The product of the Drosophila melanogaster segment polarity gene armadillo is highly conserved in sequence and expression in the housefly Musca domestica., J Mol Evol, vol. 36, no. 3, pp. 224-33, 1993.
M. Peifer and Wieschaus, E., Mutations in the Drosophila gene extradenticle affect the way specific homeo domain proteins regulate segmental identity., Genes Dev, vol. 4, no. 7, pp. 1209-23, 1990.
N. N. Pavlova, Hui, S., Ghergurovich, J. M., Fan, J., Intlekofer, A. M., White, R. M., Rabinowitz, J. D., Thompson, C. B., and Zhang, J., As Extracellular Glutamine Levels Decline, Asparagine Becomes an Essential Amino Acid., Cell Metab, vol. 27, no. 2, pp. 428-438.e5, 2018.
W. J. Pavan, Mac, S., Cheng, M., and Tilghman, S. M., Quantitative trait loci that modify the severity of spotting in piebald mice., Genome Res, vol. 5, no. 1, pp. 29-41, 1995.
W. J. Pavan and Tilghman, S. M., Piebald lethal (sl) acts early to disrupt the development of neural crest-derived melanocytes., Proc Natl Acad Sci U S A, vol. 91, no. 15, pp. 7159-63, 1994.
J. Parsch, Novozhilov, S., Saminadin-Peter, S. S., Wong, K. M., and Andolfatto, P., On the utility of short intron sequences as a reference for the detection of positive and negative selection in Drosophila., Mol Biol Evol, vol. 27, no. 6, pp. 1226-34, 2010.
S. Parks and Wieschaus, E., The Drosophila gastrulation gene concertina encodes a G alpha-like protein., Cell, vol. 64, no. 2, pp. 447-58, 1991.
J. O. Park, Tanner, L. B., Wei, M. H., Khana, D. B., Jacobson, T. B., Zhang, Z., Rubin, S. A., Li, S. Hsin- Jung, Higgins, M. B., Stevenson, D. M., Amador-Noguez, D., and Rabinowitz, J. D., Near-equilibrium glycolysis supports metabolic homeostasis and energy yield., Nat Chem Biol, vol. 15, no. 10, pp. 1001-1008, 2019.
C. Y. Park, Wong, A. K., Greene, C. S., Rowland, J., Guan, Y., Bongo, L. A., Burdine, R. D., and Troyanskaya, O. G., Functional knowledge transfer for high-accuracy prediction of under-studied biological processes., PLoS Comput Biol, vol. 9, no. 3, p. e1002957, 2013.
C. Y. Park, Krishnan, A., Zhu, Q., Wong, A. K., Lee, Y. -suk, and Troyanskaya, O. G., Tissue-aware data integration approach for the inference of pathway interactions in metazoan organisms., Bioinformatics, 2014.
C. Y. Park, Hess, D. C., Huttenhower, C., and Troyanskaya, O. G., Simultaneous genome-wide inference of physical, genetic, regulatory, and functional pathway components., PLoS Comput Biol, vol. 6, no. 11, p. e1001009, 2010.
J. O. Park, Rubin, S. A., Xu, Y. - F., Amador-Noguez, D., Fan, J., Shlomi, T., and Rabinowitz, J. D., Metabolite concentrations, fluxes and free energies imply efficient enzyme usage., Nat Chem Biol, 2016.
R. Papazyan, Sun, Z., Kim, Y. Hoon, Titchenell, P. M., Hill, D. A., Lu, W., Damle, M., Wan, M., Zhang, Y., Briggs, E. R., Rabinowitz, J. D., and Lazar, M. A., Physiological Suppression of Lipotoxic Liver Damage by Complementary Actions of HDAC3 and SCAP/SREBP., Cell Metab, vol. 24, no. 6, pp. 863-874, 2016.
D. Papatsenko and Levine, M. S., Dual regulation by the Hunchback gradient in the Drosophila embryo., Proc Natl Acad Sci U S A, vol. 105, no. 8, pp. 2901-6, 2008.
D. Papatsenko, Kislyuk, A., Levine, M., and Dubchak, I., Conservation patterns in different functional sequence categories of divergent Drosophila species., Genomics, vol. 88, no. 4, pp. 431-42, 2006.
D. Papatsenko and Levine, M., Quantitative analysis of binding motifs mediating diverse spatial readouts of the Dorsal gradient in the Drosophila embryo., Proc Natl Acad Sci U S A, vol. 102, no. 14, pp. 4966-71, 2005.
D. Papatsenko and Levine, M., Computational identification of regulatory DNAs underlying animal development., Nat Methods, vol. 2, no. 7, pp. 529-34, 2005.
D. Papatsenko, Levine, M., and Goltsev, Y., Clusters of temporal discordances reveal distinct embryonic patterning mechanisms in Drosophila and anopheles., PLoS Biol, vol. 9, no. 1, p. e1000584, 2011.
D. Papatsenko, Goltsev, Y., and Levine, M., Organization of developmental enhancers in the Drosophila embryo., Nucleic Acids Res, vol. 37, no. 17, pp. 5665-77, 2009.
A. Pane, Jiang, P., Zhao, D. Yanling, Singh, M., and Schüpbach, T., The Cutoff protein regulates piRNA cluster expression and piRNA production in the Drosophila germline., EMBO J, vol. 30, no. 22, pp. 4601-15, 2011.
V. Pachnis, Brannan, C. I., and Tilghman, S. M., The structure and expression of a novel gene activated in early mouse embryogenesis., EMBO J, vol. 7, no. 3, pp. 673-81, 1988.