publications

Raisner, R.M., Hartley, P.D., Meneghini, M.D., Bao, M.Z., Liu, C.L., Schreiber, S.L., Rando, O.J., and Madhani, H.D. (2005).

Histone variant H2A.Z marks the 5' end of both active and inactive genes in euchromatin.

Cell. 123(2): 233-248.

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Kobor, M.S., Venkatasubrahmanyam, S., Meneghini, M.D., Gin, J.G., Jennings, J.L., Link, A.J., Madhani, H.D., and Rine, J. (2004).

A Protein Complex Containing the Conserved Swi2/Snf2-Related ATPase Swr1p Deposits Histone Variant H2A.Z into Euchromatin.

PLoS Biol. 2(5): E131.

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Meneghini, M.D., Wu, M., and Madhani , H. D. (2003).

Conserved histone variant H2A.Z protects euchromatin from the ectopic spread of silent heterochromatin.

Cell. 112(5): 725-736.

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Maduro, M.F., Meneghini, M.D., Bowerman, B., Broitman-Maduro, G., and Rothman, J.H. (2001).

Restriction of mesendoderm to a single blastomere by the combined action of SKN-1 and a GSK-3ß homolog is mediated by MED-1 and -2 in C. elegans.

Molecular Cell. 7(3): 475-485.


Schlesinger, A., Shelton, C.A., Maloof, J.N., Meneghini, M., and Bowerman, B. (2000).

Wnt pathway components orient a mitotic spindle in the early Caenorhabditis elegans embryo without requiring transcription in the responding cell.

Genes & Dev. 13: 2028-2038.

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Meneghini, M.D., Ishitani, T., Carter, J.C., Hisamoto, N., Ninomiya-Tsuji, J., Thorpe, C.J., Hamill, D.R., Matsumoto, K., and Bowerman, B. (1999).

MAP kinase and Wnt pathways converge to downregulate an HMG-domain repressor in Caenorhabditis elegans.

Nature, 399:793-797.

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Ishitani, T., Ninomiya-Tsuji, J., Nagai, S., Nishita, M., Meneghini, M., Barker, N., Waterman, M., Bowerman, B., Clevers, H., Shibuya, H., and Matsumoto, K. (1999).

The TAK1-NLK-MAPK-related pathway antagonizes signalling between ß-catenin and transcription factor TCF.

Nature, 399: 798-802

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Keesee, S.K., Meneghini, M.D., Szaro, R.P., and Wu, Y.J. (1994).

Nuclear matrix proteins in human colon cancer.

Proc. Natl. Acad. Sci. U.S.A. 91: 1913-1916.

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Miller, T., Beausang, L.A., Meneghini, M., and Lidgard, G. (1993).

Death-induced changes to the nuclear matrix: the use of anti-nuclear matrix antibodies to study agents of apoptosis.

Biotechniques, 15: 1042-1047.