Reading List: Hons 2010
Elms, P., Siggers,
P., Napper, D.,
Brown, L., Paraso, M., Arkell, R. and Brown, S. (2005). In vitro analysis of partial loss-of-function ZIC2 mutations in holoprosencephaly: alanine tract expansion modulates DNA binding and transactivation. Hum Mol Genet 14, 411-20.
Warr, N., Powles-Glover, N., Chappell, A., Robson, J., Norris, D. and Arkell, R. M. (2008). Zic2-associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation. Hum Mol Genet 17, 2986-96.
Merzdorf, C. S. (2007). Emerging roles for zic genes in early development. Dev Dyn 236, 922-40.
Latchman, D. S. (1997). Transcription factors: an overview. Int J Biochem Cell Biol 29, 1305-12.
Sim, H., Argentaro, A. and Harley, V. R. (2008). Boys, girls and shuttling of SRY and SOX9. Trends Endocrinol Metab 19, 213-22.
Lyst, M. J. and Stancheva,
Gill, G. (2005a). Something about SUMO inhibits transcription. Curr Opin Genet Dev 15, 536-41.