[1] | Pennisi, D., Chiu, H. S., Kinna, G., Wilkinson, L., Simmons, D., Little, M. (2011). Altered Development of Trophoblast Lineages During Placental Development in Mice Hypomorphic for Crim1. Manuscript in preparation. * Corresponding author. |
[2] | Little, M. H., Georgas, K., Pennisi, D. J., and Wilkinson, L. (2010). Kidney development: two tales of tubulogenesis. Current Topics in Developmental Biology. 90: 193–229. |
[3] | Wilkinson, L., Gilbert, T., Sipos, A., Toma, I., Pennisi, D. J., Peti-Peterdi, J., and Little, M. H. (2009). Loss of renal microvascular integrity in postnatal Crim1 hypomorphic transgenic mice. Kidney International. 76: 1161–1171. |
[4] | Pennisi D. J.* and Mikawa T. (2009). FGFR-1 is required by epicardium-derived cells for myocardial invasion and correct coronary vascular lineage differentiation. Developmental Biology. 328: 148–159. * Corresponding author. |
[5] | Wilkinson, L., Gilbert, T., Kinna, G., Ruta, L. A., Pennisi, D. J., Kett, M., and Little, M. H. (2007). Crim1KST264/KST264 mice implicate Crim1 in the regulation of vascular endothelial growth factor-A activity during glomerular vascular development. Journal of the American Society of Nephrology. 18: 1697–1708. |
[6] | Pennisi, D. J., Wilkinson, L., Kolle, G., Sohaskey, M. L., Gillider, K., Piper, M. J., McAvoy, J. W., Lovicu, F. J., and Little, M. H. (2007). Crim1KST264/KST264 mice display a disruption of the Crim1 gene resulting in perinatal lethality with defects in multiple organ systems. Developmental Dynamics. 236: 502–511. |
[7] | Pennisi, D. J., and Mikawa, T. (2005). Normal patterning of the coronary capillary plexus is dependent on the correct transmural gradient of FGF expression in the myocardium. Developmental Biology. 279: 378–390. |
[8] | Hatcher, C. J., Diman, N. Y., Kim, M. S., Pennisi, D., Song, Y., Goldstein, M. M., Mikawa, T., and Basson, C. T. (2004). A role for Tbx5 in proepicardial cell migration during cardiogenesis. Physiological Genomics. 18: 129–140. |
[9] | Hall, C. E., Hurtado, R., Hewett, K. W., Shulimovich, M., Poma, C. P., Reckova, M., Justus, C., Pennisi, D. J., Tobita, K., Sedmera, D., Gourdie, R. G., and Mikawa, T. (2004). Hemodynamic-dependent patterning of endothelin converting enzyme 1 expression and differentiation of impulse-conducting Purkinje fibers in the embryonic heart. Development. 131: 581–592. |
[10] | Pennisi, D. J., Ballard, V. L., and Mikawa, T. (2003). Epicardium is required for the full rate of myocyte proliferation and levels of expression of myocyte mitogenic factors FGF2 and its receptor, FGFR-1, but not for transmural myocardial patterning in the embryonic chick heart. Developmental Dynamics. 228, 161–172. |
[11] | Mikawa, T., Gourdie, R. G., Takebayashi-Suzuki, K., Kanzawa, N., Hyer, J., Pennisi, D. J., Poma, C. P., Shulimovich, M., Diaz, K. G., Layliev, J., and Prasad, A. (2003). Induction and patterning of the Purkinje fibre network. Novartis Foundation Symposium. 250: 142–153. |
[12] | Pennisi, D. J., Rentschler, S., Gourdie, R. G., Fishman, G. I., and Mikawa, T. (2002). Induction and patterning of the cardiac conduction system. International Journal of Developmental Biology. 46: 765–775. |
[13] | Hosking, B. M., Wyeth, J. R., Pennisi, D. J., Wang, S. C., Koopman, P., and Muscat, G. E. (2001). Cloning and functional analysis of the Sry-related HMG box gene, Sox18. Gene. 262: 239–247. |
[14] | Pennisi, D. J., James, K. M., Hosking, B., Muscat, G. E., and Koopman, P. (2000). Structure, mapping, and expression of human SOX18. Mammalian Genome. 11: 1147–1149. |
[15] | Pennisi, D., Gardner, J., Chambers, D., Hosking, B., Peters, J., Muscat, G., Abbott, C., and Koopman, P. (2000). Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice. Nature Genetics. 24: 434-437. |
[16] | Greenfield, A., Carrel, L., Pennisi, D., Philippe, C., Quaderi, N., Siggers, P., Steiner, K., Tam, P. P., Monaco, A. P., Willard, H. F., and Koopman, P. (1998). The UTX gene escapes X inactivation in mice and humans. Human Molecular Genetics. 7: 737–742. |
[17] | Greenfield, A., Scott, D., Pennisi, D., Ehrmann, I., Ellis, P., Cooper, L., Simpson, E., and Koopman, P. (1996). An H-YDb epitope is encoded by a novel mouse Y chromosome gene. Nature Genetics. 14, 474–478. |
[18] | Monkley, S. J., Delaney, S. J., Pennisi, D. J., Christiansen, J. H., and Wainwright, B. J. (1996). Targeted disruption of the Wnt2 gene results in placentation defects. Development. 122: 3343–3353. |