Adjunct Associate Professor Edna Hardeman

Adjunct Associate Professor
Medicine, Children's Medical Research Institute

T: 02 8865 2913
F: 02 687 2120
E:

Research interests

Associate Professor Edna Hardeman is an internationally recognised expert in muscle biology and disease and more recently researches the neurodevelopmental disorder Williams Syndrome.

Publications

2011 | 2009 | 2008 | 2007

2011

   
  • Nguyen, M., Joya, J., Kee, A., Domazetovska, A., Yang, N., Hook, J., Lemckert, F., Kettle, E., Valova, V., Robinson, P., North, K., Gunning, P., Mitchell, C., Hardeman, E. (2011), Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy. Brain. 134(Pt 12), 3516-3529. [Abstract]

2009

   
  • Vlahovich, N., Kee, A., Van der Poel, C., Kettle, E., Hernandez-Deviez, D., Lucas, C., Lynch, G., Parton, R., Gunning, P., Hardeman, E. (2009), Cytoskeletal Tropomyosin Tm5NM1 Is Required for Normal Excitation-contraction Coupling in Skeletal Muscle. Molecular biology of the cell. 20(1), 400-9. [Abstract]

2008

   
  • Chang, A., Hook, J., Lemckert, F., McDonald, M., Nguyen, M., Hardeman, E., Little, D., Gunning, P., Reddel, R. (2008), The murine stanniocalcin 2 gene is a negative regulator of postnatal growth. Endocrinology. 149(5), 2403-2410. [Abstract]
  • MacArthur, D., Seto, J., Chan, S., Quinlan, K., Raftery, J., Turner, N., Nicholson, M., Kee, A., Hardeman, E., Gunning, P., Cooney, G., Head, S., Yang, N., North, K. (2008), An Actn3 knockout mouse provides mechanistic insights into the association between alpha-actinin-3 deficiency and human athletic performance. Human Molecular Genetics. 17(8), 1076-1086. [Abstract]
  • Schevzov, G., Fath, T., Vrhovski, B., Vlahovich, N., Rajan, S., Hook, J., Joya, J., Lemckert, F., Puttur, F., Lin, J., Hardeman, E., Wieczorek, D., O'Neill, G., Gunning, P. (2008), Divergent regulation of the sarcomere and the cytoskeleton. The Journal of biological chemistry. 283(1), 275-83. [Abstract]
  • Gunning, P., O'Neill, G., Hardeman, E. (2008), Tropomyosin-based regulation of the actin cytoskeleton in time and space. Physiological Reviews. 88(1), 1-35. [Abstract]
  • Nguyen, M., Hardeman, E. (2008), Mouse Models for Thin Filament Disease. In: The Sarcomere and Skeletal Muscle Disease. (pp.66-77).United States: Springer.
  • Vlahovich, N., Schevzov, G., Nair-Shaliker, V., Ilkovski, B., Artap, S., Joya, J., Kee, A., North, K., Gunning, P., Hardeman, E. (2008), Tropomyosin 4 defines novel filaments in skeletal muscle associated with muscle remodelling/regeneration in normal and diseased muscle. Cell motility and the cytoskeleton. 65(0), 73-85. [Abstract]
  • Kee, A., Hardeman, E. (2008), Tropomyosins in skeletal muscle diseases. Advances in experimental medicine and biology. 644, 143-157. [Abstract]

2007

   
  • Domazetovska, A., Ilkovski, B., Cooper, S., Ghoddusi, M., Hardeman, E., Minamide, L., Gunning, P., Bamburg, J., North, K. (2007), Mechanisms underlying intranuclear rod formation. Brain : a journal of neurology. 130(Pt 12), 3275-84. [Abstract]
  • Macarthur, D., Seto, J., Raftery, J., Quinlan, K., Huttley, G., Hook, J., Lemckert, F., Kee, A., Edwards, M., Berman, Y., Hardeman, E., Gunning, P., Easteal, S., Yang, N., North, K. (2007), Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans. Nature genetics. 39(10), 1261-5. [Abstract]
  • Chen, W., Ruell, P., Ghoddusi, M., Kee, A., Hardeman, E., Hoffman, K., Thompson, M. (2007), Ultrastructural changes and SR Ca2+ regulation in red vastus muscle following eccentric exercise in the rat. Experimental physiology. 92, 437-47. [Abstract]
  • Palmer, S., Tay, E., Santucci, N., Cuc Bach, T., Hook, J., Lemckert, F., Jamieson, R., Gunnning, P., Hardeman, E. (2007), Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development. Gene expression patterns : GEP. 7, 396-404. [Abstract]