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Preview	Issue Date	Title	Author(s)
	2001	Hormone status selects for spontaneous somatic androgen receptor variants that demonstrate specific ligand and cofactor dependent activities in autochthonous prostate cancer	Han, G.; Foster, B.; Mistry, S.; Buchanan, G.; Harris, J.; Tilley, W.; Greenberg, N.
	2001	Mutations at the boundary of the hinge and ligand binding domain of the androgen receptor confer increased transactivation function	Buchanan, G.; Yang, M.; Harris, J.; Nahm, H.; Han, G.; Moore, N.; Bentel, J.; Matusik, R.; Horsfall, D.; Marshall, V.; Greenberg, N.; Tilley, W.
	2005	Protective immunization of mice with an active-site mutant of subtilase cytotoxin of Shiga toxin-producing Escherichia coli	Talbot, U.; Paton, J.; Paton, A.
	2004	Effect of β₂‐glycoprotein I null mutation on reproductive outcome and antiphospholipid antibody‐mediated pregnancy pathology in mice	Robertson, S.; Roberts, C.; van Beijering, E.; Pensa, K.; Sheng, Y.; Shi, T.; Krilis, S.
	2001	Impaired thrombin generation in b2-glycoprotein I null mice	Sheng, Y.; Reddel, S.; Herzog, H.; Wang, Y.; Brighton, T.; France, M.; Robertson, S.; Krilis, S.
	2005	Mutation of the androgen receptor causes oncogenic transformation of the prostate	Han, G.; Buchanan, G.; Ittmann, M.; Harris, J.; Yu, X.; DeMayo, F.; Tilley, W.; Greenberg, N.
	2003	Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation	Burdon, K.; McKay, J.; Sale, M.; Russell-Eggitt, I.; Mackey, D.; Wirth, G.; Elder, J.; Nicoll, A.; Clarke, M.; FitzGerald, L.; Stankovich, J.; Shaw, M.; Sharma, S.; Gajovic, S.; Gruss, P.; Ross, S.; Thomas, P.; Voss, A.; Thomas, T.; Gecz, J.; et al.
	2009	Csf2 Null Mutation Alters Placental Gene Expression and Trophoblast Glycogen Cell and Giant Cell Abundance in Mice	Sferruzzi-Perri, A.; Macpherson, A.; Roberts, C.; Robertson, S.
	2002	Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome	Lower, K.; Turner, G.; Kerr, B.; Mathews, K.; Shaw, M.; Gedeon, A.; Schelley, S.; Hoyme, H.; White, S.; Delatycki, M.; Lampe, A.; Clayton-Smith, J.; Stewart, H.; van Ravenswaay, C.; de Vries, B.; Cox, B.; Grompe, M.; Ross, S.; Thomas, P.; Mulley, J.; et al.
	2002	Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy	Stromme, P.; Mangelsdorf, M.; Shaw, M.; Lower, K.; Lewis, S.; Bruyere, H.; Lutcherath, V.; Gedeon, A.; Wallace, R.; Scheffer, I.; Turner, G.; Partington, M.; Frints, S.; Fryns, J.; Sutherland, G.; Mulley, J.; Gecz, J.