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Preview	Issue Date	Title	Author(s)
	2006	Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation	Hagens, O.; Dubos, A.; Abidi, F.; Barbi, G.; Van Zutven, L.; Hoeltzenbein, M.; Tommerup, N.; Moraine, C.; Fryns, J.; Chelly, J.; van Bokhoven, H.; Gecz, J.; Dollfus, H.; Ropers, H.; Schwartz, C.; de Cassia Stocco dos Santos, R.; Kalscheuer, V.; Hanauer, A.
	2001	Peptide insertions in domain 4 of hbc, the shared signalling receptor subunit for GM-CSF, IL3 and IL5, induce ligand-independent activation	Jones, K.; Bagley, C.; Butcher, C.; Barry, S.; Vadas, M.; D'Andrea, R.
	2004	Role of N- and C-terminal residues of insulin-like growth factor (IGF)-binding protein-3 in regulating IGF complex formation and receptor activation	Yan, X.; Forbes, B.; McNeil, K.; Baxter, R.; Firth, S.
	2008	AIRE'S CARD revealed, a new structure for the central tolerance provokes transcriptional plasticity	Ferguson, B.; Alexander, C.; Rossi, S.; Liiv, I.; Rebane, A.; Worth, C.; Wong, J.; Laan, M.; Peterson, P.; Jenkinson, E.; Anderson, G.; Scott, H.; Cooke, A.; Rich, T.
	2003	Threonine 391 phosphorylation of the human prolactin receptor mediates a novel interaction with 14-3-3 proteins	Olayioye, M.; Guthridge, M.; Stomski, F.; Lopez, A.; Visvader, J.; Lindeman, G.
	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.
	2004	Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation	Weaving, L.; Christodoulou, J.; Williamson, S.; Friend, K.; McKenzie, O.; Archer, H.; Evans, J.; Clarke, A.; Pelka, G.; Tam, P.; Watson, C.; Lahooti, H.; Ellaway, C.; Bennetts, B.; Leonard, H.; Gecz, J.
	2006	Effect of disrupted SOX18 transcription factor function on tumor growth, vascularization, and endothelial development	Young, N.; Hahn, C.; Poh, A.; Dong, C.; Wilhelm, D.; Olsson, J.; Muscat, G.; Parsons, P.; Gamble, J.; Koopman, P.
	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.