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Preview	Issue Date	Title	Author(s)
	2003	Immunoexpression of the relaxin receptor LGR7 in breast and uterine tissues of humans and primates	Ivell, R.; Balvers, M.; Pohnke, Y.; Telgmann, R.; Bartsch, O.; Milde-Langosch, K.; Bamberger, A.; Einspanier, A.
	2003	RegR, a global LacI/GalR family regulator, modulates virulence and competence in Streptococcus pneumoniae	Chapuy-Regaud, S.; Ogunniyi, A.; Diallo, N.; Huet, Y.; Desnottes, J.; Paton, J.; Escaich, S.; Trombe, M.
	2003	Novel mesenchymal and haematopoietic cell isoforms of the SHP-2 docking receptor, PZR: identification, molecular cloning and effects on cell migration	Zannettino, A.; Roubelakis, M.; Welldon, K.; Jackson, D.; Simmons, P.; Bendall, L.; Henniker, A.; Harrison, K.; Niutta, S.; Bradstock, K.; Watt, S.
	2003	Identification and cloning of two forms of liver peroxisomal fatty Acyl CoA Oxidase from the koala (Phascolarctos cinereus)	Ngo, S.; McKinnon, R.; Stupans, I.
	2003	Family 39 a-L-iduronidases and b-D-xylosidases react through similar glycosyl-enzyme intermediates: Identification of the human iduronidase nucleophile	Nieman, C.; Wong, A.; He, S.; Clarke, L.; Hopwood, J.; Withers, S.
	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.
	2003	Role of nuclear and cytoplasmic localization in the tumour-suppressor activity of the von Hippel-Lindau protein	Lewis, M.; Roberts, B.
	2003	Resurrecting the Ancestral Steroid Receptor: Ancient Origin of Estrogen Signaling	Thornton, J.; Need, E.; Crews, D.
	2003	Novel PHF6 mutation p.D333del causes Borjeson-Forssman-Lehmann syndrome	Baumstark, A.; Lower, K.; Sinkus, A.; Andriuskeveviciute, I.; Jurkeniene, L.; Gecz, J.; Just, W.
	2003	Sodium channel α1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms	Wallace, R.; Hodgson, B.; Grinton, B.; Gardiner, R.; Robinson, R.; Rodriguez-Casero, V.; Sadleir, L.; Morgan, J.; Harkin, L.; Dibbens, L.; Yamamoto, T.; Andermann, E.; Mulley, J.; Berkovic, S.; Scheffer, I.