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PreviewIssue DateTitleAuthor(s)
2000Differences in the skin peptides of the male and female Australian tree frog Litoria splendida: The discovery of the aquatic male sex pheromone splendipherin, together with Phe8 caerulein and a new antibiotic peptide caerin 1.10Wabnitz, P.; Bowie, J.; Tyler, M.; Wallace, J.; Smith, B.
2007Kit signaling is essential for development and maintenance of interstitial cells of Cajal and electrical rhythmicity in the embryonic gastrointestinal tractSpencer, E.; Ro, S.; Bayguinov, Y.; Sanders, K.; Ward, S.
2005Identification and characterization of avihepadnaviruses isolated from exotic anseriformes maintained in captivityGuo, H.; Mason, W.; Aldrich, C.; Saputelli, J.; Miller, D.; Jilbert, A.; Newbold, J.
2000Cytochrome P450 4A, peroxisomal enzymes and nicotinamide cofactors in koala liverNgo, S.; Kong, S.; Kirlich, A.; McKinnon, R.; Stupans, I.
2009Identifying candidate serum biomarkers of exposure to tunicamycins in rats using two-dimensional electrophoresisPenno, M.; Bacic, A.; Colegate, S.; Hoffmann, P.; Michalski, W.
2001A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tardaTiller, G.; Hannig, V.; Dozier, D.; Carrel, L.; Trevarthen, K.; Wilcox, W.; Mundlos, S.; Haines, J.; Gedeon, A.; Gecz, J.
2003Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardationBurdon, 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.
2001CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsyPhillips, H.; Favre, I.; Kirkpatrick, M.; Zuberi, S.; Goudie, D.; Heron, S.; Scheffer, I.; Sutherland, G.; Berkovic, S.; Bertrand, D.; Mulley, J.
2007DMRT gene cluster analysis in the platypus: New insights into genomic organization and regulatory regionsEl-Mogharbel, N.; Wakefield, M.; Deakin, J.; Tsend-Ayush, E.; Grutzner, F.; Alsop, A.; Ezaz, T.; Graves, J.
2002Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndromeLower, 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.