1. Adelaide Research & Scholarship

Search


Current filters:



Start a new search
Add filters:

Use filters to refine the search results.

 | 
Results 1-10 of 10 (Search time: 0.006 seconds).
  • previous
  • 1
  • next
Item hits:
PreviewIssue DateTitleAuthor(s)
1996The stoned locus of drosophila melanogaster produces a dicistronic transcript and encodes two distinct polypeptidesAndrews, J.; Smith, M.; Merakovsky, J.; Coulson, M.; Hannan, F.; Kelly, L.
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.
1995Comparative toxicity and virulence of Escherichia coli clones expressing variant and chimeric Shiga-like toxin type II operonsPaton, A.; Bourne, A.; Manning, P.; Paton, J.
1999Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tardaGedeon, A.; Colley, A.; Jamieson, R.; Thompson, E.; Rogers, J.; Sillence, D.; Tiller, G.; Mulley, J.; Gecz, J.
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.
1996A novel X-linked gene, G4.5. is responsible for Barth SyndromeBione, S.; D'Adamo, P.; Maestrini, E.; Gedeon, A.; Bolhuis, P.; Toniolo, D.
1996Identification of the gene FMR2, associated with FRAXE mental retardationGecz, J.; Gedeon, A.; Sutherland, G.; Mulley, J.
1999Genomic organisation and biological characterization of the novel human CC chemokine DC-CK-1/PARC/MIP-4/SCYA18Guan, P.; Burghes, A.; Cunningham, A.; Lira, P.; Brissette, W.; Neote, K.; McColl, S.
2009Aire-Deficient C57BL/6 Mice Mimicking the Common Human 13-Base Pair Deletion Mutation Present with Only a Mild Autoimmune PhenotypeHubert, F.; Kinkel, S.; Crewther, P.; Cannon, P.; Webster, K.; Link, M.; Uibo, R.; O'Bryan, M.; Meager, A.; Forehan, S.; Smyth, G.; Mittaz, L.; Antonarakis, S.; Peterson, P.; Heath, W.; Scott, H.

Discover