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Preview	Issue Date	Title	Author(s)
	1996	The stoned locus of drosophila melanogaster produces a dicistronic transcript and encodes two distinct polypeptides	Andrews, J.; Smith, M.; Merakovsky, J.; Coulson, M.; Hannan, F.; Kelly, L.
	2005	Identification and characterization of avihepadnaviruses isolated from exotic anseriformes maintained in captivity	Guo, H.; Mason, W.; Aldrich, C.; Saputelli, J.; Miller, D.; Jilbert, A.; Newbold, J.
	2008	Antagonism of the chemokine receptors CXCR3 and CXCR4 reduces the pathology of experimental autoimmune encephalomyelitis	Kohler, R.; Comerford, I.; Townley, S.; Haylock-Jacobs, S.; Clark-Lewis, I.; McColl, S.
	2007	Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation	Tarpey, P.; Raymond, F.; Nguyen, L.; Rodriguez, J.; Hackett, A.; Vandeleur, L.; Smith, R.; Shoubridge, C.; Edkins, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Hills, K.; Jones, D.; Mironenko, T.; Perry, J.; et al.
	1999	Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda	Gedeon, A.; Colley, A.; Jamieson, R.; Thompson, E.; Rogers, J.; Sillence, D.; Tiller, G.; Mulley, J.; Gecz, J.
	1999	Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM	Friend, K.; Crimmins, D.; Phan, T.; Sue, C.; Colley, A.; Fung, V.; Morris, J.; Sutherland, G.; Richards, R.
	1999	Isolation and characterisation of zona pellucida A (ZPA) cDNAs from two species of marsupial: regulated oocyte-specific expression of ZPA transcripts	Voyle, R.; Haines, B.; Loffler, K.; Hope, R.; Rathjen, P.; Breed, W.
	1996	Induction of T cell responses to the invariant chain derived peptide CLIP in mice immunized with the group 1 allergen of house dust mite	Kristensen, N.; Hoyne, G.; Hayball, J.; Hetzel, C.; Bourne, T.; Lamb, J.
	2007	DMRT gene cluster analysis in the platypus: New insights into genomic organization and regulatory regions	El-Mogharbel, N.; Wakefield, M.; Deakin, J.; Tsend-Ayush, E.; Grutzner, F.; Alsop, A.; Ezaz, T.; Graves, J.
	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.