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Preview	Issue Date	Title	Author(s)
	2008	Conservation of small RNA pathways in platypus	Murchison, E.; Kheradpour, P.; Sachidanandam, R.; Smith, C.; Hodges, E.; Xuan, Z.; Kellis, M.; Grutzner, F.; Stark, A.; Hannon, G.
	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.
	1998	Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24	Phillips, H.; Scheffer, I.; Crossland, K.; Bhatia, K.; Fish, D.; Marsden, C.; Howell, S.; Stephenson, J.; Tolmie, J.; Plazzi, G.; Eeg-Olofsson, O.; Singh, R.; Lopes-Cendes, I.; Andermann, E.; Berkovic, S.; Mulley, J.
	2007	Kit signaling is essential for development and maintenance of interstitial cells of Cajal and electrical rhythmicity in the embryonic gastrointestinal tract	Spencer, E.; Ro, S.; Bayguinov, Y.; Sanders, K.; Ward, S.
	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.
	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.
	1995	Comparative toxicity and virulence of Escherichia coli clones expressing variant and chimeric Shiga-like toxin type II operons	Paton, A.; Bourne, A.; Manning, P.; Paton, J.
	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.
	1998	Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1B	Wallace, R.; Wang, D.; Singh, R.; Scheffer, I.; George Jnr., A.; Phillips, H.; Saar, K.; Reis, A.; Johnson, E.; Sutherland, G.; Berkovic, S.; Mulley, J.
	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.