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Preview	Issue Date	Title	Author(s)
	2002	Regulation of pacemaker frequency in the murine gastric antrum	Kim, T.; Spencer, E.; Hanna, R.; Koh, S.; Ordog, T.; Ward, S.; Sanders, K.
	2002	Epitope analysis of the FanC subunit protein of the K99 (F5) fimbriae of enterotoxigenic Escherichia coli using a recombinant fusion technique	Ogunniyi, A.; Kotlarski, I.; Morona, R.; Manning, P.
	2002	Structural organization and evolution of the marsupial zona pellucida	Breed, W.; Hope, R.; Wiebkin, O.; Spargo, S.; Chapman, J.
	2002	A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype	Cundy, T.; Hegde, M.; Naot, D.; Chong, B.; King, A.; Wallace, R.; Mulley, J.; Love, D.; Seidel, J.; Fawkner, M.; Banovic, T.; Callon, K.; Grey, A.; Reid, I.; Middleton-Hardie, C.; Cornish, J.
	2002	Sodium-channel defects in benign familial neonatal-infantile seizures	Heron, S.; Crossland, K.; Andermann, E.; Phillips, H.; Hall, A.; Bleasel, A.; Shevell, M.; Mercho, S.; Seni, M.; Guiot, M.; Mulley, J.; Berkovic, S.; Scheffer, I.
	2002	Continuous positive airway pressure treatment improves pulmonary hemodynamics in patients with obstructive sleep apnea	Sajkov, D.; Wang, T.; Saunders, N.; Bune, A.; McEvoy, R.
	2002	Mast cells, neuropeptides, histamine, and prostaglandins in UV-induced systemic immunosuppression	Hart, P.; Townley, S.; Grimbaldeston, M.; Kahlil, Z.; Finlay-Jones, J.
	2002	Truncation of the GABAA-receptor γ2 subunit in a family with generalized epilepsy with febrile seizures plus	Harkin, L.; Bowser, D.; Dibbens, L.; Singh, R.; Phillips, F.; Wallace, R.; Richards, M.; Williams, D.; Mulley, J.; Berkovic, S.; Scheffer, I.; Petrou, S.
	2002	Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome	Lower, 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.
	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.