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Preview	Issue Date	Title	Author(s)
	2005	Primary defect in UVB-induced systemic immunomodulation does not relate to immature or functionally impaired APCs in regional lymph nodes	Gorman, S.; Tan, J.; Thomas, J.; Townley, S.; Stumbles, P.; Finlay-Jones, J.; Hart, P.
	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.
	2004	Inhibition of generation of cytotoxic T lymphocyte activity by a CCL19/macrophage inflammatory protein (MIP)-3beta antagonist	Pilkington, K.; Clark-Lewis, I.; McColl, S.
	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.
	2009	Inhibition of CCR6 Function Reduces the Severity of Experimental Autoimmune Encephalomyelitis via Effects on the Priming Phase of the Immune Response	Liston, A.; Kohler, R.; Townley, S.; Haylock-Jacobs, S.; Comerford, I.; Caon, A.; Webster, J.; Harrison, J.; Swann, J.; Clark-Lewis, I.; Korner, H.; McColl, S.
	2010	A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24	Bahlo, M.; Jolly, L.; Afawi, Z.; Gardner, A.; Oliver, K.; Tan, S.; Coffey, A.; Mulley, J.; Dibbens, L.; Simri, W.; Shalata, A.; Kivity, S.; Jackson, G.; Berkovic, S.; Gecz, J.; Corbett, M.
	2007	A pneumococcal MerR-like regulator and S-nitrosoglutathione reductase are required for systemic virulence	Stroeher, U.; Kidd, S.; Stafford, S.; Jennings, M.; Paton, J.; McEwan, A.
	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.
	2006	Production and characterization of monoclonal antibodies against insulin-like growth factor type 1 receptor	Keyhanfar, M.; Forbes, B.; Cosgrove, L.; Wallace, J.; Booker, G.
	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.