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Preview	Issue Date	Title	Author(s)
	2016	High-density lipoproteins rescue diabetes-impaired angiogenesis via scavenger receptor Class B Type I	Tan, J.; Prosser, H.; Dunn, L.; Vanags, L.; Ridiandries, A.; Tsatralis, T.; Leece, L.; Clayton, Z.; Yuen, S.; Robertson, S.; Ting Lam, Y.; Celermajer, D.; Ng, M.; Bursill, C.
	2006	Wound healing is defective in mice lacking tetraspanin CD151	Cowin, A.; Adams, D.; Geary, S.; Wright, M.; Jones, J.; Ashman, L.
	2009	The ion channel TRPA1 is required for normal mechanosensation and is modulated by algesic stimuli	Brierley, S.; Hughes, P.; Page, A.; Kwan, K.; Martin, C.; O'Donnell, T.; Isaacs, N.; Harrington, A.; Adam, B.; Liebregts, T.; Holtmann, G.; Corey, D.; Rychkov, G.; Blackshaw, L.
	1997	Assignment of the Y-4 Receptor Gene (PPYR1) to Human Chromosome 10q11.2 and Mouse Chromosome 14	Darby, K.; Eyre, H.; Lapsys, N.; Copeland, N.; Gilbert, D.; Couzens, M.; Antonova, O.; Sutherland, G.; Jenkins, N.; Herzog, H.
	1997	Structural organization of the mouse and human GALR1 Galanin receptor genes (Galnr and GALNR) and chromosomal localization of the mouse gene	Jacoby, A.; Webb, G.; Liu, M.; Kofler, B.; Hort, Y.; Fathi, Z.; Bottema, C.; Shine, J.; Iismaa, T.
	2019	Purinergic receptor mediated calcium signalling in urothelial cells	Chess-Williams, R.; Sellers, D.J.; Brierley, S.M.; Grundy, D.; Grundy, L.
	2016	Ablation of type-1 IFN signaling in hematopoietic cells confers protection following traumatic brain injury	Karve, I.P.; Zhang, M.; Habgood, M.; Frugier, T.; Brody, K.M.; Sashindranath, M.; Joakim Ek, C.; Chappaz, S.; Kile, B.T.; Wright, D.; Wang, H.; Johnston, L.; Daglas, M.; Ates, R.C.; Medcalf, R.L.; Taylor, J.M.; Crack, P.J.
	2009	Aire-Deficient C57BL/6 Mice Mimicking the Common Human 13-Base Pair Deletion Mutation Present with Only a Mild Autoimmune Phenotype	Hubert, 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.
	2010	Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down Syndrome	Hewitt, C.; Ling, K.; Merson, T.; Simpson, K.; Ritchie, M.; King, S.; Pritchard, M.; Smyth, G.; Thomas, T.; Scott, H.; Voss, A.; Aziz, S.A.