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Preview	Issue Date	Title	Author(s)
	2004	Short-term synchronization between motor units in different functional subdivisions of the human flexor digitorum profundus muscle	Reilly, K.; Nordstrom, M.; Schieber, M.
	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.
	1997	High resolution characterisation of an interstitial deletion of less than 1.9Mb at 4p16.3 associated with Wolf-Hirschhorn Syndrome	Fang, Y.; Bain, S.; Haan, E.; Eyre, H.; MacDonald, M.; Wright, T.; Altherr, M.; Riess, O.; Sutherland, G.; Callen, D.
	1998	Induction of Acute Inflammation in vivo by Staphylococcal Superantigens II. Critical Role for Chemokines ICAM-i and TNF-alpha	Tessier, P.; Naccache, P.; Diener, K.; Gladue, R.; Neote, K.; Clark-Lewis, I.; McColl, S.
	1996	Gene localisation for Wilson-Turner syndrome (WTS:MIM 309585)	Gedeon, A.; Turner, G.; Mulley, J.
	1995	Plasma adrenaline responses to long-term modification of blood pressure in normotensive and hypertensive rats	Jablonskis, L.; Howe, P.
	1999	Inhibition of murine neutrophil recruitment in vivo by CXC chemokine receptor antagonists	McColl, S.; Clark-Lewis, I.
	2007	Late-onset post-traumatic Phaeoacremonium parasiticum endophthalmitis	Huynh, T.; Lee, L.; Ellis, D.
	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.
	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.