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Preview	Issue Date	Title	Author(s)
	2013	H-NS plays a role in expression of Acinetobacter baumannii virulence features	Eijkelkamp, B.; Stroeher, U.; Hassan, K.; Elbourne, L.; Paulsen, I.; Brown, M.; Payne, S.M.
	2013	Yunis-Varón Syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase	Campeau, P.; Lenk, G.; Lu, J.; Bae, Y.; Burrage, L.; Turnpenny, P.; Corona-Rivera, J.; Morandi, L.; Mora, M.; Reutter, H.; Vulto-van Silfhout, A.; Faivre, L.; Haan, E.; Gibbs, R.; Meisler, M.; Lee, B.
	2010	A proinflammatory role for proteolytically cleaved annexin A1 in neutrophil transendothelial migration	Williams, S.; Milne, I.; Bagley, C.; Gamble, J.; Vadas, M.; Pitson, S.; Khew-Goodall, Y.
	2003	Nova regulates GABA(A) receptor gamma 2 alternative splicing via a distal downstream UCAU-rich intronic splicing enhancer	Dredge, B.; Darnell, R.
	2014	Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease	Newman, M.; Wilson, L.; Verdile, G.; Lim, A.; Khan, I.; Nik, S.; Pursglove, S.; Chapman, G.; Martins, R.; Lardelli, M.
	2014	Overexpression of piRNA pathway genes in epithelial ovarian cancer	Lim, S.; Ricciardelli, C.; Oehler, M.; De Arao Tan, I.; Russell, D.; Grützner, F.; Samant, R.
	2004	Glycogen branching enzyme (GBE1) mutation causing equine glycogen storage disease IV	Ward, T.; Valberg, S.; Adelson, D.; Abbey, C.; Binns, M.; Mickelson, J.
	2001	Peptide insertions in domain 4 of hbc, the shared signalling receptor subunit for GM-CSF, IL3 and IL5, induce ligand-independent activation	Jones, K.; Bagley, C.; Butcher, C.; Barry, S.; Vadas, M.; D'Andrea, R.
	2011	A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia	Corbett, M.; Schwake, M.; Bahlo, M.; Dibbens, L.; Lin, M.; Gandolfo, L.; Vears, D.; O'Sullivan, J.; Robertson, T.; Bayly, M.; Gardner, A.; Vlaar, A.; Korenke, G.; Bloem, B.; de Coo, I.; Verhagen, J.; Lehesjoki, A.; Gecz, J.; Berkovic, 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.