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Preview	Issue Date	Title	Author(s)
	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.
	2003	Analysis of CFTR mutation screening in cases of isolated fetal echogenic bowel in the South Australian population	Nicholls, C.; Nelson, P.; Poplawski, N.; Chin, S.; Fong, B.; Solly, P.; Fietz, M.; Fletcher, J.
	2001	Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene	Bell, R.; Brice, G.; Child, A.; Murday, V.; Mansour, S.; Sandy, C.; Collin, J.; Brady, A.; Callen, D.; Burnand, K.; Mortimer, P.; Jeffery, S.
	2005	Phosphorylation-dependent translocation of sphingosine kinase to the plasma membrane drives its oncogenic signalling	Pitson, S.; Xia, P.; Leclercq, T.; Moretti, P.; Zebol, J.; Lynn, H.; Wattenberg, B.; Vadas, M.
	2008	NFκB selectivity of estrogen receptor ligands revealed by comparative crystallographic analyses	Nettles, K.; Bruning, J.; Gil, G.; Nowak, J.; Sharma, S.; Hahm, J.; Kulp, K.; Hochberg, R.; Zhou, H.; Katzenellenbogen, J.; Katzenellenbogen, B.; Kim, Y.; Joachimiak, A.; Greene, G.
	2006	De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study	Berkovic, S.; Harkin, L.; McMahon, J.; Pelekanos, J.; Zuberi, S.; Wirrell, E.; Gill, D.; Iona, X.; Mulley, J.; Scheffer, I.
	2009	Thioredoxin reductase is essential for protection of neisseria gonorrhoeae against killing by nitric oxide and for bacterial growth during interaction with cervical epithelial cells	Potter, A.; Kidd, S.; Edwards, J.; Falsetta, M.; Apicella, M.; Jennings, M.; McEwan, A.
	2008	Interference with splicing of Presenilin transcripts has potent dominant negative effects on Presenilin activity	Nornes, S.; Newman, M.; Verdile, G.; Wells, S.; Stoick-Cooper, C.; Tucker, B.; Frederich-Sleptsova, I.; Martins, R.; Lardelli, M.
	2007	A review of genome mutation and Alzheimer's disease	Thomas, P.; Fenech, M.