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Preview	Issue Date	Title	Author(s)
	2010	Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination	Pearlman, A.; Loke, J.; Le Caignec, C.; White, S.; Chin, L.; Friedman, A.; Warr, N.; Willan, J.; Brauer, D.; Farmer, C.; Brooks, E.; Oddoux, C.; Riley, B.; Shajahan, S.; Camerino, G.; Homfray, T.; Crosby, A.; Couper, J.; David, A.; Greenfield, A.; et al.
	2012	Methotrexate chemotherapy promotes osteoclast formation in the long bone of rats via increased pro-inflammatory cytokines and enhanced NF-κB activation	King, T.; Georgiou, K.; Cool, J.; Scherer, M.; Ang, E.; Foster, B.; Xu, J.; Xian, C.
	2010	Iminochromene inhibitors of dynamins I and II GTPase activity and endocytosis	Hill, T.; Mariana, A.; Gordon, C.; Odell, L.; Robertson, M.; McGeachie, A.; Chau, N.; Daniel, J.; Gorgani, N.; Robinson, P.; McCluskey, A.
	2012	Neonatal gene therapy with a gamma retroviral vector in mucopolysaccharidosis VI cats	Ponder, K.; O'Malley, T.; Wang, P.; O'Donnell, P.; Traas, A.; Knox, V.; Aguirre, G.; Ellinwood, N.; Metcalf, J.; Wang, B.; Parkinson-Lawrence, E.; Sleeper, M.; Brooks, D.; Hopwood, J.; Haskins, M.
	2011	Clinical effects and treatment of envenoming by Hoplocephalus spp. snakes in Australia: Australian Snakebite Project (ASP-12)	Isbister, G.; White, J.; Currie, B.; O'Leary, M.; Brown, S.
	2010	Disruption at the PTCHD1 locus on Xp22.11 in Autism Spectrum Disorder and intellectual disability	Gecz, J.
	2010	Determinants of the induction of cortical plasticity by non-invasive brain stimulation in healthy subjects	Ridding, M.; Ziemann, U.
	2013	Expression of an anti-CD4 single-chain antibody fragment from the donor cornea can prolong corneal allograft survival in inbred rats	Appleby, S.; Jessup, C.; Mortimer, L.; Kirk, K.; Brereton, H.; Coster, D.; Tan, C.; Williams, K.
	2010	Placental restriction increases adipose leptin gene expression and plasma leptin and alters their relationship to feeding activity in the young lamb	De Blasio, M.; Blache, D.; Gatford, K.; Robinson, J.; Owens, J.
	2014	Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth	Homan, C.; Kumar, R.; Nguyen, L.; Haan, E.; Raymond, F.; Abidi, F.; Raynaud, M.; Schwartz, C.; Wood, S.; Gecz, J.; Jolly, L.