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Preview	Issue Date	Title	Author(s)
	2010	Genome-wide identification of human FOXP3 target genes in natural regulatory T cells	Sadlon, T.; Wilkinson, B.; Pederson, S.; Brown, C.; Bresatz, S.; Gargett, T.; Melville, E.; Peng, K.; D'Andrea, R.; Glonek, G.; Goodall, G.; Zola, H.; Shannon, F.; Barry, S.
	2010	GM-CSF is an essential regulator of T cell activation competence in uterine dendritic cells during early pregnancy in mice	Moldenhauer, L.; Keenihan, S.; Hayball, J.; Robertson, S.
	2010	Lessons learnt from animal models: pathophysiology of neuropathic lysosomal storage disorders	Hemsley, K.; Hopwood, J.
	2010	Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes	Dimasi, D.; Chen, J.; Hewitt, A.; Klebe, S.; Davey, R.; Stirling, J.; Thompson, E.; Forbes, R.; Tan, T.; Savarirayan, R.; Mackey, D.; Healey, P.; Mitchell, P.; Burdon, K.; Craig, J.
	2010	Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly	Giannandrea, M.; Bianchi, V.; Mignogna, M.; Sirri, A.; Carrabino, S.; D'Elia, E.; Vecellio, M.; Russo, S.; Cogliati, F.; Larizza, L.; Ropers, H.; Tzschach, A.; Kalscheuer, V.; Oehl-Jaschkowitz, B.; Skinner, C.; Schwartz, C.; Gecz, J.; Van Esch, H.; Raynaud, M.; Chelly, J.; et al.
	2010	High-spatial resolution matrix-assisted laser desorption ionization imaging analysis of glucosylceramide in spleen sections from a mouse model of Gaucher Disease	Snel, M.; Fuller, M.
	2010	Robust, reversible gene knockdown using a single lentiviral short hairpin RNA vector	Brown, C.; Sadlon, T.; Gargett, T.; Melville, E.; Zhang, R.; Drabsch, Y.; Ling, M.; Strathdee, C.; Gonda, T.; Barry, S.
	2010	Trans-generational exposure to low levels of rhodamine B does not adversely affect litter size or liver function in murine mucopolysaccharidosis type IIIA	Derrick Roberts, A.; Fletcher, J.; Moore, L.; Byers, S.
	2010	Alterations in mouse embryo intracellular pH by DMO during culture impair implantation and fetal growth	Zander, D.; Mitchell, M.; Thompson, J.; Lane, M.
	2010	Disruption at the PTCHD1 locus on Xp22.11 in Autism Spectrum Disorder and intellectual disability	Gecz, J.