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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	Imaging blood vessels in the zebrafish	Kamei, M.; Isogai, S.; Pan, W.; Weinstein, B.M.; Detrich, H.W.; Westerfield, M.; Zon, L.I.
	2010	Augmented currents of an HCN2 variant in patients with febrile seizure syndromes	Dibbens, L.; Reid, C.; Hodgson, B.; Thomas, E.; Phillips, A.; Gazina, E.; Cromer, B.; Clarke, A.; Barram, T.; Scheffer, I.; Berkovic, S.; Petrou, S.
	2010	In vitro and in vivo characterization of putative porcine embryonic stem cells	Vassiliev, I.; Vassilieva, S.; Beebe, L.; Harrison, S.; McIlfatrick, S.; Nottle, M.
	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	Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome	Gecz, J.
	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.