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Preview	Issue Date	Title	Author(s)
	2013	Mutations in DEPDC5 cause familial focal epilepsy with variable foci	Dibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.
	2010	Comparative assessment of the osteoconductive properties of different biomaterials in vivo seeded with human or ovine mesenchymal stem/stromal cells	Zannettino, A.; Paton, S.; Itescu, S.; Gronthos, S.
	2012	Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature	Kazenwadel, J.; Secker, G.; Liu, Y.; Rosenfeld, J.; Wildin, R.; Cuellar-Rodriguez, J.; Hsu, A.; Dyack, S.; Fernandez, C.; Chong, C.; Babic, M.; Bardy, P.; Shimamura, A.; Zhang, M.; Walsh, T.; Holland, S.; Hickstein, D.; Horwitz, M.; Hahn, C.; Scott, H.; et al.
	2012	Sphingosine-1-phosphate facilitates trafficking of hematopoietic stem cells and their mobilization by CXCR4 antagonists in mice	Juarez, J.; Harun, N.; Thien, M.; Welschinger, R.; Baraz, R.; Dela Pena, A.; Pitson, S.; Rettig, M.; DiPersio, J.; Bradstock, K.; Bendall, L.
	2010	Genetic dissection of differential signaling threshold requirements for the Wnt/β-Catenin pathway in vivo	Buchert, M.; Athineos, D.; Abud, H.; Burke, Z.; Faux, M.; Samuel, M.; Jarnicki, A.; Winbanks, C.; Newton, I.; Meniel, V.; Suzuki, H.; Stacker, S.; Nathke, I.; Tosh, D.; Huelsken, J.; Clarke, A.; Heath, J.; Sansom, O.; Ernst, M.; Nusse, R.
	2011	DNMT3L is a regulator of X chromosome compaction and post-meiotic gene transcription	Zamudio, N.; Scott, H.; Wolski, K.; Lo, C.; Law, C.; Leong, D.; Kinkel, S.; Chong, S.; Jolley, D.; Smyth, G.; De Kretser, D.; Whitelaw, E.; O'Bryan, M.; Pera, M.
	2011	Successful in vitro culture of pre-antral follicles derived from vitrified murine ovarian tissue: oocyte maturation, fertilization, and live births	Wang, X.; Catt, S.; Pangesto, M.; Temple-Smith, P.
	2016	Pcdh19 loss-of-function increases neuronal migration in vitro but is dispensable for brain development in mice	Pederick, D.; Homan, C.; Jaehne, E.; Piltz, S.; Haines, B.; Baune, B.; Jolly, L.; Hughes, J.; Gecz, J.; Thomas, P.
	2010	Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down Syndrome	Hewitt, C.; Ling, K.; Merson, T.; Simpson, K.; Ritchie, M.; King, S.; Pritchard, M.; Smyth, G.; Thomas, T.; Scott, H.; Voss, A.; Aziz, S.A.