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Preview	Issue Date	Title	Author(s)
	2009	Aire-Deficient C57BL/6 Mice Mimicking the Common Human 13-Base Pair Deletion Mutation Present with Only a Mild Autoimmune Phenotype	Hubert, F.; Kinkel, S.; Crewther, P.; Cannon, P.; Webster, K.; Link, M.; Uibo, R.; O'Bryan, M.; Meager, A.; Forehan, S.; Smyth, G.; Mittaz, L.; Antonarakis, S.; Peterson, P.; Heath, W.; Scott, H.
	2014	Functional transcriptome analysis of the postnatal brain of the Ts1Cje mouse model for Down syndrome reveals global disruption of interferon-related molecular networks	Ling, K.; Hewitt, C.; Tan, K.; Cheah, P.; Vidyadaran, S.; Lai, M.; Lee, H.; Simpson, K.; Hyde, L.; Pritchard, M.; Smyth, G.; Thomas, T.; Scott, H.
	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.
	2010	Short-term inhibition of p53 combined with keratinocyte growth factor improves thymic epithelial cell recovery and enhances T-cell reconstitution after murine bone marrow transplantation	Kelly, R.; Goren, E.; Taylor, P.; Mueller, S.; Stefanski, H.; Osborn, M.; Scott, H.; Komarova, E.; Gudkov, A.; Hollander, G.; Blazar, B.
	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.
	2006	Nedd4-WW domain-binding protein 5 (Ndfip1) is associated with neuronal survival after acute cortical brain injury	Sang, Q.; Kim, M.; Kumar, S.; Bye, N.; Morganti-Kossmann, M.; Gunnersen, J.; Fuller, S.; Howitt, J.; Hyde, L.; Beissbarth, T.; Scott, H.; Silke, J.; Tan, S.
	2018	Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes	Chong, C.-E.; Venugopal, P.; Stokes, P.; Lee, Y.; Brautigan, P.; Yeung, D.; Babic, M.; Engler, G.; Lane, S.; Klingler-Hoffmann, M.; Matthews, J.; D'Andrea, R.; Brown, A.; Hahn, C.; Scott, H.