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PreviewIssue DateTitleAuthor(s)
2009Aire-Deficient C57BL/6 Mice Mimicking the Common Human 13-Base Pair Deletion Mutation Present with Only a Mild Autoimmune PhenotypeHubert, 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.
2014Functional transcriptome analysis of the postnatal brain of the Ts1Cje mouse model for Down syndrome reveals global disruption of interferon-related molecular networksLing, 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.
2010Estimating the proportion of microarray probes expressed in an RNA sampleShi, W.; de Graaf, C.; Kinkel, S.; Achtman, A.; Baldwin, T.; Schofield, L.; Scott, H.; Hilton, D.; Smyth, G.
2008Integrative analysis of RUNX1 downstream pathways and target genesMichaud, J.; Simpson, K.; Escher, R.; Buchet-Poyau, K.; Beissbarth, T.; Carmichael, C.; Ritchie, M.; Schutz, F.; Cannon, P.; Liu, M.; Shen, X.; Ito, Y.; Raskind, W.; Horwitz, M.; Osato, M.; Turner, D.; Speed, T.; Kavallaris, M.; Smyth, G.; Scott, H.
2009Molecular networks involved in mouse cerebral corticogenesis and spatio-temporal regulation of Sox4 and Sox11 novel antisense transcripts revealed by transcriptome profilingLing, K.; Hewitt, C.; Beissbarth, T.; Hyde, L.; Ghosal, K.; Cheah, P.; Cannon, P.; Hahn, C.; Thomas, P.; Smyth, G.; Tan, S.; Thomas, T.; Scott, H.
2011Aire regulates the transfer of antigen from mTECs to dendritic cells for induction of thymic toleranceHubert, F.; Kinkel, S.; Davey, G.; Phipson, B.; Mueller, S.; Liston, A.; Proietto, A.; Cannon, P.; Forehan, S.; Smyth, G.; Wu, L.; Goodnow, C.; Carbone, F.; Scott, H.; Heath, W.
2011DNMT3L is a regulator of X chromosome compaction and post-meiotic gene transcriptionZamudio, 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.
2010Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down SyndromeHewitt, C.; Ling, K.; Merson, T.; Simpson, K.; Ritchie, M.; King, S.; Pritchard, M.; Smyth, G.; Thomas, T.; Scott, H.; Voss, A.; Aziz, S.A.