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PreviewIssue DateTitleAuthor(s)
2017Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signallingHughes, J.; Dawson, R.; Tea, M.; McAninch, D.; Piltz, S.; Jackson, D.; Stewart, L.; Ricos, M.; Dibbens, L.; Harvey, N.; Thomas, P.
2010Genome-wide identification of human FOXP3 target genes in natural regulatory T cellsSadlon, 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.
2013A regulatory path associated with X-linked intellectual disability and epilepsy links KDM5C to the polyalanine expansions in ARXPoeta, L.; Fusco, F.; Drongitis, D.; Shoubridge, C.; Manganelli, G.; Filosa, S.; Paciolla, M.; Courtney, M.; Collombat, P.; Lioi, M.; Gecz, J.; Ursini, M.; Miano, M.
2012Adipokines and adipocyte function in clock mutant mice that retain melatonin rhythmicityKennaway, D.; Owens, J.; Voultsios, A.; Wight, N.
2013The influence of Flightless I on toll-like-receptor-mediated inflammation in a murine model of diabetic wound healingRuzehaji, N.; Mills, S.; Melville, E.; Arkell, R.; Fitridge, R.; Cowin, A.
2013Global loss of Bmal1 expression alters adipose tissue hormones, gene expression and glucose metabolismKennaway, D.; Varcoe, T.; Voultsios, A.; Boden, M.; Makishima, M.
2014Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout miceSen, P.; Dharmadhikari, A.; Majewski, T.; Mohammad, M.; Kalin, T.; Zabielska, J.; Ren, X.; Bray, M.; Brown, H.; Welty, S.; Thevananther, S.; Langston, C.; Szafranski, P.; Justice, M.; Kalinichenko, V.; Gambin, A.; Belmont, J.; Stankiewicz, P.; Koval, M.

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