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Results 31-40 of 89 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2013Loss of caspase-2 augments lymphomagenesis and enhances genomic instability in Atm-deficient micePuccini, J.; Shalini, S.; Voss, A.; Gatei, M.; Wilson, C.; Hiwase, D.; Lavin, M.; Dorstyn, L.; Kumar, S.
2014The neuroprotective activity of the amyloid precursor protein against traumatic brain injury is mediated via the heparin binding site in residues 96-110Corrigan, F.; Thornton, E.; Roisman, L.; Leonard, A.; Vink, R.; Blumbergs, P.; Van Den Heuvel, C.; Cappai, R.
2015Utilising the resources of the International Knockout Mouse Consortium: the Australian experienceCotton, L.; Meilak, M.; Templeton, T.; Gonzales, J.; Nenci, A.; Cooney, M.; Truman, D.; Rodda, F.; Lynas, A.; Viney, E.; Rosenthal, N.; Bianco, D.; O Bryan, M.; Smyth, I.
2015Snai1 regulates cell lineage allocation and stem cell maintenance in the mouse intestinal epitheliumHorvay, K.; Jardé, T.; Casagranda, F.; Perreau, V.M.; Haigh, K.; Nefzger, C.M.; Akhtar, R.; Gridley, T.; Berx, G.; Haigh, J.J.; Barker, N.; Polo, J.M.; Hime, G.R.; Abud, H.E.
2014SOX3 deletion in mouse and human Is associated with persistence of the craniopharyngeal canalAlatzoglou, K.; Azriyanti, A.; Rogers, N.; Ryan, F.; Curry, N.; Noakes, C.; Bignell, P.; Hall, G.; Littooij, A.; Saunders, D.; Thomas, P.; Stewart, H.; Dattani, M.
2012Relaxin increases human endothelial progenitor cell NO and migration and vasculogenesis in miceSegal, M.S.; Sautina, L.; Li, S.; Diao, Y.; Agoulnik, A.I.; Kielczewski, J.; McGuane, J.T.; Grant, M.B.; Conrad, K.P.
2015Toll-like receptor 4 Is an essential upstream regulator of on-time parturition and perinatal viability in miceWahid, H.; Dorian, C.; Chin, P.; Hutchinson, M.; Rice, K.; Olson, D.; Moldenhauer, L.; Robertson, S.
2012Characterisation of the effect of knockout of the amyloid precursor protein on outcome following mild traumatic brain injuryCorrigan, F.; Vink, R.; Blumbergs, P.; Masters, C.; Cappai, R.; Van Den Heuvel, C.
2010Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genesDimasi, 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.
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.

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