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PreviewIssue DateTitleAuthor(s)
2013A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndromeBuchovecky, C.; Turley, S.; Brown, H.; Kyle, S.; McDonald, J.; Liu, B.; Pieper, A.; Huang, W.; Katz, D.; Russell, D.; Shendure, J.; Justice, M.
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.
2009Interaction of dietary zinc and intracellular binding protein metallothionein in postnatal bone growthFong, L.; Tan, K.; Tran, C.; Cool, J.; Scherer, M.; Elovaris, R.; Coyle, P.; Foster, B.; Rofe, A.; Xian, C.
2008A mouse model of human mucopolysaccharidosis IX exhibits osteoarthritisMartin, D.; Atmuri, V.; Hemming, R.; Farley, J.; Mort, J.; Byers, S.; Hombach-Klonisch, S.; Stern, R.; Triggs-Raine, B.
2014Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growthHoman, C.; Kumar, R.; Nguyen, L.; Haan, E.; Raymond, F.; Abidi, F.; Raynaud, M.; Schwartz, C.; Wood, S.; Gecz, J.; Jolly, L.
2017Viperin is an important host restriction factor in control of Zika virus infectionVan Der Hoek, K.; Eyre, N.; Shue, B.; Khantisitthiporn, O.; Glab-Ampi, K.; Carr, J.; Gartner, M.; Jolly, L.; Thomas, P.; Adikusuma, F.; Jankovic-Karasoulos, T.; Roberts, C.; Helbig, K.; Beard, M.
2017Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesisHinze, S.; Jackson, M.; Lie, S.; Jolly, L.; Field, M.; Barry, S.; Harvey, R.; Shoubridge, C.

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