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PreviewIssue DateTitleAuthor(s)
2021The BMP antagonist Gremlin1 contributes to the development of cortical excitatory neurons, motor balance and fear responsesSuzuki, M.; Suzuki, N.; Wang, T.; Kobayashi, H.; Vrbanac, L.; Ng, J.Q.; Wright, J.A.; Lannagan, T.R.M.; Gieniec, K.A.; Lewis, M.; Ando, R.; Enomoto, A.; Koblar, S.; Thomas, P.; Worthley, D.L.; Woods, S.L.
2002Caspase-2 is not required for thymocyte or neuronal apoptosis even though cleavage of caspase-2 is dependent on both Apaf-1 and caspase-9O'Reilly, L.; Ekert, P.; Harvey, N.; Marsden, V.; Cullen, L.; Vaux, D.; Hacker, G.; Magnusson, C.; Pakusch, M.; Cecconi, F.; Kuida, K.; Strasser, A.; Huang, D.; Kumar, S.
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.
2016Pcdh19 loss-of-function increases neuronal migration in vitro but is dispensable for brain development in micePederick, D.; Homan, C.; Jaehne, E.; Piltz, S.; Haines, B.; Baune, B.; Jolly, L.; Hughes, J.; Gecz, J.; Thomas, P.
2016Mice with Sort1 deficiency display normal cognition but elevated anxiety-like behaviorRuan, C.S.; Yang, C.R.; Li, J.Y.; Luo, H.Y.; Bobrovskaya, L.; Zhou, X.F.
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.
2013Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesisStegeman, S.; Jolly, L.; Premarathne, S.; Gecz, J.; Richards, L.; Mackay-Sim, A.; Wood, S.; Alsina, B.