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PreviewIssue DateTitleAuthor(s)
2016X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesHu, H.; Haas, S.; Chelly, J.; Van Esch, H.; Raynaud, M.; De Brouwer, A.; Weinert, S.; Froyen, G.; Frints, S.; Laumonnier, F.; Zemojtel, T.; Love, M.; Richard, H.; Emde, A.; Bienek, M.; Jensen, C.; Hambrock, M.; Fischer, U.; Langnick, C.; Feldkamp, M.; et al.
2016The Nedd4-2/Ndfip1 axis is a negative regulator of IgE-mediated mast cell activationYip, K.; Kolesnikoff, N.; Hauschild, N.; Biggs, L.; Lopez, A.; Galli, S.; Kumar, S.; Grimbaldeston, M.
2016Small glutamine-rich tetratricopeptide repeat-containing protein alpha (SGTA) ablation limits offspring viability and growth in micePhilp, L.; Day, T.; Butler, M.; Laven-Law, G.; Jindal, S.; Hickey, T.; Scher, H.; Butler, L.; Tilley, W.
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.
2016Ablation of type-1 IFN signaling in hematopoietic cells confers protection following traumatic brain injuryKarve, I.P.; Zhang, M.; Habgood, M.; Frugier, T.; Brody, K.M.; Sashindranath, M.; Joakim Ek, C.; Chappaz, S.; Kile, B.T.; Wright, D.; Wang, H.; Johnston, L.; Daglas, M.; Ates, R.C.; Medcalf, R.L.; Taylor, J.M.; Crack, P.J.

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