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Results 21-30 of 71 (Search time: 0.005 seconds).
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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.
2015HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.Jolly, L.; Nguyen, L.; Domingo, D.; Sun, Y.; Barry, S.; Hancarova, M.; Plevova, P.; Vlckova, M.; Havlovicova, M.; Kalscheuer, V.; Graziano, C.; Pippucci, T.; Bonora, E.; Sedlacek, Z.; Gecz, J.
2013The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowthJolly, L.; Homan, C.; Jacob, R.; Barry, S.; Gecz, J.
2011Regulation of CRIg Expression and Phagocytosis in Human Macrophages by Arachidonate, Dexamethasone, and CytokinesGorgani, N.; Thathaisong, U.; Mukaro, V.; Poungpair, O.; Tirimacco, A.; Hii, C.; Ferrante, A.
2011Gaucher disease in sheepKarageorgos, L.; Lancaster, M.; Nimmo, J.; Hopwood, J.
2001The water-soluble components of the essential oil of Melaleuca alternifolia (tea tree oil) suppress the production of superoxide by human monocytes, but not neutrophils, activated in vitroBrand, C.; Ferrante, A.; Prager, R.; Riley, T.; Carson, C.; Finlay-Jones, J.; Hart, P.
1999Metabolism of trideuterated iso-lignoceric acid in rats in vivo and in human fibroblasts in culturePoulos, A.; Stockham, P.; Johnson, D.; Paton, B.; Beckman, K.; Singh, H.
2007N-acetylgalactosamine-6-sulfatase protein detection in MPS IVA patient and unaffected control samplesParkinson-Lawrence, E.; Muller, V.; Hopwood, J.; Brooks, D.
1995Inhibitory effects of arachidonic acid (20:4, n-6) and its monohydroxy-and hydrodrymetabolites on procoagulant activity in endothelial cellsBates, E.; Ferrante, A.; Smithers, L.; Poulos, A.; Rathjen, D.; Robinson, B.
2007Somatic FGFR and TWIST mutations are not a common cause of isolated nonsyndromic single suture craniosynostosisAnderson, P.; Cox, T.; Roscioli, T.; Elakis, G.; Smithers, L.; David, D.; Powell, B.

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