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  1. A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy

    Jadeja, S., Mort, R. L., Keighren, M., Hart, A. W., Joynson, R., Wells, S., Potter, P. K. & Jackson, I. J., 1/05/2013, In : Investigative Ophthalmology and Visual Science. 54, 5, p. 3569-3578 10 p.

    Research output: Contribution to journalJournal article

  2. Common variation in the WNK1 gene and blood pressure in childhood: the Avon Longitudinal Study of Parents and Children

    Tobin, M. D., Timpson, N. J., Wain, L. V., Ring, S., Jones, L. R., Emmett, P. M., Palmer, T. M., Ness, A. R., Samani, N. J., Smith, G. D. & Burton, P. R., 11/2008, In : Hypertension. 52, 5, p. 974-979 6 p.

    Research output: Contribution to journalJournal article

  3. A captured viral interleukin 10 gene with cellular exon structure

    Jayawardane, G., Russell, G. C., Thomson, J., Deane, D., Cox, H., Gatherer, D., Ackermann, M., Haig, D. M. & Stewart, J. P., 10/2008, In : Journal of General Virology. 89, 10, p. 2447-2455 9 p.

    Research output: Contribution to journalJournal article

  4. Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD

    Mill, J., Richards, S., Knight, J., Curran, S., Taylor, E. & Asherson, P., 08/2004, In : Molecular Psychiatry. 9, 8, p. 801-810 10 p.

    Research output: Contribution to journalJournal article

  5. Nonsense-mediated mRNA decay in Drosophila: at the intersection of the yeast and mammalian pathways

    Gatfield, D., Unterholzner, L., Ciccarelli, F. D., Bork, P. & Izaurralde, E., 1/08/2003, In : EMBO Journal. 22, 15, p. 3960-3970 11 p.

    Research output: Contribution to journalJournal article