This project has a Band 2 fee. Details of our different fee bands can be found on our website (View Website). For information on how to apply for this project, please visit the Faculty of Biology, Medicine and Health Doctoral Academy website (View Website).
Informal enquiries may be made directly to the primary supervisor.
Jenkinson, EM, et. al., O’Keefe, R.T., Crow, YJ (2016) Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts. Nature Genetics. 48(10):1185-1192
de Almeida RA, Fraczek MG, Parker S, Delneri D, O'Keefe RT. (2016) Non-coding RNAs and disease: classical ncRNAs make a comeback. Biochem Soc Trans. 44(4):1073-8
Wieczorek et al. (2014) Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome. American Journal of Human Genetics. 95(6):698-707
Hogg, R., de Almeida, RA., Ruckshanthi, J.P.D., and O’Keefe, R.T. (2014). Remodelling of U2-U6 snRNA helix I during pre-mRNA splicing by Prp16 and the nineteen complex protein Cwc2. Nucleic Acids Research. Nucleic Acids Research. 42:8008-23