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biomedical sciences research institute - Research - University of Ulster

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Publications:Lees-Murdock DJ, Lau HT, Castrillon DH, De Felici M, Walsh CP; DNA methyltransferase loading, but not de novomethylation, is an oocyte-autonomous process stimulated by SCF signaling; Developmental Biology, 321: 238-250, 2008Related ArticlesLees-Murdock DJ, Walsh CP; DNA methylation reprogramming in the germ line; Epigenetics, 3: 5-13, 2008 [Review]Presentations at conferences:Speaker, Joint UK/German Epigenetics meeting, Überherrn, Germany 2007Speaker, UK Stem Cell Network regional meeting, Antrim, 2007Speaker, XIV International Workshop on the Development and Function <strong>of</strong> the Reproductive Organs, Frascati,Italy, 2008Speaker, Cancer RRG Annual Meeting, Antrim, Northern Ireland, 2008Dr Robin W FreeburnLecturer in Haematology and ImmunologyContact details:+44 (0)28 70324606 rw.freeburn@ulster.ac.ukMain <strong>research</strong> interests:The main area <strong>of</strong> investigation in the lab is the role <strong>of</strong> Wnt proteins in lymphocytic leukaemia. Two projects are currentlylooking at chronic lymphocytic leukaemia (CLL) and acute lymphoblastic leukaemia (ALL) to identify abnormalitiesand signalling defects in the Wnt pathways that may contribute towards these leukaemias. In collaboration withBelfast City Hospital, a mix <strong>of</strong> molecular analysis, protein pathway analysis and cell based assays are used to investigateleukaemic cell lines and patient samples. Another area <strong>of</strong> interest is the regulation <strong>of</strong> intracellular signalling pathwaysin T cells, in particular the role played by inositol phosphatases in negatively regulating pathways activated by theCD28 and CD3 receptors.Immunobiology and fluorescent imaging techniques are being used to investigate the activation and control <strong>of</strong>signalling pathways such as PKB, DOK and Map kinases. Specific projects are looking at pathways downstream <strong>of</strong> PI3kinases and the role <strong>of</strong> the inositol phosphatases, SHIP and PTEN, in this regulation. PTEN is a commonly mutatedtumour suppressor gene and its role <strong>of</strong> in the leukaemogenesis <strong>of</strong> lymphocytic malignancies is another area <strong>of</strong> active<strong>research</strong>. This includes investigation into the role <strong>of</strong> genetic mutation, especially single nucleotide polymorphisms,in the pathogenesis <strong>of</strong> lymphocytic leukaemias. The expression <strong>of</strong> SHIP is<strong>of</strong>orms has been shown to change with94

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