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Dissecting the causative and collaborating roles of candidate genetic mutations in the pathogenesis of childhood ALL
Developing zebrafish models of inherited AML to interrogate secondary driver events
Role of aldehyde metabolism and DNA crosslink repair in in-utero genome stability and leukaemogenesis
Sequencing the unsequenceable: development of ground-breaking technologies to investigate the role of complex genomic sequences in childhood cancer
Characterising abnormal signalling pathway activation by PTPN11 mutations in Noonan syndrome and juvenile myelomonocytic leukaemia
Identification of infections which may play a role in the aetiology of childhood acute lymphoblastic leukaemia (ALL)