Understanding the order of genetic changes that lead to Wilms tumour to improve treatment
Ordering of driver mutations in bilateral Wilms’ tumour
We have been funding expert research since 2016, aiming to ensure that every child and young person has a safe and effective treatment for their cancer, and that they can live long and happy lives post-treatment.
Ordering of driver mutations in bilateral Wilms’ tumour
Comprehensive molecular characterization of paediatric spinal ependymomas
Histopathology of lymphomas in children with primary immune deficiency
Molecular profiling of relapsing craniopharyngioma
Defining the tumour microenvironment in extramedullary acute leukaemia
Analysis of genome-wide 5-hydroxymethylcytosine patterns in human hepatoblastoma tumours during chemotherapy treatment
Investigation of ganglioside-specific receptor expression by tumour-infiltrating immune cells
Testing the use of mebendazole and albendazole for children with acute myeloid leukaemia, and investigating how the drugs work.
Circulating molecular biomarkers for earlier identification of high risk Wilms tumour