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
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
Molecular profiling of relapsing craniopharyngioma
Defining the tumour microenvironment in extramedullary acute leukaemia
Testing the use of mebendazole and albendazole for children with acute myeloid leukaemia, and investigating how the drugs work.
Identification of new drug targets to improve treatment options and reduce treatment-related toxicity for children diagnosed with aggressive B-cell non-Hodgkin lymphoma (B-NHL)
Brain distribution models to select polymer-delivered drugs for the treatment of childhood brain cancers
Circulating molecular biomarkers for earlier identification of high risk Wilms tumour