What makes ependymoma in infants different?
Looking at molecular makeup and MRIs to characterise infant ependymoma.
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.
Looking at molecular makeup and MRIs to characterise infant ependymoma.
Understanding how proteins act inside acute myeloid leukaemia cells, to find new drug targets.
Looking at the genetics of bone marrow samples to see which genes affect resistance to treatment.
Finding which regulatory regions of the genome are causing leukaemia by acting on the wrong gene
Glo-BNHL trial is an international trial that will recruit children across the globe with relapse BNHL and assign them to the trial to receive a novel therapy. We are requesting funds to conduct biological studies alongside the trial to improve our understanding of this cancer.
Single-cell transcriptomics linked to lineage tracing to interrogate the role of intra-tumour heterogeneity in shaping therapeutic susceptibility and resistance in paediatric cancer
Deciphering the genomic landscape of childhood refractory t-cell acute lymphoblastic leukaemia
Towards chemotherapy-free treatment of paediatric post-transplant lymphoproliferative disorders
Identifying drivers of central nervous system involvement in T-cell acute lymphoblastic leukaemia