Publications by authors named "K A Fennell"

Understanding the molecular pathogenesis of MLL fusion oncoprotein (MLL-FP) leukaemia has spawned epigenetic therapies that have improved clinical outcomes in this often-incurable disease. Using genetic and pharmacological approaches, we define the individual and combined contribution of KAT6A, KAT6B and KAT7, in MLL-FP leukaemia. Whilst inhibition of KAT6A/B is efficacious in some pre-clinical models, simultaneous targeting of KAT7, with the novel inhibitor PF-9363, increases the therapeutic efficacy.

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As SARS-CoV-2 evolves, increasing in potential for greater transmissibility and immune escape, updated vaccines are needed to boost adaptive immunity to protect against COVID-19 caused by circulating strains. Here, we report features of the monovalent Omicron XBB.1.

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Article Synopsis
  • Cell therapies using mesenchymal stromal cells (MSCs), particularly human adipose-derived stromal cells (hASCs), are gaining attention as potential treatments for peripheral arterial disease (PAD) and critical limb ischemia (CLI), focusing on their ability to promote blood vessel growth.
  • This study examined the effects of different natural polysaccharide hydrogels, specifically methacrylated glycol chitosan (MGC) and methacrylated hyaluronic acid (MHA), on the survival and pro-angiogenic functions of hASCs when encapsulated within them.
  • Results showed that while hASCs maintained high viability in both hydrogels, those in MGC hydrogels secreted more pro-
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It has been proposed that adult hematopoiesis is sustained by multipotent progenitors (MPPs) specified during embryogenesis. Adult-like hematopoietic stem cell (HSC) and MPP immunophenotypes are present in the fetus, but knowledge of their functional capacity is incomplete. We found that fetal MPP populations were functionally similar to adult cells, albeit with some differences in lymphoid output.

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Cellular barcoding is a lineage-tracing methodology that couples heritable synthetic barcodes to high-throughput sequencing, enabling the accurate tracing of cell lineages across a range of biological contexts. Recent studies have extended these methods by incorporating lineage information into single-cell or spatial transcriptomics readouts. Leveraging the rich biological information within these datasets requires dedicated computational tools for dataset pre-processing and analysis.

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