About this Research Topic
The objective of this research topic is to bring together the scientific community to extend the current level of knowledge in the MDS field with manuscripts encompassing recent advances concerning relevant models (xenografts and genetically engineered) and the utility of single cell sequencing to better understand the disease heterogeneity in MDS. We will learn lessons from precursor states as well as from the pediatric clinics for those with germline MDS. Lastly, we will review current efficacy of novel therapeutics and promising combination approaches to further improve outcomes in the treatment of patients with MDS. We welcome the submission of Original Research, Review and Clinical Trial articles.
Keywords: myelodysplastic syndromes, MDS, mouse model, single cell sequencing, HSCT, clonal hematopoiesis
Important Note: All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.