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Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Projecting individualized probabilities of lifetime all-cancer riskNeel M Butala, Noor Al-Hammadi, Asiri Ediriwickrema, et al.Blood Advances|March 10, 2020
Single-cell mutational profiling enhances the clinical evaluation of AML MRDAsiri Ediriwickrema, Alexey Aleshin, Johannes G Reiter, et al.Leukemia & Lymphoma|June 17, 2020
Venetoclax and hypomethylating agent therapy in high risk myelodysplastic syndromes: a retrospective evaluation of a real-world experienceArmon Azizi, Asiri Ediriwickrema, Ritika Dutta, et al.Leukemia & Lymphoma|September 9, 2021
Clinico-genomic profiling and clonal dynamic modeling of TP53-aberrant myelodysplastic syndrome and acute myeloid leukemiaShyam A Patel, Maxwell R Lloyd, Jan Cerny, et al.Biorxiv : the Preprint Server for Biology|July 29, 2026
Single cell multi-omics enables high-resolution identification and functional purification of human acute myeloid leukemia stem cellsAsiri Ediriwickrema, Yusuke Nakauchi, Thomas Köhnke, et al.Cell Reports|September 5, 2025
A single-cell framework identifies functionally and molecularly distinct multipotent progenitors in adult human hematopoiesisAsiri Ediriwickrema, Yusuke Nakauchi, Amy C Fan, et al.Biorxiv : the Preprint Server for Biology|May 20, 2024
A single cell framework identifies functionally and molecularly distinct multipotent progenitors in adult human hematopoiesisAsiri Ediriwickrema, Yusuke Nakauchi, Amy C Fan, et al.Leukemia|March 12, 2024
Mutation order in acute myeloid leukemia identifies uncommon patterns of evolution and illuminates phenotypic heterogeneityMatthew Schwede, Katharina Jahn, Jack Kuipers, et al.Research Square|November 21, 2023
Mutation order in acute myeloid leukemia identifies uncommon patterns of evolution and illuminates phenotypic heterogeneityMatthew Schwede, Katharina Jahn, Jack Kuipers, et al.Ejhaem|November 29, 2023
Prognostic heterogeneity and clonal dynamics within distinct subgroups of myelodysplastic syndrome and acute myeloid leukemia with TP53 disruptionsShyam A Patel, Jan Cerny, William K Gerber, et al.Pageof 3