Generation and Characterization of Induced Pluripotent Stem Cells Carrying An ASXL1 Mutation
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s12015-024-10737-z.pdf
Reference55 articles.
1. Gelsi-Boyer, V., et al. (2009). Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia. British Journal of Haematology,145, 788–800. https://doi.org/10.1111/j.1365-2141.2009.07697.x
2. Magini, P., et al. (2012). Two novel patients with Bohring-Opitz syndrome caused by de novo ASXL1 mutations. American Journal of Medical Genetics. Part A,158A, 917–921. https://doi.org/10.1002/ajmg.a.35265
3. Abdel-Wahab, O., et al. (2011). Concomitant analysis of EZH2 and ASXL1 mutations in myelofibrosis, chronic myelomonocytic leukemia and blast-phase myeloproliferative neoplasms. Leukemia,25, 1200–1202. https://doi.org/10.1038/leu.2011.58
4. Bejar, R., et al. (2011). Clinical effect of point mutations in myelodysplastic syndromes. New England Journal of Medicine,364, 2496–2506. https://doi.org/10.1056/NEJMoa1013343
5. Metzeler, K. H., et al. (2011). ASXL1 mutations identify a high-risk subgroup of older patients with primary cytogenetically normal AML within the ELN Favorable genetic category. Blood,118, 6920–6929. https://doi.org/10.1182/blood-2011-08-368225
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