Cargando…
ASXL1 mutation as a surrogate marker in acute myeloid leukemia with myelodysplasia‐related changes and normal karyotype
Acute myeloid leukemia with myelodysplasia‐related changes (AML‐MRC) are poor outcome leukemias. Its diagnosis is based on clinical, cytogenetic, and cytomorphologic criteria, last criterion being sometimes difficult to assess. A high frequency of ASXL1 mutations have been described in this leukemia...
Autores principales: | Prats‐Martín, Concepción, Burillo‐Sanz, Sergio, Morales‐Camacho, Rosario M., Pérez‐López, Olga, Suito, Milagros, Vargas, Maria T., Caballero‐Velázquez, Teresa, Carrillo‐Cruz, Estrella, González, José, Bernal, Ricardo, Pérez‐Simón, José A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286456/ https://www.ncbi.nlm.nih.gov/pubmed/32216059 http://dx.doi.org/10.1002/cam4.2947 |
Ejemplares similares
-
Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo
por: Abdel-Wahab, Omar, et al.
Publicado: (2013) -
Role of ASXL1 and TP53 mutations in the molecular classification and prognosis of acute myeloid leukemias with myelodysplasia-related changes
por: Devillier, Raynier, et al.
Publicado: (2015) -
Solving the Mystery of Myelodysplasia
por: Radich, Jerald
Publicado: (2008) -
Temozolomide-Induced Myelodysplasia
por: Natelson, Ethan A., et al.
Publicado: (2010) -
Generation and Isolation of Cell Cycle-arrested Cells with Complex Karyotypes
por: Wang, Ruoxi W., et al.
Publicado: (2018)