Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes
Tumor protein p53 (TP53) is the most frequently mutated gene in cancer1,2. In patients with myelodysplastic syndromes (MDS), TP53 mutations are associated with high-risk disease3,4, rapid transformation to acute myeloid leukemia (AML)5, resistance to conventional therapies6,7,8 and dismal outcomes9....
Автори: | Bernard, E, Nannya, Y, Hasserjian, RP, Boultwood, J, Pellagatti, A |
---|---|
Формат: | Journal article |
Мова: | English |
Опубліковано: |
Springer Nature
2020
|
Схожі ресурси
Схожі ресурси
-
NRAS, FLT3 and TP53 mutations in patients with myelodysplastic syndrome and a del(5q).
за авторством: Fidler, C, та інші
Опубліковано: (2004) -
TP53 Alterations in Myelodysplastic Syndromes and Acute Myeloid Leukemia
за авторством: Ramy Rahmé, та інші
Опубліковано: (2023-04-01) -
Rare case of myelodysplastic syndrome with near-tetraploidy and TP53 mutation
за авторством: Čolović Nataša, та інші
Опубліковано: (2023-01-01) -
Clinical outcomes and characteristics of patients with TP53-mutated myelodysplastic syndromes
за авторством: Lijuan Zhang, та інші
Опубліковано: (2023-12-01) -
TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups
за авторством: Haase, D, та інші
Опубліковано: (2019)