Prognostic relevance of Wilms tumor 1 (WT1) gene Exon 7 mutations in-patient with cytogenetically normal acute myeloid leukemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12288-013-0288-6.pdf
Reference13 articles.
1. Brown P (2009) Adding WT1 to childhood AML alphabet soup. Blood 113(23):5696–5697
2. Gaidzik V, Schlenk R, Moschny S, Becker A, Bullinger L, Corbacioglu A, Krauter J, Brigitte S, Ganser A, Hartmut D, Konstanze D (2009) Prognostic impact of WT1 mutations in cytogenetically normal acute myeloid leukemia: a study of the German–Austrian AML study group. Blood 113(19):4505–4511
3. Scott R, Stiller C, Walker L (2006) Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour. J Med Genet 43:705–715
4. Mrózek K, Marcucci G, Paschka P, Whitman S, Bloomfield C (2007) Clinical relevance of mutations and gene-expression changes in adult acute myeloid leukemia with normal cytogenetics: are we ready for a prognostically prioritized molecular classification? Blood 109:431–448
5. Hohenstein P, Hastie N (2006) The many facets of the Wilms’ tumour gene, WT1. Hum Mol Genet 15:196–201
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Clinical significance of WT1 in the evaluation of therapeutic effect and prognosis of non-M3 acute myeloid leukemia;Cancer Biology & Therapy;2023-11-30
2. Genetic and Epigenetic Signatures in Acute Promyelocytic Leukemia Treatment and Molecular Remission;Frontiers in Genetics;2022-04-12
3. Wilms’ tumor 1 gene in hematopoietic malignancies: clinical implications and future directions;Leukemia & Lymphoma;2020-05-13
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