WT1mutations and single nucleotide polymorphism rs16754 analysis of patients with pediatric acute myeloid leukemia in a Chinese population
Author:
Publisher
Informa UK Limited
Subject
Cancer Research,Oncology,Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/10428194.2012.685732
Reference48 articles.
1. Mutations of the Wilms tumor 1 gene (WT1) in older patients with primary cytogenetically normal acute myeloid leukemia: a Cancer and Leukemia Group B study
2. Prevalence and prognostic implications of WT1 mutations in pediatric acute myeloid leukemia (AML): a report from the Children's Oncology Group
3. Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype
4. Favorable prognostic significance of CEBPA mutations in patients with de novo acute myeloid leukemia: a study from the Acute Leukemia French Association (ALFA)
5. CEBPA Mutations in Younger Adults With Acute Myeloid Leukemia and Normal Cytogenetics: Prognostic Relevance and Analysis of Cooperating Mutations
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1. Association between the Wilms tumor-1 rs16754 polymorphism and acute myeloid leukemia;Medicine;2020-07-02
2. GATA2 mutations and overexpression in pediatric acute myeloid leukemia;Pediatric Hematology Oncology Journal;2019-08
3. Correlation ofTET2SNP rs2454206 with improved survival in children with acute myeloid leukemia featuring intermediate-risk cytogenetics;Genes, Chromosomes and Cancer;2018-06-26
4. KITmutations correlate with adverse survival in children with core-binding factor acute myeloid leukemia;Leukemia & Lymphoma;2017-08-09
5. A systematic review and meta-analysis of the impact of WT1 polymorphism rs16754 in the effectiveness of standard chemotherapy in patients with acute myeloid leukemia;The Pharmacogenomics Journal;2015-12-08
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