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The Prognostic Impact of WT1 Expression Levels, Mutations, and SNP rs16754 in AML Patients: A Retrospective Cohort Study
Author(s) -
Shahrbanoo Rostami,
Ahmad Kazemi,
Bahram Chahardouli,
Saeed Mohammadi,
Mohsen Nikbakht,
Nasrin Alizadeh,
Asadollah Mousavi,
Kamran Alimoghaddam,
Majid Teremmahi Ardestani
Publication year - 2020
Publication title -
journal of advances in medical and biomedical research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.113
H-Index - 12
ISSN - 2676-6264
DOI - 10.30699/jambs.29.133.109
Subject(s) - retrospective cohort study , snp , oncology , cohort , medicine , genetics , single nucleotide polymorphism , biology , genotype , gene
10.30699/jambs.29.133.109 Background & Objective: The clinical outcomes and treatment options for acute myeloid leukemia (AML) patients are highly dependent upon molecular markers. In this study, Wilms tumor 1 (WT1) (exons 7 and 9) mutations, single-nucleotide polymorphism (SNP) rs16754, and WT1 expression levels in 130 random AML patients were screened; FMs-like tyrosine kinase-3 internal tandem duplication (FLT3-ITD), nucleophosmin (NPM1), and CCAAT/enhancer-binding protein alpha (CEBPA) mutations were also evaluated.

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