2006
DOI: 10.1038/sj.leu.2404399
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Association with the single-nucleotide polymorphism (Glu785Lys) of the granulocyte colony-stimulating factor receptor with myelodysplastic syndromes and acute myeloid leukemia with multlineage dysplasia

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Cited by 4 publications
(1 citation statement)
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“…A previous study detected an homozygous G-CSFR Lys785Lys genotype in a patient with secondary AML following high-risk MDS, but since DNA from non-hematopoietic cells was not studied, it remained unclear whether this base change represented a polymorphism or an acquired mutation [158]. However, analysis of another cohort of patients with MDS and AML with multilineage dysplasia (MD) did not support the relevant increased prevalence of the G-CSFR Glu785Lys polymorphism in those patients compared to the general population [159].…”
Section: Identification Of Mutations and Polymorphisms In G-csfrmentioning
confidence: 99%
“…A previous study detected an homozygous G-CSFR Lys785Lys genotype in a patient with secondary AML following high-risk MDS, but since DNA from non-hematopoietic cells was not studied, it remained unclear whether this base change represented a polymorphism or an acquired mutation [158]. However, analysis of another cohort of patients with MDS and AML with multilineage dysplasia (MD) did not support the relevant increased prevalence of the G-CSFR Glu785Lys polymorphism in those patients compared to the general population [159].…”
Section: Identification Of Mutations and Polymorphisms In G-csfrmentioning
confidence: 99%