Figure 2
Figure 2. Promoter hypermethylation of Wnt antagonists in samples from patients with ALL. (A) MSP analysis of methylated (M) and unmethylated sequences (U) in patients (UPN) with ALL at diagnosis. PB C− indicates peripheral blood lymphocytes from healthy donors; BM C−, bone marrow mononuclear cells from healthy donors; C+, human male gDNA universally methylated for all genes (used as a positive control for methylated alleles). (B) Frequency of promoter methylation for each Wnt antagonist in a series of 261 patients with ALL at diagnosis. (C) Distribution of patients included in the study according to the number of methylated genes.

Promoter hypermethylation of Wnt antagonists in samples from patients with ALL. (A) MSP analysis of methylated (M) and unmethylated sequences (U) in patients (UPN) with ALL at diagnosis. PB C− indicates peripheral blood lymphocytes from healthy donors; BM C−, bone marrow mononuclear cells from healthy donors; C+, human male gDNA universally methylated for all genes (used as a positive control for methylated alleles). (B) Frequency of promoter methylation for each Wnt antagonist in a series of 261 patients with ALL at diagnosis. (C) Distribution of patients included in the study according to the number of methylated genes.

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