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Blood, Vol. 111, Issue 9, 4716-4722, May 1, 2008 This Article Abstract Full Text Services Email this article to a friend Alert me to new issues of the journal Rights and Permissions Citing Articles Citing Articles via CrossRef Mutations in the neutral sphingomyelinase gene SMPD3 implicate the ceramide pathway in human leukemias Blood Kim et al. 111: 4716 Supplemental materials for: Kim et al Files in this Data Supplement: Table S1. PCR primers used in this study (PDF, 94 KB) Table S2. Polyphen analysis of SMPD3 mutations (PDF, 46.1 KB) Figure S1. SMPD3 mutations in primary leukemia samples (JPG, 59.5 KB) - Nucleotide sequences surrounding D194 (A) or V507 (B) in primary leukemia samples harboring mutations were demonstrated. Nucleotide sequences in sense direction were shown. Arrows indicate the position of mutation. The double peaks represent two nucleotides at the site of potential heterozygous mutations. For comparison, the corresponding wild-type sequence is also shown at the bottom. This Article Abstract Full Text Services Email this article to a friend Alert me to new issues of the journal Rights and Permissions Citing Articles Citing Articles via CrossRef

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