Ha-ras hypervariable alleles in myelodysplasia.
The somatic mutation of one of the ras oncogenes is now considered to be a critical step in the pathogenesis of many tumours. Circumstantial evidence also suggests that some individuals may be genetically predisposed to malignancy and a general method used to analyse such disease susceptibility is t...
المؤلفون الرئيسيون: | Thein, S, Oscier, D, Flint, J, Wainscoat, J |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
1986
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مواد مشابهة
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Statistical methodology in the analysis of relationships between DNA polymorphisms and disease: putative association of Ha-ras-I hypervariable alleles and cancer.
حسب: Peto, T, وآخرون
منشور في: (1988) -
Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.
حسب: Boultwood, J, وآخرون
منشور في: (1991) -
Allelic loss of IRF1 in myelodysplasia and acute myeloid leukemia: retention of IRF1 on the 5q- chromosome in some patients with the 5q- syndrome.
حسب: Boultwood, J, وآخرون
منشور في: (1993) -
Glutathione S-transferase gene deletions in myelodysplasia.
حسب: Atoyebi, W, وآخرون
منشور في: (1997) -
High-resolution genomic profiling of myelodysplasia (MDS) by microarray comparative genomic hybridization (CGH).
حسب: Esoof, N, وآخرون
منشور في: (2006)