Chromosomal deletions in myelodysplasia.
There are two major classes of genes implicated in human tumorigenesis, the oncogenes and the tumour suppressor genes. In haematological malignancies most emphasis has been placed upon the recurring translocations in which the juxtaposition of two gene sequences has resulted in the activation of an...
المؤلفون الرئيسيون: | Boultwood, J, Fidler, C |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
1995
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مواد مشابهة
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Glutathione S-transferase gene deletions in myelodysplasia.
حسب: Atoyebi, W, وآخرون
منشور في: (1997) -
Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.
حسب: Boultwood, J, وآخرون
منشور في: (1991) -
Glutathione S-transferase theta 1 (GSTT1) gene defect in myelodysplasia and acute myeloid leukaemia
حسب: Atoyebi, W, وآخرون
منشور في: (1997) -
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) -
High-resolution genomic profiling of myelodysplasia (MDS) by microarray comparative genomic hybridisation (CGH)
حسب: Esoof, N, وآخرون
منشور في: (2005)