AMPLIFICATION OF MITOCHONDRIAL-DNA IN ACUTE MYELOID-LEUKEMIA

AMPLIFICATION OF MITOCHONDRIAL-DNA IN ACUTE MYELOID-LEUKEMIA

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Boultwood, J, Fidler, C, Moss, P, Frodsham, P, Gale, R, Wainscoat, J
التنسيق:	Journal article
منشور في:	1994

مواد مشابهة

Amplification of mitochondrial DNA in acute myeloid leukaemia.
حسب: Boultwood, J, وآخرون
منشور في: (1996)

Amplification of mitochondrial DNA in CGL in transformation.
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Mutations in PTPN11 are rare in adult myelodysplastic syndromes and acute myeloid leukemia.
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Glutathione S-transferase theta 1 (GSTT1) gene defect in myelodysplasia and acute myeloid leukaemia
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BRCA2 gene deletion is rare in chronic lymphocytic leukemia.
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Allelic loss of IRF1 in myelodysplasia and acute myeloid leukemia: retention of IRF1 on the 5q- chromosome in some patients with the 5q- syndrome.
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Molecular characterization of the 7q deletion in myeloid disorders.
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Telomere length shortening in chronic myelogenous leukemia is associated with reduced time to accelerated phase.
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MOLECULAR MAPPING OF THE 7Q-DELETION IN MYELOID DISORDERS
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منشور في: (1993)

Low expression of the putative tumour suppressor gene gravin in chronic myeloid leukaemia, myelodysplastic syndromes and acute myeloid leukaemia.
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A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia.
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Intrachromosomal amplification 21: A driver of acute myeloid leukemia?
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Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia
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Analysis or telomere length in chronic myelogenous leukemia
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The human POP2 gene: identification, sequencing, and mapping to the critical region of the 5q- syndrome.
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Telomere length in myelodysplastic syndromes.
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Radiation-induced chromosome 2 rearrangement and initiation of murine acute myeloid leukemia.
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Mutation patterns of 16 genes in primary and secondary acute myeloid leukemia (AML) with normal cytogenetics
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hTERT, the catalytic component of telomerase, is downregulated in the haematopoietic stem cells of patients with chronic myeloid leukaemia.
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Gene silencing by DNA methylation in haematological malignancies.
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Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia.
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Telomere length shortening is associated with disease evolution in chronic myelogenous leukemia.
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Hematopoietic cell transplantation soon after first relapse in acute myeloid leukemia – the PROS
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Amplification of mixed lineage leukemia gene perturbs hematopoiesis and cooperates with partial tandem duplication to induce acute myeloid leukemia
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DNA methylation analysis improves the prognostication of acute myeloid leukemia
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Adherence to deferoxamine therapy: Heeding hippocrates and osler
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Gene expression profiling in the myelodysplastic syndromes.
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Genes located within the del(9q) commonly deleted region are down-regualted in acute myeloid leukaemia.
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Symposium: Radiation carcinogenesis in vivo. Radiation-induced chromosome 2 rearrangement and initiation of murine acute myeloid leukemia
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High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression.
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High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression
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