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- Bacher, Ulrike
- Haferlach, Claudia 7
- Haferlach, Torsten 7
- Kern, Wolfgang
- Schnittger, Susanne 7
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7 Einträge gefunden
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Clinical impact of FLT3 mutation load in acute promyelocytic leukemia with t(15;17)/PML-RARA.
- Schnittger, Susanne
- Bacher, Ulrike
- Haferlach, Claudia
- Kern, Wolfgang
- Alpermann, Tamara
- Haferlach, Torsten
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Comparison of genetic and clinical aspects in patients with acute myeloid leukemia and myelodysplastic syndromes all with more than 50% of bone marrow erythropoietic cells.
- Bacher, Ulrike
- Haferlach, Claudia
- Alpermann, Tamara
- Kern, Wolfgang
- Schnittger, Susanne
- Haferlach, Torsten
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CDKN1B, encoding the cyclin-dependent kinase inhibitor 1B (p27), is located in the minimally deleted region of 12p abnormalities in myeloid malignancies and its low expression is a favorable prognostic marker in acute myeloid leukemia.
- Haferlach, Claudia
- Bacher, Ulrike
- Kohlmann, Alexander
- Schindela, Sonja
- Alpermann, Tamara
- Kern, Wolfgang
- Schnittger, Susanne
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Several lymphoma-specific genetic events in parallel can be found in mature B-cell neoplasms.
- Bacher, Ulrike
- Haferlach, Torsten
- Alpermann, Tamara
- Kern, Wolfgang
- Schnittger, Susanne
- Haferlach, Claudia
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A copy number repeat polymorphism in the transactivation domain of the CEPBA gene is possibly associated with a protective effect against acquired CEBPA mutations: an analysis in 1135 patients with AML and 187 healthy controls.
- Schnittger, Susanne
- Bacher, Ulrike
- Eder, Christiane
- Lohse, Peter
- Haferlach, Claudia
- Kern, Wolfgang
- Haferlach, Torsten