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- Alpermann, Tamara 4
- Bacher, Ulrike 4
- Haferlach, Claudia 4
- Haferlach, Torsten
- Kern, Wolfgang
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4 Einträge gefunden
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Molecular analyses of 15,542 patients with suspected BCR-ABL1-negative myeloproliferative disorders allow to develop a stepwise diagnostic workflow.
- Schnittger, Susanne
- Bacher, Ulrike
- Eder, Christiane
- Dicker, Frank
- Alpermann, Tamara
- Grossmann, Vera
- Kohlmann, Alexander
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Multilineage dysplasia does not influence prognosis in CEBPA-mutated AML, supporting the WHO proposal to classify these patients as a unique entity.
- Bacher, Ulrike
- Schnittger, Susanne
- Macijewski, Katja
- Grossmann, Vera
- Kohlmann, Alexander
- Alpermann, Tamara
- Kowarsch, Andreas
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TET2 deletions are a recurrent but rare phenomenon in myeloid malignancies and are frequently accompanied by TET2 mutations on the remaining allele.
- Bacher, Ulrike
- Weissmann, Sandra
- Kohlmann, Alexander
- Schindela, Sonja
- Alpermann, Tamara
- Schnittger, Susanne
- Kern, Wolfgang
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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